| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
| rs8239772 | snp | A/G | 0.18 | 0.24 | intron-variant | Gnb5 | GRCm38.p3 | 9:75327797 | TGAGACCTTAGTTAA[A/G]AAGAAACGACCACAA | 14697 |
| rs8239773 | snp | A/G | 0.18 | 0.24 | intron-variant | Gnb5 | GRCm38.p3 | 9:75327780 | AGAAACGACCACAAC[A/G]AAACCAGACAAAAAC | 14697 |
| rs8239774 | snp | C/T | 0.18 | 0.24 | intron-variant | Gnb5 | GRCm38.p3 | 9:75327765 | AAAACCAGACAAAAA[C/T]TAAAAAGCAAAAATA | 14697 |
| rs8239775 | in-del | -/TA | 0.5 | 0 | intron-variant | Gnb5 | GRCm38.p3 | 9:75327709 | ATATTAAAAGAAAAA[-/TA]NAAAAGCCATTNNTG | 14697 |
| rs8239776 | in-del | -/A | 0.493827 | 0.0552116 | intron-variant | Gnb5 | Mm_Celera | 9:75327710 | TATTAAAAGAAAAAN[-/A]AAAAGCCATTNNTGG | 14697 |
| rs8239777 | snp | A/C | 0.18 | 0.24 | intron-variant | Gnb5 | GRCm38.p3 | 9:75327699 | AAAAAAAAAGCCATT[A/C]ATGGAATTTCAATCA | 14697 |
| rs8239778 | snp | A/G | 0.475309 | 0.108333 | intron-variant | Gnb5 | GRCm38.p3 | 9:75327698 | AAAAAAAAGCCATTC[A/G]TGGAATTTCAATCAT | 14697 |
| rs8239779 | snp | A/G | 0.21875 | 0.248039 | intron-variant | Gnb5 | GRCm38.p3 | 9:75327679 | AATTTCAATCATTAC[A/G]CCCTGCTGGAGGTAG | 14697 |
| rs8239780 | snp | C/T | 0.226843 | 0.248925 | intron-variant | Gnb5 | GRCm38.p3 | 9:75327675 | TCAATCATTACGCCC[C/T]GCTGGAGGTAGGGAA | 14697 |
| rs8239781 | in-del | -/G | 0.644636 | 0.0747315 | intron-variant | Gnb5 | Mm_Celera | 9:75327629 | TCCTTCACAAATNNN[-/G]CCTTGTAANNNNAGA | 14697 |
| rs8254952 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Gnb5 | Mm_Celera | 9:75327341 | TCAGGCGGCGAAGGA[A/G]GAAAGAGCCGTCCTG | 14697 |
| rs8254953 | snp | A/G | 0.453686 | 0.144955 | intron-variant | Gnb5 | Mm_Celera | 9:75327436 | ATTCTCCTGCAATGT[A/G]GAAGTATATGGCAGT | 14697 |
| rs8254954 | snp | C/T | 0.491493 | 0.0646602 | intron-variant | Gnb5 | Mm_Celera | 9:75327448 | TGTGGAAGTATATGG[C/T]AGTGTTTGCGCCCTT | 14697 |
| rs8254955 | snp | A/T | 0.486111 | 0.0821678 | intron-variant | Gnb5 | Mm_Celera | 9:75327455 | GTATATGGCAGTGTT[A/T]GCGCCCTTGTCTGAC | 14697 |
| rs8254956 | snp | A/G | 0.15879 | 0.232768 | intron-variant | Gnb5 | Mm_Celera | 9:75327458 | TATGGCAGTGTTTGC[A/G]CCCTTGTCTGACACG | 14697 |
| rs8254957 | snp | C/T | 0.15879 | 0.232768 | intron-variant | Gnb5 | Mm_Celera | 9:75327472 | CGCCCTTGTCTGACA[C/T]GCACTGTGCCTTGGG | 14697 |
| rs8254958 | snp | A/C | 0.496528 | 0.0415217 | intron-variant | Gnb5 | Mm_Celera | 9:75327489 | CACTGTGCCTTGGGG[A/C]TGACCCCAGCACTGG | 14697 |
| rs8259460 | snp | A/C | 0.497041 | 0.0383476 | intron-variant | Gnb5 | Mm_Celera | 9:75327536 | CACCCTGGAGAATGT[A/C]ACTGATCTCGAATTA | 14697 |
| rs8259461 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Gnb5 | GRCm38.p3 | 9:75327585 | TGGATTGTGTCTGAC[C/T]NCCTTTGATGANNNN | 14697 |
| rs8259462 | in-del | -/C | 0.345679 | 0.230967 | intron-variant | Gnb5 | GRCm38.p3 | 9:75327586 | GGATTGTGTCTGACN[-/C]CCTTTGATGANNNNN | 14697 |
| rs8259473 | in-del | -/C | 0.64 | 0.08 | intron-variant | Gnb5 | Mm_Celera | 9:75327630 | CTNNNNTTACAAGGN[-/C]NNATTTGTGAAGGAA | 14697 |
| rs8260621 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Gnb5 | Mm_Celera | 9:75328050 | ACCTCAATTTTGGAG[A/T]AATGTGTTATGCAGC | 14697 |
| rs8260622 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Gnb5 | GRCm38.p3 | 9:75328046 | CAATTTTGGAGTAAT[A/G]TGTTATGCAGCAATA | 14697 |
| rs8260623 | snp | G/T | 0.152778 | 0.230321 | intron-variant | Gnb5 | GRCm38.p3 | 9:75328044 | ATTTTGGAGTAATGT[G/T]TTATGCAGCAATACA | 14697 |
| rs8260624 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Gnb5 | Mm_Celera | 9:75327992 | AGATTAGCTGCATAG[A/G]CTATGCCAGAAGTTG | 14697 |
| rs8260625 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Gnb5 | GRCm38.p3 | 9:75327980 | TAGACTATGCCAGAA[A/G]TTGTATATTCTAAAC | 14697 |
| rs8260626 | in-del | -/G | 0.396694 | 0.202437 | intron-variant | Gnb5 | GRCm38.p3 | 9:75327954 | TAAACAGAGTTAAAT[-/G]TCTTCTTATTAAACA | 14697 |
| rs29639498 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Gnb5 | Mm_Celera | 9:75307639 | TTTTGCCCACTTTTT[A/T]AAAAATTCATTGAGC | 14697 |
| rs29640306 | snp | A/G | 0.375 | 0.216506 | intron-variant | Gnb5 | Mm_Celera | 9:75317054 | ACCTGAACCACCGAC[A/G]TGTTTGGTTTTTTTA | 14697 |
| rs29687657 | snp | A/T | 0.5 | 0 | intron-variant | Gnb5 | Mm_Celera | 9:75316842 | ACCTTGTTTTTTTTT[A/T]AAATAGGTCTCTCAT | 14697 |
| rs29695786 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Gnb5 | Mm_Celera | 9:75307500 | AGTTTTAGGAATTCT[C/T]GGGTATAGCTAATTG | 14697 |
| rs29737091 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Gnb5 | Mm_Celera | 9:75337792 | TACACCTATATACCA[C/T]GGGGAGACAGAACAG | 14697 |
| rs29738216 | snp | C/G | 0.5 | 0 | intron-variant | Gnb5 | Mm_Celera | 9:75323193 | ATAGATAGATAGATA[C/G]ATAGATAGATAGATA | 14697 |
| rs29738846 | snp | A/C | 0.475309 | 0.108333 | utr-variant-3-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant | Myo5c, Gnb5 | Mm_Celera | 9:75305259 | CCCTAGCAACCTGAC[A/C]ACCCTCCAGTCTGAT | 14697 |
| rs29782302 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Gnb5 | Mm_Celera | 9:75317377 | AAGGTTATCCTCCAC[A/G]ACATAATGAGTTTGA | 14697 |
| rs29879056 | snp | C/T | 0.432133 | 0.171253 | intron-variant, downstream-variant-500B | Gnb5, Myo5c | Mm_Celera | 9:75306529 | TCTCTACAACCTTTG[C/T]GACTTTATCTCAAAA | 14697 |
| rs29887775 | snp | A/G | 0.5 | 0 | intron-variant | Gnb5 | Mm_Celera | 9:75330556 | CTGCCGAGAAGAGAT[A/G]CTGTGACCACAGCAA | 14697 |
| rs29892234 | snp | A/C | 0.5 | 0 | intron-variant | Gnb5 | Mm_Celera | 9:75325798 | ACCATCAGCGCAGTG[A/C]CTGGGCTGTTAGTGT | 14697 |
| rs30034372 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Gnb5 | Mm_Celera | 9:75330851 | GACCAAGCATTCACA[C/T]CCATGAGTCTATGGG | 14697 |
| rs30037086 | snp | C/T | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Gnb5, LOC102636700 | Mm_Celera | 9:75312814 | AACATGACTTCTGGG[C/T]CAGCCTGCTCTACAA | 14697 |
| rs30038864 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Gnb5 | Mm_Celera | 9:75320844 | TCACCGGGCAGTGGT[A/G]GCGCACGCCTTTAAT | 14697 |
| rs30137837 | snp | C/T | 0.5 | 0 | intron-variant | Gnb5 | Mm_Celera | 9:75323049 | CACATGGCAGCTCAC[C/T]GGTCTGTAACTCCAG | 14697 |
| rs30174053 | snp | C/G | 0.5 | 0 | intron-variant | Gnb5 | Mm_Celera | 9:75323189 | ATAGATAGATAGATA[C/G]ATAGATAGATAGATA | 14697 |
| rs30183085 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Gnb5 | Mm_Celera | 9:75330949 | CCTTTTCCCTTTAAC[A/G]AAAGAGATTACTCAC | 14697 |
| rs30183473 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Gnb5 | Mm_Celera | 9:75320850 | GGCAGTGGTAGCGCA[C/T]GCCTTTAATCCCAGC | 14697 |
| rs30222952 | snp | C/G | 0.375 | 0.216506 | intron-variant, nc-transcript-variant | Gnb5, LOC102636700 | Mm_Celera | 9:75310407 | TACTGACCTCACCAA[C/G]GGGCCAAGACCTGGG | 14697 |
| rs30241458 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Gnb5, LOC102636700 | Mm_Celera | 9:75310952 | GTTTAGTGGGCAAAG[A/G]CCCCTGCCATCAAGA | 14697 |
| rs30262544 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Gnb5 | Mm_Celera | 9:75342117 | CCCCACACACCATAC[A/G]CATGCACACACACAG | 14697 |
| rs30271217 | snp | A/T | 0.46875 | 0.121031 | utr-variant-3-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant | Myo5c, Gnb5 | GRCm38.p3 | 9:75304834 | ATCTTTTTTCTGAAA[A/T]TTTTAAAACTTGTTA | 14697 |
| rs30424888 | snp | C/T | 0.5 | 0 | intron-variant | Gnb5 | Mm_Celera | 9:75317321 | GGTAATGCAGGCCTC[C/T]TACGACTCCAGCACT | 14697 |
| rs30436781 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Gnb5 | Mm_Celera | 9:75319183 | GCTGGGGGAGCTTTA[C/T]CCAGACTCTTCGCTC | 14697 |
| rs30439314 | snp | A/G | 0.498615 | 0.0262793 | intron-variant | Gnb5 | Mm_Celera | 9:75309524 | GTTACCTTTTGTGCT[A/G]TAACTCGCTCTTCAT | 14697 |
| rs30478992 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Gnb5 | Mm_Celera | 9:75330852 | ACCAAGCATTCACAC[A/C]CATGAGTCTATGGGG | 14697 |
| rs30492405 | snp | C/T | 0.429688 | 0.173817 | intron-variant | Gnb5 | Mm_Celera | 9:75320161 | TCAAAAAGAACCTGC[C/T]GGCTTCCATGTGCTG | 14697 |
| rs32951444 | snp | A/C | 0.32 | 0.24 | intron-variant | Gnb5 | Mm_Celera | 9:75309554 | TGCAAGCCTAGCAAT[A/C]GACATGATATCTCTG | 14697 |
| rs32951446 | snp | A/T | 0.142012 | 0.225474 | intron-variant | Gnb5 | Mm_Celera | 9:75309783 | TGCAAGTCAACCCTT[A/T]GCCCAACTGCACAGC | 14697 |
| rs32951448 | snp | C/T | 0.32 | 0.24 | intron-variant | Gnb5 | Mm_Celera | 9:75309807 | GCACAGCTTCTAGTT[C/T]CTTCTCTGGCCCTGT | 14697 |
| rs32951450 | snp | A/G | 0.142012 | 0.225474 | intron-variant, downstream-variant-500B | Gnb5, LOC102636700 | Mm_Celera | 9:75309934 | CAGTCCAGCTCAGGG[A/G]TGATTTCCTTGAATC | 14697 |
| rs32951452 | snp | A/C | 0.32 | 0.24 | intron-variant, downstream-variant-500B | Gnb5, LOC102636700 | Mm_Celera | 9:75309983 | GAGCAGCTATGAAAT[A/C]AGCAGGACAGAGCTG | 14697 |
| rs32951974 | snp | C/T | 0.42 | 0.183303 | intron-variant | Gnb5 | Mm_Celera | 9:75321224 | ACTGTTGTATAAAGC[C/T]TTCCACCCATGCCAA | 14697 |
| rs32951976 | snp | G/T | 0.489796 | 0.070696 | intron-variant | Gnb5 | Mm_Celera | 9:75321332 | AAAGAAGGGAGAGAG[G/T]TTCCCACCTGTCTTT | 14697 |
| rs32951978 | snp | A/C | 0.375 | 0.216506 | intron-variant | Gnb5 | Mm_Celera | 9:75321368 | ACCCCTGTTCTTATG[A/C]CTCCTTTAAATTCAG | 14697 |
| rs32951980 | snp | C/T | 0.473373 | 0.11227 | intron-variant | Gnb5 | Mm_Celera | 9:75321371 | CCTGTTCTTATGCCT[C/T]CTTTAAATTCAGGCT | 14697 |
| rs32951982 | snp | A/G/T | 0.277778 | 0.248452 | intron-variant | Gnb5 | Mm_Celera | 9:75321392 | AATTCAGGCTCTCAT[A/G/T]GCCTGCCAGCCAGGA | 14697 |
| rs32952274 | snp | A/G | 0.32 | 0.24 | intron-variant, downstream-variant-500B | Gnb5, LOC102636700 | Mm_Celera | 9:75310013 | GGCTGCTCCCTATTA[A/G]CCTCCCAGTCCTCCA | 14697 |
| rs32952276 | snp | C/T | 0.124444 | 0.216185 | intron-variant, downstream-variant-500B | Gnb5, LOC102636700 | Mm_Celera | 9:75310207 | TGTCCTCTTCCTTCC[C/T]AAGGCTGCTGTTGCT | 14697 |
| rs32952278 | snp | A/T | 0.32 | 0.24 | intron-variant | Gnb5, LOC102636700 | Mm_Celera | 9:75311158 | TCCAAGGATCCGTTG[A/T]AAGCATGATTTGTAA | 14697 |
| rs32952280 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Gnb5, LOC102636700 | Mm_Celera | 9:75311318 | AAGAGAAGGAGGCTC[C/T]GGTCTCCAGAAGCAC | 14697 |
| rs32952282 | snp | C/T | 0.32 | 0.24 | intron-variant | Gnb5, LOC102636700 | Mm_Celera | 9:75311790 | GGGGCTCTCTAAGGG[C/T]CATGTGAAGTCATGG | 14697 |
| rs32952283 | snp | A/C | 0.32 | 0.24 | intron-variant | Gnb5, LOC102636700 | Mm_Celera | 9:75311870 | TTTTTGCATCTGTCT[A/C]CTCCCAGTCTACCTA | 14697 |
| rs32952804 | snp | C/G | 0.46875 | 0.121031 | intron-variant | Gnb5 | Mm_Celera | 9:75321502 | TTGCCCTGTCTGATG[C/G]TTCCAGACTGTGCAC | 14697 |
| rs32952806 | snp | C/T | 0.497041 | 0.0383476 | intron-variant | Gnb5 | Mm_Celera | 9:75321814 | TAGAGACACCGTGGG[C/T]GCAGGTCAGGGAACA | 14697 |
| rs32952808 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Gnb5 | Mm_Celera | 9:75321940 | TGTTCTGCCAAAGAG[C/T]GGAGTCCCCTGACCG | 14697 |
| rs32952810 | snp | C/T | 0.18 | 0.24 | intron-variant | Gnb5 | Mm_Celera | 9:75322073 | CCCGTGGAGAACAAC[C/T]GTTTTAGGTGTACAA | 14697 |
| rs32952811 | snp | C/G | 0.459184 | 0.136902 | intron-variant | Gnb5 | Mm_Celera | 9:75322291 | CTCTGTGCCAGGCTT[C/G]AGTAGCTAGCAAGAA | 14697 |
| rs32952812 | snp | A/T | 0.142012 | 0.225474 | intron-variant | Gnb5 | Mm_Celera | 9:75322411 | GCAGGTGGCTCAAGC[A/T]GAACACACCGCTATC | 14697 |
| rs32952985 | snp | A/C | 0.260355 | 0.249785 | intron-variant, upstream-variant-2KB | Gnb5, LOC102636700 | Mm_Celera | 9:75312953 | ACAGAGACATAGGGA[A/C]TAAAGATGGTTGGTG | 14697 |
| rs32952987 | snp | A/G | 0.165289 | 0.235211 | intron-variant, upstream-variant-2KB | Gnb5, LOC102636700 | Mm_Celera | 9:75313464 | GGAGGAGGCCTAAGT[A/G]GAAACCTATCTGTGA | 14697 |
| rs32952988 | snp | G/T | 0.35503 | 0.226867 | intron-variant, upstream-variant-2KB | Gnb5, LOC102636700 | Mm_Celera | 9:75313536 | TGGAAGTGTGACACC[G/T]AGTGATCATGGCCCT | 14697 |
| rs32952990 | snp | A/G | 0.132653 | 0.220748 | intron-variant, upstream-variant-2KB | Gnb5, LOC102636700 | Mm_Celera | 9:75313656 | ACTGTTGCTGGAGAG[A/G]AGCCGCTGGAGTTAT | 14697 |
| rs32952992 | snp | G/T | 0.486111 | 0.0821678 | intron-variant, utr-variant-5-prime, nc-transcript-variant | Gnb5, LOC102636700 | Mm_Celera | 9:75314254 | TTGCGTTTCTCTCCC[G/T]GCTGCATCCGGACGA | 14697 |
| rs32953574 | snp | C/T | 0.459184 | 0.136902 | synonymous-codon, nc-transcript-variant | Gnb5 | Mm_Celera | 9:75334190 | GGATAATAAGTGCTC[C/T]GTGTATCCACTGACA | 14697 |
| rs32953576 | snp | C/T | 0.244898 | 0.249948 | synonymous-codon, nc-transcript-variant | Gnb5 | Mm_Celera | 9:75334208 | GTATCCACTGACATT[C/T]GACAAGAACGAGAAC | 14697 |
| rs32953578 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Gnb5 | Mm_Celera | 9:75334480 | GTCGAGTTGAGACAA[A/G]CTCTGGCTGTTGGCT | 14697 |
| rs32953580 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Gnb5 | Mm_Celera | 9:75334576 | ATGGCTGCTGAGCTG[C/T]AGGCCTGTGCActgc | 14697 |
| rs32953582 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Gnb5 | Mm_Celera | 9:75335058 | CCACAGCAGGGGCAG[C/T]ACAGCTCCAACACTC | 14697 |
| rs32953654 | snp | C/T | 0.495868 | 0.0452663 | intron-variant | Gnb5 | Mm_Celera | 9:75323423 | AGACATCTCAGTAGC[C/T]TGTGACAGTTGTTCC | 14697 |
| rs32953656 | snp | G/T | 0.375 | 0.216506 | intron-variant | Gnb5 | Mm_Celera | 9:75323485 | CCGTATAGATTTCAT[G/T]TGTGCGTGGCTGCTT | 14697 |
| rs32953658 | snp | A/C | 0.197531 | 0.244432 | intron-variant | Gnb5 | Mm_Celera | 9:75323648 | CACAGCACAGCACCA[A/C]GGGGCACAGCACAGC | 14697 |
| rs32953660 | snp | C/G | 0.493827 | 0.0552116 | intron-variant | Gnb5 | Mm_Celera | 9:75323758 | TTAGTGTTTGACTTG[C/G]AAAGAAAGTTTGAAG | 14697 |
| rs32953662 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Gnb5 | Mm_Celera | 9:75323807 | TAGAGCCAACATTGG[A/G]ACCCCAAGAAAGAAA | 14697 |
| rs32953744 | snp | A/G | 0.165289 | 0.235211 | intron-variant, upstream-variant-2KB | Gnb5, LOC102636700 | Mm_Celera | 9:75314965 | AGGCCTCAGCCTTTT[A/G]AATTCCATTTGGAGA | 14697 |
| rs32953746 | snp | G/T | 0.142012 | 0.225474 | intron-variant, upstream-variant-2KB | Gnb5, LOC102636700 | Mm_Celera | 9:75315045 | CTTGCTGGAAGTACA[G/T]AACCCTGGTTGTGTC | 14697 |
| rs32953748 | snp | C/T | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | Gnb5, LOC102636700 | Mm_Celera | 9:75315188 | TAACAAGATAAGGTC[C/T]GGTGCAGCTAGATTG | 14697 |
| rs32953750 | snp | C/T | 0.336735 | 0.234472 | intron-variant, upstream-variant-2KB | Gnb5, LOC102636700 | Mm_Celera | 9:75315458 | GTGACACAGGGTCTG[C/T]CTTCTCAGAGCCTTG | 14697 |
| rs32953752 | snp | A/T | 0.42 | 0.183303 | intron-variant, upstream-variant-2KB | Gnb5, LOC102636700 | Mm_Celera | 9:75315518 | CAGGCTTGGTATCCC[A/T]GCCTTGGACTTCTCC | 14697 |
| rs32954004 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Gnb5 | Mm_Celera | 9:75344108 | TTCCATGCCTTCCCC[A/G]GAAGACAATGACTAC | 14697 |
| rs32954006 | snp | G/T | 0.336735 | 0.234472 | utr-variant-3-prime, nc-transcript-variant | Gnb5 | Mm_Celera | 9:75344979 | ATCTTCTGACAGCGT[G/T]CAAGAATGTGTGTCC | 14697 |
| rs32954008 | snp | A/G | 0.231111 | 0.249285 | utr-variant-3-prime, nc-transcript-variant | Gnb5 | Mm_Celera | 9:75345318 | GTACCTTTTCTTGGC[A/G]TGGACTGTGGCTTCT | 14697 |
| rs32954010 | snp | A/G | 0.231111 | 0.249285 | utr-variant-3-prime, nc-transcript-variant | Gnb5 | Mm_Celera | 9:75345609 | AATTCACTTGTGATC[A/G]ATGGCAGTCTAGGCT | 14697 |
| rs32954012 | snp | C/T | 0.32 | 0.24 | utr-variant-3-prime, nc-transcript-variant | Gnb5 | Mm_Celera | 9:75345634 | TAGGCTGAGCATCCC[C/T]GACACTTGAGGGCAA | 14697 |
| rs32954264 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Gnb5 | Mm_Celera | 9:75335882 | TGGGTCTGGTCCTGT[C/T]TCTTTCCTGGAAGTG | 14697 |
| rs32954266 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Gnb5 | Mm_Celera | 9:75336031 | TCTCTTTGAATGCTG[A/C]AACTCAGGGCGTGTG | 14697 |
| rs32954268 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Gnb5 | Mm_Celera | 9:75336060 | TGTCCATCACCGTGT[A/T]TTTAAGATCCCTCAA | 14697 |
| rs32954270 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Gnb5 | Mm_Celera | 9:75336105 | TTAGCGTAACCATGG[A/G]CCATTGCGCATGTGC | 14697 |
| rs32954272 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Gnb5 | GRCm38.p3 | 9:75336235 | TGGATGCAAGAAACA[A/G]AAGAGGAACTATAGG | 14697 |
| rs32954311 | snp | A/G | 0.35503 | 0.226867 | utr-variant-3-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant | Myo5c, Gnb5 | Mm_Celera | 9:75304290 | AATTCCTGAAGGCTC[A/G]GTTTTGTTCCTGGTA | 14697 |
| rs32954313 | snp | A/G | 0.142012 | 0.225474 | utr-variant-3-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant | Myo5c, Gnb5 | Mm_Celera | 9:75304374 | TCTAGAGGCACCATG[A/G]CTCCCCCGATTTCTA | 14697 |
| rs32954334 | snp | A/T | 0.197531 | 0.244432 | intron-variant, upstream-variant-2KB | Gnb5, LOC102636700 | Mm_Celera | 9:75315546 | TCCATTTGACAGCTC[A/T]GCCCTGTGGCTTGAG | 14697 |
| rs32954336 | snp | C/T | 0.426035 | 0.177515 | intron-variant, upstream-variant-2KB | Gnb5, LOC102636700 | Mm_Celera | 9:75315694 | GAATCCCACTCTGAC[C/T]TTAGTCTTTCCCAGG | 14697 |
| rs32954338 | snp | C/T | 0.408163 | 0.193609 | intron-variant, upstream-variant-2KB | Gnb5, LOC102636700 | Mm_Celera | 9:75315753 | CCTGGAAGTCCTGCC[C/T]TGTATTCTGTCCCAT | 14697 |
| rs32954340 | snp | A/G | 0.132653 | 0.220748 | intron-variant, upstream-variant-2KB | Gnb5, LOC102636700 | Mm_Celera | 9:75315965 | CCTGCAGTGTCCTTA[A/G]TCAGCTCTCTACCCT | 14697 |
| rs32954342 | snp | A/G | 0.426035 | 0.177515 | intron-variant, upstream-variant-2KB | Gnb5, LOC102636700 | Mm_Celera | 9:75316009 | TGTTTGGCGATCTGT[A/G]GAGGTCTCTGTCCTG | 14697 |
