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
rs479929	snp	G/T	0	0	utr-variant-3-prime	RNF165	GRCh38.p7	18:46460592	CCTATTACCTCATTT[G/T]GGCGTTGTTTCTGGG	494470
rs480879	snp	A/C	0	0	utr-variant-3-prime	RNF165	GRCh38.p7	18:46460707	TTTCGTCCGAACTAT[A/C]AGGGTGTGTGATTGC	494470
rs494056	snp	G/T			intron-variant	RNF165	GRCh38.p7	18:46448061	CACCGAAAAGTCAGG[G/T]TATAGGAGGTTGAGA	494470
rs494117	snp	G/T			intron-variant	RNF165	GRCh38.p7	18:46448040	GAGGTTGAGAACACA[G/T]GGGAGCTACGTCATA	494470
rs498358	snp	A/C			intron-variant	RNF165	GRCh38.p7	18:46442307	caaagtcatgatcta[A/C]atttccgccttaaga	494470
rs503368	snp	G/T			intron-variant	RNF165	GRCh38.p7	18:46448292	GGAGCCAGGACACAA[G/T]AAGGCCAGGGCACAA	494470
rs503402	snp	G/T			intron-variant	RNF165	GRCh38.p7	18:46448284	GACACAATAAGGCCA[G/T]GGCACAAGAAGGCCA	494470
rs512934	snp	A/T			intron-variant	RNF165	GRCh38.p7	18:46443316	aaaataaaataagat[A/T]aaataaagtggtatg	494470
rs513845	snp	A/C			intron-variant	RNF165	GRCh38.p7	18:46443233	caaaaaacagacaca[A/C]attttaaaagaaaaa	494470
rs513874	snp	A/G			intron-variant	RNF165	GRCh38.p7	18:46443219	aaattttaaaagaaa[A/G]acaacaaaatgacaa	494470
rs516205	snp	C/G			downstream-variant-500B	RNF165	GRCh38.p7	18:46461431	gggcagatcacttga[C/G]atcaggagtttgaga	494470
rs525531	snp	C/G	0	0	intron-variant	RNF165	GRCh38.p7	18:46450994	TGAGAGGCCTTCCAT[C/G]TTCCCTCCTGGCCAC	494470
rs530304	snp	A/G			intron-variant	RNF165	GRCh38.p7	18:46443222	cacaaattttaaaag[A/G]aaaacaacaaaatga	494470
rs534006	snp	C/T	0	0	intron-variant	RNF165	GRCh38.p7	18:46453074	TTGACACCACCAGCA[C/T]ATGGGTTAGGGAAAA	494470
rs535750	snp	G/T	0	0	intron-variant	RNF165	GRCh38.p7	18:46445678	tctccctgctcatgg[G/T]ctggaatgtgccttc	494470
rs564978	snp	C/G			intron-variant	RNF165	GRCh38.p7	18:46441768	cccgagtagctggga[C/G]tacaggcgcccgcca	494470
rs580082	snp	G/T	0	0	intron-variant	RNF165	GRCh38.p7	18:46443075	acagagattgtcaac[G/T]gcaaaacaattgcca	494470
rs693140	snp	C/G			intron-variant	RNF165	GRCh38.p7	18:46442662	tataaatgtctctta[C/G]atcaagttagtcgac	494470
rs747575	snp	C/G	0.431769	0.17164	intron-variant	RNF165	GRCh38.p7	18:46345361	CAGGTTGTCATCTGG[C/G]CTTCTCTCCCACCTC	494470
rs753463	snp	A/T	0.484771	0.0859212	intron-variant	RNF165	GRCh38.p7	18:46438205	TGTGGGATATTCCTG[A/T]GACCCCTTTAGACAC	494470
rs753464	snp	A/G	0.124144	0.21601	intron-variant	RNF165	GRCh38.p7	18:46438296	GCTAATTTCTCTTTG[A/G]GTCAGGTCCTGGTCA	494470
