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
rs7297	snp	A/T	0.459347	0.136653	utr-variant-3-prime	TFG	GRCh38.p7	3:100748832	GGCTAAACCTCACCC[A/T]AGCATTTTAATATCC	10342
rs11353	snp	C/T	0.42058	0.182764	synonymous-codon	TFG	GRCh38.p7	3:100748174	TCAGCAGACTGGACC[C/T]CAACAACCTCAGCAG	10342
rs12128	snp	C/T	0	0	utr-variant-3-prime, downstream-variant-500B	TFG, ABI3BP	GRCh38.p7	3:100748901	ATAATATCTTGTATT[C/T]TCAAAGGGCTCTACT	10342
rs12562	snp	G/T	0.0095275	0.0683592	synonymous-codon	TFG	GRCh38.p7	3:100736589	AGGGCCACCCAGTGC[G/T]CCTGCAGAAGATCGT	10342
rs186920	snp	A/G	0	0	intron-variant	TFG	GRCh38.p7	3:100732261	ATGTTTCTTACAAAA[A/G]GAGGTAAATAATTTT	10342
rs186956	snp	C/G	0	0	intron-variant	TFG	GRCh38.p7	3:100740715	ATTATTTATTACACA[C/G]AGTAGCCAACCTCTA	10342
rs193210	snp	A/C	0	0	intron-variant	TFG	GRCh38.p7	3:100736733	TAAAATAGAGTTTAG[A/C]ACACATGTTTGGGAA	10342
rs368423	snp	A/G	0	0	intron-variant	TFG	GRCh38.p7	3:100720434	gcgactactgGTTTC[A/G]AGTATCAGACTTACA	10342
rs392104	snp	A/C			intron-variant	TFG	GRCh38.p7	3:100723100	GCATTGATTGTGACA[A/C]AATTAATAGTCTTAT	10342
rs395000	snp	G/T	0	0	intron-variant	TFG	GRCh38.p7	3:100735750	CATTCATTTCTGTGT[G/T]CATTATTTTGTAAGA	10342
rs397320	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100732195	GCTCCAAAAAAACCC[A/G]AAAAAGTAAAATGTT	10342
rs407114	snp	A/C			intron-variant	TFG	GRCh38.p7	3:100723138	AAACAATTTGGGACA[A/C]AAATACTGGGCAATA	10342
rs420281	snp	C/G	0	0	intron-variant	TFG	GRCh38.p7	3:100722928	GAAGCAATGTGAGCA[C/G]ATAAACTGTTGCTTG	10342
rs420630	snp	C/G			intron-variant	TFG	GRCh38.p7	3:100722377	aagcacacaaacaCA[C/G]GCGAAAGAGAAGTTG	10342
rs421275	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100722470	AAATACATTGAGGTA[A/G]TGACTAAAGAAATTT	10342
rs421344	snp	C/G			intron-variant	TFG	GRCh38.p7	3:100720509	ctatggaagggggca[C/G]gagaaggtttgggga	10342
rs422081	snp	A/C			intron-variant	TFG	GRCh38.p7	3:100723128	TATGGAATAAAAACA[A/C]TTTGGGACACAAATA	10342
rs423966	snp	G/T			intron-variant	TFG	GRCh38.p7	3:100720474	tgcactggaaactgg[G/T]ttcgtgtaagacagt	10342
rs424381	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100732254	TTTACCTCCTTTTGT[A/G]AGAAACATTAGATGA	10342
rs427906	snp	C/G			intron-variant	TFG	GRCh38.p7	3:100722357	tccaaagaaattaca[C/G]agtaaagcacaaaaa	10342
rs430945	snp	A/G	0.244417	0.252512	missense	TFG	GRCh38.p7	3:100736627	GCTGAGGAGGAGGAA[A/G]CAATGCTGTGGGGTG	10342