| rs32954344 | snp | A/G | 0.345679 | 0.230967 | intron-variant, nc-transcript-variant | Gnb5 | Mm_Celera | 9:75324993 | TCTGATCCTGCATCA[A/G]GGCTGAACCCTGACA | 14697 |
| rs32954346 | snp | C/G | 0.297521 | 0.245442 | intron-variant, nc-transcript-variant | Gnb5 | Mm_Celera | 9:75325133 | TTAGAATGTACAAGA[C/G]CTTTTACCGCTGAGG | 14697 |
| rs32954348 | snp | G/T | 0.497041 | 0.0383476 | intron-variant | Gnb5 | Mm_Celera | 9:75325151 | TTTACCGCTGAGGTT[G/T]TCTGTCCTTTAAGTA | 14697 |
| rs32954350 | snp | C/G/T | 0.5 | 0 | intron-variant | Gnb5 | Mm_Celera | 9:75325408 | ATAGGGCAAGAAGCC[C/G/T]GAGTTGGGAGTTCCC | 14697 |
| rs32954352 | snp | A/C | 0.375 | 0.216506 | intron-variant | Gnb5 | Mm_Celera | 9:75325597 | GGCTCCGTGCTGGAA[A/C]GATTGCCTGGTAGGC | 14697 |
| rs32954353 | snp | C/T | 0.375 | 0.216506 | intron-variant | Gnb5 | Mm_Celera | 9:75325967 | CCTGCCTGAGTGAAG[C/T]GAGAAACTGTTTGTC | 14697 |
| rs32954954 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Gnb5 | Mm_Celera | 9:75336295 | TGCTGTTGGCCTCCC[A/G]TGCATGTCTTCTCGC | 14697 |
| rs32954956 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Gnb5 | Mm_Celera | 9:75336367 | GCTCTCTGGATAGGA[C/T]CATTATCTCTGTAGA | 14697 |
| rs32954958 | snp | A/G/T | 0.142012 | 0.225474 | intron-variant | Gnb5 | GRCm38.p3 | 9:75336408 | ACATAAACTCCACTC[A/G/T]TTTTAGCATCCACCA | 14697 |
| rs32954960 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Gnb5 | Mm_Celera | 9:75336614 | ATTCAAGCTCTGTGC[A/G]GATTCATCAAAAAAA | 14697 |
| rs32954962 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Gnb5 | Mm_Celera | 9:75336927 | TTTAGACACCACCAA[C/T]CCTTCCTTTGGTGTC | 14697 |
| rs32954975 | snp | C/T | 0.336735 | 0.234472 | utr-variant-3-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant | Myo5c, Gnb5 | Mm_Celera | 9:75304375 | CTAGAGGCACCATGA[C/T]TCCCCCGATTTCTAG | 14697 |
| rs32954977 | snp | A/G | 0.32 | 0.24 | utr-variant-3-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant | Myo5c, Gnb5 | Mm_Celera | 9:75304400 | TTCTAGGGTTCCCGT[A/G]AAGTGCAGAGACATG | 14697 |
| rs32954979 | snp | A/T | 0.32 | 0.24 | utr-variant-3-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant | Myo5c, Gnb5 | Mm_Celera | 9:75304461 | ACCTTCTAGGAAAGA[A/T]TTCCACGTGGCCACT | 14697 |
| rs32954981 | snp | A/C | 0.32 | 0.24 | utr-variant-3-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant | Myo5c, Gnb5 | Mm_Celera | 9:75304544 | CTCCTACTAAAGACG[A/C]CTGGATTAGAAAACT | 14697 |
| rs32955025 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Gnb5 | Mm_Celera | 9:75317109 | TTTGTGTATGTGCAT[G/T]TTCACAGAACACAGA | 14697 |
| rs32955027 | snp | A/G | 0.32 | 0.24 | intron-variant | Gnb5 | Mm_Celera | 9:75317123 | TTTTCACAGAACACA[A/G]AAGGCTGATCGACCC | 14697 |
| rs32955029 | snp | A/C | 0.260355 | 0.249785 | intron-variant | Gnb5 | Mm_Celera | 9:75317142 | GCTGATCGACCCTAT[A/C]AAAAACTAACTCCAA | 14697 |
| rs32955031 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Gnb5 | Mm_Celera | 9:75317450 | TTTGTAAGTCAGTGC[A/G]ACAGTTGGAGATAGG | 14697 |
| rs32955033 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Gnb5 | Mm_Celera | 9:75317545 | TTAACACTCAGACCA[A/G]GGTCTTACTCTGTAG | 14697 |
| rs32955055 | snp | A/G | 0.375 | 0.216506 | intron-variant | Gnb5 | Mm_Celera | 9:75326007 | TCCTGAAAAGTTGGA[A/G]GAGCAGCACCCTATA | 14697 |
| rs32955057 | snp | G/T | 0.375 | 0.216506 | intron-variant | Gnb5 | Mm_Celera | 9:75326330 | GCAGGGCCTGTATTA[G/T]CGAGCATTAATTCCC | 14697 |
| rs32955059 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Gnb5 | Mm_Celera | 9:75326723 | TTCTACTTCCTCACC[A/G]TCAGTGCTTGACCGG | 14697 |
| rs32955061 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Gnb5 | Mm_Celera | 9:75327280 | CACAGGTACTGCACT[C/T]GTGGCTACCACACTG | 14697 |
| rs32955704 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Gnb5 | Mm_Celera | 9:75337001 | ACAGAGCTGAGGAAA[A/G]TGGATAGGAAGAGGA | 14697 |
| rs32955706 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Gnb5 | Mm_Celera | 9:75337114 | ATACACAAAAGAAAG[C/T]GTGCTAAAGAGGGAA | 14697 |
| rs32955708 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Gnb5 | Mm_Celera | 9:75337140 | GGGAAGTCACGAGCC[C/T]GCCTGCTCTGCTGTC | 14697 |
| rs32955710 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Gnb5 | Mm_Celera | 9:75337228 | CCATCCCTGTCTGGG[A/C]ACAGTCTTTGCAGTG | 14697 |
| rs32955712 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Gnb5 | Mm_Celera | 9:75337240 | GGGAACAGTCTTTGC[A/G]GTGTATAACTGCATG | 14697 |
| rs32955735 | snp | A/C | 0.32 | 0.24 | intron-variant | Gnb5 | Mm_Celera | 9:75317576 | ACTTCATTTCCCAGT[A/C]AGATCCTTGGCCAGC | 14697 |
| rs32955737 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Gnb5 | Mm_Celera | 9:75317612 | AAGCCTGAAGTAGCT[C/T]ATGTGGCTTACATGA | 14697 |
| rs32955739 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Gnb5 | Mm_Celera | 9:75317845 | GTCTGAGGACTGTTC[C/G]TTCAGGCAGTCAGAA | 14697 |
| rs32955740 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Gnb5 | Mm_Celera | 9:75317931 | CAGTCTGAGGATGCT[A/G]TGGTCCTCAGCTTCC | 14697 |
| rs32955741 | snp | A/G | 0.396694 | 0.202437 | intron-variant | Gnb5 | Mm_Celera | 9:75317968 | TGTTCTCAGTATCTA[A/G]AACAGTGGTGCTCAA | 14697 |
| rs32955743 | snp | A/G | 0.473373 | 0.11227 | intron-variant | Gnb5 | Mm_Celera | 9:75318764 | TCTGAGAGGACAGAG[A/G]GTAGCACTCGGGCTG | 14697 |
| rs32955754 | snp | A/G | 0.260355 | 0.249785 | utr-variant-3-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant | Myo5c, Gnb5 | Mm_Celera | 9:75305192 | CCTTCAGAGAACTGA[A/G]TCCTCTGATGAGCAC | 14697 |
| rs32955757 | snp | A/G | 0.32 | 0.24 | utr-variant-3-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant | Myo5c, Gnb5 | Mm_Celera | 9:75305320 | ATGGTCCTCTCTGGG[A/G]CGACCGGTTGATTGT | 14697 |
| rs32955759 | snp | A/G | 0.32 | 0.24 | utr-variant-3-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant | Myo5c, Gnb5 | Mm_Celera | 9:75305331 | TGGGGCGACCGGTTG[A/G]TTGTTCAGTACCACC | 14697 |
| rs32955761 | snp | A/G | 0.32 | 0.24 | downstream-variant-500B, upstream-variant-2KB, intron-variant | Myo5c, Gnb5 | Mm_Celera | 9:75305491 | CATTGTAGATTACAT[A/G]CCTTCTCACCGCACA | 14697 |
| rs32955763 | snp | C/T | 0.429688 | 0.173817 | downstream-variant-500B, upstream-variant-2KB, intron-variant | Myo5c, Gnb5 | Mm_Celera | 9:75305806 | AGGGCTGGACTCCAT[C/T]GTATTCTACATTTTA | 14697 |
| rs32956035 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Gnb5 | Mm_Celera | 9:75328185 | AGAGACATCATACAT[A/G]AGCACCAGTTTTTGC | 14697 |
| rs32956036 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Gnb5 | Mm_Celera | 9:75329893 | TACCTGAGAATAGAG[C/T]AGAGTTCTGACTCCC | 14697 |
| rs32956037 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Gnb5 | Mm_Celera | 9:75330459 | ATTTCCGAGCGCTCT[C/T]GGTGCATCCCTCTCT | 14697 |
| rs32956038 | snp | G/T | 0.5 | 0 | intron-variant | Gnb5 | GRCm38.p3 | 9:75331387 | TTAGCAGCAGACCTA[G/T]CTTCTACCCTAAGAG | 14697 |
| rs32956040 | snp | A/G | 0.486111 | 0.0821678 | intron-variant | Gnb5 | Mm_Celera | 9:75331450 | GCGTTCACCACCTTT[A/G]CTTCCACGAGGCTCA | 14697 |
| rs32956042 | snp | C/G | 0.5 | 0 | intron-variant | Gnb5 | Mm_Celera | 9:75331786 | GCCCATCAGGACAGG[C/G]TACTCTAAGGAGTTC | 14697 |
| rs32956043 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Gnb5 | Mm_Celera | 9:75332462 | AGAAAAGGGGATCTT[A/G]GTGCATAGTCTACTT | 14697 |
| rs32956294 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Gnb5 | Mm_Celera | 9:75337416 | CTTTACTGAGGCTTA[A/G]ATCATCCTTAGCAGG | 14697 |
| rs32956296 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Gnb5 | Mm_Celera | 9:75338113 | GCAAGCTCTCCATAA[A/G]TTGGGTTCCAGAAAA | 14697 |
| rs32956298 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Gnb5 | Mm_Celera | 9:75338787 | AACTATGTACTATGT[A/G]TTCAGATCATGGTGT | 14697 |
| rs32956300 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Gnb5 | Mm_Celera | 9:75338828 | GAGCTAAACATTGTG[A/G]ACATTTCCCATCCAC | 14697 |
| rs32956302 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Gnb5 | Mm_Celera | 9:75339962 | TCCTCTGGCCCTCAG[C/T]GTTCAGCTTTGCAAG | 14697 |
| rs32956505 | snp | A/G | 0.396694 | 0.202437 | intron-variant | Gnb5 | Mm_Celera | 9:75319020 | TTAAGACCCATCTCC[A/G]CATGCGCCGTAGGAA | 14697 |
| rs32956508 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Gnb5 | Mm_Celera | 9:75319194 | TTTATCCAGACTCTT[C/T]GCTCCTTTGAGGCAG | 14697 |
| rs32956510 | snp | C/G | 0.336735 | 0.234472 | intron-variant | Gnb5 | Mm_Celera | 9:75319394 | AATGGTTGGAGCTCT[C/G]TACTAATCTGATCTC | 14697 |
| rs32956512 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Gnb5 | Mm_Celera | 9:75319545 | CTACTGCTTCACTCT[C/G]AATGCCTGGAGCAGA | 14697 |
| rs32956565 | snp | A/C | 0.32 | 0.24 | upstream-variant-2KB, utr-variant-3-prime | Gnb5, Myo5c | Mm_Celera | 9:75306217 | GCAGGTAGTGAGAGG[A/C]CGGCAGTGAGCATGC | 14697 |
| rs32956567 | snp | C/T | 0.32 | 0.24 | intron-variant, downstream-variant-500B | Gnb5, Myo5c | Mm_Celera | 9:75306403 | ACCTCAGGGAACTTG[C/T]GCTCTCAATTTTGCA | 14697 |
| rs32956570 | snp | A/G | 0.142012 | 0.225474 | intron-variant, downstream-variant-500B | Gnb5, Myo5c | Mm_Celera | 9:75306555 | CAAAACTATAAAGGG[A/G]TTTTTTAAAAACAGA | 14697 |
| rs32956572 | snp | C/T | 0.231111 | 0.249285 | intron-variant, downstream-variant-500B | Gnb5, Myo5c | Mm_Celera | 9:75306606 | CAAATTAAACATCTT[C/T]AAAATAGCTTCATTG | 14697 |
| rs32956935 | snp | C/G | 0.152778 | 0.230321 | intron-variant | Gnb5 | Mm_Celera | 9:75332535 | CCTGGTCAAGTGAGG[C/G]CCATTTTCCAGGGCA | 14697 |
| rs32956937 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Gnb5 | Mm_Celera | 9:75332559 | CAGGGCAGAGTAACC[A/G]ACAGTCAGGCCTCTG | 14697 |
| rs32956939 | snp | A/G | 0.42 | 0.183303 | intron-variant | Gnb5 | Mm_Celera | 9:75332625 | ATTCTTACTAAGTGG[A/G]CTTTGGTTGGCACCA | 14697 |
| rs32956941 | snp | A/C | 0.396694 | 0.202437 | intron-variant | Gnb5 | Mm_Celera | 9:75332713 | TAAATGGTGACAGAT[A/C]AACAGGGACCCAGGT | 14697 |
| rs32956943 | snp | C/T | 0.5 | 0 | intron-variant | Gnb5 | Mm_Celera | 9:75332748 | CTAGTTTGTAGAAGC[C/T]TGGACATTAAGACCC | 14697 |
| rs32957014 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Gnb5 | Mm_Celera | 9:75340184 | TTCTACCAACTCTCT[G/T]CAGGTACTACCCCAG | 14697 |
| rs32957016 | snp | A/G/T | 0.132653 | 0.220748 | synonymous-codon, nc-transcript-variant | Gnb5 | GRCm38.p3 | 9:75340218 | GGATGCTTTTGCTTC[A/G/T]GGGTCGGATGATGCC | 14697 |
| rs32957018 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Gnb5 | Mm_Celera | 9:75341342 | AGGAAAAAGCAGTTT[A/G]ATGAATCCTGGCAGC | 14697 |
| rs32957020 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Gnb5 | Mm_Celera | 9:75341452 | ACTAACAAGCATTTT[C/T]CCCTAGCATATTTTC | 14697 |
| rs32957022 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Gnb5 | Mm_Celera | 9:75341475 | ATATTTTCTCAATTA[C/T]TGTCTGGTATTTCAT | 14697 |
| rs32957244 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Gnb5 | Mm_Celera | 9:75319657 | TAATGGAATCTCAGA[A/G]TATCTGGGATCTCTG | 14697 |
| rs32957246 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Gnb5 | Mm_Celera | 9:75320098 | ATTAGTCTCACAACG[C/T]CAGCTAGATAGCTCT | 14697 |
| rs32957249 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Gnb5 | Mm_Celera | 9:75320301 | GATTTCACAGCCTAG[A/G]TTCACTTTTGTGTTG | 14697 |
| rs32957251 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Gnb5 | Mm_Celera | 9:75320534 | GTGTGCATTCTGTGG[C/T]GCTCTGATCTAACTT | 14697 |
| rs32957253 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Gnb5 | Mm_Celera | 9:75320704 | AAAGACTCACGGCCA[C/T]GTTGATCCTAGTCTT | 14697 |
| rs32957444 | snp | C/T | 0.32 | 0.24 | intron-variant | Gnb5 | Mm_Celera | 9:75307010 | ATATATGTTTGTTTC[C/T]GGTCAGTTCTCTATA | 14697 |
| rs32957446 | snp | C/G | 0.32 | 0.24 | intron-variant | Gnb5 | Mm_Celera | 9:75307073 | TAGGCAATGAAAGCT[C/G]CTACATCCTCACCCA | 14697 |
| rs32957448 | snp | C/T | 0.32 | 0.24 | intron-variant | Gnb5 | Mm_Celera | 9:75308143 | TTCTGCATTTTATGC[C/T]AGTGCTGGGAACTGA | 14697 |
| rs32957450 | snp | A/T | 0.35503 | 0.226867 | intron-variant | Gnb5 | Mm_Celera | 9:75308903 | GAGTAGGAGACATTC[A/T]CCAAGCTCTGCTGAG | 14697 |
| rs32957452 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Gnb5 | Mm_Celera | 9:75308904 | AGTAGGAGACATTCT[C/T]CAAGCTCTGCTGAGC | 14697 |
| rs32957725 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Gnb5 | Mm_Celera | 9:75332906 | TTTTCCAAATGTCCC[A/G]TGAGCCACCAAAGAC | 14697 |
| rs32957727 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Gnb5 | Mm_Celera | 9:75332989 | TACAGGGCTGAACTT[C/T]TAACCACGAAAACCA | 14697 |
| rs32957728 | snp | G/T | 0.142012 | 0.225474 | intron-variant | Gnb5 | Mm_Celera | 9:75333021 | TTAGGTCCAGAATGA[G/T]AAGCCCTTAATAATA | 14697 |
| rs32957730 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Gnb5 | Mm_Celera | 9:75333059 | AAGAGCTGTCCTGAA[C/T]AATAAAAAACAGCCA | 14697 |
| rs32957732 | snp | G/T | 0.336735 | 0.234472 | intron-variant | Gnb5 | Mm_Celera | 9:75333760 | CATCTCTCCGGCCGT[G/T]AGGTTCTTAACTCCT | 14697 |
| rs32957784 | snp | A/T | 0.142012 | 0.225474 | intron-variant | Gnb5 | Mm_Celera | 9:75341501 | TTCATAGTATTGACA[A/T]ACCATCATGACCTCA | 14697 |
| rs32957785 | snp | A/C | 0.336735 | 0.234472 | intron-variant | Gnb5 | Mm_Celera | 9:75341885 | TGTTCTTGTTGCCCT[A/C]AAAAATACCCAATAT | 14697 |
| rs32957787 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Gnb5 | Mm_Celera | 9:75341914 | ATTAAAGAATGGGCT[C/T]CACTCCAAGCTGCTG | 14697 |
| rs32957789 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Gnb5 | Mm_Celera | 9:75342228 | AGGCACACATTTTCA[A/C]TATACCATTTCATGG | 14697 |
| rs32957791 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Gnb5 | Mm_Celera | 9:75342287 | CTAAGCCAATGCAAG[G/T]CAGACATCAACATGT | 14697 |
| rs32957793 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Gnb5 | Mm_Celera | 9:75342352 | TAGCTATGGGCAGTT[C/T]TACTGTGACTGCCCA | 14697 |
| rs32958065 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Gnb5 | Mm_Celera | 9:75320792 | TTCTGAGCTTTGGTT[C/T]CCTTCCTTGGAGGAG | 14697 |
| rs32958104 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Gnb5 | Mm_Celera | 9:75308959 | TGTGTTCATGAGTAT[A/G]TGCTTGTGTGCTCAT | 14697 |
| rs32958494 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Gnb5 | Mm_Celera | 9:75333833 | GCTGTGATAAAGACA[C/T]GGCACATGCATAAGG | 14697 |
| rs32958496 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Gnb5 | Mm_Celera | 9:75333952 | TCTCACACACTTGAC[A/G]TGCTGTTTTTGAATC | 14697 |
| rs32958498 | snp | A/C/T | 0.375 | 0.216506 | intron-variant | Gnb5 | Mm_Celera | 9:75334049 | CTTGAGTCAAAGGGG[A/C/T]GAGGTTGCAATGTAA | 14697 |
| rs32958500 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Gnb5 | Mm_Celera | 9:75334089 | AAGGGAAAGCATTTG[C/T]GCAGTCAGTATAAAT | 14697 |
| rs32958535 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Gnb5 | Mm_Celera | 9:75342519 | CCTAAGACCATTTAG[C/T]TCACTATTGCCTAAT | 14697 |
| rs32958537 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Gnb5 | Mm_Celera | 9:75343109 | AGAAACACACAAAAA[A/G]TGACATCCCAGACAT | 14697 |
| rs32958539 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Gnb5 | Mm_Celera | 9:75343131 | CCCAGACATTAGCAA[A/G]TACCTCTAGGACTTG | 14697 |
| rs32958541 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Gnb5 | Mm_Celera | 9:75343295 | TAGCTGTTTCTTTGA[A/G]TCCCTACTGACCCAA | 14697 |
| rs32958543 | snp | A/G | 0.375 | 0.216506 | intron-variant | Gnb5 | Mm_Celera | 9:75343356 | GATAAAATAAAAAGA[A/G]AACAAAAGAGGTTTT | 14697 |
| rs32959355 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Gnb5 | Mm_Celera | 9:75343384 | TTTCTCCTGTCACGC[C/T]TCAAACTACAGCAGG | 14697 |
| rs32959357 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Gnb5 | Mm_Celera | 9:75343440 | CCAGTAGTAATAGTA[A/G]GTGTGTGGTCTGTAC | 14697 |
| rs32959359 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon, nc-transcript-variant | Gnb5 | Mm_Celera | 9:75343543 | GGCAGATAGAGAGGT[C/T]GCCATCTACTCCAAG | 14697 |
| rs32959361 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon, nc-transcript-variant | Gnb5 | Mm_Celera | 9:75343585 | ATTTGGCGCCTCGAG[C/T]GTGGACTTCTCCCTC | 14697 |
| rs32959363 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Gnb5 | Mm_Celera | 9:75343645 | CCAGGACTGTAGGAC[C/T]AGACCTATAAAGAAC | 14697 |
| rs32959815 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Gnb5 | Mm_Celera | 9:75343689 | GCCAAGCTTCCCATC[C/G]CTGAGCTGTTGGTGA | 14697 |
| rs32959817 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Gnb5 | Mm_Celera | 9:75343697 | TCCCATCGCTGAGCT[A/G]TTGGTGAGGTGCTAT | 14697 |
| rs32959819 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Gnb5 | Mm_Celera | 9:75343752 | ACATGCCTCCCTTCA[C/T]CTCATTTCCCTGGCC | 14697 |
| rs32959821 | snp | C/T | 0.32 | 0.24 | intron-variant | Gnb5 | Mm_Celera | 9:75343917 | CCAAGCATCGAAGAC[C/T]ACTGCTCTGCCCTCA | 14697 |
| rs33678018 | snp | G/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | Gnb5, LOC102636700 | Mm_Celera | 9:75314481 | CCGGTTCCAGCGTCC[G/T]GGGTGGGAGGATGCC | 14697 |
| rs33747343 | snp | A/G | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Gnb5, LOC102636700 | Mm_Celera | 9:75312888 | ATAGATAAATGGGGG[A/G]CGGGGGGTTGTACAC | 14697 |
| rs33747708 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Gnb5 | Mm_Celera | 9:75330683 | AAGGAGCTGAGAGTT[C/T]GATCTTTGGGTCCAC | 14697 |
| rs33775122 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Gnb5 | Mm_Celera | 9:75320226 | AGAGAGCCACTGTGG[C/T]TTGCTGGCCTCCCCC | 14697 |
| rs33896930 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Gnb5 | Mm_Celera | 9:75326632 | CCACGAAGAGAGTGG[C/T]ACCCCTCAGCTGCCT | 14697 |
