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
rs295735	snp	C/T	0	0	intron-variant	HERC2	GRCh38.p7	15:28234820	TATCCAGGCAGGGAA[C/T]AGCACATCTGAAGGG	8924
rs295746	snp	A/G	0.5	0	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28229813	TGAGTACTGTTACAG[A/G]TGTTCACAAATACAA	8924
rs295757	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28217086	gtgtgcgattgagtg[C/T]GAGCATTTGTGTAAA	8924
rs415423	snp	C/T	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28205502	CAGCTCGTTCTAGGA[C/T]TGGGGGAGGCCTCCC	8924
rs916976	snp	C/T	0.185472	0.241529	intron-variant	HERC2	GRCh38.p7	15:28268367	CCAGGTGTTTTCCAA[C/T]TGCCCTGACATGTAG	8924
rs916977	snp	A/G	0.47517	0.10862	intron-variant	HERC2	GRCh38.p7	15:28268218	CTTGGCCAGCCTTCT[A/G]TCTACTCAAACTGCA	8924
rs1129038	snp	A/G	0.499894	0.00729588	utr-variant-3-prime	HERC2	GRCh38.p7	15:28111713	GCCAGGCAGCAGAGC[A/G]CTCGCTGCTGTGTAG	8924
rs1133496	snp	C/T	0.0484235	0.147875	synonymous-codon	HERC2	GRCh38.p7	15:28144734	GTGGAAGTTCATCAG[C/T]GATGGGTCTGTGAAT	8924
rs1614575	snp	C/T	0.496937	0.0390173	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28317852	CAGTATGCGCAAATA[C/T]ACAGTGACCTCTCTA	8924
rs1615773	snp	A/T	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28298036	GTGTGTGTGTGTGTG[A/T]GTGAATATTTTCAAA	8924
rs1635160	snp	A/G	0.117886	0.21224	intron-variant	LOC107987422, HERC2	GRCh38.p7	15:28315863	CAAGCTCTAGACAGT[A/G]GCATGCAGTCCCACA	8924
rs1635161	snp	A/C	0	0	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28313449	TGGGTGCGGTGGCTC[A/C]CGCCTGTAATCCCAG	8924
rs1635162	snp	C/T	0	0	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28312880	TTACTTGCCATGTCA[C/T]TTCAGAGGTGTAAGA	8924
rs1635163	snp	C/T	0.126909	0.217598	intron-variant	HERC2	GRCh38.p7	15:28310596	CTGAACCCCAGTGCA[C/T]GTATTCACTGCCCTC	8924
rs1635165	snp	C/T	0.119281	0.213102	intron-variant	HERC2	GRCh38.p7	15:28298942	CTTGGTTGAGAACCA[C/T]TGTTGAAGTTCGTTG	8924
rs1635166	snp	A/G	0.492237	0.0618148	intron-variant	HERC2	GRCh38.p7	15:28294688	gtaagaacagggtga[A/G]gtgaccttgcttccc	8924
rs1635167	snp	A/G	0.119281	0.213102	intron-variant	HERC2	GRCh38.p7	15:28290529	acataataagaatgt[A/G]gctgtgtgtggtggc	8924
rs1635168	snp	G/T	0.466721	0.124627	intron-variant	HERC2	GRCh38.p7	15:28290120	CTTACCCGTACCTGA[G/T]TATTTAGTAACTTTA	8924
rs1635169	snp	A/G	0.118235	0.212457	intron-variant	HERC2	GRCh38.p7	15:28287269	GTGGAATTTGTAGCT[A/G]TTAGAATAGCTCCTA	8924
rs1635170	snp	C/G	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28287042	TTTTACAGCGCGCAC[C/G]CACATATTCACCACC	8924
rs1635173	snp	A/G	0	0	intron-variant	HERC2	GRCh38.p7	15:28250942	AAAAAATACAAAATA[A/G]AAAGAATAGACACAA	8924
rs1667389	snp	A/G	0.118235	0.212457	intron-variant	HERC2	GRCh38.p7	15:28297829	TTTCAGGTAAAATTT[A/G]TATATAATGAAATGT	8924
rs1667390	snp	A/G	0.492287	0.0616198	intron-variant	HERC2	GRCh38.p7	15:28292555	TTGCTGAGATTTCAG[A/G]TGTGAGCCATCGCAC	8924
rs1667391	snp	C/T	0.482083	0.0929373	intron-variant	HERC2	GRCh38.p7	15:28289072	tttcacttgtcactg[C/T]ccactctcaaatggt	8924
