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
rs3826	snp	A/C	0.366885	0.220993	intron-variant, utr-variant-3-prime	FANCD2, FANCD2OS	GRCh38.p7	3:10099381	cctaccttggcctca[A/C]aaagtgctaggatta	2177
rs166485	snp	A/G/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10083849	ccaggctggagtgca[A/G/T]tggcgcgatctcggt	2177
rs174728	snp	G/T	0	0	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10092935	ggaggctgaggctgg[G/T]ggatcactagagccc	2177
rs200167	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10050554	ctcactgcaagctcc[A/G]cctcctgggttcacg	2177
rs200168	snp	A/G	0.100944	0.200705	intron-variant	FANCD2	GRCh38.p7	3:10050539	gcctcctgggttcac[A/G]ccattctcctgcctc	2177
rs200169	snp	C/G	0	0	intron-variant	FANCD2	GRCh38.p7	3:10052628	ggttcaagcgattct[C/G]ctgcctcagcctccc	2177
rs266884	snp	G/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10083892	ttttttttttttttt[G/T]ttttgagacggagtc	2177
rs266885	snp	A/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10083885	tttttttttttttga[A/G]atggagtcttgctct	2177
rs266886	snp	C/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10083875	tttgagacggagtct[C/T]gctctgtcgcccagg	2177
rs271993	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10050617	ttttttttttgagac[A/G]gagtcttgctctgtc	2177
rs271994	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10050595	tgctctgtcgcccag[A/G]ctggagtgcagtggt	2177
rs271995	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10055545	gattacaggcgtgag[C/T]caccgtgcccggcca	2177
rs271996	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10055608	agccaggatggtctc[A/G]atctcctgacctcat	2177
rs365100	snp	G/T			intron-variant	FANCD2	GRCh38.p7	3:10075240	caggctggagtgcag[G/T]ggcgcggatctccac	2177
rs375954	snp	A/G	0	0	intron-variant	FANCD2	GRCh38.p7	3:10072281	aaaaaaaaaaaaaaa[A/G]GGGAAAGGTAtatat	2177
rs401900	snp	C/T	0	0	intron-variant	FANCD2	GRCh38.p7	3:10076148	GCTATATTACACTGC[C/T]AGAAGCAGAATGGGT	2177
rs419999	snp	C/G	0.00597247	0.0543191	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10089116	tgtatttttagtagg[C/G]acagggtttcactat	2177
rs455913	snp	A/C/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10059731	gaatggcatgaagcc[A/C/G]ggaggtggagctagc	2177
rs460965	snp	A/G	0.0153892	0.0863585	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10081243	CTTAGCAGCTTCTAA[A/G]TCTAGGCTTCTGACC	2177
rs462262	snp	C/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10091435	atccaggttggagtg[C/T]agtggtgcaaacttg	2177
rs462674	snp	C/T	0.0126979	0.078662	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10091068	agaaaaaaCATATAC[C/T]GGCTGTAGCTTCTCT	2177
rs626693	snp	A/G	0.040671	0.13668	intron-variant	FANCD2	GRCh38.p7	3:10044394	GATGATTGGCCGGGC[A/G]CGGTAGCTCACGCCT	2177
rs664233	snp	A/G	0.000733235	0.0191332	intron-variant	FANCD2	GRCh38.p7	3:10043596	GCCTGGATTAAGGTG[A/G]GATCTTTGGAACTTT	2177
rs722509	snp	A/T	0.295599	0.245806	intron-variant	FANCD2	GRCh38.p7	3:10060693	CTGATTCTTTTAGAA[A/T]GCATTTTTCTTTATC	2177
rs722510	snp	C/G	0	0	intron-variant	FANCD2	GRCh38.p7	3:10060738	GCACTAGACAATGCA[C/G]GTGTCTACATTGCTG	2177
