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
rs8635	snp	A/G	0.456095	0.141508	utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	WWP1, RMDN1	GRCh38.p7	8:86467581	AATCCTTCCAATTTC[A/G]ATAATAAACTAAATA	11059
rs1865864	snp	C/T	0.105924	0.204309	intron-variant	WWP1	GRCh38.p7	8:86446845	CCATCACTTGGTGTG[C/T]GTGCTAAATAAATCT	11059
rs2917554	snp	C/G			intron-variant	WWP1	GRCh38.p7	8:86360474	TAGGTAACCCCAGGA[C/G]TAACAGTCTGGACAG	11059
rs2917558	snp	G/T			intron-variant	WWP1	GRCh38.p7	8:86433250	TTTTttttttttttg[G/T]taactacattcattc	11059
rs2953527	snp	A/G	0.00159617	0.0282053	intron-variant	WWP1	GRCh38.p7	8:86404725	TACCACCTATTTCAA[A/G]GAGTTACTGTGAGAG	11059
rs2953528	snp	C/T			intron-variant	WWP1	GRCh38.p7	8:86394983	GTTTCATGAGGTTTT[C/T]TTTACCCCAACCCCC	11059
rs2953529	snp	A/G	0.5	0	intron-variant	WWP1	GRCh38.p7	8:86364833	AGAAAGAAAGAAAGA[A/G]AGAGAGAGAGAGAGA	11059
rs3061697	in-del	-/AT	0	0	intron-variant	WWP1	GRCh38.p7	8:86397429	CTTATTAACATATCT[-/AT]CACCTCAAATACTTA	11059
rs3087641	snp	C/T	0.189576	0.242588	utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	WWP1, RMDN1	GRCh38.p7	8:86467868	ACACTAACAGAAAAT[C/T]ATTAGCCTTATATTA	11059
rs3916649	snp	A/G	0.281049	0.248064	intron-variant	WWP1	GRCh38.p7	8:86349863	GCCCATTTTCTGCAT[A/G]GGATGCTGTCTGTTC	11059
rs4332109	snp	A/G	0.0825414	0.185628	intron-variant	WWP1	GRCh38.p7	8:86373391	TTGTCTGCTTGACTT[A/G]TGATTAATTGGGATG	11059
rs4379426	snp	A/G	0.455858	0.141853	intron-variant	WWP1	GRCh38.p7	8:86400099	actttgggaggccga[A/G]gcgggcagatcatga	11059
rs4379427	snp	A/G	0.455858	0.141853	intron-variant	WWP1	GRCh38.p7	8:86400106	gaggccgaagcgggc[A/G]gatcatgaggtcagg	11059
rs4440616	snp	C/T	0.188316	0.242271	intron-variant	WWP1	GRCh38.p7	8:86429247	GAAGGATGCCCTCAC[C/T]ATGGCCTTCTGCCTA	11059
rs4443643	snp	C/T	0.106278	0.204558	intron-variant	WWP1	GRCh38.p7	8:86372356	GTAGAGACAGGTTTT[C/T]GCCGTGTTGGCCAGG	11059
rs4451291	snp	C/T	0.106278	0.204558	intron-variant	WWP1	GRCh38.p7	8:86372578	CCTTTCATATTTATG[C/T]CATTGGTCCATCTTG	11059
rs4490816	snp	C/T	0.455263	0.142713	intron-variant	WWP1	GRCh38.p7	8:86372709	tgcattgctacatct[C/T]ttatgtgggtttgtc	11059
rs4587306	snp	C/T	0.455263	0.142713	intron-variant	WWP1	GRCh38.p7	8:86373282	GTTTGTCACTCATGT[C/T]TCATGAATACCTGAG	11059
rs4961188	snp	C/T	0.455977	0.141681	intron-variant	WWP1	GRCh38.p7	8:86370804	TTCTTTTCTACTTAC[C/T]TGTTCTTTTTCTTAG	11059
rs4961189	snp	G/T	0.462909	0.131034	intron-variant	WWP1	GRCh38.p7	8:86370910	TTTCTCTGTTGCCCA[G/T]GCTGGAGTGCAGTGG	11059
