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
rs6193349	snp	A/G	0.456747	0.140554	intron-variant	Rfwd2	GRCm38.p3	1:159331443	GAGAGATAAATGCAG[A/G]TGGGTATGACATAAG	26374
rs6193771	snp	A/G	0.5	0	intron-variant	Rfwd2	Mm_Celera	1:159331510	TTGGAGGTGGTTTGG[A/G]GGTTCTTTGTTTGTT	26374
rs6230679	snp	C/T	0.5	0	intron-variant	Rfwd2	GRCm38.p3	1:159261616	gtgtgtgcgcgcgcg[C/T]gcgtatncgtatgta	26374
rs6230693	snp	A/G	0.5	0	intron-variant	Rfwd2	Mm_Celera	1:159261623	cgcgcgcgngcgtat[A/G]cgtatgtatgtgtgt	26374
rs6231338	snp	C/T	0.5	0	intron-variant	Rfwd2	GRCm38.p3	1:159261745	CTAGGCTGTCTCAGC[C/T]TCCGCAGTGCTGGGA	26374
rs6232293	snp	A/G	0.455	0.143091	intron-variant	Rfwd2	Mm_Celera	1:159261889	TACTTGTTGTTTTTC[A/G]TTAGTCCTTTTTTGA	26374
rs6250322	snp	G/T	0.5	0	intron-variant	Rfwd2	Mm_Celera	1:159335065	TTACATATTAGAAAA[G/T]TGAAAGAAAAAATAG	26374
rs6251817	snp	A/G	0.444444	0.157135	intron-variant	Rfwd2	GRCm38.p3	1:159335372	GGCATTGTTGCGGTA[A/G]ATCTCCTCCCAAATA	26374
rs6265187	snp	C/T	0.484429	0.0868505	intron-variant	Rfwd2	Mm_Celera	1:159270058	TAGCAGCCAGATGTT[C/T]ACAGCAATATTCTGT	26374
rs6284011	snp	C/T	0.5	0	intron-variant	Rfwd2	Mm_Celera	1:159237798	AAATGAACTACATTT[C/T]ATTATATCTCTCTGA	26374
rs6284510	snp	A/T	0.5	0	intron-variant	Rfwd2	Mm_Celera	1:159237885	TAGTTATTGGTACCA[A/T]AACAGTGCTATTCGT	26374
rs6339193	snp	A/C	0.5	0	intron-variant	Rfwd2	Mm_Celera	1:159241063	atcactctgggttct[A/C]atagggncttcatta	26374
rs6339197	snp	G/T	0.5	0	intron-variant	Rfwd2	Mm_Celera	1:159241070	tgggttctnataggg[G/T]cttcattaagttgga	26374
rs6370963	snp	A/T	0.444444	0.157135	intron-variant	Rfwd2	GRCm38.p3	1:159248942	TTTCACATGGTGAAA[A/T]GTTATCTTTATTGAG	26374
rs6373412	snp	C/T	0.5	0	intron-variant	Rfwd2	Mm_Celera	1:159276228	CTTTGCACACTGACT[C/T]CTCAACCCCACACCT	26374
rs6373437	snp	G/T	0.5	0	intron-variant	Rfwd2	Mm_Celera	1:159276247	AACCCCACACCTATG[G/T]AATTTTACTAATCCT	26374
rs6395862	snp	C/T	0.5	0	intron-variant	Rfwd2	Mm_Celera	1:159283385	attctggattgtagt[C/T]attccagatagagtc	26374
rs6395925	snp	C/T	0.5	0	intron-variant	Rfwd2	Mm_Celera	1:159283428	ggaagagcactacaG[C/T]CTGAAGCCCAATCCA	26374
rs6395951	snp	C/T	0.5	0	intron-variant	Rfwd2	Mm_Celera	1:159283448	AGCCCAATCCACCTC[C/T]TCTCGCTGCTCATCT	26374
rs6407858	snp	C/T	0.5	0	intron-variant	Rfwd2	Mm_Celera	1:159244492	AAATAAATGTTATAT[C/T]AGTTGTGTTGAAAGT	26374
rs6409704	snp	G/T	0.444444	0.157135	intron-variant	Rfwd2	GRCm38.p3	1:159283615	AAAGTGCTTCGTGTA[G/T]ATTTCTTATACAGAA	26374
