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
rs14137	snp	C/T	0.494007	0.0544111	synonymous-codon	KCTD3	GRCh38.p7	1:215620492	AGTACTTGGTGATGA[C/T]GCCAGATAGGGAACT	51133
rs908480	snp	C/T			intron-variant	KCTD3	GRCh38.p7	1:215590774	TGTTAAAGTATTTGT[C/T]TGCTAATATCAATAT	51133
rs1074255	snp	C/G	0.0240643	0.107019	intron-variant	KCTD3	GRCh38.p7	1:215590080	caaagtgttgattag[C/G]atgtggagaacctgg	51133
rs1342802	snp	A/G	0.000798403	0.0199641	intron-variant	KCTD3	GRCh38.p7	1:215606876	ATTAGCAAAATTGAC[A/G]TAATTGTCCAATTGA	51133
rs1819739	snp	C/G	0.43309	0.17023	intron-variant	KCTD3	GRCh38.p7	1:215591054	AAAATAAGAACTACA[C/G]CCTTGAAAAGGAGCC	51133
rs1819740	snp	A/G	0.109108	0.206518	intron-variant	KCTD3	GRCh38.p7	1:215590903	gttatgaattatgtt[A/G]cctttctttaaaagt	51133
rs2185824	snp	A/T	0	0	utr-variant-3-prime	KCTD3	GRCh38.p7	1:215620908	ATATTACCACGTCTT[A/T]ATAGGATGGTGCCCA	51133
rs2275768	snp	G/T	0.426234	0.177318	missense, utr-variant-5-prime, upstream-variant-2KB	KCTD3, LOC105372919	GRCh38.p7	1:215567710	GGGCACTGCGGCAGC[G/T]TCCCCGCGGCGGCGG	51133
rs2459573	snp	A/G	0.0178098	0.0926698	intron-variant	KCTD3	GRCh38.p7	1:215582495	TAAGATGATGGAGAG[A/G]TGAAATAACAGAGCA	51133
rs2675222	snp	C/T	0.0178098	0.0926698	intron-variant	KCTD3	GRCh38.p7	1:215570343	ATGAAACTTCATCTA[C/T]TCTACTTTCTGAATC	51133
rs2675223	snp	A/T	0.0178098	0.0926698	intron-variant	KCTD3	GRCh38.p7	1:215597033	ATACTGCAGAGATTA[A/T]TCGTACATTTGCAGT	51133
rs2675225	snp	G/T	0	0	intron-variant	KCTD3	GRCh38.p7	1:215618511	GTCAAGTACAATTCA[G/T]TTAGCCCTTACGTGA	51133
rs2675226	snp	A/T			intron-variant	KCTD3	GRCh38.p7	1:215613464	TGTCTGTTTACTCTG[A/T]TGATAGTTTCTTTTG	51133
rs2677115	snp	C/T	0.0178098	0.0926698	intron-variant	KCTD3	GRCh38.p7	1:215579622	tcctgcctcagcctc[C/T]ggagtagctgggact	51133
rs2677117	snp	A/G	0.492533	0.0606443	intron-variant	KCTD3	GRCh38.p7	1:215617663	acatgcagcaagcca[A/G]aagattttctcggag	51133
rs2797253	snp	A/G	0.0174175	0.0916809	intron-variant	KCTD3	GRCh38.p7	1:215610887	CATAGTAAGTACAGT[A/G]TAAGTATTAGCTAAT	51133
rs2797391	snp	A/G	0.0178098	0.0926698	intron-variant	KCTD3	GRCh38.p7	1:215571606	AAATTGTAAAGTTGT[A/G]TGTGGGAAGAAGTGG	51133
rs2797392	snp	A/G	0.138546	0.223781	intron-variant	KCTD3	GRCh38.p7	1:215597498	ACAGCTTTGGAAGTT[A/G]GCTCTAGAAAGGCAT	51133
rs2797393	snp	A/G	0.494855	0.0504572	intron-variant	KCTD3	GRCh38.p7	1:215600483	AGCACTGAGATGGCA[A/G]TTCTTCCCCTCTCTC	51133
