iUUCD 2.0 - integrated annotations for ubiquitin and ubiquitin-like conjugation database

Y54E10A.11

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs3138919	snp	C/T			missense	?	WS195	I:3180959	TAAAAGCCTGTGCAA[C/T]ACATGATTCTTGGAA	171893
rs193319022	snp	A/T	0.283498	0.247746	intron-variant	?	WS195	I:3179640	TTGAGCAAAAGCCGC[A/T]TTTTTTTTTTGAAAT	171893
rs193319023	snp	A/G	0.0768	0.180282	missense	?	WS195	I:3179740	ATCAATGCATTCAAA[A/G]CATTCTTGAAAAATG	171893
rs193319024	snp	C/T	0.0392	0.1344	synonymous-codon	?	WS195	I:3181104	CCGAACGAACGGAGT[C/T]GGCTGTTGATCTCGT	171893
rs193319025	snp	C/T	0.0296962	0.118179	intron-variant	?	WS195	I:3182188	GATGATTTTGTGGGT[C/T]GTTACTCCTTGCGAA	171893
rs193319026	snp	A/G	0.425408	0.178135	intron-variant	?	WS195	I:3183880	TGTCTGAAAAATTGA[A/G]AAATTTAGAAAATTT	171893
rs193319027	snp	C/T	0.020406	0.0989272	intron-variant	?	WS195	I:3183934	ACTAAAAATTCGAAA[C/T]TTTAACCAAAAATTC	171893
rs193319028	snp	A/G	0.020406	0.0989272	intron-variant	?	WS195	I:3183938	AAAATTCGAAATTTT[A/G]ACCAAAAATTCCGAT	171893
rs193319029	snp	C/T	0.43016	0.173327	intron-variant	?	WS195	I:3183957	AAAAATTCCGATTTT[C/T]CTCAAAAACTTCAAA	171893
rs193319030	snp	A/T	0.019998	0.0979748	intron-variant	?	WS195	I:3183980	ACTTCAAATCTTTTG[A/T]CTAAAAATTTATATT	171893
rs193319031	snp	C/T	0.010152	0.0705191	missense	?	WS195	I:3184329	AACAGGTAAATTGTC[C/T]CAATTTTCGTATCCA	171893
rs193319032	snp	C/G	0.0101008	0.0703445	missense	?	WS195	I:3184375	CTTCGAATTTTTGGC[C/G]TTTTTCAGGAATTCC	171893
rs193319033	snp	C/T	0.0298439	0.118454	missense	?	WS195	I:3184428	GGTGCACAACAACAG[C/T]CATCATTTATCAATT	171893
rs193319034	snp	A/G	0.18795	0.242177	missense	?	WS195	I:3186088	TTTTTTCGTTCTTCA[A/G]GGTCCTCCTTGGAAT	171893
rs193319035	snp	A/C	0.0198	0.0975088	missense	?	WS195	I:3186164	CGGCATTAGTGTCCA[A/C]CTGAATTCCCATTTT	171893
rs193319036	snp	A/G	0.0306048	0.119857	synonymous-codon	?	WS195	I:3186216	TGCAATAGCCTTTCC[A/G]TTTCTTTTCTCGTGC	171893
rs193319037	snp	A/G	0.0102038	0.070695	missense	?	WS195	I:3186419	TATCAAATCGATCGG[A/G]ATTTTCGATAAACTC	171893
rs193319038	snp	C/T	0.0101008	0.0703445	missense	?	WS195	I:3186538	GGATTTGAGAGCAAA[C/T]TTCCGTGTAAATGAG	171893
rs193572812	snp	C/T			synonymous-codon	?	WS195	I:3178237	TTTATTCTTGCACTG[C/T]TTGCACTTAATTTTC	171893
rs193572813	snp	C/G			synonymous-codon	?	WS195	I:3178252	TTTGCACTTAATTTT[C/G]GGCAACTGATGTGTC	171893
rs193572814	snp	A/T			intron-variant	?	WS195	I:3178877	TAGATTTTTCGAATT[A/T]AAAAAAAATCAAAAA	171893
rs193572815	snp	C/T			intron-variant	?	WS195	I:3180239	GTAAAAAATATATAG[C/T]CCGACAGAAATTATC	171893
rs193572816	snp	A/G			intron-variant	?	WS195	I:3180566	AAGTAATGAAAAAAT[A/G]TCAATTTTCTCTGTA	171893
rs193572818	snp	A/C			missense	?	WS195	I:3181017	CGGAATAAACTCTTG[A/C]TTCGCCACGTCATCA	171893
rs193572819	snp	A/G			intron-variant	?	WS195	I:3181388	CTACATTTTTTTTAG[A/G]CAAGAACAGTTTTTT	171893
