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
rs346432823	snp	C/T			synonymous-codon	SCD1	TAIR10	1:18139874	AGAAGAACTATGGAG[C/T]GTTATGTTTTTCACG	841327
rs346441057	snp	A/G			synonymous-codon	SCD1	TAIR10	1:18147657	AAAAATCTCTTCGAG[A/G]GAATTACGAAGAACA	841327
rs346446559	snp	C/T			intron-variant	SCD1	TAIR10	1:18140671	CATTATAGTTGAATC[C/T]GTGAGTGACATTCAA	841327
rs346451264	snp	A/T			intron-variant	SCD1	TAIR10	1:18140047	GAGCCTGCAAGAAAA[A/T]AGACAGCAACGCACT	841327
rs346472693	snp	A/T			intron-variant	SCD1	TAIR10	1:18143189	TGATGAAGCATCCTC[A/T]AGGGCAAATCGAAAA	841327
rs346472751	snp	A/C			intron-variant	SCD1	TAIR10	1:18143831	CATTTTGAGCTGATA[A/C]CAATGAATAATCATT	841327
rs346475577	snp	A/T			intron-variant	SCD1	TAIR10	1:18148272	GTTAAACTCTTAAAC[A/T]GATGACTCATTTCAC	841327
rs346490187	snp	A/C			missense	SCD1	TAIR10	1:18147640	GAAGAGAAGCAAAGA[A/C]CAAAAATCTCTTCGA	841327
rs346494369	snp	C/T			intron-variant	SCD1	TAIR10	1:18145804	AAAGACGGTTTACCA[C/T]ACTAATTGGAACAAT	841327
rs346495639	snp	A/G			intron-variant	SCD1	TAIR10	1:18140144	AGATGAAATCAGCAT[A/G]GACCTGTGATTATTC	841327
rs346498775	snp	A/T			intron-variant	SCD1	TAIR10	1:18147424	AGTTCAAACCTAAAA[A/T]TGGTGTTGTTTTTCT	841327
rs346502218	snp	C/T			intron-variant	SCD1	TAIR10	1:18143188	TTGATGAAGCATCCT[C/T]TAGGGCAAATCGAAA	841327
rs346502282	snp	A/C			intron-variant	SCD1	TAIR10	1:18140131	GAGAACTGATGGTAG[A/C]TGAAATCAGCATGGA	841327
rs346508742	snp	A/C			intron-variant	SCD1	TAIR10	1:18148039	CGAGTATGCAATATA[A/C]GGATAATCACATACC	841327
rs346510751	snp	A/G			intron-variant	SCD1	TAIR10	1:18141727	TTGACACATTGCACA[A/G]GAAAAGAAGCAGCAT	841327
rs346511939	snp	A/C			intron-variant	SCD1	TAIR10	1:18144435	TCATTCCTTGGTTTA[A/C]CAATTTCTTGCAGCG	841327
rs346514755	snp	C/T			intron-variant	SCD1	TAIR10	1:18148278	CTCTTAAACAGATGA[C/T]TCATTTCACCATGGA	841327
rs346519046	snp	A/G			intron-variant	SCD1	TAIR10	1:18145985	GACAAAAGAATCCGT[A/G]TAAGTAAGAAAAGAT	841327
rs346542897	snp	A/T			intron-variant	SCD1	TAIR10	1:18141698	TTTCAATCAATGACT[A/T]TCTCCATAAGAAGTT	841327
rs346546859	snp	A/T			intron-variant	SCD1	TAIR10	1:18141666	AGAGCAAGCTCATCA[A/T]CTCTTAAGTGAAAAC	841327
rs346554491	snp	G/T			intron-variant	SCD1	TAIR10	1:18140078	AACGTAAGCTTTGAT[G/T]TTATTTTGTGAAAAA	841327
rs346565185	snp	A/G			intron-variant	SCD1	TAIR10	1:18141656	ATCCTATTTAAGAGC[A/G]AGCTCATCATCTCTT	841327
rs346575941	snp	A/G			intron-variant	SCD1	TAIR10	1:18144879	GTTTGAAGCCATGCA[A/G]TAGCAACAGGATTAC	841327
rs346583384	snp	A/T			intron-variant	SCD1	TAIR10	1:18139538	TTAAATCCGAGATTC[A/T]GTTTCAGTGAGAATG	841327
rs346588432	snp	G/T			synonymous-codon	SCD1	TAIR10	1:18147795	AATGCAACTGACAAA[G/T]ATTTTTGATCCATCA	841327
rs346592275	snp	A/T			missense	SCD1	TAIR10	1:18145050	GGAGGGTGCCTTCCA[A/T]TGGATTCAAGAGCCC	841327
rs346599334	snp	C/T			missense	SCD1	TAIR10	1:18146283	TAGGGCACTGCTCAA[C/T]GGAATTACCAAAGCC	841327