| rs33897138 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Gnb5 | Mm_Celera | 9:75326656 | GCTGCCTACCATGGA[A/G]GGGAGTCCCTGAGCC | 14697 |
| rs45782624 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75323369 | GCTGGGGACAGCATA[C/T]AATGAATGACAGGGA | 14697 |
| rs45798959 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75330373 | CTAGGCTCTCTACCA[A/G]CTCAGTTACATCCCG | 14697 |
| rs45845683 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75328991 | TTGGCTACTCTCCAT[A/G]ACCCCATTTGTGCCT | 14697 |
| rs45908490 | snp | A/C | | | intron-variant | Gnb5 | Mm_Celera | 9:75328963 | CTCCTTCAGGGTCTC[A/C]TAGTGTCAAGCCTTG | 14697 |
| rs45962169 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75328817 | GGGTGCACCTTCACC[A/G]GCAGGCTCTTCTGGG | 14697 |
| rs46014233 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75330810 | TCCAACAAGACCACA[C/T]CTCCTAATAATGTCA | 14697 |
| rs46037967 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75328436 | GGAACTGGCATTCTA[C/T]CCTGTCTGTTATATT | 14697 |
| rs46115849 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75329001 | TCCATAACCCCATTT[A/G]TGCCTTCAAAAACAG | 14697 |
| rs46189154 | snp | C/T | | | intron-variant | Gnb5 | GRCm38.p3 | 9:75321227 | GTTGTATAAAGCTTT[C/T]CACCCATGCCAATTC | 14697 |
| rs46377880 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75321201 | AAAAAAAGACCCTAT[A/G]TCCTCAAACTGTTGT | 14697 |
| rs46591691 | snp | A/C | | | intron-variant | Gnb5 | Mm_Celera | 9:75329799 | CCTTCAGATCTAACA[A/C]GTCATGCTGTGCTTG | 14697 |
| rs46621944 | snp | G/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75321542 | GCAGAGACATCCCAT[G/T]ACAGATGGTTTGTGA | 14697 |
| rs46656807 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75321590 | GGGAATTGAACCTTT[A/G]GAAGAGTAGTCAGTG | 14697 |
| rs46665339 | snp | G/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75323778 | AAAGTTTGAAGAAAT[G/T]ATTAGAAAATGAATA | 14697 |
| rs46720971 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75329000 | CTCCATAACCCCATT[C/T]GTGCCTTCAAAAACA | 14697 |
| rs46800367 | snp | A/C | | | intron-variant | Gnb5 | Mm_Celera | 9:75332655 | AGAAGGCTGAGTCCC[A/C]TCGTCAGTGTGAAGC | 14697 |
| rs46934391 | snp | A/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75321626 | AACCACTGAGCCATC[A/T]CTCCAGCCACCAACC | 14697 |
| rs46939594 | snp | A/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75329138 | GATGCTGATCTCTCA[A/T]TAATTACTCCCAGGC | 14697 |
| rs46969824 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75321597 | GAACCTTTGGAAGAG[C/T]AGTCAGTGTTCTTAA | 14697 |
| rs47023763 | snp | A/G | | | intron-variant, upstream-variant-2KB | Gnb5, LOC102636700 | Mm_Celera | 9:75312756 | TGGGCATGGCAGTGA[A/G]CATGTTTAATCCCAG | 14697 |
| rs47045349 | snp | A/C | | | intron-variant | Gnb5 | Mm_Celera | 9:75329791 | CTGTGTGACCTTCAG[A/C]TCTAACACGTCATGC | 14697 |
| rs47088193 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75318655 | tgagcttcatcagaa[A/G]ccatgggtttacctg | 14697 |
| rs47123550 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75330221 | TCTCCTGTTTCCCAG[A/G]CTAGCCTCAAACTCT | 14697 |
| rs47200686 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75317742 | CAGATAATCCACTGT[A/G]GGGAGGGTAGCCTTC | 14697 |
| rs47212144 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75323944 | ACACTGGGACTTTTC[A/G]GAGAGTTATTGTGTG | 14697 |
| rs47259351 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75328669 | TGCAAGGCAGAACTC[C/T]AGGCAGGAACCTCCG | 14697 |
| rs47358738 | snp | A/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75318594 | ATCCTCCAATCCGCA[A/T]GGGCCTCTTTGCGAC | 14697 |
| rs47448500 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75328744 | TTTGCTCCTAGACTC[A/G]AGCCAGCTCCATGAC | 14697 |
| rs47559322 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75323709 | GGTTCTCATCTTGGA[A/G]ACAATGTAATAACTG | 14697 |
| rs47734760 | snp | C/T | | | intron-variant, upstream-variant-2KB | Gnb5, LOC102636700 | Mm_Celera | 9:75312776 | TTTAATCCCAGCACT[C/T]AAGAAGCAGAGGCAG | 14697 |
| rs47826663 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75332383 | ACCATCTGTACAGGA[C/T]AGTGCTGTCTGAGAA | 14697 |
| rs47837640 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75328289 | AGTGGCTATCGGCTG[A/G]TGCCTCTGTTTCTTG | 14697 |
| rs47837985 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75331328 | TCTTTGACCTCAGTC[A/G]TTCTTAGCATTACCC | 14697 |
| rs47839960 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75330302 | AAGTGCTAGGATTAC[A/G]GATGTGCACCGCCAC | 14697 |
| rs47843584 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75329771 | AATTTACTGTTATTA[A/G]TGTACTGTGTGACCT | 14697 |
| rs47875644 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75332021 | TGTCAGGACTCCCTG[C/T]CCCACCCCTAGAGGA | 14697 |
| rs47923074 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75329900 | GAATAGAGCAGAGTT[C/T]TGACTCCCCTGTTTC | 14697 |
| rs47975082 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75332001 | AGCCAAGGAAACAGC[A/G]ACTCTGTCAGGACTC | 14697 |
| rs48005069 | snp | A/G | | | utr-variant-3-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant | Myo5c, Gnb5 | Mm_Celera | 9:75304508 | GCCCCATCCCTGTTG[A/G]CAGGAAGGGCTCGTT | 14697 |
| rs48223587 | snp | C/T | | | intron-variant, upstream-variant-2KB | Gnb5, LOC102636700 | Mm_Celera | 9:75315397 | CCCAGGCTGAGCACA[C/T]TGCCACCCCAAAGTT | 14697 |
| rs48366723 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75332452 | TTCTCTCTGTAGAAA[A/G]GGGGATCTTAGTGCA | 14697 |
| rs48521746 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75330429 | GAAGGAGCTCTGCGG[C/T]AGGGCCGTGTGGGCA | 14697 |
| rs48635332 | snp | A/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75323905 | AGACTATGTAAAATC[A/T]TATATTAGTAAAACT | 14697 |
| rs48891192 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75327877 | TTGAGATCCACCTGC[C/T]TCCTGTCTGGGTGCT | 14697 |
| rs48941652 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75321152 | TACATGCAAATAGGG[C/T]ACTCATATAAAATGC | 14697 |
| rs48962723 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75326947 | CATCTCTGAGTGGGG[A/G]GTTTTTAGGGGGTGG | 14697 |
| rs48983941 | snp | A/G | | | intron-variant, upstream-variant-2KB | Gnb5, LOC102636700 | Mm_Celera | 9:75312634 | TATAAGCACACACAC[A/G]TACACTTATGTAGTC | 14697 |
| rs48984937 | snp | A/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75330456 | GGCATTTCCGAGCGC[A/T]CTCGGTGCATCCCTC | 14697 |
| rs49083320 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75323551 | TATCTGACTTTCTTA[C/T]TTCTTTCTCCTTCTG | 14697 |
| rs49083572 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75318737 | GTGCAAACAACACTC[C/T]TCCTCCCTTATTCTG | 14697 |
| rs49103684 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75331366 | GTAGAGAAAGATTCT[A/G]TCACTTTAGCAGCAG | 14697 |
| rs49131312 | snp | A/G | | | utr-variant-3-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant | Myo5c, Gnb5 | Mm_Celera | 9:75304305 | GGTTTTGTTCCTGGT[A/G]CCTTTGTTTTGTGGC | 14697 |
| rs49163342 | snp | A/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75327057 | AGCCCTCTGCAGGAG[A/T]CAAAGGCTTTTCTGG | 14697 |
| rs49169582 | snp | A/C | | | intron-variant | Gnb5 | Mm_Celera | 9:75318606 | GCAAGGGCCTCTTTG[A/C]GACAGAAGGTGACAT | 14697 |
| rs49185269 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75328283 | TGCTCAAGTGGCTAT[C/T]GGCTGATGCCTCTGT | 14697 |
| rs49213907 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75321485 | TACTTGGTACCTGTG[C/T]GTTGCCCTGTCTGAT | 14697 |
| rs49268469 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75321325 | AGAGAGGAAAGAAGG[A/G]AGAGAGTTTCCCACC | 14697 |
| rs49274537 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75323612 | CCTGATTCTTAAAGA[A/G]TTAAAAATTGAGGCA | 14697 |
| rs49341045 | snp | A/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75328596 | TCAACTAAAAGCAAC[A/T]TGGGGGCGGGGGTAC | 14697 |
| rs49366460 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75329883 | ATATTAATAATACCT[A/G]AGAATAGAGCAGAGT | 14697 |
| rs49582597 | snp | A/G | | | synonymous-codon, nc-transcript-variant | Gnb5 | Mm_Celera | 9:75331878 | CTCTTTCCAGGATGG[A/G]AAGGTGATTGTCTGG | 14697 |
| rs49585503 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75321535 | CCTAAGAGCAGAGAC[A/G]TCCCATGACAGATGG | 14697 |
| rs49756468 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75329867 | CATGTATCGCCCATG[C/T]ATATTAATAATACCT | 14697 |
| rs49778064 | snp | A/G | | | intron-variant | Gnb5 | GRCm38.p3 | 9:75326897 | ATCCACCTGTCACAC[A/G]GAGACAGGCGCTATA | 14697 |
| rs49823967 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75330449 | CCGTGTGGGCATTTC[C/T]GAGCGCTCTCGGTGC | 14697 |
| rs49867158 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75323655 | CAGCACCAAGGGGCA[C/T]AGCACAGCACAGTCC | 14697 |
| rs49893407 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75328745 | TTGCTCCTAGACTCG[A/G]GCCAGCTCCATGACA | 14697 |
| rs49919240 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75329836 | GTTTTATATCTATAA[C/T]AAATAAATAAATATC | 14697 |
| rs50009881 | snp | G/T | | | synonymous-codon, nc-transcript-variant | Gnb5 | Mm_Celera | 9:75331908 | GGATTCCTTCACTAC[G/T]AACAAGGTGAGGTAC | 14697 |
| rs50020397 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75318566 | CTCATGGTCCCATCT[C/T]AATATCTTTAACATC | 14697 |
| rs50021673 | snp | G/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75332590 | GCAAATGATAAAAAA[G/T]AGTGAAGCAAAATAT | 14697 |
| rs50129523 | snp | A/C | | | intron-variant | Gnb5 | Mm_Celera | 9:75329070 | CTGCCTCTGGACCAC[A/C]GCCTTCAGGTGCTGA | 14697 |
| rs50148312 | snp | A/C | | | intron-variant | Gnb5 | Mm_Celera | 9:75332640 | GCTTTGGTTGGCACC[A/C]GAAGGCTGAGTCCCA | 14697 |
| rs50526742 | snp | A/C | | | intron-variant | Gnb5 | Mm_Celera | 9:75330479 | CATCCCTCTCTGCTC[A/C]AGGATGGTAGGGGGA | 14697 |
| rs50527184 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75318722 | AGCCTCAACCTCCAG[A/G]TGCAAACAACACTCT | 14697 |
| rs50569808 | snp | C/T | | | intron-variant, upstream-variant-2KB | Gnb5, LOC102636700 | Mm_Celera | 9:75312637 | AAGCACACACACATA[C/T]ACTTATGTAGTCTGT | 14697 |
| rs50634491 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75329859 | TAAATATCCATGTAT[C/T]GCCCATGCATATTAA | 14697 |
| rs50634555 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75323733 | ATAACTGCACAATGG[C/T]AGTTCCAGATTAGTG | 14697 |
| rs50636056 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75331252 | CCATCCATGTTTGGC[C/T]ATGTAGGCAGAAATC | 14697 |
| rs50660760 | snp | A/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75329988 | TTTTGTAGGCTAAGC[A/T]GTTCTCATACTTGCA | 14697 |
| rs50721169 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75329821 | CTGTGCTTGCTTTTT[A/G]TTTTATATCTATAAC | 14697 |
| rs50752627 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75331185 | GGTGCAGAGGACCCT[C/T]GTGTGCAGACGCAGA | 14697 |
| rs50757208 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75329136 | GAGATGCTGATCTCT[C/T]AATAATTACTCCCAG | 14697 |
| rs50761659 | snp | C/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75331980 | CCCTTCTAGAGCTCT[C/G]TGAACAGCCAAGGAA | 14697 |
| rs50881759 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75323716 | ATCTTGGAGACAATG[C/T]AATAACTGCACAATG | 14697 |
| rs50899200 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75332487 | CTACTTTATTAAACA[C/T]GTTACTAGACATGGT | 14697 |
| rs51055129 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75323471 | GCCCTGTACAACAGC[C/T]GTATAGATTTCATGT | 14697 |
| rs51061242 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75333712 | AGAACTCAGGTCCTC[C/T]ATAAAAGCAGCCAGT | 14697 |
| rs51118265 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75321034 | TCAGTGGCTAAGAGC[A/G]CTACCTGCTCTTTCA | 14697 |
| rs51125805 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75330483 | CCTCTCTGCTCCAGG[A/G]TGGTAGGGGGATGTG | 14697 |
| rs51282809 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75328518 | CTCTGCTTAATAATT[C/T]CTAGGTGTGTTTTTG | 14697 |
| rs51287667 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75331986 | TAGAGCTCTGTGAAC[A/G]GCCAAGGAAACAGCG | 14697 |
| rs51301355 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75328295 | TATCGGCTGATGCCT[C/T]TGTTTCTTGCCACAT | 14697 |
| rs51368031 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75328273 | GGGGTTTCCTTGCTC[A/G]AGTGGCTATCGGCTG | 14697 |
| rs51368702 | snp | A/C | | | intron-variant | Gnb5 | Mm_Celera | 9:75318559 | CACCCAGCTCATGGT[A/C]CCATCTCAATATCTT | 14697 |
| rs51453085 | snp | A/C | | | intron-variant | Gnb5 | Mm_Celera | 9:75329853 | AATAAATAAATATCC[A/C]TGTATCGCCCATGCA | 14697 |
| rs51460916 | snp | A/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75329122 | AAAGTTCGGCCTCAG[A/T]GATGCTGATCTCTCA | 14697 |
| rs51532127 | snp | A/C | | | intron-variant, upstream-variant-2KB | Gnb5, LOC102636700 | Mm_Celera | 9:75312755 | CTGGGCATGGCAGTG[A/C]GCATGTTTAATCCCA | 14697 |
| rs51576728 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75321166 | GCACTCATATAAAAT[A/G]CATAGATAAATCAAA | 14697 |
| rs51594316 | snp | A/C | | | intron-variant | Gnb5 | Mm_Celera | 9:75333753 | ACTGAGCCATCTCTC[A/C]GGCCGTTAGGTTCTT | 14697 |
| rs51656124 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75330703 | TTTGGGTCCACAGGC[A/G]GCAGCAGAAGACTGT | 14697 |
| rs51676252 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75331355 | ACCCAGAGGTGGTAG[A/G]GAAAGATTCTATCAC | 14697 |
| rs51680106 | snp | G/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75332015 | CGACTCTGTCAGGAC[G/T]CCCTGCCCCACCCCT | 14697 |
| rs51953932 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75328937 | CTGTGACTGAGCGTT[C/T]CCAGTAGCCTCTCCT | 14697 |
| rs51980132 | snp | A/G | | | upstream-variant-2KB, intron-variant | Gnb5, Myo5c | Mm_Celera | 9:75305974 | CTTACTCGGGGCCTA[A/G]ATCACTCATGCCTAG | 14697 |
| rs51982286 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75328927 | TCCACTGCTACTGTG[A/G]CTGAGCGTTCCCAGT | 14697 |
| rs51987734 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75323940 | CAAAACACTGGGACT[C/T]TTCAGAGAGTTATTG | 14697 |
| rs52123157 | snp | C/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75323169 | ATACATACATACATA[C/G]ATAGATAGATAGATA | 14697 |
| rs52215748 | snp | C/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75323173 | ATACATACATACATA[C/G]ATAGATAGATAGATA | 14697 |
| rs52264370 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75329682 | CACGTGTAAGTAAAA[A/G]GAAAAAATTTAAATC | 14697 |
| rs52313878 | snp | A/G | | | intron-variant, upstream-variant-2KB | Gnb5, LOC102636700 | Mm_Celera | 9:75312852 | TACAGGGAAGCCAGG[A/G]CTATAAAGAGGGAGA | 14697 |
| rs52384157 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75333291 | CATGCTGTGGTGCAT[C/T]TCTCTCTCTCTCTCT | 14697 |
| rs52533601 | snp | C/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75309221 | tgtgtgtgtgtgtct[C/G]tgtgtgtgtgtgtgt | 14697 |
| rs107662917 | snp | A/G | | | intron-variant, utr-variant-5-prime, nc-transcript-variant | Gnb5, LOC102636700 | Mm_Celera | 9:75314147 | TCGCGTCACTGCCGA[A/G]GGGGCGGGCCCCGGG | 14697 |
| rs108112232 | snp | A/G | | | intron-variant | Gnb5 | GRCm38.p3 | 9:75326905 | GTCACACGGAGACAG[A/G]CGCTATAGTCTACTG | 14697 |
| rs211701555 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75337654 | TGTTTCTTAGGCATT[C/T]GTCACATGTTTATTG | 14697 |
| rs211705536 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75330453 | GTGGGCATTTCCGAG[C/T]GCTCTCGGTGCATCC | 14697 |
| rs211836556 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75330941 | ACCAGTAACCTTTTC[C/T]CTTTAACGAAAGAGA | 14697 |
| rs211872573 | snp | C/T | | | intron-variant | Gnb5 | GRCm38.p3 | 9:75326827 | CCTGGCCCAGCCTGG[C/T]TCTCAACAACTTGTA | 14697 |
| rs211903961 | in-del | -/G | | | intron-variant, upstream-variant-2KB | Gnb5, LOC102636700 | Mm_Celera | 9:75313588 | GCTTGAAGGAGGGAT[-/G]TGGGGGAGGGGGTGT | 14697 |
| rs211913940 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75321564 | GGTTTGTGAGCTACT[A/G]TGTGGTTTCTGGGAA | 14697 |
| rs211919029 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75326561 | TTTCCTAACCACCAC[C/T]ACCCCCGGTTGCTGA | 14697 |
| rs211950738 | snp | A/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75316996 | CCTGACTCATGTGCC[A/T]TCCCCTCAGCCCTAG | 14697 |
| rs212041187 | in-del | -/T | | | intron-variant | Gnb5 | GRCm38.p3 | 9:75329710 | ATCTTTTTAAAAAAA[-/T]GTGCATGGTCTAGAC | 14697 |
| rs212067374 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75322042 | ACTCAGATGACAGTA[C/T]ACCAACAGGCCACTA | 14697 |
| rs212084171 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75325903 | CTGTCATCCCAGCAC[C/T]GGGGAGGTGGAGGCG | 14697 |
| rs212115840 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75320324 | TTGTGTTGTCTAGAT[C/T]ACGTCTAGTTAGATA | 14697 |
| rs212154907 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75320639 | CTCCCATATGGGAAT[C/T]TAAGGCTGGGGTGTC | 14697 |
| rs212314762 | snp | A/G | | | intron-variant, downstream-variant-500B | Gnb5, LOC102636700 | Mm_Celera | 9:75309837 | TGGTGATGTCTGCAT[A/G]ACACTCTCCCCCACC | 14697 |
| rs212327041 | snp | A/G | | | intron-variant, upstream-variant-2KB | Gnb5, LOC102636700 | Mm_Celera | 9:75316366 | GGTCAGCTTCTTCCC[A/G]CCCCTCAGGATTCAC | 14697 |
| rs212378335 | in-del | -/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75329505 | AGAGATTTGTATTGC[-/T]TTTGCAGAGGACTCA | 14697 |
| rs212428239 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75344833 | CTGTTCAGTGGAGTG[C/T]GTGAGCGTGAATGCA | 14697 |
| rs212464171 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75336911 | GCTGTTGGCTGCTTG[A/G]TTTAGACACCACCAA | 14697 |
