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
rs193224	snp	C/G	0.0283406	0.115616	intron-variant	FAM63B	GRCh38.p7	15:58814591	aggagttcgagacca[C/G]cctgagcaatatggc	54629
rs347111	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58848629	cctcccgagtagctg[C/G]gactacaggcgcccg	54629
rs347112	snp	A/G	0.479984	0.0980171	intron-variant	FAM63B	GRCh38.p7	15:58813579	ttggtgggttatatc[A/G]taGttgcttgttggt	54629
rs347113	snp	C/T	0.0356815	0.128715	intron-variant	FAM63B	GRCh38.p7	15:58816078	caatatttacttatg[C/T]gccaggcactgttct	54629
rs347114	snp	G/T	0.0279526	0.114869	intron-variant	FAM63B	GRCh38.p7	15:58832606	tgaggcggaggttgc[G/T]gtgaactgaaatcac	54629
rs347115	snp	A/G	0.462253	0.132093	intron-variant	FAM63B	GRCh38.p7	15:58790760	accaaaaatgagata[A/G]tccttgactccactt	54629
rs347116	snp	A/C	0.194954	0.245711	intron-variant	FAM63B	GRCh38.p7	15:58790588	cttgtcttacccccc[A/C]ctaaggtctattgtc	54629
rs364439	snp	C/T	0.0356815	0.128715	intron-variant	FAM63B	GRCh38.p7	15:58821078	ACTTAAACTTTTAAG[C/T]TATAGGAAAATAAAA	54629
rs367267	snp	G/T	0.0271762	0.113356	intron-variant	FAM63B	GRCh38.p7	15:58838111	CAAGATATACTTTCA[G/T]GCCAGGTGTGGTGTG	54629
rs374865	snp	A/G	0.0356815	0.128715	intron-variant	FAM63B	GRCh38.p7	15:58791543	gattgcttgggcctg[A/G]gatccagaggctgca	54629
rs379879	snp	G/T	0.391024	0.206427	intron-variant	FAM63B	GRCh38.p7	15:58778977	ATGTTGGCCAGGCTG[G/T]TCTTGAACTCCTGAC	54629
rs384322	snp	A/C	0.0551013	0.156571	intron-variant	FAM63B	GRCh38.p7	15:58788663	ATTTATATATTTATA[A/C]TATCACCAAATAGGA	54629
rs387812	snp	C/T	0.431177	0.172264	intron-variant	FAM63B	GRCh38.p7	15:58782587	TTTCCTCATCGTGCT[C/T]CACTTTTCACTGGTC	54629
rs392739	snp	C/T	0.0352966	0.128072	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58859134	TTTGGGAAGAGATCA[C/T]GCCATACTCAAAGAA	54629
rs395601	snp	C/G	0.420733	0.18262	upstream-variant-2KB	FAM63B, LOC101928725	GRCh38.p7	15:58770997	ACAAGGGAGCTGCCC[C/G]GGAGTTCAACTTCCG	54629
rs406699	snp	A/G	0.480931	0.0957637	intron-variant	FAM63B	GRCh38.p7	15:58777655	AAAAAAAGAAAATCT[A/G]TTGAATAGTTGAGCT	54629
rs411007	snp	C/G	0.437118	0.165792	intron-variant	FAM63B	GRCh38.p7	15:58786303	GTTAAAAATTCTTCA[C/G]CAATTATTTTGTGTT	54629
rs411211	snp	A/G	0.0279526	0.114869	intron-variant	FAM63B	GRCh38.p7	15:58834729	TAATTCACGACTTTA[A/G]TAAGCCACTTTCATT	54629
rs421829	snp	C/G	0.431325	0.172108	intron-variant	FAM63B	GRCh38.p7	15:58787703	gttgcccagggtgga[C/G]tgcagtggcgcaatc	54629
rs422259	snp	C/T	0.0356815	0.128715	intron-variant	FAM63B	GRCh38.p7	15:58805409	TAGGCTCTTTGCTTA[C/T]ATTACAACTTCTGGT	54629
