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
rs11368	snp	A/G	0.499075	0.0214901	synonymous-codon	RNFT1	GRCh38.p7	17:59954051	TGTAATTACCTGACA[A/G]ATGAGAAGAATTGGC	51136
rs180511	snp	C/T	0.189576	0.242588	intron-variant	RNFT1	GRCh38.p7	17:59955087	CTTTACCCTCATGAC[C/T]GTGACTGACTTGGGT	51136
rs180512	snp	G/T	0.190205	0.242744	intron-variant	RNFT1	GRCh38.p7	17:59954470	GGGTCAAATAATACA[G/T]GGCTATAGATTTTAT	51136
rs180514	snp	C/T	0.158632	0.232706	intron-variant	RNFT1	GRCh38.p7	17:59953288	atcacttgaaccagt[C/T]gggggcggaggttgc	51136
rs767811	snp	G/T	0	0	intron-variant	RNFT1, TBC1D3P1-DHX40P1	GRCh38.p7	17:59962691	ATGTTTATTTTTAAT[G/T]TGTGTCATTGTTAGC	51136
rs975547	snp	A/C	0.190205	0.242744	intron-variant, upstream-variant-2KB	RNFT1, TBC1D3P1-DHX40P1, LOC101927755	GRCh38.p7	17:59963881	CGGGGAGGTAATATT[A/C]TTGGTGGCACCATTA	51136
rs1024637	snp	A/G	0.479502	0.0991411	intron-variant	RNFT1	GRCh38.p7	17:59961532	AAGTTACACGAGCCC[A/G]TCATATAAATCATTG	51136
rs1860294	snp	G/T	0.190205	0.242744	intron-variant	RNFT1	GRCh38.p7	17:59959484	TTGTTATTATTGGTC[G/T]TTGTTTCTGAAAGTA	51136
rs2159286	snp	A/G	0.190519	0.242821	intron-variant	RNFT1	GRCh38.p7	17:59956878	TCTCTCCATGCCTGC[A/G]CCCCTCAACCTAATA	51136
rs4968401	snp	C/T	0.487558	0.0778863	intron-variant, upstream-variant-2KB	RNFT1, TBC1D3P1-DHX40P1, LOC101927755	GRCh38.p7	17:59963369	GTATCCTTTATTCAC[C/T]AAAGGAGTAGCAAAT	51136
rs7219051	snp	A/G	0.241053	0.24984	intron-variant	RNFT1	GRCh38.p7	17:59955349	ACAAGCTTTTAAGAC[A/G]TTACTCATCTGGCAT	51136
rs7219089	snp	C/T	0.323671	0.238899	intron-variant	RNFT1	GRCh38.p7	17:59955504	TTCTTGAGAGTATTT[C/T]GGCACAAATCTTACA	51136
rs7221472	snp	C/T	0.324382	0.238678	intron-variant	RNFT1	GRCh38.p7	17:59959376	caactccagtgaaac[C/T]aGGTCTTCTAATATT	51136
rs8075105	snp	A/T	0.190205	0.242744	intron-variant	RNFT1	GRCh38.p7	17:59960329	GTTACTGTTTTATAC[A/T]ACTTTAGTGACCAAA	51136
rs8081368	snp	C/G	0.240765	0.249829	upstream-variant-2KB, intron-variant	RNFT1, TBC1D3P1-DHX40P1, LOC101927755	GRCh38.p7	17:59965245	GAAAAACCTGTCTTG[C/G]GTGGGGTATAGAGGA	51136
rs9709385	snp	G/T			upstream-variant-2KB, intron-variant	RNFT1, TBC1D3P1-DHX40P1, LOC101927755	GRCh38.p7	17:59965845	aaaatacaaaaatta[G/T]ccgggtgtggtggtg	51136
rs9709408	snp	C/T			upstream-variant-2KB, intron-variant	RNFT1, TBC1D3P1-DHX40P1, LOC101927755	GRCh38.p7	17:59965859	agccgggtgtggtgg[C/T]gcgtgcctgtaatct	51136
