iUUCD 2.0 - integrated annotations for ubiquitin and ubiquitin-like conjugation database

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs6192413	snp	A/G	0.207612	0.24638	synonymous-codon, nc-transcript-variant	Rnf149	GRCm38.p3	1:39564087	TAGAGGGAGCTGGCC[A/G]ATAACCTTCTTAGTC	67702
rs6192479	snp	A/C	0.359862	0.224567	intron-variant	Rnf149	Mm_Celera	1:39564131	TCTTGGGGAGGAAAA[A/C]AGTATTATTAAATAG	67702
rs6193073	snp	A/G	0.5	0	intron-variant	Rnf149	Mm_Celera	1:39564261	TTTATTATTATCATT[A/G]CCATTATTAAGATAT	67702
rs6193572	snp	A/G	0.5	0	intron-variant	Rnf149	Mm_Celera	1:39564357	TACCATGCCCAGCTA[A/G]GAATATATTTATTTA	67702
rs13470357	snp	A/T			missense, nc-transcript-variant	Rnf149	Mm_Celera	1:39564094	GGAAGGAGACTAAGA[A/T]GGTTATTGGCCAGCT	67702
rs13470358	snp	C/T			missense, upstream-variant-2KB, nc-transcript-variant	Rnf149	Mm_Celera	1:39576931	CGCGAGGCGGCTGCA[C/T]CTTCAAGGACAAGGT	67702
rs30493093	snp	A/G	0.255	0.24995	intron-variant	Rnf149	Mm_Celera	1:39571293	CTGTGGCCTGTAGAG[A/G]CAGTAACTAGGACTA	67702
rs30544331	snp	C/T	0.375	0.216506	upstream-variant-2KB	Rnf149	Mm_Celera	1:39578753	TTCTACCAAACAAAC[C/T]ACTAAGGAGCTGGAA	67702
rs30600252	snp	A/C	0.32	0.24	intron-variant	Rnf149	Mm_Celera	1:39570503	AGATGTTCAGTGTTA[A/C]ACGCCACCTGGAAAT	67702
rs30667837	snp	C/T	0.375	0.216506	intron-variant, upstream-variant-2KB	Rnf149	Mm_Celera	1:39574010	CCTAAAACGTCATGG[C/T]GAAAAACTTCAGCTG	67702
rs30720507	snp	C/G	0.375	0.216506	intron-variant	Rnf149	Mm_Celera	1:39563812	AAGCTAAGCCGAGCT[C/G]TACCACTGAGATACA	67702
rs30948021	snp	A/T	0.475309	0.108333	intron-variant	Rnf149	Mm_Celera	1:39566938	ACAAAGTAGTTTTTA[A/T]AAGAGAAAGAACAAC	67702
rs31290719	snp	G/T	0.375	0.216506	intron-variant	Rnf149	Mm_Celera	1:39576527	GTGAAGAGACAATGC[G/T]AGCCTGGCGGCGCCA	67702
rs31392373	snp	C/T	0.455	0.143091	intron-variant, upstream-variant-2KB	Rnf149	Mm_Celera	1:39572889	GTTGGATGAGGAGGA[C/T]AAAATTCACAATGGG	67702
rs31429712	snp	C/T	0.5	0	intron-variant	Rnf149	Mm_Celera	1:39558022	GCACAAACCCATGCA[C/T]GCATAAGCAAACACA	67702
rs31431373	snp	A/G	0.375	0.216506	intron-variant	Rnf149	Mm_Celera	1:39563817	AAGCCGAGCTCTACC[A/G]CTGAGATACACTGTT	67702
rs31515124	snp	G/T	0.444444	0.157135	intron-variant	Rnf149	Mm_Celera	1:39566060	AAAAAAAAGAGGGAC[G/T]GTGAGAGCTCTTCTG	67702
rs31595002	snp	C/T	0.5	0	intron-variant	Rnf149	Mm_Celera	1:39567845	GTGGGTTGGGGGGGA[C/T]GGCTCGGCCTGAGTG	67702
rs31771177	snp	G/T	0.33241	0.236027	intron-variant	Rnf149	Mm_Celera	1:39568473	AAAAATACTGAACCA[G/T]ACTCCCCAAATACCA	67702