rs2797394	snp	A/G	0.0174175	0.0916809	intron-variant	KCTD3	GRCh38.p7	1:215603443	TGCAATGGGGTCTGG[A/G]CACTTTTTGAAAAAA	51133
rs2886165	snp	A/G	0.0652144	0.168387	intron-variant	KCTD3	GRCh38.p7	1:215614869	GAATTTTTTACATCA[A/G]AGTTCATTATCAAAT	51133
rs2995519	snp	A/C	0	0	intron-variant	KCTD3	GRCh38.p7	1:215605584	atccaaagagttcca[A/C]accctgtatatccag	51133
rs3753836	snp	G/T	0	0	intron-variant	KCTD3	GRCh38.p7	1:215600120	ATACCAGGAAAACAT[G/T]GAGTACTTTTCAGTG	51133
rs3753837	snp	C/T	0.0452528	0.143452	intron-variant	KCTD3	GRCh38.p7	1:215581758	CAAATATGTCCTCAA[C/T]TGTCTTCCTTCGTCA	51133
rs3753838	snp	A/G	0.0452528	0.143452	intron-variant	KCTD3	GRCh38.p7	1:215581589	CGTAATAATGTGGTG[A/G]TTCTGGAAAAGAGCA	51133
rs3767251	snp	A/C	0.0475351	0.146656	utr-variant-3-prime	KCTD3	GRCh38.p7	1:215621466	CTACAAGTGAACAAA[A/C]TAGTGTTTTAATTTA	51133
rs3767252	snp	C/T	0.0475351	0.146656	utr-variant-3-prime	KCTD3	GRCh38.p7	1:215621072	TATCTGGTAAACACT[C/T]TGCAATCACAATAAG	51133
rs3767253	snp	A/G	0.0245613	0.108062	synonymous-codon	KCTD3	GRCh38.p7	1:215620513	TGAGTCAGTTCCTCC[A/G]TCGGAAGTACTTGGT	51133
rs3767255	snp	C/T	0.422158	0.181278	intron-variant	KCTD3	GRCh38.p7	1:215608232	GGTTTTATTAGTTGA[C/T]ATGCTTCTTCTGAAC	51133
rs3767256	snp	C/G	0.0463947	0.145069	intron-variant	KCTD3	GRCh38.p7	1:215602663	TTTTATTGCAATGGC[C/G]TCTAAAATGCACTGA	51133
rs3767258	snp	A/G	0.109461	0.206758	intron-variant	KCTD3	GRCh38.p7	1:215600472	AGAACTGCCATCTCA[A/G]TGCTGGTGGGTGAAG	51133
rs3767259	snp	A/T	0.0452528	0.143452	intron-variant	KCTD3	GRCh38.p7	1:215593210	AGTGGCAGGTTCATT[A/T]CTTAACCAATTCTGG	51133
rs3767260	snp	C/T	0.0463947	0.145069	intron-variant	KCTD3	GRCh38.p7	1:215585879	CTGAAGACTAGTTTT[C/T]AAAGGTCTAAATGCA	51133
rs3767261	snp	A/C/G	0.00032241	0.012693	missense	KCTD3	GRCh38.p7	1:215579011	TGTTGTTTATTTTAC[A/C/G]ACTAGGAATACCTAT	51133
rs3767262	snp	C/T	0.0452528	0.143452	intron-variant	KCTD3	GRCh38.p7	1:215574261	TTATAAAAAACTACA[C/T]ATGACAAGAAATAAA	51133
rs4655409	snp	A/G	0.00914312	0.0669923	intron-variant	KCTD3	GRCh38.p7	1:215578590	GCAAGATTTCATTTT[A/G]AAAAATGTTCCCCTG	51133
rs4655410	snp	A/C	0.0146672	0.084371	intron-variant	KCTD3	GRCh38.p7	1:215616647	cgcctgtaatcccag[A/C]tactcaggaggctga	51133
rs4655411	snp	C/T	0.0142736	0.0832652	intron-variant	KCTD3	GRCh38.p7	1:215616648	gcctgtaatcccagc[C/T]actcaggaggctgag	51133
rs6669126	snp	C/T	0.0138664	0.082103	intron-variant	KCTD3	GRCh38.p7	1:215577770	TTATGATTTGACTCA[C/T]GTATGAAAGTTGCCC	51133