rs431414	snp	C/T	0.375797	0.216044	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58855601	AGTTAGAGATAATCT[C/T]TGTGTCTTATAAAAA	54629
rs432978	snp	A/G	0.0364509	0.129988	intron-variant	FAM63B	GRCh38.p7	15:58785345	AGAAGCAAATACACA[A/G]ATATTTCGACTCACT	54629
rs442321	snp	A/T	0.0829062	0.185956	utr-variant-3-prime, downstream-variant-500B	FAM63B	GRCh38.p7	15:58854838	AAATGCTGTGTGTTG[A/T]CATTCATGAAAAATA	54629
rs446126	snp	C/T	0.430285	0.173197	intron-variant	FAM63B	GRCh38.p7	15:58820903	TAAGTAAGTTATATA[C/T]CTAATAAAACAAATA	54629
rs449243	snp	A/G	0.45762	0.139261	intron-variant	FAM63B	GRCh38.p7	15:58831041	TGTGTGTGTGTGTGT[A/G]TATATATATATATAT	54629
rs452698	snp	A/G	0.429538	0.173972	intron-variant	FAM63B	GRCh38.p7	15:58813372	tcatggcatgtgcct[A/G]taatcccagctactt	54629
rs472200	snp	A/C	0.269809	0.249214	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58860203	AACATTTTGTTTTGT[A/C]CTTCTCTAATTTATG	54629
rs474875	snp	A/C	0.461592	0.133149	intron-variant	FAM63B	GRCh38.p7	15:58794504	TCACTTTCTCCAACA[A/C]AAATCCCATAATTTT	54629
rs481309	snp	A/G	0.451856	0.147493	intron-variant	FAM63B	GRCh38.p7	15:58799766	GAGCCAGACATGGAC[A/G]TGGCTTTTTGAAGGG	54629
rs484952	snp	C/T	0.00795532	0.062565	intron-variant	FAM63B	GRCh38.p7	15:58781858	AGTGAGCCAAGATCG[C/T]GCCACTGCACTCCAG	54629
rs499269	snp	A/C	0.0283406	0.115616	intron-variant	FAM63B	GRCh38.p7	15:58811078	ggccccttgggccac[A/C]cctgcagtttatact	54629
rs500057	snp	A/G	0.446771	0.154211	intron-variant	FAM63B	GRCh38.p7	15:58822276	CCTTTATGAATGATT[A/G]CTTCTTCTTCTTTTT	54629
rs501165	snp	G/T	0.450859	0.148847	intron-variant	FAM63B	GRCh38.p7	15:58811284	ATATATCCATCACTC[G/T]AACTGTACATTTCTA	54629
rs510759	snp	A/G	0.444931	0.15653	intron-variant	FAM63B	GRCh38.p7	15:58782337	ACTATTATTTAGTGC[A/G]TCCATTTTGCCTTAC	54629
rs512146	snp	G/T	0.450609	0.149185	intron-variant	FAM63B	GRCh38.p7	15:58807529	CATGCCTGGCTAAAA[G/T]TTTTTTGTATTTTTT	54629
rs519649	snp	G/T	0	0	intron-variant	FAM63B	GRCh38.p7	15:58804230	ATTGCTAAAAATGTT[G/T]AAATATCACTGTTTT	54629
rs522391	snp	A/G	0	0	intron-variant	FAM63B	GRCh38.p7	15:58803940	TTTTTTTTTTCAGTA[A/G]AGCTGGGGTTTCACC	54629
rs523354	snp	A/G	0	0	intron-variant	FAM63B	GRCh38.p7	15:58803809	TTAttttttgaggca[A/G]agtctccctctgctg	54629
rs529301	snp	C/T	0.0283406	0.115616	intron-variant	FAM63B	GRCh38.p7	15:58804272	TATTGGAAGCTGGGA[C/T]GAGATTTCATTTGAA	54629
rs533831	snp	C/G	0	0	intron-variant	FAM63B	GRCh38.p7	15:58844777	ggagcacaccaccac[C/G]cctggctaatttttg	54629
