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
rs3663313	snp	C/G	0.492188	0.0620098	intron-variant	Herc2	GRCm38.p3	7:56132741	GTTGCCTGTGAACTA[C/G]ACTGTATTACTTGTA	15204
rs3666280	snp	C/T	0.359862	0.224567	intron-variant	Herc2	GRCm38.p3	7:56133240	CCTGATCCTGCATCT[C/T]ACATGCTACAGTACA	15204
rs3671005	snp	C/T	0.5	0	intron-variant	Herc2	Mm_Celera	7:56143439	AGAAGAATGTATATT[C/T]TTCTGTGTTTGGGTA	15204
rs3681702	snp	C/T	0.5	0	intron-variant	Herc2	GRCm38.p3	7:56052720	GTTGTCAGGTTTTGT[C/T]GGCAATGACTTACCT	15204
rs3682975	snp	G/T	0.375	0.216506	intron-variant	Herc2	Mm_Celera	7:56052909	GTGATACTGGTATTT[G/T]GCCCTTTTTAGATAT	15204
rs3691306	snp	G/T	0.5	0	intron-variant	Herc2	Mm_Celera	7:56127016	ATTTATGCTGCCCAT[G/T]ATAGATGCACTAAAA	15204
rs3714163	snp	A/T	0.495	0.0497494	intron-variant	Herc2	Mm_Celera	7:56137887	GTGAGCTAAACAAAA[A/T]GTGATAATTAGAAGG	15204
rs6216458	snp	G/T	0.5	0	intron-variant	Herc2	Mm_Celera	7:56145542	acacttaaccactgt[G/T]gtgaagatctgagtt	15204
rs6216914	snp	C/T	0.5	0	intron-variant	Herc2	GRCm38.p3	7:56145578	agttttcagcaccca[C/T]atttggtggcttaca	15204
rs6217008	snp	C/T	0.5	0	intron-variant	Herc2	Mm_Celera	7:56145632	GACATCAGAGGCCGT[C/T]TTTCAGGCTCATGTT	15204
rs6217446	snp	A/G	0.391111	0.206368	intron-variant	Herc2	Mm_Celera	7:56145689	acaTTTAGACATAGA[A/G]TTTACACATAAGTAG	15204
rs6217487	snp	C/T	0.408163	0.193609	intron-variant	Herc2	Mm_Celera	7:56145710	ACATAAGTAGTGACA[C/T]aattttaaaaaaata	15204
rs6218021	snp	A/G	0.375	0.216506	synonymous-codon	Herc2	Mm_Celera	7:56145801	GGACGACATGAATGC[A/G]TCTGCCCGGGGAGCC	15204
rs6218560	snp	A/G	0.42	0.183303	synonymous-codon	Herc2	Mm_Celera	7:56145879	GCTCCCTGTTTCAGG[A/G]CCAGAACTGGCTGCT	15204
rs6218623	snp	C/T	0.408163	0.193609	synonymous-codon	Herc2	Mm_Celera	7:56145912	GATGAAGATTGGAAC[C/T]AGGGTCATGAGAGGG	15204
rs6219128	snp	A/G	0.396694	0.202437	intron-variant	Herc2	GRCm38.p3	7:56145990	CTTAGCACATCTTAC[A/G]TATCAGTGGAAGATA	15204
rs6252440	snp	A/G	0.5	0	upstream-variant-2KB, intron-variant	Herc2, Gm34121	GRCm38.p3	7:56049389	gacccttgggagtga[A/G]tttgaagatacatac	15204
rs6252479	snp	C/T	0.5	0	upstream-variant-2KB, intron-variant	Herc2, Gm34121	GRCm38.p3	7:56049425	atgacaaaagacagg[C/T]attttaacgttgcaa	15204
rs6253472	snp	A/C	0.5	0	upstream-variant-2KB, intron-variant	Herc2, Gm34121	GRCm38.p3	7:56049599	AAAgtttaatttcca[A/C]atgcttgaagattnt	15204
rs6253491	snp	A/G	0.5	0	upstream-variant-2KB, intron-variant	Herc2, Gm34121	GRCm38.p3	7:56049613	anatgcttgaagatt[A/G]tgttatgttttattt	15204