rs4961190	snp	A/G	0.407674	0.194008	intron-variant	WWP1	GRCh38.p7	8:86402670	TTTTCCTAATAATTT[A/G]TAACTTTCTGGATTA	11059
rs4961191	snp	A/G	0.00557542	0.0525036	intron-variant	WWP1	GRCh38.p7	8:86440537	GGCCAGCCCCTTGTA[A/G]GAACCTTATTTTTCC	11059
rs5024450	snp	C/T	0.40853	0.193309	intron-variant	WWP1	GRCh38.p7	8:86352009	TGCTCTGTCAGAGTT[C/T]ATTTTTCTAGCTAGC	11059
rs6471295	snp	A/G	0.188316	0.242271	intron-variant	WWP1	GRCh38.p7	8:86362341	TCAGTATTTTTCAGG[A/G]AGAGAATGGAGGCCA	11059
rs6471296	snp	A/G	0.498034	0.0312882	intron-variant	WWP1	GRCh38.p7	8:86362425	GGAGAAAGTAGGTGT[A/G]AGGTGGCCACTGTTT	11059
rs6471309	snp	C/T	0.456095	0.141508	intron-variant	WWP1	GRCh38.p7	8:86375531	tctctcctcttaatc[C/T]cctaattcttgcata	11059
rs6471314	snp	A/G	0.455144	0.142885	intron-variant	WWP1	GRCh38.p7	8:86388230	TTAGGTAGAGTTTTA[A/G]TTTCATCAGTAGGTA	11059
rs6471315	snp	A/G	0.299664	0.245017	intron-variant	WWP1	GRCh38.p7	8:86389915	gggcggctgccgggc[A/G]gagacgctcctcact	11059
rs6471316	snp	C/G	0.455977	0.141681	intron-variant	WWP1	GRCh38.p7	8:86391358	TCTGTGTTCAGGTCA[C/G]TTGAACAACATTCCA	11059
rs6471317	snp	A/T	0.188	0.24219	intron-variant	WWP1	GRCh38.p7	8:86395366	CTGTGTTCAAATAAA[A/T]CTTTATTTATGAAAA	11059
rs6471345	snp	A/C	0.410568	0.191619	intron-variant	WWP1	GRCh38.p7	8:86445357	ctctctccctcccat[A/C]gtagtccccaggtgt	11059
rs6471349	snp	C/T	0.451732	0.147663	intron-variant	WWP1	GRCh38.p7	8:86457559	GATACACACACACAT[C/T]TAGATATAAATCTAT	11059
rs6471350	snp	A/G	0.00557542	0.0525036	intron-variant	WWP1	GRCh38.p7	8:86458973	AACTATGATACATCC[A/G]TTCTTTATAAGTCTA	11059
rs6471351	snp	C/T	0.451608	0.147832	intron-variant	WWP1	GRCh38.p7	8:86461088	tgctgggattacagg[C/T]gtgagccaccacgcc	11059
rs6981299	snp	A/G	0.451856	0.147493	intron-variant	WWP1	GRCh38.p7	8:86443220	tgagactacaggctc[A/G]caccaccatgccagc	11059
rs6988004	snp	C/T	0.00478085	0.0486577	intron-variant, nc-transcript-variant, upstream-variant-2KB	WWP1, LOC105375624	GRCh38.p7	8:86343358	ACCAAGGACTCCAGC[C/T]TTGGAACGTCTTTTT	11059
rs6988274	snp	C/T			intron-variant	WWP1	GRCh38.p7	8:86451175	ccagggaggtcaagg[C/T]tgcagtgaaccaggc	11059
rs6988382	snp	C/T	0.105924	0.204309	intron-variant	WWP1	GRCh38.p7	8:86408614	TTTTTAGTAATGTTT[C/T]TTAAAGTGTTTTCTT	11059
rs6988601	snp	A/C	0.410568	0.191619	intron-variant	WWP1	GRCh38.p7	8:86451366	TAGTGGCTATAGTGG[A/C]GCCTACAGTGATAGC	11059
rs6992287	snp	A/G	0.456095	0.141508	intron-variant	WWP1	GRCh38.p7	8:86406731	ACCAGTTCAATCCAG[A/G]TACAGAACTGTAGCA	11059
