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
rs5951419	snp	A/G	0.0292288	0.117303	upstream-variant-2KB, intron-variant	ZNF645, PTCHD1-AS	GRCh38.p7	X:22270936	TGTTGCGTTTTCACC[A/G]TTAGTGAAGTCAAGA	158506
rs5951426	snp	G/T	0.356985	0.225952	missense, intron-variant	ZNF645, PTCHD1-AS	GRCh38.p7	X:22273489	CAGTCTTTTAGGGAT[G/T]TCAGAGATTTCAGTT	158506
rs5951547	snp	C/T	0.410964	0.191287	downstream-variant-500B, intron-variant	ZNF645, PTCHD1-AS	GRCh38.p7	X:22274682	AATGTGAAATAATTA[C/T]CTACCATTTAGCTGT	158506
rs5951548	snp	A/G	0.464279	0.12878	upstream-variant-2KB, intron-variant	ZNF645, PTCHD1-AS	GRCh38.p7	X:22272415	TGTGTGCATGTATAT[A/G]TACATACACACAAAA	158506
rs6528099	snp	C/G	0.0787474	0.182133	upstream-variant-2KB, intron-variant	ZNF645, PTCHD1-AS	GRCh38.p7	X:22271034	tggatcacctgaagt[C/G]aggagtttgagacca	158506
rs6528102	snp	A/T	0.489957	0.0701457	downstream-variant-500B, intron-variant	ZNF645, PTCHD1-AS	GRCh38.p7	X:22274484	GGTTTTTATTTTTTT[A/T]TTTTTTGGTGATATG	158506
rs6629461	snp	C/T	0.310359	0.242604	synonymous-codon, intron-variant	ZNF645, PTCHD1-AS	GRCh38.p7	X:22273615	GCCACATAAGGATAT[C/T]CAGGCTCCTCCCCCA	158506
rs6633535	snp	G/T	0	0	upstream-variant-2KB, intron-variant	ZNF645, PTCHD1-AS	GRCh38.p7	X:22272392	CAAAATCTTAAAAGG[G/T]ATGTGTATTTTGTGT	158506
rs6633536	snp	G/T	0	0	upstream-variant-2KB, intron-variant	ZNF645, PTCHD1-AS	GRCh38.p7	X:22272474	ATGAGTGATTTAAGG[G/T]AGTTCACAAAAATGC	158506
rs6633537	snp	A/G	0.340069	0.233211	upstream-variant-2KB, intron-variant	ZNF645, PTCHD1-AS	GRCh38.p7	X:22272766	CACTTTCGCCTCCTA[A/G]GCTGGGGAAGATGGT	158506
rs7877302	snp	C/T	0.493176	0.0580107	upstream-variant-2KB, intron-variant	ZNF645, PTCHD1-AS	GRCh38.p7	X:22271936	AAATGTCTAGCCCAG[C/T]GAAGTTACCATCTAT	158506
rs7885426	snp	C/T	0.0560809	0.157783	upstream-variant-2KB, intron-variant	ZNF645, PTCHD1-AS	GRCh38.p7	X:22271119	gtgtggtggcacatg[C/T]ctatagtcccatcta	158506
rs12013449	snp	C/T	0.0261392	0.111294	upstream-variant-2KB, intron-variant	ZNF645, PTCHD1-AS	GRCh38.p7	X:22272513	AAAAATAAGTCAGTC[C/T]TAGAAGGCAAAGCTC	158506
rs12556801	snp	G/T	0.29094	0.246625	upstream-variant-2KB, intron-variant	ZNF645, PTCHD1-AS	GRCh38.p7	X:22271917	AGAACAGCAAATGTC[G/T]AAAAAATGTCTAGCC	158506
rs12834209	snp	A/C	0.0266548	0.112325	upstream-variant-2KB, intron-variant	ZNF645, PTCHD1-AS	GRCh38.p7	X:22270933	CATTGTTGCGTTTTC[A/C]CCATTAGTGAAGTCA	158506
rs12834646	snp	C/T			upstream-variant-2KB, intron-variant	ZNF645, PTCHD1-AS	GRCh38.p7	X:22271076	gtggtgaaaccccgt[C/T]tctactaaaaataca	158506
rs12834654	snp	C/T			upstream-variant-2KB, intron-variant	ZNF645, PTCHD1-AS	GRCh38.p7	X:22271078	ggtgaaaccccgtct[C/T]tactaaaaatacaaa	158506
