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
rs13581	snp	A/C	0.0121415	0.0769634	downstream-variant-500B, utr-variant-3-prime	SPTAN1, WDR34	GRCh38.p7	9:128633739	CACCCGCCTCCCGGG[A/C]CCCCTCAGGCCGCCA	6709
rs945829	snp	A/G	0.00597247	0.0543191	intron-variant	SPTAN1	GRCh38.p7	9:128577619	TGTCAGGTATCACCT[A/G]CAAATGCAAATCACT	6709
rs945830	snp	C/T	0.0170251	0.090679	intron-variant	SPTAN1	GRCh38.p7	9:128599633	aagcaatcctcccac[C/T]tcagcctcccaggta	6709
rs945831	snp	C/T	0.0208818	0.100024	SPTAN1	9	allele_origin=T(germline)/C(germline)	9:128600082	TTTCTTTGAATAGGA[C/T]GAAACTGATTCCAAG	6709
rs945832	snp	C/T	0.0573587	0.15934	intron-variant	SPTAN1	GRCh38.p7	9:128559022	CAATTACAGGAGACA[C/T]CAAAAAACATTATGG	6709
rs945833	snp	A/G	0.0569829	0.158885	intron-variant	SPTAN1	GRCh38.p7	9:128558792	ATGTCAGCTCAGCTC[A/G]GCCTGGGCGTGCCAC	6709
rs945834	snp	C/G	0.39979	0.200158	intron-variant	SPTAN1	GRCh38.p7	9:128558260	TTCAGCAAGTAATGC[C/G]AATCTCAGGGGGATA	6709
rs945835	snp	C/T	0.0603597	0.1629	intron-variant	SPTAN1	GRCh38.p7	9:128557268	TCAGCAAGTTGAATG[C/T]ACTGGATGTAAGAGA	6709
rs953665	snp	C/G	0.475348	0.108251	intron-variant	SPTAN1	GRCh38.p7	9:128619649	agatgaggtcattag[C/G]gtggaccctaatcca	6709
rs953666	snp	C/G	0.4628	0.13121	intron-variant	SPTAN1	GRCh38.p7	9:128619583	GTGAATAGACACACA[C/G]AGTGATGCCAAGTGA	6709
rs1048236	snp	C/T	0	0	SPTAN1	9	allele_origin=T(germline)/C(germline)	9:128605330	CAGCAGAGCGCCTGA[C/T]CCAGTCCCATCCCGA	6709
rs1129922	snp	A/G			missense	SPTAN1	GRCh38.p7	9:128584297	GACCGAATTGATGGC[A/G]TCACCATTCAGGCCC	6709
rs1129924	snp	A/T			missense	SPTAN1	GRCh38.p7	9:128612226	ACAGGGATCAAGGAC[A/T]TTGACTTCTGGCTGT	6709
rs1337555	snp	A/C			intron-variant, upstream-variant-2KB	SPTAN1	GRCh38.p7	9:128554056	TTGACCTTTCAAAAT[A/C]TAAGACATTAGTTAG	6709
rs1415568	snp	A/G	0.00813715	0.0632642	SPTAN1	9	allele_origin=G(germline)/A(germline)	9:128613422	TTATGGCAAAGACCT[A/G]GCTTCTGTGAACAAC	6709
rs1572914	snp	A/G	0.394721	0.203852	intron-variant	SPTAN1	GRCh38.p7	9:128627265	CCCCAAAGATGAGAG[A/G]AGGAGGCTGGGAGAC	6709
rs1803171	snp	G/T			utr-variant-3-prime, downstream-variant-500B	SPTAN1, WDR34	GRCh38.p7	9:128633490	ACTAACCCGCTTCCG[G/T]TCCAGTCACAATCAT	6709
rs1890101	snp	A/C					GRCh38.p7	9:128559474	GTGTATGGTGCTGTT[A/C]TGCCTCCTATCACAG	6709
rs1890102	snp	C/T	0.00358779	0.0422022			GRCh38.p7	9:128554295	TATCAGAGAATCAGT[C/T]ACTAGGCTGATGGTT	6709
rs1890103	snp	C/T	0.0583345	0.161527			GRCh38.p7	9:128578360	GTTATTCACAGGTGT[C/T]TCTCATCATGAGGAT	6709