rs31919038	snp	C/T	0.444444	0.157135	intron-variant	Rnf149	Mm_Celera	1:39576564	CACTCCTACACACTC[C/T]CCACTCAACCAACTT	67702
rs32046677	snp	C/T	0.345679	0.230967	intron-variant	Rnf149	Mm_Celera	1:39562910	AGTAAGAAATCAGTA[C/T]CTTGCATCAACTATT	67702
rs32159028	snp	C/T	0.444444	0.157135	intron-variant	Rnf149	Mm_Celera	1:39569581	CTCTTTCTTCTCCCT[C/T]TCCCCTCTCTCTCTT	67702
rs32208873	snp	G/T	0.475309	0.108333	intron-variant	Rnf149	Mm_Celera	1:39561036	GTATTAGATGACTAA[G/T]GGCTACAGACAAGCA	67702
rs32285330	snp	A/C	0.32	0.24	intron-variant	Rnf149	Mm_Celera	1:39571437	CAGCATCTGTAATCA[A/C]AGCTGCTCAGGAAGC	67702
rs32322669	snp	A/G	0.5	0	intron-variant	Rnf149	Mm_Celera	1:39575753	GCCAACAAACTCTTG[A/G]GTTCTTAAAGACCCG	67702
rs32337383	snp	G/T	0.375	0.216506	intron-variant	Rnf149	Mm_Celera	1:39574083	CCAACTCTACGACCT[G/T]AATGACTTGGCCTTT	67702
rs32337765	snp	A/C	0.375	0.216506	intron-variant	Rnf149	Mm_Celera	1:39574230	TTTTCCGGCCTGTGA[A/C]GTTATGTTTATCATT	67702
rs32350267	snp	A/T	0.444444	0.157135	intron-variant	Rnf149	Mm_Celera	1:39559627	TGAGCTCAGTGCAGC[A/T]GTCAGCACCCCCCCC	67702
rs32392029	snp	C/T	0.5	0	intron-variant	Rnf149	Mm_Celera	1:39567193	CTCTGAAAGAGTAGC[C/T]AAGTGTCCTCAAGCT	67702
rs32440755	snp	C/G	0.465374	0.126941	intron-variant	Rnf149	Mm_Celera	1:39570277	CAAATGACTTCCATT[C/G]TATAATTACCAGGTG	67702
rs32558361	snp	A/G	0.487535	0.077957	intron-variant	Rnf149	Mm_Celera	1:39563937	GACACACACATGAAG[A/G]CCTAACGAAGCATCA	67702
rs32579240	snp	C/T	0.375	0.216506	intron-variant, upstream-variant-2KB	Rnf149	Mm_Celera	1:39572602	TGGTCTCCCCAGCCT[C/T]GGGCAGGCCTCTTCC	67702
rs32607844	snp	A/G	0.5	0	intron-variant	Rnf149	Mm_Celera	1:39561194	AGGCCCAGTTTTATA[A/G]ATAGGGCTGGACAAT	67702
rs33157876	snp	A/G	0.124444	0.216185	intron-variant	Rnf149	Mm_Celera	1:39552579	CTCAGTTACACATGT[A/G]GAGACAATAATTCAA	67702
rs33157879	snp	A/G	0.231111	0.249285	intron-variant	Rnf149	Mm_Celera	1:39552660	CCCATTTTAAACTCA[A/G]CCAGCAAGAGAAATA	67702
rs33157882	snp	A/C	0.32	0.24	intron-variant	Rnf149	Mm_Celera	1:39552847	TCAAATCACAGTAGT[A/C]TATACACCGTTTGAC	67702
rs33158765	snp	A/G	0.124444	0.216185	intron-variant	Rnf149	Mm_Celera	1:39552856	AGTAGTCTATACACC[A/G]TTTGACTCAAAAGGA	67702
rs33158768	snp	A/G	0.391111	0.206368	intron-variant	Rnf149	Mm_Celera	1:39552920	ATGTTGCTTTGTAAT[A/G]TGGTTAGCCAGAGAA	67702
rs33158771	snp	C/T	0.124444	0.216185	intron-variant	Rnf149	Mm_Celera	1:39553012	TCCTTTGCCTCTTTT[C/T]TCTAATATTGGTTTA	67702
rs33159594	snp	A/T	0.408163	0.193609	intron-variant	Rnf149	Mm_Celera	1:39556048	ATGAAGGCTTCATTT[A/T]TCTGTTTTAAAAATC	67702