rs6669520	snp	A/C	0.0603597	0.1629	intron-variant	KCTD3	GRCh38.p7	1:215578352	gtgtatactacatga[A/C]gactaggtttaactg	51133
rs6674311	snp	A/G	0.0629771	0.165899	intron-variant	KCTD3	GRCh38.p7	1:215577028	TTATTAGTATTATAA[A/G]TTCTGAATCTTCCAT	51133
rs6682584	snp	A/C	0.0603597	0.1629	intron-variant	KCTD3	GRCh38.p7	1:215587626	tgaactgtgatatct[A/C]tttctgcattcaatc	51133
rs6685149	snp	G/T	0.0603597	0.1629	intron-variant	KCTD3	GRCh38.p7	1:215587623	TTTtgaactgtgata[G/T]ctatttctgcattca	51133
rs6685448	snp	A/G			intron-variant	KCTD3	GRCh38.p7	1:215601087	ggattactggcatgc[A/G]ccactacgcccagct	51133
rs7511859	snp	A/G	0.0532157	0.154195	intron-variant	KCTD3	GRCh38.p7	1:215574805	TCTCATTGATTGTAT[A/G]TATATAGTTGATCAT	51133
rs7512596	snp	A/T			intron-variant	KCTD3	GRCh38.p7	1:215569615	ttttttttttttttg[A/T]gacagagtctcgctc	51133
rs7522198	snp	A/G	0.0626037	0.165477	intron-variant	KCTD3	GRCh38.p7	1:215574846	GTTTTATTACTGGCT[A/G]CCATTTCCCTTTCTA	51133
rs7522720	snp	A/T	0.0629771	0.165899	intron-variant	KCTD3	GRCh38.p7	1:215593490	TTGTCACTGGTCTTG[A/T]GTATAGTACAGTTCT	51133
rs7528121	snp	C/G	0.415563	0.18732	intron-variant	KCTD3	GRCh38.p7	1:215588969	caaggctttattagt[C/G]tctcagcaattgggt	51133
rs7545425	snp	A/C	0.108755	0.206276	intron-variant	KCTD3	GRCh38.p7	1:215574892	CTTTAAAAGATGTTC[A/C]GTTTTTATGGCCAGA	51133
rs10218729	snp	A/G	0.00177561	0.0297431	intron-variant	KCTD3	GRCh38.p7	1:215602240	CATTCTTGACTTTTT[A/G]TCTTTTTATTCATTA	51133
rs10495002	snp	C/T	0.100231	0.200173	intron-variant	KCTD3	GRCh38.p7	1:215574581	TCAGTGCAAAAAAAT[C/T]GGTTTATCCATTTGG	51133
rs10591999	in-del	-/TC	0.5	0	intron-variant	KCTD3	GRCh38.p7	1:215591267	TTTCTTTCTTTTCTT[-/TC]TCTCTCTCTCCTTCC	51133
rs10592000	in-del	-/TTCC			intron-variant	KCTD3	GRCh38.p7	1:215591288	TCTCTCCTTCCTTCT[-/TTCC]TTCCTTCCTTCCTTC	51133
rs10612474	in-del	-/ACT	0.0599851	0.162463	intron-variant	KCTD3	GRCh38.p7	1:215608444	CTTCACATGTTAACT[-/ACT]TTTATTTATTATTAA	51133
rs11362703	in-del	-/T			intron-variant	KCTD3	GRCh38.p7	1:215593878	GAATTGGAATACAAC[-/T]TTTTTTTTTTTTTTT	51133
rs11558947	snp	A/T			utr-variant-3-prime	KCTD3	GRCh38.p7	1:215621382	AGACAGGTTAGCAAC[A/T]GGTACAGCTTTCCCT	51133
rs11558948	snp	A/G			utr-variant-3-prime	KCTD3	GRCh38.p7	1:215620741	GTAATTCTGTTAAAA[A/G]GATACTAAATGAAGT	51133
rs11581370	snp	G/T	0	0	intron-variant	KCTD3	GRCh38.p7	1:215593380	TTCTAACAATACTTA[G/T]CAGGTTTTTTGTTTT	51133
