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
rs10593	snp	A/G	0.340333	0.233109	downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant	ASAP2, ITGB1BP1	GRCh38.p7	2:9405901	TGCTGGTCTGGAACA[A/G]TGACATTGCCAACTT	8853
rs870732	snp	A/G	0.499396	0.0173617	intron-variant	ASAP2	GRCh38.p7	2:9251490	ACCCGACGGACATCA[A/G]GGATTAGCTGTTCTG	8853
rs875053	snp	A/T	0.29789	0.24537	intron-variant	ASAP2	GRCh38.p7	2:9224994	TTGAGTCAAGGTGCG[A/T]AAGTTGGAACATTGC	8853
rs875054	snp	A/C	0.149999	0.229128	intron-variant	ASAP2	GRCh38.p7	2:9226087	GGTGAGACTAGCTCG[A/C]ATGAGGCAGCACACA	8853
rs907161	snp	G/T	0.499989	0.00239614	intron-variant	ASAP2	GRCh38.p7	2:9230920	GGTCCTGTGTGACCT[G/T]GGAGGTGTGTGAGGG	8853
rs907162	snp	A/G	0.35445	0.227135	intron-variant	ASAP2	GRCh38.p7	2:9270500	ATTATTATGCACTGC[A/G]TGCCTGTATCAAAAT	8853
rs1136172	snp	C/T	0.5	0	downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant	ASAP2, ITGB1BP1	GRCh38.p7	2:9406135	AGTGACAAACACACA[C/T]TGAAGGCCTGAGGAA	8853
rs1138459	snp	C/T	0	0	utr-variant-3-prime	ASAP2	GRCh38.p7	2:9405017	TCTATTTTAACAATC[C/T]TCCTGCATCTGTATT	8853
rs1139804	snp	A/G	5.01098e-05	0.00500524	missense	ASAP2	GRCh38.p7	2:9388532	CCCCGCTTCCTCCAC[A/G]GAATGTTGGCAAAGG	8853
rs1473022	snp	A/G	0.4021	0.198407	intron-variant	ASAP2	GRCh38.p7	2:9244247	GTTGCAGTGAGCCAA[A/G]ATCGCGCCACTGCAC	8853
rs1510796	snp	C/T	0.499801	0.00998203	intron-variant	ASAP2	GRCh38.p7	2:9256874	GGTGGACAGGACAAG[C/T]GGCTAAGAGACAGTC	8853
rs1858268	snp	C/T	0.102014	0.201495	intron-variant, upstream-variant-2KB	ASAP2, LOC100506317	GRCh38.p7	2:9208017	AATTTTCAACCAAGC[C/T]TCTTCGTTCCTACGT	8853
rs1877098	snp	C/G	0.49962	0.0137727	intron-variant	ASAP2	GRCh38.p7	2:9263920	TAGAAGGCCAGGTGC[C/G]GTGTCTCACACCTGT	8853
rs1962214	snp	C/T	0.19646	0.2442	intron-variant	ASAP2	GRCh38.p7	2:9385581	GAATGGCTAATTATG[C/T]ACTTATAGGCAGCCT	8853
rs1995924	snp	C/T	0.499824	0.00938333	intron-variant	ASAP2	GRCh38.p7	2:9256385	GCTAATTTCTTTATG[C/T]ACAGTTGACACTGCC	8853
rs1995925	snp	A/G			intron-variant	ASAP2	GRCh38.p7	2:9256149	ttGCAGGGGACCCTA[A/G]AATAGTTTTTCTCCT	8853
rs2001296	snp	A/G	0.128632	0.218563	intron-variant	ASAP2	GRCh38.p7	2:9366761	TTTTTCCACGTGTCA[A/G]GGGCCGGGTTGAATT	8853
rs2136841	snp	C/G	0.499928	0.00598999	intron-variant	ASAP2	GRCh38.p7	2:9222789	GTAGGAGAAATGGCC[C/G]TTCACCTTTTCCCAT	8853
rs2136842	snp	C/T	0.499923	0.00618962	intron-variant	ASAP2	GRCh38.p7	2:9222856	CTTTTCCTTGGGGAC[C/T]GGGATGCTTATGCTG	8853