rs33159597	snp	G/T	0.124444	0.216185	intron-variant	Rnf149	Mm_Celera	1:39556567	GGTGACAGTCCCTCA[G/T]CAGTCCCACTAAAAT	67702
rs33159600	snp	A/G	0.231111	0.249285	intron-variant	Rnf149	Mm_Celera	1:39557379	AGAGGGCATGAACCA[A/G]GCCCATGAGGGAGGT	67702
rs33159603	snp	C/T	0.336735	0.234472	intron-variant	Rnf149	Mm_Celera	1:39558538	AACATGAAGTCCACC[C/T]ACTTGTCTAAGTTAT	67702
rs33160336	snp	C/T	0.124444	0.216185	intron-variant	Rnf149	Mm_Celera	1:39558995	AATATCTTCTTCAAG[C/T]CTATAAAGTGACTCA	67702
rs33160339	snp	A/G	0.124444	0.216185	intron-variant	Rnf149	Mm_Celera	1:39559811	AGCCAGGCGTGCCTC[A/G]GGGAACTGTTATTAT	67702
rs33160342	snp	A/T	0.32	0.24	intron-variant	Rnf149	Mm_Celera	1:39559851	CATTTTATTTCCTCA[A/T]CAGAGGTATCAAGAA	67702
rs33161075	snp	A/T	0.18	0.24	intron-variant	Rnf149	Mm_Celera	1:39559919	ATTAAAAAAAGAAGC[A/T]AATACAGTACTCTGC	67702
rs33161079	snp	A/G	0.231111	0.249285	intron-variant	Rnf149	Mm_Celera	1:39561597	TCTATGAGTTAGGAC[A/G]CATCAGTGGAGCCAG	67702
rs33161082	snp	G/T	0.231111	0.249285	intron-variant	Rnf149	Mm_Celera	1:39562653	ACACGTAAGGGATGA[G/T]ACTCCCTCCTAAGGA	67702
rs33161215	snp	C/T	0.124444	0.216185	intron-variant	Rnf149	Mm_Celera	1:39568242	TGCCTCCAGCTTGAG[C/T]CTACAGAGCCCTGCC	67702
rs33161218	snp	C/T	0.391111	0.206368	intron-variant	Rnf149	Mm_Celera	1:39568279	GGCTGTTAACTATGC[C/T]CAGATTTCAAACACA	67702
rs33161221	snp	A/C	0.32	0.24	intron-variant	Rnf149	Mm_Celera	1:39568304	AACACACTTGGGCTC[A/C]TTCACTGACTGTGCT	67702
rs33161223	snp	G/T	0.32	0.24	intron-variant	Rnf149	Mm_Celera	1:39568328	CTGTGCTGCAGACAA[G/T]ACCAGCATAGCTGTG	67702
rs33162015	snp	A/C	0.197531	0.244432	intron-variant	Rnf149	Mm_Celera	1:39562812	AATTACTAGAAGGAC[A/C]TTTTCTATTAATTCT	67702
rs33162018	snp	C/T	0.124444	0.216185	intron-variant	Rnf149	Mm_Celera	1:39562855	TACACATACTCTGCA[C/T]GACTAGTTATTAACT	67702
rs33162022	snp	G/T	0.32	0.24	intron-variant	Rnf149	Mm_Celera	1:39563439	GCTCCTTAACTGCTT[G/T]TAGTCTCTGACTGAG	67702
rs33162214	snp	C/G	0.231111	0.249285	intron-variant	Rnf149	Mm_Celera	1:39568367	GTGTCATACTCATAG[C/G]GATAAAAGAATTCAG	67702
rs33162217	snp	C/T	0.132653	0.220748	intron-variant	Rnf149	Mm_Celera	1:39568411	GGGACAGCAAGAACA[C/T]TTCCCTGGTAAGCAA	67702
rs33162219	snp	G/T	0.124444	0.216185	intron-variant	Rnf149	Mm_Celera	1:39568467	TGGTGCAAAAATACT[G/T]AACCAGACTCCCCAA	67702
rs33163084	snp	A/G	0.231111	0.249285	intron-variant	Rnf149	Mm_Celera	1:39568587	CTTTCTCTAGCTCTA[A/G]CCATGACAACACTGA	67702
rs33163087	snp	A/T	0.231111	0.249285	intron-variant	Rnf149	Mm_Celera	1:39568751	AAAATGACAGGGCTA[A/T]AATGGCACAGAGTAC	67702