rs11581745	snp	C/T	0.000798403	0.0199641	intron-variant	KCTD3	GRCh38.p7	1:215570944	TCATGAAGTTATATT[C/T]GAGACTGGTTTTGGG	51133
rs11582279	snp	C/T	0.5	0	intron-variant	KCTD3	GRCh38.p7	1:215571920	acaggcgtgagccac[C/T]gcgcctagccGAGAT	51133
rs11803705	snp	G/T	0.420558	0.182784	intron-variant	KCTD3	GRCh38.p7	1:215580012	CAGGTAGTGTATAAT[G/T]AATAATGCTTTGCTT	51133
rs11805855	snp	C/G	0.000798403	0.0199641	intron-variant	KCTD3	GRCh38.p7	1:215575107	aaacagaaaaattaa[C/G]ccggcatagtggcag	51133
rs12023213	snp	C/G	0.0130921	0.0798413	downstream-variant-500B	KCTD3	GRCh38.p7	1:215622195	CAAGTCAAATCGTTT[C/G]TTTCTTTTGCTTACA	51133
rs12039938	snp	C/G	0	0	intron-variant	KCTD3	GRCh38.p7	1:215579317	ATGTTGTGTAATCTT[C/G]TATCTTCTCTGAATC	51133
rs12058673	snp	A/T	0.228253	0.249052	upstream-variant-2KB, downstream-variant-500B	KCTD3, LOC105372919	GRCh38.p7	1:215566237	CCAAATTTCCTTTTT[A/T]AAAAATAATTATAAC	51133
rs12070117	snp	A/G	0.0182019	0.0936463	intron-variant	KCTD3	GRCh38.p7	1:215592409	aagtggagaataatc[A/G]ggtgccatttattct	51133
rs12071678	snp	C/T	0.0227044	0.1041	upstream-variant-2KB	KCTD3	GRCh38.p7	1:215565427	ATGCCTCAGATATCT[C/T]TATATTGTTCTGGAC	51133
rs12080379	snp	C/T	0.195526	0.243993	intron-variant	KCTD3	GRCh38.p7	1:215592206	GGGCACAGAACCAAA[C/T]TGTATCACTTAGGTC	51133
rs12090919	snp	C/T	0	0	intron-variant	KCTD3	GRCh38.p7	1:215589367	ccaggtcttgaattc[C/T]taagctttagtgatc	51133
rs12124193	snp	A/G			intron-variant	KCTD3	GRCh38.p7	1:215569891	CATTAAAAAACTTCA[A/G]AAAATTGTTAAGATA	51133
rs12129661	snp	C/T	0.0283406	0.115616	intron-variant	KCTD3	GRCh38.p7	1:215588451	tctttgatttggcct[C/T]ttatgttcttgaaag	51133
rs12568192	snp	A/G	0.5	0	intron-variant	KCTD3	GRCh38.p7	1:215617854	atatttagtatatac[A/G]taatatatattaaat	51133
rs12733007	snp	C/T			intron-variant	KCTD3	GRCh38.p7	1:215589124	ttaaaatacttaatt[C/T]tttttcttcttttct	51133
rs12741107	snp	G/T			intron-variant	KCTD3	GRCh38.p7	1:215614019	ggaactttagaatag[G/T]ttttttttttttttt	51133
rs12743895	snp	A/T	0.0486741	0.148216	intron-variant	KCTD3	GRCh38.p7	1:215602490	CAAAAAAAAAAAAAA[A/T]TCTGCACATTTGTCT	51133
rs17024959	snp	C/T	0.116488	0.211364	intron-variant	KCTD3	GRCh38.p7	1:215607502	AAAATAATGCTCAGC[C/T]TTAGTACAGAATCTT	51133
rs17024966	snp	A/G	0.108755	0.206276	intron-variant	KCTD3	GRCh38.p7	1:215608633	ATATTCTCTGATTTC[A/G]GCAAAAGGTGTATAA	51133
rs17553500	snp	C/T	0.0387552	0.1337	intron-variant	KCTD3	GRCh38.p7	1:215607245	GTTCATTGCTAATAA[C/T]AACATATTTTCTAAA	51133