rs1890104	snp	A/T	0.434976	0.168179			GRCh38.p7	9:128578531	ATTGATCCTTTGTGA[A/T]GTAAAAAGTATTTGT	6709
rs1890105	snp	C/T	0.0667028	0.170006			GRCh38.p7	9:128578595	CAGCACTTTGGAAGG[C/T]CGAGGCGGGTGGATC	6709
rs1984180	snp	C/T			intron-variant	SPTAN1	GRCh38.p7	9:128563004	atatatatatatata[C/T]atatatatatacaca	6709
rs1984181	snp	C/T			intron-variant	SPTAN1	GRCh38.p7	9:128562992	atatatatatatata[C/T]acatacatgtatata	6709
rs1984182	snp	C/T			intron-variant	SPTAN1	GRCh38.p7	9:128562990	atatatatatataca[C/T]atacatgtatatata	6709
rs1984183	snp	C/T			intron-variant	SPTAN1	GRCh38.p7	9:128562986	atatatatacacata[C/T]atgtatatatatatt	6709
rs1984184	snp	A/G	0.0573587	0.15934	intron-variant	SPTAN1	GRCh38.p7	9:128562887	AGCTCCACCTCCTGG[A/G]TTCACGCCATTCTCC	6709
rs1984185	snp	A/G	0.0573587	0.15934	intron-variant	SPTAN1	GRCh38.p7	9:128564351	TTGAACCCGGGATGC[A/G]GAGGTTTCAATGAGC	6709
rs1984186	snp	C/T	0.190205	0.242744	intron-variant	SPTAN1	GRCh38.p7	9:128564436	aaaaaaaaaaaaaat[C/T]agccagtcatggtgg	6709
rs1999831	snp	A/G	0.0569829	0.158885	intron-variant	SPTAN1	GRCh38.p7	9:128565764	TTCCAGGGTAACACA[A/G]TTTTATACCTTTTAT	6709
rs2050629	snp	A/G	0.0569829	0.158885	intron-variant	SPTAN1	GRCh38.p7	9:128558761	ATTCCTTCCACAACC[A/G]AGGCTGCATGCTGCA	6709
rs2050630	snp	G/T	0.0603597	0.1629	intron-variant	SPTAN1	GRCh38.p7	9:128556301	CTAAATTTTTTTTTT[G/T]TGAAAAAGGTCCGAC	6709
rs2065951	snp	C/T	0.0298908	0.118541	intron-variant	SPTAN1	GRCh38.p7	9:128611326	aatagaaaaattagc[C/T]gggtgtgatgtcatg	6709
rs2095668	snp	A/G	0.151001	0.229563	intron-variant	SPTAN1	GRCh38.p7	9:128589337	tctgtcacccaggct[A/G]gagtgcagtggcacg	6709
rs2152833	snp	C/T	0.471578	0.115772	intron-variant	SPTAN1	GRCh38.p7	9:128569041	CCTTAAGAAGTTACC[C/T]GAATCCTGCCTTTGT	6709
rs2184932	snp	A/G	0.474544	0.10991	intron-variant	SPTAN1	GRCh38.p7	9:128628369	CTGGGGGCTCAGGCA[A/G]GGTACAGTAAGTCCA	6709
rs2227862	snp	C/T	0.330265	0.236765	SPTAN1	9	allele_origin=G(germline)/T(germline)/C(germline)	9:128617688	CGGCCGGGACCTAAC[C/T]GGCGTGCAGAACCTG	6709
rs2227863	snp	A/G	9.88484e-05	0.00702954	missense	SPTAN1	GRCh38.p7	9:128578178	TGAAAGCCCTCATCA[A/G]TGCAGATGAGCTTGC	6709
rs2227864	snp	C/T	0.312265	0.242122	SPTAN1	9	allele_origin=G(germline)/T(germline)/C(germline)	9:128598471	GGAGTCTGAAGGTCT[C/T]ATGGCAGAGGAGGTG	6709
rs2227865	snp	A/G	0.0134005	0.0807506	SPTAN1	9	allele_origin=G(germline)/A(germline)	9:128594259	GTTGTTCCGTGAAGC[A/G]AATGAACTACAGCAA	6709
rs2228951	snp	C/T	0.0031742	0.0397118	SPTAN1	9	allele_origin=T(germline)/C(germline)	9:128608195	GGCCTTCTTGAATAC[C/T]GAAGACAAAGGAGAC	6709