rs1667392	snp	C/G	0.294631	0.247399	intron-variant	HERC2	GRCh38.p7	15:28288419	tctggctcagcctcc[C/G]gagtagctgggatta	8924
rs1667393	snp	A/G	0.118584	0.212673	intron-variant	HERC2	GRCh38.p7	15:28287493	CCTACAGTTATGGGT[A/G]GGTAACTAGACCCGA	8924
rs1667394	snp	A/G	0.471004	0.116864	HERC2	15	allele_origin=G(germline)/A(germline)	15:28285036	ctttgtttgtttggt[A/G]tatgcacgttttgaa	8924
rs1667395	snp	A/G	0.100588	0.200439	intron-variant	HERC2	GRCh38.p7	15:28282892	ccaggctggagtgca[A/G]tggacgttctcggct	8924
rs1667396	snp	A/G	0.121369	0.214369	intron-variant	HERC2	GRCh38.p7	15:28304768	acattgcgcaggtta[A/G]ttacatatgtataca	8924
rs1667399	snp	G/T	0	0	intron-variant	HERC2	GRCh38.p7	15:28299147	GCTTCCAATAAGTGT[G/T]TAATACACCCCCAAA	8924
rs1667400	snp	A/C	0.118933	0.212888	intron-variant	HERC2	GRCh38.p7	15:28299213	AAAATGCCTTCAATT[A/C]ACGTAAAACAATAAA	8924
rs1708965	snp	C/T	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28200626	tccatcaaccaaatg[C/T]agataaggcatacaa	8924
rs1802412	snp	A/T			utr-variant-3-prime	HERC2	GRCh38.p7	15:28111163	ATGCATTATGTCATC[A/T]GAATTGAGGCCTTTC	8924
rs1802413	snp	G/T			utr-variant-3-prime	HERC2	GRCh38.p7	15:28111249	TGAATGCATCCAGAG[G/T]ATATTTAAACCAAAA	8924
rs1962780	snp	A/G	0.157642	0.232314	intron-variant	HERC2	GRCh38.p7	15:28238397	TTGTTTTAATACTTG[A/G]AACTCATTTCAAGTT	8924
rs2016236	snp	A/T	0.442249	0.159814	intron-variant	HERC2	GRCh38.p7	15:28273423	GATAGAAATTAGTGT[A/T]GACATTTTGCCTCCA	8924
rs2016277	snp	A/G	0.440057	0.162414	intron-variant	HERC2	GRCh38.p7	15:28272823	ACGATTCAGTGAAAC[A/G]CACACAATGCAACAG	8924
rs2107430	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28199289	tcccttcctttatga[C/T]acaagttgatccagg	8924
rs2107431	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28199274	cacaagttgatccag[C/G]ctcttcctgtatatt	8924
rs2158400	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28199368	TTTAGGGTGTGATGT[C/T]TCCACTGTTATGTTT	8924
rs2158401	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28199356	TGTTTCCACTGTTAT[A/G]TTTTTGATGATCAGG	8924
rs2158402	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28198875	cagacgtgagccacc[A/G]tgcccAGTCAGAATT	8924
rs2238289	snp	C/T	0.49998	0.00319482	intron-variant	HERC2	GRCh38.p7	15:28208069	TGGAAGATTGGAGCC[C/T]GGGAATTGGATTGGC	8924
rs2240201	snp	C/G	0.442791	0.15916	intron-variant	HERC2	GRCh38.p7	15:28269134	CTGAAGATTGACAAA[C/G]TTCTGTTTATTGTAT	8924
rs2240202	snp	C/T	0.185816	0.24162	intron-variant	HERC2	GRCh38.p7	15:28265749	GGACTTAGTAACCGC[C/T]GTCCTATCTGTTTGA	8924
rs2240203	snp	A/G	0.443195	0.158668	intron-variant	HERC2	GRCh38.p7	15:28249056	TGTTTACATTCCTTA[A/G]ACATTGGGAATGTGG	8924
rs2240204	snp	C/T	0.260504	0.249779	intron-variant	HERC2	GRCh38.p7	15:28248886	CGCTTGTTGCAGATA[C/T]ATTGGACACACTTGG	8924
rs2240205	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28248350	TTAATTTTGTTGCCT[C/T]AATATTTAAATTCTT	8924
rs2240208	snp	C/T	0.444444	0.157135	intron-variant	HERC2	GRCh38.p7	15:28210738	CATGGGTCAGCAAGA[C/T]TGGTGGCACGCAGGT	8924
rs2245029	snp	A/G	0.000519494	0.0161083	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28299563	TCTTTAAAAATTGCA[A/G]TGTGAGTGTGAGCAC	8924