rs6409734	snp	A/C	0.5	0	intron-variant	Rfwd2	Mm_Celera	1:159283639	TACAGAATAGTAAAA[A/C]AGTGTGTGTGCCAGG	26374
rs30459689	snp	A/G	0.375	0.216506	intron-variant	Rfwd2	Mm_Celera	1:159314560	CACCTTGAGGAAGAT[A/G]CTATCTTTTTAAAAT	26374
rs30464552	snp	A/G	0.387812	0.208586	intron-variant	Rfwd2	Mm_Celera	1:159269421	TAGATTTTAGAAATA[A/G]CTTCATTTGACTATA	26374
rs30472651	snp	G/T	0.401235	0.199068	intron-variant	Rfwd2	GRCm38.p3	1:159281274	GGGAGGTGGGGAGAG[G/T]CAGGCATATTGTTTA	26374
rs30475791	snp	C/T	0.375	0.216506	intron-variant	Rfwd2	GRCm38.p3	1:159238423	CATAGATAAATGAAT[C/T]TTAGCTGGGTGTATA	26374
rs30505375	snp	C/T	0.375	0.216506	intron-variant	Rfwd2	Mm_Celera	1:159255848	AGTCTAAAAAACTAA[C/T]TAGTTTTACTCACTG	26374
rs30542577	snp	A/C	0.375	0.216506	intron-variant	Rfwd2	GRCm38.p3	1:159272430	CTTTTTCCCACTCTC[A/C]GTGACACACATTCTT	26374
rs30559774	snp	C/T	0.498615	0.0262793	intron-variant	Rfwd2	Mm_Celera	1:159242732	ATGTTTTGGTAAACG[C/T]CAAACTCTTGTCATG	26374
rs30566467	snp	C/T	0.444444	0.157135	intron-variant	Rfwd2	Mm_Celera	1:159303685	AGTGGAATCTCAGGG[C/T]TGTTTAGATTTGCAC	26374
rs30568518	snp	A/G	0.401235	0.199068	intron-variant	Rfwd2	Mm_Celera	1:159329457	CTACACTGCATGTGT[A/G]ACTTTAAGTGAAGAA	26374
rs30602182	snp	C/T	0.42	0.183303	intron-variant	Rfwd2	Mm_Celera	1:159321168	GGCAAGCAACGCAAT[C/T]CAATTGTACAACAAT	26374
rs30602938	snp	C/T	0.32	0.24	intron-variant	Rfwd2	Mm_Celera	1:159260461	TGCATGCTAGGCAGG[C/T]GCTCTACCCGAGCTC	26374
rs30603446	snp	A/G	0.444444	0.157135	intron-variant	Rfwd2	Mm_Celera	1:159233104	GAGTGCTTAAGGATA[A/G]AGATGGAGGTCCAGT	26374
rs30606380	snp	A/T	0.375	0.216506	intron-variant	Rfwd2	Mm_Celera	1:159241179	GGAAGTTACCAGAGT[A/T]GTTAGTGTCCTGAGC	26374
rs30607177	snp	C/T	0.459184	0.136902	intron-variant	Rfwd2	Mm_Celera	1:159259116	TGTAAAAACATCAAG[C/T]AATTGTGTGTACTAA	26374
rs30609330	snp	A/G	0.375	0.216506	intron-variant	Rfwd2	GRCm38.p3	1:159336532	AAATGTCTCCCATTA[A/G]ACATTTGCCTAGACC	26374
rs30660948	snp	A/G	0.387812	0.208586	intron-variant	Rfwd2	Mm_Celera	1:159285256	CATGCGATCTCATGT[A/G]TATGATAGGATAAGA	26374
rs30663386	snp	A/G	0.5	0	intron-variant	Rfwd2	Mm_Celera	1:159252722	ATTTAAAAGCATTTA[A/G]TTTAGTCTTCCCTTT	26374
rs30693835	snp	A/G	0.375	0.216506	intron-variant	Rfwd2	GRCm38.p3	1:159335757	TTAACATCAAACATA[A/G]TTGTCCAGTAGGTAG	26374
rs30705670	snp	A/G	0.231111	0.249285	intron-variant	Rfwd2	Mm_Celera	1:159318624	TTAGAAAAGACATAA[A/G]CCAAACCAAATTGTT	26374