rs2228952	snp	A/C/T	0.0146655	0.0843685	SPTAN1, WDR34	9	allele_origin=T(germline)/C(germline)	9:128633289	CCGCGAGCTCCCCAC[A/C/T]GCGTTCGACTACGTG	6709
rs2275257	snp	C/G/T	0.0295035	0.117819	intron-variant	SPTAN1	GRCh38.p7	9:128566561	AGGGGAATGGATGGC[C/G/T]GTTTTTAATAAAGAA	6709
rs2275258	snp	A/G	0.0345262	0.126772	intron-variant	SPTAN1	GRCh38.p7	9:128576719	CTTGTGATTCTCTTC[A/G]GAGTGGTGATTTGCT	6709
rs2275259	snp	A/G	0.0345262	0.126772	intron-variant	SPTAN1	GRCh38.p7	9:128582048	ACATGCTATCTCGTT[A/G]AAGACATAATACAAC	6709
rs2297767	snp	C/T	0.0905309	0.192535	intron-variant	SPTAN1	GRCh38.p7	9:128575023	CTGAGACAGAAATGC[C/T]GTGAACTCAACCTCT	6709
rs2297768	snp	C/T	0.471004	0.116864	intron-variant	SPTAN1	GRCh38.p7	9:128575110	AAGCTAACATGGCTC[C/T]GTCCCTAATGTGTCT	6709
rs2297769	snp	A/C	0.02845	0.115836	SPTAN1	9	allele_origin=A(germline)/C(germline)	9:128575382	GCTTCTCACAACATT[A/C]TTATGTTAACTTTTT	6709
rs2297770	snp	A/G	0.0345262	0.126772	intron-variant	SPTAN1	GRCh38.p7	9:128575398	TTATGTTAACTTTTT[A/G]GTATATTCAGGATAA	6709
rs2297771	snp	A/G	0.458545	0.137872	intron-variant	SPTAN1	GRCh38.p7	9:128575564	GGAAGGGCAGAGTTC[A/G]TTTGATCTGTTTCCT	6709
rs3737308	snp	A/G	0.33004	0.236841	SPTAN1	9	allele_origin=G(germline)/A(germline)	9:128626364	AGAGACTGAGTTGGC[A/G]GAGTCGCCAGGGCTG	6709
rs3750332	snp	C/G	0.440333	0.16209	intron-variant	SPTAN1	GRCh38.p7	9:128617870	CAGGTTTGGACTGAG[C/G]GGTCATGAACACTTT	6709
rs3750333	snp	G/T	0.045811	0.144246	SPTAN1	9	allele_origin=G(germline)/T(germline)	9:128617719	GTTCTGCTTCCAGCC[G/T]CTTGTGCTTCTTCCT	6709
rs3763599	snp	A/G	0.372391	0.217992	intron-variant	SPTAN1	GRCh38.p7	9:128569171	GTGAATTTAACATTT[A/G]TAAGTGGCAGTGAGA	6709
rs3793450	snp	C/G	0.00755907	0.0610114	intron-variant	SPTAN1	GRCh38.p7	9:128604651	AGCCACCACGCCCAG[C/G]CTAAAAAAATTTATT	6709
rs3814530	snp	A/G	0.139903	0.224452	intron-variant	SPTAN1	GRCh38.p7	9:128591710	GCTTAGGCGTGTCCT[A/G]AGGCTCCTGGAGCCC	6709
rs3814531	snp	A/G	0.0345262	0.126772	intron-variant	SPTAN1	GRCh38.p7	9:128600312	GAGTGTCTGTCAAAT[A/G]CTCAGTACAGTTAGG	6709
rs3818829	snp	A/G	0.00119737	0.0244387	intron-variant	SPTAN1	GRCh38.p7	9:128608795	TCACCCAAAATAACT[A/G]TCCTTTTCTCAAGAC	6709
rs4240431	snp	A/G	0.0520825	0.152737	intron-variant	SPTAN1	GRCh38.p7	9:128584200	TCCTCTCAGGAATGG[A/G]AAAAAGACCTTATCA	6709
rs4307429	snp	A/G	0.0176395	0.0922421	SPTAN1	9	allele_origin=G(germline)/A(germline)	9:128588767	TAGATGACTCAGCGC[A/G]GACGTGTTTTTACCA	6709