rs2263809	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28303732	gaaaactgtaaaaca[G/T]tgatgcagaaaattg	8924
rs2269900	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28299054	GTAAGACTATCATTA[G/T]GTTGTTCATAACAGT	8924
rs2345304	snp	A/T	0.00199481	0.0315187	intron-variant	LOC107987422, HERC2	GRCh38.p7	15:28315965	AAATGCCCATGTTGG[A/T]CCTCTGCCCTGGACC	8924
rs2345305	snp	C/T			intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28318727	TTGCTGGATGTAGGG[C/T]CCTAGGCCTGACGTA	8924
rs2345414	snp	C/T			intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28300033	actcagcctgagtga[C/T]aagagcgagactcgg	8924
rs2346039	snp	C/G	0.260504	0.249779	intron-variant	HERC2	GRCh38.p7	15:28293265	TTGGGAAGCCATGGC[C/G]GGTGGATCACAAGGT	8924
rs2346040	snp	C/T	0	0	intron-variant	HERC2	GRCh38.p7	15:28294687	tgggaagcaaggtca[C/T]ctcaccctgttctta	8924
rs2346041	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28294699	tcacctcaccctgtt[C/G]ttactacaaaatgtg	8924
rs2346042	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28296689	TGAATTACTGATACA[G/T]AAAAAAAAAAAAAAA	8924
rs2346045	snp	G/T	0	0	intron-variant	HERC2	GRCh38.p7	15:28296700	CAGCAACCTTTTTTT[G/T]TTTTTTTTTTATGTA	8924
rs2346046	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28294697	cattttgtagtaaga[A/G]cagggtgaagtgacc	8924
rs2346047	snp	C/G	0	0	intron-variant	HERC2	GRCh38.p7	15:28294696	attttgtagtaagaa[C/G]agggtgaagtgacct	8924
rs2346049	snp	A/G	0.00557542	0.0525036	intron-variant	HERC2	GRCh38.p7	15:28294600	tggggtcgggtttcc[A/G]cgataaggaggttgt	8924
rs2346050	snp	A/G	0.444533	0.157025	intron-variant	HERC2	GRCh38.p7	15:28277538	GACTTAGGGTTGGTG[A/G]ATTAATTGGAATGTA	8924
rs2346051	snp	C/T	0.25912	0.249834	intron-variant	HERC2	GRCh38.p7	15:28277456	TTTTTTTTAGATAAT[C/T]GTGGATTCACATACA	8924
rs2346083	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28237130	CCTCAGATTGATGAT[G/T]AAATTTATTTTTCCA	8924
rs2346084	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28237127	CAGATTGATGATGAA[A/G]TTTATTTTTCCAGCC	8924
rs2346085	snp	A/G/T	0.00125398	0.0250084	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28237078	CATACCAGATCTGGG[A/G/T]AGTCTCTCTTCACCT	8924
rs2346086	snp	A/G	0	0	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28237017	CTTCTCGGATTACAC[A/G]CTTCGTATTTGGCAA	8924
rs2346090	snp	C/T	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28236596	tctctttaaaaaaaG[C/T]AGGAGATagccaggc	8924
rs2346091	snp	C/T	0.0879971	0.190408	intron-variant	HERC2	GRCh38.p7	15:28236448	caaaaattagctggg[C/T]gtggtgacgggtgcc	8924
rs2346092	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28236424	gggtgcctgtaatcc[C/T]agttactcgggaggc	8924
rs2346093	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28236421	tgcctgtaatcccag[G/T]tactcgggaggctga	8924
rs2346094	snp	C/T	0.248188	0.249993	intron-variant	HERC2	GRCh38.p7	15:28236360	gaggttgcagtgagc[C/T]gagatcgcgccactg	8924
rs2346095	snp	A/G	0.248188	0.249993	intron-variant	HERC2	GRCh38.p7	15:28236353	cagtgagccgagatc[A/G]cgccactgcactcca	8924