rs533904	snp	C/G			intron-variant	FAM63B	GRCh38.p7	15:58844750	TTTGTATTTTTAGTA[C/G]AGATGGAGTTTCACC	54629
rs533907	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58844748	TGTATTTTTAGTAGA[A/G]ATGGAGTTTCACCAT	54629
rs534646	snp	A/G	0.277778	0.248452	intron-variant	FAM63B	GRCh38.p7	15:58844699	gaactcctgacctca[A/G]atgatccaccgcctc	54629
rs535679	snp	A/G	0.297128	0.245518	intron-variant	FAM63B	GRCh38.p7	15:58843296	CAGGTGTAGTGGTAC[A/G]TGCCTGTAGTCTCAG	54629
rs546116	snp	A/C	0.0283406	0.115616	intron-variant	FAM63B	GRCh38.p7	15:58808740	gtgggcacctgtagt[A/C]ccagctactcgggag	54629
rs551943	snp	A/T	0.0356815	0.128715	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58855214	GATCATGGAGCTTAG[A/T]TTTAATTTAGATAGC	54629
rs556082	snp	C/G	0.0283406	0.115616	intron-variant	FAM63B	GRCh38.p7	15:58784876	CTGGGCTCAAGTGAT[C/G]CTTTCACTTCAGCCT	54629
rs556256	snp	C/T	0.445724	0.155538	intron-variant	FAM63B	GRCh38.p7	15:58802565	GCTAAAAATGGATTT[C/T]ATATTTTTAAAGAGG	54629
rs561903	snp	C/T	0.44638	0.154709	intron-variant	FAM63B	GRCh38.p7	15:58783631	TGTAATTCTTAATCA[C/T]CTAAAGAGTAAAGTA	54629
rs567876	snp	G/T	0.0364509	0.129988	intron-variant	FAM63B	GRCh38.p7	15:58799432	ATTAGCCAGGCGTGG[G/T]GGCGGGTGCCTGTAG	54629
rs571030	snp	C/G	0.0209421	0.100162	intron-variant	FAM63B	GRCh38.p7	15:58851005	gcctgggcgacagag[C/G]aagactcagtcgtga	54629
rs574683	snp	C/T	0.448452	0.152042	intron-variant	FAM63B	GRCh38.p7	15:58816117	aatgCAGCATACATG[C/T]GTGCATCCATTAACT	54629
rs596094	snp	A/G	0.44638	0.154709	intron-variant	FAM63B	GRCh38.p7	15:58783004	TGGGCCCAGAAGACA[A/G]AGGCTGCAGTGAGTA	54629
rs597112	snp	C/T	0.446771	0.154211	intron-variant	FAM63B	GRCh38.p7	15:58818486	GGAGGACGGCTTCAG[C/T]CCAGGAATTTGAGAC	54629
rs601795	snp	C/G	0.451732	0.147663	intron-variant	FAM63B	GRCh38.p7	15:58797951	CCCCTCTGAACATTG[C/G]TTTCCTCTTCTGTAA	54629
rs610877	snp	G/T	0.461481	0.133325	intron-variant	FAM63B	GRCh38.p7	15:58811129	ctaaatcttggcatt[G/T]ctgtaccaataggag	54629
rs618684	snp	C/T	0.461259	0.133677	intron-variant	FAM63B	GRCh38.p7	15:58823723	AAAAGAGTTGTCAGA[C/T]GAATCAATGATCAAC	54629
rs620284	snp	C/T	0.0283406	0.115616	intron-variant	FAM63B	GRCh38.p7	15:58811985	AAGTTTACAATTAAC[C/T]AATATTATTTTGAAA	54629
rs624536	snp	G/T	0.447032	0.153878	intron-variant	FAM63B	GRCh38.p7	15:58834299	GATTAAGGAGTGAGA[G/T]ATtgtggggaaaaga	54629
rs625312	snp	C/T	0.450734	0.149016	intron-variant	FAM63B	GRCh38.p7	15:58781080	CCTGGGCAACAAGAA[C/T]GAAACACTGTCTGGA	54629