rs4384085	snp	A/G	0.00358779	0.0422022	intron-variant	SPTAN1	GRCh38.p7	9:128582299	TGATATCTGACTGGT[A/G]ACATCAAGCAAAATC	6709
rs4395990	snp	C/G	0.45762	0.139261	intron-variant	SPTAN1	GRCh38.p7	9:128568240	GCTTTAGGTACAATC[C/G]CTGCCTGGCAGGCCC	6709
rs4506330	snp	A/T	0.458775	0.137524	intron-variant	SPTAN1	GRCh38.p7	9:128562132	TTGTTTTTTATATTT[A/T]TTATTTTTTTGACAG	6709
rs4560891	snp	C/T	0.0569829	0.158885	intron-variant	SPTAN1	GRCh38.p7	9:128563321	CTCAGGAGGCTGAGG[C/T]GGGAGGATCGCTGGA	6709
rs4836615	snp	A/G	0.0178853	0.0928588	SPTAN1	9	allele_origin=G(germline)/A(germline)	9:128584886	TTGGTGCTGCTCCTC[A/G]TGTCTCCCCTTCTTG	6709
rs4837277	snp	G/T	0.104859	0.203554	intron-variant	SPTAN1	GRCh38.p7	9:128561587	agaatggcatgaacc[G/T]gggaggcggagcttg	6709
rs4837278	snp	A/G	0.0283406	0.115616	intron-variant	SPTAN1	GRCh38.p7	9:128561620	gtgagccgaaattgc[A/G]ccactgcactccagc	6709
rs4837279	snp	A/G	0.458315	0.13822	intron-variant	SPTAN1	GRCh38.p7	9:128567804	TTGCTCTTATTGCCC[A/G]AGTTGGAGTGCAATG	6709
rs4837280	snp	A/G	0.0584853	0.160693	intron-variant	SPTAN1	GRCh38.p7	9:128578027	TAGACATTTGAGAAC[A/G]TAGAATTCAGAGCTT	6709
rs4837281	snp	C/T	0.0581099	0.160244	intron-variant	SPTAN1	GRCh38.p7	9:128578566	ccaggcacggtggct[C/T]atgtctgtaatccca	6709
rs4837282	snp	C/T	0.0581099	0.160244	intron-variant	SPTAN1	GRCh38.p7	9:128578596	agcactttggaaggc[C/T]gaggcgggtggatca	6709
rs4837283	snp	A/G	0.0905309	0.192535	intron-variant	SPTAN1	GRCh38.p7	9:128578679	actaaaaatgcaaca[A/G]ttagctggtcatggt	6709
rs4837284	snp	C/T	0.328505	0.237354	SPTAN1	9	allele_origin=T(germline)/C(germline)	9:128584890	TGCTGCTCCTCGTGT[C/T]TCCCCTTCTTGCCGA	6709
rs4837285	snp	A/G	0.0955749	0.196603	intron-variant	SPTAN1	GRCh38.p7	9:128587166	tcacgactccctaca[A/G]ctttgacctcctgtg	6709
rs4837286	snp	A/G	0.201418	0.245234	intron-variant	SPTAN1	GRCh38.p7	9:128587833	ATTTACAGAGTTTAA[A/G]ATAAGatttatttat	6709
rs4837287	snp	A/C	0.0955749	0.196603	intron-variant	SPTAN1	GRCh38.p7	9:128587926	cctcggctcactgca[A/C]cctccgcctcctggg	6709
rs4837288	snp	G/T	0.00358779	0.0422022	intron-variant	SPTAN1	GRCh38.p7	9:128601973	AACTTGGTCATTGAT[G/T]ATATGAATGGGCAAC	6709
rs4837289	snp	A/G	0.473909	0.111197	intron-variant	SPTAN1	GRCh38.p7	9:128603791	CCTGGTCAAGAGCCT[A/G]CCAGTTCTCAACAGT	6709
rs4837290	snp	C/T	0.0614824	0.164198	intron-variant	SPTAN1	GRCh38.p7	9:128618715	GTCTCGATCTCCTGA[C/T]CTCGTGATCTGCCCG	6709
rs5900805	in-del	-/T			intron-variant	SPTAN1	GRCh38.p7	9:128556479	TGTTTTGAGTCATAG[-/T]AACAATAAGGAACTT	6709