rs30708227	snp	A/G	0.444444	0.157135	intron-variant	Rfwd2	Mm_Celera	1:159334211	AGAGGTAGGCTATGG[A/G]TTTAGTGGAGCGTTT	26374
rs30717010	snp	G/T	0.375	0.216506	intron-variant	Rfwd2	Mm_Celera	1:159286131	AATCCTTTATCAAAT[G/T]TCTATAATAGTTTAT	26374
rs30744819	snp	A/G	0.304688	0.243945	intron-variant	Rfwd2	GRCm38.p3	1:159268000	AGGGAATCCTTGAGA[A/G]GTTTGATAAAAAGCT	26374
rs30750944	snp	C/T	0.498615	0.0262793	intron-variant	Rfwd2	Mm_Celera	1:159286391	ACTGAATAATTTGCT[C/T]TGGAAGATGCAGATT	26374
rs30761774	snp	A/G	0.415225	0.187619	intron-variant	Rfwd2	Mm_Celera	1:159253566	AGATAATACGTGAAG[A/G]TAATTCTCTGCTCTT	26374
rs30800756	snp	A/C	0.415225	0.187619	intron-variant	Rfwd2	GRCm38.p3	1:159317790	TCTTCATACATTTAC[A/C]TTTATTTCATTATGA	26374
rs30801802	snp	C/T	0.33241	0.236027	intron-variant	Rfwd2	GRCm38.p3	1:159276757	GACTATATGATTGAA[C/T]ACATAGAACCTGATA	26374
rs30805967	snp	C/T	0.375	0.216506	intron-variant	Rfwd2	Mm_Celera	1:159267223	AGTTCAGATTACTTA[C/T]AGAAATTCATTGGGA	26374
rs30808693	snp	A/G	0.5	0	intron-variant, upstream-variant-2KB	Rfwd2	GRCm38.p3	1:159257197	ACATTGTTGGTGGAC[A/G]TTCGAGTGGTTTTTA	26374
rs30853589	snp	A/G	0.415225	0.187619	intron-variant	Rfwd2	GRCm38.p3	1:159253622	AATCTGAGTTTTTCA[A/G]ATCCCTTTAGGAGCC	26374
rs30931405	snp	A/G	0.345679	0.230967	intron-variant	Rfwd2	Mm_Celera	1:159243890	TTGGTCAATTTGTAT[A/G]TGTAATTTAGGTTGC	26374
rs30944623	snp	A/G	0.432133	0.171253	intron-variant	Rfwd2	Mm_Celera	1:159329686	ACAGTAGCAACTAAA[A/G]AGGCATAGGAAATAT	26374
rs30951884	snp	C/T	0.290657	0.246672	intron-variant	Rfwd2	Mm_Celera	1:159295045	TGGAATTAAAGTAAG[C/T]GATAAAATAATCAGT	26374
rs30980274	snp	C/T	0.345679	0.230967	intron-variant	Rfwd2	Mm_Celera	1:159241334	AGTATTTCTTTTGTC[C/T]ATATTGGAAGTTGTG	26374
rs30987837	snp	A/G	0.277778	0.248452	intron-variant	Rfwd2	GRCm38.p3	1:159310490	GATTTAATGTATAGT[A/G]GTAATAGTGCCTAAC	26374
rs30996612	snp	A/T	0.444444	0.157135	intron-variant	Rfwd2	GRCm38.p3	1:159334419	TTCAAGCCACTGCGC[A/T]GAGAGGTAGAACAAT	26374
rs31000308	snp	C/T	0.375	0.216506	intron-variant	Rfwd2	GRCm38.p3	1:159304531	CATGTTGGTGTTCCT[C/T]CTTCTTGATTTTCTT	26374
rs31000988	snp	A/C	0.444444	0.157135	intron-variant	Rfwd2	GRCm38.p3	1:159323939	GGTTCCCACCCCCAA[A/C]CTTTATGTGTGCTAT	26374
rs31013660	snp	C/T	0.32	0.24	intron-variant	Rfwd2	Mm_Celera	1:159260103	TTTGCTAGTTTGATG[C/T]ATCATAATGAAACAC	26374
rs31048982	snp	C/G	0.415225	0.187619	intron-variant	Rfwd2	GRCm38.p3	1:159248077	CTCACGATAATTAGA[C/G]TTATTTGTAGAGTGG	26374