rs346607059	snp	A/T			intron-variant	SCD1	TAIR10	1:18140062	TAGACAGCAACGCAC[A/T]AACGTAAGCTTTGAT	841327
rs346607435	snp	A/C			intron-variant	SCD1	TAIR10	1:18145026	TCCAAGCAAATCAGG[A/C]TGTACCTTGGAGGGT	841327
rs346634421	snp	A/C			utr-variant-3-prime	SCD1	TAIR10	1:18139242	TTTCATACATTTTAA[A/C]ACGCCAAAGTTTATT	841327
rs346638322	snp	C/T			intron-variant	SCD1	TAIR10	1:18141437	AACTCCCGAGAGCCA[C/T]CAAGGTGAATAAGAA	841327
rs346647825	snp	C/T			intron-variant	SCD1	TAIR10	1:18148553	GCTGATTCCACATTT[C/T]ATCGCCGTTTAACAA	841327
rs346660397	snp	C/T			intron-variant	SCD1	TAIR10	1:18140065	ACAGCAACGCACTAA[C/T]GTAAGCTTTGATGTT	841327
rs346670399	snp	C/G			missense	SCD1	TAIR10	1:18145946	TCTTCAGAAACGCAT[C/G]AGTGCTAAAAACTTT	841327
rs346672135	snp	A/T			intron-variant	SCD1	TAIR10	1:18140069	CAACGCACTAACGTA[A/T]GCTTTGATGTTATTT	841327
rs346680151	snp	C/T			utr-variant-5-prime	SCD1	TAIR10	1:18148957	CAATTCGGCCTCCTT[C/T]GTTTTTTTGGCCAAG	841327
rs346694064	snp	G/T			intron-variant	SCD1	TAIR10	1:18140969	GGTAAGTCACCATAA[G/T]TATCGCTTCTTCTTT	841327
rs346733694	snp	C/T			utr-variant-5-prime	SCD1	TAIR10	1:18148830	GATCCGTCCCATTGT[C/T]TTCCTTCGAGATCTA	841327
rs346735354	snp	A/G			utr-variant-3-prime, intron-variant	SCD1	TAIR10	1:18141824	ACGACTGTGGTAACA[A/G]TAAAAGCAAAATAAT	841327
rs346736532	snp	C/G			intron-variant	SCD1	TAIR10	1:18141620	TAAATTTCAAGAAAT[C/G]AAAGTGTGAAAGACT	841327
rs346736991	snp	A/C			missense, intron-variant	SCD1	TAIR10	1:18142095	CCAATCAAGCATTTT[A/C]TACCGACCAGACAGT	841327
rs346744280	snp	C/G			intron-variant	SCD1	TAIR10	1:18148517	TTAGCAAATACAGAA[C/G]AAACCTAACAACTAG	841327
rs346753850	snp	A/G			intron-variant	SCD1	TAIR10	1:18147825	ACCCTCTGTGCAAAA[A/G]TTATTAAGATAAAAT	841327
rs346771850	snp	A/T			synonymous-codon	SCD1	TAIR10	1:18139745	TTGTGGTACTCTATA[A/T]AGTTGCCAGCCTGAG	841327
rs346774162	snp	A/G			intron-variant	SCD1	TAIR10	1:18142691	ATTAAAAAGCTTGAA[A/G]TTTGTAAATGTATGG	841327
rs346787425	snp	C/T			synonymous-codon	SCD1	TAIR10	1:18139883	ATGGAGTGTTATGTT[C/T]TTCACGCATTTAATG	841327
rs346798649	snp	A/C			intron-variant	SCD1	TAIR10	1:18144140	TGCAGGAAATAAATC[A/C]ACTATACAGTAAGGT	841327
rs346827765	snp	A/G			intron-variant	SCD1	TAIR10	1:18141790	GTTATTCTTCCAAAT[A/G]TTCTAATTTACTATA	841327
rs346828695	snp	A/C			intron-variant	SCD1	TAIR10	1:18143444	CTTTTATTTTCATCA[A/C]AAAACGTGATAAGGA	841327
rs346832547	snp	A/T			missense	SCD1	TAIR10	1:18142108	TTATACCGACCAGAC[A/T]GTCTGTACTACCGCT	841327
rs346836206	snp	A/G			intron-variant	SCD1	TAIR10	1:18140124	ATCTTTTGAGAACTG[A/G]TGGTAGATGAAATCA	841327
rs346839780	snp	C/T			intron-variant	SCD1	TAIR10	1:18145678	CCAACTGAAAACAAT[C/T]GGAAGAGTACCAATA	841327
rs346849193	snp	A/C			intron-variant	SCD1	TAIR10	1:18139644	CAGGATCTCATAAGA[A/C]TTATCAAACCGCATG	841327
rs346853388	snp	C/G			intron-variant	SCD1	TAIR10	1:18139711	AAAAGAGGGAGGGTC[C/G]TACCACGGCGGCTGT	841327
