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
rs80374365	snp	C/G			intron-variant	Tomosyn	Release_6_plus_ISO1_MT	X:12642353	CAACATGAACAACAG[C/G]GACAACATAAATATG	32217
rs80375167	snp	A/T			intron-variant	Tomosyn	Release_6_plus_ISO1_MT	X:12642599	GATATACATATTTAT[A/T]ACCTAATTCGAATTG	32217
rs80379379	in-del	-/T			intron-variant	Tomosyn	Release_6_plus_ISO1_MT	X:12642379	TATGTTTCTCCCCCC[-/T]CTCTCTCTCTCTCTC	32217
rs80386349	snp	A/T			intron-variant	Tomosyn	Release_6_plus_ISO1_MT	X:12642343	ACAATCGAAACAACA[A/T]GAACAACAGCGACAA	32217
rs202248648	snp	A/T			intron-variant	Tomosyn	Release_6_plus_ISO1_MT	X:12638298	TATAAGATATATTGT[A/T]TAATATGAAATAATT	32217
rs202254400	snp	C/T			upstream-variant-2KB, utr-variant-3-prime	Tomosyn, Aven, CG2540	Release_6_plus_ISO1_MT	X:12631075	TTATTTATTCATTAT[C/T]ATATATGAAAACATA	32217
rs202254491	snp	G/T			intron-variant, upstream-variant-2KB	Tomosyn	Release_6_plus_ISO1_MT	X:12632652	CAATCCGAAATCAAA[G/T]CCAGCGACAACCATA	32217
rs202255410	snp	A/G			intron-variant, upstream-variant-2KB	Tomosyn, mir-970	Release_6_plus_ISO1_MT	X:12635121	CAAAAGAAATCGAAG[A/G]GAGGGAAGCAAACAA	32217
rs202340112	snp	C/T			intron-variant, upstream-variant-2KB	Tomosyn, CkIalpha	Release_6_plus_ISO1_MT	X:12652224	TAATACATATATCAA[C/T]GTTCCCTTCATTCCA	32217
rs202372029	snp	A/G			intron-variant	Tomosyn	Release_6_plus_ISO1_MT	X:12642816	TCAGCTAACTAAGTC[A/G]TTGCCTAAAGTTAAA	32217
rs202388245	snp	A/G			intron-variant, downstream-variant-500B	Tomosyn, mir-970	Release_6_plus_ISO1_MT	X:12636513	GTGATTAGTACGTTT[A/G]ATCCAATTTCTTCTC	32217
rs202433151	snp	A/C			intron-variant	Tomosyn	Release_6_plus_ISO1_MT	X:12651436	AGTGATAAAGCCACG[A/C]ACATAAATGAAAACC	32217
rs202443893	snp	C/G			intron-variant	Tomosyn	Release_6_plus_ISO1_MT	X:12648011	GAATAAGAAAAAATG[C/G]ATAGAAATCGGGATA	32217
rs202446873	snp	A/T			intron-variant	Tomosyn	Release_6_plus_ISO1_MT	X:12650503	TAGTACAAAAACAAT[A/T]AATATTACAAAATAA	32217
rs202447213	snp	C/T			intron-variant	Tomosyn	Release_6_plus_ISO1_MT	X:12650140	TTCTCTCTCTATATT[C/T]TCTCTCGGTATTTGT	32217
rs202450919	snp	C/T			intron-variant	Tomosyn	Release_6_plus_ISO1_MT	X:12646880	AAGATTGTTGCAAAA[C/T]CGATGAAGAGAAATC	32217
rs202453732	snp	A/T			intron-variant	Tomosyn	Release_6_plus_ISO1_MT	X:12647585	GCGGACAACACTGTA[A/T]ATTGATCAAACTACA	32217
rs202456183	snp	A/G			intron-variant, synonymous-codon	Tomosyn	Release_6_plus_ISO1_MT	X:12648911	GCATCAATTACAGCA[A/G]CTACAGCAGCAATCG	32217
rs202457736	snp	A/G			synonymous-codon, intron-variant	Tomosyn	Release_6_plus_ISO1_MT	X:12644031	GCTGCTCAGCGGATC[A/G]GCAGCGGCAACGGCG	32217
rs202459826	snp	A/G			intron-variant	Tomosyn	Release_6_plus_ISO1_MT	X:12643268	ATTACAAATTATTTG[A/G]GATTTATTTCTATGA	32217
