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

TRIM3

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs561479405	snp	G/T			intron-variant	TRIM3	GRCh38.p7	11:6469216	TCCTGCTGGGGTAGC[G/T]GGATGCCAGGCTCCA	10612
rs561671977	snp	A/G	5.138e-05	0.00506827	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6457703	GTGCCTACCGGCCAC[A/G]CACAGCCTCGAGCTG	10612
rs561673882	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6464283	CCCTACCAGGCTTCC[C/T]CCAGGCCTCTTACCT	10612
rs561735237	snp	A/G	3.38123e-05	0.00411157	missense, utr-variant-5-prime, nc-transcript-variant	TRIM3	GRCh38.p7	11:6458132	GGGTGGGGGTCCTCC[A/G]GGTCGTGGGCCCCAT	10612
rs561799505	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6470505	AACTCCTGGGCTCAA[C/T]TAATCCTCCTGCCTT	10612
rs561921319	snp	A/T	0.000798403	0.0199641	intron-variant	TRIM3	GRCh38.p7	11:6469880	TTTAGTAACTCCTAA[A/T]GAAAGTAACGTTCAA	10612
rs562065667	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6452918	ATTTCCAGGTCACTT[C/T]TTCAGAGAAGACTAA	10612
rs562213162	snp	A/C	0.000798403	0.0199641	intron-variant	TRIM3	GRCh38.p7	11:6457998	CCCAGCCACTCGGCA[A/C]CCCCCAATGCCTCTC	10612
rs562422353	snp	A/T	0.00279162	0.0372561	intron-variant	TRIM3	GRCh38.p7	11:6469949	TCAGGAGGCTGAATC[A/T]GACACTGTGATGGGA	10612
rs562442430	snp	A/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6471489	TGAAATTCATGGCCA[A/T]CTCCCCCAACATTGC	10612
rs562473417	in-del	-/TTCAGTGCG	0.00159617	0.0282053	intron-variant	TRIM3	GRCh38.p7	11:6455499	CAGAAACCATGTTCA[-/TTCAGTGCG]TTCAGTGCGGTTGAT	10612
rs562614263	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6470636	AGTGGAGAGGTCCAG[C/T]TGGCAGTTGGAAAGA	10612
rs562679669	snp	A/G	0.0023933	0.0345097	intron-variant	TRIM3	GRCh38.p7	11:6455515	TTCAGTGCGGTTGAT[A/G]CCATAATCAGGTGTA	10612
rs562710689	snp	A/G			intron-variant	TRIM3	GRCh38.p7	11:6466704	CTGGCCCCTTTTCCT[A/G]GCTGATGTGACACCT	10612
rs562770801	snp	C/T	0.000399281	0.0141238	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	TRIM3	GRCh38.p7	11:6458233	CTCTGGGAGGATGGA[C/T]GTCTGCCGGCATACT	10612
rs562935396	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6455439	ACAAGAAACAGAGGG[A/G]AAAAAAGGCACATTT	10612
rs563196566	snp	C/T	0.000798403	0.0199641	intron-variant	TRIM3	GRCh38.p7	11:6449247	TCTGTTTTGGGGGAA[C/T]GGGCATATGGGACAC	10612
rs563210952	snp	A/G			intron-variant	TRIM3	GRCh38.p7	11:6468006	AAATATTCATTGGCC[A/G]AGCAAGGTGGCTCAC	10612
rs563478472	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6468422	GGCACTTTCAGCAAT[A/G]AGAAGACATGAGCCC	10612
rs563535577	snp	A/G	0.000798403	0.0199641	intron-variant	TRIM3	GRCh38.p7	11:6462237	CAAGCTGCAGCTCTC[A/G]TTTTCTTGATTGCTT	10612
rs563801731	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6457167	GCCCACAGCACCTAC[C/T]GAGGGCATGTCAGGA	10612
rs563863888	snp	C/G	1.6525e-05	0.00287441	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6450940	CAAAACGGCCAACCA[C/G]TTTGCCATTGGGCTG	10612
rs563863960	snp	C/T	0.00119737	0.0244387	intron-variant	TRIM3	GRCh38.p7	11:6457539	GAACTTTCCCTTCTC[C/T]CTGGGGAACCTACTG	10612
rs563888817	snp	A/T	0.0111196	0.0737302	utr-variant-3-prime, upstream-variant-2KB	ARFIP2, TRIM3	GRCh38.p7	11:6475680	CCTTCAGGTCTCAGC[A/T]TTTTTTTTTTTTTTT	10612
rs563951036	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime, upstream-variant-2KB, downstream-variant-500B	ARFIP2, TRIM3	GRCh38.p7	11:6476247	TTTGCTGTATGAATG[A/C]ATGCATGATGAAGGT	10612
rs564072081	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6469772	GATGAGGAAGCACCA[A/G]TTGCTCCAGGAGTAC	10612
rs564318768	snp	A/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6457225	GAGCTGGTGTGGAAG[A/T]CAGAGGAACAATGGA	10612
rs564504825	snp	A/G	0.00119737	0.0244387	intron-variant	TRIM3	GRCh38.p7	11:6452242	CCTCTCCCTTCTCCA[A/G]CCTCCTCTAATTTAG	10612
rs564505767	snp	C/T			intron-variant	TRIM3	GRCh38.p7	11:6467270	GGGAGAAAAATGGTA[C/T]GGGTGAGGGTGAGAA	10612
rs565004247	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6454284	TAGTCCCAGCTACTC[A/G]GGAGGCTGAAGTAGG	10612
rs565063867	snp	G/T			intron-variant	TRIM3	GRCh38.p7	11:6458382	ATGGGTGCCAACCCC[G/T]TCCCTCACAGGTGTG	10612
rs565255732	snp	C/G	9.91309e-05	0.00703958	intron-variant	TRIM3	GRCh38.p7	11:6449277	CACCAGGAAACCGCC[C/G]CCTCATGTCATTCCC	10612
rs565287476	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime, upstream-variant-2KB, downstream-variant-500B	ARFIP2, TRIM3	GRCh38.p7	11:6474234	AGTCGGTCTCAGGGA[C/T]TGAGATGAGACTCCG	10612
rs565348922	snp	A/G	0.00119737	0.0244387	utr-variant-3-prime, upstream-variant-2KB	ARFIP2, TRIM3	GRCh38.p7	11:6475018	TATCCATGACAAAGG[A/G]CAAAGTCATGCCTGT	10612
rs565412268	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6467672	TGGGAGGCTGAGGTG[A/G]GAGGATTGCTTGAGC	10612
rs565542696	snp	A/C			intron-variant	TRIM3	GRCh38.p7	11:6472426	CCTCCCCTCCACACT[A/C]CCCCTGCCCCCTCGC	10612
rs565751057	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TRIM3	GRCh38.p7	11:6473416	TGGAGGTGTCTGCAC[C/G]AGGGAGAAAAGAGCC	10612
rs565808549	snp	C/G			intron-variant	TRIM3	GRCh38.p7	11:6470174	AAAATAGTTTAAAGG[C/G]CAAGGACGGAAAATT	10612
rs565941351	snp	G/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime, upstream-variant-2KB, downstream-variant-500B	ARFIP2, TRIM3	GRCh38.p7	11:6474390	CTGACCAGGAAGACG[G/T]AGAAACCGTCTGTAC	10612
rs566017949	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6467070	GTGTTAGGAATGGAA[C/T]GATAAAACAGACAGG	10612
rs566077674	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TRIM3	GRCh38.p7	11:6448875	ATAAAGTGCAACCGT[G/T]GGGGTGGGGGTAGGA	10612
rs566081095	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6461186	GCTGGGATTACAGGC[A/G]TGAGCCACCATGCCC	10612
rs566479745	snp	G/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6458423	TCATTTTAAAACCTC[G/T]CTGCTTGACACATCT	10612
rs566535225	snp	A/C	6.63163e-05	0.00575793	intron-variant	TRIM3	GRCh38.p7	11:6457851	AAACTCCATCGTCTG[A/C]GGTACAAGGACTCCA	10612
rs566546361	snp	A/G			utr-variant-3-prime, upstream-variant-2KB, downstream-variant-500B	ARFIP2, TRIM3	GRCh38.p7	11:6476438	TTTTGACTTGATAGG[A/G]TTCTGGTGTTTGATT	10612
rs566546411	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6452520	TGGTCTCCCCGCCCC[A/G]GCCCCACCCCAACTC	10612
rs566733422	snp	C/G	0.000399281	0.0141238	missense, intron-variant, utr-variant-5-prime, nc-transcript-variant	TRIM3	GRCh38.p7	11:6465620	ACTGGTACCGATCCA[C/G]GCAGATGCTGCATAC	10612
rs566797259	snp	C/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6459658	AGACCTGGATTTAGG[C/G]AATAGTAATGTAGAC	10612
rs566870458	in-del	-/A	0.00159617	0.0282053	intron-variant	TRIM3	GRCh38.p7	11:6470253	CAATTTTGCAGGGGG[-/A]TATCAACTGAACTTG	10612
rs567033555	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6463693	TGGGAGTGGGGTAAC[A/G]GGAGCCAGGAGTGGA	10612
rs567087935	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6453830	GAAAACGGTCATGTC[A/G]TGAGGACCCCAATCC	10612
rs567129053	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6453404	AGAATCTGCTGGTGT[C/T]CTAGTTTGGTCCTTA	10612
rs567273633	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6458458	TGCCAGCAGGTATAA[C/T]GGCCTTGCCCCTTAC	10612
rs567276838	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6453141	CACTTGCAGCACTGA[C/T]ATGGCATTTGGCACA	10612
rs567334736	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6458842	TACTGTATGACCCCT[A/G]ACAAGTTACATAACT	10612
rs567462043	snp	A/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6459712	AAGTGTTTAAGAAGG[A/T]GGGAAGGTGGGAGGT	10612
rs567524535	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6460236	ACTGAATTTGGCAAA[C/T]GTGAGGGTACTTTGT	10612
rs567524670	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6453904	CCCAGCCCATGCCAG[C/T]CCTAAGGACTCCAGA	10612
rs567584736	snp	A/G	0.00119737	0.0244387	intron-variant	TRIM3	GRCh38.p7	11:6454436	CCCCTCACCAGGACA[A/G]ACAAAGTGGCACTTG	10612
rs567605316	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6471876	TGAGAAACTAAGAAA[C/T]ATGGAACAGATGGAC	10612
rs567789625	snp	C/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6466062	GACATAGTGCCTGTT[C/G]AGTGCATGGTACAGA	10612
rs567797305	snp	A/G			intron-variant, utr-variant-5-prime, upstream-variant-2KB	TRIM3	GRCh38.p7	11:6473189	GAGGTCAGAACCAGG[A/G]AGGGGCCTGGGGTCC	10612
rs567897470	snp	A/C	0.000399281	0.0141238	downstream-variant-500B	TRIM3	GRCh38.p7	11:6448172	GTCAGGGCTCCAGGG[A/C]TTCAGGGATGACTTT	10612
rs567933513	snp	C/T			intron-variant	TRIM3	GRCh38.p7	11:6471054	CAAGCAAGAAGCTGA[C/T]TGTGAACAAATGAAG	10612
rs568009927	snp	A/C			intron-variant	TRIM3	GRCh38.p7	11:6466541	TAACTTTGCCCCATA[A/C]CTTTTCTACAACCTC	10612
rs568092733	in-del	-/TTCTGCAGCAAATCATCCCC	0.00438332	0.0466095	intron-variant	TRIM3	GRCh38.p7	11:6472874	CAGCTCTGATTCCAA[-/TTCTGCAGCAAATCATCCCC]TTCTGCAGCAAATCA	10612
rs568101529	snp	C/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6469129	CGGAAGGACCAGGAG[C/G]CGGGAGGCAAGCTGA	10612
rs568350753	snp	C/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6451799	ACAAAGTCCAGTATG[C/G]GCACCACTTGAGGAC	10612
rs568369956	snp	A/C	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6451212	TGACCACCAAGAGGC[A/C]CTAGACTGGTCAGTT	10612
rs568519882	snp	C/T	0.00438332	0.0466095	intron-variant	TRIM3	GRCh38.p7	11:6470104	GGAAAACTTTGGTAG[C/T]GGTGAGGGCTATTAA	10612
rs568635626	snp	G/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6470716	GTTGGTGCAGAGATG[G/T]TTCCTGAAGCCATGG	10612
rs568644600	snp	C/T	1.64977e-05	0.00287203	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6457385	GGTCCTCGAACGCTG[C/T]ACTGATCTGGGCCAG	10612
rs568657437	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6470227	AATAGCAAAGACAGG[C/T]CAAGATAAATCAATT	10612
rs568780174	snp	G/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6451834	CCAGTGTGGCTGGAC[G/T]GCAGGGAGCACCCAG	10612
rs568811632	snp	G/T	1.66388e-05	0.00288429	intron-variant	TRIM3	GRCh38.p7	11:6457872	AAGGACTCCAGTCGG[G/T]TAATGGCTAGACATC	10612
rs568933987	snp	G/T			intron-variant	TRIM3	GRCh38.p7	11:6464182	GAAATTCCCTAACAG[G/T]TCTACAAAGCCCTAG	10612
rs569053840	snp	G/T	0.000798403	0.0199641	intron-variant	TRIM3	GRCh38.p7	11:6470751	GGATGACATTACCCT[G/T]AGAGGGTAAAGAGAG	10612
rs569055919	snp	A/G			intron-variant	TRIM3	GRCh38.p7	11:6462823	GCTACTCAGGAGGCT[A/G]AGGCAGGAGGATCAC	10612
rs569465156	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB, downstream-variant-500B	ARFIP2, TRIM3	GRCh38.p7	11:6474533	TCCTGAGGAAATTCT[A/G]GTTCAGACCATCCAG	10612
rs569480572	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6458892	TCCTTTGTAAGATGG[A/G]GAAGTACAGACTTCA	10612
rs569977384	snp	C/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6461735	ATCCCCTTCCTATTT[C/G]TCAAGTGTACCTGGC	10612
rs570070238	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6455664	ACTCCAGACAGACTA[C/T]ATACATTCAGGAGCC	10612
rs570134944	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6449741	AGTCACTCTTGACTC[C/T]AATTTCTTCTCTGTT	10612
rs570198532	snp	A/G	0.00358779	0.0422022	utr-variant-3-prime, upstream-variant-2KB	ARFIP2, TRIM3	GRCh38.p7	11:6475256	CAGCAGGAGCTTTGG[A/G]AACCGCCTCAACCTC	10612
rs570241695	snp	C/T			downstream-variant-500B	TRIM3	GRCh38.p7	11:6448516	CTTGGGAAGCTGGGT[C/T]CCTTGCCTGCCTGCT	10612
rs570298478	snp	A/G	0.000798403	0.0199641	intron-variant	TRIM3	GRCh38.p7	11:6468656	GTGGTGGGGTGGCAG[A/G]GGCAGAAGCCACGTC	10612
rs570324134	snp	A/G	0.000798403	0.0199641	intron-variant	TRIM3	GRCh38.p7	11:6468530	AAAGAGAACCCAGAG[A/G]AATGGTAGGAAAACC	10612
rs570330349	in-del	-/TG			intron-variant	TRIM3	GRCh38.p7	11:6469955	GGCTGAATCAGACAC[-/TG]TGATGGGAGGGCTAA	10612
rs570349815	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime, upstream-variant-2KB	ARFIP2, TRIM3	GRCh38.p7	11:6475813	AGCCTCCCGAGTAGC[C/T]GGGACTACAGGACTA	10612
