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
rs10890	snp	C/T	0.49168	0.063958	utr-variant-3-prime, intron-variant	FXN	GRCh38.p7	9:69073008	CTCCCTCACATGATA[C/T]CCCTTATCTTTTATA	2395
rs944348	snp	A/G	0.497586	0.0346604	intron-variant	FXN	GRCh38.p7	9:69069343	CAGTCTCACTCTGTC[A/G]CCCAGGATGGAGTGC	2395
rs953588	snp	A/G	0.417359	0.185718	intron-variant	FXN	GRCh38.p7	9:69089911	TTTCTAAAATCCTTG[A/G]AAGATCCCACTAGGG	2395
rs1045632	snp	C/T	0.489665	0.0711382	utr-variant-3-prime, intron-variant	FXN	GRCh38.p7	9:69078861	CATGTCCTCAGCATA[C/T]CATGTTTGTCTTTCC	2395
rs1052186	snp	C/G	0	0	utr-variant-3-prime, intron-variant	FXN	GRCh38.p7	9:69072916	AGGAGGCAACACATT[C/G]TTTCTACAGAGCTGT	2395
rs1052187	snp	C/G	0	0	utr-variant-3-prime, intron-variant	FXN	GRCh38.p7	9:69072912	GGCAACACATTCTTT[C/G]TACAGAGCTGTGACA	2395
rs1052188	snp	C/G	0	0	utr-variant-3-prime, intron-variant	FXN	GRCh38.p7	9:69072886	TGACACATAGCCCAA[C/G]TGTCCTCAAAAGCAG	2395
rs1052189	snp	C/G	0	0	utr-variant-3-prime, intron-variant	FXN	GRCh38.p7	9:69072833	CAACAACAAAAAACA[C/G]ACCTCAGCTGCATAA	2395
rs1052194	snp	C/G			synonymous-codon, intron-variant, utr-variant-3-prime	FXN	GRCh38.p7	9:69072735	TCCGGAATAGGCCAA[C/G]GAAGACAAGTCCAGT	2395
rs1052195	snp	C/G	0.00486615	0.0490856	missense, intron-variant, utr-variant-3-prime	FXN	GRCh38.p7	9:69072734	CCGGAATAGGCCAAG[C/G]AAGACAAGTCCAGTT	2395
rs1052201	snp	A/T	0	0	missense, intron-variant	FXN	GRCh38.p7	9:69072653	ACGCCGTCGTGGGAG[A/T]ACACCCAGTTTTTCC	2395
rs1330843	snp	A/T	0	0	intron-variant	FXN	GRCh38.p7	9:69066869	TATATATATATATAT[A/T]TTTTTTTTTTGAGGA	2395
rs1411675	snp	C/T	0.491732	0.0637633	intron-variant	FXN	GRCh38.p7	9:69072136	CAACCACTACCTCTG[C/T]CTAGCTTCAAAACAT	2395
rs1411676	snp	C/T	0.49168	0.063958	intron-variant	FXN	GRCh38.p7	9:69072002	TGATATGAAATGGTA[C/T]GATACATGCATCTAA	2395
rs1544306	snp	C/T	0.482309	0.0923707	upstream-variant-2KB	FXN	GRCh38.p7	9:69034854	gcttactgcaacttc[C/T]ccctcccgggctcaa	2395
rs1800651	snp	C/T	0.316726	0.240931	intron-variant	FXN	GRCh38.p7	9:69036689	AAGACTTTATCTATG[C/T]TATTCCCATTTAATC	2395
rs1800652	snp	C/T	0.390464	0.206809	intron-variant	FXN	GRCh38.p7	9:69046200	ctcttctcctctccc[C/T]tggttcccggtttcc	2395
rs1815427	snp	C/T	0.490782	0.0672626	intron-variant	FXN	GRCh38.p7	9:69069254	TCTCAGTCTCCCAAG[C/T]AGCTGGGATTACAGG	2395
rs1888334	snp	C/T	0.497829	0.0328757			GRCh38.p7	9:69074499	GGAGTCTCGCTCTGT[C/T]GCTCAGGTACGATCT	2395
rs1971625	snp	A/G	0.0505692	0.150756	upstream-variant-2KB	FXN	GRCh38.p7	9:69035052	actgggactacaggc[A/G]cccgccaccatgcct	2395