rs6992346	snp	C/T	0.0209421	0.100162	intron-variant	WWP1	GRCh38.p7	8:86461703	GTGCAACATGTTCTA[C/T]TATTTAAGCAGTTGT	11059
rs6992944	snp	G/T	0.456095	0.141508	intron-variant	WWP1	GRCh38.p7	8:86407079	AAGTAAGGCTTGGGA[G/T]ATGTTCATTCAGAAC	11059
rs6993497	snp	G/T	0.188	0.24219	intron-variant	WWP1	GRCh38.p7	8:86400247	tgaagcaggagaatt[G/T]cttgaacccgggagg	11059
rs6993612	snp	A/C	0.188316	0.242271	intron-variant	WWP1	GRCh38.p7	8:86372811	ACATTTATTTATCTT[A/C]GTGTTTTCTAAGAAG	11059
rs6994529	snp	C/T	0.455977	0.141681	intron-variant	WWP1	GRCh38.p7	8:86426995	GTGAAACCCCCATCT[C/T]TACTAAAAATACAAA	11059
rs6996052	snp	C/G	0.410568	0.191619	intron-variant	WWP1	GRCh38.p7	8:86417643	TAACTCAGGATAAAA[C/G]AGAAAAGGGCTTCAT	11059
rs7005799	snp	A/G	0.453697	0.14494	intron-variant	WWP1	GRCh38.p7	8:86389911	gacggggcggctgcc[A/G]ggcggagacgctcct	11059
rs7006017	snp	G/T	0.460702	0.134554	intron-variant	WWP1	GRCh38.p7	8:86399325	TTCCCTCAGACATCA[G/T]TCTACCATTTCAGAA	11059
rs7007855	snp	G/T	0.455977	0.141681	intron-variant	WWP1	GRCh38.p7	8:86417262	AGAGGGTGGAGCAGG[G/T]CAGGAGTCTCTTTTT	11059
rs7008034	snp	C/T	0.106278	0.204558	intron-variant	WWP1	GRCh38.p7	8:86377054	GACTCCAAGTTGTTG[C/T]TCCTTTTATTAGATT	11059
rs7009442	snp	C/T	0	0	intron-variant	WWP1	GRCh38.p7	8:86424921	TCTGTTTTCTGATAA[C/T]TTGGAATTCTGTAAG	11059
rs7011820	snp	C/T	0.00199481	0.0315187	intron-variant	WWP1	GRCh38.p7	8:86443219	ctgagactacaggct[C/T]acaccaccatgccag	11059
rs7012745	snp	A/T	0.121101	0.214208	intron-variant	WWP1	GRCh38.p7	8:86448132	TTTAAATAAAATTTT[A/T]CATTTTTCTTTGCAG	11059
rs7015160	snp	A/G	0.106278	0.204558	intron-variant	WWP1	GRCh38.p7	8:86376809	AAAGAATGATCATGG[A/G]CCTGTGCTAAATGGC	11059
rs7015490	snp	A/G	0.411746	0.190626	upstream-variant-2KB, intron-variant	WWP1, LOC105375624	GRCh38.p7	8:86342081	ATTGTGCGGACACGT[A/G]TACTCGGTCAATAAG	11059
rs7015772	snp	A/G	0.187053	0.241946	intron-variant	WWP1	GRCh38.p7	8:86369942	TTGAGTGTACCAGAT[A/G]ATATGTAACATATGC	11059
rs7017706	snp	C/T	0.451252	0.148316	utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	RMDN1, WWP1	GRCh38.p7	8:86468661	TCAGGGTGCTGGTCT[C/T]CCTCAAGTAAGAAAT	11059
rs7017716	snp	G/T	0.456095	0.141508	intron-variant	WWP1	GRCh38.p7	8:86416772	GGTAATTTGCACCTA[G/T]TTGAGGGGTGTTCAT	11059
rs7018101	snp	A/G	0.106278	0.204558	intron-variant	WWP1	GRCh38.p7	8:86447120	tgaaatacaactgtc[A/G]gtcatagagcagtca	11059
rs7460342	snp	C/T	0.456214	0.141336	intron-variant	WWP1	GRCh38.p7	8:86462908	agaaaaaggcaagtt[C/T]gttgaagttctttat	11059