| rs212519833 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75317885 | CTGACTGCGTGACTG[A/G]GTGAGCCATTCCCTA | 14697 |
| rs212532351 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75316659 | CTGTGTCCCACCAAG[C/T]TCCAACAGCCTCCCA | 14697 |
| rs212556740 | snp | G/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75318398 | CCTGAGCCAAGCATA[G/T]AGAAACTATCACACT | 14697 |
| rs212569556 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75309370 | GCATATATGTGGACA[C/T]CTTCATGCATCCTTC | 14697 |
| rs212643685 | in-del | -/C | | | utr-variant-3-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant | Myo5c, Gnb5 | Mm_Celera | 9:75305081 | AAAAAAAAAAAACAA[-/C]AACAGAAGATATGGG | 14697 |
| rs212656136 | snp | C/T | | | intron-variant, downstream-variant-500B | Gnb5, LOC102636700 | Mm_Celera | 9:75309886 | ACCTCCACCCAAACA[C/T]ACCTCTCTCAAATTC | 14697 |
| rs212658204 | snp | G/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75340276 | CCTCTCCAGGCAGGG[G/T]GGGGGGGTAATATCT | 14697 |
| rs212686702 | snp | A/G | | | intron-variant, downstream-variant-500B | Gnb5, Myo5c | Mm_Celera | 9:75306477 | GGTGGGTGCACAGTG[A/G]GGGGTGCTTATGTTC | 14697 |
| rs212729362 | snp | A/G | | | intron-variant, upstream-variant-2KB | Gnb5, LOC102636700 | Mm_Celera | 9:75313468 | GAGGCCTAAGTGGAA[A/G]CCTATCTGTGACGCT | 14697 |
| rs212867720 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75333758 | GCCATCTCTCCGGCC[A/G]TTAGGTTCTTAACTC | 14697 |
| rs212883832 | snp | A/T | | | utr-variant-3-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant | Myo5c, Gnb5 | Mm_Celera | 9:75304596 | AGGGTATTCAGTCTA[A/T]GAGCAGGTCATGGTA | 14697 |
| rs212888908 | snp | A/G | | | intron-variant | Gnb5, LOC102636700 | Mm_Celera | 9:75310973 | GCCATCAAGACCCCT[A/G]ACAACCTGAAATCTA | 14697 |
| rs212952706 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75320016 | ACCCACTGCCAGTTA[C/T]TCAGTGTCACCTGAA | 14697 |
| rs213054703 | snp | A/C | | | intron-variant | Gnb5 | Mm_Celera | 9:75338843 | AACATTTCCCATCCA[A/C]CCTTTCTGTCCTCAC | 14697 |
| rs213088179 | snp | A/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75339370 | GCAGAGTGCTTAACT[A/T]ATGTACGTGGTCCTG | 14697 |
| rs213130667 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75307053 | CTTTGTACCCACACC[A/G]GATGTAGGCAATGAA | 14697 |
| rs213214652 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75327860 | TGTAGATCAGACTTT[C/T]CTTGAGATCCACCTG | 14697 |
| rs213226946 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75341216 | CTGGGATTTAAAGAC[A/G]TGCACCACCACTGCC | 14697 |
| rs213331745 | in-del | -/AG | | | intron-variant | Gnb5 | GRCm38.p3 | 9:75330198 | TCTTTTTTAAAAAAA[-/AG]GACAGGGTCTCCTGT | 14697 |
| rs213336751 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75308686 | CTTTGTCCCTGGAGA[C/T]GCTCTCAGCCTTCAC | 14697 |
| rs213412603 | in-del | -/AGCCTCTGAG | | | intron-variant | Gnb5 | Mm_Celera | 9:75344813 | GAGAAAATAGGCTGA[-/AGCCTCTGAG]AGCCCTGTTCAGTGG | 14697 |
| rs213435776 | snp | A/G | | | synonymous-codon, nc-transcript-variant | Gnb5 | Mm_Celera | 9:75335767 | GGACCTGGCCCCCTC[A/G]GAAACAGGAAACACC | 14697 |
| rs213470274 | snp | G/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75336255 | GGAACTATAGGAATC[G/T]CCATATAGGCCCTAA | 14697 |
| rs213470411 | snp | A/C | | | intron-variant | Gnb5 | Mm_Celera | 9:75329510 | ATTTGTATTGCTTTG[A/C]AGAGGACTCAGCTTC | 14697 |
| rs213503735 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75329855 | TAAATAAATATCCAT[A/G]TATCGCCCATGCATA | 14697 |
| rs213513952 | snp | A/G | | | utr-variant-3-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant | Myo5c, Gnb5 | Mm_Celera | 9:75305322 | GGTCCTCTCTGGGGC[A/G]ACCGGTTGATTGTTC | 14697 |
| rs213531842 | in-del | -/AAAA | | | utr-variant-3-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant | Myo5c, Gnb5 | GRCm38.p3 | 9:75305061 | AAATTTTTTTTCACG[-/AAAA]AAAAAAAAAAAAACA | 14697 |
| rs213543214 | in-del | -/A | | | intron-variant, downstream-variant-500B | Gnb5, Myo5c | Mm_Celera | 9:75306510 | GTCTGTGTAAATTCT[-/A]ATTTCTCTACAACCT | 14697 |
| rs213666743 | in-del | -/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75317083 | AGTTTTCTAAATTAC[-/T]TTTTTTTTTATTTGT | 14697 |
| rs213683431 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75334123 | AAAGATGCACATGTC[C/T]GTATCCTTCCATGCC | 14697 |
| rs213742323 | snp | C/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75328221 | TATGAGGTCACCAAA[C/G]AGGCAGGTGTGGCCA | 14697 |
| rs213768895 | snp | A/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75342725 | GACCAAAAAGCACGT[A/T]GGGGAGGAAAGGGGT | 14697 |
| rs213769201 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75334527 | TGCCCTGGGTGGGTG[A/G]GAGTCAGAATGCTGC | 14697 |
| rs213816027 | snp | A/C | | | intron-variant | Gnb5 | Mm_Celera | 9:75328945 | GAGCGTTCCCAGTAG[A/C]CTCTCCTTCAGGGTC | 14697 |
| rs213914249 | in-del | -/AT | | | intron-variant | Gnb5 | Mm_Celera | 9:75324505 | TGATGTGCGTGTGAG[-/AT]ATGTGTGAGATGAGT | 14697 |
| rs213918148 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75329504 | GGAGAGATTTGTATT[A/G]CTTTGCAGAGGACTC | 14697 |
| rs214019351 | in-del | -/ACAC | | | intron-variant | Gnb5 | GRCm38.p3 | 9:75337503 | TATATACACACTCAT[-/ACAC]ACACACACACACACA | 14697 |
| rs214036531 | snp | G/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75307747 | CAGTCTTTGCTGTTA[G/T]TTAACTCAGGGTACC | 14697 |
| rs214052672 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75326001 | AACTGCTCCTGAAAA[A/G]TTGGAGGAGCAGCAC | 14697 |
| rs214057613 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75331562 | AGTGTTCAAGGTCAT[C/T]CTTGGCTACATATCG | 14697 |
| rs214112231 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75319856 | TAGTTTCCTCCTGCT[A/G]TGTACAGGAGAACCT | 14697 |
| rs214153324 | snp | G/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75320192 | TCCTTGCATTGGCCT[G/T]GTCCTTCCCTGAGAG | 14697 |
| rs214226516 | snp | A/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75320725 | TCCTAGTCTTAAAGG[A/T]ATGTAAATCTGTTCT | 14697 |
| rs214290988 | snp | G/T | | | intron-variant | Gnb5, LOC102636700 | Mm_Celera | 9:75311109 | AAAAGGTAATGTTAA[G/T]AAATTAACTGCATTG | 14697 |
| rs214329315 | snp | C/T | | | intron-variant | Gnb5, LOC102636700 | Mm_Celera | 9:75311757 | GGTGAGATAGAAATG[C/T]TAACAGATTCGTACT | 14697 |
| rs214447006 | snp | A/T | | | intron-variant, upstream-variant-2KB | Gnb5, LOC102636700 | Mm_Celera | 9:75316062 | GCAGAAAATGGAAGA[A/T]AAAAGTAAGAGACCT | 14697 |
| rs214449377 | snp | C/T | | | intron-variant, nc-transcript-variant | Gnb5 | Mm_Celera | 9:75325080 | ATCACTCAGCATTTC[C/T]AGGCCCTGTAGCAAG | 14697 |
| rs214482434 | snp | C/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75316459 | ACAGACAGACAGACA[C/G]ACACAGGCACACACA | 14697 |
| rs214493249 | snp | A/C | | | intron-variant | Gnb5 | Mm_Celera | 9:75319700 | ATAATGCGAAGGAGG[A/C]GTTTCTTTAACAGCC | 14697 |
| rs214590618 | snp | A/C | | | intron-variant | Gnb5 | Mm_Celera | 9:75317427 | ACAAGCAGATATAGA[A/C]ATAAATATTTGTAAG | 14697 |
| rs214613610 | snp | A/G | | | intron-variant, downstream-variant-500B | Gnb5, LOC102636700 | Mm_Celera | 9:75309951 | GATTTCCTTGAATCT[A/G]AAGGTGGGGCTCTCT | 14697 |
| rs214650287 | snp | A/G | | | intron-variant, downstream-variant-500B | Gnb5, LOC102636700 | Mm_Celera | 9:75310269 | GATTTTAAATGGTTC[A/G]CTATATTTCCAACCT | 14697 |
| rs214837572 | snp | A/G | | | intron-variant, upstream-variant-2KB | Gnb5, LOC102636700 | Mm_Celera | 9:75312890 | AGATAAATGGGGGGC[A/G]GGGGGTTGTACACAG | 14697 |
| rs214913927 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75307083 | AAGCTGCTACATCCT[C/T]ACCCATGCTTTGTAT | 14697 |
| rs214929577 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75322001 | CACTGCAGTCAAGGA[C/T]AAACACAAAAAGATA | 14697 |
| rs215010908 | in-del | -/C | | | intron-variant | Gnb5 | Mm_Celera | 9:75329576 | CCTGTAATTCCAGCT[-/C]CGGGGGACTGAGTCA | 14697 |
| rs215017871 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | Gnb5 | Mm_Celera | 9:75345549 | CTGGGGGAGTCTTTA[A/G]AAATGAAACGGACAC | 14697 |
| rs215051516 | snp | G/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75307528 | TTGTGTCACATTGTG[G/T]TTTTAACCTCTGACT | 14697 |
| rs215178373 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75337679 | TTATTGAGGGAATTA[C/T]ATGCATACATGCATT | 14697 |
| rs215272305 | snp | A/T | | | downstream-variant-500B, upstream-variant-2KB, intron-variant | Myo5c, Gnb5 | Mm_Celera | 9:75305456 | TATTGAGCAAATTGG[A/T]TGCACCATTTTTTTC | 14697 |
| rs215349432 | in-del | -/TTTATAAAGCTCCCTCGCTCCCC | | | intron-variant | Gnb5 | Mm_Celera | 9:75331707 | AAATGGAAAGCTGAG[-/TTTATAAAGCTCCCTCGCTCCCC]CCTTTATTCACGGGC | 14697 |
| rs215384583 | in-del | -/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75341862 | TAAGAGAAAACATAA[-/T]TTTTTTTTGTTCTTG | 14697 |
| rs215422302 | snp | C/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75328232 | CAAAGAGGCAGGTGT[C/G]GCCATGGTTGGCTGA | 14697 |
| rs215436352 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75336969 | CCCCCCACCCCATGC[A/G]CCAACACCTGCTTGC | 14697 |
| rs215452730 | snp | C/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75323629 | TAAAAATTGAGGCAC[C/G]GGGCACAGCACAGCA | 14697 |
| rs215568771 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75344693 | ACAGAGAGGACGGGT[A/G]GTGGCCTTCCTGAGC | 14697 |
| rs215734097 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75335185 | TGCTGGACAGGAAGC[C/T]TGGCAAGGTGTGGGT | 14697 |
| rs215735836 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75318860 | TCACCGTGTTCTAGA[A/G]AGCAGAGATTTTTCT | 14697 |
| rs215740264 | snp | A/C | | | intron-variant | Gnb5 | Mm_Celera | 9:75326041 | TCTCAGAATCCATCC[A/C]CAGACGGTACTTTTT | 14697 |
| rs215768004 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75339468 | GGTGGAGGCACTAGG[A/G]TCTGAAGTTCAAGGT | 14697 |
| rs215773377 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75326516 | ATTACCCATGAAAGA[A/G]ACACTCTTCCCACCC | 14697 |
| rs215782602 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75321139 | TGTCATGCAGGCATA[C/T]ATGCAAATAGGGCAC | 14697 |
| rs215787135 | snp | A/G | | | intron-variant, upstream-variant-2KB | Gnb5, LOC102636700 | Mm_Celera | 9:75313531 | CTTCCTGGAAGTGTG[A/G]CACCTAGTGATCATG | 14697 |
| rs215812354 | snp | C/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75321230 | GTATAAAGCTTTCCA[C/G]CCATGCCAATTCAAC | 14697 |
| rs215813636 | snp | C/T | | | intron-variant | Gnb5 | GRCm38.p3 | 9:75326779 | TCCCCTCTTCTCCTC[C/T]CCTCTCCCAAAAGAT | 14697 |
| rs215950034 | snp | C/T | | | intron-variant | Gnb5 | GRCm38.p3 | 9:75329443 | ACCTTTTTTTTTTTT[C/T]TTTTGTAACTTTTGT | 14697 |
| rs215954220 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75325152 | TTACCGCTGAGGTTG[C/T]CTGTCCTTTAAGTAT | 14697 |
| rs215959768 | snp | A/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75341875 | AATTTTTTTTTGTTC[A/T]TGTTGCCCTAAAAAA | 14697 |
| rs216197809 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75308919 | CCAAGCTCTGCTGAG[C/T]ACATTCTTCCATGTC | 14697 |
| rs216215665 | snp | G/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75318530 | CTATAAAACCCTCAG[G/T]GTTACATTGGGTTCA | 14697 |
| rs216234776 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75309321 | TATGTGTGTTTATGG[A/G]TACATATGTGTGTTG | 14697 |
| rs216261903 | in-del | -/TGTGTG | | | intron-variant | Gnb5 | Mm_Celera | 9:75335310 | TAGGGTGTGTGTTCC[-/TGTGTG]TGTGTGTGTGTGTGT | 14697 |
| rs216276174 | snp | C/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75342785 | ATCAAAGGAAGCCAG[C/G]ACAGGAACTCAAACC | 14697 |
| rs216302212 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75343660 | TAGACCTATAAAGAA[C/T]GAACCAGCGCTCTGC | 14697 |
| rs216356004 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75322133 | TGTCTAGAATTACAT[C/T]ACACCTTTGGACTTT | 14697 |
| rs216357201 | in-del | -/C | | | utr-variant-3-prime, nc-transcript-variant | Gnb5 | Mm_Celera | 9:75345305 | GCACTTTAAACTGTA[-/C]CCTTTTCTTGGCGTG | 14697 |
| rs216371250 | snp | C/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75340099 | GTGGAGCTTCTGGCT[C/G]TGTGACCTAGGATGC | 14697 |
| rs216388699 | snp | A/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75322871 | TTTTTCTTTCTTTTT[A/T]AGGGATGTTGAAAAG | 14697 |
| rs216399075 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75336833 | GGTGAGGTACAGGTC[A/G]CCCAAAGGAACCCCA | 14697 |
| rs216446809 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75330387 | AGCTCAGTTACATCC[C/T]GGCTCTTGTGTGCCA | 14697 |
| rs216514669 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75317870 | TCAGAAGTGTAACCT[C/T]TGACTGCGTGACTGG | 14697 |
| rs216526548 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75322071 | TACCCGTGGAGAACA[A/G]CCGTTTTAGGTGTAC | 14697 |
| rs216533510 | in-del | -/CACACACACACACA | | | intron-variant | Gnb5 | Mm_Celera | 9:75333340 | TCTCTCTCTCTCTCT[-/CACACACACACACA]CACACACACACACAC | 14697 |
| rs216541522 | snp | C/T | | | downstream-variant-500B, upstream-variant-2KB, intron-variant | Myo5c, Gnb5 | Mm_Celera | 9:75305551 | GAAAGGTGTTAGAAT[C/T]CCACAAGTCACAGTC | 14697 |
| rs216548828 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75318273 | TCTTTATCTGAAGGC[C/T]ACTAGCAGAATACTG | 14697 |
| rs216563507 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75324349 | TAGAGAGCATGAGAC[A/G]agagaatgagagagc | 14697 |
| rs216632176 | snp | A/G | | | intron-variant | Gnb5 | GRCm38.p3 | 9:75324562 | CAGAGGTGTGTATGA[A/G]TGTGGGAGTTCAAGA | 14697 |
| rs216652456 | in-del | -/A | | | intron-variant | Gnb5 | Mm_Celera | 9:75331706 | TAAAATGGAAAGCTG[-/A]GCCTTTATTCACGGG | 14697 |
| rs216719254 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75336310 | GTGCATGTCTTCTCG[C/T]TGGGCCTTTGCAGAA | 14697 |
| rs216791634 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75319738 | TCTAGACACCTCTTT[C/T]CATGCTTTGATATAT | 14697 |
| rs217058571 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75320577 | CAGAGGTCAGGCTCG[A/G]ACCAGACAGTCTCTT | 14697 |
| rs217059279 | in-del | -/AT/T/TT | | | intron-variant | Gnb5 | GRCm38.p3 | 9:75321181 | GCATAGATAAATCAA[-/AT/T/TT]AAAAAAAAAAGACCC | 14697 |
| rs217111239 | in-del | -/ACACTT | | | intron-variant | Gnb5 | GRCm38.p3 | 9:75329350 | ATGTTTTACACACAC[-/ACACTT]ACACACACACACACA | 14697 |
| rs217125482 | snp | C/G | | | intron-variant, upstream-variant-2KB | Gnb5, LOC102636700 | Mm_Celera | 9:75315839 | GACTCTGTCCCTCCT[C/G]CCTCCTCCCCAGCCA | 14697 |
| rs217154415 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75341982 | TTGAAGAGATGGCTC[A/G]GAGATTAGAGAGCTT | 14697 |
| rs217177069 | snp | A/C | | | intron-variant | Gnb5 | Mm_Celera | 9:75334555 | TGCGTGTAAGGCAGG[A/C]AGTATATGGCTGCTG | 14697 |
| rs217179540 | snp | C/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75342585 | GCCATGTAGATCGTC[C/G]TCTTTGAAGACTAAT | 14697 |
| rs217197935 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75316513 | AGGCACACATACACA[C/T]ATACACATGTGCACA | 14697 |
| rs217206120 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75335254 | TAAGTTGTATGGAGC[C/T]GCTTCTGTCTTCTGG | 14697 |
| rs217454944 | snp | A/C | | | intron-variant | Gnb5 | Mm_Celera | 9:75340954 | GGGAAGCAGCCCACA[A/C]CCCTGCACCTGGGAT | 14697 |
| rs217466579 | snp | A/G | | | intron-variant, upstream-variant-2KB | Gnb5, LOC102636700 | Mm_Celera | 9:75315098 | GAAGGGGCTGCAAGC[A/G]CCTGTGTGGCTTAGA | 14697 |
| rs217483343 | snp | A/G | | | intron-variant | Gnb5, LOC102636700 | Mm_Celera | 9:75311304 | CGTGTGGAGGCAGGA[A/G]GAGAAGGAGGCTCCG | 14697 |
| rs217487539 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75324229 | TTCTTGATTCTTTGT[A/G]GGACGTGGTTATTCT | 14697 |
| rs217501492 | in-del | -/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75317335 | TTACGACTCCAGCAC[-/T]TTGGGAGGTCAAGGC | 14697 |
| rs217633481 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75319677 | TGGGATCTCTGTGGG[A/G]CAGTTAGATAATGCG | 14697 |
| rs217638631 | in-del | -/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75327744 | GTGTATTTGTTTGGG[-/T]TTTTTTATTTTTGCT | 14697 |
| rs217765481 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75320846 | ACCGGGCAGTGGTAG[C/T]GCATGCCTTTAATCC | 14697 |
| rs217796800 | snp | A/G | | | intron-variant, upstream-variant-2KB | Gnb5, LOC102636700 | Mm_Celera | 9:75316210 | AAGAACCTATGGGCT[A/G]GGAGCAAGCGGAGGC | 14697 |
| rs217798301 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75321261 | ACATGGGGGATAGTG[C/T]CCAAATACATCAAAA | 14697 |
| rs217804987 | snp | C/T | | | intron-variant | Gnb5, LOC102636700 | Mm_Celera | 9:75311894 | CTACCTAATGAGCCA[C/T]CAAGCTAGAAGAAAT | 14697 |
| rs217829543 | snp | A/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75325306 | CACTGACACAGCTGG[A/T]GCTTTTATAGGGACT | 14697 |
| rs217831125 | snp | A/C | | | intron-variant | Gnb5 | Mm_Celera | 9:75316585 | GCACACACATGTACA[A/C]ACAGACATCCACACA | 14697 |
| rs217885652 | in-del | -/AAAAGAAAG | | | intron-variant | Gnb5 | Mm_Celera | 9:75324860 | AGAAAAGAAAAAAGA[-/AAAAGAAAG]AAAAGAAAGAAAGAG | 14697 |
| rs217933670 | snp | C/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75322921 | GAAACAAGAGAAACT[C/G]CAATAATATGGGCAT | 14697 |
| rs217959460 | snp | G/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75337150 | GAGCCTGCCTGCTCT[G/T]CTGTCCTAGGAAGGT | 14697 |
| rs218057968 | in-del | -/TA | | | intron-variant | Gnb5 | Mm_Celera | 9:75339216 | TGTTAGCAATTTTTT[-/TA]TATACTATTATCTTC | 14697 |
| rs218094693 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75316931 | CTCTGCCTCCCTAGA[C/T]TGGACTGACAAGCAC | 14697 |