rs570767214	snp	C/G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TRIM3	GRCh38.p7	11:6474087	ACCCGCACGCCCCCC[C/G/T]GCCAACGCCTCCACC	10612
rs570851102	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6450256	CCTTCCCACAGTTCC[C/T]TGCACCTTCCTATCA	10612
rs570916487	snp	C/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6451160	CTGGGGAAAGAACAG[C/G]GAGTAGGAGGAGGTA	10612
rs571209914	snp	A/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6463270	AAGTTACATTAAAAA[A/T]TTAAAATAAAAAAAT	10612
rs571258009	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6453348	TTCTTGACATTTGAC[A/G]ATTTAGCAAAATCTG	10612
rs571319875	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6453820	GTCCAAAAGAGAAAA[C/T]GGTCATGTCGTGAGG	10612
rs571534401	snp	C/T			intron-variant	TRIM3	GRCh38.p7	11:6455916	GGTGGCTGGTGGGTG[C/T]GTAAGGGGTGATCCT	10612
rs571562351	snp	C/T	0.000436967	0.0147747	utr-variant-3-prime, nc-transcript-variant	TRIM3	GRCh38.p7	11:6448853	CACCAAAGCAAGAAC[C/T]GAATAAATAAAGTGC	10612
rs571565906	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6465792	TCCCCACCCAATCCC[C/T]GCCACTCAAATCCCC	10612
rs571676114	snp	C/T	0.000798403	0.0199641	intron-variant	TRIM3	GRCh38.p7	11:6466178	TCCTCTAACTACCTG[C/T]AGCTCTTCCATTTAT	10612
rs571746332	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6461046	GAGCAGCTGGGATTA[C/T]AGGCTCACACCATCA	10612
rs571807555	snp	G/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6454989	CCCTATAGGATAAAA[G/T]CAAAATTCCACACTC	10612
rs572023888	snp	C/T			intron-variant	TRIM3	GRCh38.p7	11:6467429	GTGAGTTTGGGAAGA[C/T]AGGTAGAGATGAGAT	10612
rs572156156	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6472487	GTCACCTGTGACACT[C/T]TATGAACGCTCTCTA	10612
rs572222663	snp	C/T	0.00597247	0.0543191	intron-variant	TRIM3	GRCh38.p7	11:6465489	ACACATGCTCCCTCA[C/T]CCTCCCCACAGGGGA	10612
rs572229363	snp	A/C			intron-variant	TRIM3	GRCh38.p7	11:6464516	GTTATATTTATCTAT[A/C]ATCTGGCTATATGAT	10612
rs572282806	snp	A/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6465886	CAGGGTGATGTGACC[A/T]CTGAGCCTGGTGTTC	10612
rs572284608	snp	C/T	0.000798403	0.0199641	intron-variant	TRIM3	GRCh38.p7	11:6459324	TTATCCTGCCAGCAA[C/T]AGGAAGCTGCAAGAG	10612
rs572348620	snp	C/G	0.000798403	0.0199641	intron-variant	TRIM3	GRCh38.p7	11:6460040	TAGACAGTGATAAGA[C/G]AGAGGGACAGAGCAC	10612
rs572367971	snp	A/G			intron-variant	TRIM3	GRCh38.p7	11:6471820	ACAAATAGGACATTG[A/G]TACGTACATTGGGAA	10612
rs572477665	snp	C/T	0.00438332	0.0466095	downstream-variant-500B	TRIM3	GRCh38.p7	11:6448349	CCCTCACCCCCCCAA[C/T]CCCACAATCCTTCCC	10612
rs572692511	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime, upstream-variant-2KB	ARFIP2, TRIM3	GRCh38.p7	11:6474784	CCCCAGACGTTAGCC[A/C]TCATCACTCAGCTAG	10612
rs572825327	snp	G/T	1.69424e-05	0.00291048	intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6451478	GAGCAGGTAGGAGGG[G/T]AGACACTGTGGGCAC	10612
rs572916470	snp	A/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6464239	AGCTTCATCCCATAA[A/T]ACTCTCAGTCACACT	10612
rs572979041	snp	A/C	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6464706	TCAGTTTTTAAAAAG[A/C]GTAAGCACGGTAGCT	10612
rs573019517	in-del	-/CAGC	0.00438332	0.0466095	intron-variant	TRIM3	GRCh38.p7	11:6461713	AAACACCTTCTAATT[-/CAGC]AATATCCCCTTCCTA	10612
rs573275029	snp	C/T			intron-variant	TRIM3	GRCh38.p7	11:6454283	GTAGTCCCAGCTACT[C/T]GGGAGGCTGAAGTAG	10612
rs573294675	snp	A/G	0.000798403	0.0199641	intron-variant	TRIM3	GRCh38.p7	11:6458611	AGGCACCCCCTGCCC[A/G]ACTTCTTTAACTCAT	10612
rs573325917	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6452265	TAATTTAGCTGCCCA[A/G]TATGCTCAGGTCTCC	10612
rs573381614	snp	C/G			intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6451532	AGGGAGGAGACCCCC[C/G]CACCACCATTTATTC	10612
rs573559611	snp	A/C	0.000798403	0.0199641	intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6452012	AGTCAGAGGCTGTTG[A/C]AGTATTCCAGTTGAG	10612
rs573600691	snp	C/T			intron-variant	TRIM3	GRCh38.p7	11:6460032	AGAAAGCATAGACAG[C/T]GATAAGAGAGAGGGA	10612
rs573714613	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6458715	TTAAAATACTTCCCA[C/T]CTACAGAGAAAAAAG	10612
rs573777323	snp	G/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6459175	GGTGCAGGCAGAGGG[G/T]GAAGGGTAGTCCAGA	10612
rs573870978	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6464332	ACATGAGCTTTTCCA[A/G]TGGTCTTTCTTCTGT	10612
rs573905992	snp	A/C	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6464741	CCTGTAATCCCAGCA[A/C]TTTGGGAGGCCGAGG	10612
rs573994901	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6465348	TTCTTGACAGGAACC[A/G]TGGCCCAGTGTTATG	10612
rs574049355	snp	G/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6467331	TAGGCTGAAGAAACA[G/T]CATGATAAAGGTTCT	10612
rs574112429	snp	A/C	0.00119737	0.0244387	intron-variant	TRIM3	GRCh38.p7	11:6461477	TCTCTTCTTCCATTA[A/C]CCCCCGCACCACTCT	10612
rs574232721	snp	C/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6455909	GGAATGGGGTGGCTG[C/G]TGGGTGCGTAAGGGG	10612
rs574387700	snp	A/G			intron-variant	TRIM3	GRCh38.p7	11:6465138	CCATAGAAGCCTAGA[A/G]GCTGGGACAGGTTGC	10612
rs574427524	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6455321	TAGTATGTGACAGAG[C/T]TAGGATTCAAGCTCA	10612
rs574585611	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6449893	GATCACTGCAAAAGA[C/T]TGATCTTCCTGTCTC	10612
rs574692997	snp	C/T	0.00159617	0.0282053	intron-variant	TRIM3	GRCh38.p7	11:6459661	CCTGGATTTAGGCAA[C/T]AGTAATGTAGACTAT	10612
rs574708082	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime, upstream-variant-2KB	ARFIP2, TRIM3	GRCh38.p7	11:6475481	TTTCTGCTTAAAACA[A/C]TTCTCAGCTCCTTCT	10612
rs574802645	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, upstream-variant-2KB	ARFIP2, TRIM3	GRCh38.p7	11:6475928	TCTCCTGACCTGGTG[A/G]TCCGCCCGCCTCGGC	10612
rs574868603	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6468825	TTGTCTGTGCTGTTG[A/G]ATGCATTATGAGCCT	10612
rs574890354	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6469588	CCTGTATTGGTTATT[C/T]CCACCATACTTTATG	10612
rs574961013	snp	A/T	0.000798403	0.0199641	intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6449939	TGAGTGATCTAAGAC[A/T]CACAGGACTGCATCA	10612
rs574964767	snp	C/T	1.69666e-05	0.00291256	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456875	CGCTCCGGGAAGGCC[C/T]GTGCCGCCAATGCAG	10612
rs575040368	snp	C/T	0.000798403	0.0199641	intron-variant	TRIM3	GRCh38.p7	11:6462805	CCTGCACCTGTAATC[C/T]CAGCTACTCAGGAGG	10612
rs575104316	snp	A/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6463394	TACATGGTAGCTACT[A/G]TTATTACAATTTCTC	10612
rs575118326	snp	A/C	0.000798403	0.0199641	intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6451572	ACAAGCACTTACTGA[A/C]AAAATCAAACATGGC	10612
rs575166591	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6455005	CAAAATTCCACACTC[C/T]ATCTCCAAAACCAAT	10612
rs575414612	in-del	-/A	0.0130921	0.0798413	intron-variant	TRIM3	GRCh38.p7	11:6452969	CCCTACCAAATCAAT[-/A]TGCACATATAAACTT	10612
rs575488756	in-del	-/T	0.00119737	0.0244387	intron-variant	TRIM3	GRCh38.p7	11:6463209	ACTCTGTCTCAAAAA[-/T]AACAAAAACAAAAAC	10612
rs575676523	snp	C/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6463483	TCCAATTTCAGCTCT[C/G]ATCCAACATTGAGCT	10612
rs575694372	snp	A/G	0.00795532	0.062565	intron-variant	TRIM3	GRCh38.p7	11:6464167	TCTCAGGGTAAAGGT[A/G]AAATTCCCTAACAGG	10612
rs575758090	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6457975	TAATCCAGAGCAGTA[C/T]CCTGTCACCCAGCCA	10612
rs575950709	snp	A/T	0.00676609	0.0577691	intron-variant	TRIM3	GRCh38.p7	11:6471998	AAATAAATAAATAAA[A/T]AAAAGGCACCACCAC	10612
rs575968673	snp	C/G	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6472581	TTGCTCAAGTTCTCT[C/G]GGCAAGAATGCCATT	10612
rs576042344	snp	A/G			intron-variant	TRIM3	GRCh38.p7	11:6468015	TTGGCCGAGCAAGGT[A/G]GCTCACATCTGTAAT	10612
rs576247682	snp	C/T			intron-variant	TRIM3	GRCh38.p7	11:6463989	AGAGCCAGGTTTCCG[C/T]TGGGGCAGAAGGCAG	10612
rs576301900	snp	G/T	0.0023933	0.0345097	downstream-variant-500B	TRIM3	GRCh38.p7	11:6448388	GGCAGATAGGCAAAG[G/T]ACTTGCCTACTTCTG	10612
rs576391937	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TRIM3	GRCh38.p7	11:6448903	GGAGAGGGAGGGCAC[C/T]GGGTGCACCCATGCC	10612
rs576410393	snp	A/G	0.00199481	0.0315187	intron-variant	TRIM3	GRCh38.p7	11:6454619	TCATTACTCCCCCGC[A/G]ATCCCCTCCTCACTA	10612
rs576451646	snp	A/G	0.000798403	0.0199641	intron-variant	TRIM3	GRCh38.p7	11:6466538	GCTTAACTTTGCCCC[A/G]TACCTTTTCTACAAC	10612
rs576656382	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6468235	GTGATGGGCCATGAA[C/T]AGAGACAGTGAAAGC	10612
rs576706047	snp	A/G			intron-variant	TRIM3	GRCh38.p7	11:6471534	TGAATGAACCATTCA[A/G]TCAAACTTCTCTGGG	10612
rs576731196	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime, upstream-variant-2KB	ARFIP2, TRIM3	GRCh38.p7	11:6475359	CTTGCAGTTTTGGGC[G/T]GGGGCTACTATGCTA	10612
rs577325384	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, upstream-variant-2KB	ARFIP2, TRIM3	GRCh38.p7	11:6475865	GGCTAATTTTCTTGC[A/G]TTTTTAGTAGAGATG	10612
rs577379584	snp	C/G	0.000798403	0.0199641	intron-variant	TRIM3	GRCh38.p7	11:6462127	TCAGGTCAAATGTCA[C/G]CTCCTCAGGGAAGCC	10612
rs577452612	snp	A/G/T	1.65616e-05	0.00287759	intron-variant	TRIM3	GRCh38.p7	11:6450647	AAAGTGGTCTTCAGG[A/G/T]CAGTAAGCTGGGATG	10612
rs577466509	snp	C/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6468307	AAGTACAATGTGTCT[C/T]TCTGATGTCCAGGTA	10612
rs577597291	snp	C/T	0.00119737	0.0244387	intron-variant	TRIM3	GRCh38.p7	11:6462761	CTTAGTTTCCTCCTC[C/T]CTAATATGGGGATAC	10612
rs577687831	snp	A/G	0.00199481	0.0315187	intron-variant	TRIM3	GRCh38.p7	11:6454006	GAAGTAGAAGCAAGA[A/G]GAGGACTGCTATAGA	10612
rs577752902	snp	A/T			intron-variant	TRIM3	GRCh38.p7	11:6465078	ACAGGGTCTGGCACA[A/T]AGTAGTTGCTCAATA	10612
rs577846077	snp	G/T	0.000399281	0.0141238	intron-variant	TRIM3	GRCh38.p7	11:6465421	TTTCCTGCAGGTTGG[G/T]GTTCACCTGCTCTCC	10612
rs745344433	snp	G/T			intron-variant	TRIM3	GRCh38.p7	11:6460481	GGAGAAGATCTTGAG[G/T]ATTGGGGAGTGCCTC	10612
rs745371333	snp	A/G	1.65927e-05	0.00288029	intron-variant	TRIM3	GRCh38.p7	11:6451224	GGCACTAGACTGGTC[A/G]GTTCAGCTGGACACC	10612
rs745399688	snp	A/G			intron-variant	TRIM3	GRCh38.p7	11:6462172	TATAGAATAGTTCTT[A/G]CCCCAAACACCCCTA	10612
rs745519689	snp	A/G			intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6449531	GGGTGAAGCCCCAGG[A/G]CTGAGAACCCCCACC	10612
rs745564179	snp	C/T			utr-variant-3-prime, upstream-variant-2KB	ARFIP2, TRIM3	GRCh38.p7	11:6475613	CATTATATGCTAGCC[C/T]CTCTGCCTGGGATGC	10612
rs745571148	snp	A/G			intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6450473	AAAGGGGAAAAGGAG[A/G]AGGTAAAATAGAGAG	10612
rs745581812	snp	C/T	1.64966e-05	0.00287194	intron-variant	TRIM3	GRCh38.p7	11:6465533	CCTCCCCACAGGGTC[C/T]TCATCCCTCCCCAGT	10612
rs745669893	snp	A/G	1.66225e-05	0.00288287	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456950	GCCGAGCCCAGGCGC[A/G]GTGCCTGCTCTGCAA	10612
rs745700856	snp	C/T			intron-variant	TRIM3	GRCh38.p7	11:6453829	AGAAAACGGTCATGT[C/T]GTGAGGACCCCAATC	10612
rs745708737	snp	A/T			intron-variant	TRIM3	GRCh38.p7	11:6462238	AAGCTGCAGCTCTCG[A/T]TTTCTTGATTGCTTA	10612
rs745784724	snp	A/C			intron-variant, utr-variant-5-prime, upstream-variant-2KB, downstream-variant-500B	ARFIP2, TRIM3	GRCh38.p7	11:6474326	GCCTCCTGGAGGCGC[A/C]CTTTCCGGCTTCCTT	10612
rs745870273	snp	A/G	0.000149329	0.00863958	utr-variant-3-prime, nc-transcript-variant	TRIM3	GRCh38.p7	11:6448979	AGACCCTCTTGTCCA[A/G]TCACCCCAATGTCTG	10612
