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
rs6683	snp	C/T	0.474091	0.11083	utr-variant-3-prime, intron-variant	ECHDC1, RNF146	GRCh38.p7	6:127288876	GGTAAAAATAACTTG[C/T]ATTTGCCTTACCATC	81847
rs13981	snp	A/G	0.0110494	0.0735024	utr-variant-3-prime, intron-variant	ECHDC1, RNF146	GRCh38.p7	6:127288950	TTGACCTCTTGTGAT[A/G]AGTCAGAACTAGAAC	81847
rs15131	snp	G/T	0	0	intron-variant, utr-variant-3-prime, downstream-variant-500B	ECHDC1, RNF146	GRCh38.p7	6:127288269	CTATAAGACTAGACA[G/T]CAAAGCCTATGGGAA	81847
rs877102	snp	C/T	0.465892	0.126058	upstream-variant-2KB	RNF146	GRCh38.p7	6:127265941	CCTGAAATAAACTGA[C/T]TTCAGAGGAATAACA	81847
rs877661	snp	A/C	0.408871	0.193029	utr-variant-5-prime, upstream-variant-2KB, intron-variant	RNF146	GRCh38.p7	6:127266770	CCGCACCGGCGAGCT[A/C]ACTCCGGCGCCTCAT	81847
rs1013640	snp	A/G	0.0162398	0.0886349	intron-variant	RNF146	GRCh38.p7	6:127272419	TTTTCCTTCCCCAGC[A/G]TTTATCCAGTTAGTC	81847
rs2038378	snp	C/T	0.41141	0.19091	intron-variant	RNF146	GRCh38.p7	6:127269255	GACTGCTAATTAAAG[C/T]ATTTAGAACTTAGAA	81847
rs2144742	snp	A/C	0.41141	0.19091	intron-variant	RNF146	GRCh38.p7	6:127274641	ACACTAGAGGTTTTA[A/C]CATTCAATCAATTAG	81847
rs2180341	snp	A/G	0.41141	0.19091	intron-variant	RNF146	GRCh38.p7	6:127279485	ttggtgtatttatct[A/G]tcctatgccagcacc	81847
rs2326567	snp	A/G	0.41141	0.19091	intron-variant, utr-variant-5-prime	RNF146	GRCh38.p7	6:127285015	TTCCATAGGTTAGGA[A/G]AAAGTTGTACTTTCT	81847
rs2875972	snp	C/T	0.44638	0.154709	upstream-variant-2KB	RNF146	GRCh38.p7	6:127264377	ACACAAATGTGGTTT[C/T]TGGGGtttttttgag	81847
rs3055106	in-del	-/TT	0.411578	0.190768	intron-variant	RNF146	GRCh38.p7	6:127273069	TTGTAATGGCATGAC[-/TT]TTCTTGGCTTCTTGG	81847
rs3756992	snp	C/T	0.00358779	0.0422022	intron-variant	RNF146	GRCh38.p7	6:127285981	ataaGGCAGAAATTA[C/T]AAATTTTATGTCAGT	81847
rs4266509	snp	C/G	0	0	intron-variant	RNF146	GRCh38.p7	6:127286499	TCATATCCCCATTGT[C/G]TAGTATGTGGCTTGC	81847
rs4502958	snp	A/G	0.474	0.111014	intron-variant	RNF146	GRCh38.p7	6:127271968	TTTATTATTAATGTG[A/G]CTAATAGAAAATTTG	81847
rs4897207	snp	C/T	0.41141	0.19091	intron-variant, utr-variant-5-prime	RNF146	GRCh38.p7	6:127284753	ATAGTGCTTAACATA[C/T]TAAGACGTCCTATTA	81847
rs5879845	in-del	-/A	0.199254	0.244796	intron-variant	RNF146	GRCh38.p7	6:127274453	AGAGAGGAATAAATT[-/A]GATTGGTTACAGATA	81847
rs6569477	snp	A/T	0.411074	0.191194	intron-variant	RNF146	GRCh38.p7	6:127268157	CCAAAGATGATAGGG[A/T]ACGCTTTGTTCTTTG	81847
rs6569478	snp	A/G	0.41141	0.19091	intron-variant	RNF146	GRCh38.p7	6:127277474	GGCAGTGTTCTCTAG[A/G]GGGACAGAACTAATA	81847