rs6254034	snp	C/T	0.5	0	upstream-variant-2KB, intron-variant	Herc2, Gm34121	GRCm38.p3	7:56049705	TTTCTTACTCCCGCA[C/T]CCCCATNCCCCCAGg	15204
rs6254045	snp	C/T	0.5	0	upstream-variant-2KB, intron-variant	Herc2, Gm34121	GRCm38.p3	7:56049712	CTCCCGCANCCCCAT[C/T]CCCCCAGggtctctt	15204
rs6254095	snp	C/T	0.5	0	upstream-variant-2KB, intron-variant	Herc2, Gm34121	GRCm38.p3	7:56049738	ctcttaacccagaat[C/T]cacctgcttctgcct	15204
rs6254545	snp	A/C	0.5	0	upstream-variant-2KB, nc-transcript-variant	Herc2, Gm34121	GRCm38.p3	7:56049794	tactaccaggcccgg[A/C]TCAATTACTTTTTCT	15204
rs6254602	snp	A/G	0.5	0	upstream-variant-2KB, nc-transcript-variant	Herc2, Gm34121	Mm_Celera	7:56049825	TAAATTTCCTCTTCT[A/G]TCCACTGACTCAAAG	15204
rs6255098	snp	A/C	0.5	0	upstream-variant-2KB, nc-transcript-variant	Herc2, Gm34121	Mm_Celera	7:56049874	TTAAAGCACAGGGAG[A/C]CTCGAGAACNTCGTC	15204
rs6255113	snp	C/T	0.5	0	upstream-variant-2KB, nc-transcript-variant	Herc2, Gm34121	Mm_Celera	7:56049884	GGGAGNCTCGAGAAC[C/T]TCGTCCCGCTGCAAA	15204
rs6270685	snp	A/G	0.5	0	intron-variant	Herc2	Mm_Celera	7:56128373	tctctggagtgtaca[A/G]ccacacattggatat	15204
rs6270757	snp	G/T	0.5	0	intron-variant	Herc2	Mm_Celera	7:56128414	ccctacccactccag[G/T]gcttatggaccatca	15204
rs6270791	snp	G/T	0.5	0	intron-variant	Herc2	Mm_Celera	7:56128434	atggaccatcatgga[G/T]agggtgtagacatat	15204
rs6284320	snp	A/G	0.5	0	intron-variant	Herc2	Mm_Celera	7:56128647	AGCTAGGGAGAGTCA[A/G]TGGTGtcacttttct	15204
rs6284710	snp	C/T	0.444444	0.157135	intron-variant	Herc2	Mm_Celera	7:56128675	TCTTTGTGGGTGTGG[C/T]TCCTGGACTCAAGTA	15204
rs6305806	snp	A/G	0.5	0	intron-variant	Herc2	Mm_Celera	7:56097112	tgtacatgagtagct[A/G]cagctgtcttcagac	15204
rs6306262	snp	A/G	0.5	0	intron-variant	Herc2	Mm_Celera	7:56097186	accatgtggttgctg[A/G]gaantgaactcagga	15204
rs6306282	snp	C/G	0.5	0	intron-variant	Herc2	Mm_Celera	7:56097190	tgtggttgctgngaa[C/G]tgaactcaggatgtc	15204
rs6341883	snp	A/G	0.48	0.0979796	intron-variant	Herc2	Mm_Celera	7:56099180	ATGGAACCATTTTAT[A/G]TTGTGTTGTTTTAAG	15204
rs6341971	snp	A/T	0.493827	0.0552116	intron-variant	Herc2	Mm_Celera	7:56099226	AGACTTGGCAGTAGG[A/T]GGGTGTGCTATTCCC	15204
rs6369437	snp	G/T	0.5	0	intron-variant	Herc2	Mm_Celera	7:56172509	tttattatttaccag[G/T]tgctgcatttaggtt	15204
rs6369481	snp	A/T	0.5	0	intron-variant	Herc2	Mm_Celera	7:56172533	ttaggtttagtttgt[A/T]tttatttttattttt	15204
rs6370480	snp	A/G	0.5	0	intron-variant	Herc2	Mm_Celera	7:56172680	acagtctgcagccca[A/G]ttcccaacaatggtt	15204