rs9709409	snp	C/T			upstream-variant-2KB, intron-variant	RNFT1, TBC1D3P1-DHX40P1, LOC101927755	GRCh38.p7	17:59965863	gggtgtggtggtgcg[C/T]gcctgtaatctcagc	51136
rs9912341	snp	A/G	0.139564	0.224285	upstream-variant-2KB, intron-variant	RNFT1, TBC1D3P1-DHX40P1, LOC101927755	GRCh38.p7	17:59965927	acccgggaggcggag[A/G]ttgcagtgagccggg	51136
rs11079391	snp	C/T	0.0952156	0.196321	intron-variant	RNFT1	GRCh38.p7	17:59960424	TATGTTTCAAAGAAG[C/T]CAAGTCTTCTCTCaa	51136
rs11406596	in-del	-/A/AA	0.5	0	intron-variant	RNFT1	GRCh38.p7	17:59960437	GCCAAGTCTTCTCTC[-/A/AA]AAAAAAAAAAAAAAA	51136
rs11554818	snp	C/T	0	0	utr-variant-3-prime	RNFT1	GRCh38.p7	17:59952652	TCAGGAAAGAATACC[C/T]GAGTTCTCTAAAACC	51136
rs11868009	snp	A/C	0.487113	0.0792303	intron-variant	RNFT1	GRCh38.p7	17:59959138	tttcttatcaattct[A/C]cttagcctctcaaac	51136
rs12051810	snp	C/G			intron-variant	RNFT1	GRCh38.p7	17:59955863	TAGGAACCTTTCAGG[C/G]TACTAAGTGGTAAAT	51136
rs12600680	snp	C/T	0.324619	0.238604	intron-variant	RNFT1	GRCh38.p7	17:59960013	TAAGATACAAAGTGC[C/T]ATGAAATATATGATT	51136
rs16943969	snp	A/G	0.24134	0.24985	intron-variant	RNFT1	GRCh38.p7	17:59953792	ATCCAATTATAAAAT[A/G]GCCTGTTTTTTAATC	51136
rs17850123	snp	A/G	0	0	synonymous-codon, nc-transcript-variant, upstream-variant-2KB	RNFT1, TBC1D3P1-DHX40P1, LOC101927755	GRCh38.p7	17:59963188	ATCCTCACTGCTTCC[A/G]GTTCCTGGAGGACTG	51136
rs28733789	snp	A/G			intron-variant	RNFT1	GRCh38.p7	17:59961322	AGATTACAGGCATGA[A/G]CCACTGTGCCTTGCC	51136
rs34068842	in-del	-/T	0.494315	0.0530107	intron-variant	RNFT1	GRCh38.p7	17:59953191	GAATGAAAGGGATTC[-/T]TTTTTTTTTTTTTTT	51136
rs34229958	in-del	-/G			intron-variant	RNFT1	GRCh38.p7	17:59959143	TATCAATTCTCCTTA[-/G]CCTCTCAAACTTAAC	51136
rs34511510	in-del	-/T	0	0	intron-variant	RNFT1, TBC1D3P1-DHX40P1	GRCh38.p7	17:59961903	TTTTTTTTTTTTTTT[-/T]GAGATGGAGTCTCGT	51136
rs34533381	in-del	-/A			intron-variant	RNFT1	GRCh38.p7	17:59956682	ATATGTCACATCTAA[-/A]TCATTTTGTGCTGAG	51136
rs34816517	in-del	-/C			downstream-variant-500B	RNFT1	GRCh38.p7	17:59952217	TTTTCTATACTATTC[-/C]AAATCATCAAGTAAG	51136
rs35264935	in-del	-/C			intron-variant	RNFT1	GRCh38.p7	17:59957769	GAACTGCCTGAACCC[-/C]AGGAGGCGGAGGTTG	51136
rs35344838	in-del	-/C			intron-variant	RNFT1	GRCh38.p7	17:59956147	ACAAACAAAGCCCCC[-/C]ATTTGTGGATTAAAA	51136