rs6569479	snp	C/T	0.41141	0.19091	intron-variant	RNF146	GRCh38.p7	6:127285443	ATTCATTTTAAGCTT[C/T]CAATCTCTGACATCT	81847
rs6906717	snp	A/C	0.41141	0.19091	intron-variant	RNF146	GRCh38.p7	6:127275637	GCATGTGATAAATTC[A/C]GTAATAGAAAAACAT	81847
rs7755329	snp	C/T			intron-variant	RNF146	GRCh38.p7	6:127270826	ttccttatgattttt[C/T]ttttttttgagatgg	81847
rs7764180	snp	A/C	0.366266	0.221319	intron-variant, utr-variant-5-prime	RNF146	GRCh38.p7	6:127284522	ATTTTCAGGAATTTT[A/C]TGGAAACTAACTTTT	81847
rs7766270	snp	A/G	0	0	intron-variant	RNF146	GRCh38.p7	6:127279520	tgtcttgttacctta[A/G]ctttgtagtaagttt	81847
rs7773637	snp	A/G			intron-variant	RNF146	GRCh38.p7	6:127270864	ctctgtcattaggct[A/G]gagtgcagtggtgcg	81847
rs7773638	snp	C/G			intron-variant	RNF146	GRCh38.p7	6:127270865	tctgtcattaggctg[C/G]agtgcagtggtgcga	81847
rs7773643	snp	A/G			intron-variant	RNF146	GRCh38.p7	6:127270875	ggctggagtgcagtg[A/G]tgcgatcttggctca	81847
rs7773646	snp	A/G			intron-variant	RNF146	GRCh38.p7	6:127270877	ctggagtgcagtggt[A/G]cgatcttggctcact	81847
rs7774468	snp	C/G	0.411242	0.191052	intron-variant	RNF146	GRCh38.p7	6:127271356	aactgTATAAATTCT[C/G]AGAGTTAATAGGTGA	81847
rs7775667	snp	C/T	0.474	0.111014	intron-variant	RNF146	GRCh38.p7	6:127277599	CCAAAACTGAAGAAC[C/T]TGGAGTCTGATGTTC	81847
rs9321072	snp	C/T	0.366266	0.221319	intron-variant, utr-variant-5-prime	RNF146	GRCh38.p7	6:127285204	GTGTTGCTTCCTTTA[C/T]TAGAAAATTGCCATC	81847
rs9321073	snp	C/T	0.41141	0.19091	intron-variant, utr-variant-3-prime, downstream-variant-500B	ECHDC1, RNF146	GRCh38.p7	6:127288546	TGTGTATATAATAAA[C/T]ATGTATGGAAATAAA	81847
rs9372861	snp	C/T	0.380529	0.213219	intron-variant	RNF146	GRCh38.p7	6:127280050	tctgtatgcctttat[C/T]tcttttccctaattt	81847
rs9372862	snp	C/T	0.366266	0.221319	intron-variant	RNF146	GRCh38.p7	6:127280101	catgttgaatagcag[C/T]ggtaaaagcatgcat	81847
rs9375498	snp	A/G	0.380529	0.213219	intron-variant	RNF146	GRCh38.p7	6:127274296	ACAGCTTATTTGGGT[A/G]TTCAAATATGGGTTC	81847
rs9385419	snp	A/G	0.41141	0.19091	intron-variant	RNF146	GRCh38.p7	6:127276446	CACAAAGTAGTTAAG[A/G]CATGAAACCTGAGAT	81847
rs9388557	snp	G/T	0.366266	0.221319	intron-variant	RNF146	GRCh38.p7	6:127269802	TATGTATATATAATT[G/T]TTTTTGAGTTGTGTA	81847
rs9388558	snp	A/T	0.366266	0.221319	intron-variant	RNF146	GRCh38.p7	6:127275441	AAATCTAATCCTTTG[A/T]TATTCTGTTCCTCAC	81847
rs9388559	snp	A/G	0.36606	0.221428	intron-variant, utr-variant-5-prime	RNF146	GRCh38.p7	6:127280572	ACTGAAGACACAGGA[A/G]TTTGCTCAAAGAATG	81847