rs435035	snp	A/C			intron-variant	TFG	GRCh38.p7	3:100732228	GATGAAAAAAATACA[A/C]GCTCCTTGATAAAGA	10342
rs447236	snp	C/G			intron-variant	TFG	GRCh38.p7	3:100735290	TCTGATGTATCCCCA[C/G]AACTTACCACAGTAT	10342
rs448493	snp	G/T			intron-variant	TFG	GRCh38.p7	3:100723096	ATGAGCATTGATTGT[G/T]ACAAAATTAATAGTC	10342
rs448919	snp	A/C	0	0	intron-variant	TFG	GRCh38.p7	3:100732289	AACAGAAGATGAACA[A/C]AAGCTTTCCAAAAAA	10342
rs453716	snp	C/T	0	0	intron-variant	TFG	GRCh38.p7	3:100735355	TGCCATATAAGTACT[C/T]GCTATTATCAGCAGA	10342
rs497835	snp	G/T	0	0	intron-variant	TFG	GRCh38.p7	3:100737494	CTGGAAGGCACCCTA[G/T]AGATTAGTTAAGTAC	10342
rs571403	snp	A/C			downstream-variant-500B	TFG, ABI3BP	GRCh38.p7	3:100749037	AAGACCACCACACCA[A/C]TAAGGACTTCTGAAA	10342
rs571521	snp	G/T			downstream-variant-500B	TFG, ABI3BP	GRCh38.p7	3:100748996	TTTTTCACATAATGT[G/T]AGTGACTAAATTAAA	10342
rs572352	snp	A/T	0	0	utr-variant-3-prime, downstream-variant-500B	TFG, ABI3BP	GRCh38.p7	3:100748931	TTAACCTATCATCAG[A/T]GTTACATTTTATACA	10342
rs573376	snp	G/T			utr-variant-3-prime	TFG	GRCh38.p7	3:100748798	GGACAAGGGAAGCTA[G/T]AAAGTCAAGTCAATC	10342
rs574795	snp	A/T			intron-variant	TFG	GRCh38.p7	3:100718542	aaaaaaaCCCTTGAA[A/T]TACAAAGTTGTAACT	10342
rs591728	snp	A/G	0.239614	0.249784	intron-variant	TFG	GRCh38.p7	3:100714748	ACTCCTACAATAAAG[A/G]AACACTTTTGTCTTT	10342
rs628268	snp	A/C/G/T	0	0	utr-variant-3-prime	TFG	GRCh38.p7	3:100748830	GAGGATATTAAAATG[A/C/G/T]TAGGGTGAGGTTTAG	10342
rs664333	snp	A/T	0.101403	0.201045	intron-variant	TFG	GRCh38.p7	3:100736422	TGGAGCAAAGGAAAA[A/T]ATAAAGTACATACAT	10342
rs665230	snp	G/T	0	0	missense	TFG	GRCh38.p7	3:100736624	GAACACCCGACAGCA[G/T]TGCTTCCTCCTCCTC	10342
rs931206	snp	A/G	0.427575	0.175975	intron-variant	TFG	GRCh38.p7	3:100735434	TTATAAGCCCATGCT[A/G]TAAGCTCTTGTAAAC	10342
rs967308	snp	C/T	0.0577344	0.159793	upstream-variant-2KB	TFG	GRCh38.p7	3:100708832	TTGGCTATAAATTCC[C/T]ACTTACTCATACTGT	10342
rs967309	snp	C/T	0.0577344	0.159793	upstream-variant-2KB	TFG	GRCh38.p7	3:100708894	AGAGTACGTAGGACA[C/T]ACTCAAATGCCTTAT	10342
rs1012364	snp	A/T	0.420733	0.18262	intron-variant	TFG	GRCh38.p7	3:100734067	agtttttttttttgc[A/T]tttttttttgcaaag	10342
rs1015198	snp	A/C			intron-variant	TFG	GRCh38.p7	3:100734560	AAACCAGAGGAGTTT[A/C]CCCCAATAAAATTAG	10342
