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
rs1060782	snp	A/C	0	0	upstream-variant-2KB, intron-variant, nc-transcript-variant, downstream-variant-500B	LBX2, PCGF1, LBX2-AS1	GRCh38.p7	2:74504612	TCCTGTGGCCCCACT[A/C]CATTTGTTTTTTAGA	84759
rs2240442	snp	A/G	0.133435	0.221162	intron-variant	PCGF1	GRCh38.p7	2:74506646	TTTGGTAGGACTCAC[A/G]TAGGCAGAAGGCCAA	84759
rs2240443	snp	A/C	0.405732	0.19557	upstream-variant-2KB, intron-variant, downstream-variant-500B	LBX2, PCGF1, LBX2-AS1	GRCh38.p7	2:74505288	TTCAGACTCCCCCCA[A/C]CCATCCTACAGTCCT	84759
rs3192661	snp	C/T	8.61735e-05	0.00656348	intron-variant	PCGF1	GRCh38.p7	2:74507192	GGAAGGCGCACGGGT[C/T]GGGGTTTGAGGGTGG	84759
rs3806607	snp	A/G	0.493703	0.0557558	upstream-variant-2KB, nc-transcript-variant	PCGF1	GRCh38.p7	2:74508487	TTTTTAAGTACCCAG[A/G]GCCGGCGGTGTAGAG	84759
rs5024139	snp	A/C	0.5	0	upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	LBX2, PCGF1, LBX2-AS1	GRCh38.p7	2:74505085	AATAAAGCTGCAGTT[A/C]ATTTCACATAAATAT	84759
rs5024140	snp	A/T	0.5	0	upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	LBX2, PCGF1, LBX2-AS1	GRCh38.p7	2:74505091	GCTGCAGTTCATTTC[A/T]CATAAATATCTGGGG	84759
rs5024141	snp	C/T	0.5	0	upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	LBX2, PCGF1, LBX2-AS1	GRCh38.p7	2:74505092	CTGCAGTTCATTTCA[C/T]ATAAATATCTGGGGA	84759
rs5024143	snp	A/G	0.5	0	upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	LBX2, PCGF1, LBX2-AS1	GRCh38.p7	2:74505131	GAGTGGGATGGGGTG[A/G]GGGCTTGGCCCCTAC	84759
rs5024144	snp	C/T	0.5	0	upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	LBX2, PCGF1, LBX2-AS1	GRCh38.p7	2:74505135	GGGATGGGGTGGGGG[C/T]TTGGCCCCTACCTCC	84759
rs17010004	snp	C/G	0.148996	0.228688	intron-variant	PCGF1	GRCh38.p7	2:74507239	TCCTTCATCACACTA[C/G]ACGGCCAAGCCCCGC	84759
rs35595209	in-del	-/A			frameshift-variant, nc-transcript-variant	PCGF1	GRCh38.p7	2:74506813	CAGTGGCTGTGTCTC[-/A]GTGGATCTTAATGTT	84759
rs41285989	snp	C/T	0.000494291	0.0157131	intron-variant	PCGF1	GRCh38.p7	2:74506164	GGGTCTTTACTGTCC[C/T]GCGGCCAAGGACATA	84759
rs41285991	snp	C/T	0.151251	0.229671	intron-variant	PCGF1	GRCh38.p7	2:74506707	AGTCCTCAAGAGGCC[C/T]CTCAAAGTCAGGTTG	84759
rs72818086	snp	G/T	0.00924125	0.0673441	missense, downstream-variant-500B, nc-transcript-variant	PCGF1, LBX2-AS1	GRCh38.p7	2:74505365	AGCGGGAGAGCCATA[G/T]CTGCTTCATTGTCAT	84759
rs72818087	snp	A/G	1.64741e-05	0.00286998	synonymous-codon, nc-transcript-variant	PCGF1	GRCh38.p7	2:74506814	CAGTGGCTGTGTCTC[A/G]TGGATCTTAATGTTG	84759