rs2175335	snp	C/G/T	0.133777	0.221342	intron-variant	ASAP2	GRCh38.p7	2:9222979	TCCAGACCCTCCAAG[C/G/T]CCTGTGTTTTCTCTT	8853
rs2271333	snp	A/G	0.498794	0.0245311	intron-variant	ASAP2	GRCh38.p7	2:9233121	GAGATACGGCTTTGA[A/G]ACAGTTTGAGTCATC	8853
rs2356779	snp	A/G	0.26271	0.249677	intron-variant	ASAP2	GRCh38.p7	2:9251562	GTCAGATGAGGTAAT[A/G]CGTTTTAGTAAAGTG	8853
rs2666205	snp	A/C	0.0592355	0.161582	intron-variant	ASAP2	GRCh38.p7	2:9215988	TTCAGCAGAGCTGCA[A/C]ATTGGACCTTCTGAG	8853
rs2666206	snp	A/G	0.163892	0.234703	intron-variant	ASAP2	GRCh38.p7	2:9241698	GGAAAATTACAGTAC[A/G]TATCTTTGGTGAGGC	8853
rs2666207	snp	C/T	0.499902	0.00698814	intron-variant	ASAP2	GRCh38.p7	2:9241137	CATCCAGATAcagta[C/T]taccctcttatccac	8853
rs2666208	snp	G/T	0.49998	0.00319482	intron-variant	ASAP2	GRCh38.p7	2:9240553	aaaaatcattaactt[G/T]tgggaggggctgggc	8853
rs2666209	snp	C/T	0.499897	0.00718776	intron-variant	ASAP2	GRCh38.p7	2:9240042	TGACTAGTTTTTTCA[C/T]CCTGACTTAATTTCT	8853
rs2666210	snp	A/G	0.304188	0.244057	intron-variant	ASAP2	GRCh38.p7	2:9271039	TTGGGAGGCCGAGGC[A/G]GGTGGATCACGAGGT	8853
rs2666211	snp	A/G	0.153	0.230415	intron-variant	ASAP2	GRCh38.p7	2:9270850	agccgagatcgcgcc[A/G]ctgcactccagcctg	8853
rs2666212	snp	C/T	0.438246	0.16451	intron-variant	ASAP2	GRCh38.p7	2:9251499	ACAAAACCCACCCGA[C/T]GGACATCAGGGATTA	8853
rs2666213	snp	C/T	0.499984	0.00279548	intron-variant	ASAP2	GRCh38.p7	2:9250300	CAGGAAGTCTGTGGT[C/T]AAATACCATTTGCTG	8853
rs2666214	snp	A/C	0.492087	0.0623997	intron-variant	ASAP2	GRCh38.p7	2:9249683	AATCTCAGCCCAGCG[A/C]CCAGTCTCACTCAGG	8853
rs2666215	snp	A/C	0.0498117	0.149749	intron-variant	ASAP2	GRCh38.p7	2:9249110	GTGTGGCCTCAGCCA[A/C]AAGACAGCCTCTCAG	8853
rs2666216	snp	A/C	0.174288	0.23826	intron-variant	ASAP2	GRCh38.p7	2:9268479	GGCCTGGCTTTATTC[A/C]CACAAGGGGGGAGGT	8853
rs2666217	snp	A/G	0.163892	0.234703	intron-variant	ASAP2	GRCh38.p7	2:9262711	TTTTTAAAGGAACAC[A/G]GCACACAAATGTGAC	8853
rs2666218	snp	A/G	0.411746	0.190626	intron-variant	ASAP2	GRCh38.p7	2:9262859	GGAATCAAAGTCCTC[A/G]GTCTCTTTCACGCGG	8853
rs2666219	snp	C/T	0.406123	0.195258	intron-variant	ASAP2	GRCh38.p7	2:9263693	GAGGCTGCAGCCTCT[C/T]GTTGTTCATGCGTCG	8853
rs2709559	snp	C/T	0.431029	0.17242	intron-variant, utr-variant-3-prime	ASAP2	GRCh38.p7	2:9390671	CTCCTTCCCATGGGC[C/T]GTGGGAGTCACCACC	8853
rs2709560	snp	C/T	0.17461	0.238362	intron-variant, synonymous-codon	ASAP2	GRCh38.p7	2:9389915	AGGATCTGGGAGAGG[C/T]GGGGAGAAAGCCGCA	8853