rs202463815	snp	A/C			intron-variant	Tomosyn	Release_6_plus_ISO1_MT	X:12646246	TCACTAAACAACACT[A/C]TAAACACCACACTCT	32217
rs202467071	snp	A/T			intron-variant	Tomosyn	Release_6_plus_ISO1_MT	X:12641545	AAGTACTTAGACCCC[A/T]GTCCATTTATATCTA	32217
rs202471596	snp	A/G			upstream-variant-2KB, missense	Tomosyn, Aven, CG2540	Release_6_plus_ISO1_MT	X:12630884	CACTGCAAGCTAAAA[A/G]CAAGTCGTGACACCA	32217
rs202473245	snp	C/T			intron-variant	Tomosyn	Release_6_plus_ISO1_MT	X:12640865	TCGCTCTCTCTCTCT[C/T]TCTTTCTCTCTCTCT	32217
rs202474304	snp	C/G			intron-variant	Tomosyn	Release_6_plus_ISO1_MT	X:12638582	TTGATTCAATAATTC[C/G]TGTGCTTTAGGTTGG	32217
rs202478242	snp	C/T			intron-variant	Tomosyn	Release_6_plus_ISO1_MT	X:12637904	ACCATAAAGCAATTT[C/T]ACAATAATATTTCAA	32217
rs202481238	snp	A/T			intron-variant, upstream-variant-2KB	Tomosyn, mir-970	Release_6_plus_ISO1_MT	X:12635302	AAGCATATTTTCTAT[A/T]TGAACTGCTATTGAA	32217
rs202488728	snp	A/G			intron-variant, upstream-variant-2KB	Tomosyn	Release_6_plus_ISO1_MT	X:12631865	GGTATTTAGTGGGTG[A/G]TTGTGTTGCGGAATG	32217
rs202493646	snp	A/T			intron-variant	Tomosyn	Release_6_plus_ISO1_MT	X:12645204	GCATAAACGCAGTAC[A/T]TCCGCTCTCGACGTC	32217
rs202510028	snp	C/T			intron-variant	Tomosyn	Release_6_plus_ISO1_MT	X:12640147	AGGGTTTCGTATTTG[C/T]GTTTCGGTATTTAAT	32217
rs202512134	snp	A/C			intron-variant	Tomosyn	Release_6_plus_ISO1_MT	X:12634331	TTTCCATCCCCCGCA[A/C]CCCAGTTGCTCTGCA	32217
rs202521703	snp	A/G			intron-variant, utr-variant-5-prime, upstream-variant-2KB	Tomosyn	Release_6_plus_ISO1_MT	X:12633599	AGTAGAGACAGTAGA[A/G]GCAGTAAAAGCAGCA	32217
rs202533464	snp	A/T			intron-variant, missense	Tomosyn	Release_6_plus_ISO1_MT	X:12648631	AACAGCAGCAGCAGC[A/T]ACAGCAGCAACAGCA	32217
rs202542309	snp	A/G			intron-variant	Tomosyn	Release_6_plus_ISO1_MT	X:12647996	AAACATTTTTGTTGG[A/G]AATAAGAAAAAATGC	32217
rs202548497	snp	C/T			missense, intron-variant	Tomosyn	Release_6_plus_ISO1_MT	X:12643934	CGGAGGCTGGCGAAA[C/T]ATCGGCCCACGATGG	32217
rs202554810	snp	A/C			intron-variant	Tomosyn	Release_6_plus_ISO1_MT	X:12639743	ACCTGATAACCCCTG[A/C]CACGCCCCCCCCCCC	32217
rs202559245	snp	C/T			intron-variant	Tomosyn	Release_6_plus_ISO1_MT	X:12643224	CTTCAATTTGCTGTA[C/T]TTATACACCCTCAAT	32217
rs202566729	snp	G/T			intron-variant	Tomosyn	Release_6_plus_ISO1_MT	X:12638539	CAGTGAGTTTTACAC[G/T]CACCCAATTTTCGTT	32217
rs202568847	snp	C/T			upstream-variant-2KB, utr-variant-3-prime	Tomosyn, Aven, CG2540	Release_6_plus_ISO1_MT	X:12631006	TGCAACGACGTGTTA[C/T]AGAGGCTTCTGACGA	32217
rs202568873	snp	C/T			intron-variant, upstream-variant-2KB	Tomosyn	Release_6_plus_ISO1_MT	X:12632730	CGTGCCAGTGTGTTT[C/T]TGTGTGTGTGTGAGT	32217