| rs218163146 | snp | A/G | | | intron-variant, nc-transcript-variant | Gnb5, LOC102636700 | Mm_Celera | 9:75310372 | TAGATTAGCAAACAA[A/G]GCTTCAGGGGAGTCA | 14697 |
| rs218193806 | snp | A/G | | | intron-variant, upstream-variant-2KB | Gnb5, LOC102636700 | Mm_Celera | 9:75314665 | CAGAAGGAAGCAGAC[A/G]TGCTTTCTGCGTCCG | 14697 |
| rs218228796 | snp | C/T | | | intron-variant, upstream-variant-2KB | Gnb5, LOC102636700 | GRCm38.p3 | 9:75315202 | CTGGTGCAGCTAGAT[C/T]GTTGTCATTTATTTA | 14697 |
| rs218269459 | snp | C/G | | | intron-variant | Gnb5, LOC102636700 | Mm_Celera | 9:75310942 | TGGCAAGATTGTTTA[C/G]TGGGCAAAGACCCCT | 14697 |
| rs218321611 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75343064 | GTTGACGTAAAACTA[C/T]CCAGCACACACACAT | 14697 |
| rs218351251 | in-del | -/TTT | | | intron-variant | Gnb5 | Mm_Celera | 9:75324278 | TGATTATGCAATGTC[-/TTT]TTTTTTTTTAACCTG | 14697 |
| rs218439355 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75336040 | ATGCTGAAACTCAGG[A/G]CGTGTGTCCATCACC | 14697 |
| rs218471546 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75336433 | CCACCAGGAGGTTGA[A/G]GGTCCTTGGATCTCT | 14697 |
| rs218587447 | snp | A/G | | | intron-variant | Gnb5, LOC102636700 | Mm_Celera | 9:75311995 | TCTTGCCCAGCCTAA[A/G]CAGAGAGCAAAACTA | 14697 |
| rs218604309 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75332361 | CTCTGGTTGCAGGCC[A/G]GAGTCCACCATCTGT | 14697 |
| rs218643957 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75339090 | AGGACAGTGAAAGAA[C/T]CTGACTCAAAGGAGG | 14697 |
| rs218678082 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75339669 | AATAGCCACTGTTCA[C/T]TGAGGCTTTTTAGTT | 14697 |
| rs218717168 | snp | A/C | | | intron-variant | Gnb5 | Mm_Celera | 9:75307630 | CACAAATATTTTTGC[A/C]CACTTTTTAAAAAAT | 14697 |
| rs218729190 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75329399 | ACACACATCTGGCTC[C/T]TGGTTCAGCTTTTTT | 14697 |
| rs218767092 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75337858 | CTCCAAACCGGCCTG[A/G]AGGATGAAGAGCCAG | 14697 |
| rs218804922 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75308513 | TTCCAGTTATTTATA[A/G]TGAACATTATAAACG | 14697 |
| rs218837145 | snp | G/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75333228 | AATCCTGGATCCTAC[G/T]GGAAGGAGTAAACTG | 14697 |
| rs218903512 | in-del | -/CACCAAG | | | intron-variant | Gnb5 | Mm_Celera | 9:75308901 | CGAGTAGGAGACATT[-/CACCAAG]CTCCAAGCTCTGCTG | 14697 |
| rs219003211 | snp | A/G | | | intron-variant, upstream-variant-2KB | Gnb5, LOC102636700 | GRCm38.p3 | 9:75313827 | GAGGCACgtgtgtgt[A/G]tgtgtgtgtgtgtgt | 14697 |
| rs219049970 | in-del | -/A | | | upstream-variant-2KB, downstream-variant-500B | Gnb5, Myo5c | Mm_Celera | 9:75306277 | GCTGCAAGTCCAGAT[-/A]AAAGGGATTAGGTGA | 14697 |
| rs219061533 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75334764 | TCTGAGCCATCACAC[C/T]AACCTTTATGTACTA | 14697 |
| rs219090587 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75325639 | ATGGGGCAAAAAGAA[A/G]TAATAGAAACTGATT | 14697 |
| rs219230841 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75317493 | ATCGATCGATCGATC[A/G]ATTCCTGATCCAAAC | 14697 |
| rs219241381 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75333149 | GCACCCACATGGAAC[A/G]CCACACAGAGACCCT | 14697 |
| rs219301099 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75333690 | GCTGCCATGTGGGTC[C/T]TGGGATAGAACTCAG | 14697 |
| rs219442488 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75318591 | AACATCCTCCAATCC[A/G]CAAGGGCCTCTTTGC | 14697 |
| rs219459220 | snp | A/C | | | intron-variant, upstream-variant-2KB | Gnb5, LOC102636700 | GRCm38.p3 | 9:75314777 | AAACTTGCCAGCAGG[A/C]TGGCATTCCAGGGAC | 14697 |
| rs219461851 | snp | A/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75328274 | GGGTTTCCTTGCTCA[A/T]GTGGCTATCGGCTGA | 14697 |
| rs219501611 | in-del | -/GCTGC | | | intron-variant, utr-variant-5-prime, nc-transcript-variant | Gnb5, LOC102636700 | GRCm38.p3 | 9:75314255 | TGCGTTTCTCTCCCG[-/GCTGC]ATCCGGACGAAGATG | 14697 |
| rs219549082 | snp | A/G | | | intron-variant, upstream-variant-2KB | Gnb5, LOC102636700 | Mm_Celera | 9:75313026 | CAGACATTGCCTAGA[A/G]TATCCTCCAGAGCAT | 14697 |
| rs219581470 | snp | A/T | | | intron-variant, upstream-variant-2KB | Gnb5, LOC102636700 | Mm_Celera | 9:75313646 | AGCCCAGGGAACTGT[A/T]GCTGGAGAGGAGCCG | 14697 |
| rs219709211 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75333922 | TCATTTGTATTCAGC[C/T]GGTTCTGCCTTCGCT | 14697 |
| rs219823317 | snp | A/G | | | intron-variant, upstream-variant-2KB | Gnb5, LOC102636700 | Mm_Celera | 9:75313579 | TGCATCTGTAGCTTG[A/G]AGGAGGGATTGGGGG | 14697 |
| rs219903928 | snp | C/T | | | intron-variant, downstream-variant-500B | Gnb5, LOC102636700 | Mm_Celera | 9:75310114 | ACTTCCTCCTCTTCC[C/T]TATGCTCGGTCCAAG | 14697 |
| rs219936778 | snp | A/G | | | intron-variant, nc-transcript-variant | Gnb5, LOC102636700 | Mm_Celera | 9:75310526 | ACAGGCTGGGGCCCT[A/G]GGTGTTCGGCTGGTG | 14697 |
| rs220039949 | in-del | -/C | | | intron-variant | Gnb5 | Mm_Celera | 9:75329205 | TAGAGGCAAGAGGAT[-/C]AGGGGTTCCGGTCGT | 14697 |
| rs220090686 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | Gnb5 | Mm_Celera | 9:75345705 | ACAGAACCTTCTGGC[A/G]TGGGAAGACAGGCCA | 14697 |
| rs220217636 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75308072 | TTGTTTACCTAAAAG[C/T]AATGCTACTTCAAAC | 14697 |
| rs220233692 | snp | A/C | | | intron-variant, downstream-variant-500B | Gnb5, LOC102636700 | Mm_Celera | 9:75310093 | GTCATCATCCCTTCA[A/C]GTCTCACTTCCTCCT | 14697 |
| rs220324709 | snp | A/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75308993 | AACACGTGTGTGTGA[A/T]CATGAGTATGTGCTT | 14697 |
| rs220353691 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | Gnb5 | Mm_Celera | 9:75345131 | CTGGAAACACTCGGA[C/T]AGGCCGTGGCACTTC | 14697 |
| rs220356644 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75309433 | TCTCCCTCTCTTTGG[C/T]CTTCAACTACACTGC | 14697 |
| rs220496469 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75330009 | CATACTTGCAATCCT[C/T]CTGCTTCAGCCTCTT | 14697 |
| rs220529681 | snp | A/C | | | intron-variant | Gnb5 | GRCm38.p3 | 9:75329709 | AATCTTTTTAAAAAA[A/C]TGTGCATGGTCTAGA | 14697 |
| rs220583406 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75325758 | GTGGAAGGAGTGGTG[A/G]GCTTAGGAAAAGCAC | 14697 |
| rs220628874 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75326180 | AGTTGTTTCCCTGTG[A/G]GGTTCCTGACAAGTG | 14697 |
| rs220714658 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75308977 | CTTGTGTGCTCATAG[A/G]AACACGTGTGTGTGA | 14697 |
| rs220718807 | in-del | -/TTT | | | intron-variant | Gnb5 | GRCm38.p3 | 9:75330191 | CCATGCCTCTTTTTT[-/TTT]AAAAAAAGACAGGGT | 14697 |
| rs220738383 | snp | A/T | | | intron-variant, downstream-variant-500B | Gnb5, Myo5c | Mm_Celera | 9:75306561 | TATAAAGGGATTTTT[A/T]AAAAACAGATTAGTG | 14697 |
| rs220740637 | snp | C/T | | | downstream-variant-500B, upstream-variant-2KB, intron-variant | Myo5c, Gnb5 | Mm_Celera | 9:75305617 | CTGGGGCCCCCTGGC[C/T]CCCTGGCAGGATGGG | 14697 |
| rs220745274 | snp | C/T | | | downstream-variant-500B, upstream-variant-2KB, intron-variant | Myo5c, Gnb5 | Mm_Celera | 9:75305710 | GCTAAGGTTCTGGTT[C/T]TCTGGCTTGAATTCA | 14697 |
| rs220766920 | in-del | -/AAAGCAACAG | | | intron-variant | Gnb5 | Mm_Celera | 9:75340342 | AATTTTATTTAAAGC[-/AAAGCAACAG]AAAGGAACAGAAAAT | 14697 |
| rs220778389 | snp | C/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75327051 | GGTAAAAGCCCTCTG[C/G]AGGAGTCAAAGGCTT | 14697 |
| rs220815203 | in-del | -/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75307119 | AGTTTTTGTCTTAGA[-/T]TCTTTTTTTAATTAT | 14697 |
| rs220865332 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75328367 | TCCCTTACAGCAGGT[A/G]ACCCAAGAGAGAGAA | 14697 |
| rs220884378 | in-del | -/CCA | | | intron-variant | Gnb5 | Mm_Celera | 9:75307775 | ACCCCGTCCCCCACC[-/CCA]CCCCCAAATCCCATT | 14697 |
| rs220941426 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75329935 | ATTATCCTAATTAAA[C/T]TTTATTTATTGTTTA | 14697 |
| rs220988748 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75328719 | GCCATGAAGGGTCAC[C/T]GCTTGCTGGTTTGCT | 14697 |
| rs221040488 | snp | C/T | | | utr-variant-3-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant | Myo5c, Gnb5 | Mm_Celera | 9:75305018 | GTTTTTTTTTCCTCT[C/T]TCTAATCAGTGTTCT | 14697 |
| rs221159710 | in-del | -/A | | | intron-variant | Gnb5 | Mm_Celera | 9:75338054 | GGGGCTATTTCAGTC[-/A]AAAAAAAACCCCTAT | 14697 |
| rs221201238 | in-del | -/ATAA | | | intron-variant | Gnb5 | Mm_Celera | 9:75334099 | ATTTGCGCAGTCAGT[-/ATAA]ATGAGAAAGATGCAC | 14697 |
| rs221264135 | snp | A/G | | | intron-variant | Gnb5, LOC102636700 | Mm_Celera | 9:75311351 | ACTGTCTTTCTCCAC[A/G]CCCTGTTCATTCTTT | 14697 |
| rs221267204 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75325749 | TCACCGGGTGTGGAA[A/G]GAGTGGTGGGCTTAG | 14697 |
| rs221333039 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75320771 | GTGTACATAAAATTC[C/T]CAGTCTTCTGAGCTT | 14697 |
| rs221367961 | in-del | -/A | | | intron-variant, upstream-variant-2KB | Gnb5, LOC102636700 | Mm_Celera | 9:75312139 | CTTCAGATTATCACC[-/A]AAAAAATGTATTCAG | 14697 |
| rs221423565 | snp | G/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75344203 | TATTGTGTGGATGGT[G/T]GGGTAGCTAGGTGAG | 14697 |
| rs221430490 | snp | A/G | | | intron-variant, upstream-variant-2KB | Gnb5, LOC102636700 | Mm_Celera | 9:75312283 | CAGGTGTGAGCGCAC[A/G]TGGTATACAGACATA | 14697 |
| rs221463458 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75328132 | AGTTTCATGCCTGGC[A/G]CTGAAACAAATTACC | 14697 |
| rs221526903 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75323300 | GGGGGCTTGTGTAAA[C/T]GGCCTGCAAGAATTC | 14697 |
| rs221567178 | in-del | -/A | | | intron-variant | Gnb5 | Mm_Celera | 9:75319842 | CACATCTATCTCAAT[-/A]GTTTCCTCCTGCTAT | 14697 |
| rs221584053 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75307289 | GCTCTAACTACTGAG[C/T]CATCTCTCCAGCCCC | 14697 |
| rs221609393 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75308005 | CCTGCTTCATGGACA[C/T]GCTATGTTTTCTCTG | 14697 |
| rs221655643 | in-del | -/C | | | intron-variant | Gnb5 | Mm_Celera | 9:75336954 | TGTCACAAACCTTGA[-/C]CCCCCACCCCATGCA | 14697 |
| rs221698718 | snp | A/C | | | intron-variant | Gnb5 | Mm_Celera | 9:75309098 | ATGTGAGTGTGTGTT[A/C]ATGGGTACATGTGTG | 14697 |
| rs221700573 | snp | C/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75329161 | TCCCAGGCAAGGCAG[C/G]GCACGCCTGCAATAG | 14697 |
| rs221775466 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75320367 | AAAAGTGGAGGGATA[C/T]GTCTGCAGCTAAAAT | 14697 |
| rs221784054 | in-del | -/ATAGATAGATAGATAGATAG | | | intron-variant | Gnb5 | Mm_Celera | 9:75323170 | TACATACATACATAC[-/ATAGATAGATAGATAGATAG]ATAGATAGATAGATA | 14697 |
| rs221848270 | snp | G/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75327036 | TAAGAATAAGAAGAG[G/T]GTAAAAGCCCTCTGC | 14697 |
| rs221859122 | snp | A/C | | | intron-variant | Gnb5 | Mm_Celera | 9:75325315 | AGCTGGTGCTTTTAT[A/C]GGGACTCCGTACCTT | 14697 |
| rs221861086 | in-del | -/C | | | intron-variant, utr-variant-5-prime, nc-transcript-variant | Gnb5, LOC102636700 | Mm_Celera | 9:75314169 | GCCCCGGGCGGCGTT[-/C]GGGGTCACGGAGGCT | 14697 |
| rs221886026 | snp | C/T | | | utr-variant-3-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant | Myo5c, Gnb5 | Mm_Celera | 9:75304894 | TTTAATTTTTAAATA[C/T]AGCTATTTCTTTTAA | 14697 |
| rs221911849 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75319914 | ATCTCATGTATCCCA[C/T]TGCGGTCGGTCTCGG | 14697 |
| rs221915645 | snp | A/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75321872 | CTGCAGTCACATCAG[A/T]CTTAGAGGGACCACA | 14697 |
| rs222049644 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | Gnb5 | Mm_Celera | 9:75345098 | CCGTCCAGTGTCTCC[A/G]TGAAATCTGCCCCCT | 14697 |
| rs222078675 | in-del | -/AC | | | intron-variant | Gnb5 | GRCm38.p3 | 9:75334809 | ACAAAACAAAACAAA[-/AC]AAACAAACAAACAAA | 14697 |
| rs222167529 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75323747 | GCAGTTCCAGATTAG[C/T]GTTTGACTTGCAAAG | 14697 |
| rs222232132 | in-del | -/GC | | | intron-variant | Gnb5 | Mm_Celera | 9:75316455 | CAGACAGACAGACAG[-/GC]ACACACACAGGCACA | 14697 |
| rs222288753 | in-del | -/A | | | intron-variant | Gnb5 | Mm_Celera | 9:75343798 | TCTGAAAGCCCCTGC[-/A]ACCCTGCCCACACCT | 14697 |
| rs222406976 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75325683 | TACAGTAGAATCCAC[A/G]AAGTCCATACTGCTG | 14697 |
| rs222418643 | snp | A/G | | | downstream-variant-500B, upstream-variant-2KB | Gnb5, Bcl2l10 | Mm_Celera | 9:75346226 | TCTCTGTGTGTGGTC[A/G]TGAATACACAGGCCA | 14697 |
| rs222447816 | snp | G/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75333878 | GGAGAGATGCACATG[G/T]GCACCCGGTCTACTT | 14697 |
| rs222450982 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75320339 | CACGTCTAGTTAGAT[A/G]TTGCCTCTAAGAAAA | 14697 |
| rs222456125 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75338177 | ACCACGCACAGCATG[A/G]CTAAATATAAAACAT | 14697 |
| rs222500508 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75307193 | GGAGACCAGAAGAGG[A/G]TGCTGGATCCCCTGG | 14697 |
| rs222588147 | snp | A/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75338968 | GCTTCAGTCTCTGGC[A/T]TCCACATGCATAGTA | 14697 |
| rs222601723 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75341519 | CATCATGACCTCAAA[A/G]AATCTTCCATCTGGA | 14697 |
| rs222629545 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75339624 | GCATCCATACTTCCC[A/G]CTGAGCACCGAGAAG | 14697 |
| rs222741500 | in-del | -/GATC | | | intron-variant | Gnb5 | Mm_Celera | 9:75317477 | TAGGAAACCGGAAGG[-/GATC]GATCGATCGATCAAT | 14697 |
| rs222813842 | snp | C/T | | | intron-variant, downstream-variant-500B | Gnb5, Myo5c | Mm_Celera | 9:75306763 | CTTGAATCCAGTCCA[C/T]TTCTGGTGAACATGC | 14697 |
| rs222869672 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75323255 | AATAAATCTTTTAAA[A/G]GAATTAAATAGGACG | 14697 |
| rs222874454 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | Gnb5 | Mm_Celera | 9:75345194 | AAACTCTGCTAAGTT[C/T]TGTCTGTTTTTGAAA | 14697 |
| rs222908610 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75318004 | CTAATGCTTTCACCC[C/T]TTAACACAGCTCCTC | 14697 |
| rs222908700 | snp | C/T | | | intron-variant | Gnb5 | GRCm38.p3 | 9:75323714 | TCATCTTGGAGACAA[C/T]GTAATAACTGCACAA | 14697 |
| rs222923078 | snp | A/C | | | intron-variant | Gnb5 | Mm_Celera | 9:75317040 | CTGAAGCCCGAGTGA[A/C]CTGAACCACCGACGT | 14697 |
| rs222943295 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75342057 | AGGTGGCTTACAACC[A/G]CCTGTAACTTCTGTT | 14697 |
| rs223008720 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75325391 | AGAAAAGAATGGTTC[A/G]CATAGGGCAAGAAGC | 14697 |
| rs223026087 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75316675 | TCCAACAGCCTCCCA[C/T]TGTAACCCCATCTTC | 14697 |
| rs223060764 | snp | A/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75326954 | GAGTGGGGAGTTTTT[A/T]GGGGGTGGGGGGAGG | 14697 |
| rs223096768 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75340528 | ACTGGAATTGCAGAT[A/G]GTTGGGAGCCACCAT | 14697 |
| rs223100513 | snp | C/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75321733 | CTTCGGACTACGCTG[C/G]TTCCAGAATATTCAG | 14697 |
| rs223127682 | in-del | -/TTT | | | intron-variant | Gnb5 | Mm_Celera | 9:75330185 | TCACTCCCATGCCTC[-/TTT]TTTTTTAAAAAAAGA | 14697 |
| rs223135081 | snp | G/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75338922 | CTGGGCCTGGGGGCA[G/T]AGCTCATTTGGTAAG | 14697 |
| rs223148351 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75320406 | GAAAACCACTGTTCC[A/G]TGTGTGCGCTCAGCA | 14697 |
| rs223149666 | snp | A/G | | | intron-variant, upstream-variant-2KB | Gnb5, LOC102636700 | Mm_Celera | 9:75314939 | GCACACCTCCTCCCC[A/G]CCTTCCTAATAGGCC | 14697 |
| rs223179027 | in-del | -/TCTC | | | intron-variant | Gnb5 | GRCm38.p3 | 9:75327628 | ATGCATCTTACAAGG[-/TCTC]ATTTGTGAAGGAACC | 14697 |
| rs223198851 | snp | A/C | | | intron-variant | Gnb5 | Mm_Celera | 9:75320265 | TGGAGTTAGCCTTAA[A/C]GCCCAGTTATTCTCT | 14697 |
| rs223217816 | in-del | -/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75329186 | AATAGCGGCACCTGA[-/G]AAGTAGAGGCAAGAG | 14697 |
| rs223268657 | in-del | -/CCATG | | | intron-variant | Gnb5 | Mm_Celera | 9:75325809 | GTGACTGGGCTGTTA[-/CCATG]GTGTGTGGTACCATG | 14697 |
| rs223274195 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75343165 | TGACTTTCATTTCCT[C/T]GTGTGTGAATTTCTA | 14697 |
| rs223285894 | snp | A/G | | | downstream-variant-500B, upstream-variant-2KB | Gnb5, Bcl2l10 | Mm_Celera | 9:75346011 | TTTTAGAAACTCTTC[A/G]TGTAATGAGATGCCA | 14697 |
| rs223321788 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75336094 | AAGTTTGCATCTTAG[C/T]GTAACCATGGACCAT | 14697 |
| rs223416402 | in-del | -/TC | | | intron-variant | Gnb5 | Mm_Celera | 9:75308993 | ACACGTGTGTGTGAA[-/TC]CATGAGTATGTGCTT | 14697 |
| rs223442498 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75319319 | TAATCAATTGGGGCC[A/G]ATGACTTTTCTGTTT | 14697 |
| rs223467646 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75336746 | GGGGTGACTTGCTAC[C/T]CTCTCCCCTAATTGT | 14697 |
| rs223470226 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75319868 | GCTATGTACAGGAGA[A/G]CCTATTTTTGGGAGA | 14697 |
| rs223501350 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75330163 | CACCCACTGTCAGGG[A/G]TTTTCTGTCACTCCC | 14697 |
| rs223531422 | snp | G/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75326176 | AGTCAGTTGTTTCCC[G/T]GTGGGGTTCCTGACA | 14697 |