rs920781	snp	G/T	0.448066	0.152544	intron-variant	RNF165	GRCh38.p7	18:46340784	AGGTGCCTAGGATGT[G/T]CTAGACAGTTGCCCC	494470
rs948596	snp	A/T	0.450231	0.149691	intron-variant	RNF165	GRCh38.p7	18:46346484	TCGGCCCCCAAGAAG[A/T]CCCAGCAAACACAGC	494470
rs1197784	snp	C/T	0	0	intron-variant	RNF165	GRCh38.p7	18:46446701	TTTCTTTTTTTTTTT[C/T]ttttccttttttttt	494470
rs1197949	snp	G/T			intron-variant	RNF165	GRCh38.p7	18:46439857	gcgacagagcgagac[G/T]ccgtctcaaaaaaac	494470
rs1206885	snp	A/G			intron-variant	RNF165	GRCh38.p7	18:46451773	ctgttgtccaggcta[A/G]aatgcagtggtgcaa	494470
rs1376080	snp	A/G	0.429688	0.173817	intron-variant	RNF165	GRCh38.p7	18:46450081	ATTAATAAAGTGACA[A/G]CTAACCTTCAtggca	494470
rs1470324	snp	A/G	0.499683	0.0125759	intron-variant	RNF165	GRCh38.p7	18:46378210	AGCAAGTTTGAGGTC[A/G]TGGTGTCCAAAAGCA	494470
rs1580009	snp	A/C	0.494855	0.0504572	intron-variant	RNF165	GRCh38.p7	18:46449691	agaatgagtgccaag[A/C]gaatggggaggtccc	494470
rs1668049	snp	C/T			intron-variant	RNF165	GRCh38.p7	18:46445934	aaaacagcctggatt[C/T]ttcaacaaatacatt	494470
rs1788264	snp	A/T			intron-variant	RNF165	GRCh38.p7	18:46445987	gatttaaggggttgc[A/T]tttttgtgttgtcat	494470
rs1788265	snp	A/G			intron-variant	RNF165	GRCh38.p7	18:46446070	ggcttgagtaaattc[A/G]ggttcaactcttatt	494470
rs1893974	snp	C/G/T	0.139903	0.224452			GRCh38.p7	18:46346840	CTGACTGCCCAAGGG[C/G/T]CTGCTTTGCACTCCC	494470
rs1964444	snp	C/T	0.493881	0.054972	intron-variant	RNF165	GRCh38.p7	18:46364356	TAATGTTGTTAACTT[C/T]TGTGAATTTTTGACC	494470
rs2000707	snp	C/T	0.317451	0.240729	intron-variant	RNF165	GRCh38.p7	18:46342682	TCCCCTTCCTGAGGC[C/T]TTGAGCCCCAAGATG	494470
rs2008211	snp	C/T	0.353371	0.227628	intron-variant	RNF165	GRCh38.p7	18:46341124	CTCAGAGCACAACTC[C/T]AGGAGTTAAGCAGCA	494470
rs2044221	snp	A/G	0.367091	0.220884	intron-variant	RNF165	GRCh38.p7	18:46379022	GGCCTGGAGTAGGGA[A/G]GGAGCGGGGCACCAG	494470
rs2053957	snp	A/G	0.464629	0.128197	intron-variant	RNF165	GRCh38.p7	18:46385481	CAGTAGAGCCACGCT[A/G]GAAAAGCTCCTGGGT	494470
rs2167198	snp	A/T	0	0	intron-variant	RNF165	GRCh38.p7	18:46438739	CTTGGAGCCAGTTGG[A/T]TGCAAACTTAGAAAT	494470
rs2364833	snp	G/T			upstream-variant-2KB	RNF165	GRCh38.p7	18:46333875	GGNCTGACCCCTCCC[G/T]CGCGCCCCGCAGCGG	494470
rs2364834	snp	A/G	0.203882	0.245709	intron-variant	RNF165	GRCh38.p7	18:46359327	GAACGTGACAAAGGG[A/G]GTGTGCAGGCAGCTG	494470
rs2364835	snp	C/T	0.497776	0.0332724	intron-variant	RNF165	GRCh38.p7	18:46360102	CAGAATACCCTGAGA[C/T]GCATCACAAGTCCAT	494470