rs6370630	snp	C/T	0.415225	0.187619	intron-variant	Herc2	Mm_Celera	7:56172764	tacTAGAGGCTTATC[C/T]TGTCTGATACATTGT	15204
rs6371055	snp	A/C	0.415225	0.187619	intron-variant	Herc2	Mm_Celera	7:56172812	TTGGCATTTTTCTCC[A/C]TCATTTCTTCAGTGA	15204
rs6371074	snp	A/G	0.391111	0.206368	intron-variant	Herc2	GRCm38.p3	7:56172828	TCATTTCTTCAGTGA[A/G]TCAATCAAACTAATT	15204
rs6371108	snp	A/T	0.244898	0.249948	intron-variant	Herc2	Mm_Celera	7:56172847	ATCAAACTAATTGTT[A/T]AATCATCAAGTATTT	15204
rs6371628	snp	A/G	0.375	0.216506	intron-variant	Herc2	Mm_Celera	7:56172944	TCAGGGATTATTtct[A/G]tatctttgtttctgt	15204
rs6372060	snp	C/G	0.415225	0.187619	intron-variant	Herc2	Mm_Celera	7:56172997	CTTGATTGCTTTGTG[C/G]CCTGTAACATGATCA	15204
rs6372134	snp	A/G	0.415225	0.187619	intron-variant	Herc2	Mm_Celera	7:56173052	ctatagatacctatt[A/G]agtccatttgatcta	15204
rs31009431	snp	G/T	0.444444	0.157135	intron-variant	Herc2	Mm_Celera	7:56222081	GCAACCAGGGATTCA[G/T]AGTCGGAAAATGCTC	15204
rs31011246	snp	A/G	0.444444	0.157135	utr-variant-3-prime	Herc2	Mm_Celera	7:56231235	AGAATACCACTCCTT[A/G]AAATGTGTGGAAGAG	15204
rs31018590	snp	C/G	0.444444	0.157135	intron-variant	Herc2	GRCm38.p3	7:56130782	ATCTGGGTTTTAGGC[C/G]AGCCAAGGCTATATA	15204
rs31040538	snp	A/G	0.33241	0.236027	intron-variant	Herc2	Mm_Celera	7:56090701	AATCCTACACACTGA[A/G]GGAAGCACCCCCCAA	15204
rs31040960	snp	A/C	0.429688	0.173817	intron-variant	Herc2	Mm_Celera	7:56132185	AATTTAGAATCTTTC[A/C]CCCAGGGTTCTCCTC	15204
rs31042396	snp	A/G	0.444444	0.157135	intron-variant	Herc2	Mm_Celera	7:56114095	TTAAGTTCGTCAGGG[A/G]GAAAGTGGGTGCTAA	15204
rs31042399	snp	C/G	0.444444	0.157135	intron-variant	Herc2	GRCm38.p3	7:56158076	CAGTTACCTTGGAAG[C/G]TGAAAGCAGGAAGAT	15204
rs31047956	snp	A/G	0.444444	0.157135	intron-variant	Herc2	Mm_Celera	7:56195499	AGTCTTGTTTTATTT[A/G]AAATGATTTCTTTAA	15204
rs31048166	snp	C/G	0.456747	0.140554	intron-variant	Herc2	Mm_Celera	7:56159799	TCAGTTATTGGGTAC[C/G]TACTCATCTTGCTTG	15204
rs31048758	snp	A/G	0.5	0	intron-variant	Herc2	GRCm38.p3	7:56170541	CTTACTTTTAGTAAC[A/G]ATTATTTGATTTCTT	15204
rs31052877	snp	G/T	0.375	0.216506	intron-variant	Herc2	Mm_Celera	7:56186877	AGTCATGGAGGGTGG[G/T]TCATAGGACTACATA	15204
rs31053275	snp	A/G	0.444444	0.157135	intron-variant	Herc2	GRCm38.p3	7:56136287	AAACAGAAGCAGTGG[A/G]AGAGTGCTGATTGCT	15204
rs31056130	snp	A/G	0.375	0.216506	intron-variant	Herc2	Mm_Celera	7:56141293	AGATTAAGCTGCACA[A/G]CTGTAACATATGTGT	15204