rs2709561	snp	C/T	0.0490535	0.14873	intron-variant	ASAP2	GRCh38.p7	2:9228274	TGACATAAGTATATT[C/T]TTAACACTGAAGGAA	8853
rs2709562	snp	A/G	0.446118	0.155041	intron-variant	ASAP2	GRCh38.p7	2:9251851	GCCCATCTCTGCTCC[A/G]TCCATCACTGCCAGA	8853
rs2709563	snp	A/G	0.499968	0.00399348	intron-variant	ASAP2	GRCh38.p7	2:9251836	ATCCATCACTGCCAG[A/G]AAACTCACATTCAGT	8853
rs2709564	snp	C/T	0.155987	0.23165	intron-variant	ASAP2	GRCh38.p7	2:9240178	CTAGTTCAATATTAG[C/T]TGGCTGCAGGCATCC	8853
rs2709565	snp	A/C	0.499996	0.00139776	intron-variant	ASAP2	GRCh38.p7	2:9239912	TTAAACATGACAAAA[A/C]CTCATCTCTACAAAA	8853
rs2709566	snp	A/C	0.3748	0.216622	intron-variant	ASAP2	GRCh38.p7	2:9239739	CTCATCTAAAACAAA[A/C]AAAAAAAGATGCTGC	8853
rs2709567	snp	A/G	0.5	0.00019968	intron-variant	ASAP2	GRCh38.p7	2:9244833	CTCAGAAAGGATCTA[A/G]TGAAAAGGGTTTGCC	8853
rs2709568	snp	A/G	0.499631	0.0135733	intron-variant	ASAP2	GRCh38.p7	2:9243343	AGGTGGGTGGATCAC[A/G]AGGTCAGGAGATCGA	8853
rs2709569	snp	A/G	0.0158469	0.0875917	intron-variant	ASAP2	GRCh38.p7	2:9249012	ATACATAGGATGCTA[A/G]AATTTTAGGTCTAGA	8853
rs2709570	snp	C/T	0.494651	0.0514399	intron-variant	ASAP2	GRCh38.p7	2:9249337	CCCATTCTGCCCTCA[C/T]GTCTCTAGAGAGGAC	8853
rs2709571	snp	A/G	0.216048	0.247684	intron-variant	ASAP2	GRCh38.p7	2:9367004	GCAAAGGAGTTAACA[A/G]ACATGCTTTGGGAGA	8853
rs2709572	snp	C/G	0.239326	0.249772	intron-variant	ASAP2	GRCh38.p7	2:9366038	GGGGCAGGAAGGTGG[C/G]TGTCGACCTGAGCCC	8853
rs2709573	snp	C/T	0.243919	0.249926	intron-variant	ASAP2	GRCh38.p7	2:9363687	GCTACCCAGAAGGAT[C/T]GCATGAGCCTGGGAG	8853
rs2709574	snp	C/T	0.195526	0.243993	intron-variant	ASAP2	GRCh38.p7	2:9361606	GACTCCAGCCTGGGT[C/T]ATGGAGTGAGACCCT	8853
rs2709575	snp	A/G	0.0479149	0.147179	intron-variant	ASAP2	GRCh38.p7	2:9361204	TTTAAAACTCTGGAA[A/G]CAATTAGATTTTGAA	8853
rs2709576	snp	A/G	0.448323	0.15221	intron-variant	ASAP2	GRCh38.p7	2:9359248	GAAATCGCTGGTGAT[A/G]AGGGAAAACAAGTAC	8853
rs2709577	snp	G/T	0.0471551	0.14613	intron-variant	ASAP2	GRCh38.p7	2:9367789	GTGTTAATTTAATGT[G/T]TAACATGTCAGAAGA	8853
rs2709578	snp	A/T	0.196149	0.244131	intron-variant	ASAP2	GRCh38.p7	2:9368779	AGAGCCTCACTCGCC[A/T]CTGGTGGGTGGAAGA	8853
rs2709579	snp	A/C/T	0.0479342	0.147301	intron-variant	ASAP2	GRCh38.p7	2:9369910	gcaatgatgtgatct[A/C/T]ggctcactgcagcat	8853
rs2709580	snp	C/T	0.427727	0.175821	intron-variant	ASAP2	GRCh38.p7	2:9374444	CCTGAATAAGAAGGG[C/T]GTGGAGGTGACGAGG	8853
rs2709581	snp	C/G			intron-variant	ASAP2	GRCh38.p7	2:9387917	aaggcagttttccct[C/G]ctctcgcttgctctc	8853