rs12843875	snp	G/T			upstream-variant-2KB, intron-variant	ZNF645, PTCHD1-AS	GRCh38.p7	X:22271961	ATCTATTCACTCCTG[G/T]TTTTTTTTTTTTTTT	158506
rs12843876	snp	G/T			upstream-variant-2KB, intron-variant	ZNF645, PTCHD1-AS	GRCh38.p7	X:22271962	TCTATTCACTCCTGT[G/T]TTTTTTTTttttttt	158506
rs12860105	snp	C/T	0.00394476	0.0442359	missense, intron-variant	ZNF645, PTCHD1-AS	GRCh38.p7	X:22273851	ATGCGCCACCTCCAT[C/T]TCCATCATCACCAGT	158506
rs16981921	snp	C/T	0.0500702	0.150094	upstream-variant-2KB, intron-variant	ZNF645, PTCHD1-AS	GRCh38.p7	X:22270926	ATTGGGGCATTGTTG[C/T]GTTTTCACCATTAGT	158506
rs16981925	snp	A/G	0.0348667	0.127349	upstream-variant-2KB, intron-variant	ZNF645, PTCHD1-AS	GRCh38.p7	X:22271823	GTTGCTGTTTTTACG[A/G]TCCAGTTTGTACTTA	158506
rs34516956	in-del	-/T	0.483247	0.0899768	downstream-variant-500B, intron-variant	ZNF645, PTCHD1-AS	GRCh38.p7	X:22274925	GTTACTTGTTAATGC[-/T]TTTTTTTTTTTTTTT	158506
rs56006398	snp	G/T	0.00158814	0.0281345	utr-variant-3-prime, intron-variant	ZNF645, PTCHD1-AS	GRCh38.p7	X:22274325	AAAACCTTCAAGTTC[G/T]ATACTGTACTGTGGA	158506
rs57690843	snp	C/G			upstream-variant-2KB, intron-variant	ZNF645, PTCHD1-AS	GRCh38.p7	X:22272268	AGGAGTGAGCCAAGG[C/G]GCCTGACACTATTCA	158506
rs59090833	snp	A/G/T	0.00581083	0.0535878	upstream-variant-2KB, intron-variant	ZNF645, PTCHD1-AS	GRCh38.p7	X:22272107	CCTGCCTCCTGAGTA[A/G/T]CTGAGATTACAGGCG	158506
rs73636821	snp	C/T	0.0245906	0.108123	downstream-variant-500B, intron-variant	ZNF645, PTCHD1-AS	GRCh38.p7	X:22274790	AGAAGCACCAAAATA[C/T]ATCAGAATTCCAGTA	158506
rs75062800	snp	A/G	0.00618021	0.0552441	synonymous-codon, intron-variant	ZNF645, PTCHD1-AS	GRCh38.p7	X:22274158	AATGGATCATAGAAG[A/G]TGGCCTGCATGGAAA	158506
rs111333157	snp	A/G/T	2.34775e-05	0.0034261	missense, intron-variant	ZNF645, PTCHD1-AS	GRCh38.p7	X:22274247	CACATCATTCACACC[A/G/T]GAGAAGACATAGACG	158506
rs112059840	snp	C/T	0.128718	0.218611	downstream-variant-500B, intron-variant	ZNF645, PTCHD1-AS	GRCh38.p7	X:22274692	GGTAGATAATTATTT[C/T]ACATTTTAGGAACTG	158506
rs112235331	snp	A/C/G	0.00385373	0.0437266	synonymous-codon, intron-variant	ZNF645, PTCHD1-AS	GRCh38.p7	X:22273636	TCCTCCCCCAGAACT[A/C/G]TCTCTAAGTCTGCCT	158506
rs113181888	snp	A/G	0.5	0	missense, intron-variant	ZNF645, PTCHD1-AS	GRCh38.p7	X:22273298	TATCCTGTGCTGAGA[A/G]TTGAGGCGCATAAAC	158506
rs113259855	snp	C/T	0	0	upstream-variant-2KB, intron-variant	ZNF645, PTCHD1-AS	GRCh38.p7	X:22272144	ACCATGCCTAGCTAA[C/T]TCTTGTATTTTTAGT	158506
rs113314974	snp	A/T	0.00239573	0.0345271	missense, intron-variant	ZNF645, PTCHD1-AS	GRCh38.p7	X:22273530	ACCATCTAAGCTATA[A/T]TCCACCAGAACAGCA	158506