rs31056488	snp	A/T	0.387812	0.208586	intron-variant	Herc2	Mm_Celera	7:56195461	CTACTCTTAAATTCT[A/T]ATATGCATTTGGATT	15204
rs31056822	snp	A/C	0.387812	0.208586	intron-variant	Herc2	GRCm38.p3	7:56147164	GATTGATTGATTGAA[A/C]GTTGAAATACAGAGA	15204
rs31058101	snp	G/T	0.359862	0.224567	intron-variant	Herc2	GRCm38.p3	7:56069128	CGACTGCATATATGG[G/T]CTGGCCGACTGCATA	15204
rs31059180	snp	C/T	0.444444	0.157135	intron-variant	Herc2	Mm_Celera	7:56108064	TGACTTCAGTGTTTT[C/T]CCTGATTACAGGTTT	15204
rs31060442	snp	G/T	0.444444	0.157135	intron-variant	Herc2	Mm_Celera	7:56122211	AGAGCCAAAGGCTGA[G/T]GGTAAATTGTTCTTT	15204
rs31063374	snp	C/T	0.444444	0.157135	intron-variant	Herc2	GRCm38.p3	7:56149352	CCTCACTGAGCTCTA[C/T]AGGAAGGTCCCCTTT	15204
rs31064930	snp	A/G	0.5	0	intron-variant	Herc2	GRCm38.p3	7:56061042	TCTTCCTTTCTGGAT[A/G]GAAAGTTTGAGTTCT	15204
rs31086909	snp	A/G	0.5	0	intron-variant	Herc2	GRCm38.p3	7:56189060	AACATGCACAAAATG[A/G]GAACTAATGAAGGTA	15204
rs31097086	snp	A/G	0.489796	0.070696	intron-variant	Herc2	Mm_Celera	7:56147531	TTTGGAAGTGGATCC[A/G]AGCTATAGAGTGTGC	15204
rs31100194	snp	C/T	0.444444	0.157135	intron-variant	Herc2	Mm_Celera	7:56092203	AGTCATCTAAGAGCT[C/T]TTCTTTTAACATGTT	15204
rs31133992	snp	A/G	0.375	0.216506	intron-variant	Herc2	Mm_Celera	7:56058530	GCTTATAGAAGATAG[A/G]GGTTCCAGGACAGCC	15204
rs31134213	snp	A/G	0.359862	0.224567	intron-variant	Herc2	Mm_Celera	7:56063636	ATCAATAATATTTCC[A/G]TGATGTCTATAGGAC	15204
rs31135402	snp	A/G	0.345679	0.230967	intron-variant	Herc2	GRCm38.p3	7:56068502	GAGTGAATAGCTTTT[A/G]GTTTAAACTGAAACA	15204
rs31137392	snp	A/T	0.387812	0.208586	intron-variant	Herc2	Mm_Celera	7:56182299	CTGTGGCTAAGGTAA[A/T]TAGAAACTAACAGCT	15204
rs31143061	snp	C/T	0.444444	0.157135	intron-variant	Herc2	Mm_Celera	7:56167821	TGCATGCCTGATACC[C/T]GTGGAAGCCAGAAAA	15204
rs31146126	snp	C/T	0.375	0.216506	intron-variant	Herc2	Mm_Celera	7:56193376	TCCTTGCAAGGCTCC[C/T]GGTGTGGACCAGACA	15204
rs31160201	snp	C/T	0.375	0.216506	intron-variant	Herc2	Mm_Celera	7:56122517	TTTTTTTTTTTTAAT[C/T]TTTCTTTTACTTTGA	15204
rs31160626	snp	A/T	0.32	0.24	upstream-variant-2KB, intron-variant	Herc2, Gm34121	Mm_Celera	7:56048408	CAAACCAGCGAGTTT[A/T]GAGAGAGAGAACTAC	15204
rs31163338	snp	A/G	0.401235	0.199068	intron-variant	Herc2	Mm_Celera	7:56219094	AAGAGATACCTAGTG[A/G]CTGAATGATCTCCCT	15204
rs31180182	snp	A/G	0.415225	0.187619	intron-variant	Herc2	Mm_Celera	7:56158159	CTGGTTAAAATACAA[A/G]TAAACATTCTGGGCC	15204