rs2709582	snp	C/G			intron-variant	ASAP2	GRCh38.p7	2:9387916	aggcagttttccctg[C/G]tctcgcttgctctct	8853
rs2709583	snp	A/C	0.42666	0.176893	intron-variant	ASAP2	GRCh38.p7	2:9382821	tgtcaggcgactaca[A/C]ttggtgtatggggtc	8853
rs2709584	snp	G/T	0.499563	0.0147699	intron-variant	ASAP2	GRCh38.p7	2:9265521	TTTGATAATTTTTTC[G/T]AATTAAAGAAAATGA	8853
rs2709585	snp	A/G	0.173965	0.238157	intron-variant	ASAP2	GRCh38.p7	2:9263212	ACTAGCTCAGGAAAA[A/G]AATCACAAACAAGAG	8853
rs2709586	snp	C/T	0.425123	0.178415	intron-variant	ASAP2	GRCh38.p7	2:9377518	GGACTCCCAGATCTG[C/T]GGTAAACTGCCTGTG	8853
rs2709587	snp	A/G	0.488302	0.0755777	intron-variant	ASAP2	GRCh38.p7	2:9260303	CAGATTCTGGATCCC[A/G]CCTCATCCTCATGAC	8853
rs2709588	snp	C/G	0.382085	0.212258	intron-variant	ASAP2	GRCh38.p7	2:9259637	AGGGGGCCTGAGAGC[C/G]CCAAGGAGCAAGGTG	8853
rs2709589	snp	C/T	0.498774	0.02473	intron-variant	ASAP2	GRCh38.p7	2:9258987	GCAGGCCCAGGGTCC[C/T]GGTCTGGCCCCGCGA	8853
rs2709590	snp	C/T	0.499984	0.00279548	intron-variant	ASAP2	GRCh38.p7	2:9258715	CTGTTCCTCAAGAGA[C/T]CTAAAGAAGTTGCAA	8853
rs2709591	snp	C/T	0.49277	0.0596899	intron-variant	ASAP2	GRCh38.p7	2:9356162	AATTTAACACAGCGT[C/T]GCTCTTGTTTTTCTA	8853
rs2709592	snp	C/T	0.35574	0.226537	intron-variant	ASAP2	GRCh38.p7	2:9376131	AGCTCAGAGCCTGCA[C/T]GGACATGCCTGTTAC	8853
rs2709593	snp	A/G			intron-variant	ASAP2	GRCh38.p7	2:9268751	TGTCCCTTCTTCTCA[A/G]GCTGGCCTTTCGTCC	8853
rs2709594	snp	A/T	0.17138	0.237316	intron-variant	ASAP2	GRCh38.p7	2:9270431	TCAGTATTTTTTTTT[A/T]AATTTTTGATTATTG	8853
rs2709595	snp	C/T	0.472989	0.113031	intron-variant	ASAP2	GRCh38.p7	2:9270828	gacggagtctcgctc[C/T]gtcgcccaggctgga	8853
rs2709596	snp	A/G	0.464309	0.12873	intron-variant	ASAP2	GRCh38.p7	2:9271090	GAGCCACCGCGCCCG[A/G]CCCTGTTTTCATTTT	8853
rs2709597	snp	A/G	0.0490535	0.14873	intron-variant	ASAP2	GRCh38.p7	2:9375481	tgtaatcattccatg[A/G]tgtaaacatagatca	8853
rs2715855	snp	C/T	0.0482946	0.147699	intron-variant	ASAP2	GRCh38.p7	2:9376693	CTTCTCATTTATTTC[C/T]CATGGAGTCAGGAGA	8853
rs2715856	snp	C/T	0.177824	0.239355	intron-variant	ASAP2	GRCh38.p7	2:9377427	GATTAGAAACCAGAG[C/T]ACTGGATTATGGGTG	8853
rs2715857	snp	C/T	0.0479149	0.147179	intron-variant	ASAP2	GRCh38.p7	2:9381626	ctgtagccccagtta[C/T]ccaggaggctaaggt	8853
rs2715858	snp	C/T	0.425586	0.17796	intron-variant	ASAP2	GRCh38.p7	2:9383619	gcagaattcagaccc[C/T]tcccataatcctaat	8853