rs7460650	snp	A/G	0.442579	0.159415	intron-variant	WWP1	GRCh38.p7	8:86461856	TACATGGTAAGTTCA[A/G]GAATCCTAAATACGA	11059
rs7461413	snp	C/G	0.455977	0.141681	intron-variant	WWP1	GRCh38.p7	8:86458749	GTTATAGTACACTTT[C/G]CAAAAGTTGCATCTT	11059
rs7461668	snp	A/G	0.455977	0.141681	intron-variant	WWP1	GRCh38.p7	8:86463401	aacctctgcctccca[A/G]gttcaagcgattctc	11059
rs7461904	snp	C/T	0.274393	0.248807	intron-variant	WWP1	GRCh38.p7	8:86440089	atattgcatctatta[C/T]gagtttatctcaatt	11059
rs7462792	snp	A/T	0.107694	0.205546	intron-variant	WWP1	GRCh38.p7	8:86421834	tctcaaaaaaaaaaa[A/T]TTTTTTTTGAAAATA	11059
rs7464360	snp	C/G	0.254944	0.249951	intron-variant	WWP1	GRCh38.p7	8:86457733	CATGGGTAAAATAAA[C/G]TACCAGAGAATCCTT	11059
rs7812422	snp	C/G	0.245346	0.249957	intron-variant	WWP1	GRCh38.p7	8:86387241	CTTCCATTAGCAGTG[C/G]TCCTGTGTATTAGGC	11059
rs7815082	snp	C/T	0.00914312	0.0669923	intron-variant, upstream-variant-2KB	WWP1	GRCh38.p7	8:86367043	ATTGAGTTTTAAATT[C/T]GGTGCTTGATAAAAT	11059
rs7816275	snp	A/G	0.456095	0.141508	intron-variant	WWP1	GRCh38.p7	8:86361175	GAAGAGTGGGGCAGG[A/G]AGACCATTTAGCAAG	11059
rs7818436	snp	A/G	0.18989	0.242666	intron-variant	WWP1	GRCh38.p7	8:86466022	ACATGGGAAAATGAA[A/G]GTACAGAAGGGTTCT	11059
rs7819020	snp	C/T	0.0209421	0.100162	intron-variant	WWP1	GRCh38.p7	8:86363012	CATTTATATAGTACT[C/T]GATAATTCATAAAGT	11059
rs7819454	snp	A/G	0.40853	0.193309	intron-variant, upstream-variant-2KB	WWP1, LOC105375624	GRCh38.p7	8:86344120	TAGTAAATTAGCTGC[A/G]ACTAGAAATGATCAT	11059
rs7822494	snp	C/T	0.495174	0.0488838	intron-variant	WWP1	GRCh38.p7	8:86464210	taatatccataatta[C/T]ctgacaagatgagta	11059
rs7825890	snp	A/G	0.0839998	0.186933	intron-variant	WWP1	GRCh38.p7	8:86450914	ATTATGTATTAGACT[A/G]TGTCTTAAAAGATGC	11059
rs7830128	snp	A/G	0.4628	0.13121	intron-variant	WWP1	GRCh38.p7	8:86361011	GATAAAGAGGAGAAG[A/G]AAGAGGTGGGGCAAC	11059
rs7830480	snp	C/T	0.455977	0.141681	intron-variant	WWP1	GRCh38.p7	8:86390908	GTTAAGGCTCCCTAT[C/T]GTTTTCTCGTATATT	11059
rs7832493	snp	A/C	0.456095	0.141508	intron-variant	WWP1	GRCh38.p7	8:86359304	TCTGGAACCTATGCT[A/C]TAAACAACTCTAACA	11059
rs7833049	snp	C/T	0.45574	0.142025	intron-variant	WWP1	GRCh38.p7	8:86433669	ttgaaatcaccttgt[C/T]atggtggctcacgcc	11059
rs7833543	snp	A/G	0.0832709	0.186283	intron-variant	WWP1	GRCh38.p7	8:86346766	GCATTGGAAAATCCA[A/G]TAAATTGCCCTTTAT	11059
rs7835743	snp	A/G	0.390464	0.206809	intron-variant	WWP1	GRCh38.p7	8:86365089	TTAGAGAGTAAGAGA[A/G]AACAGAACCAAAAGG	11059