rs2364836	snp	A/C/T	0.000798403	0.0199641	intron-variant	RNF165	GRCh38.p7	18:46384771	ctgtaatcccagtgn[A/C/T]tttgggagaccgaag	494470
rs2365331	snp	G/T	0.219947	0.248187	intron-variant	RNF165	GRCh38.p7	18:46402519	TCTACATGTGTGTGT[G/T]TTTTTTTCTTTTCGA	494470
rs2365332	snp	A/G	0.469346	0.119947	downstream-variant-500B, utr-variant-3-prime	RNF165	GRCh38.p7	18:46461187	ATGACAGACGTCCCA[A/G]TGACCTTGAGCAAGT	494470
rs2365333	snp	A/G	0.463343	0.130326	downstream-variant-500B	RNF165	GRCh38.p7	18:46461432	GGCAGATCACTTGAG[A/G]TCAGGAGTTTGAGAC	494470
rs2365334	snp	C/T	0.463343	0.130326	downstream-variant-500B	RNF165	GRCh38.p7	18:46461519	GCGTGGTGGTAGGCG[C/T]CTGTAATCCCAGCTA	494470
rs2365335	snp	C/G	0.473266	0.112482	downstream-variant-500B	RNF165	GRCh38.p7	18:46461709	AGGAGAAAAGGAGAG[C/G]AAAGAAGAAGAGAAG	494470
rs2601041	snp	G/T					GRCh38.p7	18:46389925	gtagagacagggttt[G/T]gccatgttgcccagg	494470
rs2601042	snp	A/C					GRCh38.p7	18:46404980	gctccgtttggctcc[A/C]aagtctctgttgttt	494470
rs2601043	snp	A/C					GRCh38.p7	18:46405048	TGGCAAGACCCCACC[A/C]ATTTTTTTTTTGGTA	494470
rs2601044	snp	A/C	0	0			GRCh38.p7	18:46429716	TTACAAATTCTTACC[A/C]AACTCTCTATCACAT	494470
rs2852085	snp	G/T			intron-variant, nc-transcript-variant	RNF165, LOC105372095	GRCh38.p7	18:46389786	caggctgcagtgcag[G/T]ggtgcaatcttggct	494470
rs2852086	snp	G/T			intron-variant, upstream-variant-2KB	RNF165, LOC105372095	GRCh38.p7	18:46389854	ccacctcagcctccc[G/T]ggtagttgggactat	494470
rs2852087	snp	G/T			intron-variant, upstream-variant-2KB	RNF165, LOC105372095	GRCh38.p7	18:46389900	tacccagctaagttt[G/T]gtattttttgtagag	494470
rs2852088	snp	A/C			intron-variant	RNF165	GRCh38.p7	18:46405045	ATATGGCAAGACCCC[A/C]CCCATTTTTTTTTTG	494470
rs2886191	snp	A/G			intron-variant	RNF165	GRCh38.p7	18:46344329	AGTGGAAGGGAAGGG[A/G]TNGGAGGCGCTCTCC	494470
rs2886344	snp	A/G	0.420892	0.182472	intron-variant	RNF165	GRCh38.p7	18:46417717	caatagaagtataac[A/G]taaggccgggagcgg	494470
rs3220798	microsatellite	(CA)20/21/22/23/24/25	0.5576	0.26408	intron-variant	RNF165	GRCh38.p7	18:46348901	TATGCTTCTAGAAAT[(CA)20/21/22/23/24/25]GAAAGAGAGAGAGAG	494470
rs3844039	snp	A/G	0.147321	0.227941	intron-variant	RNF165	GRCh38.p7	18:46424995	ACAGGACAGCCGGCC[A/G]CAGGGCTGGAGAGGC	494470
rs3850524	snp	A/G	0.497959	0.0318836	intron-variant	RNF165	GRCh38.p7	18:46364223	CAGTGGCTCATGGCT[A/G]TAATCCCAGCACTTT	494470
rs3850525	snp	C/T	0.0221141	0.102801	intron-variant	RNF165	GRCh38.p7	18:46385431	TGCAACACCTTCCTC[C/T]TCAGAATCCCTCCCT	494470
