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
rs9886	snp	C/G	0.264084	0.249603	utr-variant-3-prime, downstream-variant-500B	INPPL1, PHOX2A	GRCh38.p7	11:72238621	CTCTGGTGCTGTCCT[C/G]TTTTACTGGACCCCG	3636
rs655423	snp	C/G	0	0	splice-donor-variant	INPPL1	GRCh38.p7	11:72234616	CGCCAGCTGCCCACG[C/G]TGAGGCTGTGGGCAG	3636
rs655513	snp	G/T	0	0	intron-variant	INPPL1	GRCh38.p7	11:72234677	GGGGTACATAAGAGT[G/T]TATTGGAGAGCCTGC	3636
rs714548	snp	A/G	0.0523653	0.153103	intron-variant	INPPL1	GRCh38.p7	11:72233198	TCATCGCAGGCCTGC[A/G]GTCCCCCAAGGCCCA	3636
rs1006488	snp	C/T	0.0166325	0.0896639	intron-variant	INPPL1	GRCh38.p7	11:72233623	GGTGGGAATATTCCC[C/T]CTGAGTCCCCATTCC	3636
rs1049472	snp	C/G	0.0444215	0.142258	missense	INPPL1	GRCh38.p7	11:72237585	TCCTGGGGGAAGTGG[C/G]CAGTGGGGATGACCG	3636
rs1801031	snp	A/C			synonymous-codon	INPPL1	GRCh38.p7	11:72228425	CCAGCCCAACCAGGG[A/C]CTTGTGTGCGCCCTG	3636
rs2276046	snp	A/G	0.169583	0.236713	intron-variant	INPPL1	GRCh38.p7	11:72235289	CACACTCCCCTGAGG[A/G]GCAGATGGGACAAAC	3636
rs2276047	snp	C/T	0.408986	0.192934	intron-variant	INPPL1	GRCh38.p7	11:72230337	GGAGGACCGGTCACA[C/T]GGGCCTGTGCCCCTA	3636
rs2276048	snp	C/T	0.37518	0.216402	synonymous-codon	INPPL1	GRCh38.p7	11:72230168	CAGCGTGAACTTCTG[C/T]GACTTCCCAATCTTG	3636
rs3210036	snp	C/T	0.030527	0.119715	utr-variant-3-prime, downstream-variant-500B	INPPL1, PHOX2A	GRCh38.p7	11:72238908	GGGGTGGGGCAGGAT[C/T]TCACCCATAAAGTGC	3636
rs3210037	snp	C/G			utr-variant-3-prime, downstream-variant-500B	INPPL1, PHOX2A	GRCh38.p7	11:72238912	TGGGGCAGGATTTCA[C/G]CCATAAAGTGCCAGT	3636
rs3216093	in-del	-/C			intron-variant	INPPL1	GRCh38.p7	11:72235044	CCTACGCGCTGCCCC[-/C]TGACACCACTCAATC	3636
rs4329713	snp	C/T	0.343701	0.231776	upstream-variant-2KB	INPPL1	GRCh38.p7	11:72223659	AGGCCCGGTGCCGAG[C/T]GCGGTACGAGCTCGG	3636
rs10751199	snp	A/G	0.487495	0.0780784	intron-variant	INPPL1	GRCh38.p7	11:72236778	GACTGTGGGTGCCTC[A/G]AGAGGCTTTCCAAAC	3636
rs11235470	snp	C/T	0.00716266	0.059414	downstream-variant-500B, upstream-variant-2KB	FOLR2, INPPL1	GRCh38.p7	11:72222179	ACAGGAGCTGTTGCC[C/T]AGAAAGCCCGTGAGC	3636
rs11235471	snp	C/T	0.00716266	0.059414	intron-variant	INPPL1	GRCh38.p7	11:72227041	ACGTGGGCGATCAGA[C/T]GTGGGCAATATCTTA	3636
rs11235472	snp	C/G	0.314787	0.241459	intron-variant	INPPL1	GRCh38.p7	11:72238020	GGCACTCAGCTCCCC[C/G]TGACATGCCCTGTTT	3636
rs11548491	snp	C/G	0.179731	0.239922	missense	INPPL1	GRCh38.p7	11:72237492	GGGGCCGTGGTGGGG[C/G]TGAGGCCCGTGGCCC	3636
rs11548492	snp	C/G			utr-variant-3-prime, downstream-variant-500B	INPPL1, PHOX2A	GRCh38.p7	11:72238902	TTGGTTGGGGTGGGG[C/G]AGGATCTCAGCCATA	3636