rs745876002	snp	C/T	4.9423e-05	0.00497082	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456146	CACCTTGTAAATTGG[C/T]GAATTCACCTTTCTC	10612
rs745886008	in-del	-/GA			intron-variant	TRIM3	GRCh38.p7	11:6464881	GTCCCAGCTACTCCG[-/GA]GAGGCTGAGGCAGGA	10612
rs746067831	snp	C/T			intron-variant	TRIM3	GRCh38.p7	11:6465207	GAAGGACAGACCTAA[C/T]TTCAAATATCCTCCA	10612
rs746119245	snp	C/T			intron-variant	TRIM3	GRCh38.p7	11:6452938	GAGAAGACTAATGAC[C/T]AAGTACCACCCTCCG	10612
rs746146371	snp	A/G			intron-variant	TRIM3	GRCh38.p7	11:6467027	GATTTCAGGAATTCA[A/G]TAAATATTTACTGCC	10612
rs746155042	snp	A/C	1.64982e-05	0.00287208	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6457386	GTCCTCGAACGCTGC[A/C]CTGATCTGGGCCAGG	10612
rs746158822	snp	A/G			intron-variant	TRIM3	GRCh38.p7	11:6467492	TGATTTTGGCTGGGT[A/G]CAGTGGCTCATACCT	10612
rs746182709	snp	A/G			intron-variant	TRIM3	GRCh38.p7	11:6470536	GGCCTGCCAAAGCGT[A/G]GGGGTTGCAGGCATG	10612
rs746225488	snp	A/C/T	4.94558e-05	0.00497251	intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6450526	ATGTTGGGACAGTGG[A/C/T]CACGGAGGGAGGGAA	10612
rs746239862	snp	A/G	1.6473e-05	0.00286988	intron-variant	TRIM3	GRCh38.p7	11:6450667	AAGCTGGGATGCTGA[A/G]TGGGATGGGGAAGAG	10612
rs746417812	snp	C/G	1.7238e-05	0.00293576	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456685	CCCGTCCTTGTCTTT[C/G]GTAGTGACAGTGAGC	10612
rs746442221	snp	A/C			intron-variant	TRIM3	GRCh38.p7	11:6453435	ACATCTCTCTCCTAT[A/C]CCATGGTATCTGAAA	10612
rs746461721	snp	A/C	1.65463e-05	0.00287626	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6457826	TGGCCGTCTCACAGG[A/C]CTCACAGTAAAACTC	10612
rs746510715	in-del	-/AC	1.65985e-05	0.00288079	frameshift-variant, utr-variant-5-prime, nc-transcript-variant	TRIM3	GRCh38.p7	11:6458231	GCTCTGGGAGGATGG[-/AC]ACGTCTGCCGGCATA	10612
rs746525323	snp	A/G	3.77302e-05	0.00434323	intron-variant	TRIM3	GRCh38.p7	11:6458048	TCCCGGCCTCACTGG[A/G]CCTCGCTTGGGCCCA	10612
rs746540613	snp	C/T	3.50287e-05	0.00418487	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456565	CGCTGTGTACACTAG[C/T]TCATATGTGCCATTC	10612
rs746661369	snp	A/G			intron-variant	TRIM3	GRCh38.p7	11:6460034	AAAGCATAGACAGTG[A/G]TAAGAGAGAGGGACA	10612
rs746680990	snp	C/T			intron-variant	TRIM3	GRCh38.p7	11:6461914	AAAATAAAATCCAAA[C/T]ACTTTCTGAAAACCT	10612
rs746724078	snp	C/T	1.78083e-05	0.00298393	intron-variant	TRIM3	GRCh38.p7	11:6457065	AGTGGGTGAGCAGAC[C/T]GGCACAGGGGGAGTC	10612
rs746728770	snp	C/T	1.65198e-05	0.00287395	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6451407	CCTCGGACCCCAAAA[C/T]GGAACTTGAACTGGC	10612
rs746761295	snp	C/T			intron-variant	TRIM3	GRCh38.p7	11:6464231	ACCTCTCCAGCTTCA[C/T]CCCATAATACTCTCA	10612
rs746815680	snp	C/G/T	3.30231e-05	0.00406333	intron-variant	TRIM3	GRCh38.p7	11:6451261	AGTAAAGTGACAGCA[C/G/T]GCCTCTCACCTTGAA	10612
rs746833836	snp	C/T	0.000116041	0.00761624	intron-variant	TRIM3	GRCh38.p7	11:6456040	TGAAAACTCTTATTT[C/T]GGTGGTGGAGGAGAG	10612
rs746834690	snp	A/G	1.65542e-05	0.00287695	stop-gained, nc-transcript-variant	TRIM3	GRCh38.p7	11:6457301	CAAGACACACCTTCT[A/G]TTTGGCCCCACAAAT	10612
rs746922487	snp	A/G	1.64743e-05	0.00287	synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant	TRIM3	GRCh38.p7	11:6465584	CACAGAAGGTGTGCA[A/G]GCAAGGAAGAACCTT	10612
rs747078637	snp	C/T	1.65446e-05	0.00287612	utr-variant-3-prime, nc-transcript-variant	TRIM3	GRCh38.p7	11:6449007	CTGTCCCTCCACAAG[C/T]CAGGCAGGGCCTCTG	10612
rs747082474	snp	A/G	1.8725e-05	0.00305976	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456429	GGGACTTGACACGGC[A/G]CTTCACATCGTCCGG	10612
rs747276515	snp	A/G	3.64604e-05	0.00426953	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456346	GTCCTTTCGTTTGCC[A/G]CCTGTGCTGTACATG	10612
rs747286598	snp	G/T			intron-variant	TRIM3	GRCh38.p7	11:6462444	ATAGAGCCTCTCTCT[G/T]TCACCCAGGCTAGAG	10612
rs747347021	snp	A/G			intron-variant	TRIM3	GRCh38.p7	11:6469115	AGATTGAAGGTTGGC[A/G]GAAGGACCAGGAGGC	10612
rs747385356	snp	A/G	1.64852e-05	0.00287094	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6450992	CTTGTTGTCGACCAC[A/G]ATGATATGTCCATTC	10612
rs747521044	snp	A/G/T	3.37008e-05	0.00410481	intron-variant	TRIM3	GRCh38.p7	11:6450857	TTCTCTGGAACAGGG[A/G/T]TATCAGCATAGATCT	10612
rs747672385	snp	A/G			intron-variant	TRIM3	GRCh38.p7	11:6471007	CATGTGGTTTTCAGG[A/G]GATGGAGGACAGGAA	10612
rs747763244	in-del	-/A	3.3027e-05	0.00406355	intron-variant	TRIM3	GRCh38.p7	11:6456196	GAAGGGACAGGAGGG[-/A]AAAACAAAATAATTC	10612
rs747865466	snp	C/G	1.81793e-05	0.00301485	synonymous-codon, splice-donor-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6458068	GCTTGGGCCCACCTT[C/G]CCTTCATGGTTGGGG	10612
rs747891102	snp	C/G	1.65455e-05	0.00287619	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6451420	AACGGAACTTGAACT[C/G]GCCCTCATTGGAGAA	10612
rs748083778	snp	A/G			intron-variant	TRIM3	GRCh38.p7	11:6464163	TGGCTCTCAGGGTAA[A/G]GGTGAAATTCCCTAA	10612
rs748102504	snp	A/G			intron-variant	TRIM3	GRCh38.p7	11:6450831	CTTTACAGCTGGGGT[A/G]TCTAGGGGAGTTCTC	10612
rs748115703	snp	C/T	1.66319e-05	0.00288369	utr-variant-5-prime, intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6465724	GGCTCCCGCCACTCA[C/T]ACCAGCCTCTGTATG	10612
rs748140665	snp	C/T	1.6507e-05	0.00287284	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6457323	CCCACAAATGGTCTC[C/T]AGGTCGCTGACCAGA	10612
rs748354829	snp	C/G	3.71354e-05	0.00430886	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456532	CAGCACCGAGAGGAG[C/G]AGCTCGCCTTCCGTG	10612
rs748366592	snp	A/G			missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456359	CCGCCTGTGCTGTAC[A/G]TGGAGCTGGGCCTAC	10612
rs748407632	snp	C/G	4.94344e-05	0.00497139	intron-variant	TRIM3	GRCh38.p7	11:6449201	GAAGGAGTGCAGAAA[C/G]GAGGGAGAGGCAAGA	10612
rs748483914	snp	A/G	4.94491e-05	0.00497213	intron-variant	TRIM3	GRCh38.p7	11:6449225	GGCAAGATCAGGCAG[A/G]TGAGAGTCTGTTTTG	10612
rs748496226	snp	C/G			intron-variant, utr-variant-5-prime, upstream-variant-2KB, downstream-variant-500B	ARFIP2, TRIM3	GRCh38.p7	11:6474377	GCTAGTCTATCGGCT[C/G]ACCAGGAAGACGTAG	10612
rs748564572	snp	A/G	1.89292e-05	0.0030764	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456443	CGCTTCACATCGTCC[A/G]GGGAAGGTGGCAGGT	10612
rs748734710	snp	A/G	1.66399e-05	0.00288438	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456946	CGGGGCCGAGCCCAG[A/G]CGCAGTGCCTGCTCT	10612
rs748773096	snp	A/C	1.66969e-05	0.00288932	intron-variant	TRIM3	GRCh38.p7	11:6450883	GATCTTGGAGCTGTC[A/C]CCCTATACCTGCAAA	10612
rs748779976	snp	C/T	1.64849e-05	0.00287092	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6451005	ACAATGATATGTCCA[C/T]TCCGGTCTACGGCCA	10612
rs748808029	snp	A/C/G	1.64819e-05	0.00287066	intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6450537	GTGGTCACGGAGGGA[A/C/G]GGAAGACACTGACCT	10612
rs748914270	snp	A/G	1.6615e-05	0.00288223	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	TRIM3	GRCh38.p7	11:6458212	CTGCAGTGCCGAGAC[A/G]CCCTGCTCTGGGAGG	10612
rs748931053	snp	C/G			intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6451789	TGTAAAAGGCACAAA[C/G]TCCAGTATGGGCACC	10612
rs749002569	snp	G/T	1.70656e-05	0.00292104	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456844	GACCAGTTCCAGCTG[G/T]GCATTCTCATGTGGC	10612
rs749114158	snp	A/G			intron-variant	TRIM3	GRCh38.p7	11:6462249	CTCGTTTTCTTGATT[A/G]CTTACTGTCAGTCAC	10612
rs749117549	snp	C/T			utr-variant-3-prime, upstream-variant-2KB	ARFIP2, TRIM3	GRCh38.p7	11:6475805	CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGACTA	10612
rs749189062	in-del	-/T	1.67133e-05	0.00289074	intron-variant	TRIM3	GRCh38.p7	11:6450881	TAGATCTTGGAGCTG[-/T]CCCCCTATACCTGCA	10612
rs749223150	snp	A/G			intron-variant	TRIM3	GRCh38.p7	11:6462351	TCTGCAGTGAAAACT[A/G]GATTCAGATCTCAGC	10612
rs749256535	snp	A/C	6.5987e-05	0.00574362	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6457341	GTCGCTGACCAGAGC[A/C]TGCTTGCGCTGCTGC	10612
rs749313976	snp	A/C			intron-variant	TRIM3	GRCh38.p7	11:6465294	TTAGGTGGTGTCAAA[A/C]GCTGCCTTGAGGTTT	10612
rs749371038	snp	A/G			intron-variant	TRIM3	GRCh38.p7	11:6467381	GAACCTGAAAGGACT[A/G]TGTGGTTGGAGCCAA	10612
rs749406224	snp	C/T	4.9489e-05	0.00497414	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6457380	CTCCAGGTCCTCGAA[C/T]GCTGCACTGATCTGG	10612
rs749519115	snp	C/T	1.64906e-05	0.00287142	intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6449496	GCCTCAGGCAGAGGG[C/T]AGGGCTTTGGAGGAG	10612
rs749625878	snp	C/G			intron-variant	TRIM3	GRCh38.p7	11:6459796	CAAATTCCTAGCTTT[C/G]ATAACTGAGTGGATA	10612
rs749691043	snp	C/T	1.65482e-05	0.00287643	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6449379	ACTCCTGTGGGGGCA[C/T]TGAACTGCCCATTGC	10612
rs749808503	snp	A/G			downstream-variant-500B	TRIM3	GRCh38.p7	11:6448215	TGGAGTCTCCCACAC[A/G]TAGCTACCACCTGGG	10612
rs749887981	snp	C/G	1.67744e-05	0.00289602	intron-variant	TRIM3	GRCh38.p7	11:6457278	ACGATGGTAGGAAAG[C/G]GTGAACACAAGACAC	10612
rs749940749	snp	C/G	1.64966e-05	0.00287194	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6451379	GGGGCGCTGCAGCTG[C/G]CCAGGTGAGCGTCCT	10612
rs749954630	snp	C/G	1.64966e-05	0.00287194	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6457358	GCTTGCGCTGCTGCA[C/G]TGCTTGCTCCAGGTC	10612
rs749986227	snp	C/T			intron-variant	TRIM3	GRCh38.p7	11:6463663	GATATCTATATTGTA[C/T]CGAAAGTGGTGTAAT	10612
rs750004607	snp	A/G	1.64735e-05	0.00286993	intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6449452	CACTGTACACCTGGC[A/G]GGGGAAGGGGCTAGG	10612
rs750032942	in-del	-/AA/AAA			intron-variant	TRIM3	GRCh38.p7	11:6454386	CAGAGACCCTGTCTC[-/AA/AAA]AAAAAAAAAAAAAAA	10612
rs750112619	snp	A/G			intron-variant	TRIM3	GRCh38.p7	11:6463889	GACAGGAAAACTGAG[A/G]CCATTTCCAGTTGAT	10612
rs750232343	snp	C/T	5.88992e-05	0.00542643	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456497	CGGAAGGGGCTGCCG[C/T]GCACTGGCTGTCCGT	10612
rs750246770	snp	A/G	1.65146e-05	0.0028735	intron-variant	TRIM3	GRCh38.p7	11:6449295	TCATGTCATTCCCAG[A/G]CCTTACTCACCTGGA	10612
rs750330331	snp	A/C			intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6449566	TCTACAGCTACAGCC[A/C]AAATCTGCTTCATAG	10612
rs750335182	snp	A/G			intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6452121	TGAGACTTAGTAGCA[A/G]ACTGGAATGGGGTAG	10612
rs750413045	snp	C/T	1.66874e-05	0.0028885	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6457740	CAGGGCCGCCTTGTG[C/T]TGCTCCACCACATCC	10612
rs750437243	snp	C/T			intron-variant	TRIM3	GRCh38.p7	11:6471555	CTTCTCTGGGCACAC[C/T]GTGGGCCAGGTCCTT	10612
rs750495638	in-del	-/ACTC	0.000198157	0.00995185	intron-variant	TRIM3	GRCh38.p7	11:6449300	TCATTCCCAGGCCTT[-/ACTC]ACCTGGATGCGGCTG	10612
rs750501622	snp	A/G	3.3168e-05	0.00407221	intron-variant	TRIM3	GRCh38.p7	11:6451067	AATCTTGGTCTGGAG[A/G]AAGAGAATATCCATA	10612
rs750550656	snp	A/G			intron-variant	TRIM3	GRCh38.p7	11:6461367	GCTCCTTTGAAGCTC[A/G]TGCCTTCTATCTCTA	10612
rs750626193	snp	A/G	3.3083e-05	0.00406699	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6450931	CACGGCCCCCAAAAC[A/G]GCCAACCAGTTTGCC	10612
rs750742558	snp	A/G	0.000125012	0.00790509	intron-variant	TRIM3	GRCh38.p7	11:6458335	AACAGAGTGGGTGGG[A/G]TGGCATAAGTGCACC	10612
rs750762527	snp	A/G/T	6.69843e-05	0.00578692	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456915	CTCGCATGTGCTTGC[A/G/T]CACCAGCAACACCTC	10612
rs750787647	snp	A/G			intron-variant	TRIM3	GRCh38.p7	11:6454940	CCAGTAAAATGTTTC[A/G]AAGAAGTAAAGTGCA	10612
rs750829499	snp	C/T			intron-variant	TRIM3	GRCh38.p7	11:6453327	CCAGTCCACAAAGTC[C/T]TGCCATTCTTGACAT	10612
rs750892904	snp	A/G	0.000760167	0.0194809	utr-variant-3-prime, nc-transcript-variant	TRIM3	GRCh38.p7	11:6448820	CATCCTTGGGACCAC[A/G]GTCCAGGCTCACCCA	10612