rs202664000	snp	A/G			intron-variant	Tomosyn	Release_6_plus_ISO1_MT	X:12647070	CGCCCGCATAGCCAC[A/G]TGTCTACCTCTCGCT	32217
rs202668824	snp	A/G			intron-variant	Tomosyn	Release_6_plus_ISO1_MT	X:12649997	TGAATATGTTCTCTC[A/G]ATCTGTCTCGCTCGC	32217
rs202673984	snp	A/C			intron-variant	Tomosyn	Release_6_plus_ISO1_MT	X:12644797	AGCGAAAGGATCATC[A/C]TCCATCTTATCCAAA	32217
rs202679133	snp	A/T			intron-variant, upstream-variant-2KB	Tomosyn, CkIalpha	Release_6_plus_ISO1_MT	X:12652191	TAATTTGTTGTAATT[A/T]GTGCAATTGATTGTA	32217
rs202683096	snp	G/T			intron-variant	Tomosyn	Release_6_plus_ISO1_MT	X:12647703	TTCTTACCTAGAAAA[G/T]CTTTGTGTCAAATAA	32217
rs202685439	snp	C/T			intron-variant	Tomosyn	Release_6_plus_ISO1_MT	X:12646794	CCTTTATTTTCATTT[C/T]CGATTTTGCTTAGCG	32217
rs202686894	snp	A/T			intron-variant	Tomosyn	Release_6_plus_ISO1_MT	X:12650654	AATATTTGAAACACT[A/T]AAATTCTGCGAGCGA	32217
rs202691547	snp	A/C			intron-variant, upstream-variant-2KB	Tomosyn	Release_6_plus_ISO1_MT	X:12632547	AGAAAAGAGAAAAGG[A/C]AATTTGGGGAGCTTC	32217
rs202692455	snp	A/C			intron-variant	Tomosyn	Release_6_plus_ISO1_MT	X:12645259	TCTAAACCCTTTCTC[A/C]CACCCAGTCTCCCCT	32217
rs202695055	snp	G/T			intron-variant	Tomosyn	Release_6_plus_ISO1_MT	X:12651240	TGGTAAGACTGATCG[G/T]TGATTAGATTATATC	32217
rs202697020	snp	C/T			intron-variant	Tomosyn	Release_6_plus_ISO1_MT	X:12646215	CACACATCACAGTTT[C/T]ACACATCACCACAAT	32217
rs202699331	snp	A/G			intron-variant	Tomosyn	Release_6_plus_ISO1_MT	X:12642074	AATTTTATTTGATTT[A/G]GATGGATTGGATTGG	32217
rs202704839	snp	A/C			intron-variant	Tomosyn	Release_6_plus_ISO1_MT	X:12642914	TGTTGATACAATATT[A/C]CCCCAGTCCCCCCCC	32217
rs202708061	snp	A/C			intron-variant	Tomosyn	Release_6_plus_ISO1_MT	X:12641402	TTGTAGCCAATGAAA[A/C]TTTTGTTTTGGTTTG	32217
rs202711921	snp	A/T			intron-variant, upstream-variant-2KB	Tomosyn, mir-970	Release_6_plus_ISO1_MT	X:12635726	CCATTCTCTCCCTCA[A/T]TGCAGCAAATATTTC	32217
rs202714601	snp	C/T			intron-variant, upstream-variant-2KB	Tomosyn	Release_6_plus_ISO1_MT	X:12632040	GCTTTTCAATATCAA[C/T]CATCACATCACCGTT	32217
rs202720680	snp	C/G			intron-variant, upstream-variant-2KB	Tomosyn, mir-970	Release_6_plus_ISO1_MT	X:12635226	TATTTCCTCATTTCC[C/G]TTCCAAGAAATGCAA	32217
rs202728643	snp	A/T			intron-variant	Tomosyn	Release_6_plus_ISO1_MT	X:12646303	GCATTTTAAAAAATA[A/T]TATCCAAAATCGAAA	32217
rs202729339	snp	C/G			intron-variant	Tomosyn	Release_6_plus_ISO1_MT	X:12640572	TTAAGTTATTATCCT[C/G]ATGACGAATAGTTTC	32217
rs202734168	snp	C/T			intron-variant	Tomosyn	Release_6_plus_ISO1_MT	X:12650593	CGCTGAAGAATGGCT[C/T]AAAAAGTTTTAAATG	32217