rs12280967	snp	G/T	0.00716266	0.059414	upstream-variant-2KB	INPPL1	GRCh38.p7	11:72223374	GGGCTCCGCCCCCTT[G/T]GCGGCTGCCGCGTCC	3636
rs12288631	snp	C/T	0.349233	0.229462	intron-variant	INPPL1	GRCh38.p7	11:72227802	CACGTTGCCCGTGTG[C/T]GCAAATGGGCTAACC	3636
rs12361913	snp	C/T	0.359311	0.224836	intron-variant	INPPL1	GRCh38.p7	11:72230768	TCCTGGATGCCTACC[C/T]GCCCCTGAGTGGCTG	3636
rs12417459	snp	A/G	0.0704125	0.17392	intron-variant	INPPL1	GRCh38.p7	11:72236225	TTAAAAATGGAATGC[A/G]AAATTGTTTCTAAGA	3636
rs12795135	snp	C/T	0.0165985	0.0895754	intron-variant	INPPL1	GRCh38.p7	11:72229605	TTCGTGTTCTGGAGC[C/T]GGGTGGGAGGCTCTG	3636
rs17162083	snp	A/G	0.00478085	0.0486577	intron-variant	INPPL1	GRCh38.p7	11:72230731	GAGCCAACTGGCAGG[A/G]TATCCCTGTGGACGG	3636
rs17162091	snp	C/T	0.0468649	0.145726	synonymous-codon	INPPL1	GRCh38.p7	11:72231060	GGGGAAGACCCTGGA[C/T]GAGGTCACAGTGACC	3636
rs17847213	snp	G/T	0	0	intron-variant	INPPL1	GRCh38.p7	11:72238205	GGCCCCGGGGGCGGA[G/T]CTGGGGCCCTCAGGA	3636
rs17847214	snp	A/G	0.000270925	0.0116357	missense	INPPL1	GRCh38.p7	11:72229205	CTCACCCGTACCCTC[A/G]CTACCTCATGCCGGA	3636
rs17847215	snp	C/G	0.0194172	0.0966001	missense	INPPL1	GRCh38.p7	11:72229989	GCCATCCACACGTAA[C/G]GCCAAGACCATCCCC	3636
rs17847219	snp	A/C	0.0487262	0.148286	intron-variant	INPPL1	GRCh38.p7	11:72231216	TCATCTTGTCCAGGA[A/C]CCTGTCCTCACACAC	3636
rs17847220	snp	A/C	0.00119737	0.0244387	intron-variant	INPPL1	GRCh38.p7	11:72231926	CTCCTGATTTTCGGT[A/C]TGGTGCTCTCCCAGG	3636
rs17847221	snp	G/T	0.0517044	0.152246	intron-variant	INPPL1	GRCh38.p7	11:72228551	CCCTTGGCTCTACCT[G/T]CCTCTTCCCATCCCC	3636
rs17847222	snp	A/C	0.00016515	0.00908558	missense	INPPL1	GRCh38.p7	11:72237230	GGGGTCCCGCACCAG[A/C]TGCTGCCCCCGGAGC	3636
rs34620751	in-del	-/C			utr-variant-3-prime, downstream-variant-500B, upstream-variant-2KB	FOLR2, INPPL1	GRCh38.p7	11:72221947	TGTTTTCTAATAATT[-/C]CCATGTCTGTGGAAT	3636
rs34634942	in-del	-/G			frameshift-variant, intron-variant	INPPL1	GRCh38.p7	11:72238071	GGCGGGCGGGCCAGC[-/G]GGGCTGGGCGAGGCA	3636
rs35233954	snp	G/T	0	0	upstream-variant-2KB, intron-variant	INPPL1	GRCh38.p7	11:72224652	GGCACCGTCCCCGCA[G/T]GAGGAGCTGGGGGCA	3636
rs35322067	snp	A/T	0.5	0	intron-variant	INPPL1	GRCh38.p7	11:72234734	GAGAGAGAGAGAGAG[A/T]GTGTGTGTGTGTGTG	3636
rs35437876	snp	C/T	0.0121596	0.0770191	intron-variant	INPPL1	GRCh38.p7	11:72237108	CCTGGCTTAGTCGTT[C/T]TGCTTCCACACCCAG	3636
rs35524893	in-del	-/C			frameshift-variant	INPPL1	GRCh38.p7	11:72233723	AGGTTGGAGTTACCT[-/C]CCCAGTTCATCTCCA	3636
rs35752296	in-del	-/G			intron-variant	INPPL1	GRCh38.p7	11:72236559	AACTATTAACGTTCT[-/G]GGGGAATTAGTGCTC	3636