rs138094158	snp	A/G	0.0033452	0.0407604	synonymous-codon, intron-variant	ZNF645, PTCHD1-AS	GRCh38.p7	X:22273825	TCATATTATACCTCA[A/G]AAACAGCATTATGCG	158506
rs138176282	snp	A/T	0.0022018	0.0331067	missense, intron-variant	ZNF645, PTCHD1-AS	GRCh38.p7	X:22273089	GAAAAAAGAAAAAAA[A/T]TCCTGGTTACCGTTG	158506
rs138673057	snp	C/G	0.000319019	0.0126257	missense, intron-variant	ZNF645, PTCHD1-AS	GRCh38.p7	X:22273925	AACTCGGTTCGTAGC[C/G]AAGTGCCAGCTCTAA	158506
rs139423670	snp	A/C	0.0168099	0.0901243	downstream-variant-500B, intron-variant	ZNF645, PTCHD1-AS	GRCh38.p7	X:22274514	GTTAACCTGTGTAAA[A/C]GGGTTAAATTTCAAT	158506
rs139621376	snp	A/G	0.0013226	0.0256817	missense, intron-variant	ZNF645, PTCHD1-AS	GRCh38.p7	X:22273452	CGCTTGAAAAAGTTC[A/G]TCCTCATATTGCTCC	158506
rs140897254	snp	C/G	0.0389457	0.134	upstream-variant-2KB, intron-variant	ZNF645, PTCHD1-AS	GRCh38.p7	X:22272273	TGAGCCAAGGCGCCT[C/G]ACACTATTCACTGCC	158506
rs140922897	snp	A/T	1.64727e-05	0.00286986	missense, intron-variant	ZNF645, PTCHD1-AS	GRCh38.p7	X:22274091	TTAACATTTTACCTC[A/T]GTTCACCGAAAATCA	158506
rs141135903	snp	A/G	0.103655	0.20269	upstream-variant-2KB, intron-variant	ZNF645, PTCHD1-AS	GRCh38.p7	X:22272052	CAGTGACGCGATCTC[A/G]GCTCACTGCAACCTC	158506
rs141246738	snp	C/T	0.00263281	0.0361866	missense, intron-variant	ZNF645, PTCHD1-AS	GRCh38.p7	X:22273743	ACTCAGATTCTGGTG[C/T]TAAGAAGCCAACACC	158506
rs141295358	snp	A/C	0.0302564	0.119217	upstream-variant-2KB, intron-variant	ZNF645, PTCHD1-AS	GRCh38.p7	X:22272612	TTGAGTACTGAAGAG[A/C]AGCATCAGCAACCTC	158506
rs141753613	snp	G/T	4.55809e-05	0.00477372	missense, intron-variant	ZNF645, PTCHD1-AS	GRCh38.p7	X:22273866	CTCCATCATCACCAG[G/T]AAACCATCAAATGCC	158506
rs142294017	snp	C/G	0.000136924	0.00827304	missense, intron-variant	ZNF645, PTCHD1-AS	GRCh38.p7	X:22273340	TTCATGTGTAGTATT[C/G]TTCAGCAGTGCAAGA	158506
rs142781082	snp	C/G	0.000189982	0.00974449	missense, intron-variant	ZNF645, PTCHD1-AS	GRCh38.p7	X:22273000	AAGGAATATGAACAA[C/G]ATGCCTGCTGGTGAA	158506
rs142874640	snp	C/T	0.000251408	0.011209	missense, intron-variant	ZNF645, PTCHD1-AS	GRCh38.p7	X:22274193	TGTCACCTTGTCCAC[C/T]AACGCGGAGTCCACC	158506
rs143029068	snp	A/G	4.57661e-05	0.0047834	synonymous-codon, intron-variant	ZNF645, PTCHD1-AS	GRCh38.p7	X:22273687	CGTTAGTATTTTTAC[A/G]AGAAAACATGGCAAT	158506
rs144175358	snp	C/T	0.000189982	0.00974449	missense, intron-variant	ZNF645, PTCHD1-AS	GRCh38.p7	X:22273271	GGATATAAAGTATGT[C/T]CGCGCTGTCGTTATC	158506
rs144353133	snp	C/T	0.00581083	0.0535878	upstream-variant-2KB, intron-variant	ZNF645, PTCHD1-AS	GRCh38.p7	X:22271417	TACTTAACAAGAATA[C/T]CACCTTCCCCATCAA	158506