rs5900806	in-del	-/TAAA			intron-variant	SPTAN1	GRCh38.p7	9:128564588	CAAAAACAAATAAAT[-/TAAA]AAATAAATAAAAATC	6709
rs5900808	in-del	-/A	0.0923359	0.194016	intron-variant	SPTAN1	GRCh38.p7	9:128582329	CTCAAAAGTTATGAG[-/A]AAAAATGTCATCACC	6709
rs5900810	in-del	-/TTG/TTT	0	0	intron-variant	SPTAN1	GRCh38.p7	9:128588328	TTTTTTTTTTTTTTT[-/TTG/TTT]GAGATGGAGTTTCAC	6709
rs5900811	in-del	-/A			intron-variant	SPTAN1	GRCh38.p7	9:128599686	ACAAAGCACAGCTCT[-/A]AAAAAAAAAAAAAAA	6709
rs6478836	snp	C/T	0.444444	0.157135	intron-variant	SPTAN1	GRCh38.p7	9:128555623	AATTTGCAAAGCCTT[C/T]TTTTTTTTTTTTTTT	6709
rs6478837	snp	C/T	0.444444	0.157135	intron-variant	SPTAN1	GRCh38.p7	9:128555624	ATTTGCAAAGCCTTT[C/T]TTTTTTTTTTTTTTT	6709
rs6478838	snp	A/G	0.0452528	0.143452	intron-variant	SPTAN1	GRCh38.p7	9:128555792	TCCTAGATATTTGGA[A/G]AAAATAATCTGAAAA	6709
rs6478841	snp	C/G	0.199873	0.244923	intron-variant	SPTAN1	GRCh38.p7	9:128603297	GAATTGTGGTTTTTA[C/G]CATTCTTTTTTCACT	6709
rs6478842	snp	C/T	0.0581099	0.160244	intron-variant	SPTAN1	GRCh38.p7	9:128607118	AAACTGGATCAAATG[C/T]ATGCCCAGGCCTAGG	6709
rs7019666	snp	C/G	0.0581099	0.160244	intron-variant	SPTAN1	GRCh38.p7	9:128580393	GTTTTGAAGTATCTT[C/G]GAGTATAAAATTGCC	6709
rs7021150	snp	A/T	0	0	utr-variant-3-prime, downstream-variant-500B	SPTAN1, WDR34	GRCh38.p7	9:128633419	GTGCTCTCACTTTCC[A/T]CTGTAACCTTAAGCC	6709
rs7023384	snp	A/G	0.0287284	0.116357	intron-variant	SPTAN1	GRCh38.p7	9:128563957	CAACCAACATTTCTT[A/G]ATGACCTCTGTATGC	6709
rs7024498	snp	C/G	0.0175809	0.0920943	SPTAN1	9	allele_origin=G(germline)/C(germline)	9:128611886	CAGGGAGGAAGATGA[C/G]CACCGTCACTGTCAA	6709
rs7026966	snp	A/G	0.0581099	0.160244	intron-variant	SPTAN1	GRCh38.p7	9:128587434	TTGTCCCAAAAGATG[A/G]GAATCCTGAAAAACT	6709
rs7027388	snp	A/G	0.0962929	0.197165	intron-variant	SPTAN1	GRCh38.p7	9:128587494	GCAGGAGGTGATTAC[A/G]TCATTGTGCAACTGA	6709
rs7027510	snp	C/T	0.367297	0.220775	intron-variant	SPTAN1	GRCh38.p7	9:128578672	catctctactaaaaa[C/T]gcaacagttagctgg	6709
rs7028880	snp	A/G	0.0298908	0.118541	intron-variant	SPTAN1	GRCh38.p7	9:128605718	CAAAAACggccaggc[A/G]cagtggctcacgtct	6709
rs7031524	snp	C/T	0.0581099	0.160244	intron-variant	SPTAN1	GRCh38.p7	9:128579363	gacaGAGCCCTGGAA[C/T]GAAAGAGAGCTCAGA	6709
rs7032787	snp	C/T			intron-variant	SPTAN1	GRCh38.p7	9:128616990	cgcctataatcccaa[C/T]actttgggagaccga	6709
rs7032911	snp	A/G	0.0905309	0.192535	intron-variant	SPTAN1	GRCh38.p7	9:128576321	ACTCAGGCTGACAAG[A/G]CAGGATCACTTGAGA	6709

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