rs73949674	snp	A/G	0.5	0	upstream-variant-2KB	PCGF1	GRCh38.p7	2:74509281	GAGCTTCCCTTTTCA[A/G]TCAGAATGAAAGTCA	84759
rs75600937	snp	A/C/G/T	0.0131133	0.0801018	upstream-variant-2KB, nc-transcript-variant	PCGF1	GRCh38.p7	2:74507861	AATTAAGGAGTGGGG[A/C/G/T]GGGGGGAGCACAGGG	84759
rs76022282	snp	C/G	0.5	0	upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	LBX2, PCGF1, LBX2-AS1	GRCh38.p7	2:74505108	ATAAATATCTGGGGA[C/G]GGAAGGGGAGTGGGA	84759
rs76860347	snp	A/C			splice-acceptor-variant, downstream-variant-500B	PCGF1, LBX2-AS1	GRCh38.p7	2:74505420	AAAAAGGAGCTGCAC[A/C]TAGGAGGGAGATGGG	84759
rs77154120	snp	C/T	0.5	0	upstream-variant-2KB, utr-variant-3-prime, nc-transcript-variant	LBX2, PCGF1, LBX2-AS1	GRCh38.p7	2:74505059	GCTTTTTAAAAGTTT[C/T]TATTTCAAAAAATAA	84759
rs77597989	snp	A/C/G	0.000129157	0.00803505	upstream-variant-2KB, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	LBX2, PCGF1, LBX2-AS1	GRCh38.p7	2:74505104	TCACATAAATATCTG[A/C/G]GGAGGGAAGGGGAGT	84759
rs77847000	snp	A/G	0.101315	0.20098	upstream-variant-2KB, missense, downstream-variant-500B, nc-transcript-variant	LBX2, PCGF1, LBX2-AS1	GRCh38.p7	2:74505189	AAAAGCAAAGGGGAT[A/G]GCTAAGGAGAGAATG	84759
rs78352764	snp	C/G	0.5	0	upstream-variant-2KB	PCGF1	GRCh38.p7	2:74509444	AGGCTGCTGTAATCA[C/G]TCTAGATGAATAACA	84759
rs78921032	snp	C/T	0.300288	0.24489	missense, intron-variant	PCGF1	GRCh38.p7	2:74505997	TCATCATAGCGATAG[C/T]AGTGGGCTTTAGAGT	84759
rs79220597	snp	C/T	0.00886798	0.0659951	intron-variant	PCGF1	GRCh38.p7	2:74506926	AGGCCCTCTGGAAAC[C/T]GGATTCATGGGCTGG	84759
rs80278338	snp	C/T	0.0248432	0.108648	upstream-variant-2KB, nc-transcript-variant	PCGF1	GRCh38.p7	2:74507971	GCGAAAGACTGCCCC[C/T]TCCTACCCCCAAAGG	84759
rs111643889	snp	C/T	0.00993419	0.0697739	upstream-variant-2KB	PCGF1	GRCh38.p7	2:74508942	GGTCCGAGCCACTAT[C/T]ATCTGTCCTCTGTAG	84759
rs111794312	snp	C/T	0.5	0	synonymous-codon, nc-transcript-variant	PCGF1	GRCh38.p7	2:74507609	CATCTTGTACACTGA[C/T]TGGAGCTGGTTCCGA	84759
rs112122276	snp	C/G	0.00263655	0.0362122	intron-variant, downstream-variant-500B	PCGF1, LBX2-AS1	GRCh38.p7	2:74505471	CTGGCAGGTCAAAAA[C/G]TACCCTGGTCCACCC	84759
rs113463685	snp	A/C			intron-variant	PCGF1	GRCh38.p7	2:74507152	CGAACCTCCTCCTGA[A/C]GATACACCCTCCGTC	84759
rs114370770	snp	A/G	0.0111196	0.0737302	upstream-variant-2KB, nc-transcript-variant	PCGF1	GRCh38.p7	2:74508032	GGTCGTCGGTCTTCT[A/G]TGACGACGACCCTGC	84759
rs115156451	snp	A/G	0.0119091	0.0762411	intron-variant	PCGF1	GRCh38.p7	2:74507242	TTCATCACACTAGAC[A/G]GCCAAGCCCCGCGCC	84759