rs2346096	snp	C/G	0.0298908	0.118541	intron-variant	HERC2	GRCh38.p7	15:28236313	acaagagcgagactc[C/G]gtctcaaaaGGAGAG	8924
rs2346097	snp	A/C	0.021333	0.101051	intron-variant	HERC2	GRCh38.p7	15:28236296	tctcaaaaGGAGAGG[A/C]GGATTCAACACAGCT	8924
rs2346098	snp	C/T	0.040671	0.13668	intron-variant	HERC2	GRCh38.p7	15:28236282	GCGGATTCAACACAG[C/T]TGATGATGATAAAAA	8924
rs2346099	snp	C/T	0	0	intron-variant	HERC2	GRCh38.p7	15:28236272	CACAGCTGATGATGA[C/T]AAAAATAATAATAAT	8924
rs2346100	snp	A/T			intron-variant	HERC2	GRCh38.p7	15:28236266	TGATGATGATAAAAA[A/T]AATAATAATAAGGAT	8924
rs2346101	snp	A/T	0.0111196	0.0737302	intron-variant	HERC2	GRCh38.p7	15:28236263	TGATGATAAAAATAA[A/T]AATAATAAGGATAGT	8924
rs2428632	snp	C/T	0.00874735	0.0655527	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28215556	CTGAAGTTCCCTGCC[C/T]TCAGAGTCAGGGGCC	8924
rs2428635	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28207451	AGCCGTGAGTGAACA[C/T]GAAAGAGAGTGTGTA	8924
rs2428636	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28207416	aggcatggtggctta[C/T]gcctgtaatcccaac	8924
rs2428637	snp	C/G	1.66668e-05	0.00288672	intron-variant	HERC2	GRCh38.p7	15:28196578	CAGGTGATTTCTGTT[C/G]TGTCCTAGCTTTCAG	8924
rs2428638	snp	A/G			splice-acceptor-variant, intron-variant	HERC2	GRCh38.p7	15:28196571	TTTCTGTTCTGTCCT[A/G]GCTTTCAGTGCCAAT	8924
rs2428639	snp	C/T			synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28196538	AAAAGATATCATTGT[C/T]GACTTTCCCCAGCAG	8924
rs2428640	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28196020	AAATCAGGATGGGGT[A/G]TCGGGGAAGAATTAG	8924
rs2428641	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28309503	ggaaaaagggagagg[C/T]aaatggaaatcacaa	8924
rs2428642	snp	C/G/T	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28309477	cacaaaagagcatag[C/G/T]ggttatatcagacca	8924
rs2428643	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28303779	atacgtaggaataaa[A/C]ctaacccaagaagtg	8924
rs2428647	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28235354	GGCAGGGCTGGCGAG[C/T]TCCAGGGCAGAGGGT	8924
rs2428648	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28235313	CTGGCAGGTGGGTCC[A/G]ATCCACAGGAGGATC	8924
rs2428649	snp	A/G	0.000299847	0.0122407	intron-variant	HERC2	GRCh38.p7	15:28230324	TGGCTGAATAGAATC[A/G]TAGCATGTAGCACAG	8924
rs2428650	snp	A/G	0.172997	0.237846	intron-variant	HERC2	GRCh38.p7	15:28230224	TGCTTCATGAACTTG[A/G]CTTATGATGTCCTGG	8924
rs2442398	snp	C/G	0.00438332	0.0466095	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28321611	GGGGAGAGAGGGAAA[C/G]AGGGAAGAGATGGAG	8924
rs2442400	snp	A/T			intron-variant	HERC2	GRCh38.p7	15:28283208	taaatctacagatct[A/T]aggtaagcaaaccct	8924
rs2442401	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28283337	gccttaactatcgtg[C/G]attaacaagtcaaat	8924
rs2525893	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28226555	gagtccaacctgttt[C/T]ttttgatgatctgat	8924
rs2525894	snp	A/T	0.00358779	0.0422022	intron-variant	HERC2	GRCh38.p7	15:28226549	aacctgttttttttg[A/T]tgatctgattgtttc	8924

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