rs3850526	snp	A/C			intron-variant, upstream-variant-2KB	RNF165, LOC105372095	GRCh38.p7	18:46391469	GGTTGCCGCTATTCC[A/C]CCCTCAGTGTCCTCA	494470
rs3850527	snp	G/T	0.279991	0.248195	intron-variant	RNF165	GRCh38.p7	18:46425379	CCGGGGCTACCCCAG[G/T]GATGATGGCCTTCTG	494470
rs3861807	snp	A/G	0.490063	0.0697833	intron-variant	RNF165	GRCh38.p7	18:46419460	CACTTCCTGTCTCTG[A/G]ACTTCAGCTTTCCAA	494470
rs3861808	snp	C/G	0.4862	0.0819127	intron-variant	RNF165	GRCh38.p7	18:46422357	ATGAAATCCGAATTT[C/G]TCCCAGGCTAGAAAA	494470
rs3861809	snp	A/G	0.461037	0.134028	intron-variant	RNF165	GRCh38.p7	18:46428057	AGCCCTCCCGCAGCC[A/G]TCCACACTGGTCTAC	494470
rs3889358	snp	G/T	0.0629771	0.165899	intron-variant	RNF165	GRCh38.p7	18:46364857	CAGCCGCCTGCTGAG[G/T]CCCCAAGCCTCCTGC	494470
rs3889748	snp	A/G	0.146314	0.227484	intron-variant	RNF165	GRCh38.p7	18:46396786	GCCCTGAGCTGTCCC[A/G]ACATAGGCGTGGTGC	494470
rs3889942	snp	C/T	0.238749	0.249747	intron-variant	RNF165	GRCh38.p7	18:46426440	GTGACCCACAAATGC[C/T]TGGGGACTGCTGGCT	494470
rs3894151	snp	A/G	0.485049	0.0851591	intron-variant	RNF165	GRCh38.p7	18:46379740	CTGAAGTCACATGTC[A/G]CTTTAGATTCAGAAA	494470
rs3897684	snp	A/T	0	0	intron-variant	RNF165	GRCh38.p7	18:46364441	AGTCGTAGAACACGC[A/T]TTCTAAAGTAACTGG	494470
rs3902741	snp	A/G	0.108402	0.206034	intron-variant	RNF165	GRCh38.p7	18:46420892	AGTAAATTAAAAGCA[A/G]AAAAGCAAATCTCCA	494470
rs3911129	snp	A/T	0.472522	0.113946	intron-variant	RNF165	GRCh38.p7	18:46415599	TCTCAATAAAGGGCC[A/T]AGTGCACCAGGGAGG	494470
rs3911130	snp	A/C	0.381503	0.21262	intron-variant	RNF165	GRCh38.p7	18:46411566	TCCGTGAGGCAGAAC[A/C]TCAGCTGTCCAGCTC	494470
rs3911131	snp	A/C	0.495407	0.0477027	intron-variant	RNF165	GRCh38.p7	18:46411393	AGCATACGTCCTATT[A/C]AGGATAGTCACATAG	494470
rs3916035	snp	A/C	0	0	intron-variant	RNF165	GRCh38.p7	18:46422161	TCAGAGATGAAGAAA[A/C]CGAAAGTGGGCCATC	494470
rs3930378	snp	C/T			intron-variant, upstream-variant-2KB	RNF165, LOC105372095	GRCh38.p7	18:46390129	TATGCTCCTCTCCCT[C/T]TTCCTGACCTCCCCA	494470
rs4020476	in-del	-/GA			intron-variant	RNF165	GRCh38.p7	18:46364745	GCTCACATACTGATG[-/GA]NGNGGNTGGCCTTTT	494470
rs4020477	in-del	-/GA			intron-variant	RNF165	GRCh38.p7	18:46364747	CACATACTGATGGAN[-/GA]GGNTGGCCTTTTCTG	494470
rs4101620	snp	C/T	0.251578	0.249995	intron-variant	RNF165	GRCh38.p7	18:46415508	GACAGATCCTTGTTC[C/T]GTCGCCCAGGCTGGA	494470