| rs223553303 | in-del | -/TA | | | intron-variant | Gnb5 | Mm_Celera | 9:75317092 | AATTACTTTTTTTTT[-/TA]ATTTGTGTATGTGCA | 14697 |
| rs223651902 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75324302 | TAACCTGCTTTTGGG[A/G]TATCAATAAAAGACT | 14697 |
| rs223654760 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75336484 | TCTCAGGGTCCTATC[C/T]CCCATGGCAGGTGCT | 14697 |
| rs223656567 | snp | C/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75320886 | GGAGGCAGAGGCAGG[C/G]AGATCTCTGAGTTCG | 14697 |
| rs223877405 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75340438 | GTATGGACGTTTTGT[C/T]TGAATATATGACTTT | 14697 |
| rs223924768 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75333414 | ATTTACTTTATTTTA[C/T]GTGTGTGAATGTTTG | 14697 |
| rs223943736 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75339780 | AGGAAACCAGGCTGG[A/G]AAAGATGATGTCACT | 14697 |
| rs223967273 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75332784 | GAAGGGCCTTATTCA[C/T]CCCCGATTGGTTCTA | 14697 |
| rs224011488 | in-del | -/TATAGTA | | | intron-variant | Gnb5 | Mm_Celera | 9:75344909 | ATTAAACTCAACTCT[-/TATAGTA]TAAACTATTAACTAT | 14697 |
| rs224039527 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75336642 | AAAATCTCCCAGAAT[C/T]GGAACCCCATAATAT | 14697 |
| rs224109218 | in-del | -/TATGTGT | | | intron-variant, upstream-variant-2KB | Gnb5, LOC102636700 | Mm_Celera | 9:75312360 | AATTTTAATTAAAAA[-/TATGTGT]ATATATATATACATA | 14697 |
| rs224247920 | in-del | -/CG | | | intron-variant | Gnb5 | Mm_Celera | 9:75329386 | ACACACACACACACA[-/CG]CACATCTGGCTCCTG | 14697 |
| rs224253285 | in-del | -/GAGAGAG | | | intron-variant | Gnb5 | Mm_Celera | 9:75324634 | AAGCTGAGAGAGACA[-/GAGAGAG]AGAGAGAGAAGAGAG | 14697 |
| rs224332836 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75341670 | GGTGATCCTTAGCTA[A/G]GGAGGGGCACACAGC | 14697 |
| rs224369407 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75317713 | TCCTCCCTAGAGCCT[C/T]CCACCCCCATCGGCA | 14697 |
| rs224391226 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75335029 | CATTAAGTCTGTGCC[C/T]TACTTTGCATAAACC | 14697 |
| rs224400024 | snp | A/C | | | intron-variant | Gnb5 | Mm_Celera | 9:75322415 | GTGGCTCAAGCTGAA[A/C]ACACCGCTATCTTCC | 14697 |
| rs224431562 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75317559 | AGGGTCTTACTCTGT[A/G]GACTTCATTTCCCAG | 14697 |
| rs224469685 | in-del | -/TCTG | | | intron-variant | Gnb5 | Mm_Celera | 9:75306901 | GTTTCTCTCTCTCTC[-/TCTG]TGTGTCTCTCTCTCT | 14697 |
| rs224504182 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75323098 | CTTCTTCTGGCCTCT[A/G]AGGACACTGTCTACA | 14697 |
| rs224621028 | snp | A/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75329677 | ACACACACGTGTAAG[A/T]AAAAGGAAAAAATTT | 14697 |
| rs224708954 | snp | C/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75338293 | ACACCAGATGACTCA[C/G]AACTGCCTCTAACTG | 14697 |
| rs224778958 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75332149 | AATCAAAATTCTGTC[C/T]TTTGTCCCCTCTCTA | 14697 |
| rs224846328 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75322203 | CGTGCAGATATCACC[C/T]TACAGCCCAGTACAG | 14697 |
| rs224858604 | snp | C/G | | | intron-variant, upstream-variant-2KB | Gnb5, LOC102636700 | Mm_Celera | 9:75316102 | GTGAGATGGCTCAGT[C/G]GTTAAGAGCACTGAC | 14697 |
| rs224965716 | in-del | -/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75318667 | AAGCCATGGGTTTAC[-/T]CTGTCAACAGGCCTT | 14697 |
| rs224965735 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75329187 | AATAGCGGCACCTGA[A/G]AGTAGAGGCAAGAGG | 14697 |
| rs224995963 | snp | A/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75309455 | CTACACTGCCCAGCC[A/T]ATGAGTCCCAGAGAT | 14697 |
| rs225068363 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75329654 | CACACACACACACAC[A/G]CACACACACACACAC | 14697 |
| rs225157578 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75341652 | AGAGGAACAGATATT[C/T]AAGGTGATCCTTAGC | 14697 |
| rs225166254 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75316416 | TTCCTCCATCTCTCC[A/G]CCTCAGCCTGTCTCT | 14697 |
| rs225182849 | snp | C/T | | | intron-variant, upstream-variant-2KB | Gnb5, LOC102636700 | Mm_Celera | 9:75314622 | ATTCCCATCTCTCCA[C/T]TGTCCTTGGGGGCAG | 14697 |
| rs225200949 | snp | C/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75316853 | TTTTAAAATAGGTCT[C/G]TCATTTTTCCTGAAC | 14697 |
| rs225235217 | snp | G/T | | | intron-variant, downstream-variant-500B | Gnb5, LOC102636700 | Mm_Celera | 9:75310259 | GGGGCAGCGTGATTT[G/T]AAATGGTTCGCTATA | 14697 |
| rs225260459 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75319306 | TAATCAGAGGATTTA[A/G]TCAATTGGGGCCAAT | 14697 |
| rs225313875 | snp | G/T | | | intron-variant, upstream-variant-2KB | Gnb5, LOC102636700 | Mm_Celera | 9:75313719 | CTTCATCCCAGAGGA[G/T]AGGACGCCCCTGACC | 14697 |
| rs225332740 | snp | A/G | | | intron-variant | Gnb5, LOC102636700 | Mm_Celera | 9:75311678 | CTGGCATCCTGGACT[A/G]CATGCTATCCTGGGC | 14697 |
| rs225334212 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75318121 | CTGTGAACAGACACC[A/G]TGACCAAGGCAGCTG | 14697 |
| rs225338562 | snp | G/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75337655 | GTTTCTTAGGCATTC[G/T]TCACATGTTTATTGA | 14697 |
| rs225367639 | snp | C/T | | | intron-variant, nc-transcript-variant | Gnb5, LOC102636700 | Mm_Celera | 9:75310839 | TGGAGGAAGGAGGAT[C/T]GAGATGTTCCAGGAT | 14697 |
| rs225378700 | snp | A/C | | | intron-variant, upstream-variant-2KB | Gnb5, LOC102636700 | Mm_Celera | 9:75312625 | TGTACACTTTATAAG[A/C]ACACACACATACACT | 14697 |
| rs225400340 | snp | G/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75317071 | GTTTGGTTTTTTTAG[G/T]TTTCTAAATTACTTT | 14697 |
| rs225443826 | snp | A/G | | | intron-variant, nc-transcript-variant | Gnb5, LOC102636700 | Mm_Celera | 9:75310711 | CTCTCCAGGCTGGAG[A/G]GAGCTGGGTAGGTAG | 14697 |
| rs225512291 | in-del | -/TGGCTGT | | | intron-variant | Gnb5 | Mm_Celera | 9:75334484 | AGTTGAGACAAACTC[-/TGGCTGT]TGGCTGTTGTAGAGA | 14697 |
| rs225562989 | snp | A/G | | | intron-variant, upstream-variant-2KB | Gnb5, LOC102636700 | Mm_Celera | 9:75313476 | AGTGGAAACCTATCT[A/G]TGACGCTGAACTGCC | 14697 |
| rs225638983 | snp | A/C | | | intron-variant | Gnb5 | Mm_Celera | 9:75333004 | CTAACCACGAAAACC[A/C]ATTAGGTCCAGAATG | 14697 |
| rs225640741 | snp | A/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75307488 | CTAAATATAATAAGT[A/T]TTAGGAATTCTTGGG | 14697 |
| rs225678406 | snp | G/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75328229 | CACCAAAGAGGCAGG[G/T]GTGGCCATGGTTGGC | 14697 |
| rs225679991 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75333596 | TTGTATAGTCTATGC[A/G]TTGCATGTATGCCTG | 14697 |
| rs225692965 | in-del | -/ATAC | | | intron-variant | Gnb5 | Mm_Celera | 9:75316514 | GGCACACATACACAT[-/ATAC]ACATGTGCACACACA | 14697 |
| rs225716909 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75328525 | TAATAATTCCTAGGT[A/G]TGTTTTTGGGTTAGA | 14697 |
| rs225728292 | in-del | -/AAAGAG | | | intron-variant | Gnb5 | Mm_Celera | 9:75343350 | TGAAGGATAAAATAA[-/AAAGAG]AAAGAGAACAAAAGA | 14697 |
| rs225741703 | snp | C/T | | | synonymous-codon, nc-transcript-variant | Gnb5 | Mm_Celera | 9:75334187 | TCTGGATAATAAGTG[C/T]TCTGTGTATCCACTG | 14697 |
| rs225769476 | in-del | -/AG | | | intron-variant | Gnb5 | Mm_Celera | 9:75324887 | GAAAGAAAGAGAGAA[-/AG]AGGAAAATTTTCCTG | 14697 |
| rs225771589 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75309293 | CATAGGTACATATGC[A/G]TGCATTCATAGGTAT | 14697 |
| rs225778494 | snp | G/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75308206 | TGGCATGTATTTTTT[G/T]ACTCTGCATGTATCT | 14697 |
| rs225811917 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75309636 | TAATTCCTCTGTTCT[C/T]TCAGCTTTCACATGA | 14697 |
| rs225938430 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75337095 | GTCTTACTCTAACTC[A/G]GAAATACACAAAAGA | 14697 |
| rs225981526 | snp | G/T | | | intron-variant | Gnb5, LOC102636700 | Mm_Celera | 9:75311154 | GCTCTCCAAGGATCC[G/T]TTGAAAGCATGATTT | 14697 |
| rs225998106 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75330308 | TAGGATTACAGATGT[A/G]CACCGCCACAGCCAG | 14697 |
| rs226034471 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75330780 | ACATACTTCCTCCAA[C/T]AATGCCACACCTACT | 14697 |
| rs226036426 | snp | A/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75326487 | GCTATAGGGTAGGGG[A/T]AGCCCGCCACCATAT | 14697 |
| rs226073690 | snp | C/T | | | intron-variant | Gnb5 | GRCm38.p3 | 9:75326771 | CCCTCCTCTCCCCTC[C/T]TCTCCTCTCCTCTCC | 14697 |
| rs226277794 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75307136 | CTTTTTTTAATTATG[C/T]GCATGTTGGGGTGCG | 14697 |
| rs226328742 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75336643 | AAATCTCCCAGAATC[A/G]GAACCCCATAATATG | 14697 |
| rs226348456 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75333460 | GTGCACCATGAGTGT[A/G]CCTAGTGCCCCCTAA | 14697 |
| rs226380077 | snp | C/G/T | | | intron-variant | Gnb5 | GRCm38.p3 | 9:75330069 | ATGCCCAAGTTACCT[C/G/T]TCTAGAGCACTTCTG | 14697 |
| rs226476361 | in-del | -/AAACAAC | | | intron-variant | Gnb5 | GRCm38.p3 | 9:75331671 | TCTAGACAAAAAAAA[-/AAACAAC]AAAAAAAAAAGAGTA | 14697 |
| rs226507896 | in-del | -/T/TT | | | intron-variant | Gnb5 | Mm_Celera | 9:75327705 | AATTCCATGAATGGC[-/T/TT]TTTTTTTTTCTTTTA | 14697 |
| rs226510889 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75329094 | GTGCTGACCCTGAGG[A/G]AAAACTCCCTAGAAA | 14697 |
| rs226666396 | snp | G/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75335164 | ATCTGGTTTGGGACC[G/T]GACAGTGCTGGACAG | 14697 |
| rs226671818 | snp | G/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75325206 | GGGGCCAGGTAGTCA[G/T]GATATAACTCTGGCT | 14697 |
| rs226684566 | snp | G/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75316743 | AGTACAGCAAAAATA[G/T]TCCCCTGCCTCAGCT | 14697 |
| rs226740589 | snp | C/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75329762 | GAAATTATTAATTTA[C/G]TGTTATTAATGTACT | 14697 |
| rs227004185 | snp | C/T | | | intron-variant, upstream-variant-2KB | Gnb5, LOC102636700 | Mm_Celera | 9:75312447 | GAACCATGGGCATAA[C/T]TGGTGTCAACAGGGC | 14697 |
| rs227118190 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75327764 | TTATTTTTGCTTTTT[A/G]GTTTTTGTCTGGTTT | 14697 |
| rs227145754 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75328161 | CCCCCAAATTAAGCA[A/G]CCTAGCACAGAGACA | 14697 |
| rs227150231 | snp | G/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75322739 | GACACGGAGAGAAAA[G/T]ATAATTGATGGTTGG | 14697 |
| rs227188217 | snp | C/T | | | intron-variant, upstream-variant-2KB | Gnb5, LOC102636700 | GRCm38.p3 | 9:75313953 | CTTAGAGCCAGGGAC[C/T]AGAGTTGGGGCCAGC | 14697 |
| rs227301266 | in-del | -/C | | | intron-variant | Gnb5 | GRCm38.p3 | 9:75334810 | CAAAACAAAACAAAA[-/C]AAACAAACAAACAAA | 14697 |
| rs227354093 | in-del | -/TT | | | intron-variant | Gnb5 | Mm_Celera | 9:75309138 | GTAAATGAGTGTGTG[-/TT]TTCATGGGGGTCTGT | 14697 |
| rs227403731 | snp | G/T | | | stop-lost, nc-transcript-variant | Gnb5 | Mm_Celera | 9:75344962 | TCTCAGGTTTGGGCA[G/T]AATCTTCTGACAGCG | 14697 |
| rs227446064 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75309185 | TGGGCACATGTGTGT[A/G]TGTTCATGAGTTCGT | 14697 |
| rs227482530 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75342523 | AGACCATTTAGTTCA[C/T]TATTGCCTAATAGAT | 14697 |
| rs227504207 | snp | C/T | | | intron-variant, upstream-variant-2KB | Gnb5, LOC102636700 | Mm_Celera | 9:75312931 | AGACAGAGACAAAGA[C/T]AGACAAACAGAGACA | 14697 |
| rs227560323 | snp | A/G | | | intron-variant, downstream-variant-500B | Gnb5, LOC102636700 | Mm_Celera | 9:75310332 | TCCCATGACAACCCT[A/G]CACGGTTTAAAGATA | 14697 |
| rs227602814 | snp | C/T | | | intron-variant, nc-transcript-variant | Gnb5, LOC102636700 | Mm_Celera | 9:75310896 | GCCTGGGCTGGGCTA[C/T]CTGAAACCTGTATCA | 14697 |
| rs227645694 | snp | C/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75306901 | GGTTTCTCTCTCTCT[C/G]TGTGTCTCTCTCTCT | 14697 |
| rs227675049 | snp | G/T | | | intron-variant, downstream-variant-500B | Gnb5, Myo5c | Mm_Celera | 9:75306658 | GCAATCAAACCCCAT[G/T]CGTACAGCTGATGGA | 14697 |
| rs227693885 | snp | C/T | | | utr-variant-3-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant | Myo5c, Gnb5 | Mm_Celera | 9:75305171 | TCCCTCAAACTGTTT[C/T]CCTTCCCTTCAGAGA | 14697 |
| rs227695323 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75307358 | ACCAGCAAGATGGCT[C/T]AGCAGGCCAAGCTAA | 14697 |
| rs227856667 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75308530 | GAACATTATAAACGC[C/T]GTCTATGACTTGGAA | 14697 |
| rs227857830 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75328555 | ATATTGTCCGAGTTA[A/G]GTTTCTATTGCTGTG | 14697 |
| rs227887245 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75324207 | AAACTTTGGAGAACA[A/G]TTGCAATTCTTGATT | 14697 |
| rs227889745 | snp | A/C | | | intron-variant | Gnb5 | Mm_Celera | 9:75328863 | AGATAACCCTGCCAC[A/C]TCGAGGCATGCCTTA | 14697 |
| rs227922016 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75324807 | GTGAGTTCCAGGACA[A/G]CCAGGGCTACACAGA | 14697 |
| rs227934176 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75307535 | ACATTGTGGTTTTAA[C/T]CTCTGACTCTGACCA | 14697 |
| rs227950721 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75319603 | TCCTTCCTTCTCCTG[A/G]TCTGTTGATTGGAGC | 14697 |
| rs227970571 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75308330 | CTCAGGTTGTCAGCC[C/T]TGGCAGCAGGCACCT | 14697 |
| rs228045857 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75344336 | GGTAGATAGGTGAGT[A/G]GGTGGGCGGAAGGGT | 14697 |
| rs228064100 | snp | A/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75329243 | TACAGGAGTTTAAGA[A/T]CCTCCTGGGCTACAT | 14697 |
| rs228126870 | snp | C/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75325458 | AGGAAGTCCTGAGAA[C/G]CCACATGATGGGGCT | 14697 |
| rs228132691 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75338166 | GTTCAGAAGGTACCA[C/T]GCACAGCATGGCTAA | 14697 |
| rs228232737 | in-del | -/AAGG | | | intron-variant | Gnb5 | Mm_Celera | 9:75318521 | GTTGACTCCTATAAA[-/AAGG]ACCCTCAGGGTTACA | 14697 |
| rs228255851 | in-del | -/C | | | intron-variant | Gnb5 | Mm_Celera | 9:75327584 | GTGGATTGTGTCTGA[-/C]CCCCTTTGATGACAA | 14697 |
| rs228309717 | snp | C/T | | | intron-variant | Gnb5 | GRCm38.p3 | 9:75326785 | CTTCTCCTCTCCTCT[C/T]CCAAAAGATATAAAA | 14697 |
| rs228313527 | in-del | -/TTGT | | | intron-variant, upstream-variant-2KB | Gnb5, LOC102636700 | Mm_Celera | 9:75315201 | TCTGGTGCAGCTAGA[-/TTGT]TGTCATTTATTTACC | 14697 |
| rs228363175 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75344702 | ACGGGTGGTGGCCTT[C/T]CTGAGCAATCTCTGC | 14697 |
| rs228364399 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75321552 | CCCATGACAGATGGT[C/T]TGTGAGCTACTGTGT | 14697 |
| rs228384909 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | Gnb5 | Mm_Celera | 9:75345279 | TTTCCTTGGATCTAG[C/T]CTGTCTTCAGAGCAC | 14697 |
| rs228402409 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75337631 | TTTATCCTCCCAAAG[C/T]GAGCCACTGTTTCTT | 14697 |
| rs228471753 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75327332 | TATTTCTAATCAGGC[A/G]GCGAAGGAAGAAAGA | 14697 |
| rs228486713 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75328933 | GCTACTGTGACTGAG[C/T]GTTCCCAGTAGCCTC | 14697 |
| rs228545873 | snp | A/G | | | intron-variant, nc-transcript-variant | Gnb5 | Mm_Celera | 9:75325037 | AGGAGTGTCTCTGAG[A/G]GGACAGTGGTGGGCT | 14697 |
| rs228606642 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75321064 | AGAGGTCCTGAGTTC[A/G]ATTCCCAACAACCTC | 14697 |
| rs228644159 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75325880 | AAGCCAGGCATGGGG[A/G]CACATGTCTGTCATC | 14697 |
| rs228681937 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75326224 | GCTCATTGTGAGTGA[A/G]CACCAGACAGGGACT | 14697 |
| rs228683656 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75320583 | TCAGGCTCGGACCAG[A/G]CAGTCTCTTAACTAA | 14697 |
| rs228714097 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75323206 | tagatagatagatag[A/G]taggcaggcacttgt | 14697 |
| rs228764582 | in-del | -/TTTATTTATTTATTTA | | | intron-variant | Gnb5 | GRCm38.p3 | 9:75341053 | ATACCTTAATTTTAT[-/TTTATTTATTTATTTA]TTTATTTATTTATTT | 14697 |
| rs228781124 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75326362 | GATGTGGGTCACTAA[A/G]TCTATGGTTCTGTAA | 14697 |
| rs228848483 | in-del | -/ATAT | | | intron-variant | Gnb5 | Mm_Celera | 9:75338599 | AATACACATACACGC[-/ATAT]ATACACACACACACA | 14697 |
| rs228874138 | snp | C/T | | | utr-variant-3-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant | Myo5c, Gnb5 | Mm_Celera | 9:75304445 | TGAGTTCCATGCCTA[C/T]ACCTTCTAGGAAAGA | 14697 |
| rs228932010 | in-del | -/C | | | utr-variant-3-prime, nc-transcript-variant | Gnb5 | Mm_Celera | 9:75345174 | AAGCCCTTCTGTCAT[-/C]TCAAAAACTCTGCTA | 14697 |
| rs229026263 | snp | A/C | | | intron-variant | Gnb5 | Mm_Celera | 9:75327725 | TTTTTCTTTTAATAT[A/C]AGAGTGTATTTGTTT | 14697 |
| rs229045967 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75318339 | AAGCCCACAGTGACA[C/T]ACCTACTCCAACAAG | 14697 |
| rs229047961 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75324019 | TTAACTTGATTCTTT[C/T]TGGCCACTGCCTGGC | 14697 |
| rs229083406 | in-del | -/AA | | | intron-variant | Gnb5 | Mm_Celera | 9:75334800 | AAAACAAAACAAAAC[-/AA]AAAACAAAACAAACA | 14697 |
| rs229153145 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75326441 | TGGAAGATGACCATG[A/G]GGGGCACAGTTGTCA | 14697 |
