iUUCD 2.0 - integrated annotations for ubiquitin and ubiquitin-like conjugation database

KCTD7

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs777890772	snp	A/G	3.29614e-05	0.00405951	missense	KCTD7	GRCh38.p7	7:66638928	GCTTTGCCAAGCTCA[A/G]GGTCTGTGTCTTCAA	154881
rs778046189	in-del	-/C			intron-variant	KCTD7	GRCh38.p7	7:66638218	GCCCAGGAGCATAAG[-/C]TCCTTGTCACCGACC	154881
rs778155909	snp	A/G	1.64746e-05	0.00287002	missense	KCTD7	GRCh38.p7	7:66638357	GGCCCCTCCTGGAGC[A/G]GCTGGAGAACATGCA	154881
rs778245978	snp	G/T	1.66418e-05	0.00288455	intron-variant	KCTD7	GRCh38.p7	7:66638814	CTGCTGCCCTGTCCT[G/T]CCTCTTCACCCTAGT	154881
rs778513261	snp	C/T	4.64177e-05	0.00481733	synonymous-codon	KCTD7	GRCh38.p7	7:66629130	CATGTCCAGCTCTGA[C/T]GCCGAAGACGACTTT	154881
rs778647590	in-del	-/CGGCCACGCAGG	4.36005e-05	0.00466887	cds-indel	KCTD7	GRCh38.p7	7:66629165	AGCCGGCCACGCCGA[-/CGGCCACGCAGG]CGGGGCACGCGCTGC	154881
rs778676871	snp	A/G	0.000212472	0.0103049	intron-variant	KCTD7	GRCh38.p7	7:66629216	CACAGGAGGTACCCG[A/G]GCGGGCGGCGGGCCG	154881
rs778715078	snp	A/G					GRCh38.p7	7:66627933	TCAGGTGATCCACCC[A/G]CATCGCTTACCAAAG	154881
rs778718424	snp	A/T	1.6537e-05	0.00287545			GRCh38.p7	7:66639174	TGTGTGACAAGCACC[A/T]CGTGAACCACTACTA	154881
rs778782270	snp	A/G			intron-variant	KCTD7	GRCh38.p7	7:66635462	ATAGCTGCTGCACAG[A/G]CTTGTCAAAGAGGAT	154881
rs778804133	snp	C/T			utr-variant-3-prime	KCTD7	GRCh38.p7	7:66642631	TATTTGATTCCAATA[C/T]ACATTATTAAGCTTT	154881
rs779019733	snp	A/G			intron-variant, utr-variant-3-prime	KCTD7	GRCh38.p7	7:66639868	ATAGCTGCCAAAGCT[A/G]TGCACCCAGTTGGCC	154881
rs779076635	snp	C/T			intron-variant	KCTD7	GRCh38.p7	7:66638797	TGTTTCTCTGTGCAT[C/T]TCTGCTGCCCTGTCC	154881
rs779291721	snp	A/C/G	3.2973e-05	0.00406025	intron-variant	KCTD7	GRCh38.p7	7:66638203	ACACTGTGTGGCACT[A/C/G]CCCAGGAGCATAAGC	154881
rs779492935	snp	C/T			utr-variant-3-prime	KCTD7	GRCh38.p7	7:66642861	GGTGGGAACAAACAG[C/T]GAGTATGGGAACAGG	154881
rs779584948	snp	C/G			upstream-variant-2KB	KCTD7	GRCh38.p7	7:66628146	ACTTTGTCTTTTAAA[C/G]AAAGGAGAAAATGGC	154881
rs779759931	snp	G/T	1.65899e-05	0.00288005	intron-variant	KCTD7	GRCh38.p7	7:66638838	CCCTAGTGATAGGTG[G/T]TGTGTTCATCCTTAT	154881
rs779862565	snp	C/T	1.66344e-05	0.0028839	intron-variant	KCTD7	GRCh38.p7	7:66633238	CCAGCTCTCATTCCC[C/T]GTTGCCTGCCTGAGA	154881
rs779871558	snp	A/G	1.66045e-05	0.00288132	missense	KCTD7	GRCh38.p7	7:66639194	AACCACTACTACTGC[A/G]AGCGCCCCATCTATG	154881
rs779953354	snp	G/T	0.000170372	0.00922806	intron-variant, utr-variant-3-prime	KCTD7	GRCh38.p7	7:66640357	TGTTTTACTCCTCAC[G/T]CCTGTATATTTTGGT	154881
rs779961219	snp	A/C			intron-variant	KCTD7	GRCh38.p7	7:66630219	CTGCAGTGAGCTGTA[A/C]TTGTGCCACTGTACT	154881
rs780330313	snp	A/G	4.94556e-05	0.00497246	intron-variant	KCTD7	GRCh38.p7	7:66638213	GCACTGCCCAGGAGC[A/G]TAAGCTCCTTGTCAC	154881