rs9401945	snp	C/G	0.366266	0.221319	intron-variant	RNF146	GRCh38.p7	6:127276531	GATAAAGATATGAGG[C/G]GGCCAAGGGTTCTGT	81847
rs9401946	snp	C/G	0.0174175	0.0916809	intron-variant	RNF146	GRCh38.p7	6:127276910	TTCCTAGGTTTAAAC[C/G]TATGTCTACTGGCCT	81847
rs9401947	snp	C/T	0.380529	0.213219	intron-variant	RNF146	GRCh38.p7	6:127280916	CATATTTAACTTCAC[C/T]GTATTGATGAAACAT	81847
rs9482781	snp	A/G	0.0524604	0.153226	intron-variant	RNF146	GRCh38.p7	6:127270679	cgtgtagttccactt[A/G]tacaatacttttttt	81847
rs9482782	snp	A/G	0.0524604	0.153226	intron-variant	RNF146	GRCh38.p7	6:127277417	CTAAAGTCAGAGTAA[A/G]ACAAAAAGGTTACTT	81847
rs9482783	snp	G/T	0.0217236	0.101931	intron-variant	RNF146	GRCh38.p7	6:127277447	TAGAAACCTTGTTTA[G/T]TCAGtatattaggca	81847
rs9482784	snp	C/T	0.0524604	0.153226	intron-variant	RNF146	GRCh38.p7	6:127279898	ttgtctcctggtgta[C/T]cagaacacaactgat	81847
rs9491721	snp	A/C	0.0217236	0.101931	upstream-variant-2KB	RNF146	GRCh38.p7	6:127265675	taataTTAGCATTAC[A/C]TCTTCAAGCTGGAAT	81847
rs9491722	snp	A/C	0.00478085	0.0486577	intron-variant	RNF146	GRCh38.p7	6:127275636	TGCATGTGATAAATT[A/C]CGTAATAGAAAAACA	81847
rs9491723	snp	G/T	0.0134861	0.0810011	intron-variant	RNF146	GRCh38.p7	6:127275713	AGAAAATGGTAGAGA[G/T]AACCATTTCTGTGTA	81847
rs9491724	snp	A/G	0.0799831	0.183287	intron-variant	RNF146	GRCh38.p7	6:127277261	ATATATAGGGAGTGT[A/G]TGAAAATGTGCAGTT	81847
rs9491725	snp	A/G	0.0524604	0.153226	intron-variant	RNF146	GRCh38.p7	6:127278679	caattctattgctat[A/G]tccctgggagtggca	81847
rs9784840	snp	C/T	0.243919	0.249926	upstream-variant-2KB	RNF146	GRCh38.p7	6:127265597	tacctcatagtttat[C/T]atgagaattaagtgg	81847
rs10081141	snp	C/T	0.00301857	0.0387321	missense	RNF146	GRCh38.p7	6:127286686	AAAGCGAACGAGTCC[C/T]GTTCTAATACTGCAC	81847
rs10583480	in-del	-/AG	0.117886	0.21224	intron-variant	RNF146	GRCh38.p7	6:127285416	GCAGAATTAGCTGGC[-/AG]AGAGATTGTCATTCA	81847
rs10669927	in-del	-/TTTTT			intron-variant	RNF146	GRCh38.p7	6:127285530	TCTTTTTTTTTTTTT[-/TTTTT]TTTTACCATGGGGAA	81847
rs12175928	snp	C/T	0.366266	0.221319	intron-variant	RNF146	GRCh38.p7	6:127273262	AATTcataatagcaa[C/T]aggaaattattacag	81847
rs12192111	snp	A/G	0.243919	0.249926	intron-variant	RNF146	GRCh38.p7	6:127269684	TGATGAGGGCTAAAA[A/G]TTGAGACATTAGGGC	81847
rs12199451	snp	C/G	0.474	0.111014	intron-variant	RNF146	GRCh38.p7	6:127276635	AGATGGTCAAGAGAT[C/G]GTAGGTCCCCATGAA	81847
rs12210968	snp	A/G	0.474	0.111014	intron-variant	RNF146	GRCh38.p7	6:127275840	ACTATGAGTAATTTT[A/G]TACAACTAGATTATT	81847
rs12661321	snp	A/G	0	0	intron-variant	RNF146	GRCh38.p7	6:127274454	GAGAGGAATAAATTA[A/G]ATTGGTTACAGATAA	81847