rs780961	snp	C/G			intron-variant	FANCD2	GRCh38.p7	3:10079339	ccagcctgggagaca[C/G]agcgagactccgtct	2177
rs781871	snp	A/T	0.31503	0.241394	upstream-variant-2KB, intron-variant	FANCD2, CIDECP	GRCh38.p7	3:10025121	ACTGCACCTGGCTAA[A/T]GTTTAAATTTTTTTG	2177
rs803334	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10030793	cctgcctcagcctcc[C/T]gagtagctgagatta	2177
rs803335	snp	A/C	0.0905309	0.192535	intron-variant	FANCD2	GRCh38.p7	3:10043351	ATAAACTTGCACTGT[A/C]GTCTGTCTGGGATTG	2177
rs803336	snp	A/G	0.332568	0.235971	intron-variant	FANCD2	GRCh38.p7	3:10054673	acacggtgaaacccc[A/G]actctactaaaaata	2177
rs803341	snp	A/G	0.0611083	0.163768	intron-variant	FANCD2	GRCh38.p7	3:10053361	caaagtccccagagt[A/G]tgatgttccccttcc	2177
rs803342	snp	A/T	0	0	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10090444	aaaaaaaaaaaaaaa[A/T]TCAGCAACTTCCAAG	2177
rs812380	snp	C/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10083883	tttttttttttgaga[C/T]ggagtcttgctctgt	2177
rs1008636	snp	G/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10092684	aaaaaaaaaaaaaaa[G/T]ACATGAAAGAGGTGG	2177
rs1066724	snp	A/C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10069309	acccatttttcaatc[A/C/T]gaataattttttttc	2177
rs1151609	snp	C/G			intron-variant	FANCD2	GRCh38.p7	3:10041049	gtaccaccacgccca[C/G]ctaatttttgtatgt	2177
rs1179924	snp	C/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10089281	tttttttttttgaga[C/T]ggagtttcgctcttg	2177
rs1552244	snp	A/G	0.381308	0.21274	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10093893	ATGTGGGAGATGGGC[A/G]AGTTGGAGAGAGGAG	2177
rs1642642	snp	C/G	0	0	intron-variant	FANCD2	GRCh38.p7	3:10055072	TGCTAAATGCAAAAG[C/G]TAAGATGTAGAACAA	2177
rs1703145	snp	A/G	0	0	intron-variant	FANCD2	GRCh38.p7	3:10036278	TGGCAGGCTAAAAAA[A/G]AAGACATAGGGAGTT	2177
rs1798959	snp	A/C/G	0.5	0	intron-variant	FANCD2	GRCh38.p7	3:10055236	tggttgtataacatt[A/C/G]tgaatatacttaatg	2177
rs1798960	snp	A/C			intron-variant	FANCD2	GRCh38.p7	3:10055152	tattttatcaaaatt[A/C]aaaaataaaaTAAAA	2177
rs1798966	snp	A/G	0	0	intron-variant	FANCD2	GRCh38.p7	3:10036275	CAGGCTAAAAAAAAA[A/G]ACATAGGGAGTTAGG	2177
rs1983415	snp	C/G	0.267091	0.249415	intron-variant	FANCD2	GRCh38.p7	3:10046275	AGTCAGGATGGTCTC[C/G]ATCTCCTGACCTTGT	2177
rs1983416	snp	A/G	0.0618563	0.164627	intron-variant	FANCD2	GRCh38.p7	3:10046327	CAAAGTGCTGGGATT[A/G]CAGATGTGAGCCACT	2177
rs2075310	snp	A/G	0.459801	0.135955	upstream-variant-2KB, intron-variant	FANCD2, CIDECP	GRCh38.p7	3:10025967	GCAGGCGTTGTGTCA[A/G]TTTGCCTAGGTTCAC	2177
rs2160869	snp	C/T	0.333952	0.235483	intron-variant	FANCD2	GRCh38.p7	3:10037571	TCCAATTTTAGTATA[C/T]GTGCTGCCAAAGCAA	2177
rs2241276	snp	A/G	0.0146672	0.084371	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088704	GTATAAAACAGAACC[A/G]GAGGATCTTAAGATC	2177
rs2272123	snp	C/T	0.310632	0.242536	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10098431	TTGGTGACTCTAAGT[C/T]GATGCTGAACATGGT	2177
rs2272124	snp	A/G	0.303931	0.244114	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10096505	ACAAAGAATAAGAGT[A/G]GGGGATTATCACTAG	2177