rs35957078	in-del	-/C			intron-variant	RNFT1	GRCh38.p7	17:59955075	GATGTAAGAACACCC[-/C]AAGTCAGTCACGGTC	51136
rs58997167	snp	A/C	0.0387552	0.1337	intron-variant	RNFT1	GRCh38.p7	17:59957861	AAACAAAACAAAACC[A/C]AAAAAAAAGATACAA	51136
rs59767604	snp	C/G	0.240765	0.249829	intron-variant, upstream-variant-2KB	RNFT1, TBC1D3P1-DHX40P1, LOC101927755	GRCh38.p7	17:59963978	AGGTAACTCTTTAGT[C/G]TGAATAAGCAGTTAC	51136
rs61751975	snp	A/G	0.0121533	0.0769997	synonymous-codon, nc-transcript-variant, upstream-variant-2KB	RNFT1, TBC1D3P1-DHX40P1, LOC101927755	GRCh38.p7	17:59963203	AGTTCCTGGAGGACT[A/G]TGCAGTTGGCTACGA	51136
rs61752305	snp	A/G/T	0.000576407	0.016967	synonymous-codon, missense, nc-transcript-variant	RNFT1, TBC1D3P1-DHX40P1	GRCh38.p7	17:59962995	TGTGGGAGTGACCCC[A/G/T]TAAGCGACTGTGTAC	51136
rs62081840	snp	A/T			intron-variant, upstream-variant-2KB	RNFT1, TBC1D3P1-DHX40P1, LOC101927755	GRCh38.p7	17:59963509	CAAAAAAAAAAAAGT[A/T]GAGCTGCAAATGCTT	51136
rs71370154	in-del	-/T	0.5	0	intron-variant	RNFT1, TBC1D3P1-DHX40P1	GRCh38.p7	17:59961882	TGCCTGGCCCAGGTC[-/T]TTTTTTTTTTTTTTT	51136
rs73318983	snp	A/C	0.000267206	0.0115556	missense	RNFT1	GRCh38.p7	17:59954106	GAACAAATATCATCC[A/C]CATCTGAACACTGTC	51136
rs74346234	snp	A/C			intron-variant	RNFT1	GRCh38.p7	17:59955428	AGACTTGAACAAATC[A/C]AAGTATTGATGACTG	51136
rs74348089	snp	G/T	0.00159617	0.0282053	intron-variant	RNFT1	GRCh38.p7	17:59953855	TTTTCCCCTTCATAC[G/T]CTCCTCTGCATAAAA	51136
rs74555505	snp	C/T	0.00676609	0.0577691	intron-variant, upstream-variant-2KB	RNFT1, TBC1D3P1-DHX40P1, LOC101927755	GRCh38.p7	17:59963807	CTGCACTTAGGTGAC[C/T]TACAAATTAGATTTT	51136
rs75137032	snp	G/T	0	0	intron-variant	RNFT1	GRCh38.p7	17:59953207	TTTTTTTTTTTTTTT[G/T]AGATGGAGACTGAAG	51136
rs75400693	snp	A/C/T	0.5	0	upstream-variant-2KB, intron-variant	RNFT1, TBC1D3P1-DHX40P1, LOC101927755	GRCh38.p7	17:59966287	AGGAGACCCCCACCT[A/C/T]AAAAAAAAACACATT	51136
rs75421338	snp	C/T	0.0232847	0.105357	utr-variant-5-prime, intron-variant, upstream-variant-2KB	RNFT1, TBC1D3P1-DHX40P1, LOC101927755	GRCh38.p7	17:59964722	CCGCAAGCTCTTCTC[C/T]CAGCCCGGCGGCAAC	51136
rs75460876	snp	C/T	0.00358779	0.0422022	intron-variant, upstream-variant-2KB	RNFT1, TBC1D3P1-DHX40P1, LOC101927755	GRCh38.p7	17:59963718	AGTATTTTTTAATGG[C/T]TGGAAATGTTAGGAA	51136