rs28576514	snp	A/C			intron-variant	KCTD3	GRCh38.p7	1:215603009	GCTCTTTTTGATACC[A/C]CTGTCTTTGGATGTT	51133
rs33997368	in-del	-/G			frameshift-variant	KCTD3	GRCh38.p7	1:215620503	TGGCATCATCACCAA[-/G]TACTTCCGATGGAGG	51133
rs34006906	in-del	-/C			intron-variant	KCTD3	GRCh38.p7	1:215579527	TTTTGAGACGGAGTC[-/C]TCGCTCTGTCGCTCA	51133
rs34019406	in-del	-/C			frameshift-variant, utr-variant-5-prime	KCTD3	GRCh38.p7	1:215577710	ATGAAGCAGAATTTT[-/C]ACGGGATCACTCCAT	51133
rs34191564	in-del	-/T			upstream-variant-2KB	KCTD3	GRCh38.p7	1:215565965	AGTGTATTTTATGTG[-/T]GGCCAAAGACAATTC	51133
rs34318346	in-del	-/C			intron-variant	KCTD3	GRCh38.p7	1:215587049	AGACCAGACATTCCC[-/C]AAACTTTTTGGTTTC	51133
rs34340618	in-del	-/C			intron-variant	KCTD3	GRCh38.p7	1:215590523	GGGTTGTGGGAGCCC[-/C]TGATTTTTTATTTCA	51133
rs34352533	snp	A/G	0.0744748	0.178019	intron-variant	KCTD3	GRCh38.p7	1:215600504	CCCCTCTCTCCTGTG[A/G]TTGTATTGTAGTCTA	51133
rs34444725	in-del	-/C			intron-variant	KCTD3	GRCh38.p7	1:215618566	TATCCCATTGTTTCC[-/C]TGATCCGTCAATGTG	51133
rs34449729	in-del	-/C			intron-variant	KCTD3	GRCh38.p7	1:215597260	AAATGTTTCAGTTTC[-/C]TTGTTTCCTTTTTTT	51133
rs34486061	in-del	-/G			intron-variant	KCTD3	GRCh38.p7	1:215579305	TTTTATTTAAAATGT[-/G]TGTGTAATCTTCTAT	51133
rs34694239	in-del	-/G			intron-variant	KCTD3	GRCh38.p7	1:215575071	GCATGGCCAACATGG[-/G]TGAAACCCCCTCTCT	51133
rs34765174	in-del	-/T			intron-variant	KCTD3	GRCh38.p7	1:215588656	ACTATTTCAGCACTT[-/T]CCTGTGTTTGTAGCT	51133
rs34889977	in-del	-/G			frameshift-variant	KCTD3	GRCh38.p7	1:215620518	GTACTTCCGATGGAG[-/G]AACTGACTCACCTGG	51133
rs34983781	in-del	-/C			intron-variant	KCTD3	GRCh38.p7	1:215609907	AAGAACTTAACTAGA[-/C]AGTTATGTTTATGAG	51133
rs35036763	in-del	-/T			intron-variant	KCTD3	GRCh38.p7	1:215597423	CCCAAGTTGATATTT[-/T]AAATTTAGATTTATA	51133
rs35074372	in-del	-/T			intron-variant	KCTD3	GRCh38.p7	1:215569946	TGGTATGGCCCGTAG[-/T]AAAACAACATCCGAC	51133
rs35128670	in-del	-/G			frameshift-variant	KCTD3	GRCh38.p7	1:215620277	AAGGGGCAACAGGGG[-/G]AATGTAATATATCTG	51133
rs35231115	snp	A/C/T	0.000230713	0.0107381	synonymous-codon	KCTD3	GRCh38.p7	1:215604217	AAGCTGAGGACCTGA[A/C/T]CCAACTGTCTCTGGG	51133
rs35331520	in-del	-/C			intron-variant	KCTD3	GRCh38.p7	1:215606619	TAATGTTATTGTGGG[-/C]ATGTGATACCAAGGA	51133
rs35450006	in-del	-/G			intron-variant	KCTD3	GRCh38.p7	1:215616548	GGCGGATCACCTGAG[-/G]TCGGGAGTTCAAGAT	51133

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