rs31052830	snp	G/T	0.49827	0.0293608	intron-variant	Rfwd2	Mm_Celera	1:159288182	TGTTTTTAGTTCTTT[G/T]GGAAAAGTTTAAAAT	26374
rs31101439	snp	C/T	0.387812	0.208586	intron-variant	Rfwd2	Mm_Celera	1:159284852	TTTCTCATTCCAGAA[C/T]GTTTTATCGTTCCAG	26374
rs31112472	snp	A/T	0.444444	0.157135	intron-variant	Rfwd2	GRCm38.p3	1:159248088	TAGAGTTATTTGTAG[A/T]GTGGATCATTTCATT	26374
rs31154774	snp	A/G	0.32	0.24	intron-variant	Rfwd2	Mm_Celera	1:159321891	TATAGGCAGTCACCT[A/G]GGAGCTGAGCCTCTG	26374
rs31157265	snp	A/G	0.387812	0.208586	intron-variant	Rfwd2	Mm_Celera	1:159262167	TCTTGTGATTTATCT[A/G]TACTGATTTCTTTGC	26374
rs31160783	snp	A/G	0.375	0.216506	intron-variant	Rfwd2	GRCm38.p3	1:159238510	GAGTCCCAGGCTAGC[A/G]TGGGCTACATAAAGA	26374
rs31177156	snp	A/T	0.32	0.24	intron-variant	Rfwd2	GRCm38.p3	1:159271150	AAGCATATATAAACC[A/T]TCACAGGTGTCATGC	26374
rs31189680	snp	C/T	0.444444	0.157135	intron-variant	Rfwd2	Mm_Celera	1:159299543	CCATCTACTTGATTT[C/T]AAAGAACGTACACCT	26374
rs31196850	snp	G/T	0.444444	0.157135	intron-variant	Rfwd2	Mm_Celera	1:159334135	CACTTGACAGAAAAT[G/T]AACATCCAGAATATG	26374
rs31198913	snp	A/C	0.375	0.216506	intron-variant	Rfwd2	Mm_Celera	1:159277255	GAAATGCCTCTGAGG[A/C]CACCCTGGTCTATAC	26374
rs31214457	snp	A/C	0.5	0	intron-variant	Rfwd2	Mm_Celera	1:159289820	CGGGAAAAAAAAAAA[A/C]AAAAAAACAAACTTC	26374
rs31230448	snp	A/G	0.375	0.216506	intron-variant	Rfwd2	Mm_Celera	1:159271476	AGATCAGTCTTAGTC[A/G]GTGATCTATTGCTGT	26374
rs31232172	snp	C/T	0.375	0.216506	intron-variant, upstream-variant-2KB	Rfwd2	Mm_Celera	1:159258036	ACATCCATGTATATA[C/T]GTGCTCATGCCCCTG	26374
rs31257634	snp	C/T	0.42	0.183303	intron-variant	Rfwd2	Mm_Celera	1:159274263	TTGGAAATGCTTTTT[C/T]TATTGACTTATAATT	26374
rs31258065	snp	A/T	0.426035	0.177515	intron-variant	Rfwd2	Mm_Celera	1:159249106	AATTTGGGACTCTGT[A/T]AAGTTAAGATAAAAA	26374
rs31259858	snp	A/T	0.48	0.0979796	intron-variant	Rfwd2	Mm_Celera	1:159328147	TATAAGTGTTTTTTT[A/T]AAATATAAATTCTTT	26374
rs31265834	snp	C/T	0.375	0.216506	intron-variant	Rfwd2	Mm_Celera	1:159259856	TGTGGTGATCTTCTG[C/T]CCTTTATTACCACTC	26374
rs31284026	snp	A/G	0.375	0.216506	intron-variant	Rfwd2	Mm_Celera	1:159290747	TTTGGAAGAGCAGTC[A/G]GTGCTCTTAACCACT	26374
rs31287041	snp	A/G	0.5	0	intron-variant	Rfwd2	Mm_Celera	1:159252854	ACAGGGTTTCTCTGT[A/G]TAGCTCTGGCTGTCC	26374
rs31311724	snp	C/T	0.432133	0.171253	intron-variant	Rfwd2	GRCm38.p3	1:159337316	GCTTTCAGAATGCCA[C/T]GAATTTATCTATAGC	26374