rs76147107	snp	G/T	0.5	0	intron-variant, upstream-variant-2KB	RNFT1, TBC1D3P1-DHX40P1, LOC101927755	GRCh38.p7	17:59963507	ACCAAAAAAAAAAAA[G/T]TTGAGCTGCAAATGC	51136
rs76419616	snp	C/T	0.356383	0.226236	upstream-variant-2KB, intron-variant	RNFT1, TBC1D3P1-DHX40P1, LOC101927755	GRCh38.p7	17:59964765	CGCGCTCCCCGGACG[C/T]TCTCACGCGCGCGCG	51136
rs76525517	snp	A/C	0	0	upstream-variant-2KB, intron-variant	RNFT1, TBC1D3P1-DHX40P1, LOC101927755	GRCh38.p7	17:59966288	GGAGACCCCCACCTC[A/C]AAAAAAAACACATTG	51136
rs77495043	snp	A/C	1.67719e-05	0.0028958	missense	RNFT1	GRCh38.p7	17:59956514	AAAATATTCGTAAAA[A/C]CTGTCTGAAAGTTCT	51136
rs77530104	snp	A/C			splice-acceptor-variant	RNFT1	GRCh38.p7	17:59957383	CATATACCAGTAACC[A/C]TAAAAAATAAGAAGA	51136
rs78095669	snp	A/G	0.5	0	intron-variant, upstream-variant-2KB	RNFT1, TBC1D3P1-DHX40P1, LOC101927755	GRCh38.p7	17:59963506	CACCAAAAAAAAAAA[A/G]GTTGAGCTGCAAATG	51136
rs78261818	snp	A/G	0.00159617	0.0282053	intron-variant	RNFT1	GRCh38.p7	17:59956067	GACATGATTTTTGGC[A/G]GTGAGCTTTCTAAAC	51136
rs78349854	snp	A/G			intron-variant	RNFT1	GRCh38.p7	17:59955425	AGGAGACTTGAACAA[A/G]TCCAAGTATTGATGA	51136
rs78559369	snp	A/C	0.5	0	intron-variant, upstream-variant-2KB	RNFT1, TBC1D3P1-DHX40P1, LOC101927755	GRCh38.p7	17:59963495	GGGAACATTTGCACC[A/C]AAAAAAAAAAAGTTG	51136
rs79006987	snp	A/G			intron-variant	RNFT1	GRCh38.p7	17:59953247	GTCACCCAGGCCGGA[A/G]TGCAATGGCACCATC	51136
rs79015397	snp	A/G	0.5	0	intron-variant	RNFT1	GRCh38.p7	17:59959929	AGAAAAAAAAAAAAA[A/G]AGCTCTCGCTTATGA	51136
rs111339435	snp	A/C	0.029116	0.117091	intron-variant	RNFT1	GRCh38.p7	17:59961498	AAGGTGAAATTTTAG[A/C]AACTCATCCTCTTTT	51136
rs111857062	snp	C/T	0.069869	0.173358	intron-variant	RNFT1	GRCh38.p7	17:59960052	AATGTAATTGTGTAT[C/T]TGGACCTCTAATTAC	51136
rs111918363	snp	A/G	0.239037	0.24976	intron-variant	RNFT1	GRCh38.p7	17:59953393	TTTAGTAGAGACAGG[A/G]TTTCACCATGTTGGT	51136
rs111953367	snp	A/G	0.444444	0.157135	intron-variant, upstream-variant-2KB	RNFT1, TBC1D3P1-DHX40P1, LOC101927755	GRCh38.p7	17:59963383	CTAAAGGAGTAGCAA[A/G]TAATCACAACAGATG	51136
rs112263224	snp	C/T	0.5	0	intron-variant	RNFT1	GRCh38.p7	17:59953949	CCACTAAACACTAGA[C/T]TTTTTTTTTTTTGCC	51136
rs112345334	snp	C/T	0.000798403	0.0199641	intron-variant	RNFT1	GRCh38.p7	17:59959342	CCTCCAAACTATATC[C/T]CAGATTTGCCCATCT	51136