rs750964913	snp	A/T			intron-variant	TRIM3	GRCh38.p7	11:6473023	CCTGAGTTTCTGTTG[A/T]CCACATCAGAGAACC	10612
rs750980669	snp	A/G	1.67801e-05	0.00289651	missense, utr-variant-5-prime, nc-transcript-variant	TRIM3	GRCh38.p7	11:6458151	CGTGGGCCCCATCAG[A/G]TGCCTGCTGCATTGC	10612
rs751005352	snp	A/C			intron-variant	TRIM3	GRCh38.p7	11:6459423	AGGGAATGAGACAGC[A/C]GATGGGGTTGGGGGG	10612
rs751029245	snp	G/T	1.65201e-05	0.00287398	intron-variant	TRIM3	GRCh38.p7	11:6456051	ATTTTGGTGGTGGAG[G/T]AGAGCGGTAAAGGTG	10612
rs751113447	snp	A/C	1.65157e-05	0.0028736	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6457414	AGGGCCTCTGCCTTG[A/C]GCTCCTGCAGCTGCT	10612
rs751150240	snp	A/G			intron-variant	TRIM3	GRCh38.p7	11:6454831	AAAGGACCTTAGCAG[A/G]GCTGGATCGATGACA	10612
rs751208002	snp	C/G			utr-variant-3-prime, upstream-variant-2KB	ARFIP2, TRIM3	GRCh38.p7	11:6475059	GCACTATGGGAATCT[C/G]CTGAGTGGGTCTTCC	10612
rs751279359	in-del	-/T			intron-variant	TRIM3	GRCh38.p7	11:6461861	ATTTCCCTGTATATA[-/T]ATATTTTTAAAAACT	10612
rs751290712	snp	A/G			utr-variant-3-prime, nc-transcript-variant	TRIM3	GRCh38.p7	11:6448929	ATGCCCACAGCCCAC[A/G]TTCAGTGCTGCCAGG	10612
rs751309783	snp	C/G	1.64963e-05	0.00287192	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6457367	GCTGCAGTGCTTGCT[C/G]CAGGTCCTCGAACGC	10612
rs751350770	snp	A/C	1.81543e-05	0.00301277	intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6449477	GCTAGGGACTGGGGA[A/C]CTGGCCTCAGGCAGA	10612
rs751451090	snp	A/G	1.65113e-05	0.00287322	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6449312	CTTACTCACCTGGAT[A/G]CGGCTGTTGCCCCAG	10612
rs751545075	snp	C/T	5.17032e-05	0.00508418	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456619	AAGGCGCGTGCCGTC[C/T]GGGCCGGTGATCTCT	10612
rs751551964	snp	A/G			intron-variant	TRIM3	GRCh38.p7	11:6468173	CATCAAGATGAACTG[A/G]GTGTGAGAGGGATGT	10612
rs751600250	snp	A/G			intron-variant	TRIM3	GRCh38.p7	11:6453772	ATGCTGGTTCCACTC[A/G]GTGAGGTCTGCCTCA	10612
rs751645746	snp	A/G	1.89608e-05	0.00307896	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456519	GCTGTCCGTAGAGCA[A/G]CACCGAGAGGAGCAG	10612
rs751650268	snp	C/T	1.6577e-05	0.00287893	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6457780	ACTGTGCCATGCTCA[C/T]GATGCTCCCCGGCGC	10612
rs751716871	snp	A/C			intron-variant	TRIM3	GRCh38.p7	11:6472792	AAGCTTTTCCACAGC[A/C]GAAAGTAGCAAGTGC	10612
rs751732845	snp	C/G			intron-variant	TRIM3	GRCh38.p7	11:6454833	AGGACCTTAGCAGAG[C/G]TGGATCGATGACATG	10612
rs751740572	snp	A/C			intron-variant	TRIM3	GRCh38.p7	11:6459037	TTAATATAAGGAATG[A/C]TAGAAAGTGATAAGG	10612
rs751874039	snp	C/T	1.68046e-05	0.00289862	intron-variant	TRIM3	GRCh38.p7	11:6451099	GAGGCTTTATTCTGA[C/T]AGTGGGGAAAGTAGT	10612
rs751881567	in-del	-/AA			utr-variant-3-prime, upstream-variant-2KB	ARFIP2, TRIM3	GRCh38.p7	11:6475020	TCCATGACAAAGGGC[-/AA]AGTCATGCCTGTGAG	10612
rs751940292	snp	A/G			intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6451667	GAATGGTGAGAAAAG[A/G]CTCCAAGAGAAGAAG	10612
rs751998972	in-del	-/AG			intron-variant	TRIM3	GRCh38.p7	11:6463187	TCCAGCCTGGGTGAC[-/AG]AGAGAGACTCTGTCT	10612
rs752097911	snp	G/T	0.000181313	0.00951965	synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant	TRIM3	GRCh38.p7	11:6465669	TGGCTGGACCTCTGG[G/T]CCAGGGCTGTCCTCC	10612
rs752143932	snp	A/C	1.77398e-05	0.00297818	utr-variant-3-prime, nc-transcript-variant	TRIM3	GRCh38.p7	11:6448841	GGCTCACCCAGTCAC[A/C]AAAGCAAGAACCGAA	10612
rs752144613	snp	C/T	6.68103e-05	0.00577933	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456931	CACCAGCAACACCTC[C/T]GGGGCCGAGCCCAGG	10612
rs752157801	snp	C/G			intron-variant	TRIM3	GRCh38.p7	11:6471584	TTCAGCTGTGAAATA[C/G]AGACACAAAGCTGAA	10612
rs752226015	snp	C/G			intron-variant	TRIM3	GRCh38.p7	11:6453703	AGGACATAATATATA[C/G]AAATCAAATTATTAA	10612
rs752251596	snp	A/C	3.6706e-05	0.00428388	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456392	ACTGCCTTCTGGCGC[A/C]CATGGCTGCCGGGGC	10612
rs752278464	snp	C/T			intron-variant	TRIM3	GRCh38.p7	11:6466195	GCTCTTCCATTTATA[C/T]CCTGACCCACCTCTT	10612
rs752442084	snp	A/C	3.5392e-05	0.00420651	intron-variant	TRIM3	GRCh38.p7	11:6456261	CACCCACTACCTGAG[A/C]CTGGCCCATCTGGCT	10612
rs752478685	snp	A/C/G	6.59874e-05	0.00574369	missense, synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6457377	TTGCTCCAGGTCCTC[A/C/G]AACGCTGCACTGATC	10612
rs752482754	in-del	-/GAGT			intron-variant	TRIM3	GRCh38.p7	11:6468859	CTAAAGACTGTGAAT[-/GAGT]GAATGAATGAATGAA	10612
rs752517633	snp	A/G			intron-variant, utr-variant-5-prime, upstream-variant-2KB	TRIM3	GRCh38.p7	11:6473174	AATTGCAGAAGGGAG[A/G]AGGTCAGAACCAGGG	10612
rs752523158	snp	A/G			intron-variant	TRIM3	GRCh38.p7	11:6458931	TAGAGGATTACATGT[A/G]AAGTACTTACTTATA	10612
rs752724316	snp	C/T	5.14196e-05	0.00507022	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456786	TCGTGGTGAGCAGTG[C/T]GCCCAGATTGAGCAC	10612
rs752724347	snp	A/G			intron-variant	TRIM3	GRCh38.p7	11:6470204	TAAGAAACTGCCTTG[A/G]TTAGGAGAATAGCAA	10612
rs752744626	snp	C/T			intron-variant	TRIM3	GRCh38.p7	11:6471378	ACTGCAGGTTACAGT[C/T]TTTGGGCTTTCTCTG	10612
rs752748088	snp	C/T			intron-variant	TRIM3	GRCh38.p7	11:6452743	AGAAGTGAGGGGGCA[C/T]TAAAAGGTACAGTTT	10612
rs752774607	snp	A/G	3.73559e-05	0.00432164	intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6449491	ACCTGGCCTCAGGCA[A/G]AGGGTAGGGCTTTGG	10612
rs752808682	snp	C/T	3.44347e-05	0.00414923	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456638	CCGGTGATCTCTGCA[C/T]GCAGCTCAGCGCTGC	10612
rs752809928	snp	A/G	3.39541e-05	0.00412018	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	TRIM3	GRCh38.p7	11:6458122	TACACTGAGGGGGTG[A/G]GGGTCCTCCGGGTCG	10612
rs753054514	snp	C/T	1.64846e-05	0.0028709	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6451357	TGGTGTCCACTGCCA[C/T]ACCTGTGGGGCGCTG	10612
rs753082195	snp	C/T			intron-variant	TRIM3	GRCh38.p7	11:6463692	ATGGGAGTGGGGTAA[C/T]GGGAGCCAGGAGTGG	10612
rs753143225	in-del	-/T			intron-variant	TRIM3	GRCh38.p7	11:6462598	TTCTTTTTTAGAGAC[-/T]GCATCTCACTATGTT	10612
rs753182719	snp	A/G			intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6450332	CTTCCCTACTAGACT[A/G]TAATCAAGAAGACAC	10612
rs753206806	snp	A/G			intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6451585	GACAAAATCAAACAT[A/G]GCAGCAGGTCTGGGG	10612
rs753248745	snp	A/G	1.68542e-05	0.0029029	intron-variant	TRIM3	GRCh38.p7	11:6451103	CTTTATTCTGACAGT[A/G]GGGAAAGTAGTCCTA	10612
rs753369575	snp	C/G	1.6519e-05	0.00287388	intron-variant	TRIM3	GRCh38.p7	11:6449291	CCCCTCATGTCATTC[C/G]CAGGCCTTACTCACC	10612
rs753377828	snp	A/G	1.73739e-05	0.00294731	intron-variant	TRIM3	GRCh38.p7	11:6457039	CAACACCTGATGAGG[A/G]GTAGGGGAGGAGTGG	10612
rs753384739	snp	C/G	2.00262e-05	0.00316429	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456494	ACGCGGAAGGGGCTG[C/G]CGCGCACTGGCTGTC	10612
rs753399592	snp	A/G			intron-variant	TRIM3	GRCh38.p7	11:6464007	GGGCAGAAGGCAGAG[A/G]AAAAGTGCGGATAGA	10612
rs753427401	snp	A/G			intron-variant	TRIM3	GRCh38.p7	11:6464756	CTTTGGGAGGCCGAG[A/G]TAGGCGGATTGCCTG	10612
rs753489834	snp	C/T	1.64768e-05	0.00287021	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6449130	TGGACCATACAGTGG[C/T]TCTGCAGATGTGTTG	10612
rs753560845	snp	C/G	3.2981e-05	0.00406071	intron-variant	TRIM3	GRCh38.p7	11:6456274	AGCCTGGCCCATCTG[C/G]CTCTGCCCTCGGCTG	10612
rs753881199	snp	C/G	1.66147e-05	0.0028822	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6450921	TCAGTGGCCCCACGG[C/G]CCCCAAAACGGCCAA	10612
rs753962365	snp	A/G	6.75596e-05	0.00581165	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456889	CTGTGCCGCCAATGC[A/G]GCCAGCCGCTCTCGC	10612
rs754057241	snp	C/T			intron-variant	TRIM3	GRCh38.p7	11:6468668	CAGGGGCAGAAGCCA[C/T]GTCAGAGTGACTGAA	10612
rs754110172	snp	C/G			intron-variant	TRIM3	GRCh38.p7	11:6470165	GCTATGTGGAAAATA[C/G]TTTAAAGGGCAAGGA	10612
rs754163124	snp	C/G	1.71352e-05	0.00292699	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456788	GTGGTGAGCAGTGCG[C/G]CCAGATTGAGCACCG	10612
rs754197621	snp	A/G	1.95651e-05	0.00312764	intron-variant	TRIM3	GRCh38.p7	11:6458032	CTCCTCCCACCCCAA[A/G]TCCCGGCCTCACTGG	10612
rs754211134	snp	C/G			intron-variant	TRIM3	GRCh38.p7	11:6459880	GTTCAGCCTTGTCCT[C/G]GTTGAATTTACTGTA	10612
rs754235527	snp	A/G			utr-variant-3-prime, upstream-variant-2KB	ARFIP2, TRIM3	GRCh38.p7	11:6474906	GGCCCATTAAGTGGC[A/G]GCTCATATAAGGACC	10612
rs754286991	snp	C/T			utr-variant-3-prime, upstream-variant-2KB, downstream-variant-500B	ARFIP2, TRIM3	GRCh38.p7	11:6476197	TTCCCCAGGGCCTAA[C/T]GCAGTCCCTGGCAAA	10612
rs754366101	snp	C/T			intron-variant	TRIM3	GRCh38.p7	11:6461686	TCACTGAATCTAGTG[C/T]TTCCCCATGCAAAAC	10612
rs754443142	snp	A/C			utr-variant-3-prime, nc-transcript-variant	TRIM3	GRCh38.p7	11:6448890	GGGGGTGGGGGTAGG[A/C]GAGGGAGGGCACCGG	10612
rs754454785	snp	C/T			intron-variant	TRIM3	GRCh38.p7	11:6455399	CTACCCTGGTGCCCA[C/T]TGTACTAGGCTCTGA	10612
rs754559037	snp	A/G	1.65225e-05	0.00287419	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6451408	CTCGGACCCCAAAAC[A/G]GAACTTGAACTGGCC	10612
rs754572536	snp	A/G			intron-variant	TRIM3	GRCh38.p7	11:6464762	GAGGCCGAGGTAGGC[A/G]GATTGCCTGAGTTCA	10612
rs754627548	snp	G/T			intron-variant	TRIM3	GRCh38.p7	11:6452657	CTTGGGTTCTGCAGT[G/T]GTCCCCTGTGGCAGG	10612
rs754747895	in-del	-/T	1.66801e-05	0.00288787	intron-variant	TRIM3	GRCh38.p7	11:6450887	TTGGAGCTGTCCCCC[-/T]ATACCTGCAAAGTGG	10612
rs754773960	snp	C/G	1.6528e-05	0.00287467	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6457309	ACCTTCTGTTTGGCC[C/G]CACAAATGGTCTCCA	10612
rs754875188	snp	C/T	3.44305e-05	0.00414898	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456624	GCGTGCCGTCCGGGC[C/T]GGTGATCTCTGCACG	10612
rs754877406	snp	G/T	4.99422e-05	0.00499686	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6449319	ACCTGGATGCGGCTG[G/T]TGCCCCAGTCAGCCA	10612
rs754946691	snp	A/T			intron-variant	TRIM3	GRCh38.p7	11:6463968	GGGAAGCAGTATCTC[A/T]GGTGCAGAGCCAGGT	10612
rs754966175	snp	C/T	3.64199e-05	0.00426716	intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6449479	TAGGGACTGGGGACC[C/T]GGCCTCAGGCAGAGG	10612
rs754999159	snp	C/T	1.64969e-05	0.00287196	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456522	GTCCGTAGAGCAGCA[C/T]CGAGAGGAGCAGCTC	10612
rs755061476	snp	G/T			intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6450188	CATTTAATTCCCACT[G/T]GTGCTTGAGGTCCTC	10612
rs755092746	snp	A/C			intron-variant	TRIM3	GRCh38.p7	11:6468689	AGTGACTGAAGAGTA[A/C]ATGGGAGATGAAGTT	10612
rs755221954	snp	C/T			intron-variant	TRIM3	GRCh38.p7	11:6455095	GCTCCTTCCAGTTCC[C/T]TGAACCACCTCCTCC	10612
rs755229178	snp	G/T	1.73375e-05	0.00294422	intron-variant	TRIM3	GRCh38.p7	11:6457688	CCAGGACCCTGCCCA[G/T]TGCCTACCGGCCACG	10612
rs755303014	snp	A/G			intron-variant	TRIM3	GRCh38.p7	11:6459991	TAGATGGCTTCGGTA[A/G]CACTGGGAGAGGATG	10612
rs755329548	snp	C/G	1.68179e-05	0.00289977	intron-variant	TRIM3	GRCh38.p7	11:6451101	GGCTTTATTCTGACA[C/G]TGGGGAAAGTAGTCC	10612
rs755453060	snp	A/G	1.64849e-05	0.00287092	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6450993	TTGTTGTCGACCACA[A/G]TGATATGTCCATTCC	10612
rs755470661	snp	A/G	1.66693e-05	0.00288693	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456934	CAGCAACACCTCCGG[A/G]GCCGAGCCCAGGCGC	10612
rs755485446	snp	A/C/T	0.000186185	0.00964676	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6457006	CTGACCCTGGCGCAG[A/C/T]GTGTCCAGCTGGCTT	10612
rs755512086	snp	C/T			utr-variant-3-prime, nc-transcript-variant	TRIM3	GRCh38.p7	11:6448932	CCCACAGCCCACATT[C/T]AGTGCTGCCAGGTCT	10612