rs35874549	in-del	-/G			intron-variant	INPPL1	GRCh38.p7	11:72234733	AGAGAGAGAGAGAGA[-/G]TGTGTGTGTGTGTGT	3636
rs35908322	in-del	-/G			intron-variant	INPPL1	GRCh38.p7	11:72232586	TCTGGCCCTGACCCT[-/G]GGGGATCTACCCCTC	3636
rs41298113	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B	INPPL1, PHOX2A	GRCh38.p7	11:72238592	GTTGCCATGGTTACC[A/G]AGGACCCTGGTTACT	3636
rs45506896	snp	A/G	0.0517204	0.152267	intron-variant	INPPL1	GRCh38.p7	11:72229589	ACCTCTGGGAGGTGC[A/G]TTCGTGTTCTGGAGC	3636
rs56353029	snp	C/G	0.0381591	0.132753	intron-variant	INPPL1	GRCh38.p7	11:72228861	AGGTGAGACCCCCAT[C/G]CCATCCACTGAACAG	3636
rs56787483	snp	A/C	0.000399281	0.0141238	downstream-variant-500B, utr-variant-3-prime	INPPL1, PHOX2A	GRCh38.p7	11:72239366	TTTCCTGATCACCAG[A/C]GTAAGGGGTGACCCA	3636
rs57191897	snp	A/C	0.134119	0.221521	upstream-variant-2KB, intron-variant	INPPL1	GRCh38.p7	11:72224396	TGCAGCCAAGCTGTA[A/C]GGGGGACGAGAGGAA	3636
rs57578058	snp	A/T			intron-variant	INPPL1	GRCh38.p7	11:72234736	GAGAGAGAGAGAGTG[A/T]GTGTGTGTGTGTGTG	3636
rs58062215	snp	A/C			upstream-variant-2KB, intron-variant	INPPL1	GRCh38.p7	11:72224521	CCGAAGTGTCGGGGC[A/C]AGGATGGGGGGACTC	3636
rs61729392	snp	A/C	0.117188	0.211804	missense	INPPL1	GRCh38.p7	11:72235144	TGGCTGATATCGAGT[A/C]CCTGCAGGACCAGCA	3636
rs61731648	snp	A/C	0.0688775	0.172321	missense	INPPL1	GRCh38.p7	11:72234530	CCCCCACCCCAGAAT[A/C]CAAGAAGAGCTTTGA	3636
rs61735633	snp	A/G	0.0253123	0.109615	synonymous-codon	INPPL1	GRCh38.p7	11:72228830	TCCTGAGACTCCCAC[A/G]GCTCCAGCTGCTGAG	3636
rs61736300	snp	G/T	0.0407986	0.136875	missense	INPPL1	GRCh38.p7	11:72229710	GAGCCTGGTGCTGAA[G/T]CTGTCAGTGCTAAAG	3636
rs61736312	snp	A/G	0.178793	0.239645	synonymous-codon	INPPL1	GRCh38.p7	11:72234288	CTCCTCAGGGCTCTC[A/G]AAGACTTCAGACCAG	3636
rs61749194	snp	A/C	0.0465407	0.145281	synonymous-codon	INPPL1	GRCh38.p7	11:72232916	AGAGTTTGAGCCCCT[A/C]CTCAGGGTGGACCAG	3636
rs61749195	snp	A/C	0.046474	0.14518	missense	INPPL1	GRCh38.p7	11:72232917	GAGTTTGAGCCCCTC[A/C]TCAGGGTGGACCAGC	3636
rs62625974	snp	A/G			utr-variant-3-prime, downstream-variant-500B	INPPL1, PHOX2A	GRCh38.p7	11:72238662	CCAGGGGTGCCTGTG[A/G]GGGTCCATTTGGGTA	3636
rs70940819	snp	C/T	0.000424892	0.0145693	missense	INPPL1	GRCh38.p7	11:72235868	AGCCGCAAGCCAGCC[C/T]TCACAGAGGCCTCCT	3636
rs70940820	snp	A/T	0.00279162	0.0372561	intron-variant	INPPL1	GRCh38.p7	11:72236074	TCAGGGTTGGCCTGG[A/T]GATCATCAGCTGCTT	3636
rs70940821	snp	A/G	0.000165656	0.00909949	missense	INPPL1	GRCh38.p7	11:72237189	CCAAGAACAGCTTCA[A/G]TAACCCTGCCTACTA	3636