rs1055213	snp	A/G	0.19459	0.243782	intron-variant	TFG	GRCh38.p7	3:100746432	TGCAGAATGATACAG[A/G]GAAATACTGAACTGA	10342
rs1059363	snp	C/G	0.409041	0.192888	intron-variant, utr-variant-5-prime, upstream-variant-2KB	TFG	GRCh38.p7	3:100709616	CGAAGGGCAACCGAG[C/G]GGGCCGTGACCACCG	10342
rs1059503	snp	A/G	0.123105	0.215401	utr-variant-3-prime	TFG	GRCh38.p7	3:100748829	GGAGGATATTAAAAT[A/G]CTAGGGTGAGGTTTA	10342
rs1065628	snp	A/C/T	1.6504e-05	0.00287258	missense	TFG	GRCh38.p7	3:100713729	AGCTAATCATCAAAG[A/C/T]TCAACTTGGGGAGGA	10342
rs1133721	snp	A/T			intron-variant	TFG	GRCh38.p7	3:100746301	cccagagattttgaa[A/T]ttcatttgattgggt	10342
rs1143775	snp	A/T	0.295088	0.245901	intron-variant	TFG	GRCh38.p7	3:100728572	AGTAACTTTTTTTTT[A/T]AAAAAAAAGAATTCT	10342
rs1143776	snp	A/G	0.227369	0.248974	upstream-variant-2KB	TFG	GRCh38.p7	3:100709274	AATACCCGCTTTCGA[A/G]AAAACCGGAAGTGCG	10342
rs1143777	snp	A/T	0.127599	0.217986	upstream-variant-2KB	TFG	GRCh38.p7	3:100708090	agaaggactccatac[A/T]tctatacttgaatcc	10342
rs1144104	snp	G/T	0.251578	0.249995	intron-variant	TFG	GRCh38.p7	3:100729339	ATGGTATGTTGTAAA[G/T]TTGAAACACAGTTTT	10342
rs1144105	snp	C/T	0.228547	0.249078	intron-variant	TFG	GRCh38.p7	3:100724075	AAAAACTTGGTTACA[C/T]AGAAGTCATTATCTA	10342
rs1144106	snp	C/T	0.241627	0.24986	intron-variant	TFG	GRCh38.p7	3:100723542	TCTTTTCCTAGCCCT[C/T]TACTTTCAAGCTTTG	10342
rs1144107	snp	C/T	0.240478	0.249819	intron-variant	TFG	GRCh38.p7	3:100722872	TAACAGTGGTCTTCA[C/T]CAAGAAGGAAATTTA	10342
rs1384198	snp	C/G	0.409212	0.192748	intron-variant	TFG	GRCh38.p7	3:100729920	TCTGAAATAGAAGTG[C/G]AACTAGGAATAATCA	10342
rs1402252	snp	C/G	0.459347	0.136653	intron-variant	TFG	GRCh38.p7	3:100729644	TTTCATAGTTTAAAA[C/G]TGTCCATATTGTGAA	10342
rs1503838	snp	A/G	0.446972	0.153955	intron-variant	TFG	GRCh38.p7	3:100719940	CTGAAAATTTAAAAA[A/G]TTAAAAAACAACCTT	10342
rs1520649	snp	C/T	0.427575	0.175975	intron-variant	TFG	GRCh38.p7	3:100723634	TTCTTTTTATCATCA[C/T]AAAGTGACTATTACT	10342
rs1628175	snp	C/G			intron-variant	TFG	GRCh38.p7	3:100729399	ACAAACAGTACATGT[C/G]ATTATACAATGGGGA	10342
rs1718279	snp	A/C	0.228547	0.249078	intron-variant	TFG	GRCh38.p7	3:100741122	aatatagtatagtaa[A/C]ttcacaaatgagtaa	10342
rs1809962	snp	C/G			intron-variant	TFG	GRCh38.p7	3:100734973	CCCTCCTTCCCACTG[C/G]CACATTCATTATTCT	10342
rs1812160	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100735285	GCATAATACTGTGGT[A/G]AGTTGTGGGGACACA	10342