rs2715859	snp	C/T	0.425894	0.177655	intron-variant	ASAP2	GRCh38.p7	2:9384836	tcttcccccagggta[C/T]agggtgagaccctct	8853
rs2715860	snp	C/G	0.454722	0.143489	missense	ASAP2	GRCh38.p7	2:9388407	AAACCTTGCCAAGGA[C/G]AAGCAGAGGGCTTTC	8853
rs2715861	snp	C/T	0.0162398	0.0886349	intron-variant, missense	ASAP2	GRCh38.p7	2:9390139	CCTTTTTCTTTTTGC[C/T]GTTCCTGTCCCTAGC	8853
rs2715862	snp	C/T	0.0535932	0.154675	intron-variant, utr-variant-3-prime	ASAP2	GRCh38.p7	2:9390301	GCCTTGCATTTGGGG[C/T]GGACCTGGCTCCCCA	8853
rs2715863	snp	C/T	0.216649	0.247765	intron-variant	ASAP2	GRCh38.p7	2:9353417	TTAAAAATAGTGCAG[C/T]ATGGTGACATGTGCC	8853
rs2715864	snp	A/G	0.24932	0.249999	intron-variant	ASAP2	GRCh38.p7	2:9353832	GGTGGAATTGGGGCC[A/G]GGGGCAGTGGCTCAC	8853
rs2715865	snp	C/T	0.222035	0.248431	intron-variant	ASAP2	GRCh38.p7	2:9354061	TTCTGGGAGCTCATC[C/T]AATCCATTGCCTGCA	8853
rs2715866	snp	A/G	0.448066	0.152544	intron-variant	ASAP2	GRCh38.p7	2:9355520	TAAAACTGTGCTGAC[A/G]CCAGCAGTATGTAAG	8853
rs2715867	snp	C/T	0.21725	0.247846	intron-variant	ASAP2	GRCh38.p7	2:9359667	ATGTAGGGAATTTAA[C/T]GTCAAGAGCAATAGT	8853
rs2715868	snp	A/G	0.0766824	0.180169	intron-variant	ASAP2	GRCh38.p7	2:9359730	TCCTCTCAAGGGGCC[A/G]TCAGTCTTATTGATG	8853
rs2715869	snp	A/G	0.200801	0.245111	intron-variant	ASAP2	GRCh38.p7	2:9360539	CCGTCCCCAACAAAT[A/G]TTTAACAGTCAACTC	8853
rs2715870	snp	C/T	0.239326	0.249772	intron-variant	ASAP2	GRCh38.p7	2:9363197	aaatccattcgtcca[C/T]tggtggcatttaggt	8853
rs2715871	snp	A/T	0.0766824	0.180169	intron-variant	ASAP2	GRCh38.p7	2:9363495	AACAGGTGTGAGATG[A/T]TCGTGGTTTTAATTT	8853
rs2715872	snp	A/G	0.239326	0.249772	intron-variant	ASAP2	GRCh38.p7	2:9365058	TGAGCACCAAAGCAT[A/G]TACTTACTTACATAT	8853
rs2715873	snp	A/G	0.00358779	0.0422022	intron-variant	ASAP2	GRCh38.p7	2:9366154	TCTATGGGCTGAAAC[A/G]TAAACTGGAACTTGG	8853
rs2715874	snp	C/T	0.21695	0.247806	intron-variant	ASAP2	GRCh38.p7	2:9367284	CCGATCCACCCGCCT[C/T]GGCCTCCCAAAGTGG	8853
rs2715875	snp	C/T	0.0471551	0.14613	intron-variant	ASAP2	GRCh38.p7	2:9368020	tTAGCTTTCCTGGCT[C/T]AGTGCCGCTTCACTC	8853
rs2715876	snp	G/T	0.0726307	0.176182	intron-variant	ASAP2	GRCh38.p7	2:9370640	GCATTGGGGGCATGA[G/T]CGGGATGATGGGGTC	8853
rs2715877	snp	C/T	0.193966	0.243639	intron-variant	ASAP2	GRCh38.p7	2:9370654	AGCGGGATGATGGGG[C/T]CAGACATGTGGTGCT	8853
rs2715878	snp	G/T	0.490836	0.0670685	intron-variant	ASAP2	GRCh38.p7	2:9375405	TAGAATAAACTAGGG[G/T]TTTTTCTTTTCAGTA	8853

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