rs1984002	snp	A/G	0.49168	0.063958	utr-variant-3-prime, intron-variant	FXN	GRCh38.p7	9:69074717	AGATAGGATCTTGCT[A/G]TGTTGCCCAGGCTGA	2395
rs1984003	snp	C/T	0.49168	0.063958	utr-variant-3-prime, intron-variant	FXN	GRCh38.p7	9:69074549	TTAATACAAACTTCT[C/T]ATTAATAAACCCTCC	2395
rs1984004	snp	C/T	0.49168	0.063958	utr-variant-3-prime, intron-variant	FXN	GRCh38.p7	9:69074459	GTAACCTCCTCCGCC[C/T]GGGGTCAAGCAATTC	2395
rs1984005	snp	C/T	0.0111196	0.0737302	intron-variant	FXN	GRCh38.p7	9:69056147	acacacctgtaatcc[C/T]ggtgctttgggaggc	2395
rs2309393	snp	A/G	0.425277	0.178263	intron-variant	FXN	GRCh38.p7	9:69061172	TTTCCTATCGGAATT[A/G]GAAATCTTTTGAGTG	2395
rs2309394	snp	C/T	0.493386	0.0571263	intron-variant	FXN	GRCh38.p7	9:69056200	ttagaaatagtcctc[C/T]tttctaaatttatag	2395
rs2481598	snp	A/G	0.00112412	0.0236812	FXN	9	allele_origin=G(germline)/A(germline)	9:69035836	GGCGTCACCCAGCCC[A/G]GCCCAGGCCCAGACC	2395
rs2481599	snp	A/C	0.493703	0.0557558	intron-variant	FXN	GRCh38.p7	9:69039128	tgtggtggcactcac[A/C]tgtaatcccagctac	2395
rs2481600	snp	C/T	0.499996	0.00139776	intron-variant	FXN	GRCh38.p7	9:69051935	tcactgcaacctccg[C/T]cccctggattcaaga	2395
rs2481601	snp	G/T	0.451732	0.147663	intron-variant	FXN	GRCh38.p7	9:69070992	TTTGTTTGTTTGTTT[G/T]TTTTAATTTGACAAG	2395
rs2498419	snp	A/G	0.0298908	0.118541	intron-variant	FXN	GRCh38.p7	9:69037043	TTGTACTTTAGGCTT[A/G]AACTTCCCACACGTG	2395
rs2498425	snp	C/T	0.125528	0.21681	intron-variant	FXN	GRCh38.p7	9:69045317	CCTAAAATACTTTAA[C/T]ATAGggctgggtgcg	2395
rs2498426	snp	C/T	0.0111196	0.0737302	intron-variant	FXN	GRCh38.p7	9:69045549	agtgagccgagatcg[C/T]gccactgcactccag	2395
rs2498427	snp	A/C	0.5	0.000399361	intron-variant	FXN	GRCh38.p7	9:69045622	aaaaccaaaaaaaaa[A/C]aCTTCAGCATGATTA	2395
rs2498428	snp	A/T	0.390464	0.206809	intron-variant	FXN	GRCh38.p7	9:69050181	tgtgtatttctttct[A/T]tcacaatgatgtttg	2395
rs2498429	snp	A/T	0.115438	0.210697	intron-variant	FXN	GRCh38.p7	9:69082287	AAAATATGTATATAC[A/T]TTTTACTTAGGGAAT	2395
rs2498430	snp	C/T	0.498611	0.0263212	intron-variant	FXN	GRCh38.p7	9:69069786	GCAGTAGGCATCCTC[C/T]TCCGTGGACTCCCGC	2395
rs2498431	snp	A/G	0.490673	0.0676508	intron-variant	FXN	GRCh38.p7	9:69069675	GTGCCCTTGCACCCT[A/G]CAGAGGCCTACTCTC	2395
rs2498432	snp	C/T	0.0952156	0.196321	intron-variant	FXN	GRCh38.p7	9:69069453	AGAACTCACAGTAGC[C/T]GCTTAGCACGAGGAG	2395
rs2498433	snp	A/G	0.497271	0.0368399	intron-variant	FXN	GRCh38.p7	9:69067070	GAGAGCTTGTCCTCA[A/G]GGCCCGCTTCTCTGC	2395