rs70940822	snp	C/T	0.00249463	0.0352292	intron-variant	INPPL1	GRCh38.p7	11:72238189	AGGTGGGGGAGGGGC[C/T]GGCCCCGGGGGCGGA	3636
rs70940823	snp	C/T	0.00795532	0.062565	utr-variant-3-prime, downstream-variant-500B	INPPL1, PHOX2A	GRCh38.p7	11:72238680	GTCCATTTGGGTACG[C/T]CTGGGCCCCCACTTT	3636
rs70940824	snp	G/T	0.242314	0.250171	utr-variant-3-prime, downstream-variant-500B	INPPL1, PHOX2A	GRCh38.p7	11:72238968	TCTGTGCTGCCCTGC[G/T]CTGGGGATGCACGGC	3636
rs70940825	snp	C/T	0.130694	0.219696	intron-variant	INPPL1	GRCh38.p7	11:72230643	GAGGGTGGATAACAT[C/T]TGCCAGCACTGTTAT	3636
rs70940826	snp	A/C/G	0.000115748	0.00760671	intron-variant	INPPL1	GRCh38.p7	11:72230910	ATGGGTCAGGCCCGG[A/C/G]CTGGGGCTGGGGCGG	3636
rs70940827	snp	A/G	0.0768	0.180282	upstream-variant-2KB, intron-variant	INPPL1	GRCh38.p7	11:72224558	CGATGGGGATTTGGG[A/G]ACTGGATCTCCTCGG	3636
rs70940828	snp	C/G	0.0767999	0.180282	intron-variant	INPPL1	GRCh38.p7	11:72232558	ACTTCTTCCCTTTAT[C/G]CCTATCCCTGACTTC	3636
rs70940829	snp	A/C	0.0392	0.1344	intron-variant	INPPL1	GRCh38.p7	11:72233177	GGGTGAGCCAAGAAA[A/C]CGGCATGGGCCTTGG	3636
rs70940830	in-del	-/AAGT	0.0392	0.1344	utr-variant-3-prime	INPPL1, PHOX2A	GRCh38.p7	11:72239092	TGTCTTCAATAAATT[-/AAGT]TTTATTTGGATTGAG	3636
rs71477718	snp	C/T	0.5	0	intron-variant	INPPL1	GRCh38.p7	11:72231237	CCTCACACACCACCT[C/T]CAAACTAGCCTACTT	3636
rs71477719	snp	C/T	3.31928e-05	0.00407373	intron-variant	INPPL1	GRCh38.p7	11:72232601	TGGGGATCTACCCCT[C/T]CCCACCACGCACCCC	3636
rs71726140	in-del	-/GAAG	0.0279526	0.114869	utr-variant-3-prime, downstream-variant-500B	INPPL1, PHOX2A	GRCh38.p7	11:72238800	TGTCCGTCCGGAAAT[-/GAAG]GAATAGCCCGAGGAC	3636
rs72968867	snp	C/T			intron-variant	INPPL1	GRCh38.p7	11:72233273	CCAGCCTCCATGGCC[C/T]CTCTGAGGCCTTTGG	3636
rs73528804	snp	C/G	0.0872718	0.189788	intron-variant	INPPL1	GRCh38.p7	11:72227730	GTGCCCTAGACATAC[C/G]CGACTCCAGCAGAGC	3636
rs73528809	snp	A/G	0.00159617	0.0282053	intron-variant	INPPL1	GRCh38.p7	11:72229857	TTGGCCCCAAGGTCA[A/G]TTGTGTCCCTCCCTG	3636
rs73545661	snp	A/G	0.0260105	0.111035	intron-variant	INPPL1	GRCh38.p7	11:72226556	CGGGGATACTGCTAA[A/G]CATTCTACAGTGCAC	3636
rs74374875	snp	A/G	0.5	0	intron-variant	INPPL1	GRCh38.p7	11:72230324	GGAGCCCCTGGCCTA[A/G]GGGCACAGGCCCATG	3636
rs74635729	snp	A/G	0.127254	0.217792	upstream-variant-2KB	INPPL1	GRCh38.p7	11:72223408	TTCCGCCCTCGGCTG[A/G]AGGGGAGGAAGCTAG	3636
rs75144009	snp	C/T	0.00755907	0.0610114	intron-variant	INPPL1	GRCh38.p7	11:72229294	TCCTCACCTGCTTCC[C/T]GGCTGCACAGGTGCC	3636
rs76160915	snp	C/T	0.00557542	0.0525036	utr-variant-3-prime, downstream-variant-500B	INPPL1, PHOX2A	GRCh38.p7	11:72238656	CCAGCCCCAGGGGTG[C/T]CTGTGGGGGTCCATT	3636