rs116112081	snp	A/G	0.0655868	0.168795	upstream-variant-2KB	PCGF1	GRCh38.p7	2:74509676	TTTTTTTCCTCTGTT[A/G]TGTTCACAGATATAG	84759
rs116551748	snp	A/C	0.00914312	0.0669923	intron-variant	PCGF1	GRCh38.p7	2:74507256	CGGCCAAGCCCCGCG[A/C]CCTGCGCCATCAGCC	84759
rs117505699	snp	A/C/T	3.29697e-05	0.00406005	missense, nc-transcript-variant	PCGF1	GRCh38.p7	2:74505574	GGGTTTAGCATCAAG[A/C/T]GGTGACACAGGACCC	84759
rs117835471	snp	A/C	8.79159e-05	0.0066295	utr-variant-5-prime, nc-transcript-variant	PCGF1	GRCh38.p7	2:74507673	GGAGACGCCATCTTA[A/C]AGGCTGATCCCAGCC	84759
rs138216462	snp	A/C	0.00636936	0.0560724	upstream-variant-2KB, nc-transcript-variant	PCGF1	GRCh38.p7	2:74507916	TGTAGAAATCATCAT[A/C]ATAGGCCCTACGCGA	84759
rs140632466	snp	A/G	0.000177226	0.00941179	synonymous-codon, nc-transcript-variant	PCGF1	GRCh38.p7	2:74507624	CTGGAGCTGGTTCCG[A/G]AGCCTCATCGCGATC	84759
rs142233300	snp	C/G	0.000152805	0.00873951	upstream-variant-2KB, intron-variant, downstream-variant-500B	LBX2, PCGF1, LBX2-AS1	GRCh38.p7	2:74505312	GTCTGAAGGGGGTGT[C/G]ATCCCAGGGAGGGTG	84759
rs143031369	snp	C/G	0.00119737	0.0244387	upstream-variant-2KB, nc-transcript-variant	PCGF1	GRCh38.p7	2:74508467	GCGGGGTGCTCGCTC[C/G]AGAGCTCTACACCGC	84759
rs143464189	snp	A/G	1.64895e-05	0.00287132	missense, downstream-variant-500B, nc-transcript-variant	PCGF1, LBX2-AS1	GRCh38.p7	2:74505559	CTACTCACATGCTGA[A/G]GGTTTAGCATCAAGC	84759
rs143569594	snp	A/G	9.89266e-05	0.00703232	intron-variant	PCGF1	GRCh38.p7	2:74506912	AAAAGCAGATTCTCA[A/G]GCCCTCTGGAAACTG	84759
rs144121264	snp	C/T	1.64876e-05	0.00287116	missense, nc-transcript-variant	PCGF1	GRCh38.p7	2:74505567	ATGCTGAGGGTTTAG[C/T]ATCAAGCGGTGACAC	84759
rs144134701	snp	C/T	0.00027651	0.0117549	missense, downstream-variant-500B, nc-transcript-variant	PCGF1, LBX2-AS1	GRCh38.p7	2:74505352	ACCTTGCCGAACCAG[C/T]GGGAGAGCCATATCT	84759
rs145551425	snp	C/G/T	0.00402715	0.0446924	intron-variant	PCGF1	GRCh38.p7	2:74505805	GGTTAGGGAATCCTA[C/G/T]CTTTCCTCCTCTTCC	84759
rs145617098	snp	C/T	0.00279162	0.0372561	upstream-variant-2KB, nc-transcript-variant	PCGF1	GRCh38.p7	2:74507819	TGCTCACCTGAGCCC[C/T]ACCGGCCCCTCCCCT	84759
rs147573775	snp	C/T	5.10243e-05	0.0050507	upstream-variant-2KB, intron-variant, downstream-variant-500B	LBX2, PCGF1, LBX2-AS1	GRCh38.p7	2:74505228	GTAGTCAGTGGGGAA[C/T]GTTCTTATATTATTC	84759
rs148319271	snp	C/T	0.000798403	0.0199641	intron-variant	PCGF1	GRCh38.p7	2:74507468	GCGCACTGGGCACTC[C/T]GTCTCTGCGCAGGCG	84759