rs193572820	snp	A/G			intron-variant	?	WS195	I:3181586	TTCAGAGAATCGGTT[A/G]GGATGTTTGTGGAGG	171893
rs193572821	snp	A/G			intron-variant	?	WS195	I:3185014	AATTAATTTATTTTC[A/G]AATATTTATATTTAG	171893
rs193572822	snp	G/T			intron-variant	?	WS195	I:3185021	TTATTTTCGAATATT[G/T]ATATTTAGCGATATT	171893
rs193572823	snp	A/C			missense	?	WS195	I:3186623	TCTCGGGTGGAGCAA[A/C]TTCGTAAATGGAGGT	171893
rs193572824	snp	A/T			intron-variant	?	WS195	I:3186783	AATCTGGAAAAAGTT[A/T]AAAATTTTTTGGAAA	171893
rs193572825	snp	A/G			intron-variant	?	WS195	I:3186997	TTGTTAAATGCAAAA[A/G]GGTATGCACCTTTAA	171893
rs193572826	snp	C/G			intron-variant	?	WS195	I:3187021	CCTTTAAAGAGAGTA[C/G]TGTAATTAAATTTTT	171893
rs193572827	snp	G/T			intron-variant	?	WS195	I:3187581	CGGAGTTTCGAGAGT[G/T]TGTCGATTTTTGAAT	171893
rs193572828	snp	A/G			synonymous-codon	?	WS195	I:3188058	AATCGAAGTAATCAG[A/G]GCAGGATTTTCCAAC	171893
rs193572829	snp	A/G			missense	?	WS195	I:3188159	GAATCAAATTCAGAA[A/G]TCTTGGATATATTCC	171893
rs193572834	snp	A/T			missense	?	WS195	I:3190353	GCCAAATCAAAGGTA[A/T]TCGGCACAAAGAGCT	171893
rs193572835	snp	C/T			intron-variant	?	WS195	I:3191388	ATTTTTCGTTTTTTT[C/T]CTCATCTTTATGGAT	171893
rs193572836	snp	C/T			intron-variant	?	WS195	I:3191563	CTGCGGGATATCTTG[C/T]GCGTAAGATATGGCG	171893
rs193572837	snp	A/T			intron-variant	?	WS195	I:3191679	ATCGAAATTTTAATT[A/T]AAAAGTGGAAAACGT	171893
rs193572838	snp	A/T			intron-variant	?	WS195	I:3191847	AAAATGGCAAAAAAA[A/T]TTTTTTGAGCATTTT	171893
rs193572839	snp	C/T			intron-variant	?	WS195	I:3192241	AATAAAGGTTAAAAA[C/T]AAAGGAAAAATATTG	171893
rs353102012	snp	A/T			intron-variant	?	WS195	I:3180440	ATTCAAATTTCAGTA[A/T]AAAATCATAATTTTC	171893
rs353104052	in-del	-/T			intron-variant	?	WS195	I:3179955	AGAAAATATTTAGAA[-/T]TTTTTTTTCAATTTT	171893
rs353104698	snp	A/G			intron-variant	?	WS195	I:3191833	CCGAAAAGTGCTCAA[A/G]AATGGCAAAAAAAAT	171893
rs353104997	in-del	-/A			intron-variant	?	WS195	I:3191102	TACTTATCCATCTAC[-/A]AAAAATCGTCATATC	171893
rs353109174	snp	A/C			intron-variant	?	WS195	I:3185028	CGAATATTTATATTT[A/C]GCGATATTCCATCTT	171893
rs353110475	snp	A/T			intron-variant	?	WS195	I:3189775	GAACTTAATTTTTAT[A/T]TATTCATCACTTTTT	171893
rs353111536	snp	A/G			intron-variant	?	WS195	I:3183695	TCAAACCGTAATGGG[A/G]CAGCCTGACACCACA	171893
rs353115734	snp	A/G			intron-variant	?	WS195	I:3179556	AAAAAAATTGTTATC[A/G]AAATCCCCCATTTTT	171893
rs353119186	in-del	-/T			intron-variant	?	WS195	I:3189406	ATATAAAATCTCGGA[-/T]TTTTTTTTTCGATTT	171893
rs353120216	in-del	-/A			intron-variant	?	WS195	I:3178129	TTTCAGAGTTTTTTT[-/A]AAAAATATTTTTGCA	171893
rs353120461	snp	C/T			intron-variant	?	WS195	I:3179293	TGTAATTTCACTTTC[C/T]GGAAATTTCACCAAT	171893
rs353122799	in-del	-/T/TTT			intron-variant, cds-indel	?	WS195	I:3182989	AAATTTTTAAAGCTG[-/T/TTT]TTTTTTTTTTGGAAT	171893