rs33163090	snp	A/G	0.391111	0.206368	intron-variant	Rnf149	Mm_Celera	1:39568767	AATGGCACAGAGTAC[A/G]TAAGTGCACAGGGTG	67702
rs33163093	snp	A/T	0.391111	0.206368	intron-variant	Rnf149	Mm_Celera	1:39568874	TCCTTAGCCAACCCA[A/T]CAGAGGGCCCATGGA	67702
rs33163115	snp	A/G	0.124444	0.216185	intron-variant	Rnf149	Mm_Celera	1:39563513	TCCTTTCTCTCCTCT[A/G]GAAATGTTCAGTACG	67702
rs33163118	snp	A/G	0.124444	0.216185	intron-variant	Rnf149	Mm_Celera	1:39563874	ACTAAGGGCTGCCAC[A/G]ATGGTCCTTCACTCA	67702
rs33163121	snp	A/G	0.124444	0.216185	intron-variant	Rnf149	Mm_Celera	1:39563889	GATGGTCCTTCACTC[A/G]TTATACTCCTGTCAA	67702
rs33163726	snp	A/T	0.124444	0.216185	intron-variant	Rnf149	Mm_Celera	1:39569330	GAGCAGAAAGTCCTA[A/T]GAATAGTTTGGTCTC	67702
rs33163729	snp	C/T	0.124444	0.216185	intron-variant	Rnf149	Mm_Celera	1:39569334	AGAAAGTCCTATGAA[C/T]AGTTTGGTCTCAAAG	67702
rs33163731	snp	A/C	0.132653	0.220748	intron-variant	Rnf149	Mm_Celera	1:39570017	AAATTACAAGGTACA[A/C]GCTAAAAGCCTTTTT	67702
rs33163856	snp	G/T	0.124444	0.216185	intron-variant, downstream-variant-500B	Rnf149	Mm_Celera	1:39550844	GGGCACTAATGCATA[G/T]GTAACACACGGAACA	67702
rs33163859	snp	A/C	0.336735	0.234472	downstream-variant-500B	Rnf149	Mm_Celera	1:39551161	TCACTGAAGTGTAAA[A/C]TATTTTGATCAAGAA	67702
rs33163862	snp	C/G	0.124444	0.216185	utr-variant-3-prime, nc-transcript-variant	Rnf149	Mm_Celera	1:39551432	AACAGTCTTCAAAGA[C/G]TTTCACCAGCGAGAA	67702
rs33163900	snp	C/T	0.132653	0.220748	intron-variant	Rnf149	Mm_Celera	1:39564672	GAAGAAAGAGTCCTG[C/T]CTGGTTATCAGGCCA	67702
rs33163903	snp	A/G	0.124444	0.216185	synonymous-codon, nc-transcript-variant	Rnf149	Mm_Celera	1:39565138	TATAATAGAATATCA[A/G]CCATGCTAATGAGAT	67702
rs33164647	snp	A/G	0.231111	0.249285	intron-variant	Rnf149	Mm_Celera	1:39570768	GCAATTAGAACACAA[A/G]TAACTATAGATATGA	67702
rs33164650	snp	A/G	0.231111	0.249285	intron-variant	Rnf149	Mm_Celera	1:39570822	ATCTTTTCCTGAGAG[A/G]AATATTTACATTTTA	67702
rs33164775	snp	C/G	0.152778	0.230321	utr-variant-3-prime, nc-transcript-variant	Rnf149	Mm_Celera	1:39551545	AACAACAGAATCAAA[C/G]TTTTAATTAAGTATT	67702
rs33164778	snp	A/G	0.124444	0.216185	utr-variant-3-prime, nc-transcript-variant	Rnf149	Mm_Celera	1:39552015	GAACTCAAGCTCCTC[A/G]GGCCTCAGCCACAGT	67702
rs33164781	snp	A/G	0.391111	0.206368	utr-variant-3-prime, nc-transcript-variant	Rnf149	GRCm38.p3	1:39552026	CCTCGGGCCTCAGCC[A/G]CAGTTTGCACCACTG	67702
rs33164896	snp	A/G	0.124444	0.216185	intron-variant	Rnf149	Mm_Celera	1:39566568	AAAAGTACATAGCAA[A/G]TGATAACACAAGTCA	67702