rs2498434	snp	C/T	0.499663	0.0129749	intron-variant	FXN	GRCh38.p7	9:69061135	GGTATCAGGCCACTC[C/T]TTTTCAAAGGGCATA	2395
rs2871218	snp	C/T	0.497829	0.0328757	utr-variant-3-prime, intron-variant	FXN	GRCh38.p7	9:69074129	TGGCACGATCTCGGC[C/T]CACTGCAACCTCCAC	2395
rs2871219	snp	C/T	0.425277	0.178263	intron-variant	FXN	GRCh38.p7	9:69061440	GTTGTGTGTTGCACC[C/T]TATACTGGGGGGCCA	2395
rs2871220	snp	C/T	0.438105	0.164671	intron-variant	FXN	GRCh38.p7	9:69055649	AAACTTAGCCCTGTA[C/T]TGTGGTACATGTCTG	2395
rs3066311	in-del	-/TTT	0.49168	0.063958	utr-variant-3-prime, intron-variant	FXN	GRCh38.p7	9:69074200	tattattattattat[-/TTT]attgttattattatt	2395
rs3066313	in-del	-/CA	0.49168	0.063958	intron-variant	FXN	GRCh38.p7	9:69072484	ACACAAAATGAGCTA[-/CA]GTGTATATCTGCCTT	2395
rs3793451	snp	C/T	0.212425	0.24716	intron-variant	FXN	GRCh38.p7	9:69044364	GCTGCCCTCTCACTT[C/T]TTCAGAGACATGTGT	2395
rs3793452	snp	C/T	0.0652144	0.168387	intron-variant	FXN	GRCh38.p7	9:69044694	CCCCTGTCACCTCCC[C/T]TGCATCTCCCTACTC	2395
rs3793453	snp	C/T	0.0185938	0.0946107	intron-variant	FXN	GRCh38.p7	9:69044704	CTCCCCTGCATCTCC[C/T]TACTCCAGCTGCACC	2395
rs3793454	snp	A/G	0.000798403	0.0199641	intron-variant	FXN	GRCh38.p7	9:69046568	GTTTTCTTCCTGAGC[A/G]GCAACAATCTTAGGC	2395
rs3793455	snp	C/T	0.171704	0.237423	intron-variant	FXN	GRCh38.p7	9:69058114	TAATCCAGATACACC[C/T]AAGAGGACATCTGTT	2395
rs3793456	snp	A/G	0.443598	0.158176	intron-variant	FXN	GRCh38.p7	9:69058117	TCCAGATACACCCAA[A/G]AGGACATCTGTTCTT	2395
rs3793457	snp	A/G	0.5	0.000399361	intron-variant	FXN	GRCh38.p7	9:69060045	TTTTGCTCCTACATG[A/G]GTAGGGCTGATCTTG	2395
rs3793458	snp	A/G	0.419135	0.184101	intron-variant	FXN	GRCh38.p7	9:69060196	ACACGGTGAAACCCC[A/G]TCTCTACTAAAAAAA	2395
rs3793459	snp	C/G	0.497695	0.0338674	intron-variant	FXN	GRCh38.p7	9:69060295	AGAATGGCGTGAACC[C/G]GGGAGGCAGAGCTTG	2395
rs3793460	snp	C/G	0.499	0.0223418	intron-variant	FXN	GRCh38.p7	9:69060304	TGAACCCGGGAGGCA[C/G]AGCTTGCAGTGAACC	2395
rs3793461	snp	G/T	0.429087	0.174436	intron-variant	FXN	GRCh38.p7	9:69060548	AAGAGAAAGCCCTCT[G/T]TATCTGGTCTATTTG	2395
rs3793464	snp	A/G	0.0154538	0.0865337	intron-variant	FXN	GRCh38.p7	9:69061317	TTGCCCTGAGTCCTC[A/G]AAGGAGGCAGGAGAG	2395
rs3793465	snp	A/G	0.444267	0.157354	intron-variant	FXN	GRCh38.p7	9:69064522	CATGTCTGATGTTTG[A/G]GTTGACGTGGTACTC	2395
rs3793466	snp	C/T	0.446771	0.154211	intron-variant	FXN	GRCh38.p7	9:69066324	GACATCATTTTTAGG[C/T]AATTAATATTTTCCC	2395
rs3793467	snp	A/C	0.467439	0.123371	intron-variant	FXN	GRCh38.p7	9:69066337	GGTAATTAATATTTT[A/C]CCATTTATTATTCTG	2395