rs755614612	snp	A/C	1.64781e-05	0.00287033	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6449081	CAGCATCAGCCACCA[A/C]CACATGGCCATCCGA	10612
rs755666712	snp	C/T			intron-variant	TRIM3	GRCh38.p7	11:6465520	GGAGGATCCTCATCC[C/T]CCCCACAGGGTCCTC	10612
rs755683197	snp	A/G			intron-variant	TRIM3	GRCh38.p7	11:6463062	ATGCAAAAATTAACC[A/G]GATGTGGTGGCGTGC	10612
rs755791471	snp	C/G			intron-variant	TRIM3	GRCh38.p7	11:6463911	CCAGTTGATAAAGGA[C/G]AGTGGGCAGTGGAGC	10612
rs755797035	snp	C/G	3.55999e-05	0.00421885	intron-variant	TRIM3	GRCh38.p7	11:6456271	CTGAGCCTGGCCCAT[C/G]TGGCTCTGCCCTCGG	10612
rs755885544	snp	A/C	1.76602e-05	0.0029715	utr-variant-3-prime, nc-transcript-variant	TRIM3	GRCh38.p7	11:6448842	GCTCACCCAGTCACC[A/C]AAGCAAGAACCGAAT	10612
rs755992857	snp	C/T			intron-variant	TRIM3	GRCh38.p7	11:6454902	GTTTAGAAGTAAGGA[C/T]CTTCAGCGAAAAGTT	10612
rs756104137	snp	A/G	1.87078e-05	0.00305836	intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6449492	CCTGGCCTCAGGCAG[A/G]GGGTAGGGCTTTGGA	10612
rs756177459	in-del	-/A			intron-variant	TRIM3	GRCh38.p7	11:6471582	CTTCAGCTGTGAAAT[-/A]AGAGACACAAAGCTG	10612
rs756304376	snp	A/C	1.72136e-05	0.00293369	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456640	GGTGATCTCTGCACG[A/C]AGCTCAGCGCTGCCT	10612
rs756307761	in-del	-/AG	0.000130268	0.0080695	intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6449490	GACCTGGCCTCAGGC[-/AG]AGGGTAGGGCTTTGG	10612
rs756328311	snp	A/G			utr-variant-3-prime, nc-transcript-variant	TRIM3	GRCh38.p7	11:6448879	AGTGCAACCGTGGGG[A/G]TGGGGGTAGGAGAGG	10612
rs756351130	snp	C/T	3.69911e-05	0.00430049	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456535	CACCGAGAGGAGCAG[C/T]TCGCCTTCCGTGCGC	10612
rs756399381	snp	C/T	1.67598e-05	0.00289476	intron-variant	TRIM3	GRCh38.p7	11:6457895	TAGACATCACACTTC[C/T]TTGTCCCCTCCCCAC	10612
rs756478196	snp	A/G			intron-variant, utr-variant-5-prime, upstream-variant-2KB	TRIM3	GRCh38.p7	11:6473198	ACCAGGGAGGGGCCT[A/G]GGGTCCTCCAGGCAG	10612
rs756492027	snp	C/T			intron-variant	TRIM3	GRCh38.p7	11:6471751	TAACTCTGAGGATGG[C/T]ACAGAATAAAGAAGG	10612
rs756669130	snp	C/T	1.64887e-05	0.00287125	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6451368	GCCACACCTGTGGGG[C/T]GCTGCAGCTGCCCAG	10612
rs756705717	snp	A/G	1.74616e-05	0.00295474	intron-variant	TRIM3	GRCh38.p7	11:6457046	TGATGAGGGGTAGGG[A/G]AGGAGTGGGTGAGCA	10612
rs756843900	snp	A/C	1.65037e-05	0.00287256	intron-variant	TRIM3	GRCh38.p7	11:6465525	ATCCTCATCCTCCCC[A/C]CAGGGTCCTCATCCC	10612
rs756887264	snp	C/T			intron-variant	TRIM3	GRCh38.p7	11:6461969	TATTCTCTCCAATTT[C/T]ACCTCATCCCACTTT	10612
rs756938509	snp	C/T	3.30502e-05	0.00406497	utr-variant-5-prime, intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6465698	CCCTCTTTGCCATGG[C/T]GCCCACAGATGGCTC	10612
rs756964309	snp	A/G	3.69604e-05	0.0042987	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456403	GCGCACATGGCTGCC[A/G]GGGCCGCCAGGGGAC	10612
rs757335002	snp	A/C			intron-variant	TRIM3	GRCh38.p7	11:6472860	CTACTGTCAGGCCTG[A/C]AGCTCTGATTCCAAT	10612
rs757344745	snp	A/C/T	3.30886e-05	0.00406736	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6450930	CCACGGCCCCCAAAA[A/C/T]GGCCAACCAGTTTGC	10612
rs757482301	snp	G/T	1.65685e-05	0.00287819	intron-variant	TRIM3	GRCh38.p7	11:6450658	CAGGGCAGTAAGCTG[G/T]GATGCTGAGTGGGAT	10612
rs757495139	snp	A/G			intron-variant	TRIM3	GRCh38.p7	11:6454840	TAGCAGAGCTGGATC[A/G]ATGACATGAGTACTC	10612
rs757523393	snp	C/T	1.7129e-05	0.00292647	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456794	AGCAGTGCGCCCAGA[C/T]TGAGCACCGATCGCC	10612
rs757557573	snp	C/G			intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6451762	AAAGGCATTCAAGCA[C/G]AGTGAACAGATTGTA	10612
rs757574916	snp	C/G			intron-variant	TRIM3	GRCh38.p7	11:6453347	ATTCTTGACATTTGA[C/G]GATTTAGCAAAATCT	10612
rs757593762	snp	A/G	1.68946e-05	0.00290638	missense, utr-variant-5-prime, nc-transcript-variant	TRIM3	GRCh38.p7	11:6458133	GGTGGGGGTCCTCCG[A/G]GTCGTGGGCCCCATC	10612
rs757648121	snp	C/T	1.72362e-05	0.00293561	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456668	CCTGTGCGCACCAAC[C/T]GCCCGTCCTTGTCTT	10612
rs757687296	snp	C/T	1.65408e-05	0.00287578	intron-variant	TRIM3	GRCh38.p7	11:6456046	CTCTTATTTTGGTGG[C/T]GGAGGAGAGCGGTAA	10612
rs757715831	in-del	-/AGGCTCAACACCTG			utr-variant-3-prime, upstream-variant-2KB	ARFIP2, TRIM3	GRCh38.p7	11:6475223	ACAAGGTTCAGATTT[-/AGGCTCAACACCTG]GGTGCAGCAGGAGCT	10612
rs757791376	snp	C/T			intron-variant	TRIM3	GRCh38.p7	11:6452761	AAAGGTACAGTTTAG[C/T]GGTGAGGTAATGCCC	10612
rs757844231	snp	C/T	1.94165e-05	0.00311575	intron-variant	TRIM3	GRCh38.p7	11:6458036	TCCCACCCCAAGTCC[C/T]GGCCTCACTGGGCCT	10612
rs757886137	snp	C/T	3.30055e-05	0.00406222	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6451389	AGCTGCCCAGGTGAG[C/T]GTCCTCGGACCCCAA	10612
rs757913287	snp	A/G			intron-variant	TRIM3	GRCh38.p7	11:6460929	TTTTTTTTTTGAGAC[A/G]GAGTCCTGCTCTGTC	10612
rs757925771	snp	G/T			intron-variant	TRIM3	GRCh38.p7	11:6466324	GTTACTACCCCTAAT[G/T]CAGGCAACCATCTGT	10612
rs757983865	snp	A/C	3.55454e-05	0.00421562	intron-variant	TRIM3	GRCh38.p7	11:6457061	GAGGAGTGGGTGAGC[A/C]GACTGGCACAGGGGG	10612
rs758048764	snp	G/T			intron-variant	TRIM3	GRCh38.p7	11:6453763	TGTCAACTGATGCTG[G/T]TTCCACTCAGTGAGG	10612
rs758063228	snp	C/T	1.65201e-05	0.00287398	intron-variant	TRIM3	GRCh38.p7	11:6449296	CATGTCATTCCCAGG[C/T]CTTACTCACCTGGAT	10612
rs758084490	snp	A/T	1.67601e-05	0.00289478	intron-variant	TRIM3	GRCh38.p7	11:6457280	GATGGTAGGAAAGGG[A/T]GAACACAAGACACAC	10612
rs758301500	snp	C/G	1.86604e-05	0.00305448	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456423	CGCCAGGGGACTTGA[C/G]ACGGCGCTTCACATC	10612
rs758303478	snp	A/G	1.66449e-05	0.00288482	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6457752	GTGCTGCTCCACCAC[A/G]TCCCTCAGCAGCACT	10612
rs758391984	snp	A/G	0.000117578	0.00766649	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456498	GGAAGGGGCTGCCGC[A/G]CACTGGCTGTCCGTA	10612
rs758420067	snp	A/G	1.64773e-05	0.00287026	intron-variant	TRIM3	GRCh38.p7	11:6449185	CTGTCGAATACCTGG[A/G]GAAGGAGTGCAGAAA	10612
rs758424852	snp	A/C	1.75533e-05	0.00296249	intron-variant	TRIM3	GRCh38.p7	11:6457663	ACACCATCCCTGTGG[A/C]CCCACCAGCCCAGGA	10612
rs758444852	snp	A/T			intron-variant	TRIM3	GRCh38.p7	11:6470358	GAAGAGCAGTTTGGA[A/T]GAGAGGGTGATAAGT	10612
rs758565275	snp	A/C	5.83017e-05	0.00539884	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456480	GACGCAGGGCACGCA[A/C]GCGGAAGGGGCTGCC	10612
rs758603484	snp	C/T			synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6450581	ATGGAAGTCCGTTAC[C/T]ACAATTTCATTCTTG	10612
rs758656508	snp	A/G			intron-variant	TRIM3	GRCh38.p7	11:6452819	CTCAATACTGATGAG[A/G]CTTTGGGATGTCTTG	10612
rs758796306	snp	C/T	6.63438e-05	0.00575912	intron-variant	TRIM3	GRCh38.p7	11:6450668	AGCTGGGATGCTGAG[C/T]GGGATGGGGAAGAGT	10612
rs758807446	snp	C/G	0.000664231	0.0182119	utr-variant-3-prime, nc-transcript-variant	TRIM3	GRCh38.p7	11:6448826	TGGGACCACAGTCCA[C/G]GCTCACCCAGTCACC	10612
rs758828714	snp	C/T	3.35289e-05	0.0040943	missense, utr-variant-5-prime, nc-transcript-variant	TRIM3	GRCh38.p7	11:6458154	GGGCCCCATCAGGTG[C/T]CTGCTGCATTGCCTC	10612
rs758919729	snp	C/T			intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6451637	GGGATTGTGAGAACA[C/T]GAAGGGATGAAGGGG	10612
rs758961744	snp	A/G	0.000339805	0.0130302	intron-variant	TRIM3	GRCh38.p7	11:6458337	CAGAGTGGGTGGGGT[A/G]GCATAAGTGCACCCT	10612
rs758997395	in-del	-/TG			intron-variant	TRIM3	GRCh38.p7	11:6454483	AGCAGTGAGCACACC[-/TG]TGTGTGTGCACAACA	10612
rs759078989	snp	C/G			intron-variant	TRIM3	GRCh38.p7	11:6465953	CAAACCTGGCTCAGT[C/G]TCTCACCAGCTATGT	10612
rs759259818	snp	C/G			intron-variant	TRIM3	GRCh38.p7	11:6471452	GAATCCTTTAAATAA[C/G]ATTAGCAGGGAAGGA	10612
rs759272381	snp	A/G	3.30398e-05	0.00406434	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6457415	GGGCCTCTGCCTTGC[A/G]CTCCTGCAGCTGCTG	10612
rs759394530	snp	A/T			intron-variant	TRIM3	GRCh38.p7	11:6457601	TCCCTGAGACTTCCA[A/T]CTCTGCCCTTCCCAG	10612
rs759445381	snp	C/T	1.71531e-05	0.00292852	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456772	GTGTGCAGTGGCGCT[C/T]GTGGTGAGCAGTGCG	10612
rs759486247	snp	A/C			intron-variant	TRIM3	GRCh38.p7	11:6463416	CAATTTCTCAGCCAG[A/C]TTTTCTCCAGGAGTG	10612
rs759539419	snp	A/G			intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6451461	AGAGGAGCAAGGGGA[A/G]GGAGCAGGTAGGAGG	10612
rs759608189	snp	A/G	4.99513e-05	0.00499731	intron-variant	TRIM3	GRCh38.p7	11:6457877	CTCCAGTCGGGTAAT[A/G]GCTAGACATCACACT	10612
rs759655523	snp	C/T	1.64811e-05	0.00287059	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6451342	CAATTATGTCTCCAT[C/T]GGTGTCCACTGCCAC	10612
rs759731962	snp	C/T	3.29897e-05	0.00406125	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6457345	CTGACCAGAGCCTGC[C/T]TGCGCTGCTGCAGTG	10612
rs760012445	snp	A/G			utr-variant-3-prime, upstream-variant-2KB, downstream-variant-500B	ARFIP2, TRIM3	GRCh38.p7	11:6476240	GTAAATATTTGCTGT[A/G]TGAATGAATGCATGA	10612
rs760030045	snp	C/T	3.29766e-05	0.00406045	missense, intron-variant, utr-variant-5-prime, nc-transcript-variant	TRIM3	GRCh38.p7	11:6465676	ACCTCTGGGCCAGGG[C/T]TGTCCTCCCTCTTTG	10612
rs760107465	snp	A/G			intron-variant	TRIM3	GRCh38.p7	11:6458647	CTACTGTCTACTCTT[A/G]CCAAATTTATGCCAA	10612
rs760121855	snp	A/G			intron-variant	TRIM3	GRCh38.p7	11:6472082	TTTCACCTTTCAGAT[A/G]CAAGCTATGACTACA	10612
rs760162365	snp	C/T	3.32984e-05	0.00408021	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6449403	CCATTGCCCTCGCCA[C/T]GGGAGCCAAACTTGA	10612
rs760181903	snp	C/G/T	0.000118888	0.00770923	intron-variant	TRIM3	GRCh38.p7	11:6457513	CCAGAGTTGCTGAGG[C/G/T]TGGCTTTGCCGAACT	10612
rs760301696	snp	A/G	5.09083e-05	0.00504495	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6457713	GCCACGCACAGCCTC[A/G]AGCTGGCGCTGCAGG	10612
rs760418938	snp	C/T			intron-variant	TRIM3	GRCh38.p7	11:6469203	GTGGTCTGCTGGGTC[C/T]TGCTGGGGTAGCTGG	10612
rs760460780	snp	C/T	1.83781e-05	0.00303129	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456395	GCCTTCTGGCGCACA[C/T]GGCTGCCGGGGCCGC	10612
rs760507659	snp	C/G			intron-variant	TRIM3	GRCh38.p7	11:6451143	CAAAGCAGAATCTTG[C/G]GCTGGGGAAAGAACA	10612
rs760508275	snp	A/G	1.69089e-05	0.0029076	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456885	AGGCCTGTGCCGCCA[A/G]TGCAGCCAGCCGCTC	10612
rs760584439	snp	A/C			intron-variant	TRIM3	GRCh38.p7	11:6471141	CTTTTCAGTTTCTCC[A/C]AATTCTCAAATAGCA	10612
rs760734929	snp	C/T	1.66103e-05	0.00288182	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456961	GCGCAGTGCCTGCTC[C/T]GCAAAGCTGCAGCTA	10612
rs760797760	snp	A/G	1.66932e-05	0.002889	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	TRIM3	GRCh38.p7	11:6458275	CGTCAGGCTCTGGGC[A/G]GGGATATAGTTTTGG	10612
rs760883267	snp	A/C/G	3.30143e-05	0.00406279	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6457397	CTGCACTGATCTGGG[A/C/G]CAGGGCCTCTGCCTT	10612
rs760955244	snp	G/T			intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6450135	CTTGGCTCTTCCTGT[G/T]TCTTTTGTCTCAAAC	10612
rs760957194	snp	A/G			intron-variant	TRIM3	GRCh38.p7	11:6463359	ACTTAGCCAGTCCCT[A/G]GCAAACAGTAAGCAA	10612
rs760990411	snp	A/G	1.69605e-05	0.00291204	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	TRIM3	GRCh38.p7	11:6458125	ACTGAGGGGGTGGGG[A/G]TCCTCCGGGTCGTGG	10612
rs761052622	snp	A/G			intron-variant	TRIM3	GRCh38.p7	11:6467779	GTCTCAAAAAAAAAA[A/G]GTGATTTTATCCTAA	10612
rs761171625	snp	A/C	1.71064e-05	0.00292454	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6449437	GGAACTCTCCATCGG[A/C]ACTGTACACCTGGCG	10612