rs148848478	snp	C/T	0.000153988	0.00877328	missense, downstream-variant-500B, nc-transcript-variant	PCGF1, LBX2-AS1	GRCh38.p7	2:74505404	GGAGAACTTCATTGT[C/T]AAAAAGGAGCTGCAC	84759
rs148881124	snp	C/T	0.00121947	0.0246627	intron-variant	PCGF1	GRCh38.p7	2:74505918	CTGGGTCATTGGCAC[C/T]GTCACCTCCTGCAAC	84759
rs149397277	snp	C/T	0.00358779	0.0422022	upstream-variant-2KB	PCGF1	GRCh38.p7	2:74509478	CACCCACCCTTTCAC[C/T]TCCTTGCTCTTTTTT	84759
rs149582140	snp	C/T	0.00289716	0.0379498	missense, intron-variant	PCGF1	GRCh38.p7	2:74506202	CAGTGGGCTGGGTGA[C/T]CCGGTCCAAACCTCG	84759
rs150786268	snp	A/G			upstream-variant-2KB, intron-variant, nc-transcript-variant, downstream-variant-500B	LBX2, PCGF1, LBX2-AS1	GRCh38.p7	2:74504896	GTTTCACACATATAG[A/G]GATCCTCTACCCTTC	84759
rs150874982	snp	A/C/T	0.000131836	0.008118	missense, nc-transcript-variant	PCGF1	GRCh38.p7	2:74505601	ACCCTCCGGAGATGG[A/C/T]GTACCTCAGCTCTAA	84759
rs180955861	snp	G/T	0.00993419	0.0697739	upstream-variant-2KB, nc-transcript-variant	PCGF1	GRCh38.p7	2:74508177	GCTTTGCAGAGTCTC[G/T]GAGAGGGTGCCGGGG	84759
rs181340250	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	PCGF1, LBX2-AS1	GRCh38.p7	2:74505482	AAAACTACCCTGGTC[C/T]ACCCTAGACTCTGTC	84759
rs181766336	snp	A/G	0.00159617	0.0282053	upstream-variant-2KB, intron-variant, nc-transcript-variant, downstream-variant-500B	LBX2, PCGF1, LBX2-AS1	GRCh38.p7	2:74504675	TTATAAAACTATAAT[A/G]CAATTCTTTGGATTT	84759
rs182625168	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	PCGF1	GRCh38.p7	2:74509249	GTTGTTCCTTTTTTA[C/T]GTTTAAAACCTGTTG	84759
rs182797844	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB	PCGF1	GRCh38.p7	2:74508878	CAAGAAGTTATGAGA[A/T]TAGTGATTAATCAAT	84759
rs183212992	snp	A/G			upstream-variant-2KB	PCGF1	GRCh38.p7	2:74508662	TGGTGAAATAGAAAG[A/G]ACGTGGAGGGGAATG	84759
rs184354450	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB, intron-variant, nc-transcript-variant, downstream-variant-500B	LBX2, PCGF1, LBX2-AS1	GRCh38.p7	2:74504858	ACCTTCCCATCACCA[A/G]AAAGAGTGGTGTGGG	84759
rs185419211	snp	C/T	3.30546e-05	0.00406524	intron-variant, downstream-variant-500B	PCGF1, LBX2-AS1	GRCh38.p7	2:74505522	TTAGCCCCTTCTCCC[C/T]CTCAAGAAACCTACT	84759
rs185950692	snp	A/G	3.29462e-05	0.00405857	synonymous-codon, intron-variant	PCGF1	GRCh38.p7	2:74506038	GCTGAAGGGGAGGCC[A/G]AGGTTGCTCAGTGCT	84759
rs185950710	snp	C/T	0.00318978	0.0398085	upstream-variant-2KB, nc-transcript-variant	PCGF1	GRCh38.p7	2:74508211	GGGGAGTGAGAGACC[C/T]CCAGGGACTTGGTAG	84759
rs187670961	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	PCGF1	GRCh38.p7	2:74508668	AATAGAAAGGACGTG[G/T]AGGGGAATGACCAGA	84759