rs144357703	snp	A/G	2.28128e-05	0.00337726	synonymous-codon, intron-variant	ZNF645, PTCHD1-AS	GRCh38.p7	X:22273468	TCCTCATATTGCTCC[A/G]CCACAAACTGAAATC	158506
rs145057529	snp	C/T	0.000529661	0.016265	upstream-variant-2KB, intron-variant	ZNF645, PTCHD1-AS	GRCh38.p7	X:22272676	CCCTCACTAGAGTGG[C/T]GGGACAGGGTAGGTG	158506
rs146303957	snp	A/G/T	0.000296252	0.0121677	synonymous-codon, missense, intron-variant	ZNF645, PTCHD1-AS	GRCh38.p7	X:22273981	ATATATTATTGTAAA[A/G/T]GTGCCACCTGATATG	158506
rs146331121	snp	C/T	9.13096e-05	0.00675622	stop-gained, intron-variant	ZNF645, PTCHD1-AS	GRCh38.p7	X:22273415	CGCCATAAGAGAGCT[C/T]GAAAACAAGTTACCA	158506
rs146611118	snp	A/G	2.28097e-05	0.00337703	synonymous-codon, intron-variant	ZNF645, PTCHD1-AS	GRCh38.p7	X:22273474	TATTGCTCCGCCACA[A/G]ACTGAAATCTCTGAC	158506
rs146977013	snp	A/C	2.28136e-05	0.00337732	missense, intron-variant	ZNF645, PTCHD1-AS	GRCh38.p7	X:22273805	CCAGCGGTATCGTCC[A/C]CTCATCATATTATAC	158506
rs147382653	snp	C/T	0.00235482	0.0342325	missense, intron-variant	ZNF645, PTCHD1-AS	GRCh38.p7	X:22274198	CCTTGTCCACCAACG[C/T]GGAGTCCACCTCCTT	158506
rs147408051	snp	A/G/T	0.00113649	0.0238112	missense, intron-variant	ZNF645, PTCHD1-AS	GRCh38.p7	X:22273088	AGAAAAAAGAAAAAA[A/G/T]TTCCTGGTTACCGTT	158506
rs147787234	snp	C/T	0.000114553	0.00756725	missense, intron-variant	ZNF645, PTCHD1-AS	GRCh38.p7	X:22273719	TAACAGTTGATCATA[C/T]TCAGAATAACTCAGA	158506
rs148712606	snp	A/G	6.84611e-05	0.00585029	synonymous-codon, intron-variant	ZNF645, PTCHD1-AS	GRCh38.p7	X:22273273	ATATAAAGTATGTCC[A/G]CGCTGTCGTTATCCT	158506
rs149337344	snp	A/C	0.00186705	0.0304965	missense, intron-variant	ZNF645, PTCHD1-AS	GRCh38.p7	X:22273926	ACTCGGTTCGTAGCC[A/C]AGTGCCAGCTCTAAC	158506
rs149542720	snp	C/T	4.61782e-05	0.00480489	missense, intron-variant	ZNF645, PTCHD1-AS	GRCh38.p7	X:22273100	AAAATTCCTGGTTAC[C/T]GTTGGGGGGACATTA	158506
rs150664878	snp	A/C/G	0.000114082	0.00755179	synonymous-codon, intron-variant	ZNF645, PTCHD1-AS	GRCh38.p7	X:22273801	TCAACCAGCGGTATC[A/C/G]TCCCCTCATCATATT	158506
rs150907787	snp	G/T	0.0605624	0.163136	upstream-variant-2KB, intron-variant	ZNF645, PTCHD1-AS	GRCh38.p7	X:22270962	CAAGAGTCAACAACT[G/T]GGCCAGGCGCGGTGG	158506
rs151015591	snp	C/T	0.00633741	0.0559334	upstream-variant-2KB, intron-variant	ZNF645, PTCHD1-AS	GRCh38.p7	X:22272228	ACGATCTGCCTGCCT[C/T]GGCCTTCCAAAGTGC	158506
rs180830452	snp	C/G	0.000529661	0.016265	upstream-variant-2KB, intron-variant	ZNF645, PTCHD1-AS	GRCh38.p7	X:22271868	TGTGAGGAAATGTGG[C/G]CTAAATACCCATAAC	158506