rs3829062	snp	C/T	0.499347	0.0180537	intron-variant	FXN	GRCh38.p7	9:69053281	TCTTGACTTCTTTTA[C/T]TTTTCTGTTTCCCCC	2395
rs3829063	snp	A/G	0.18325	0.240924	intron-variant	FXN	GRCh38.p7	9:69053458	CCTGGGTGACAGAGC[A/G]AGACTCTGTCATAGA	2395
rs3829064	snp	C/T	0.498253	0.0295011	intron-variant	FXN	GRCh38.p7	9:69063550	CATCATTTCTATACA[C/T]TTGTTTTTGAATCAG	2395
rs3838715	in-del	-/T	0.375	0.216506	intron-variant	FXN	GRCh38.p7	9:69063721	GAGACAGGATCTCTG[-/T]TCGCCCAGTCTGGTG	2395
rs4069737	snp	C/T	0.195837	0.244062	intron-variant	FXN	GRCh38.p7	9:69086258	AATGGCGTTTAGCAA[C/T]GGAGAGGGTATAACA	2395
rs4304388	snp	C/T	0.171704	0.237423	intron-variant	FXN	GRCh38.p7	9:69057942	GTCCATTCTTTGATC[C/T]CAGTGTCTGGAACAG	2395
rs4596713	snp	C/T	0.442385	0.15965	intron-variant	FXN	GRCh38.p7	9:69084300	CTTGCTAAAGTTCCA[C/T]GTCACCAAACCAAAG	2395
rs4744786	snp	A/G	0.478437	0.10157	intron-variant	FXN	GRCh38.p7	9:69039039	gggcggatcacctga[A/G]gtcaggagtttgaga	2395
rs4744787	snp	A/G	0.479502	0.0991411	intron-variant	FXN	GRCh38.p7	9:69039723	CCTCTTAAATACCGG[A/G]GACAGCTTCGAGAAG	2395
rs4744795	snp	A/G	0.429688	0.173817	intron-variant	FXN	GRCh38.p7	9:69053511	GATGGATGGATGGAT[A/G]GATAGATAGATAGAT	2395
rs4744806	snp	C/T	0.491732	0.0637633	utr-variant-3-prime, intron-variant	FXN	GRCh38.p7	9:69073302	ACTCACACGGGAAGA[C/T]CATTTCTTATTTGTG	2395
rs4744807	snp	A/G	0.497803	0.033074	utr-variant-3-prime, intron-variant	FXN	GRCh38.p7	9:69073384	TGCTGTTTCTCCCAC[A/G]TATTCACATACGTGT	2395
rs4744808	snp	C/T	0.49168	0.063958	utr-variant-3-prime, intron-variant	FXN	GRCh38.p7	9:69073395	CCACATATTCACATA[C/T]GTGTCTGTGTGTATA	2395
rs4744810	snp	A/G	0.491577	0.0643472	utr-variant-3-prime, intron-variant	FXN	GRCh38.p7	9:69074088	TACTTGGGAGGCTGA[A/G]GCGGAAGAATCGCTT	2395
rs4744811	snp	A/C	0.497803	0.033074	downstream-variant-500B, intron-variant	FXN	GRCh38.p7	9:69079223	TTTCCCATTTTCTCT[A/C]CTGGATTCCCATTGC	2395
rs4745543	snp	C/T	0.448323	0.15221	intron-variant	FXN	GRCh38.p7	9:69039765	ATGTTTCTTAGTCCA[C/T]TTTCTGTTGCTTGTG	2395
rs4745553	snp	A/G	0.5	0.000399361	intron-variant	FXN	GRCh38.p7	9:69047106	GGAAAAAGCCGGCAC[A/G]GCATTCCCCATGGAA	2395
rs4745577	snp	A/G	0.491629	0.0641526	utr-variant-3-prime, intron-variant	FXN	GRCh38.p7	9:69073185	CCTGCTCACTGTTCT[A/G]TCTCCAAATGAGACA	2395
rs4745578	snp	C/T	0.491577	0.0643472	utr-variant-3-prime, intron-variant	FXN	GRCh38.p7	9:69074077	GTAATCCCAGCTACT[C/T]GGGAGGCTGAAGCGG	2395
rs4745580	snp	C/T	0.497695	0.0338674	utr-variant-3-prime, intron-variant	FXN	GRCh38.p7	9:69074840	TGAGTCTGATGGAAA[C/T]GTTTAAGTGCAGTAG	2395