rs31182047	snp	C/T	0.487535	0.077957	synonymous-codon	Herc2	GRCm38.p3	7:56153423	TAACTCCCAGCTTTG[C/T]TCTGTCACACAAAGC	15204
rs31182052	snp	C/T	0.265928	0.249492	intron-variant	Herc2	GRCm38.p3	7:56205865	ATTTTTTGCTGACTG[C/T]AGGTGCTAGTAGCTC	15204
rs31186208	snp	G/T	0.444444	0.157135	intron-variant	Herc2	Mm_Celera	7:56210405	AGGGATGGCTCAGCC[G/T]TTAAAATCACTGGCT	15204
rs31192953	snp	A/T	0.444444	0.157135	intron-variant	Herc2	Mm_Celera	7:56213264	GATTTACATTTTCAT[A/T]TAAATATAAATTTAT	15204
rs31217635	snp	A/G	0.375	0.216506	intron-variant	Herc2	Mm_Celera	7:56190918	AAGTCATAGTTTAAT[A/G]TATATAATCCATTGT	15204
rs31228772	snp	A/T	0.277778	0.248452	intron-variant	Herc2	Mm_Celera	7:56188418	AACTGTATGTACTCA[A/T]GTTCTCTGGATACAT	15204
rs31229024	snp	A/T	0.46875	0.121031	intron-variant	Herc2	Mm_Celera	7:56159896	AATGCTTTTGGATTT[A/T]TCAGCTCAGGTTTTC	15204
rs31230505	snp	C/G	0.444444	0.157135	intron-variant	Herc2	Mm_Celera	7:56222079	GGGCAACCAGGGATT[C/G]ATAGTCGGAAAATGC	15204
rs31231358	snp	C/T	0.493827	0.0552116	intron-variant	Herc2	Mm_Celera	7:56206054	GTGTGTGTTAATTAA[C/T]TAATTTTTGGAATTC	15204
rs31231830	snp	C/T	0.432133	0.171253	intron-variant	Herc2	Mm_Celera	7:56138643	ATAGATCTGCCCTAA[C/T]CACATTATGTGGAAA	15204
rs31232190	snp	C/T	0.444444	0.157135	intron-variant	Herc2	GRCm38.p3	7:56116346	CATACACACACACAC[C/T]CCAATAGATTTTTCC	15204
rs31233452	snp	C/T	0.444444	0.157135	intron-variant	Herc2	GRCm38.p3	7:56182746	ACATCGTGAGCAGTT[C/T]CTCATAAGCTTTTGC	15204
rs31234093	snp	A/G	0.444444	0.157135	intron-variant	Herc2	Mm_Celera	7:56171438	TTCTATTATGATTTT[A/G]TATACTATGTCTTTA	15204
rs31235454	snp	A/G	0.375	0.216506	intron-variant	Herc2	Mm_Celera	7:56220106	ATAGAATGCTTACTT[A/G]CTTGGCATGCACAAA	15204
rs31239156	snp	C/G	0.387812	0.208586	intron-variant	Herc2	Mm_Celera	7:56225358	TGCTCTCCTCTGGGA[C/G]CACGAATCCTTTCAA	15204
rs31240501	snp	C/T	0.498615	0.0262793	intron-variant	Herc2	Mm_Celera	7:56223399	TCCAGTTTAATAACC[C/T]AGTATTGCTAACATT	15204
rs31240749	snp	C/T	0.345679	0.230967	intron-variant	Herc2	Mm_Celera	7:56157090	TGAAGCAGTCAGCAG[C/T]GTTATTTGACTATCA	15204
rs31246933	snp	A/G	0.432133	0.171253	intron-variant	Herc2	Mm_Celera	7:56228018	AGAGCAGAGAAAAGT[A/G]TGCATCTGAGAGAGT	15204
rs31247625	snp	C/T	0.459184	0.136902	intron-variant	Herc2	GRCm38.p3	7:56148445	ACTGAGTTCAGGTAG[C/T]CACCTATTCTAAGTT	15204
rs31249357	snp	C/T	0.498615	0.0262793	intron-variant	Herc2	Mm_Celera	7:56109783	TTTCTCCCTTCAGGG[C/T]ATGTGAGATTAAAGT	15204

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