| rs229187458 | snp | A/C | | | intron-variant | Gnb5 | Mm_Celera | 9:75322500 | CCAGTGTGCTCCTCG[A/C]GTCTTATAAAATTAA | 14697 |
| rs229208871 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75341185 | CAGAAATCCGCCTGC[C/T]TCTGCCTCCCAAGTG | 14697 |
| rs229251986 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | Gnb5 | Mm_Celera | 9:75345477 | AATTATCTTTTTTCA[A/G]CCTGTTCAGTTGTCT | 14697 |
| rs229259871 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75322473 | AACCAGTTAGCATTC[C/T]TACTGTAGAAACCAG | 14697 |
| rs229353529 | snp | A/T | | | utr-variant-3-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant | Myo5c, Gnb5 | Mm_Celera | 9:75304572 | ACTACTCCCTTTAGA[A/T]ACTCTAAGAGGGTAT | 14697 |
| rs229383732 | in-del | -/ACAC | | | intron-variant | Gnb5 | Mm_Celera | 9:75316553 | CACACAGGCACACAT[-/ACAC]ACACATATACACATG | 14697 |
| rs229440618 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75326748 | GACCGGCATTAGCCA[C/T]GCCTCTCCCCTCCTC | 14697 |
| rs229504394 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75339336 | GATTAAAGACTTACC[A/G]AGGGATGTAGCTCAG | 14697 |
| rs229536606 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75339847 | TGATGTGGCTCTGTC[C/T]TTCTGACTCCGTTGT | 14697 |
| rs229569685 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75324723 | GCAATGTTGGCGCAC[A/G]CCTTTAATCCCAGCA | 14697 |
| rs229615469 | in-del | -/TACCCC | | | intron-variant | Gnb5 | Mm_Celera | 9:75343898 | GCAGCCACTTTCTGG[-/TACCCC]TACCCAAGCATCGAA | 14697 |
| rs229680139 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75341994 | CTCGGAGATTAGAGA[A/G]CTTGGTGCCCTCCCA | 14697 |
| rs229713308 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75342652 | AGCAGTGAACACCCA[A/G]CCCATCGATTTCCAC | 14697 |
| rs229714857 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75334630 | CCTACATGTATGCAT[C/T]GCCTGTGGAGGCCAG | 14697 |
| rs229740236 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75324168 | TTATTACTTTGGCTA[C/T]AGGCCTGGGAATAGG | 14697 |
| rs229750511 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75335284 | GGAACAGTATTTCCT[A/G]GAGCAAGTAGCTAGG | 14697 |
| rs229878212 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75320326 | GTGTTGTCTAGATCA[C/T]GTCTAGTTAGATATT | 14697 |
| rs229905335 | snp | A/C | | | intron-variant | Gnb5 | Mm_Celera | 9:75322004 | TGCAGTCAAGGACAA[A/C]CACAAAAAGATAGAT | 14697 |
| rs229913771 | in-del | -/TGTGTGTGTGTGTGTCTCTGTGTG | | | intron-variant | Gnb5 | GRCm38.p3 | 9:75309204 | TCATGAGTTCGTGTC[-/TGTGTGTGTGTGTGTCTCTGTGTG]TGTGTGTGTGTGTGT | 14697 |
| rs229927055 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75318832 | TCTAGTACAGGTCAC[C/T]CTTCTCCATGTTTCA | 14697 |
| rs230134873 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75341822 | AGTTTTGTTACAAGT[A/G]GCAAATTATATTGAT | 14697 |
| rs230199509 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75319040 | CGCCGTAGGAAGGAC[A/G]GAGTTTTAGGATGGT | 14697 |
| rs230294894 | snp | C/T | | | intron-variant | Gnb5 | GRCm38.p3 | 9:75326796 | CTCTCCCAAAAGATA[C/T]AAAAGATAAAATCCT | 14697 |
| rs230324852 | snp | G/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75319690 | GGGCAGTTAGATAAT[G/T]CGAAGGAGGAGTTTC | 14697 |
| rs230328271 | snp | G/T | | | intron-variant, upstream-variant-2KB | Gnb5, LOC102636700 | Mm_Celera | 9:75313589 | GCTTGAAGGAGGGAT[G/T]GGGGGAGGGGGTGTG | 14697 |
| rs230338983 | in-del | -/CTACCTG/TCTCTACCTG | | | intron-variant | Gnb5 | Mm_Celera | 9:75316691 | GTAACCCCATCTTCT[-/CTACCTG/TCTCTACCTG]TCTATGCCTCCCCAG | 14697 |
| rs230355066 | snp | C/T | | | intron-variant, upstream-variant-2KB | Gnb5, LOC102636700 | Mm_Celera | 9:75314391 | CGTGGAGCGTGAGTG[C/T]GAGCAGGGGGTGGAA | 14697 |
| rs230391363 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75340843 | CCCTCTGACAAGTTC[C/T]CGGAATTCCAAACAT | 14697 |
| rs230395747 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75325324 | TTTTATAGGGACTCC[A/G]TACCTTTGCTCTTCT | 14697 |
| rs230470084 | snp | G/T | | | upstream-variant-2KB, intron-variant | Gnb5, Myo5c | Mm_Celera | 9:75306047 | GCACAAGGATGTCAG[G/T]TTTGTTCCATGGAGT | 14697 |
| rs230522202 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75329335 | TTCTTATATCAATAT[A/G]TGTTTTACACACACA | 14697 |
| rs230557217 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75317029 | CTTGAGATTTCCTGA[A/G]GCCCGAGTGACCTGA | 14697 |
| rs230616246 | snp | G/T | | | intron-variant, upstream-variant-2KB | Gnb5, LOC102636700 | Mm_Celera | 9:75315207 | GCAGCTAGATTGTTG[G/T]CATTTATTTACCCAG | 14697 |
| rs230616297 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75320654 | CTAAGGCTGGGGTGT[C/T]CCCAGTGCCTGAATG | 14697 |
| rs230660626 | snp | A/G | | | intron-variant, upstream-variant-2KB | Gnb5, LOC102636700 | Mm_Celera | 9:75315554 | ACAGCTCAGCCCTGT[A/G]GCTTGAGCAGTCTTT | 14697 |
| rs230665338 | in-del | -/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75319844 | CATCTATCTCAATAG[-/T]TTCCTCCTGCTATGT | 14697 |
| rs230672872 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75344378 | GGGTAGATAGATGGA[C/T]GGATGATGAAATTAA | 14697 |
| rs230682602 | in-del | -/GTGTAC | | | intron-variant | Gnb5 | Mm_Celera | 9:75324461 | AGGTGCATATGGAGT[-/GTGTAC]GTGTGAGTGAAAGGA | 14697 |
| rs230690290 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75317395 | ATAATGAGTTTGAAG[C/T]CAGCCCCTGTTTAAA | 14697 |
| rs230691935 | snp | A/G | | | intron-variant, nc-transcript-variant | Gnb5, LOC102636700 | Mm_Celera | 9:75310508 | CATTCTGCGCACACA[A/G]CTACAGGCTGGGGCC | 14697 |
| rs230694459 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75336815 | TTCCCAGGTCAGCAT[A/G]CTGGTGAGGTACAGG | 14697 |
| rs230724599 | snp | A/G | | | intron-variant | Gnb5, LOC102636700 | Mm_Celera | 9:75310996 | GAAATCTATTCCCTG[A/G]CTCCCCCAACTCATT | 14697 |
| rs230743171 | snp | A/G | | | intron-variant, upstream-variant-2KB | Gnb5, LOC102636700 | Mm_Celera | 9:75316222 | GCTGGGAGCAAGCGG[A/G]GGCCAGAGGGAGCAG | 14697 |
| rs230843673 | snp | A/G | | | intron-variant, upstream-variant-2KB | Gnb5, LOC102636700 | Mm_Celera | 9:75316047 | TTTACTTCTTCCTCC[A/G]CAGAAAATGGAAGAA | 14697 |
| rs230952969 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75332068 | GATAGGGCACAGCAA[A/G]ATAAACCTGTTAAAC | 14697 |
| rs231004242 | in-del | -/CC | | | intron-variant | Gnb5 | GRCm38.p3 | 9:75326769 | CCCCTCCTCTCCCCT[-/CC]CTTCTCCTCTCCTCT | 14697 |
| rs231026621 | snp | G/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75336462 | CTCAGTCTGTCCTCA[G/T]TGAGACTCTCAGGGT | 14697 |
| rs231079468 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75336923 | TTGATTTAGACACCA[C/T]CAACCCTTCCTTTGG | 14697 |
| rs231126630 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75325815 | TGGGCTGTTAGTGTG[C/T]GGTACCATGAGGGTG | 14697 |
| rs231129061 | in-del | -/AA | | | intron-variant | Gnb5 | Mm_Celera | 9:75306971 | CACACACACACACAC[-/AA]ACACACACACACAGC | 14697 |
| rs231135219 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75330454 | TGGGCATTTCCGAGC[A/G]CTCTCGGTGCATCCC | 14697 |
| rs231209731 | snp | A/T | | | intron-variant, upstream-variant-2KB | Gnb5, LOC102636700 | Mm_Celera | 9:75312202 | ACCAGGCTGCACGCA[A/T]AGCTATGGCTCACTA | 14697 |
| rs231227595 | in-del | -/G | | | intron-variant, upstream-variant-2KB | Gnb5, LOC102636700 | Mm_Celera | 9:75312883 | CAAATATAGATAAAT[-/G]GGGGGCGGGGGGTTG | 14697 |
| rs231256627 | snp | C/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75320446 | CTCAAGCTGTATGCA[C/G]GTAGGACTGGCTGTC | 14697 |
| rs231400705 | in-del | -/TTTTTC | | | intron-variant | Gnb5 | GRCm38.p3 | 9:75329438 | GCCCAACCTTTTTTT[-/TTTTTC]TTTTGTAACTTTTGT | 14697 |
| rs231404128 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75325488 | TTCTCCTGAACCATG[C/T]AGACAATTCGAGTGT | 14697 |
| rs231477374 | in-del | -/GTCCCT | | | downstream-variant-500B, upstream-variant-2KB | Gnb5, Bcl2l10 | Mm_Celera | 9:75345946 | CCTGTGTATTACAAG[-/GTCCCT]GCTTTTTCTTCCTTT | 14697 |
| rs231483179 | in-del | -/ATAA | | | utr-variant-3-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant | Myo5c, Gnb5 | Mm_Celera | 9:75304757 | TAGATAGATAGATAG[-/ATAA]ATAGATAAATAGATA | 14697 |
| rs231507706 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75338858 | CCCTTTCTGTCCTCA[C/T]CCACTTCTGTCAGAA | 14697 |
| rs231612579 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75333355 | TCACACACACACACA[C/T]ACACACAAACAATAC | 14697 |
| rs231702014 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75328684 | TAGGCAGGAACCTCC[A/G]GGCAGGAACTGGAGC | 14697 |
| rs231738907 | snp | A/C/T | | | intron-variant | Gnb5 | GRCm38.p3 | 9:75329414 | CTGGTTCAGCTTTTT[A/C/T]AAAAGAGGGCCCAAC | 14697 |
| rs231800703 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75332212 | GAGCACATGGCAGGT[A/G]AGGCAGGAAACTGCA | 14697 |
| rs231805681 | snp | A/C/T | | | intron-variant | Gnb5 | GRCm38.p3 | 9:75316912 | GTTTGAGGGATCCCC[A/C/T]TGTCTCTGCCTCCCT | 14697 |
| rs231899091 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75342018 | CCTCCCAGAGGACCC[A/G]AGTTCAATGCCAGCA | 14697 |
| rs231908061 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75329584 | TCCAGCTCCGGGGGA[C/T]TGAGTCACCTCCTTT | 14697 |
| rs231931873 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75319799 | TAAACACTCTTGGGA[C/T]TGTATTAAATGTATT | 14697 |
| rs231939781 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75325729 | TAGACCATTGTGGGA[A/G]GCAGTCACCGGGTGT | 14697 |
| rs231969681 | snp | C/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75338774 | ACATCGCTTTAAAAA[C/G]TATGTACTATGTATT | 14697 |
| rs232004404 | snp | A/G | | | intron-variant | Gnb5 | GRCm38.p3 | 9:75331694 | AAAAAAAAAGAGTAA[A/G]ATGGAAAGCTGAGCC | 14697 |
| rs232012330 | in-del | -/CC | | | intron-variant | Gnb5 | Mm_Celera | 9:75339567 | AAACAAACAAATTAA[-/CC]CCCCACACACACTCT | 14697 |
| rs232087471 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75318201 | CATTATCATCAAGAC[A/G]GGAACACAGCATCCA | 14697 |
| rs232134395 | snp | A/G | | | intron-variant, upstream-variant-2KB | Gnb5, LOC102636700 | Mm_Celera | 9:75312647 | ACATACACTTATGTA[A/G]TCTGTTTTATCCATG | 14697 |
| rs232139978 | in-del | -/AAACAAAACAAAC | | | intron-variant | Gnb5 | GRCm38.p3 | 9:75334802 | AAACAAAACAAAACA[-/AAACAAAACAAAC]AAACAAACAAACAAA | 14697 |
| rs232168067 | in-del | -/ACACACACACTT | | | intron-variant | Gnb5 | GRCm38.p3 | 9:75329344 | CAATATATGTTTTAC[-/ACACACACACTT]ACACACACACACACA | 14697 |
| rs232169953 | snp | G/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75320053 | AAGACAGCTCTGTCC[G/T]GATGGATGGTTGGTC | 14697 |
| rs232201025 | snp | C/T | | | intron-variant, upstream-variant-2KB | Gnb5, LOC102636700 | Mm_Celera | 9:75314914 | CTTATGTGCAGTTCC[C/T]CCACCCACGGCACAC | 14697 |
| rs232282580 | snp | C/T | | | intron-variant | Gnb5 | GRCm38.p3 | 9:75317906 | CCATTCCCTACACCC[C/T]CTACACCCGCAGTCT | 14697 |
| rs232335272 | snp | G/T | | | intron-variant, upstream-variant-2KB | Gnb5, LOC102636700 | Mm_Celera | 9:75314527 | GGCGGGTGGAGAGGC[G/T]CAGGCTGCAGGTGCC | 14697 |
| rs232342943 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75321968 | CCGGGTTCCCTCCCC[A/G]GTGTCATCCCTAGAC | 14697 |
| rs232356560 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75336175 | GCTCAGGGCTTGGGA[C/T]GCTCCCATCCCACAT | 14697 |
| rs232381486 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75317273 | CTATGTAAAGGTCTG[A/G]GTTCCATTCTCTGCA | 14697 |
| rs232421657 | snp | A/G | | | intron-variant, upstream-variant-2KB | Gnb5, LOC102636700 | Mm_Celera | 9:75313115 | GAAATGGAAGCTCCC[A/G]GAATCTCACCCAAAA | 14697 |
| rs232423325 | in-del | -/CCACC | | | utr-variant-5-prime, downstream-variant-500B | Gnb5, Myo5c | Mm_Celera | 9:75306346 | CTCGTTTCTGGCCAG[-/CCACC]CCAGGTGTTCATTGC | 14697 |
| rs232459866 | snp | C/T | | | intron-variant, upstream-variant-2KB | Gnb5, LOC102636700 | Mm_Celera | 9:75315091 | AAGTTGGGAAGGGGC[C/T]GCAAGCGCCTGTGTG | 14697 |
| rs232461725 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75307801 | TCCCATTGGCATGGA[A/G]CTATCTCTGATTCTC | 14697 |
| rs232488109 | snp | G/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75340125 | GATGCCTTCCTGGGG[G/T]TCCTGAGCGGGGTCA | 14697 |
| rs232497869 | snp | C/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75308740 | TCTTAATCTCTCCCT[C/G]TGGTTCATCTCCCTG | 14697 |
| rs232595268 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75339154 | CCCTCCACCTTCTAC[A/G]TCTACACAAACATAT | 14697 |
| rs232707348 | snp | C/T | | | intron-variant | Gnb5, LOC102636700 | Mm_Celera | 9:75311125 | AAATTAACTGCATTG[C/T]AATGTTTTTTATGGC | 14697 |
| rs232802469 | snp | C/T | | | downstream-variant-500B, upstream-variant-2KB, intron-variant | Myo5c, Gnb5 | Mm_Celera | 9:75305471 | ATGCACCATTTTTTT[C/T]CTACCATTGTAGATT | 14697 |
| rs232804958 | snp | C/G | | | intron-variant, upstream-variant-2KB | Gnb5, LOC102636700 | GRCm38.p3 | 9:75314021 | CCCCCACCCCACCCC[C/G]ACTCCCATCCCCTCA | 14697 |
| rs232835816 | snp | A/T | | | utr-variant-3-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant | Myo5c, Gnb5 | Mm_Celera | 9:75304835 | TCTTTTTTCTGAAAT[A/T]TTTAAAACTTGTTAT | 14697 |
| rs232885793 | in-del | -/TGTG | | | intron-variant | Gnb5 | Mm_Celera | 9:75329636 | ACCTGCACACACACA[-/TGTG]CACACACACACACAC | 14697 |
| rs232991252 | in-del | -/A | | | intron-variant | Gnb5 | Mm_Celera | 9:75326071 | TCATGATATAGGAGG[-/A]GGGGTGGCATCTGAT | 14697 |
| rs233003172 | in-del | -/AGATAGATCTGTATCACTC | | | intron-variant | Gnb5 | Mm_Celera | 9:75322012 | AGGACAAACACAAAA[-/AGATAGATCTGTATCACTC]AGATGACAGTACACC | 14697 |
| rs233023746 | snp | C/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75335193 | AGGAAGCCTGGCAAG[C/G]TGTGGGTCTTTAAAT | 14697 |
| rs233077737 | snp | A/T | | | intron-variant | Gnb5 | GRCm38.p3 | 9:75329447 | TTTTTTTTTTTCTTT[A/T]GTAACTTTTGTAAAA | 14697 |
| rs233140801 | in-del | -/TG | | | intron-variant, upstream-variant-2KB | Gnb5, LOC102636700 | Mm_Celera | 9:75312390 | ATACATACATATACA[-/TG]TACATATACAAATGA | 14697 |
| rs233193625 | in-del | -/A | | | intron-variant | Gnb5 | Mm_Celera | 9:75336623 | CTGTGCAGATTCATC[-/A]AAAAAAATCTCCCAG | 14697 |
| rs233234003 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75323930 | AAAACTAAGTCAAAA[C/T]ACTGGGACTTTTCAG | 14697 |
| rs233282941 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75340898 | AGTTGGTAAAACCAC[A/G]CTTTTGCTAGAGCAC | 14697 |
| rs233329083 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75333673 | GTTACAGATGGTTGT[A/G]AGCTGCCATGTGGGT | 14697 |
| rs233335999 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75341392 | AATATCTATTTGTAT[A/G]TTTGTCTTTTTCACA | 14697 |
| rs233463358 | snp | A/G | | | intron-variant, upstream-variant-2KB | Gnb5, LOC102636700 | Mm_Celera | 9:75316250 | CAGGGCTGGAGCAAG[A/G]GGGAGAACGGGAAGT | 14697 |
| rs233531749 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75327365 | CGTCCTGTCCACAGG[C/T]CCCGTCTCCTCTTTA | 14697 |
| rs233635098 | in-del | -/CAAAT | | | intron-variant | Gnb5 | Mm_Celera | 9:75339559 | AAAGAAAGAAACAAA[-/CAAAT]TAACCCCCCACACAC | 14697 |
| rs233644654 | snp | G/T | | | intron-variant, downstream-variant-500B | Gnb5, LOC102636700 | Mm_Celera | 9:75310193 | AGCCCTTCTGGCTGT[G/T]TCCTCTTCCTTCCCA | 14697 |
| rs233689983 | in-del | -/GAGT | | | intron-variant | Gnb5 | Mm_Celera | 9:75344407 | AATTGGTGAATGAGA[-/GAGT]GAGTGAGTGAGTGAA | 14697 |
| rs233725265 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75336872 | TCTGCTGAAGGTTGG[C/T]TCTACAACGCCAACA | 14697 |
| rs233735964 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75323222 | TAGGCAGGCACTTGT[A/G]CACATTAAATAAAAA | 14697 |
| rs233738771 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75328251 | ATGGTTGGCTGACTG[C/T]GTGACTGGGGTTTCC | 14697 |
| rs233854131 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75323635 | TTGAGGCACGGGGCA[C/T]AGCACAGCACCAAGG | 14697 |
| rs233958451 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75309452 | CAACTACACTGCCCA[A/G]CCAATGAGTCCCAGA | 14697 |
| rs233974356 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75331411 | CTAAGAGGTATTTTC[C/T]AGCCCGATCTTCCGA | 14697 |
| rs234033343 | snp | A/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75327102 | CCTCAGCGCCTGGCC[A/T]CAGCGCCTAATTGTG | 14697 |
| rs234059939 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75326046 | GAATCCATCCCCAGA[C/T]GGTACTTTTTCATGA | 14697 |
| rs234093553 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75326521 | CCATGAAAGAGACAC[C/T]CTTCCCACCCCACTG | 14697 |
| rs234139887 | snp | A/G | | | downstream-variant-500B, upstream-variant-2KB, intron-variant | Myo5c, Gnb5 | Mm_Celera | 9:75305881 | CGATGACAAGGGTTC[A/G]AGTGTAGGAGACCTT | 14697 |
| rs234180503 | in-del | -/ACTGAG | | | intron-variant | Gnb5 | Mm_Celera | 9:75330029 | TTCAGCCTCTTAGGT[-/ACTGAG]ACTACAGGCCTACAT | 14697 |
| rs234229957 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75321233 | TAAAGCTTTCCACCC[A/G]TGCCAATTCAACACA | 14697 |
| rs234237722 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75327789 | TGGTTTTGTTGTGGT[C/T]GTTTCTTTTTAACTA | 14697 |
| rs234336479 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75331221 | GCTGTATTGCGAATG[A/G]CTGGCTTTGCTAACC | 14697 |
| rs234361289 | snp | C/T | | | intron-variant, upstream-variant-2KB | Gnb5, LOC102636700 | Mm_Celera | 9:75315873 | GTGTATGCACCCTCC[C/T]ACCTCCTCCTGTTGA | 14697 |
| rs234374158 | snp | G/T | | | intron-variant | Gnb5 | GRCm38.p3 | 9:75326907 | CACACGGAGACAGGC[G/T]CTATAGTCTACTGTC | 14697 |
| rs234503657 | in-del | -/A | | | utr-variant-3-prime, nc-transcript-variant | Gnb5 | Mm_Celera | 9:75345578 | ACATGCAGAAAACAG[-/A]AAAAAAAAACTGTAT | 14697 |