rs12661323	snp	G/T			intron-variant	RNF146	GRCh38.p7	6:127274486	GTGTAAATGCATTCA[G/T]GAGATAAGGAGAATT	81847
rs17054498	snp	A/G	0.0209421	0.100162	intron-variant, utr-variant-5-prime	RNF146	GRCh38.p7	6:127283154	ACTCTTATTAGTCTG[A/G]CAGAAATATTTCACA	81847
rs34022547	in-del	-/G			intron-variant	RNF146	GRCh38.p7	6:127271604	CCACTAGCCACATGG[-/G]AGTTATTGAGCACTT	81847
rs34183554	in-del	-/G			intron-variant	RNF146	GRCh38.p7	6:127277303	TAGGCTGCAGCAAGG[-/G]AAATGAACATAGCCT	81847
rs34276067	in-del	-/C			intron-variant	RNF146	GRCh38.p7	6:127273490	ATACCTAATTTTTTC[-/C]TTTTCCTTTTTTTGA	81847
rs34446709	in-del	-/C			intron-variant	RNF146	GRCh38.p7	6:127272322	TTGTGAAGAGCTCCC[-/C]AGGTAGTGCTGATAG	81847
rs34452528	in-del	-/T			intron-variant	RNF146	GRCh38.p7	6:127269659	TCTTAGCTAATTTTT[-/T]AGCAGGAGATGATGA	81847
rs34779419	in-del	-/T			utr-variant-5-prime	RNF146	GRCh38.p7	6:127280297	CTGGTGAAGAAAATG[-/T]CTTTATTTTTGTGGC	81847
rs34966816	in-del	-/T			intron-variant	RNF146	GRCh38.p7	6:127279685	ACTTTGGGTAGTATT[-/T]GTCATTTTAATATGT	81847
rs35122403	in-del	-/T			intron-variant	RNF146	GRCh38.p7	6:127277885	CAGTCAGTTACTTTT[-/T]GAAAGTTCTCTGATT	81847
rs35162965	snp	A/T			intron-variant	RNF146	GRCh38.p7	6:127273489	ATATACCTAATTTTT[A/T]CTTTTCCTTTTTTTG	81847
rs35268158	in-del	-/GTTT	0.5	0	intron-variant	RNF146	GRCh38.p7	6:127279558	GGATTTTTCAAGATT[-/GTTT]GGGTTACTTAGGGTC	81847
rs35314752	in-del	-/A			intron-variant, utr-variant-5-prime	RNF146	GRCh38.p7	6:127283891	ATGATGGAACCAAAA[-/A]TACCTGCACAAACAG	81847
rs35895333	in-del	-/G			intron-variant	RNF146	GRCh38.p7	6:127273304	TTAATTTTATACAGC[-/G]TATGATTCATACTGC	81847
rs36121662	in-del	-/C	0.190205	0.242744	intron-variant	RNF146	GRCh38.p7	6:127274758	GCAGGACTTTGTGGA[-/C]CAAAAAACTTCAAGT	81847
rs41285264	snp	G/T	0.138207	0.223612	intron-variant, utr-variant-3-prime, downstream-variant-500B	ECHDC1, RNF146	GRCh38.p7	6:127288413	GAAACATTTTGACAT[G/T]TGTGACCAAAGGTCA	81847
rs45456292	snp	A/G	0.0162398	0.0886349	utr-variant-3-prime	RNF146	GRCh38.p7	6:127287822	GGTATGGGAAGGATA[A/G]ACTCATAATTAAAAT	81847
rs55949622	snp	G/T	0.0023933	0.0345097	intron-variant	RNF146	GRCh38.p7	6:127269918	TAAATGGCAAAAATC[G/T]TATTAAACATTAGCT	81847
rs56803126	snp	C/T	0.0209421	0.100162	upstream-variant-2KB	RNF146	GRCh38.p7	6:127264611	ACTGACCTCGTGATC[C/T]GCCCACTTCGGCCTC	81847
rs57592897	in-del	-/T/TTTTT	0.625	0.125	intron-variant	RNF146	GRCh38.p7	6:127285546	TTTTTTTTTTTTTTT[-/T/TTTTT]ACCATGGGGAAAAAA	81847