rs76170479	snp	C/G	0.000399281	0.0141238	intron-variant	INPPL1	GRCh38.p7	11:72225284	CCAGACCCGCCTCCA[C/G]CCCCCAGAGTGGGAG	3636
rs76870980	snp	G/T	0.137867	0.223442	upstream-variant-2KB, utr-variant-5-prime, intron-variant	INPPL1	GRCh38.p7	11:72224157	AGAGGCTCGAGAACG[G/T]CGCACCTCGTCTGGG	3636
rs77348083	snp	A/C	0.133435	0.221162	upstream-variant-2KB	INPPL1	GRCh38.p7	11:72222947	GGTGGCTGATGAGAA[A/C]GGTGGCACAGATTGT	3636
rs77490552	snp	C/G	0.0138799	0.0821421	intron-variant	INPPL1	GRCh38.p7	11:72230652	TAACATTTGCCAGCA[C/G]TGTTATATGCTTGAG	3636
rs77987571	snp	G/T	0.0685596	0.171987	intron-variant, synonymous-codon	INPPL1	GRCh38.p7	11:72225532	TCCCGTTTGGATAGG[G/T]ACTGAGTGGTGAGCA	3636
rs78176749	snp	G/T	0.02016	0.0983543	upstream-variant-2KB	INPPL1	GRCh38.p7	11:72223403	CCCCCTTCCGCCCTC[G/T]GCTGGAGGGGAGGAA	3636
rs79023399	snp	C/T	0.0410537	0.137264	intron-variant	INPPL1	GRCh38.p7	11:72234101	GGTTGTCTCTTTGCT[C/T]TGGTCCAGGGTCTGG	3636
rs79054886	snp	A/G	0.133777	0.221342	upstream-variant-2KB, utr-variant-5-prime, intron-variant	INPPL1	GRCh38.p7	11:72224150	CTGCGTGAGAGGCTC[A/G]AGAACGTCGCACCTC	3636
rs79304956	snp	A/G	0.031825	0.122064	intron-variant	INPPL1	GRCh38.p7	11:72226839	GTCAGCTGTTGAGTG[A/G]GAGGGGGACAGCTGG	3636
rs80156982	snp	C/T	0.000399281	0.0141238	synonymous-codon	INPPL1	GRCh38.p7	11:72229705	CTAGAGAGCCTGGTG[C/T]TGAAGCTGTCAGTGC	3636
rs80340347	snp	C/T	0.0142736	0.0832652	downstream-variant-500B, utr-variant-3-prime	INPPL1, PHOX2A	GRCh38.p7	11:72239346	CGAGGGGTGGGGCAG[C/T]GGGCTTTCCTGATCA	3636
rs80351327	snp	C/T	0.5	0	intron-variant	INPPL1	GRCh38.p7	11:72226651	CTCTAGCCTAGGCAA[C/T]TGACCCAACAAGGAA	3636
rs111332650	snp	C/T	0.5	0	intron-variant	INPPL1	GRCh38.p7	11:72230056	CAGGGCCAAGGGTGG[C/T]TGGAGGTGACCAGGG	3636
rs111670945	snp	C/G	0.5	0	intron-variant	INPPL1	GRCh38.p7	11:72230670	TTATATGCTTGAGCA[C/G]TGGGTATGCAGTGGA	3636
rs111718440	snp	A/C/T	0	0	splice-acceptor-variant	INPPL1	GRCh38.p7	11:72231496	ATGCACTCTCTACCC[A/C/T]GATTGCCATGCAATC	3636
rs112117090	snp	C/G			utr-variant-3-prime, downstream-variant-500B	INPPL1, PHOX2A	GRCh38.p7	11:72238823	AGCCCGAGGACCGGG[C/G]TGGGGTTTATTTAAA	3636
rs112327379	snp	C/T	0.5	0	missense	INPPL1	GRCh38.p7	11:72232924	AGCCCCTCCTCAGGG[C/T]GGACCAGCTCAACCT	3636
rs112721877	snp	C/T	1.64795e-05	0.00287045	synonymous-codon	INPPL1	GRCh38.p7	11:72233470	GCCCTCATGGTGTGA[C/T]CGGATTCTGTGGAAA	3636
rs112903949	in-del	-/GT	0.5	0	intron-variant	INPPL1	GRCh38.p7	11:72234752	TGTGTGTGTGTGTGT[-/GT]GTGTGTGTGTGTATG	3636

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