rs180904294	snp	A/G	0.000529661	0.016265	downstream-variant-500B, intron-variant	ZNF645, PTCHD1-AS	GRCh38.p7	X:22274544	TACAGCTGTAAAAAT[A/G]CTATTTTATGTGAAC	158506
rs181036832	snp	G/T			upstream-variant-2KB, intron-variant	ZNF645, PTCHD1-AS	GRCh38.p7	X:22272034	GTCGCCCAGGCTGGA[G/T]TGCAGTGACGCGATC	158506
rs181797502	snp	C/G	0.00528398	0.051128	upstream-variant-2KB, intron-variant	ZNF645, PTCHD1-AS	GRCh38.p7	X:22271707	GGAGGGCACGGAGTA[C/G]GGGTTGACAGCCAAC	158506
rs183525998	snp	A/G	0.00105904	0.0229869	upstream-variant-2KB, intron-variant	ZNF645, PTCHD1-AS	GRCh38.p7	X:22272691	TGGGACAGGGTAGGT[A/G]AGGAGAGAAGGAAGC	158506
rs183894704	snp	A/G	0.00633741	0.0559334	upstream-variant-2KB, intron-variant	ZNF645, PTCHD1-AS	GRCh38.p7	X:22271109	AATTAGCCAGGTGTG[A/G]TGGCACATGCCTATA	158506
rs184196652	snp	C/T	0.00105904	0.0229869	upstream-variant-2KB, intron-variant	ZNF645, PTCHD1-AS	GRCh38.p7	X:22271550	CCTGAAACCACCCAA[C/T]TTAGTCCCTAATAAC	158506
rs184448876	snp	A/C	0.00791544	0.0624105	upstream-variant-2KB, intron-variant	ZNF645, PTCHD1-AS	GRCh38.p7	X:22271327	TAATCCATGTTGAGA[A/C]TAAGCAAACTTAGCT	158506
rs184716539	snp	A/T	0.00105904	0.0229869	downstream-variant-500B, intron-variant	ZNF645, PTCHD1-AS	GRCh38.p7	X:22274482	GTGGTTTTTATTTTT[A/T]TATTTTTTGGTGATA	158506
rs185237932	snp	G/T	0.00158814	0.0281345	upstream-variant-2KB, intron-variant	ZNF645, PTCHD1-AS	GRCh38.p7	X:22271890	ACCCATAACCCTTTT[G/T]AAAATTAAGCAAGAA	158506
rs185501024	snp	C/G	0.0287145	0.11633	upstream-variant-2KB, intron-variant	ZNF645, PTCHD1-AS	GRCh38.p7	X:22272124	TGAGATTACAGGCGC[C/G]TGCCACCATGCCTAG	158506
rs185586921	snp	C/G	0.00158814	0.0281345	upstream-variant-2KB, intron-variant	ZNF645, PTCHD1-AS	GRCh38.p7	X:22271734	CAACGAAGCTAAAAG[C/G]GTGAATGTCTGCACA	158506
rs186622393	snp	C/G	2.29621e-05	0.00338829	missense, intron-variant	ZNF645, PTCHD1-AS	GRCh38.p7	X:22273138	CATCATAGGTGAAAA[C/G]GATGATTTACCAATT	158506
rs187097397	snp	A/C	0.00317376	0.039709	upstream-variant-2KB, intron-variant	ZNF645, PTCHD1-AS	GRCh38.p7	X:22271463	TCTCCTCCTGCTATG[A/C]CCACCAATCTACAGC	158506
rs187258946	snp	C/T	2.28851e-05	0.00338261	missense, intron-variant	ZNF645, PTCHD1-AS	GRCh38.p7	X:22273563	CCATGGTGTCACTAC[C/T]GTCTGTGCAACATAT	158506
rs187271405	snp	C/T	0.00475684	0.0485365	upstream-variant-2KB, intron-variant	ZNF645, PTCHD1-AS	GRCh38.p7	X:22272811	ATGCGCACGTGTTAC[C/T]GGCACATGACTCCCG	158506
rs188835886	snp	A/G	0.00211696	0.0324653	upstream-variant-2KB, intron-variant	ZNF645, PTCHD1-AS	GRCh38.p7	X:22271253	TACTGAAACCAACAT[A/G]ATTCTCTGTCGCTGT	158506