rs31311725	snp	C/T	0.124444	0.216185	intron-variant	Rfwd2	Mm_Celera	1:159337248	TCGGGAGCTGTTTAT[C/T]CTCACACATGTCCAG	26374
rs31311726	snp	C/T	0.124444	0.216185	intron-variant	Rfwd2	Mm_Celera	1:159337234	TGGAAAGCAAATGCT[C/T]GGGAGCTGTTTATCC	26374
rs31311727	snp	C/T	0.391111	0.206368	intron-variant	Rfwd2	GRCm38.p3	1:159337067	TGCTTCTGTCCATTG[C/T]CCTCTTCATGTAGGC	26374
rs31311728	snp	C/T	0.444444	0.157135	intron-variant	Rfwd2	GRCm38.p3	1:159337052	TAAAAAGATTTTTCA[C/T]GCTTCTGTCCATTGT	26374
rs31311729	snp	C/T	0.21875	0.248039	intron-variant	Rfwd2	GRCm38.p3	1:159336944	CCACCCTACCAAGTG[C/T]TTCTCTTCAGAGTCT	26374
rs31311730	snp	G/T	0.5	0	intron-variant	Rfwd2	Mm_Celera	1:159336927	TTCAGATTGCCATTT[G/T]TCCACCCTACCAAGT	26374
rs31311731	snp	A/T	0.391111	0.206368	intron-variant	Rfwd2	GRCm38.p3	1:159336795	GCTTGATGTGCTCAG[A/T]CTTAAGTTTCCTGCA	26374
rs31311732	snp	A/G	0.124444	0.216185	intron-variant	Rfwd2	Mm_Celera	1:159336681	AAGTGTGGGTCTCCC[A/G]GTTTCAAAGGTGGTC	26374
rs31311733	snp	C/G	0.459184	0.136902	intron-variant	Rfwd2	Mm_Celera	1:159336382	TGGAGGCTGCAATTG[C/G]TTGCTTGGTTGGATT	26374
rs31312254	snp	A/G	0.401235	0.199068	intron-variant	Rfwd2	Mm_Celera	1:159249013	AGTAATAGAAGTTGT[A/G]GTAGTAATAAGTATA	26374
rs31312424	snp	A/G	0.497041	0.0383476	intron-variant	Rfwd2	Mm_Celera	1:159313526	GCATGCACCACCATA[A/G]CCCATCCTATAGTAT	26374
rs31312425	snp	A/G	0.408163	0.193609	intron-variant	Rfwd2	GRCm38.p3	1:159312876	TACAATAATTGACCA[A/G]GAGGGTAGCTTGTCA	26374
rs31312426	snp	C/T	0.48	0.0979796	intron-variant	Rfwd2	Mm_Celera	1:159312794	TAATAATTCAGTGAA[C/T]TGCCTGCAGTGCTGA	26374
rs31312427	snp	A/G	0.459184	0.136902	intron-variant	Rfwd2	Mm_Celera	1:159312660	TCTCTCCCACACACC[A/G]CTCACATTCTAAAAA	26374
rs31312428	snp	C/G	0.32	0.24	intron-variant	Rfwd2	Mm_Celera	1:159312398	ATTTATATATATGTT[C/G]TATGTAATATGTTTC	26374
rs31312429	snp	C/T	0.391111	0.206368	intron-variant	Rfwd2	GRCm38.p3	1:159312346	TCTTCTTGGTCTCCT[C/T]GGGTTATGGGTTATG	26374
rs31312430	snp	A/T	0.459184	0.136902	intron-variant	Rfwd2	Mm_Celera	1:159311935	TGTTTTAAAATTTCC[A/T]CTCATAGCTGGGCGT	26374
rs31312431	snp	C/T	0.391111	0.206368	intron-variant	Rfwd2	Mm_Celera	1:159311826	TGCTTCATTCACTTT[C/T]TTCTAAGCACTGTTG	26374
rs31312432	snp	A/T	0.345679	0.230967	intron-variant	Rfwd2	GRCm38.p3	1:159311504	CCTCCAGTCAGCCCC[A/T]CTCACTCAGTCCCTG	26374

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