rs187882706	snp	C/T	0.00517822	0.0506191	upstream-variant-2KB	PCGF1	GRCh38.p7	2:74509052	GATTCTGATAAAACA[C/T]GAAACACAAAGGACA	84759
rs188933540	snp	A/G	5.68037e-05	0.00532903	intron-variant, downstream-variant-500B	PCGF1, LBX2-AS1	GRCh38.p7	2:74505327	GATCCCAGGGAGGGT[A/G]GCCTGGCTTACCTTG	84759
rs190465152	snp	A/T			upstream-variant-2KB, intron-variant, nc-transcript-variant, downstream-variant-500B	LBX2, PCGF1, LBX2-AS1	GRCh38.p7	2:74504639	TAGACTTCTCCCTCC[A/T]TTTTGTCCCCATCCC	84759
rs190595537	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	PCGF1	GRCh38.p7	2:74508866	GTGAATATGCAGCAA[C/G]AAGTTATGAGATTAG	84759
rs191140721	snp	C/T	0.00159617	0.0282053	intron-variant	PCGF1	GRCh38.p7	2:74506404	AACATGGTGAAACCC[C/T]GTCTCTACTAAAAAA	84759
rs191999052	snp	C/G	0.0115144	0.0749975	upstream-variant-2KB, nc-transcript-variant	PCGF1	GRCh38.p7	2:74508251	TCCCCCATTCTCCCC[C/G]CTGCTGCCGGGGATG	84759
rs192852437	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB	PCGF1	GRCh38.p7	2:74509075	AAAGGACAAAGGACA[A/G]TTTTTGAGATGTGGA	84759
rs199697372	snp	C/T	0.0515954	0.152104	missense, intron-variant	PCGF1	GRCh38.p7	2:74505973	CGCTCCAGGCACAGG[C/T]TCAACTGCTCATCAT	84759
rs200118363	snp	C/T	0.071262	0.174793	missense, intron-variant	PCGF1	GRCh38.p7	2:74506045	GGGAGGCCGAGGTTG[C/T]TCAGTGCTGGCTCTG	84759
rs200377150	snp	C/G	0.000165333	0.00909061	intron-variant, downstream-variant-500B	PCGF1, LBX2-AS1	GRCh38.p7	2:74505514	CTCCTTTCTTAGCCC[C/G]TTCTCCCCCTCAAGA	84759
rs200556348	snp	A/G	1.64741e-05	0.00286998	missense, intron-variant	PCGF1	GRCh38.p7	2:74506048	AGGCCGAGGTTGCTC[A/G]GTGCTGGCTCTGAGA	84759
rs200641357	snp	G/T	0.280878	0.248086	missense, intron-variant	PCGF1	GRCh38.p7	2:74506000	TCATAGCGATAGTAG[G/T]GGGCTTTAGAGTGGT	84759
rs200678431	snp	A/G	0.0813875	0.18458	synonymous-codon, intron-variant	PCGF1	GRCh38.p7	2:74505977	CCAGGCACAGGTTCA[A/G]CTGCTCATCATAGCG	84759
rs200707864	snp	C/G	0.0610156	0.163661	missense, intron-variant	PCGF1	GRCh38.p7	2:74506049	GGCCGAGGTTGCTCA[C/G]TGCTGGCTCTGAGAA	84759
rs200862116	snp	A/G	0.000149245	0.00863714	intron-variant	PCGF1	GRCh38.p7	2:74506268	CTAGAAGAAGGTGAA[A/G]TATGAGAATAAAGTA	84759
rs200904086	snp	A/G			missense, nc-transcript-variant	PCGF1	GRCh38.p7	2:74505614	GGCGTACCTCAGCTC[A/G]AACAGAACATCGGAC	84759
rs201019641	snp	A/G	2.00914e-05	0.00316943	intron-variant, downstream-variant-500B	PCGF1, LBX2-AS1	GRCh38.p7	2:74505467	CTTTCTGGCAGGTCA[A/G]AAACTACCCTGGTCC	84759