rs626228	snp	A/G	0.0130921	0.0798413	intron-variant	FAM63B	GRCh38.p7	15:58810007	ggcggatcacttgag[A/G]tcaggagtttgagac	54629
rs633585	snp	A/T			intron-variant	FAM63B	GRCh38.p7	15:58785350	TTTTTAGAAGCAAAT[A/T]CACAGATATTTCGAC	54629
rs634116	snp	A/C	0.00717551	0.0594665	intron-variant	FAM63B	GRCh38.p7	15:58830646	tagacaaaggctgtg[A/C]tgtgccttatagaga	54629
rs634565	snp	A/G	0.00874735	0.0655527	intron-variant	FAM63B	GRCh38.p7	15:58830516	tcttttggattttgg[A/G]atgtctgcattatac	54629
rs635349	snp	A/G	0.0356815	0.128715	intron-variant	FAM63B	GRCh38.p7	15:58784924	TAACAGGCTGGGTAC[A/G]GTGGCTCACGTCTAC	54629
rs637918	snp	C/T	0.385741	0.209939	intron-variant	FAM63B	GRCh38.p7	15:58846071	cattaaccatccatc[C/T]tgcctgcctccaaat	54629
rs640045	snp	C/T	0.293551	0.246177	intron-variant	FAM63B	GRCh38.p7	15:58852262	CTTGCTCTATCATCC[C/T]GACTGGAGTGTAGTG	54629
rs648432	snp	C/G	0.0970103	0.197722	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58861645	CCTCCCAAAGTGAAA[C/G]TTTTGAAACTGATGA	54629
rs650013	snp	C/T	0.0283406	0.115616	intron-variant	FAM63B	GRCh38.p7	15:58809925	gggcatggtggcatg[C/T]gcctgtagtcccagc	54629
rs650731	snp	A/G	0.131038	0.219882	intron-variant	FAM63B	GRCh38.p7	15:58773460	GTACTGTCTTCACTT[A/G]AAACATCTCAGTGCC	54629
rs652193	snp	C/T	0.446641	0.154377	intron-variant	FAM63B	GRCh38.p7	15:58773115	GAAACATTGCATCTA[C/T]AGATATAATTATCAA	54629
rs654857	snp	C/T	0.450859	0.148847	intron-variant	FAM63B	GRCh38.p7	15:58814545	caaaaaattaaaaag[C/T]gagcagggtatggtg	54629
rs654870	snp	A/G	0.457037	0.140127	intron-variant	FAM63B	GRCh38.p7	15:58808145	GGGGAAGCTGTGTGT[A/G]TGGGGTTAGGAGGAA	54629
rs655312	snp	A/C	0.0879971	0.190408	intron-variant	FAM63B	GRCh38.p7	15:58851169	ctggccaacatggta[A/C]aaccccgtctctatt	54629
rs656317	snp	A/G			intron-variant	FAM63B	GRCh38.p7	15:58804229	TTGCTAAAAATGTTT[A/G]AATATCACTGTTTTA	54629
rs657649	snp	A/T	0	0	intron-variant	FAM63B	GRCh38.p7	15:58803942	ttttttttttttcag[A/T]aaagctggggtttca	54629
rs661367	snp	C/T	0.270351	0.24917	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58861104	AGGAAAAGATTCACA[C/T]GCACTAGCTTTAGGA	54629
rs661852	snp	C/T	0.00597247	0.0543191	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58860961	TGAATCTGTAACAAG[C/T]TGTCATTTATTAAGC	54629
rs662149	snp	C/G	0	0	intron-variant	FAM63B	GRCh38.p7	15:58791855	gaccttttcttttat[C/G]tactacattccttcc	54629
rs664783	snp	C/G	0.14665	0.227637	intron-variant	FAM63B	GRCh38.p7	15:58808905	tttaaagatgaaaaa[C/G]tggctgggcacggtg	54629
rs664909	snp	A/C			intron-variant	FAM63B	GRCh38.p7	15:58782922	aaaaaaaaaaaaaaa[A/C]aaaaaaaaaaCAGAG	54629