rs353126939	snp	C/T			intron-variant	?	WS195	I:3189743	TGTTTGCCAACTTCT[C/T]GGTGTCGCAGCTTCT	171893
rs353127638	in-del	-/A			intron-variant	?	WS195	I:3176578	GAACCATTTGTACTG[-/A]AAAAAAAAGAAAATT	171893
rs353128079	snp	C/T			intron-variant	?	WS195	I:3191198	TCTGGCTGCATTTTT[C/T]GAACTTAATTTTTTT	171893
rs353129920	in-del	-/T			intron-variant	?	WS195	I:3187503	ATACAAAAAAAAAAG[-/T]TTTTTTTCACTTCAA	171893
rs353131811	snp	A/C			missense	?	WS195	I:3178621	TTCCTGTTCAATGAG[A/C]AACCGGCTCGCGTAC	171893
rs353137527	snp	A/T			intron-variant	?	WS195	I:3184901	ACTAAAACAACATAT[A/T]TGACGCGCAAATATC	171893
rs353138966	in-del	-/T			intron-variant	?	WS195	I:3186952	AATTTTCGATTTTCG[-/T]TTTTTTTTTGGTCTC	171893
rs353140072	snp	C/T			synonymous-codon	?	WS195	I:3186024	AAAATGCTCCAATTT[C/T]GGCTCATCTTCCGCA	171893
rs353146183	snp	A/C			intron-variant	?	WS195	I:3189784	TTTTATATATTCATC[A/C]CTTTTTAATAAATAT	171893
rs353150390	in-del	-/A			intron-variant	?	WS195	I:3179539	GATTTTCTAAAAATC[-/A]AAAAAAAATTGTTAT	171893
rs353151731	snp	C/G			intron-variant	?	WS195	I:3189747	TGCCAACTTCTCGGT[C/G]TCGCAGCTTCTGGAA	171893
rs353153838	snp	A/T			intron-variant	?	WS195	I:3180439	TATTCAAATTTCAGT[A/T]TAAAATCATAATTTT	171893
rs353154327	snp	A/G			intron-variant	?	WS195	I:3183019	TTTGATGGAAAATAT[A/G]TCAAAATTTGCGTTT	171893
rs353155702	in-del	-/T			intron-variant	?	WS195	I:3185070	TCGTATTATTTTCTC[-/T]TTTTTTTTTTGCTTA	171893
rs353156618	snp	A/T			intron-variant	?	WS195	I:3189135	ATTATTTTCGTCGAA[A/T]TCAATTTTTTTTAAC	171893
rs353157159	snp	A/G			intron-variant	?	WS195	I:3188623	TTTTCAAAAATCGAG[A/G]CACCACGTTTTCAAA	171893
rs353159635	in-del	-/A			intron-variant	?	WS195	I:3177094	ATCGATTTTTGCAGG[-/A]AAAAAATTCAGAAAA	171893
rs353160485	in-del	-/T			intron-variant	?	WS195	I:3185777	CTGGATAAAAATTCA[-/T]TTTTTTTTTGCTTAC	171893
rs353165996	in-del	-/G			intron-variant	?	WS195	I:3181645	AATGAAATTTTTTTT[-/G]TTGTTTTTTCGGATA	171893
rs353168108	snp	C/T			intron-variant	?	WS195	I:3191957	CAAAATAGCCTCTCA[C/T]CTCGAAAATATTCAT	171893
rs353171255	in-del	-/T			intron-variant	?	WS195	I:3190798	TATAATGCAATTCAA[-/T]TTTTTTTTCTGAAAA	171893
rs353174229	snp	C/G			intron-variant	?	WS195	I:3179523	TTTCGTTCGAATTTC[C/G]GATTTTCTAAAAATC	171893
rs353174975	snp	A/G			intron-variant	?	WS195	I:3180256	CGACAGAAATTATCT[A/G]CTTTAATAACTCGAT	171893
rs353176482	snp	A/G			synonymous-codon	?	WS195	I:3190586	ATCTGTGGTCAACTG[A/G]GCGACGAGTCCACAG	171893
rs353179717	snp	A/T			intron-variant	?	WS195	I:3187855	AAAAATCGATTTTTT[A/T]AAACCTTTTTTTAAT	171893
rs353179829	snp	A/G			intron-variant	?	WS195	I:3191190	CGGACCGCTCTGGCT[A/G]CATTTTTCGAACTTA	171893
rs353182069	snp	C/T			intron-variant	?	WS195	I:3189807	ATAAATATTGCGGTT[C/T]TTTATTAGCCGTTTA	171893
rs353182775	snp	A/G			intron-variant	?	WS195	I:3182061	TTGAATGGCAAAGTC[A/G]CCAGAAAGATGGATG	171893