rs780533210	snp	C/T			intron-variant	KCTD7	GRCh38.p7	7:66630053	GAGGTGGGAGGATTG[C/T]TTGATCCCAGCAGTT	154881
rs780590290	snp	C/T			intron-variant	KCTD7	GRCh38.p7	7:66631310	AAAAGGATGCATGGC[C/T]ATAATCCCAGCACTT	154881
rs780612080	snp	A/G			intron-variant	KCTD7	GRCh38.p7	7:66632900	AATATATATATATAT[A/G]CAAAAAATTAGCCGG	154881
rs780685090	snp	A/G			intron-variant	KCTD7	GRCh38.p7	7:66630285	AAACAAACAAAAACA[A/G]AAAAAGCAAGAGAAG	154881
rs780710316	snp	A/G	3.29565e-05	0.00405921	missense	KCTD7	GRCh38.p7	7:66633404	ATCCCCACGGACTCC[A/G]AGGGCCGGTACTTCA	154881
rs781014688	snp	G/T	1.65954e-05	0.00288053	intron-variant	KCTD7	GRCh38.p7	7:66633242	CTCTCATTCCCCGTT[G/T]CCTGCCTGAGAGCCC	154881
rs781181088	snp	A/T			intron-variant, utr-variant-3-prime	KCTD7	GRCh38.p7	7:66639975	GGGTTATCTTCTCAC[A/T]GGGCTGGAATGCAAA	154881
rs781343567	snp	A/C			intron-variant	KCTD7	GRCh38.p7	7:66634395	GGAGATAGGGTCTTG[A/C]TATGTTGCCCAGGGT	154881
rs781426628	snp	A/C	0.000203604	0.0100876	utr-variant-3-prime	KCTD7	GRCh38.p7	7:66640404	TTCAGAAATTGAAAA[A/C]GATCCCCAAGGATCT	154881
rs781560681	snp	A/G			utr-variant-3-prime	KCTD7	GRCh38.p7	7:66641138	CACGTTCTGAGATAT[A/G]CGCTCTCTCTATTGT	154881
rs781612364	snp	C/T			utr-variant-3-prime	KCTD7	GRCh38.p7	7:66642985	GTTCATGTACCTGTC[C/T]GTGAGTGCTTTGGTG	154881
rs781613111	in-del	-/G	1.68026e-05	0.00289845	intron-variant	KCTD7	GRCh38.p7	7:66638453	TCAGCTGCCCAGGAT[-/G]GGTGGGTATGTGGGA	154881
rs781725855	snp	A/G	1.64749e-05	0.00287005	missense	KCTD7	GRCh38.p7	7:66638341	CAGTACTATGCCATC[A/G]GGCCCCTCCTGGAGC	154881
rs796052686	snp	A/G			synonymous-codon	KCTD7	GRCh38.p7	7:66638394	GAAGGGCGAGAAGGT[A/G]CGCCAAGCGTTTCTG	154881
rs796052687	snp	A/G			missense	KCTD7	GRCh38.p7	7:66629204	TGCCCCTGCTGCCAC[A/G]GGAGGTACCCGGGCG	154881
rs796052688	in-del	-/TCCAGCGG			frameshift-variant	KCTD7	GRCh38.p7	7:66638898	CCCGGCTGCGTGCGG[-/TCCAGCGG]AAGGCCCGCTTTGCC	154881
rs796052689	snp	C/G			missense	KCTD7	GRCh38.p7	7:66639066	TGTCTTTTGGGCCCT[C/G]GGAGGCTGTGGCTGA	154881
rs796052690	snp	C/T			missense	KCTD7	GRCh38.p7	7:66629114	GTCGTCAGGACGGTG[C/T]CATGTCCAGCTCTGA	154881
rs796485508	in-del	-/A			intron-variant	KCTD7	GRCh38.p7	7:66631706	GCAGTGCAAAACAGG[-/A]AAAAAAAAAAAAGCC	154881
rs796511904	in-del	-/TG			intron-variant	KCTD7	GRCh38.p7	7:66634137	ATATATATATATATA[-/TG]TATATATATGAGCTC	154881
rs796725334	snp	A/G			intron-variant, utr-variant-3-prime	KCTD7	GRCh38.p7	7:66640135	AATCCAGTTTGTGGT[A/G]AACCTCTTTGGAAGG	154881
rs796799547	in-del	-/A			intron-variant	KCTD7	GRCh38.p7	7:66631282	TCACTGGAGCAGGAG[-/A]GATGTAATATTGAAA	154881
rs797005416	in-del	-/AT			intron-variant	KCTD7	GRCh38.p7	7:66633593	TATTGAAAGAGATCA[-/AT]TTTTTTTTTTTTTTT	154881

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