rs60034087	snp	C/T	0.0174175	0.0916809	upstream-variant-2KB	RNF146	GRCh38.p7	6:127264618	TCGTGATCCGCCCAC[C/T]TCGGCCTCCTAAAGT	81847
rs60312390	snp	C/T	0.0126979	0.078662	intron-variant, utr-variant-5-prime	RNF146	GRCh38.p7	6:127283578	AGCCTTGAAGTATGT[C/T]TTATAGGTAGACTAG	81847
rs60598629	in-del	-/T			intron-variant	RNF146	GRCh38.p7	6:127269997	TTTGTCTTTGTTTTT[-/T]ATATGTATTTATATT	81847
rs60988696	snp	C/T	0.0425829	0.139564	intron-variant	RNF146	GRCh38.p7	6:127272912	CTAAAGGAAAATAAA[C/T]TCCTAAGGAAGAAAA	81847
rs61326477	snp	A/G/T	0.00159649	0.0282165	intron-variant, utr-variant-5-prime	RNF146	GRCh38.p7	6:127283692	AAGAAATATCACTAA[A/G/T]TTTTTCTGCCCATTT	81847
rs62438529	snp	C/T			intron-variant	RNF146	GRCh38.p7	6:127267596	TCTCTCGCTCTTCCT[C/T]CTTTTTTTTCTCCTG	81847
rs67358768	in-del	-/T	0.380529	0.213219	intron-variant	RNF146	GRCh38.p7	6:127278313	TAGATTTTCCACAAC[-/T]TTTTTTTTAGCATTA	81847
rs71024769	in-del	-/CAAA	0	0	intron-variant	RNF146	GRCh38.p7	6:127279559	GGACCCTAAGTAACC[-/CAAA]CAATCTTGAAAAATC	81847
rs72961049	snp	C/T	0.108402	0.206034	intron-variant	RNF146	GRCh38.p7	6:127281113	GACATAAAACTCTTG[C/T]TTTCTACTCTTCCAG	81847
rs73579964	snp	C/G	0.0119091	0.0762411	upstream-variant-2KB, utr-variant-5-prime	RNF146	GRCh38.p7	6:127266433	TCCCCTCCGTCCCCC[C/G]CCTCCCCATTTTTTT	81847
rs74454300	snp	C/G	0.5	0	intron-variant	RNF146	GRCh38.p7	6:127276261	TGAACAATAGTCCAG[C/G]TGAGAGTTATGTAGG	81847
rs74842472	snp	A/T			intron-variant	RNF146	GRCh38.p7	6:127278322	CCACAACTTTTTTTT[A/T]GCATTACAAACAGAA	81847
rs75060469	snp	A/G	0.00318978	0.0398085	intron-variant	RNF146	GRCh38.p7	6:127276510	TTGTAAAATGTGTGT[A/G]TATGAGATAAAGATA	81847
rs75330094	snp	G/T			stop-gained	RNF146	GRCh38.p7	6:127286815	GGAGCTTCATGGCTT[G/T]GAAAGCGGTGTGCTC	81847
rs75562683	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	RNF146	GRCh38.p7	6:127287735	AAGGTTGAAAGGGTT[A/G]CCTGTAAATTTCTGC	81847
rs75673629	snp	A/G	0.0134861	0.0810011	utr-variant-3-prime, intron-variant	ECHDC1, RNF146	GRCh38.p7	6:127288756	GTAGTTTTTACATCT[A/G]TGGCCAAATAGTATT	81847
rs75997766	snp	A/T	0.5	0	utr-variant-3-prime, intron-variant	ECHDC1, RNF146	GRCh38.p7	6:127288985	TTCTTTGACTTTCAC[A/T]TTTTTTAAAAAGTGT	81847
rs76295519	snp	C/T	0.5	0	intron-variant	RNF146	GRCh38.p7	6:127285529	CCCCTTTTAAAATGT[C/T]TTTTTTTTTTTTTTT	81847
rs76406607	snp	A/G	0.0644693	0.167566	intron-variant	RNF146	GRCh38.p7	6:127268543	ATAGATTTTGGATGT[A/G]TTTGTTTTGGTGCCT	81847
rs76426484	snp	A/T	0.0755793	0.179102	intron-variant	RNF146	GRCh38.p7	6:127272141	GGTAAGTCATTTAAC[A/T]TCCTGAGCTTAGGCT	81847

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