rs761228283	snp	C/T	1.64953e-05	0.00287182	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6457354	GCCTGCTTGCGCTGC[C/T]GCAGTGCTTGCTCCA	10612
rs761269355	snp	C/T			utr-variant-3-prime, upstream-variant-2KB	ARFIP2, TRIM3	GRCh38.p7	11:6474869	GGAGACTCGGTACCT[C/T]TCATGTTGAAAAATC	10612
rs761324547	snp	C/G			intron-variant	TRIM3	GRCh38.p7	11:6469581	TGCTATCCCTGTATT[C/G]GTTATTCCCACCATA	10612
rs761434194	snp	A/G	0.000115966	0.00761377	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6457846	CAGTAAAACTCCATC[A/G]TCTGCGGTACAAGGA	10612
rs761439756	snp	C/T	1.73525e-05	0.0029455	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456587	GTGCCATTCTTGTGG[C/T]CCACCACTGGCACCG	10612
rs761539746	snp	G/T			intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6452090	GGACTCAAGACATAT[G/T]TAGGAGGTAGGCTCA	10612
rs761617065	snp	A/T			utr-variant-3-prime, nc-transcript-variant	TRIM3	GRCh38.p7	11:6448831	CCACAGTCCAGGCTC[A/T]CCCAGTCACCAAAGC	10612
rs761629806	snp	G/T			intron-variant	TRIM3	GRCh38.p7	11:6468371	CAAGAGAAAAGTCTG[G/T]ACTGGTTATTGATTT	10612
rs761648821	snp	C/T			intron-variant	TRIM3	GRCh38.p7	11:6462590	TTTTTAAATTCTTTT[C/T]TAGAGACTGCATCTC	10612
rs761739298	in-del	-/AGA			intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6451675	AGAAAAGGCTCCAAG[-/AGA]AGAAGATGTCTGAAC	10612
rs761850166	snp	G/T			utr-variant-3-prime, nc-transcript-variant	TRIM3	GRCh38.p7	11:6448990	TCCAATCACCCCAAT[G/T]TCTGTCCCTCCACAA	10612
rs761883704	snp	C/T	1.65081e-05	0.00287293	intron-variant	TRIM3	GRCh38.p7	11:6451264	AAAGTGACAGCAGGC[C/T]TCTCACCTTGAACTT	10612
rs761983386	snp	A/G			missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456743	CGCAGGCCCTCTCCC[A/G]TGGCCACCGTTTCGT	10612
rs762006556	snp	A/G	1.65531e-05	0.00287686	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6451059	CCAGCTCCAATCTTG[A/G]TCTGGAGGAAGAGAA	10612
rs762028401	snp	A/G	1.82433e-05	0.00302016	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456364	TGTGCTGTACATGGA[A/G]CTGGGCCTACGCACT	10612
rs762109636	snp	C/T	9.5109e-05	0.00689532	utr-variant-3-prime, nc-transcript-variant	TRIM3	GRCh38.p7	11:6448797	AGGGTAGGGTGAAGC[C/T]CTGCACACATCCTTG	10612
rs762184285	snp	C/G	1.68117e-05	0.00289923	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456903	CAGCCAGCCGCTCTC[C/G]CATGTGCTTGCGCAC	10612
rs762303170	snp	C/T			intron-variant	TRIM3	GRCh38.p7	11:6465396	ACAGGTTCTTGCCCT[C/T]AAAACCTCATTTCCT	10612
rs762332953	snp	A/T	1.64955e-05	0.00287184	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6457362	GCGCTGCTGCAGTGC[A/T]TGCTCCAGGTCCTCG	10612
rs762362326	snp	C/T	1.65094e-05	0.00287305	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6457404	GATCTGGGCCAGGGC[C/T]TCTGCCTTGCGCTCC	10612
rs762567513	snp	A/G	1.72445e-05	0.00293632	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456733	TAGCGCCTGGCGCAG[A/G]CCCTCTCCCGTGGCC	10612
rs762608565	snp	A/C			intron-variant	TRIM3	GRCh38.p7	11:6467972	CTGAGCTACAAGCAA[A/C]AAGCTGGACTGATTT	10612
rs762665364	snp	C/T			intron-variant	TRIM3	GRCh38.p7	11:6460621	GATTCAGGGGCCTGA[C/T]GATGGCTCAGATTAG	10612
rs762672434	snp	A/G	1.72451e-05	0.00293637	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456611	GGCACCGGAAGGCGC[A/G]TGCCGTCCGGGCCGG	10612
rs762692979	snp	C/G	3.2963e-05	0.00405961	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	TRIM3	GRCh38.p7	11:6458089	ATGGTTGGGGCAGGA[C/G]AGAGGGCGGCCAGCC	10612
rs762763007	snp	A/T			intron-variant	TRIM3	GRCh38.p7	11:6458935	GGATTACATGTAAAG[A/T]ACTTACTTATATTTG	10612
rs762831120	snp	A/G	1.76558e-05	0.00297113	intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6449458	ACACCTGGCGGGGGA[A/G]GGGGCTAGGGACTGG	10612
rs762938990	snp	G/T	1.66217e-05	0.0028828	intron-variant	TRIM3	GRCh38.p7	11:6457867	GGTACAAGGACTCCA[G/T]TCGGGTAATGGCTAG	10612
rs763042966	snp	C/T			intron-variant	TRIM3	GRCh38.p7	11:6454804	GGGTCAGAGAGTAGC[C/T]GTCACTGAGGGAAAG	10612
rs763058510	snp	A/G	1.648e-05	0.0028705	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6451310	GATGCTGACCCAACG[A/G]TTGTCATAGTCTGCC	10612
rs763067089	snp	A/G	0.000185265	0.00962279	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6457002	GTTCCTGACCCTGGC[A/G]CAGTGTGTCCAGCTG	10612
rs763323426	snp	A/G	8.32868e-05	0.00645263	intron-variant	TRIM3	GRCh38.p7	11:6451080	AGGAAGAGAATATCC[A/G]TAAGAGGCTTTATTC	10612
rs763436861	in-del	-/CGC			intron-variant, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	TRIM3	GRCh38.p7	11:6473910	CTCCGCCTGTCCCCG[-/CGC]CGCCGGCGCCGCCGC	10612
rs763490500	snp	C/T	1.82901e-05	0.00302402	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456382	GGGCCTACGCACTGC[C/T]TTCTGGCGCACATGG	10612
rs763650093	snp	G/T	1.64898e-05	0.00287135	missense, intron-variant, utr-variant-5-prime, nc-transcript-variant	TRIM3	GRCh38.p7	11:6465678	CTCTGGGCCAGGGCT[G/T]TCCTCCCTCTTTGCC	10612
rs763740821	snp	C/T			intron-variant	TRIM3	GRCh38.p7	11:6454823	ACTGAGGGAAAGGAC[C/T]TTAGCAGAGCTGGAT	10612
rs763745606	snp	C/T	1.68886e-05	0.00290586	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6457720	ACAGCCTCGAGCTGG[C/T]GCTGCAGGGCCGCCT	10612
rs763748898	snp	A/G	1.65168e-05	0.00287369	intron-variant	TRIM3	GRCh38.p7	11:6449282	GGAAACCGCCCCCTC[A/G]TGTCATTCCCAGGCC	10612
rs763840735	snp	C/T	1.94808e-05	0.0031209	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456482	CGCAGGGCACGCACG[C/T]GGAAGGGGCTGCCGC	10612
rs763862185	snp	A/C	1.71982e-05	0.00293237	intron-variant	TRIM3	GRCh38.p7	11:6457522	CTGAGGGTGGCTTTG[A/C]CGAACTTTCCCTTCT	10612
rs763865804	snp	C/G			intron-variant	TRIM3	GRCh38.p7	11:6455540	GGTGTATGAGGTTAT[C/G]GGAGAGGCAGTGGGA	10612
rs763867953	snp	A/G	1.64781e-05	0.00287033	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6449095	ACCACATGGCCATCC[A/G]AGGTCAGTGCCAGGC	10612
rs763883653	snp	A/C			utr-variant-3-prime, upstream-variant-2KB	ARFIP2, TRIM3	GRCh38.p7	11:6475950	CGCCTCGGCCTCCCA[A/C]AGTGCTGGGATTACA	10612
rs763949137	snp	C/G			intron-variant	TRIM3	GRCh38.p7	11:6460681	TAGAAACAGACATCA[C/G]AACTGAAGGCAGCTG	10612
rs763968458	snp	C/G			intron-variant, upstream-variant-2KB	TRIM3	GRCh38.p7	11:6473538	AACACACACAAGCTC[C/G]CAAACCCCGCGCTCC	10612
rs764118096	snp	A/C/G	3.31336e-05	0.00407012	intron-variant	TRIM3	GRCh38.p7	11:6450655	CTTCAGGGCAGTAAG[A/C/G]TGGGATGCTGAGTGG	10612
rs764133621	snp	A/G			intron-variant	TRIM3	GRCh38.p7	11:6466348	CATCTGTTCTCTCCT[A/G]GAATACAGCAATAGC	10612
rs764199742	snp	C/T			intron-variant	TRIM3	GRCh38.p7	11:6471571	GTGGGCCAGGTCCTT[C/T]AGCTGTGAAATAGAG	10612
rs764311440	snp	C/T	3.38152e-05	0.00411175	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456886	GGCCTGTGCCGCCAA[C/T]GCAGCCAGCCGCTCT	10612
rs764344270	snp	C/T	0.000439858	0.0148235	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	TRIM3	GRCh38.p7	11:6458131	GGGGTGGGGGTCCTC[C/T]GGGTCGTGGGCCCCA	10612
rs764434165	snp	A/T	1.69392e-05	0.00291021	missense, utr-variant-5-prime, nc-transcript-variant	TRIM3	GRCh38.p7	11:6458296	ATAGTTTTGGAGACA[A/T]CTGTCCAGGAAGGAG	10612
rs764453292	snp	C/T	1.64961e-05	0.00287189	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6457356	CTGCTTGCGCTGCTG[C/T]AGTGCTTGCTCCAGG	10612
rs764491038	snp	A/G	1.6501e-05	0.00287232	intron-variant	TRIM3	GRCh38.p7	11:6456187	CTGCCTGTGGGAAGG[A/G]ACAGGAGGGAAAACA	10612
rs764541660	snp	C/T			intron-variant	TRIM3	GRCh38.p7	11:6464630	TACTTGATTGTTACC[C/T]ATTCTATGCTTGTGT	10612
rs764617582	snp	C/T	1.6585e-05	0.00287962	intron-variant	TRIM3	GRCh38.p7	11:6456039	TTGAAAACTCTTATT[C/T]TGGTGGTGGAGGAGA	10612
rs764715392	in-del	-/G			intron-variant	TRIM3	GRCh38.p7	11:6462969	CCCAGAACTTTGGGA[-/G]GCTGAGGCGGGCAGA	10612
rs764870240	snp	A/G	3.35694e-05	0.00409678	intron-variant	TRIM3	GRCh38.p7	11:6457277	GACGATGGTAGGAAA[A/G]GGTGAACACAAGACA	10612
rs764980978	snp	A/G	1.96585e-05	0.0031351	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456496	GCGGAAGGGGCTGCC[A/G]CGCACTGGCTGTCCG	10612
rs765180298	snp	C/T			intron-variant, utr-variant-5-prime, nc-transcript-variant	TRIM3	GRCh38.p7	11:6473084	CTCAGTCGAACTGAC[C/T]TCCCTGGGGTGCAGC	10612
rs765391483	snp	C/T			intron-variant	TRIM3	GRCh38.p7	11:6471474	AGGGAAGGAAAGCAA[C/T]GAAATTCATGGCCAT	10612
rs765457750	snp	A/G	3.31351e-05	0.00407019	intron-variant	TRIM3	GRCh38.p7	11:6451064	TCCAATCTTGGTCTG[A/G]AGGAAGAGAATATCC	10612
rs765553176	snp	A/C			utr-variant-3-prime, upstream-variant-2KB, downstream-variant-500B	ARFIP2, TRIM3	GRCh38.p7	11:6476420	GCTGCCTGGCCCCAG[A/C]TCTTTTGACTTGATA	10612
rs765637165	snp	A/C	1.64825e-05	0.00287071	stop-gained, nc-transcript-variant	TRIM3	GRCh38.p7	11:6449043	CTACTGGAGGTAGCG[A/C]TAGGCTTTAAAGCAG	10612
rs765675504	snp	C/T			intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6450210	GAGGTCCTCCTCATA[C/T]AGTCTTTCCTGAATC	10612
rs765739252	snp	C/T	2.10662e-05	0.0032454	utr-variant-3-prime, nc-transcript-variant	TRIM3	GRCh38.p7	11:6448809	AGCTCTGCACACATC[C/T]TTGGGACCACAGTCC	10612
rs765789195	snp	A/G			intron-variant	TRIM3	GRCh38.p7	11:6463579	CACAGGGTCCAGGAT[A/G]GGCAGGAAAGACAGG	10612
rs765791752	in-del	-/A			intron-variant	TRIM3	GRCh38.p7	11:6460657	ATGGGAGAGCAGAGG[-/A]ACACTTACTAGAAAC	10612
rs765801651	snp	A/G			intron-variant	TRIM3	GRCh38.p7	11:6459987	CATTTAGATGGCTTC[A/G]GTAGCACTGGGAGAG	10612
rs765851143	snp	A/C	1.65138e-05	0.00287343	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6457410	GGCCAGGGCCTCTGC[A/C]TTGCGCTCCTGCAGC	10612
rs765981493	snp	C/G			intron-variant	TRIM3	GRCh38.p7	11:6469816	CCTAGATCTGGAGCA[C/G]GGGTGGGTCCAGAGG	10612
rs766001275	snp	C/T	1.65111e-05	0.0028732	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6450594	ACTACAATTTCATTC[C/T]TGTTGTTCACAGCCA	10612
rs766057877	snp	C/G			intron-variant	TRIM3	GRCh38.p7	11:6464753	GCACTTTGGGAGGCC[C/G]AGGTAGGCGGATTGC	10612
rs766080596	snp	C/T	1.64963e-05	0.00287192	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6457365	CTGCTGCAGTGCTTG[C/T]TCCAGGTCCTCGAAC	10612
rs766094790	in-del	-/G			intron-variant	TRIM3	GRCh38.p7	11:6453864	GTACTGAGAGGAGGA[-/G]GGGGGATCAGACCTC	10612
rs766132326	snp	A/G			intron-variant	TRIM3	GRCh38.p7	11:6470062	CGCTTACCTGCTAGG[A/G]GATGAAGGATTTATC	10612
rs766199914	snp	C/T	3.44602e-05	0.00415077	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456736	CGCCTGGCGCAGGCC[C/T]TCTCCCGTGGCCACC	10612
rs766200168	snp	A/G	1.78567e-05	0.00298798	intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6449466	CGGGGGAAGGGGCTA[A/G]GGACTGGGGACCTGG	10612
rs766248520	snp	A/G			intron-variant	TRIM3	GRCh38.p7	11:6465854	TAGGGGCAAGACAGG[A/G]CAGTGACTGGAAGGA	10612
rs766249286	snp	A/G	3.84593e-05	0.00438499	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456511	GCGCACTGGCTGTCC[A/G]TAGAGCAGCACCGAG	10612
rs766257186	snp	C/G			intron-variant	TRIM3	GRCh38.p7	11:6471167	TAGCATTAATTTTCC[C/G]CAGGACTTCCTCCTA	10612
rs766322893	snp	A/G	3.4481e-05	0.00415202	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456616	CGGAAGGCGCGTGCC[A/G]TCCGGGCCGGTGATC	10612
rs766517242	snp	C/G	1.65899e-05	0.00288005	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6457771	CTCAGCAGCACTGTG[C/G]CATGCTCACGATGCT	10612
rs766553711	snp	G/T			intron-variant	TRIM3	GRCh38.p7	11:6462781	TATGGGGATACCTGG[G/T]TGTGGTAGCCTGCAC	10612
rs766563497	snp	C/T	1.67239e-05	0.00289166	intron-variant	TRIM3	GRCh38.p7	11:6451091	ATCCATAAGAGGCTT[C/T]ATTCTGACAGTGGGG	10612
rs766703556	snp	C/T	1.64776e-05	0.00287028	synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant	TRIM3	GRCh38.p7	11:6465654	GAACTGCTTGTCCAT[C/T]GGCTGGACCTCTGGG	10612
rs766731764	snp	C/G			intron-variant	TRIM3	GRCh38.p7	11:6451148	CAGAATCTTGGGCTG[C/G]GGAAAGAACAGGGAG	10612