rs112481698	snp	A/G	0.000547995	0.0165438	intron-variant	RNFT1	GRCh38.p7	17:59958731	AACTCATCAATACCA[A/G]ACATCTGCTGTGTTT	51136
rs112664639	snp	A/C	0.5	0	intron-variant	RNFT1	GRCh38.p7	17:59957855	ATCTCAAAACAAAAC[A/C]AAACCAAAAAAAAAG	51136
rs112808730	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT1	GRCh38.p7	17:59956139	TTAATAGGAACAAAC[A/G]AAGCCCCCATTTGTG	51136
rs112835092	snp	A/G/T	0.000216245	0.0103963	missense, nc-transcript-variant	RNFT1, TBC1D3P1-DHX40P1	GRCh38.p7	17:59962562	AAAACCTGATTTACA[A/G/T]TGCTTTTGTTTGCAT	51136
rs113104342	snp	C/G	0.0562307	0.157967	intron-variant	RNFT1	GRCh38.p7	17:59957809	AAGATCACACCACTG[C/G]ACTCCAGCCTGGGCA	51136
rs113341992	snp	A/G	0.5	0	intron-variant	RNFT1	GRCh38.p7	17:59958167	CTAAGCTGAAATAAT[A/G]CAGATAATTAAGCTA	51136
rs113569159	snp	G/T	0.00953873	0.0683987	intron-variant	RNFT1	GRCh38.p7	17:59958589	TTCACAATAATGGAA[G/T]GGAGGATCATTTTGC	51136
rs113699640	snp	A/G	0.00874735	0.0655527	intron-variant	RNFT1	GRCh38.p7	17:59957917	GTAAAACCTATGTGA[A/G]TATGTTTTTGCTGAT	51136
rs114788792	snp	A/G	0.0865458	0.189163	intron-variant	RNFT1	GRCh38.p7	17:59955881	CTAAGTGGTAAATTA[A/G]GGTTCTCTATGACAT	51136
rs115039364	snp	G/T	0.000263535	0.011476	synonymous-codon, nc-transcript-variant	RNFT1, TBC1D3P1-DHX40P1	GRCh38.p7	17:59963008	CCGTAAGCGACTGTG[G/T]ACACATCCATGGGCA	51136
rs115215316	snp	A/T	0.00914312	0.0669923	utr-variant-3-prime	RNFT1	GRCh38.p7	17:59952634	TTTATTCTGAAAACA[A/T]TGTCAGGAAAGAATA	51136
rs115465451	snp	A/C/T	0.00279162	0.0372561	intron-variant	RNFT1	GRCh38.p7	17:59956927	CTAGTTTAAGAATTA[A/C/T]GTGTATGACAATGTT	51136
rs117634246	snp	C/T	0.0023933	0.0345097	intron-variant	RNFT1	GRCh38.p7	17:59955702	CTGGCCAGTTAGTCT[C/T]GTTTACTTTGTAGAC	51136
rs138113380	snp	C/T	8.4679e-05	0.00650633	splice-acceptor-variant	RNFT1	GRCh38.p7	17:59958446	TTAAAAAAATTAAGC[C/T]ACCAAAAGAAAAACA	51136
rs138189792	snp	C/T	0.00438332	0.0466095	intron-variant	RNFT1	GRCh38.p7	17:59958878	TCCCTGAATAATTTT[C/T]TTTCTAGACTTTTAA	51136
rs138794420	snp	C/T	0.0120912	0.0768076	missense	RNFT1	GRCh38.p7	17:59957277	GACTCCATCTAGTTA[C/T]GTTACCAAACTCCCC	51136
rs139402154	snp	A/G	0.0111196	0.0737302	intron-variant	RNFT1	GRCh38.p7	17:59954361	TAATAGGATTTTGAA[A/G]GATTGTTAGATCTAC	51136
rs139407842	snp	A/C	0.000399281	0.0141238	intron-variant	RNFT1, TBC1D3P1-DHX40P1	GRCh38.p7	17:59962189	CATGCCCAGCCACTA[A/C]AAGTTTTTCATGATG	51136