rs4286190	snp	A/G	0.194278	0.243711	intron-variant	RNF165	GRCh38.p7	18:46421998	ATAGATAGAGAGGGA[A/G]GAAAGCAGACCCATG	494470
rs4290554	snp	A/G	0.101658	0.201233	utr-variant-3-prime	RNF165	GRCh38.p7	18:46460596	TTACCTCATTTTGGC[A/G]TTGTTTCTGGGAGTG	494470
rs4580283	snp	C/G	0.000399281	0.0141238	intron-variant	RNF165	GRCh38.p7	18:46374641	CTTTGTGCTCTAATT[C/G]TTTGGTTTTTAAACT	494470
rs4602126	snp	C/T	0.473634	0.111748	intron-variant	RNF165	GRCh38.p7	18:46368619	ACAGCTCTATGGAGT[C/T]GAGTCTTAATCAGTT	494470
rs4890325	snp	A/G	0.269267	0.249256	intron-variant	RNF165	GRCh38.p7	18:46413901	CATGGATCCTTCCAG[A/G]AATCATCTGCATGTT	494470
rs4890326	snp	C/G	0.491783	0.0635686	intron-variant	RNF165	GRCh38.p7	18:46427389	CTCCTAATGAGGCTC[C/G]AGAGAAACCTGAAGG	494470
rs4890327	snp	C/T	0.0209421	0.100162	intron-variant	RNF165	GRCh38.p7	18:46428876	acattataattctgt[C/T]ggacagtgctgGGTG	494470
rs4890328	snp	C/T	0.492435	0.0610346	intron-variant	RNF165	GRCh38.p7	18:46452393	caagcaattctccca[C/T]gtcagcctcccaagc	494470
rs4890643	snp	G/T	0.331874	0.236213	upstream-variant-2KB	RNF165	GRCh38.p7	18:46333162	GAATTTGCAGGAGCC[G/T]CAGAGCCTGATGTTA	494470
rs4890644	snp	C/T	0.454423	0.143914	intron-variant	RNF165	GRCh38.p7	18:46374408	TGTCCCCATTAAACA[C/T]GAACTCCCCATTCTC	494470
rs4890645	snp	C/T	0.47934	0.0995154	intron-variant	RNF165	GRCh38.p7	18:46380870	CAGCCTTCCTTCCCA[C/T]GTCTCAGCACTGCAG	494470
rs4890646	snp	C/G	0.479904	0.0982045	intron-variant	RNF165	GRCh38.p7	18:46381201	GGCATTGGGATAAGG[C/G]CAGGCACTGCCTTTG	494470
rs4890647	snp	C/T	0.357024	0.225933	intron-variant	RNF165	GRCh38.p7	18:46381315	CCACAAGAGCAGGTT[C/T]AGCCGCAAGAAACAG	494470
rs4890648	snp	G/T	0.480064	0.0978296	intron-variant	RNF165	GRCh38.p7	18:46403991	GGATTCTACTGCCCT[G/T]TGTGATTAACAATTC	494470
rs4890649	snp	A/T	0.479502	0.0991411	intron-variant	RNF165	GRCh38.p7	18:46403992	GATTCTACTGCCCTG[A/T]GTGATTAACAATTCC	494470
rs4890650	snp	A/G	0.489318	0.0722982	intron-variant	RNF165	GRCh38.p7	18:46417980	ctgcactccagcctg[A/G]gcaacagagcaagac	494470
rs4890651	snp	C/T	0.460365	0.13508	intron-variant	RNF165	GRCh38.p7	18:46419301	TTGAGCCATCCTCCG[C/T]AGCCAGCCCTAGGCC	494470
rs4890652	snp	A/T	0.124837	0.216412	intron-variant	RNF165	GRCh38.p7	18:46426973	CATGGACCCAGATAT[A/T]CTATCCTGGGAGTTT	494470
rs5824623	in-del	-/G	0.490007	0.0699769	intron-variant	RNF165	GRCh38.p7	18:46346443	GCTCCCTTGGGTTTA[-/G]GGGCCTCCTCCCAGG	494470

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