rs2272125	snp	A/C	0.30382	0.244138	synonymous-codon, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10096385	GACTCTGCAAACTAA[A/C]AGTTCCAGGGTCTTT	2177
rs2276798	snp	C/G	0.00159617	0.0282053	intron-variant	FANCD2	GRCh38.p7	3:10060658	CCCATTTTGTGCAAA[C/G]ATTTCTAGAATTTTA	2177
rs2287435	snp	A/C	0.00398564	0.0444627	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10090218	GGAAGAACCAGGAAC[A/C]AAAAGTAGCTTCCTT	2177
rs2287439	snp	A/C	0.115088	0.210473	intron-variant	FANCD2	GRCh38.p7	3:10044132	TGGCTTCTTTGACTG[A/C]ACCTTGATGTGCTTG	2177
rs2302844	snp	A/G	3.36831e-05	0.00410371	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10095190	ATCTTCCTATAACCA[A/G]TAAGTTTATAAATGC	2177
rs2347581	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10064196	AAAAGAGAGAGTGCA[C/T]AAAAAGCACTTAGCA	2177
rs2347582	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10064195	AAAGAGAGAGTGCAT[A/G]AAAAGCACTTAGCAC	2177
rs2347583	snp	G/T			intron-variant	FANCD2	GRCh38.p7	3:10064183	CATAAAAAGCACTTA[G/T]CACAAGGCCCAGCAC	2177
rs2347584	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10064173	ACTTAGCACAAGGCC[C/T]AGCACAGAATAGGGC	2177
rs2347585	snp	C/T	0.0501905	0.150254	intron-variant	FANCD2	GRCh38.p7	3:10064163	AGGCCCAGCACAGAA[C/T]AGGGCTCTCAGACAG	2177
rs2347586	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10064103	TCTCTTCTTTACTAT[C/T]GTGATTGTTATTAAG	2177
rs2600013	snp	C/G	0	0			GRCh38.p7	3:10101748	CCTGAGCCAGGGACT[C/G]TGATGGTGTTAGACA	2177
rs2600014	snp	A/C/G					GRCh38.p7	3:10101700	GTTAATAAAGACCCC[A/C/G]CTTTAAGAACAAAAT	2177
rs2662144	snp	A/C	0	0	intron-variant	FANCD2	GRCh38.p7	3:10061801	AGAATTCTGACTTCC[A/C]TAGGGTAGGGTAAAG	2177
rs2662145	snp	A/C	0.00576364	0.0533723	intron-variant	FANCD2	GRCh38.p7	3:10061615	AGTGCATATTATGTA[A/C]TAAACATtgttctaa	2177
rs2687893	snp	A/G	0.114387	0.210022	intron-variant	FANCD2	GRCh38.p7	3:10047230	TAAAATAATACAACC[A/G]TTAAATCTATTCCTA	2177
rs3095773	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10041071	gagtagctagaatta[C/T]aagtgcgtaccacca	2177
rs3100098	snp	A/C	0.497907	0.0322805	intron-variant	FANCD2	GRCh38.p7	3:10031320	GAGACGGGGTTTCAC[A/C]ATGTTAGCCAAGATG	2177
rs3105784	snp	A/G	0.499382	0.017561	intron-variant	FANCD2	GRCh38.p7	3:10031319	AGACGGGGTTTCACC[A/G]TGTTAGCCAAGATGG	2177
rs3107667	snp	A/C	0.496034	0.0443518	intron-variant	FANCD2	GRCh38.p7	3:10031344	CCGTCTCTACTAAAA[A/C]TACAAAAAATTAGCC	2177
rs3172417	snp	C/T	0.44092	0.161398	utr-variant-3-prime, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10101265	TGACTCTGATTAGAC[C/T]CCAGATAAATTGTTG	2177
rs3732974	snp	C/G	0.0131889	0.080128	utr-variant-5-prime	FANCD2	GRCh38.p7	3:10028652	TGGAAACCATTTTGA[C/G]CAATGTCTTGTGCAC	2177
rs3843378	snp	C/G/T	0	0	intron-variant	FANCD2	GRCh38.p7	3:10073491	AGGAGATTACTCCAA[C/G/T]GCCTAAGAGAGTTTT	2177
rs3846170	snp	A/T			intron-variant, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10026746	GCTTTTCTGGAAGCC[A/T]GATGGTATCGCACGT	2177
rs3846171	snp	C/G			intron-variant, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10026747	CTTTTCTGGAAGCCA[C/G]ATGGTATCGCACGTG	2177
rs3846172	snp	A/T			intron-variant, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10026748	TTTTCTGGAAGCCAG[A/T]TGGTATCGCACGTGT	2177