rs202736095	snp	A/C			intron-variant	Tomosyn	Release_6_plus_ISO1_MT	X:12637688	TAAATATATTTGATT[A/C]GATTTATGTATGCTT	32217
rs202740993	snp	C/G			intron-variant	Tomosyn	Release_6_plus_ISO1_MT	X:12645256	TTCTCTAAACCCTTT[C/G]TCCCACCCAGTCTCC	32217
rs202741296	snp	A/C			intron-variant	Tomosyn	Release_6_plus_ISO1_MT	X:12649929	TCTCTCTCTCTCTCT[A/C]TCTCTCTGTCTTTCT	32217
rs202741622	snp	A/G			intron-variant	Tomosyn	Release_6_plus_ISO1_MT	X:12634153	TCTCTCCCTGCCCAA[A/G]CCCACTCGCATTCTC	32217
rs202743428	snp	A/C			intron-variant	Tomosyn	Release_6_plus_ISO1_MT	X:12640952	CCGAATCGCAGTGAA[A/C]CGCGCGTACAAACAT	32217
rs202759598	snp	A/T			intron-variant, upstream-variant-2KB	Tomosyn, mir-970	Release_6_plus_ISO1_MT	X:12634389	AGTATGCCAACGATT[A/T]GCTTGTCCTTCTCCA	32217
rs202884465	snp	A/C			utr-variant-3-prime, upstream-variant-2KB	Tomosyn, CkIalpha	Release_6_plus_ISO1_MT	X:12653297	AAGTACACTTATTTA[A/C]TTTCTGTTTTCAAGT	32217
rs202904537	snp	G/T			downstream-variant-500B, upstream-variant-2KB, utr-variant-5-prime	Tomosyn, CkIalpha	Release_6_plus_ISO1_MT	X:12653743	CCGATAGTTTAGCAG[G/T]GTGCCACGGTGAAGT	32217
rs202904720	snp	A/G			intron-variant	Tomosyn	Release_6_plus_ISO1_MT	X:12648047	TCTAAAGTGCACTAC[A/G]AACATATAGGCTAAA	32217
rs202906790	snp	A/G			intron-variant	Tomosyn	Release_6_plus_ISO1_MT	X:12646976	TATATATGTATATAT[A/G]TATATATATGTATAT	32217
rs202907008	snp	C/T			synonymous-codon, intron-variant	Tomosyn	Release_6_plus_ISO1_MT	X:12644739	CAGCAGCGGCATTGG[C/T]GGAAGCGTCGCTGGA	32217
rs202907218	snp	C/T			intron-variant	Tomosyn	Release_6_plus_ISO1_MT	X:12647768	TGGAAAAGTAAGTTT[C/T]TGATTTCAATATAAT	32217
rs202913008	snp	A/T			intron-variant	Tomosyn	Release_6_plus_ISO1_MT	X:12642939	CCCCCCCCCCTTAGC[A/T]ACCCAATAACCCCGT	32217
rs202914330	snp	C/T			intron-variant	Tomosyn	Release_6_plus_ISO1_MT	X:12647275	ATAATCGTGTTCTCG[C/T]GTTTTAATTGTATCC	32217
rs202917694	snp	A/C			intron-variant	Tomosyn	Release_6_plus_ISO1_MT	X:12641863	TTTTATGGTCAAGTA[A/C]AATAAAATGTGGCCA	32217
rs202919101	snp	A/C			intron-variant	Tomosyn	Release_6_plus_ISO1_MT	X:12651450	GCACATAAATGAAAA[A/C]CTTTTTAAATATCTT	32217
rs202920031	snp	A/T			intron-variant	Tomosyn	Release_6_plus_ISO1_MT	X:12647646	CTAATTTTTTTAATT[A/T]TATTTTATTTAAATA	32217
rs202921343	snp	A/T			intron-variant	Tomosyn	Release_6_plus_ISO1_MT	X:12639618	CAAAAAAAAAAAAAA[A/T]TTACTTAGACCGTAG	32217
rs202922790	snp	A/G			intron-variant	Tomosyn	Release_6_plus_ISO1_MT	X:12642256	GTCGATTTCGAGTCG[A/G]TTCGATTTGAGTTGA	32217
rs202923102	snp	C/T			intron-variant	Tomosyn	Release_6_plus_ISO1_MT	X:12643419	CAATGTAAATACTAA[C/T]AATGTCATAAAGCAT	32217
rs202924728	snp	C/T			intron-variant	Tomosyn	Release_6_plus_ISO1_MT	X:12637218	CTTAGTGACCTAAAC[C/T]GACCGCATTAAGTTC	32217