rs188918118	snp	C/T	0.000529661	0.016265	upstream-variant-2KB, intron-variant	ZNF645, PTCHD1-AS	GRCh38.p7	X:22271700	TTTTAGGGGAGGGCA[C/T]GGAGTAGGGGTTGAC	158506
rs190500499	snp	A/G	0.00475684	0.0485365	upstream-variant-2KB, intron-variant	ZNF645, PTCHD1-AS	GRCh38.p7	X:22271788	ATTATGGGTGGAGTG[A/G]AGGCAGAAAAATATG	158506
rs190506241	snp	A/G	0.00158814	0.0281345	upstream-variant-2KB, intron-variant	ZNF645, PTCHD1-AS	GRCh38.p7	X:22270927	TTGGGGCATTGTTGC[A/G]TTTTCACCATTAGTG	158506
rs190603898	snp	C/T	0.000227884	0.0106719	synonymous-codon, intron-variant	ZNF645, PTCHD1-AS	GRCh38.p7	X:22274152	AGATGCAATGGATCA[C/T]AGAAGGTGGCCTGCA	158506
rs191471321	snp	A/G	2.28217e-05	0.00337792	missense, intron-variant	ZNF645, PTCHD1-AS	GRCh38.p7	X:22273355	GTTCAGCAGTGCAAG[A/G]GAACATACTTGTCTC	158506
rs191695581	snp	C/G			upstream-variant-2KB, intron-variant	ZNF645, PTCHD1-AS	GRCh38.p7	X:22272652	GCTTTTTCTTTCTCT[C/G]CCCAAATTCCCTCAC	158506
rs191904272	snp	C/T	0.00581083	0.0535878	upstream-variant-2KB, intron-variant	ZNF645, PTCHD1-AS	GRCh38.p7	X:22271484	AATCTACAGCTATTA[C/T]GTCACAAAATCTACC	158506
rs192067453	snp	A/G	0.000794774	0.0199187	utr-variant-5-prime, intron-variant	ZNF645, PTCHD1-AS	GRCh38.p7	X:22272972	GACAAACCTAAATAT[A/G]TGTCTGAACTCCAAG	158506
rs192607182	snp	C/T			upstream-variant-2KB, intron-variant	ZNF645, PTCHD1-AS	GRCh38.p7	X:22271285	TAAAACAATAACAGA[C/T]GTGGGAATAGTTTTC	158506
rs200078401	snp	A/G	0.000529661	0.016265	missense, intron-variant	ZNF645, PTCHD1-AS	GRCh38.p7	X:22273527	GGGACCATCTAAGCT[A/G]TATTCCACCAGAACA	158506
rs200330462	snp	A/C			upstream-variant-2KB, intron-variant	ZNF645, PTCHD1-AS	GRCh38.p7	X:22272537	AAAGCTCTGCAGGGC[A/C]TGCTGGGAATTTATT	158506
rs200644599	in-del	-/G	0.0525796	0.153379	upstream-variant-2KB, intron-variant	ZNF645, PTCHD1-AS	GRCh38.p7	X:22271141	CCCATCTACTTGGAA[-/G]GGAAAAAAAAAAAAA	158506
rs200886998	snp	C/G	2.28264e-05	0.00337826	missense, intron-variant	ZNF645, PTCHD1-AS	GRCh38.p7	X:22273433	AAACAAGTTACCAGC[C/G]CTTCGCTTGAAAAAG	158506
rs201219167	in-del	-/A			downstream-variant-500B, intron-variant	ZNF645, PTCHD1-AS	GRCh38.p7	X:22274484	GGTTTTTATTTTTTT[-/A]TTTTTTGGTGATATG	158506
rs201362226	in-del	-/G			upstream-variant-2KB, intron-variant	ZNF645, PTCHD1-AS	GRCh38.p7	X:22271959	CATCTATTCACTCCT[-/G]GTTTTTTTTTTTTTT	158506
rs201655784	snp	A/G	4.58432e-05	0.00478743	missense, intron-variant	ZNF645, PTCHD1-AS	GRCh38.p7	X:22273740	ATAACTCAGATTCTG[A/G]TGCTAAGAAGCCAAC	158506
rs201682184	snp	A/G	6.83659e-05	0.00584622	missense, intron-variant	ZNF645, PTCHD1-AS	GRCh38.p7	X:22274102	CCTCAGTTCACCGAA[A/G]ATCAAGAAACCTTGA	158506

Full records

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