rs3846173	snp	G/T			intron-variant, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10026749	TTTCTGGAAGCCAGA[G/T]GGTATCGCACGTGTT	2177
rs3846174	snp	A/G			intron-variant, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10026751	TCTGGAAGCCAGATG[A/G]TATCGCACGTGTTAA	2177
rs3846175	snp	A/T			intron-variant, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10026752	CTGGAAGCCAGATGG[A/T]ATCGCACGTGTTAAA	2177
rs3846176	snp	A/G			intron-variant, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10026753	TGGAAGCCAGATGGT[A/G]TCGCACGTGTTAAAG	2177
rs3846177	snp	G/T	0.329783	0.236927	intron-variant, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10026888	TTTAGCACAGGGCCC[G/T]GTACCTCGTAAATGT	2177
rs3864015	snp	C/T	0.0238492	0.106564	intron-variant	FANCD2	GRCh38.p7	3:10064460	CTGCTGGCTTGGTTG[C/T]ACTGGTGAAGTTACA	2177
rs3864017	snp	A/G	0.26124	0.249747	FANCD2	3	allele_origin=G(germline)/A(germline)	3:10064848	TCCTGTGAGGTCACC[A/G]GACCCCCATCTTTTG	2177
rs3895942	snp	C/G	0.32955	0.237006	intron-variant	FANCD2	GRCh38.p7	3:10067061	CAACAACGTGGTATA[C/G]AGAAAAAAAATCTCT	2177
rs3930484	snp	C/T	0.0607341	0.163335	intron-variant	FANCD2	GRCh38.p7	3:10046157	CTCCCGGGTTCACGC[C/T]ATTCTCCTGCCTCAG	2177
rs3936531	snp	C/T	0.0418186	0.138422	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10085398	CTTTTTTCTTTCTTT[C/T]TTTTTTTTTTTTGAG	2177
rs4019705	snp	A/G	0.00279162	0.0372561	intron-variant	FANCD2	GRCh38.p7	3:10071102	caaatccccctctgc[A/G]agaaacacccaagaa	2177
rs4019706	snp	A/G	0.342358	0.232314	intron-variant	FANCD2	GRCh38.p7	3:10071178	tggcttttatccaaa[A/G]gacaggcaataacag	2177
rs4019707	snp	A/G	0.295343	0.245854	intron-variant	FANCD2	GRCh38.p7	3:10071366	aaagaaaggaaatca[A/G]tataccaaggagata	2177
rs4019708	snp	A/C	0.295343	0.245854	intron-variant	FANCD2	GRCh38.p7	3:10071387	caaggagatatctgc[A/C]ctcccatgtttattg	2177
rs4019772	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10064977	AAAAAGTTTCTCTCG[A/G]GACAAATGGTATTTG	2177
rs4019779	snp	C/G			intron-variant	FANCD2	GRCh38.p7	3:10064079	GGCTCTTCTCTGAGG[C/G]CTCCTTCACTTAATA	2177
rs4019780	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10064102	ACTTAATAACAATCA[C/T]GATAGTAAAGAAGAG	2177
rs4019781	snp	G/T			intron-variant	FANCD2	GRCh38.p7	3:10064120	TAGTAAAGAAGAGAT[G/T]GACTTTGTTAATGAT	2177
rs4019782	snp	C/T	1.64803e-05	0.00287052	intron-variant	FANCD2	GRCh38.p7	3:10064682	GTTTTCCCTGTAGCC[C/T]TGCGTATTCCTGAGC	2177
rs4019783	snp	A/G	0.000428491	0.0146309	intron-variant	FANCD2	GRCh38.p7	3:10064702	TATTCCTGAGCTGCA[A/G]CATCAGATTCTGGTT	2177
rs4019784	snp	A/C/T	0.00478114	0.0486627	intron-variant	FANCD2	GRCh38.p7	3:10064724	ATTCTGGTTTTTCTC[A/C/T]GCAGTGACTTTCCAT	2177
rs4019785	snp	C/T	0.169463	0.236672	intron-variant	FANCD2	GRCh38.p7	3:10064924	TGTTTTGAATGTTCA[C/T]GGGGAATTCCACAGC	2177
rs4019786	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10064939	TGGGGAATTCCACAG[C/T]TCTTGGTGGGGAAGT	2177
rs4019792	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10064058	TTCTGCCCTACCCTG[C/T]CTCACGGCTCTTCTC	2177

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