rs4745581	snp	A/G	0.49168	0.063958	utr-variant-3-prime, intron-variant	FXN	GRCh38.p7	9:69074964	AGAACTCGGTGACAT[A/G]ATGTACTCCTTTATC	2395
rs4745582	snp	C/T	0.491783	0.0635686	utr-variant-3-prime, intron-variant	FXN	GRCh38.p7	9:69075228	TTTGGGAGGCTGAGG[C/T]AAGTGTATCACCTGA	2395
rs4745583	snp	C/T	0.491629	0.0641526	utr-variant-3-prime, intron-variant	FXN	GRCh38.p7	9:69075266	AGTTCAAGACCAGCC[C/T]GGCCAACATGGCAAA	2395
rs4745585	snp	C/T	0.490175	0.0693959	downstream-variant-500B, intron-variant	FXN	GRCh38.p7	9:69079168	TACCTCACACAGGCA[C/T]GGAAAAACTTGAACC	2395
rs6560541	snp	G/T	0.02016	0.0983543	utr-variant-3-prime, intron-variant	FXN	GRCh38.p7	9:69075768	CAGGATCTCACTTTG[G/T]CACTCAGGCTGGAGG	2395
rs6560545	snp	C/T	0.490175	0.0693959	intron-variant	FXN	GRCh38.p7	9:69081224	aggaacttaaatcaa[C/T]aagcaaaaaccaaat	2395
rs6560546	snp	A/G	0.490287	0.0690083	intron-variant	FXN	GRCh38.p7	9:69081495	atacattcaaccact[A/G]tggagaacagtttgg	2395
rs6560547	snp	A/G	0.49681	0.0398085	intron-variant	FXN	GRCh38.p7	9:69081769	aaagaatgtaatcat[A/G]tattttgcagcaata	2395
rs6560550	snp	C/T	0.498632	0.0261223	intron-variant	FXN	GRCh38.p7	9:69083000	ACTGTACAGGAAGGG[C/T]TTTCCAACCTCCTCT	2395
rs6560551	snp	A/G	0.496517	0.0415876	intron-variant	FXN	GRCh38.p7	9:69083286	TATGGTGACTTCTTC[A/G]GGTCTACATTTGCTT	2395
rs7020927	snp	C/G	0.0267878	0.112589	intron-variant	FXN	GRCh38.p7	9:69040968	tcttggatttcccac[C/G]ctccaggactctaag	2395
rs7022681	snp	A/C	0.164873	0.23506	intron-variant	FXN	GRCh38.p7	9:69047262	CCACCTCCGAGTCCA[A/C]GATTTCCAGGTGACA	2395
rs7024295	snp	C/T	0.490453	0.0684267	utr-variant-3-prime, intron-variant	FXN	GRCh38.p7	9:69078565	AGCCTGAAAAATGTG[C/T]TTTTCTGACTGAACT	2395
rs7025834	snp	C/T	0.497829	0.0328757	intron-variant	FXN	GRCh38.p7	9:69072524	GAGCTTTACTCCAGT[C/T]AATTTCTTGGGGGCA	2395
rs7026473	snp	A/G	0.479824	0.098392	intron-variant	FXN	GRCh38.p7	9:69040602	gaacccgggaggcag[A/G]gcttgcagtgatccg	2395
rs7026584	snp	A/G	0.0279526	0.114869	intron-variant	FXN	GRCh38.p7	9:69040668	gcgagactgcatctc[A/G]aaGaaaaaaataaat	2395
rs7027359	snp	C/T	0.431621	0.171796	intron-variant	FXN	GRCh38.p7	9:69094895	tttgaactcctgggc[C/T]cgagcagtcctccta	2395
rs7027499	snp	A/G	0.49706	0.0382258	intron-variant	FXN	GRCh38.p7	9:69092986	GTAAGTCCAAAGAAG[A/G]GTGTGAAGCATCTGT	2395
rs7028835	snp	C/T	0.490287	0.0690083	intron-variant	FXN	GRCh38.p7	9:69079676	tggagtgcagtggcg[C/T]gatctcgactcactg	2395

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