rs7837581	snp	A/G	0.185788	0.241613	intron-variant	WWP1	GRCh38.p7	8:86353186	AAAGGTTTGAATTTT[A/G]AATTAATGAAAGAAA	11059
rs7837618	snp	A/C	0.188	0.24219	intron-variant	WWP1	GRCh38.p7	8:86353245	TGTTATTTAGGGCCA[A/C]AGTGATGACACCTAC	11059
rs7839096	snp	A/G	0.188316	0.242271	intron-variant	WWP1	GRCh38.p7	8:86348323	tcctgggttcaagag[A/G]ttctcctgcctcagc	11059
rs7839610	snp	A/T	0.25045	0.25	intron-variant	WWP1	GRCh38.p7	8:86376273	GAGTTCTTAGGTAAA[A/T]TAAGAAAAAACTAgg	11059
rs7841007	snp	A/T	0.245061	0.249951	intron-variant	WWP1	GRCh38.p7	8:86394133	actcagcaatagata[A/T]TACATTGTTTGAGCA	11059
rs7841690	snp	C/T	0.456095	0.141508	intron-variant	WWP1	GRCh38.p7	8:86353130	CTTATAGGGAAAAGC[C/T]TTTGCTTAGGGTAAG	11059
rs7841939	snp	A/G	0.281049	0.248064	intron-variant	WWP1	GRCh38.p7	8:86358546	gagtgcagtggtgcc[A/G]tcacaactcaccact	11059
rs7842042	snp	C/T	0.455977	0.141681	intron-variant	WWP1	GRCh38.p7	8:86460970	gcccgacaccacgcc[C/T]ggctaattttttgta	11059
rs7842293	snp	G/T	0.0941369	0.195465	intron-variant	WWP1	GRCh38.p7	8:86351522	tttttttttttttta[G/T]tagagatgttgccca	11059
rs7843266	snp	A/G	0.030278	0.119257	intron-variant	WWP1	GRCh38.p7	8:86348839	aacagccctaaacca[A/G]gtgacttaaaacaac	11059
rs7843272	snp	C/T	0.188	0.24219	intron-variant	WWP1	GRCh38.p7	8:86348235	ttttctttttttttt[C/T]gagacggagtttccc	11059
rs7843399	snp	A/G	0.18989	0.242666	intron-variant	WWP1	GRCh38.p7	8:86412639	TGAAACTGCACTTCT[A/G]GATGTCTCTACACTA	11059
rs7843434	snp	C/T	0.0174175	0.0916809	intron-variant, upstream-variant-2KB	WWP1	GRCh38.p7	8:86368148	attgagtctttactt[C/T]gtgtcatatactcta	11059
rs7844592	snp	A/G	0.00159617	0.0282053	intron-variant	WWP1	GRCh38.p7	8:86398866	aaagtatacatttta[A/G]tcgtttttaatatat	11059
rs7846090	snp	A/T	0.455977	0.141681	intron-variant	WWP1	GRCh38.p7	8:86455495	gggtacaatgttaat[A/T]ctttaaaaatcaatc	11059
rs7846468	snp	A/C	0.269538	0.249235	intron-variant, upstream-variant-2KB	WWP1, LOC105375624	GRCh38.p7	8:86343795	ATTTGATAAGTTTAA[A/C]AAATTTTTTTCTGTG	11059
rs9297913	snp	C/T	0.18989	0.242666	intron-variant	WWP1	GRCh38.p7	8:86466317	AGACAAAGAAACATA[C/T]ATATTTGTTAATTGA	11059
rs9642913	snp	A/G	0.4628	0.13121	intron-variant	WWP1	GRCh38.p7	8:86377719	AAGTGTATTATCTTC[A/G]ATATTTTAGATTTTA	11059
rs9656826	snp	A/T	0.255224	0.249945	intron-variant	WWP1	GRCh38.p7	8:86430524	ttaagtaatcctccc[A/T]ccttgccctcccaag	11059
rs9656828	snp	A/G	0.299664	0.245017	intron-variant	WWP1	GRCh38.p7	8:86443504	tatttatttatttac[A/G]tatttatttaCACTT	11059

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