rs1903744	snp	C/T	0.459347	0.136653	intron-variant	TFG	GRCh38.p7	3:100728321	GAGCTTTTTAAGTTA[C/T]ATAATTTTTATTAAA	10342
rs1915309	snp	A/G	0.434253	0.168969	intron-variant	TFG	GRCh38.p7	3:100716575	atcgaactaacacac[A/G]attcagcgatgccac	10342
rs2126540	snp	A/C	0.409212	0.192748	intron-variant	TFG	GRCh38.p7	3:100743683	CTACCCAGCACTAAA[A/C]ACTTAGACACGTATA	10342
rs2126541	snp	A/C	0.41023	0.191902	downstream-variant-500B	TFG, ABI3BP	GRCh38.p7	3:100749273	AGTGATTTTCCTTCT[A/C]GATAAAAGGTATAGT	10342
rs2139691	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100724589	TGAATTAGTGTATAT[C/T]CCCTCTTTGCCTATG	10342
rs2272082	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100736550	AAAAAAAAGTCAGTT[C/T]AGTATCCAACACAAG	10342
rs2293030	snp	G/T	0.427879	0.175668	intron-variant	TFG	GRCh38.p7	3:100744424	CTTCCTAAAGCACTG[G/T]ATTTGCCCTCTAAAG	10342
rs2316942	snp	A/T			intron-variant	TFG	GRCh38.p7	3:100728368	aaatttaataaatat[A/T]taaGAACAGCATGAA	10342
rs2447456	snp	A/G	0.251578	0.249995	intron-variant	TFG	GRCh38.p7	3:100715498	AACTTATACTGTGGA[A/G]GAGAAGTGTAAATCA	10342
rs2449252	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100718516	TAACTAATTGGGGAA[A/G]ACAAACTACAACGAG	10342
rs2455873	snp	G/T	0	0	intron-variant	TFG	GRCh38.p7	3:100729493	AACACATACTTAAAG[G/T]TCAGTCCACATTTTA	10342
rs2455874	snp	G/T	0.00199481	0.0315187	intron-variant	TFG	GRCh38.p7	3:100718618	GCTGGAGTACAGTGG[G/T]GTGATCTTGGCTCAC	10342
rs2460720	snp	A/T	0	0	intron-variant	TFG	GRCh38.p7	3:100732131	TGGGCACTCTGGAAA[A/T]AATAATTATAGGAAC	10342
rs2929616	snp	G/T			intron-variant	TFG	GRCh38.p7	3:100722401	AAATATTCTGGATGT[G/T]CTCATTTTCAACTTC	10342
rs2947093	snp	G/T	0.5	0	intron-variant	TFG	GRCh38.p7	3:100718550	CTTTGTATTTCATGG[G/T]TTTTTTTTTTTTTTT	10342
rs3057194	in-del	-/TTTA	0.375	0.216506	intron-variant	TFG	GRCh38.p7	3:100728367	TAAATTTAATAAATA[-/TTTA]AGAACAGCATGAAAT	10342
rs3087787	snp	A/T	0.443598	0.158176	intron-variant	TFG	GRCh38.p7	3:100742598	GTTAGGTTACTTAGC[A/T]TGTCTAAATGATCTC	10342
rs3101519	snp	A/C			intron-variant	TFG	GRCh38.p7	3:100718471	ttttgtccgttggtc[A/C]cagttcatggaccct	10342
rs3102101	snp	A/T			intron-variant	TFG	GRCh38.p7	3:100718479	TCAAGCTAAGGGTCC[A/T]TGAACTGGGACCAAC	10342
rs3773921	snp	A/G	0.427575	0.175975	intron-variant	TFG	GRCh38.p7	3:100736295	CATGTCTGCAATGCC[A/G]ATATCCCCCTACTCC	10342