rs139462395	snp	C/G/T	6.59201e-05	0.00574078	missense, nc-transcript-variant	RNFT1, TBC1D3P1-DHX40P1	GRCh38.p7	17:59962904	AGCCACTTGAAGAGA[C/G/T]AGCGGAATTCTGAGA	51136
rs140037039	in-del	-/A	0.0130921	0.0798413	intron-variant	RNFT1	GRCh38.p7	17:59959433	TCCCATTTGACATGG[-/A]AGACTTATCAGCTAC	51136
rs140111904	snp	A/C	0.00557542	0.0525036	intron-variant	RNFT1	GRCh38.p7	17:59954699	AGTGCAATATGAAGA[A/C]GACTTAGGGACCACT	51136
rs140131960	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT1	GRCh38.p7	17:59959735	ACCAACATGGTGAAA[C/T]TCCGTCTCTATTAAA	51136
rs140134307	in-del	-/T	0.0865458	0.189163	downstream-variant-500B	RNFT1	GRCh38.p7	17:59952033	TAATTATAAGGGCAA[-/T]TTTTTTATAAGATTT	51136
rs141254111	snp	A/G	0.000216071	0.0103918	synonymous-codon	RNFT1	GRCh38.p7	17:59958351	GCATTTTAAGCCCAT[A/G]AAAAAGAATTTCAGA	51136
rs141412497	snp	A/G	0.00398564	0.0444627	intron-variant	RNFT1	GRCh38.p7	17:59953903	GACAAAACTTAGCCA[A/G]TCCACTAGTATGTAC	51136
rs141521142	snp	C/T	0.00914312	0.0669923	intron-variant	RNFT1	GRCh38.p7	17:59959753	CGTCTCTATTAAAAA[C/T]ACAAAAATTTGCCAG	51136
rs142057142	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT1	GRCh38.p7	17:59955992	TTTCATGCCATGAAC[A/G]TATTTATGCACATAT	51136
rs142118872	snp	A/G	0.000399281	0.0141238	intron-variant	RNFT1	GRCh38.p7	17:59956999	ACTTAGATAATCCAC[A/G]CTATGTGAAGGTCGA	51136
rs142157351	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	RNFT1, TBC1D3P1-DHX40P1, LOC101927755	GRCh38.p7	17:59963764	ATCTTAATGCCTTAT[C/T]ATCATCATAGGTAAC	51136
rs142393490	snp	A/G	3.29647e-05	0.00405971	missense, nc-transcript-variant, upstream-variant-2KB	RNFT1, TBC1D3P1-DHX40P1, LOC101927755	GRCh38.p7	17:59963205	TTCCTGGAGGACTGT[A/G]CAGTTGGCTACGATT	51136
rs142527640	in-del	-/AAC	0.079617	0.182947	intron-variant, upstream-variant-2KB	RNFT1, TBC1D3P1-DHX40P1, LOC101927755	GRCh38.p7	17:59963738	AATGTTAGGAAAAAA[-/AAC]AACATTAAATCTTAA	51136
rs142631280	snp	A/G	0.000399208	0.0141225	synonymous-codon, nc-transcript-variant	RNFT1, TBC1D3P1-DHX40P1	GRCh38.p7	17:59962564	AACCTGATTTACAAT[A/G]CTTTTGTTTGCATAC	51136
rs143076700	snp	C/T	0.000399281	0.0141238	intron-variant	RNFT1	GRCh38.p7	17:59959271	AACCCAGAGGTCATT[C/T]TTGCTTCTCTCCACC	51136

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