rs766757188	snp	A/G			utr-variant-3-prime, upstream-variant-2KB	ARFIP2, TRIM3	GRCh38.p7	11:6474878	GTACCTTTCATGTTG[A/G]AAAATCCCCAGTGGC	10612
rs766781718	snp	C/G	4.94368e-05	0.00497152	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6449058	ATAGGCTTTAAAGCA[C/G]TGGTTGCCAGCATCA	10612
rs766872340	snp	C/T	3.29544e-05	0.00405908	missense, intron-variant, utr-variant-5-prime, nc-transcript-variant	TRIM3	GRCh38.p7	11:6465653	GGAACTGCTTGTCCA[C/T]TGGCTGGACCTCTGG	10612
rs766909063	snp	C/T	1.65255e-05	0.00287445	intron-variant	TRIM3	GRCh38.p7	11:6449272	GGACACACCAGGAAA[C/T]CGCCCCCTCATGTCA	10612
rs766923385	snp	C/T			utr-variant-3-prime, upstream-variant-2KB, downstream-variant-500B	ARFIP2, TRIM3	GRCh38.p7	11:6476162	ACTGTGGGCAGGGAC[C/T]GTGTTTTATTCACTG	10612
rs767172065	snp	A/C	1.83219e-05	0.00302665	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456389	CGCACTGCCTTCTGG[A/C]GCACATGGCTGCCGG	10612
rs767223640	snp	C/T			intron-variant	TRIM3	GRCh38.p7	11:6463492	AGCTCTGATCCAACA[C/T]TGAGCTTCTATTGCA	10612
rs767288892	snp	A/G			intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6452097	AGACATATGTAGGAG[A/G]TAGGCTCATGAGACT	10612
rs767296856	snp	C/T	1.68838e-05	0.00290544	intron-variant	TRIM3	GRCh38.p7	11:6457504	TATCTCATTCCAGAG[C/T]TGCTGAGGGTGGCTT	10612
rs767345417	snp	A/G	1.65866e-05	0.00287976	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6450911	AAAGTGGCGGTCAGT[A/G]GCCCCACGGCCCCCA	10612
rs767373172	snp	C/T			intron-variant	TRIM3	GRCh38.p7	11:6469607	CCATACTTTATGGCT[C/T]AGTTCTCAAGGCACC	10612
rs767391489	snp	A/C			intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6449552	AACCCCCACCCAGAT[A/C]TACAGCTACAGCCCA	10612
rs767394294	in-del	-/C			intron-variant	TRIM3	GRCh38.p7	11:6454424	AGGAAGTTCAGCCCC[-/C]TCACCAGGACAGACA	10612
rs767454416	snp	A/G			intron-variant	TRIM3	GRCh38.p7	11:6468430	CAGCAATGAGAAGAC[A/G]TGAGCCCACCTAGGG	10612
rs767469858	snp	A/G	3.31153e-05	0.00406898	intron-variant	TRIM3	GRCh38.p7	11:6450645	ACAAAGTGGTCTTCA[A/G]GGCAGTAAGCTGGGA	10612
rs767557176	snp	A/G	1.72178e-05	0.00293404	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456625	CGTGCCGTCCGGGCC[A/G]GTGATCTCTGCACGC	10612
rs767676975	snp	A/G			utr-variant-3-prime, upstream-variant-2KB	ARFIP2, TRIM3	GRCh38.p7	11:6474777	TCTTGCTCCCCAGAC[A/G]TTAGCCCTCATCACT	10612
rs767757801	snp	A/G			intron-variant	TRIM3	GRCh38.p7	11:6465499	CCTCACCCTCCCCAC[A/G]GGGGAGGAGGATCCT	10612
rs767805640	snp	G/T			intron-variant	TRIM3	GRCh38.p7	11:6461210	CATGCCCAGTGTAAC[G/T]TATTTAATTGTGACT	10612
rs767850851	snp	A/G			intron-variant	TRIM3	GRCh38.p7	11:6452602	CTTTCTTCTAATGTG[A/G]ACCTTCTACTAAGCT	10612
rs767863512	snp	A/G			intron-variant	TRIM3	GRCh38.p7	11:6462650	CTCCTAGGCTCAAGT[A/G]ATCCTCCCACCTTGG	10612
rs767884063	snp	A/G			intron-variant	TRIM3	GRCh38.p7	11:6457127	ATAAAATACAAGAGG[A/G]TGCCTGTGGACAGAG	10612
rs767909646	snp	A/G			intron-variant	TRIM3	GRCh38.p7	11:6453229	CATCTCCACTTGAAT[A/G]CCGCATAGCTATCTC	10612
rs767964059	snp	A/G	1.64814e-05	0.00287061	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6451346	TATGTCTCCATTGGT[A/G]TCCACTGCCACACCT	10612
rs768141767	snp	C/T	1.65545e-05	0.00287697	intron-variant	TRIM3	GRCh38.p7	11:6450643	ATACAAAGTGGTCTT[C/T]AGGGCAGTAAGCTGG	10612
rs768162947	snp	C/T			intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6451942	AGATCAATTTTGCTT[C/T]TAAGAAAGAACATTC	10612
rs768168256	snp	A/G			intron-variant	TRIM3	GRCh38.p7	11:6454164	CAGGAGGATAGCTTG[A/G]GCCTAGGAGTTCCAG	10612
rs768200540	snp	A/G			intron-variant	TRIM3	GRCh38.p7	11:6473013	TAGGGCCAGTCCTGA[A/G]TTTCTGTTGTCCACA	10612
rs768224336	snp	C/T	4.96397e-05	0.0049817	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6457827	GGCCGTCTCACAGGC[C/T]TCACAGTAAAACTCC	10612
rs768327330	snp	C/T			intron-variant	TRIM3	GRCh38.p7	11:6469304	ATGTCCAAGGACCAA[C/T]AGCTCCTCCCCCACT	10612
rs768424830	in-del	-/A			intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6450238	ATCATACACTTCTGT[-/A]TCCCTTCCCACAGTT	10612
rs768431687	snp	G/T			intron-variant	TRIM3	GRCh38.p7	11:6470597	TAATGTGATGAATCT[G/T]AGGTGCCTATGGGAT	10612
rs768485897	snp	A/C	0.00061106	0.0174687	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6451046	GCCCATGAGGCGGCC[A/C]GCTCCAATCTTGGTC	10612
rs768497947	snp	A/T			intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6449876	ACATCATTTCTCATC[A/T]GGATCACTGCAAAAG	10612
rs768570218	snp	C/T			utr-variant-3-prime, upstream-variant-2KB	ARFIP2, TRIM3	GRCh38.p7	11:6475843	ACAGGCGCCAGCCAC[C/T]GTGCCGGGCTAATTT	10612
rs768657176	snp	C/T			intron-variant	TRIM3	GRCh38.p7	11:6463142	CCCAGGAGGCAGAGA[C/T]TGCAGTGAGCCAAGA	10612
rs768723254	snp	A/G	1.79226e-05	0.00299349	intron-variant	TRIM3	GRCh38.p7	11:6457073	AGCAGACTGGCACAG[A/G]GGGAGTCTCTGTGAT	10612
rs768864995	snp	C/T	1.82277e-05	0.00301886	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456349	CTTTCGTTTGCCGCC[C/T]GTGCTGTACATGGAG	10612
rs768881445	snp	A/T	1.87898e-05	0.00306505	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456436	GACACGGCGCTTCAC[A/T]TCGTCCGGGGAAGGT	10612
rs768952931	snp	C/T			intron-variant	TRIM3	GRCh38.p7	11:6468411	AGCATATAAATGGCA[C/T]TTTCAGCAATGAGAA	10612
rs769161440	snp	C/G			intron-variant	TRIM3	GRCh38.p7	11:6465312	TGCCTTGAGGTTTGG[C/G]AAAGGACAGAGAAGG	10612
rs769199712	snp	C/T			downstream-variant-500B	TRIM3	GRCh38.p7	11:6448236	ACCACCTGGGCTAGC[C/T]TCAATTCCCTTGCCC	10612
rs769230965	snp	C/T			downstream-variant-500B	TRIM3	GRCh38.p7	11:6448475	TCTTGCTCTTCTCTA[C/T]GGAAGTTTCAAAATA	10612
rs769302628	snp	A/G	1.71026e-05	0.00292421	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456817	CGATCGCCGCAGACC[A/G]TCCACCTCAAGGACC	10612
rs769338273	snp	C/G/T	8.62916e-05	0.00656805	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456721	AGGCTGGCCCACTAG[C/G/T]GCCTGGCGCAGGCCC	10612
rs769428206	snp	A/T			intron-variant	TRIM3	GRCh38.p7	11:6462241	CTGCAGCTCTCGTTT[A/T]CTTGATTGCTTACTG	10612
rs769602140	snp	C/T	1.65045e-05	0.00287263	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6457328	AAATGGTCTCCAGGT[C/T]GCTGACCAGAGCCTG	10612
rs769748543	snp	C/T			intron-variant	TRIM3	GRCh38.p7	11:6460523	AAGAGGAGGACTGGA[C/T]GTCAGTCTCTGAATG	10612
rs769817505	snp	C/T			intron-variant	TRIM3	GRCh38.p7	11:6452201	TGACAAGGAAACCTT[C/T]CTCCTACACAGAGTG	10612
rs769855508	snp	A/G	1.67287e-05	0.00289207	intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6451455	TGGAGCAGAGGAGCA[A/G]GGGGAGGGAGCAGGT	10612
rs769933836	in-del	-/GCT			cds-indel, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456896	CCAATGCAGCCAGCC[-/GCT]GCTCTCGCATGTGCT	10612
rs769970130	snp	C/T			intron-variant	TRIM3	GRCh38.p7	11:6465236	CAACTAGTCATAAAT[C/T]GCTGATGCCAAAGCT	10612
rs770050631	snp	A/G	1.79935e-05	0.00299941	intron-variant	TRIM3	GRCh38.p7	11:6457076	AGACTGGCACAGGGG[A/G]AGTCTCTGTGATTAC	10612
rs770260270	snp	C/T			intron-variant	TRIM3	GRCh38.p7	11:6464824	AAACCCCATCTGTAA[C/T]AAAATACAAAAAGTT	10612
rs770362678	snp	C/T	1.82563e-05	0.00302123	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456370	GTACATGGAGCTGGG[C/T]CTACGCACTGCCTTC	10612
rs770363275	snp	C/T	1.68055e-05	0.0028987	intron-variant	TRIM3	GRCh38.p7	11:6457494	GGAGGGGGAATATCT[C/T]ATTCCAGAGTTGCTG	10612
rs770417232	in-del	-/C	3.30205e-05	0.00406314	intron-variant	TRIM3	GRCh38.p7	11:6465521	GAGGATCCTCATCCT[-/C]CCCACAGGGTCCTCA	10612
rs770477999	snp	C/T			intron-variant	TRIM3	GRCh38.p7	11:6460117	CAGGAAGAGCAGCTG[C/T]GTTAGGGCAGAAAAC	10612
rs770523441	snp	C/T			downstream-variant-500B	TRIM3	GRCh38.p7	11:6448329	TGTGCTGGGCAGAGG[C/T]CATTCCCTCACCCCC	10612
rs770553781	snp	A/G	1.70246e-05	0.00291754	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456861	CATTCTCATGTGGCC[A/G]CTCCGGGAAGGCCTG	10612
rs770574279	snp	A/C	4.99172e-05	0.00499561	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456947	GGGGCCGAGCCCAGG[A/C]GCAGTGCCTGCTCTG	10612
rs770574395	snp	A/C	3.33717e-05	0.0040847	intron-variant	TRIM3	GRCh38.p7	11:6450885	TCTTGGAGCTGTCCC[A/C]CTATACCTGCAAAGT	10612
rs770768881	snp	A/G	0.000115315	0.00759236	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456132	GCTGGCTGCGGACAC[A/G]CCTTGTAAATTGGTG	10612
rs770793294	snp	A/G	1.75965e-05	0.00296613	missense, utr-variant-5-prime, nc-transcript-variant	TRIM3	GRCh38.p7	11:6458090	TGGTTGGGGCAGGAG[A/G]GAGGGCGGCCAGCCA	10612
rs770797841	snp	C/T	1.65946e-05	0.00288046	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	TRIM3	GRCh38.p7	11:6458239	GAGGATGGACGTCTG[C/T]CGGCATACTGGACAG	10612
rs770860335	snp	C/T			intron-variant	TRIM3	GRCh38.p7	11:6472081	CTTTCACCTTTCAGA[C/T]ACAAGCTATGACTAC	10612
rs770895807	in-del	-/TG			intron-variant	TRIM3	GRCh38.p7	11:6455269	TCCTAATTTTACACA[-/TG]AGTTAACTGAAGCTC	10612
rs770911098	snp	C/T			intron-variant	TRIM3	GRCh38.p7	11:6452774	AGCGGTGAGGTAATG[C/T]CCCTCCAGTTTGAGC	10612
rs770956889	snp	A/C			intron-variant	TRIM3	GRCh38.p7	11:6463361	TTAGCCAGTCCCTGG[A/C]AAACAGTAAGCAATC	10612
rs770963103	snp	A/G	1.64982e-05	0.00287208	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6457381	TCCAGGTCCTCGAAC[A/G]CTGCACTGATCTGGG	10612
rs771092262	snp	C/G	3.35847e-05	0.00409771	intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6451462	GAGGAGCAAGGGGAG[C/G]GAGCAGGTAGGAGGG	10612
rs771149059	snp	A/C	1.65759e-05	0.00287883	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6449387	GGGGGCATTGAACTG[A/C]CCATTGCCCTCGCCA	10612
rs771155896	snp	A/G	4.94817e-05	0.00497377	intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6450504	GAGTCTTGTGGAAGA[A/G]GAAAGGATGTTGGGA	10612
rs771208925	snp	C/T			intron-variant	TRIM3	GRCh38.p7	11:6464293	CTTCCTCCAGGCCTC[C/T]TACCTGACATATTTT	10612
rs771215017	snp	C/T	1.64972e-05	0.00287199	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6457342	TCGCTGACCAGAGCC[C/T]GCTTGCGCTGCTGCA	10612
rs771286689	snp	A/G			intron-variant	TRIM3	GRCh38.p7	11:6450723	GTTAGGAGAGGGGTG[A/G]GGTCTCCAGGACTGA	10612
rs771375853	snp	C/T			intron-variant	TRIM3	GRCh38.p7	11:6457060	GGAGGAGTGGGTGAG[C/T]AGACTGGCACAGGGG	10612
rs771376691	snp	C/G			intron-variant	TRIM3	GRCh38.p7	11:6455338	AGGATTCAAGCTCAG[C/G]TGTCTGGTTTCAGAG	10612
rs771407563	snp	C/T			intron-variant	TRIM3	GRCh38.p7	11:6469130	GGAAGGACCAGGAGG[C/T]GGGAGGCAAGCTGAA	10612
rs771550712	snp	A/G	3.86466e-05	0.00439566	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456468	GCAGGTCCCCCGGAC[A/G]CAGGGCACGCACGCG	10612
rs771567130	snp	C/T	1.80468e-05	0.00300384	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456546	GCAGCTCGCCTTCCG[C/T]GCGCGCTGTGTACAC	10612
rs771609572	snp	A/G			intron-variant	TRIM3	GRCh38.p7	11:6471113	GGACATCTGCAAAGG[A/G]TGTGTTTCAAGGCTT	10612
rs771682148	in-del	-/CACT	1.7505e-05	0.00295841	intron-variant	TRIM3	GRCh38.p7	11:6456250	CCTTCCCTCCCCACC[-/CACT]ACCTGAGCCTGGCCC	10612
rs771706428	snp	A/G	1.65053e-05	0.0028727	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6451035	ACTCCCTTGGGGCCC[A/G]TGAGGCGGCCAGCTC	10612
rs771729036	snp	A/T	3.31587e-05	0.00407164	intron-variant	TRIM3	GRCh38.p7	11:6451237	TCAGTTCAGCTGGAC[A/T]CCAGGGTAAGTAAAG	10612
rs771746757	snp	A/G	1.70554e-05	0.00292017	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6457708	TACCGGCCACGCACA[A/G]CCTCGAGCTGGCGCT	10612
rs771876967	snp	C/T	0.000232323	0.0107753	utr-variant-3-prime, nc-transcript-variant	TRIM3	GRCh38.p7	11:6448983	CCTCTTGTCCAATCA[C/T]CCCAATGTCTGTCCC	10612
rs771919613	in-del	-/T			intron-variant	TRIM3	GRCh38.p7	11:6460898	TGTTTTTTTGGTGGC[-/T]TTTTTTTTTTTTTTT	10612
rs771950716	snp	C/T	1.66183e-05	0.00288251	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456952	CGAGCCCAGGCGCAG[C/T]GCCTGCTCTGCAAAG	10612
rs771987951	snp	G/T			intron-variant	TRIM3	GRCh38.p7	11:6463295	AAAAATAAAATGAAG[G/T]TAATAAAGTATCTGT	10612