| rs234549508 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75307084 | AGCTGCTACATCCTC[A/G]CCCATGCTTTGTATA | 14697 |
| rs234592943 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75329476 | AAGTATGAAGGTGTA[C/T]ATGTTCTGGGATGGA | 14697 |
| rs234596763 | in-del | -/TTTTA | | | intron-variant | Gnb5 | Mm_Celera | 9:75307323 | TATCAATTTTTTTTT[-/TTTTA]AATTAGGTATCCTAG | 14697 |
| rs234629206 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75325657 | ATAGAAACTGATTAT[A/G]ATCTGGCAGGTACAG | 14697 |
| rs234649784 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75328189 | ACATCATACATGAGC[A/G]CCAGTTTTTGCTCCA | 14697 |
| rs234685369 | in-del | -/AAAC | | | intron-variant | Gnb5 | Mm_Celera | 9:75339552 | AATAAGTAAAGAAAG[-/AAAC]AAACAAATTAACCCC | 14697 |
| rs234763620 | snp | C/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75325181 | ATTTTCGCTTTGTTT[C/G]TTTTGTTTTGGGGCC | 14697 |
| rs234831286 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75328602 | AAAAGCAACATGGGG[A/G]CGGGGGTACTTCAGC | 14697 |
| rs234837477 | in-del | -/TTT | | | downstream-variant-500B, upstream-variant-2KB | Gnb5, Bcl2l10 | Mm_Celera | 9:75346196 | TATTCATCTATTTGA[-/TTT]TTTTTTTTTAATTCT | 14697 |
| rs234868521 | snp | G/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75324265 | ATTTGATTTGACAGT[G/T]ATTATGCAATGTCTT | 14697 |
| rs234956426 | snp | C/G | | | intron-variant, upstream-variant-2KB | Gnb5, LOC102636700 | Mm_Celera | 9:75313428 | GATCCTCCTTCCCAT[C/G]CTAAAGTTCACAGAA | 14697 |
| rs235071241 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75324465 | GCATATGGAGTGTGT[A/G]CGTGTGAGTGAAAGG | 14697 |
| rs235124429 | in-del | -/C | | | intron-variant | Gnb5 | Mm_Celera | 9:75321235 | AGCTTTCCACCCATG[-/C]CCAATTCAACACATG | 14697 |
| rs235182480 | snp | A/C | | | intron-variant | Gnb5 | Mm_Celera | 9:75322123 | GTTCCTCTGCTGTCT[A/C]GAATTACATCACACC | 14697 |
| rs235196719 | snp | C/T | | | intron-variant | Gnb5, LOC102636700 | Mm_Celera | 9:75311529 | AGAGATCGTGAGTTC[C/T]GCTTTTCATCTTGTT | 14697 |
| rs235207810 | snp | C/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75326573 | CACCACCCCCGGTTG[C/G]TGAAAGGCATAGGAG | 14697 |
| rs235247356 | in-del | -/TGTCTC | | | intron-variant | Gnb5 | Mm_Celera | 9:75306904 | TTCTCTCTCTCTCTG[-/TGTCTC]TCTCTCTCTGTGTCT | 14697 |
| rs235247571 | snp | G/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75321271 | TAGTGTCCAAATACA[G/T]CAAAAGTCTTGGCAC | 14697 |
| rs235259404 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | Gnb5 | Mm_Celera | 9:75345105 | GTGTCTCCATGAAAT[C/G]TGCCCCCTCCCTGGA | 14697 |
| rs235322704 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75337793 | ACACCTATATACCAT[A/G]GGGAGACAGAACAGG | 14697 |
| rs235352772 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75338835 | ACATTGTGAACATTT[C/T]CCATCCACCCTTTCT | 14697 |
| rs235393418 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | Gnb5 | Mm_Celera | 9:75345728 | ACAGGCCACTAAACT[A/G]ATTTAAAAGCCTGCT | 14697 |
| rs235558422 | in-del | -/AAC | | | intron-variant | Gnb5 | Mm_Celera | 9:75338061 | TTTCAGTCAAAAAAA[-/AAC]CCCTATCCAGCCAGG | 14697 |
| rs235574482 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75337765 | TCAGGAAACAAAGCA[A/G]ATACAAAAAGATACA | 14697 |
| rs235582424 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75333475 | ACCTAGTGCCCCCTA[A/G]GTCAGAAGAAATGCC | 14697 |
| rs235590132 | in-del | -/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75336235 | TGGATGCAAGAAACA[-/G]AAGAGGAACTATAGG | 14697 |
| rs235597913 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75320069 | GATGGATGGTTGGTC[C/T]CCCAGACTGAGAGAT | 14697 |
| rs235606099 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75309416 | CCTGTTTTGAAATAG[A/G]ATCTCCCTCTCTTTG | 14697 |
| rs235619804 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75333884 | ATGCACATGTGCACC[C/T]GGTCTACTTAGAAGT | 14697 |
| rs235662140 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75343842 | CAGAAGCCAAGCCAG[C/T]GTTGAGGGGACACCG | 14697 |
| rs235844553 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75342845 | GGGTTGCGCTTACTG[A/G]CACGCTCCTCCTGGC | 14697 |
| rs235852725 | snp | A/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75318414 | AGAAACTATCACACT[A/T]TAAGAGGTCACAGCC | 14697 |
| rs235897136 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75343669 | AAAGAACGAACCAGC[A/G]CTCTGCCAAGCTTCC | 14697 |
| rs235986700 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75323269 | AAGAATTAAATAGGA[C/T]GTGCTCCCTAGTGGT | 14697 |
| rs235988563 | snp | G/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75317614 | GCCTGAAGTAGCTCA[G/T]GTGGCTTACATGACA | 14697 |
| rs235991189 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75329100 | ACCCTGAGGGAAAAC[C/T]CCCTAGAAAGTTCGG | 14697 |
| rs236021510 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75318046 | ACCCCCACCACAAAA[C/T]TATTTCACTGCTATT | 14697 |
| rs236108210 | snp | C/T | | | intron-variant | Gnb5 | GRCm38.p3 | 9:75317480 | GAAACCGGAAGGGAT[C/T]GATCGATCGATCAAT | 14697 |
| rs236113553 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75325271 | CTCCTGGGTGCTGGG[A/G]TTACAGATGTGCACC | 14697 |
| rs236118604 | snp | A/C | | | intron-variant | Gnb5 | Mm_Celera | 9:75341239 | CCACTGCCTGGCTTA[A/C]TTTTATTTTTTTTAA | 14697 |
| rs236141267 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75317877 | TGTAACCTCTGACTG[C/T]GTGACTGGGTGAGCC | 14697 |
| rs236167139 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75339858 | TGTCCTTCTGACTCC[A/G]TTGTCCCTGTGCTCT | 14697 |
| rs236207610 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75340566 | CTAGTACTTAACCCT[A/G]ATTCCTTGAACTAAC | 14697 |
| rs236211777 | snp | G/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75325966 | ACCTGCCTGAGTGAA[G/T]CGAGAAACTGTTTGT | 14697 |
| rs236288571 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75339648 | CGAGAAGAAGATGAC[C/T]GCAGGAATAGCCACT | 14697 |
| rs236338945 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75339377 | GCTTAACTTATGTAC[A/G]TGGTCCTGAGTTCTC | 14697 |
| rs236362722 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75333206 | TGCAGGTTGATGACC[C/T]AAGTCCAATCCTGGA | 14697 |
| rs236397264 | snp | C/T | | | intron-variant, upstream-variant-2KB | Gnb5, LOC102636700 | Mm_Celera | 9:75315618 | AGCCCCCCACTGTAG[C/T]ACAGTTCTGCAGCCC | 14697 |
| rs236406524 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75328281 | CTTGCTCAAGTGGCT[A/G]TCGGCTGATGCCTCT | 14697 |
| rs236435350 | snp | A/G | | | intron-variant, upstream-variant-2KB | Gnb5, LOC102636700 | Mm_Celera | 9:75316220 | GGGCTGGGAGCAAGC[A/G]GAGGCCAGAGGGAGC | 14697 |
| rs236437947 | in-del | -/A | | | intron-variant | Gnb5 | Mm_Celera | 9:75326075 | ATATAGGAGGAGGGG[-/A]TGGCATCTGATGGGC | 14697 |
| rs236476409 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75309543 | CTCGCTCTTCATGCA[A/G]GCCTAGCAATCGACA | 14697 |
| rs236476708 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75316608 | TCCACACAGAGGCAT[C/T]CACACATACACGCAC | 14697 |
| rs236517570 | snp | C/T | | | intron-variant, downstream-variant-500B | Gnb5, LOC102636700 | Mm_Celera | 9:75310095 | CATCATCCCTTCAAG[C/T]CTCACTTCCTCCTCT | 14697 |
| rs236548831 | in-del | -/T | | | intron-variant, nc-transcript-variant | Gnb5, LOC102636700 | Mm_Celera | 9:75310596 | GCCACACAAATGGCC[-/T]TTTCCCCTCTGGCTG | 14697 |
| rs236580152 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75323570 | TTTCTCCTTCTGCTC[C/T]GATGAATTCTGTGAA | 14697 |
| rs236592217 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75336751 | GACTTGCTACCCTCT[C/T]CCCTAATTGTTCAAT | 14697 |
| rs236662874 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75342747 | GAAAGGGGTCTTTGG[C/T]TTACACTTGCATATC | 14697 |
| rs236700133 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75335857 | GATGCTGGCAGTTGG[C/T]TCTTGTTCTTGGGTC | 14697 |
| rs236750461 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75307150 | GTGCATGTTGGGGTG[C/T]GGGGTAGGTATAATA | 14697 |
| rs236791989 | in-del | -/G | | | intron-variant | Gnb5, LOC102636700 | Mm_Celera | 9:75311258 | TGAACTGCGTGCACA[-/G]GAAGTCAGCACTCAC | 14697 |
| rs236883069 | in-del | -/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75335945 | ACCCACAGCAGTCTC[-/G]GCACCCCTTCCTCCG | 14697 |
| rs236942266 | snp | C/T | | | intron-variant | Gnb5 | GRCm38.p3 | 9:75326896 | TATCCACCTGTCACA[C/T]GGAGACAGGCGCTAT | 14697 |
| rs236955064 | snp | G/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75320729 | AGTCTTAAAGGAATG[G/T]AAATCTGTTCTCAAG | 14697 |
| rs236992579 | snp | C/T | | | intron-variant, upstream-variant-2KB | Gnb5, LOC102636700 | Mm_Celera | 9:75316084 | AAGAGACCTGGGGGG[C/T]TGGTGAGATGGCTCA | 14697 |
| rs237111453 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75319344 | CTGTTTGTTCTAAGT[A/G]TGTTTTTGTGACAGG | 14697 |
| rs237145698 | snp | A/T | | | intron-variant, upstream-variant-2KB | Gnb5, LOC102636700 | GRCm38.p3 | 9:75313792 | TCATTTTTAAAAGAA[A/T]TTTTCGATTAGTGGG | 14697 |
| rs237183250 | snp | C/T | | | intron-variant, upstream-variant-2KB | Gnb5, LOC102636700 | Mm_Celera | 9:75314682 | GCTTTCTGCGTCCGC[C/T]GGCTCAGTTTGCGGT | 14697 |
| rs237191263 | snp | G/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75319702 | AATGCGAAGGAGGAG[G/T]TTCTTTAACAGCCCC | 14697 |
| rs237372819 | in-del | -/CACACACA | | | intron-variant | Gnb5 | GRCm38.p3 | 9:75329626 | CACTAGACTCACCTG[-/CACACACA]CACACACACACACAC | 14697 |
| rs237447985 | snp | C/T | | | intron-variant, downstream-variant-500B | Gnb5, LOC102636700 | Mm_Celera | 9:75309889 | TCCACCCAAACACAC[C/T]TCTCTCAAATTCTCC | 14697 |
| rs237490290 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | Gnb5 | Mm_Celera | 9:75344971 | TGGGCATAATCTTCT[C/G]ACAGCGTTCAAGAAT | 14697 |
| rs237598554 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75321670 | AAAGTATCTGCCGTG[A/G]TATTTAACACCCAGC | 14697 |
| rs237631205 | snp | C/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75317051 | GTGACCTGAACCACC[C/G]ACGTGTTTGGTTTTT | 14697 |
| rs237645410 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75337929 | CCACACTATAAAAAC[A/G]CTGAGCTCAGGAAGC | 14697 |
| rs237645518 | snp | A/C | | | intron-variant | Gnb5 | Mm_Celera | 9:75330760 | CCTCAAGCCCTCCCC[A/C]AGTGACATACTTCCT | 14697 |
| rs237648880 | in-del | -/A | | | intron-variant | Gnb5 | GRCm38.p3 | 9:75334810 | AAAACAAAACAAAAC[-/A]AAACAAACAAACAAA | 14697 |
| rs237683178 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75331346 | CTTAGCATTACCCAG[A/G]GGTGGTAGAGAAAGA | 14697 |
| rs237809886 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75338953 | CCATTCGAAGAGCCA[A/G]CTTCAGTCTCTGGCA | 14697 |
| rs237853574 | in-del | -/CA | | | intron-variant | Gnb5 | Mm_Celera | 9:75337501 | ACATATATACACACT[-/CA]TACACACACACACAC | 14697 |
| rs237900069 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75340362 | GAACAGAAAATACTA[C/T]AGGAAAACATCAGGC | 14697 |
| rs237938752 | in-del | -/CATTGCCTGGTCAAGTGAGGGC | | | intron-variant | Gnb5 | Mm_Celera | 9:75332515 | GGTTAGCAGCTGCAG[-/CATTGCCTGGTCAAGTGAGGGC]CATTTTCCAGGGCAG | 14697 |
| rs238017484 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | Gnb5 | Mm_Celera | 9:75344986 | GACAGCGTTCAAGAA[C/T]GTGTGTCCTCTCGTG | 14697 |
| rs238058746 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75328833 | GCAGGCTCTTCTGGG[C/T]CCTAGTCAGGGGCTA | 14697 |
| rs238152628 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75342249 | CATTTCATGGAAACC[A/G]TTCTGCTCTAAGGGC | 14697 |
| rs238193221 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75335055 | AAACCACAGCAGGGG[C/T]AGTACAGCTCCAACA | 14697 |
| rs238207553 | snp | A/G | | | utr-variant-3-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant | Myo5c, Gnb5 | Mm_Celera | 9:75304616 | AGGTCATGGTAACCC[A/G]TAACTAGAATCCCAG | 14697 |
| rs238336567 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75336041 | TGCTGAAACTCAGGG[C/T]GTGTGTCCATCACCG | 14697 |
| rs238372939 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75329715 | TTTAAAAAAATGTGC[A/G]TGGTCTAGACAGTGT | 14697 |
| rs238409446 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75329986 | TGTTTTGTAGGCTAA[A/G]CAGTTCTCATACTTG | 14697 |
| rs238532039 | snp | A/G | | | intron-variant, upstream-variant-2KB | Gnb5, LOC102636700 | Mm_Celera | 9:75313057 | GTAATTCTCATAAAA[A/G]CCCTTGGATCCAGAT | 14697 |
| rs238547043 | snp | C/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75323067 | TCTGTAACTCCAGTG[C/G]CACGGGATATGACCC | 14697 |
| rs238574103 | snp | G/T | | | intron-variant, upstream-variant-2KB | Gnb5, LOC102636700 | Mm_Celera | 9:75313650 | CAGGGAACTGTTGCT[G/T]GAGAGGAGCCGCTGG | 14697 |
| rs238574475 | snp | A/C | | | intron-variant | Gnb5 | Mm_Celera | 9:75306866 | ATGTATTTCTATTGA[A/C]CTCAGGAGTAGTATT | 14697 |
| rs238587073 | snp | A/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75332150 | ATCAAAATTCTGTCT[A/T]TTGTCCCCTCTCTAT | 14697 |
| rs238611986 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75307223 | GAGCAGGAGCTACAG[C/T]AGTTGTCTACCTCAC | 14697 |
| rs238679587 | in-del | -/A | | | intron-variant | Gnb5 | Mm_Celera | 9:75316653 | ACTTCACTGTGTCCC[-/A]CCAAGCTCCAACAGC | 14697 |
| rs238727687 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75332743 | TTTTTCTAGTTTGTA[A/G]AAGCTTGGACATTAA | 14697 |
| rs238764523 | snp | A/C | | | intron-variant | Gnb5 | Mm_Celera | 9:75328148 | CTGAAACAAATTACC[A/C]CCAAATTAAGCAGCC | 14697 |
| rs238817205 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75333083 | ACAGCCAGAGGCCCA[A/G]GGAGATGGCTCAGTG | 14697 |
| rs238971498 | snp | A/G | | | intron-variant, downstream-variant-500B | Gnb5, LOC102636700 | Mm_Celera | 9:75310161 | TCTTAGCAAGCCTTC[A/G]TGTCTATCTGACCAT | 14697 |
| rs239019619 | snp | C/T | | | intron-variant, nc-transcript-variant | Gnb5, LOC102636700 | Mm_Celera | 9:75310563 | ACAGATACAAATGTG[C/T]ACTTTGTAGGAAGCC | 14697 |
| rs239082034 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75318907 | TGGATAAAGGCCAAG[C/T]GTTAGCCAGTGTGCT | 14697 |
| rs239159672 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75336316 | GTCTTCTCGCTGGGC[C/T]TTTGCAGAACTGCAT | 14697 |
| rs239160572 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75319221 | GCAGCTATTAATTTT[A/G]TTAAGAAGCAAAACT | 14697 |
| rs239223174 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75317157 | AAAAAACTAACTCCA[A/G]TTTCTTTTAAAACTT | 14697 |
| rs239229131 | in-del | -/A | | | intron-variant | Gnb5, LOC102636700 | Mm_Celera | 9:75311086 | CAATGTATATAAATG[-/A]AAAAAATAAAAGGTA | 14697 |
| rs239261514 | snp | A/G | | | intron-variant, nc-transcript-variant | Gnb5, LOC102636700 | Mm_Celera | 9:75310862 | TCCAGGATACTCTCC[A/G]GTGCTTCACAAATTT | 14697 |
| rs239300818 | snp | G/T | | | intron-variant | Gnb5, LOC102636700 | Mm_Celera | 9:75311314 | CAGGAAGAGAAGGAG[G/T]CTCCGGTCTCCAGAA | 14697 |
| rs239380334 | in-del | -/GGGGT | | | intron-variant | Gnb5 | Mm_Celera | 9:75336729 | GTTGAGGCTGGGGTG[-/GGGGT]GGGGGTGACTTGCTA | 14697 |
| rs239382358 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75342095 | ACCTGACACCCTCTT[C/T]TGTCCTCCCCACACA | 14697 |
| rs239449993 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75316524 | CACATATACACATGT[A/G]CACACACATGCACAC | 14697 |
| rs239464136 | snp | A/C | | | intron-variant | Gnb5 | Mm_Celera | 9:75319869 | CTATGTACAGGAGAA[A/C]CTATTTTTGGGAGAA | 14697 |
| rs239488741 | snp | A/G | | | intron-variant, downstream-variant-500B | Gnb5, LOC102636700 | Mm_Celera | 9:75310035 | AGTCCTCCAGCTCCA[A/G]GCTACCACATCCCAT | 14697 |
| rs239563617 | in-del | -/AAAAAAAAACAAC | | | utr-variant-3-prime, upstream-variant-2KB, intron-variant, nc-transcript-variant | Myo5c, Gnb5 | Mm_Celera | 9:75305069 | TTTCACGAAAAAAAA[-/AAAAAAAAACAAC]AACAGAAGATATGGG | 14697 |
| rs239633096 | snp | C/T | | | intron-variant, upstream-variant-2KB | Gnb5, LOC102636700 | Mm_Celera | 9:75314784 | CCAGCAGGCTGGCAT[C/T]CCAGGGACTCTCGGC | 14697 |
| rs239672315 | snp | C/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75308280 | TTCTTGGGAGTCTGT[C/T]CTCTCCTTCTACCCT | 14697 |
| rs239691471 | snp | G/T | | | intron-variant, upstream-variant-2KB | Gnb5, LOC102636700 | Mm_Celera | 9:75315156 | TGTTGGGGTTTTGTT[G/T]TATTTTGTTTTGTTT | 14697 |
| rs239708688 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75309001 | TGTGTGAACATGAGT[A/G]TGTGCTTGTGTGTTC | 14697 |
| rs239720115 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75317428 | CAAGCAGATATAGAC[A/G]TAAATATTTGTAAGT | 14697 |
| rs239731696 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75308920 | CAAGCTCTGCTGAGC[A/G]CATTCTTCCATGTCC | 14697 |
| rs239812168 | in-del | -/G | | | intron-variant, upstream-variant-2KB | Gnb5, LOC102636700 | Mm_Celera | 9:75316350 | TGCTCCTTCCTGTAA[-/G]GGTCAGCTTCTTCCC | 14697 |
| rs240006475 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75316470 | GACACACACAGGCAC[A/G]CACACACATACACAT | 14697 |
| rs240020569 | in-del | -/T | | | intron-variant | Gnb5 | Mm_Celera | 9:75317062 | CACCGACGTGTTTGG[-/T]TTTTTTAGTTTTCTA | 14697 |
| rs240143959 | snp | C/T | | | intron-variant | Gnb5 | GRCm38.p3 | 9:75327617 | TCATGTCTCTCTATG[C/T]ATCTTACAAGGATTT | 14697 |
| rs240181486 | snp | A/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75322421 | CAAGCTGAACACACC[A/G]CTATCTTCCTGAAGC | 14697 |
| rs240256747 | snp | C/G | | | intron-variant | Gnb5 | Mm_Celera | 9:75332693 | CATGCCTTGCCACTG[C/G]CGTGTAAATGGTGAC | 14697 |
| rs240286924 | snp | A/G | | | intron-variant, downstream-variant-500B | Gnb5, Myo5c | Mm_Celera | 9:75306416 | TGTGCTCTCAATTTT[A/G]CATCAATGCCTGGAT | 14697 |