rs664936	snp	C/T	0.453331	0.145452	intron-variant, upstream-variant-2KB	FAM63B, LOC101928725	GRCh38.p7	15:58772587	TACTTTCTCCAATTC[C/T]TCACTTTTTTGCATA	54629
rs670920	snp	C/G	0.39009	0.207062	intron-variant	FAM63B	GRCh38.p7	15:58849895	ACAAAAATTAGCCGG[C/G]TGTGGTGGCACATGC	54629
rs673813	snp	A/T	0.470618	0.117591	intron-variant	FAM63B	GRCh38.p7	15:58784972	TGGCAGTCTGTCTGA[A/T]TTTCTAAATTTTAAG	54629
rs677933	snp	C/G	0.410737	0.191478	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58859717	ATGAACTAAAATTTA[C/G]ATAGATATTCAAAGT	54629
rs678020	snp	C/T	0.0356815	0.128715	intron-variant	FAM63B	GRCh38.p7	15:58795977	TTCTCCAGTATTCAA[C/T]ACCCTTTCTCCTTTC	54629
rs682619	snp	A/G	0.476052	0.106772	intron-variant	FAM63B	GRCh38.p7	15:58806574	AATATTAAAACAACT[A/G]AGTTAACACCATTTG	54629
rs684505	snp	C/G	0.448708	0.151707	intron-variant	FAM63B	GRCh38.p7	15:58821443	ACTTTATTTCTTAAG[C/G]TCATAAACATGTATT	54629
rs688343	snp	A/T	0.446641	0.154377	intron-variant	FAM63B	GRCh38.p7	15:58819867	GGATAAGATTCTATG[A/T]ACATTGCACAAAAAA	54629
rs688756	snp	G/T	0.402982	0.197728	intron-variant	FAM63B	GRCh38.p7	15:58784073	CTCGCAAATTGCTGG[G/T]ATTACAGGTGTGAGC	54629
rs793571	snp	C/T	0.459347	0.136653	intron-variant	FAM63B	GRCh38.p7	15:58849507	CCAGtttttttcttt[C/T]ttgagacggagtctt	54629
rs793572	snp	C/T	0.0685596	0.171987	intron-variant	FAM63B	GRCh38.p7	15:58849269	gtgatcggcccgcct[C/T]ggcctcccaaagtgc	54629
rs809904	snp	C/T			utr-variant-3-prime	FAM63B	GRCh38.p7	15:58855830	cgggttcaagcaatt[C/T]tcctgcctcagccct	54629
rs812659	snp	A/G	0	0	intron-variant	FAM63B	GRCh38.p7	15:58844584	actgtcaacaatgca[A/G]atttttttttttttt	54629
rs813219	snp	C/T	0.39527	0.203462	intron-variant	FAM63B	GRCh38.p7	15:58849500	ttttctttcttgaga[C/T]ggagtcttgctctgt	54629
rs813220	snp	A/C	0.386884	0.209196	intron-variant	FAM63B	GRCh38.p7	15:58844489	tcttgggtcactgca[A/C]cctccgcctcctggg	54629
rs814252	snp	A/G	0	0	intron-variant	FAM63B	GRCh38.p7	15:58844557	tttttttttttttga[A/G]acggagtctcgctct	54629
rs1047390	snp	C/T	0	0	missense, upstream-variant-2KB, nc-transcript-variant	FAM63B, LOC101928725	GRCh38.p7	15:58771652	CCACTGTCCTTCAAG[C/T]CCAAACCCGCGGAGG	54629
rs1053420	snp	A/G	0.496517	0.0415876	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58861609	AATTATTTTAAAACT[A/G]CTTAATTCTTAAAAA	54629
rs1054991	snp	A/G	0.495407	0.0477027	utr-variant-3-prime	FAM63B	GRCh38.p7	15:58857201	ATGAAATGTTCAATT[A/G]TATTAAAACAAACAA	54629

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