rs3773922	snp	A/G	0.459574	0.136304	intron-variant	TFG	GRCh38.p7	3:100730657	CACATTTCTTGGTGA[A/G]GGTAAGCCACAGGTT	10342
rs3773924	snp	C/T	0.42803	0.175514	intron-variant	TFG	GRCh38.p7	3:100729865	TATCATTAACATAAT[C/T]CCATATGACTATTAG	10342
rs3796275	snp	C/G	0.00199481	0.0315187	intron-variant	TFG	GRCh38.p7	3:100747134	TGACTATTTCCATAT[C/G]TCTCAATCAAATTCA	10342
rs3796276	snp	C/T	0.443464	0.15834	intron-variant	TFG	GRCh38.p7	3:100746765	CACCTGAAATCTGAA[C/T]TGTTTTTTTTTAACT	10342
rs3821726	snp	C/T	0.137867	0.223442	intron-variant	TFG	GRCh38.p7	3:100711924	ACACAACCAACTCTT[C/T]GCCTTCTGCAATGCC	10342
rs3830581	in-del	-/C	0.419944	0.183355	intron-variant	TFG	GRCh38.p7	3:100736766	CAATGCTGTAATAAA[-/C]ACTTCTACACATGTA	10342
rs3832236	in-del	-/A	0.448323	0.15221	intron-variant	TFG	GRCh38.p7	3:100747343	GCATTAAAAAAAAAA[-/A]GGATTGAATGAATTT	10342
rs3839089	in-del	-/T			intron-variant	TFG	GRCh38.p7	3:100747032	GACCCTGACTAAATT[-/T]ATTAAGAGCAAGCTT	10342
rs3841652	in-del	-/T	0.0626037	0.165477	intron-variant	TFG	GRCh38.p7	3:100732184	TTTTTTGGTTTTTTT[-/T]GGAGCCCAATAACCT	10342
rs4928085	snp	C/T	0.428182	0.17536	intron-variant	TFG	GRCh38.p7	3:100733729	AGTGACTTGGACTTA[C/T]ATTCTTTTGAGGATT	10342
rs4928086	snp	G/T	0.42803	0.175514	intron-variant	TFG	GRCh38.p7	3:100741759	taccattttttatct[G/T]ttttgccatattttc	10342
rs5851219	in-del	-/C			intron-variant	TFG	GRCh38.p7	3:100735569	ACAGCTAGTGAGTGA[-/C]AGCACTAGGATTTGA	10342
rs5851220	in-del	-/AAAC	0.5	0	downstream-variant-500B	TFG, ABI3BP	GRCh38.p7	3:100749209	GTTAATTTAGGACAT[-/AAAC]AAACAAACAGTAGAT	10342
rs6772054	snp	A/C	0.00265044	0.036307	missense	TFG	GRCh38.p7	3:100748418	CCAAGACCAGGTTTT[A/C]CTTCACTTCCTGGAA	10342
rs6773482	snp	C/G	0.409041	0.192888	intron-variant, upstream-variant-2KB, utr-variant-5-prime	TFG	GRCh38.p7	3:100710003	CCAGGAGGCGCGCCT[C/G]GGGGGCTCCGGGAGG	10342
rs6775161	snp	A/G	0.481087	0.0953875	intron-variant	TFG	GRCh38.p7	3:100719048	AATGTGTTTATGAAA[A/G]TTGAACATTAAACAA	10342
rs6777552	snp	A/G	0.0456336	0.143994	intron-variant	TFG	GRCh38.p7	3:100711664	TTCTAGGTGCTGCTG[A/G]GAATAGATAGTACCA	10342
rs6777763	snp	A/G	0.459687	0.136129	intron-variant	TFG	GRCh38.p7	3:100711831	ATATTTACCATCTTG[A/G]TGAAGTAATTATACT	10342
rs6806786	snp	C/T	0.459118	0.137002	upstream-variant-2KB	TFG	GRCh38.p7	3:100708142	gcttaacagacaaga[C/T]tgaaaacctaactta	10342

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