rs201054134	snp	A/C/G	4.94173e-05	0.00497053	missense, intron-variant	PCGF1	GRCh38.p7	2:74505992	ACTGCTCATCATAGC[A/C/G]ATAGTAGTGGGCTTT	84759
rs201312933	snp	C/T	3.31334e-05	0.00407009	intron-variant	PCGF1	GRCh38.p7	2:74505816	CCTATCTTTCCTCCT[C/T]TTCCCCACCCAGAGC	84759
rs201383050	snp	C/T	0.00199804	0.031544	missense, intron-variant	PCGF1	GRCh38.p7	2:74505958	TCTCCTCACCTCAGC[C/T]GCTCCAGGCACAGGT	84759
rs201559196	snp	A/G/T	7.45666e-05	0.00610555	missense, downstream-variant-500B, nc-transcript-variant	PCGF1, LBX2-AS1	GRCh38.p7	2:74505353	CCTTGCCGAACCAGC[A/G/T]GGAGAGCCATATCTG	84759
rs201679071	snp	A/G	0.000560113	0.0167255	intron-variant	PCGF1	GRCh38.p7	2:74506149	AAGAAGAATGCTCTG[A/G]GGTCTTTACTGTCCC	84759
rs201836803	snp	A/G	3.29919e-05	0.00406138	missense, intron-variant	PCGF1	GRCh38.p7	2:74506219	CGGTCCAAACCTCGG[A/G]ACTGGTAGAATTCCC	84759
rs201906065	snp	A/C	0.000527313	0.0162289	intron-variant	PCGF1	GRCh38.p7	2:74506897	AGACTGCAGGAAAAG[A/C]AAAGCAGATTCTCAG	84759
rs202099071	snp	A/C	0.00339088	0.0410358	intron-variant	PCGF1	GRCh38.p7	2:74507559	CGACCACAGCAGTAA[A/C]CCTGCCGCCCTTGCA	84759
rs202141276	snp	A/C/G	1.64789e-05	0.0028704	intron-variant	PCGF1	GRCh38.p7	2:74505671	AGGGAAGAGGGCAAG[A/C/G]TGTGTGAGGGAAGGA	84759
rs368170536	snp	A/C/G	0.000769544	0.0196005	intron-variant	PCGF1	GRCh38.p7	2:74507197	CTCAAACCCCAACCC[A/C/G]TGCGCCTTCCCACCT	84759
rs368396183	snp	A/G			upstream-variant-2KB, intron-variant, nc-transcript-variant, downstream-variant-500B	LBX2, PCGF1, LBX2-AS1	GRCh38.p7	2:74504592	AAGCCTCCATTTCTG[A/G]CAATTCCTGTGGCCC	84759
rs368528693	snp	A/G	3.30202e-05	0.00406313	intron-variant	PCGF1	GRCh38.p7	2:74506935	GGAAACTGGATTCAT[A/G]GGCTGGGTGGGGTGC	84759
rs368548736	snp	C/T	1.64795e-05	0.00287045	intron-variant	PCGF1	GRCh38.p7	2:74506144	TGGGCAAGAAGAATG[C/T]TCTGGGGTCTTTACT	84759
rs369013269	snp	A/G	8.23988e-05	0.00641815	missense, nc-transcript-variant	PCGF1	GRCh38.p7	2:74505602	CCCTCCGGAGATGGC[A/G]TACCTCAGCTCTAAC	84759
rs369110833	snp	A/G	0.000181259	0.00951824	intron-variant	PCGF1	GRCh38.p7	2:74506165	GGTCTTTACTGTCCC[A/G]CGGCCAAGGACATAC	84759
rs369200306	snp	A/G	0.000153988	0.00877328	upstream-variant-2KB, synonymous-codon, downstream-variant-500B, nc-transcript-variant	LBX2, PCGF1, LBX2-AS1	GRCh38.p7	2:74505167	CTTCTCTTTCACACT[A/G]TATTGTAAAAGCAAA	84759
rs369371639	snp	C/T	4.37646e-05	0.00467765	intron-variant, downstream-variant-500B	PCGF1, LBX2-AS1	GRCh38.p7	2:74505432	CACCTAGGAGGGAGA[C/T]GGGGGCATAATTTTA	84759

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