rs202929755	snp	C/T			intron-variant, upstream-variant-2KB	Tomosyn, mir-970	Release_6_plus_ISO1_MT	X:12635670	ATTGTAATTGAAGCT[C/T]TCAACTTGTTTTCAT	32217
rs202931467	snp	A/T			intron-variant	Tomosyn	Release_6_plus_ISO1_MT	X:12642836	CTAAAGTTAAACCCC[A/T]ATCCGATGTTTGTTA	32217
rs202931514	snp	A/G/T			intron-variant	Tomosyn	Release_6_plus_ISO1_MT	X:12637994	CTCATTAAAAATTTA[A/G/T]AATCTTTTAATTTGC	32217
rs202937590	snp	A/T			upstream-variant-2KB, downstream-variant-500B	Tomosyn, Aven, CG2540	Release_6_plus_ISO1_MT	X:12631443	AATTAGGCAAGTAAC[A/T]TAAAGGATTTTAATT	32217
rs202958391	snp	A/C			upstream-variant-2KB, utr-variant-5-prime	Tomosyn, Aven, CG2540	Release_6_plus_ISO1_MT	X:12629954	TGGCTAACGAAGCAC[A/C]GGTGATGTTGGACTT	32217
rs202959792	snp	C/T			intron-variant	Tomosyn	Release_6_plus_ISO1_MT	X:12640179	TTGTTTTTTGTTTTT[C/T]ATTTTTTAATGTGAT	32217
rs202964259	snp	A/C			missense, downstream-variant-500B	Tomosyn, mir-970	Release_6_plus_ISO1_MT	X:12636830	TCACCGCCGATGACA[A/C]CATTCACTTGTGGAG	32217
rs202967232	snp	G/T			intron-variant	Tomosyn	Release_6_plus_ISO1_MT	X:12641337	ACATTATATAATCTA[G/T]ATATATATATATTTA	32217
rs202971141	snp	C/T			intron-variant, upstream-variant-2KB	Tomosyn	Release_6_plus_ISO1_MT	X:12632254	CAAGAGTTGCCAACC[C/T]CCCCCCCCCTCTGAC	32217
rs202974561	snp	A/G/T			intron-variant, utr-variant-5-prime	Tomosyn	Release_6_plus_ISO1_MT	X:12633755	AAAACTAAAGCGAAC[A/G/T]TCTTGAAGCCATTAA	32217
rs202974608	snp	A/G			upstream-variant-2KB, utr-variant-5-prime	Tomosyn, Aven, CG2540	Release_6_plus_ISO1_MT	X:12629620	GATGGATAATGCGGC[A/G]AACAGCTGTTCCCTT	32217
rs203065830	snp	A/C			missense, upstream-variant-2KB	Tomosyn, CkIalpha	Release_6_plus_ISO1_MT	X:12651801	GCGGCGGTGGTGGTG[A/C]CGGCGGTGGTGCGGC	32217
rs203083610	snp	C/T			intron-variant	Tomosyn	Release_6_plus_ISO1_MT	X:12649372	AAAAAAAAAACAATT[C/T]GCATATTTTTTTTTA	32217
rs203086078	snp	G/T			intron-variant	Tomosyn	Release_6_plus_ISO1_MT	X:12648174	AAATTTGTCTTTGTT[G/T]GCACACTAGTTTTGC	32217
rs203092180	snp	G/T			intron-variant	Tomosyn	Release_6_plus_ISO1_MT	X:12645023	ATGTGAGGGTGTTCT[G/T]TGGATTCTGTGTATT	32217
rs203093681	snp	C/G			intron-variant	Tomosyn	Release_6_plus_ISO1_MT	X:12648078	AATGAAACTTCACAA[C/G]AACAAAGTAAAAATT	32217
rs203094294	snp	A/T			intron-variant	Tomosyn	Release_6_plus_ISO1_MT	X:12646451	GTAAGCATTTCAAGA[A/T]GGTTACACTTAATTG	32217
rs203094421	snp	A/T			intron-variant	Tomosyn	Release_6_plus_ISO1_MT	X:12643546	TATTTTCTTACGTAT[A/T]TTCACCTCACTTTTC	32217
rs203102548	snp	A/G			missense, intron-variant	Tomosyn	Release_6_plus_ISO1_MT	X:12644450	CTGATGAGGGCGCCA[A/G]CAGTAGCATTGCCAG	32217

Full records

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