rs33164899	snp	C/T	0.231111	0.249285	intron-variant	Rnf149	Mm_Celera	1:39566796	ATCCATCTAGAGGTT[C/T]TTAAATAGCTGTGAT	67702
rs33165584	snp	C/T	0.124444	0.216185	utr-variant-3-prime, nc-transcript-variant	Rnf149	Mm_Celera	1:39552423	GTAAAAAACTGAATG[C/T]CCTGTTCAAGCCAAG	67702
rs33165587	snp	C/G	0.124444	0.216185	utr-variant-3-prime, nc-transcript-variant	Rnf149	Mm_Celera	1:39552444	TCAAGCCAAGGCTCT[C/G]TCGGTGAGGCTGTCA	67702
rs33165655	snp	A/T	0.32	0.24	intron-variant	Rnf149	Mm_Celera	1:39571522	AAGCCTGATCAATAT[A/T]CCCAGAACAATTCTC	67702
rs33165658	snp	C/G	0.32	0.24	intron-variant, upstream-variant-2KB	Rnf149	Mm_Celera	1:39572270	TCTCCTAAACTTTCA[C/G]GGTTTTTTTATAAGT	67702
rs33165660	snp	A/G	0.124444	0.216185	intron-variant, upstream-variant-2KB	Rnf149	Mm_Celera	1:39572347	CAAAACCAAGGTGTA[A/G]CACAAGCCCAGTTTA	67702
rs33165663	snp	C/T	0.231111	0.249285	intron-variant, upstream-variant-2KB	Rnf149	Mm_Celera	1:39572395	TGCTCTACCTGTAGA[C/T]ACTGTCATCAATTTT	67702
rs33165924	snp	A/T	0.124444	0.216185	intron-variant	Rnf149	Mm_Celera	1:39568200	AAAGAGATCTAAAGA[A/T]ATCCATTAGGTCTCA	67702
rs33166466	snp	A/G	0.124444	0.216185	intron-variant, upstream-variant-2KB	Rnf149	Mm_Celera	1:39572804	GCAAGAGGAGTTAGG[A/G]TAGAGGAAATTAATC	67702
rs33166470	snp	A/G	0.124444	0.216185	intron-variant, upstream-variant-2KB	Rnf149	Mm_Celera	1:39573210	ATCACAAGTAAACAT[A/G]AAAACACAAAACAAC	67702
rs45759793	snp	A/C			intron-variant	Rnf149	Mm_Celera	1:39558032	ATGCATGCATAAGCA[A/C]ACACACACACAGAGG	67702
rs46704514	snp	A/C			intron-variant	Rnf149	Mm_Celera	1:39558826	TGCCTTGAACTCAGA[A/C]TCCTTGTACCTATGC	67702
rs47745889	snp	A/C/G			intron-variant	Rnf149	GRCm38.p3	1:39558065	GCTACCATATGCAGA[A/C/G]CTATACTTCGGAATT	67702
rs50722826	snp	C/T			intron-variant	Rnf149	Mm_Celera	1:39554936	CCTTCCTTCCTCTCA[C/T]TGTGGATAAACTGTG	67702
rs211741201	in-del	-/TG			utr-variant-3-prime, nc-transcript-variant	Rnf149	Mm_Celera	1:39551930	TCCCTCTCTCTCTCT[-/TG]CTCTCTCTCTCTCTC	67702
rs212024993	snp	A/G			intron-variant	Rnf149	Mm_Celera	1:39558078	GAGCTATACTTCGGA[A/G]TTACAGATTGGGGAA	67702
rs212098864	snp	G/T			intron-variant	Rnf149	Mm_Celera	1:39576629	GGGTTCGGGAATCTG[G/T]AGAGTTACTGAACTC	67702
rs212111272	snp	A/G			intron-variant	Rnf149	Mm_Celera	1:39567318	ATAATATCAAACTCC[A/G]GAAGCTTTCAATGAG	67702
rs212211465	snp	A/C			intron-variant	Rnf149	Mm_Celera	1:39566426	AAGAAATGACCAGGG[A/C]TGATGATGATGCCTT	67702
rs212259623	snp	G/T			upstream-variant-2KB	Rnf149	Mm_Celera	1:39577774	TTTTGTTACAAACTC[G/T]GTAATATATTAAATT	67702

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