rs346866505	snp	C/G			intron-variant	SCD1	TAIR10	1:18145194	ATCAGAACATGATCC[C/G]AAACTCAGTAGACGG	841327
rs346870657	snp	A/G			intron-variant	SCD1	TAIR10	1:18140645	ATTTGCAACCCTGAT[A/G]ATTATCCAATCATTA	841327
rs346888070	snp	C/G			intron-variant	SCD1	TAIR10	1:18141736	TGCACAGGAAAAGAA[C/G]CAGCATGCGGGTTAT	841327
rs346903218	snp	A/C/G			intron-variant	SCD1	TAIR10	1:18140325	TGCAGAATTGACACA[A/C/G]TTTGATCAAACAAGT	841327
rs346916813	snp	C/T			intron-variant	SCD1	TAIR10	1:18140979	CATAAGTATCGCTTC[C/T]TCTTTGGTGCCTTAT	841327
rs346922884	snp	A/G			intron-variant	SCD1	TAIR10	1:18139673	TGACCAGAAAAATTT[A/G]GAGCAACTATCCAAC	841327
rs346928848	snp	C/G			synonymous-codon	SCD1	TAIR10	1:18145493	TTCAACTTCTGGCTC[C/G]GCTATTGTGATTATT	841327
rs346982877	snp	A/G			intron-variant	SCD1	TAIR10	1:18139966	TTGATAATTGTGTTT[A/G]GATCCAGGTTAATAA	841327
rs347023171	snp	A/G			utr-variant-3-prime, intron-variant	SCD1	TAIR10	1:18141920	TCTTTAGGCCTAACA[A/G]ATAGTGAATGCAACC	841327
rs347029999	snp	C/T			synonymous-codon	SCD1	TAIR10	1:18143795	CGACAAATCGCTTCT[C/T]GAAGCAGCACGGCCC	841327
rs347079571	snp	C/G			intron-variant	SCD1	TAIR10	1:18140039	CATCCGCCGAGCCTG[C/G]AAGAAAATAGACAGC	841327
rs347179147	snp	A/G			synonymous-codon	SCD1	TAIR10	1:18140200	AGATTGTACTGGCCC[A/G]GCATGGCATGCCAAA	841327
rs347179150	snp	C/T			intron-variant	SCD1	TAIR10	1:18141069	TTGTCGTTGAACATT[C/T]TGTCAAATGGGATTC	841327
rs347202382	snp	A/G			intron-variant	SCD1	TAIR10	1:18139968	GATAATTGTGTTTAG[A/G]TCCAGGTTAATAATG	841327
rs347206514	snp	C/T			synonymous-codon	SCD1	TAIR10	1:18140004	CTCACCTTCGTCATT[C/T]TCCCAAAAGCGTAGC	841327
rs347214306	snp	A/G			missense	SCD1	TAIR10	1:18143781	GCATCCCGCACTGTC[A/G]ACAAATCGCTTCTTG	841327
rs347248932	snp	A/G			intron-variant	SCD1	TAIR10	1:18148025	AGCATACAAAACTCC[A/G]AGTATGCAATATACG	841327
rs347284367	snp	G/T			intron-variant	SCD1	TAIR10	1:18141009	TGAGTTATGACTGAC[G/T]GATAGTTAATAATTG	841327
rs347358957	snp	A/C/T			intron-variant	SCD1	TAIR10	1:18142882	AAGAGCATAAAGTAA[A/C/T]GTGAAGACATATTAA	841327
rs347388587	snp	G/T			intron-variant	SCD1	TAIR10	1:18143414	AGCCAATATATCAAG[G/T]ATGCTACAGATCGAC	841327
rs347417711	snp	A/G			intron-variant	SCD1	TAIR10	1:18143619	TTTCTGAGCAGCACC[A/G]AAAAATTCATTAAAT	841327
rs347432930	snp	A/C			intron-variant	SCD1	TAIR10	1:18140973	AGTCACCATAAGTAT[A/C]GCTTCTTCTTTGGTG	841327
rs347435937	snp	A/C			intron-variant	SCD1	TAIR10	1:18147882	AAGCAGGTGTATTCA[A/C]AACAAACCAACTTAA	841327
rs347451569	snp	A/G			intron-variant	SCD1	TAIR10	1:18146882	ATTAGTGTGGTGATT[A/G]AATAGAGATAGTATG	841327
rs347460006	snp	C/T			intron-variant	SCD1	TAIR10	1:18140341	TTTGATCAAACAAGT[C/T]GCAGATTCTGAGATA	841327
rs347461176	snp	A/G			intron-variant	SCD1	TAIR10	1:18143163	AAGTATGTTGACAAC[A/G]ATGGAAAAGTTGATG	841327
rs347465380	snp	C/T			intron-variant	SCD1	TAIR10	1:18140684	TCCGTGAGTGACATT[C/T]AATACAGCAAATCCA	841327

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