rs772041431	snp	C/G			intron-variant	TRIM3	GRCh38.p7	11:6464175	TAAAGGTGAAATTCC[C/G]TAACAGGTCTACAAA	10612
rs772074421	snp	C/T			intron-variant	TRIM3	GRCh38.p7	11:6455305	AGGTCATGTGACTTG[C/T]TAGTATGTGACAGAG	10612
rs772075758	snp	A/G			intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6452032	TTCCAGTTGAGAAAT[A/G]ATGATGGCTTGGACC	10612
rs772287339	snp	C/T	1.65773e-05	0.00287895	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6457454	CCCCGACTAAGGCAA[C/T]TGCTGCGGACAGCTG	10612
rs772423223	snp	C/G			intron-variant	TRIM3	GRCh38.p7	11:6449235	GGCAGATGAGAGTCT[C/G]TTTTGGGGGAACGGG	10612
rs772578878	snp	A/G			intron-variant	TRIM3	GRCh38.p7	11:6469169	CTGGTGAAGGGAAAG[A/G]CTGGGAGGAAGAGTG	10612
rs772588510	snp	A/G			intron-variant	TRIM3	GRCh38.p7	11:6454535	AACTTTTATGCCAGG[A/G]AGCATTCCCAGCCTA	10612
rs772627879	snp	A/G			synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6457401	ACTGATCTGGGCCAG[A/G]GCCTCTGCCTTGCGC	10612
rs772629148	snp	G/T	1.72445e-05	0.00293632	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456691	CTTGTCTTTGGTAGT[G/T]ACAGTGAGCGAGGCA	10612
rs772654554	snp	A/C	1.67041e-05	0.00288994	intron-variant	TRIM3	GRCh38.p7	11:6450882	AGATCTTGGAGCTGT[A/C]CCCCTATACCTGCAA	10612
rs772706128	snp	A/G	6.78472e-05	0.005824	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6449432	GAAGAGGAACTCTCC[A/G]TCGGCACTGTACACC	10612
rs772975847	snp	C/T			intron-variant	TRIM3	GRCh38.p7	11:6454380	TGGACAACAGAGACC[C/T]TGTCTCAAAAAAAAA	10612
rs772991219	in-del	-/G			intron-variant	TRIM3	GRCh38.p7	11:6460562	GAGGAAAGGAGAGGA[-/G]GATATAGAGAGGCAC	10612
rs773028912	in-del	-/AAGGAACGGTACTATCTGT			intron-variant	TRIM3	GRCh38.p7	11:6455948	TGATTCACTGCTCTT[-/AAGGAACGGTACTATCTGT]AGGGTTCCATCTTCC	10612
rs773109332	snp	C/T			intron-variant	TRIM3	GRCh38.p7	11:6451093	CCATAAGAGGCTTTA[C/T]TCTGACAGTGGGGAA	10612
rs773158681	snp	A/G	1.79919e-05	0.00299927	intron-variant	TRIM3	GRCh38.p7	11:6457078	ACTGGCACAGGGGGA[A/G]TCTCTGTGATTACTG	10612
rs773236129	snp	A/G			intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6452069	ATTGGCTGGAGGGAC[A/G]CAGATGGACTCAAGA	10612
rs773350227	snp	A/G	3.29951e-05	0.00406159	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6457339	AGGTCGCTGACCAGA[A/G]CCTGCTTGCGCTGCT	10612
rs773351321	snp	C/T	1.65403e-05	0.00287574	intron-variant	TRIM3	GRCh38.p7	11:6465746	CTCTGTATGGAGAGA[C/T]GGTCAGCACCAGGGA	10612
rs773363944	snp	C/T			intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6450046	CACTCTCAGCTTTCA[C/T]GGTCCCCTCCTCAAG	10612
rs773414582	in-del	-/T			intron-variant	TRIM3	GRCh38.p7	11:6462399	CCTTGGAAATATTTC[-/T]TTTTTTTTTATTTGT	10612
rs773416791	snp	C/G	1.64806e-05	0.00287054	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6449046	CTGGAGGTAGCGATA[C/G]GCTTTAAAGCAGTGG	10612
rs773436993	snp	A/G	1.648e-05	0.0028705	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6451309	AGATGCTGACCCAAC[A/G]GTTGTCATAGTCTGC	10612
rs773480355	snp	C/T			intron-variant	TRIM3	GRCh38.p7	11:6467653	ACCTGTAGTCCAGGC[C/T]ACTTGGGAGGCTGAG	10612
rs773533358	snp	C/T			intron-variant	TRIM3	GRCh38.p7	11:6454616	ACCTCATTACTCCCC[C/T]GCAATCCCCTCCTCA	10612
rs773539755	snp	C/T	3.65197e-05	0.004273	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456371	TACATGGAGCTGGGC[C/T]TACGCACTGCCTTCT	10612
rs773625148	snp	C/T			intron-variant	TRIM3	GRCh38.p7	11:6463311	TAATAAAGTATCTGT[C/T]GCAGGGATTAAGGAA	10612
rs773634161	snp	A/G	1.64727e-05	0.00286986	synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant	TRIM3	GRCh38.p7	11:6465621	CTGGTACCGATCCAG[A/G]CAGATGCTGCATACC	10612
rs773683200	snp	A/G	1.64849e-05	0.00287092	intron-variant	TRIM3	GRCh38.p7	11:6449229	AGATCAGGCAGATGA[A/G]AGTCTGTTTTGGGGG	10612
rs773732164	snp	C/T			intron-variant	TRIM3	GRCh38.p7	11:6472038	CACACAAGCGAGAAC[C/T]CTGGTAGTCTTCTCA	10612
rs773752077	snp	A/G			intron-variant	TRIM3	GRCh38.p7	11:6469449	TCCCACTGTGCTCTA[A/G]AGATTTGCCCCCAAG	10612
rs773892975	snp	A/C			intron-variant	TRIM3	GRCh38.p7	11:6454182	CTAGGAGTTCCAGAC[A/C]AGCCCAAACAATATA	10612
rs773998446	snp	C/T	3.36768e-05	0.00410333	intron-variant	TRIM3	GRCh38.p7	11:6457498	GGGGAATATCTCATT[C/T]CAGAGTTGCTGAGGG	10612
rs774001004	snp	C/T			intron-variant	TRIM3	GRCh38.p7	11:6470749	GTGGATGACATTACC[C/T]TGAGAGGGTAAAGAG	10612
rs774015299	snp	C/G			intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6451987	AGTCAAGACTACAAG[C/G]TAGCTGCCCAGTCAG	10612
rs774092539	snp	C/T			intron-variant	TRIM3	GRCh38.p7	11:6455670	GACAGACTACATACA[C/T]TCAGGAGCCAGGCAT	10612
rs774124535	snp	A/G	1.71699e-05	0.00292996	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456764	ACCGTTTCGTGTGCA[A/G]TGGCGCTCGTGGTGA	10612
rs774141247	in-del	-/TT	8.63044e-05	0.00656846	intron-variant	TRIM3	GRCh38.p7	11:6457528	GTGGCTTTGCCGAAC[-/TT]TCCCTTCTCCCTGGG	10612
rs774145028	snp	C/T	1.70182e-05	0.00291699	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456864	TCTCATGTGGCCGCT[C/T]CGGGAAGGCCTGTGC	10612
rs774145037	snp	A/G	8.27547e-05	0.00643199	intron-variant	TRIM3	GRCh38.p7	11:6450637	CTGAAAATACAAAGT[A/G]GTCTTCAGGGCAGTA	10612
rs774200839	snp	C/T			intron-variant	TRIM3	GRCh38.p7	11:6457164	GATGCCCACAGCACC[C/T]ACCGAGGGCATGTCA	10612
rs774221743	snp	A/G			utr-variant-3-prime, upstream-variant-2KB, downstream-variant-500B	ARFIP2, TRIM3	GRCh38.p7	11:6476160	GCACTGTGGGCAGGG[A/G]CCGTGTTTTATTCAC	10612
rs774282696	snp	C/T			intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6449880	CATTTCTCATCTGGA[C/T]CACTGCAAAAGATTG	10612
rs774382370	snp	G/T			intron-variant	TRIM3	GRCh38.p7	11:6454271	TGGCATGCGCCTGTA[G/T]TCCCAGCTACTCGGG	10612
rs774385766	snp	C/G	1.64974e-05	0.00287201	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6457343	CGCTGACCAGAGCCT[C/G]CTTGCGCTGCTGCAG	10612
rs774392923	snp	A/G	1.8069e-05	0.00300569	missense, utr-variant-5-prime, nc-transcript-variant	TRIM3	GRCh38.p7	11:6458097	GGCAGGAGAGAGGGC[A/G]GCCAGCCACTACACT	10612
rs774474685	snp	A/G			missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456729	CCACTAGCGCCTGGC[A/G]CAGGCCCTCTCCCGT	10612
rs774545919	snp	A/T	1.64743e-05	0.00287	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456140	CGGACACACCTTGTA[A/T]ATTGGTGAATTCACC	10612
rs774706119	snp	C/T			utr-variant-3-prime, upstream-variant-2KB, downstream-variant-500B	ARFIP2, TRIM3	GRCh38.p7	11:6474696	TAGCCACTTTACATA[C/T]ATTATTTAATAGTCA	10612
rs774716924	snp	C/T			intron-variant	TRIM3	GRCh38.p7	11:6464675	TGTTCCCCATAAATA[C/T]GTAAACTATTGTGTA	10612
rs774757254	snp	A/G			utr-variant-3-prime, upstream-variant-2KB	ARFIP2, TRIM3	GRCh38.p7	11:6475844	CAGGCGCCAGCCACC[A/G]TGCCGGGCTAATTTT	10612
rs774792510	snp	G/T			intron-variant	TRIM3	GRCh38.p7	11:6465273	GTCTGAGCACTGTTT[G/T]ATTTCTTAGGTGGTG	10612
rs774892751	snp	C/T			intron-variant	TRIM3	GRCh38.p7	11:6453164	TTGGCACATAGTAGG[C/T]ATTCAACAAATGAAT	10612
rs774894779	snp	A/G			intron-variant	TRIM3	GRCh38.p7	11:6467473	ATAACCGCCATTAAG[A/G]ATGTGATTTTGGCTG	10612
rs774955780	snp	A/G	4.95716e-05	0.00497829	intron-variant	TRIM3	GRCh38.p7	11:6449274	ACACACCAGGAAACC[A/G]CCCCCTCATGTCATT	10612
rs774957592	snp	A/G	1.79974e-05	0.00299973	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456547	CAGCTCGCCTTCCGT[A/G]CGCGCTGTGTACACT	10612
rs774961980	snp	C/G			intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6449598	CTTCACATCCATGTG[C/G]CCTACTGCCTAGTAG	10612
rs775118490	snp	C/T	1.66084e-05	0.00288165	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456956	CCCAGGCGCAGTGCC[C/T]GCTCTGCAAAGCTGC	10612
rs775129168	snp	A/G			intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6451770	TCAAGCAGAGTGAAC[A/G]GATTGTAAAAGGCAC	10612
rs775151876	snp	A/G	1.94271e-05	0.0031166	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456477	CCGGACGCAGGGCAC[A/G]CACGCGGAAGGGGCT	10612
rs775208666	snp	C/T	3.30289e-05	0.00406366	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6451041	TTGGGGCCCATGAGG[C/T]GGCCAGCTCCAATCT	10612
rs775253246	snp	A/G			intron-variant	TRIM3	GRCh38.p7	11:6459046	GGAATGATAGAAAGT[A/G]ATAAGGAAATGCATC	10612
rs775263265	in-del	-/AC			intron-variant	TRIM3	GRCh38.p7	11:6471587	AGCTGTGAAATAGAG[-/AC]ACAAAGCTGAATCAG	10612
rs775321090	snp	A/G	0.000199256	0.0099794	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6450917	GCGGTCAGTGGCCCC[A/G]CGGCCCCCAAAACGG	10612
rs775351128	snp	A/G			intron-variant	TRIM3	GRCh38.p7	11:6460600	ATAGGAGAGTGAAGG[A/G]TGGAGGATTCAGGGG	10612
rs775360507	snp	A/C			intron-variant	TRIM3	GRCh38.p7	11:6462337	TTGACAGTGAAGGCT[A/C]TGCAGTGAAAACTGG	10612
rs775374183	snp	A/G			intron-variant, upstream-variant-2KB, downstream-variant-500B	ARFIP2, TRIM3	GRCh38.p7	11:6474508	GGCTTTGGGCGCTTC[A/G]GGAGCCCCCTCCTGA	10612
rs775513715	snp	C/T			intron-variant	TRIM3	GRCh38.p7	11:6452989	CATATAAACTTAGGT[C/T]ACCAGGATATATGCT	10612
rs775611149	snp	A/C			intron-variant	TRIM3	GRCh38.p7	11:6452213	CTTCCTCCTACACAG[A/C]GTGAACCTTTCAACC	10612
rs775613549	snp	A/G			intron-variant	TRIM3	GRCh38.p7	11:6472718	AGATGCAAAAGTAAT[A/G]GCAGTAACAAGACAA	10612
rs775651527	snp	C/G/T	3.29616e-05	0.00405954	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456169	CCTTTCTCCCTTCCA[C/G/T]GACTGCCTGTGGGAA	10612
rs775709454	snp	C/G	3.31549e-05	0.0040714	utr-variant-3-prime, nc-transcript-variant	TRIM3	GRCh38.p7	11:6448992	CAATCACCCCAATGT[C/G]TGTCCCTCCACAAGC	10612
rs775716378	snp	C/G	1.66485e-05	0.00288513	missense, utr-variant-5-prime, nc-transcript-variant	TRIM3	GRCh38.p7	11:6458269	GGATAGCGTCAGGCT[C/G]TGGGCAGGGATATAG	10612
rs775829317	snp	C/T	1.64958e-05	0.00287187	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6457348	ACCAGAGCCTGCTTG[C/T]GCTGCTGCAGTGCTT	10612
rs775845847	snp	C/G	0.000148548	0.00861695	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6457392	GAACGCTGCACTGAT[C/G]TGGGCCAGGGCCTCT	10612
rs775847859	snp	G/T	1.68898e-05	0.00290596	intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6451475	AGGGAGCAGGTAGGA[G/T]GGGAGACACTGTGGG	10612
rs776067275	snp	C/T	1.72341e-05	0.00293543	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456693	TGTCTTTGGTAGTGA[C/T]AGTGAGCGAGGCAGG	10612
rs776073986	snp	C/T	4.94605e-05	0.0049727	intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6450529	TTGGGACAGTGGTCA[C/T]GGAGGGAGGGAAGAC	10612
rs776089201	snp	C/T			intron-variant	TRIM3	GRCh38.p7	11:6460165	GGAGGGAATGAGTAG[C/T]CATCAGCGTTAAAAG	10612
rs776268474	snp	C/T	3.3024e-05	0.00406336	intron-variant	TRIM3	GRCh38.p7	11:6451263	TAAAGTGACAGCAGG[C/T]CTCTCACCTTGAACT	10612
rs776294933	snp	A/G	0.000151723	0.00870854	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6457721	CAGCCTCGAGCTGGC[A/G]CTGCAGGGCCGCCTT	10612
rs776299762	snp	C/T			downstream-variant-500B	TRIM3	GRCh38.p7	11:6448343	GTCATTCCCTCACCC[C/T]CCCAACCCCACAATC	10612
rs776299859	snp	C/T	0.000115958	0.00761352	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6457845	ACAGTAAAACTCCAT[C/T]GTCTGCGGTACAAGG	10612
rs776303658	in-del	-/T			intron-variant	TRIM3	GRCh38.p7	11:6468859	TCTAAAGACTGTGAA[-/T]GAATGAATGAATGAA	10612
rs776343735	snp	C/T	3.40553e-05	0.00412632	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6449434	AGAGGAACTCTCCAT[C/T]GGCACTGTACACCTG	10612
rs776442475	snp	A/T			intron-variant	TRIM3	GRCh38.p7	11:6471248	GTAACCAAGGCATTG[A/T]TGAAAATGGATGCGA	10612
rs776592116	snp	A/C	1.65241e-05	0.00287433	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6451048	CCATGAGGCGGCCAG[A/C]TCCAATCTTGGTCTG	10612
rs776661439	snp	C/T			intron-variant	TRIM3	GRCh38.p7	11:6464394	TTAACTCCTATTCAT[C/T]CTCTGAATTGCTCCT	10612
rs776668851	snp	C/G	1.64784e-05	0.00287035	intron-variant	TRIM3	GRCh38.p7	11:6449197	TGGGGAAGGAGTGCA[C/G]AAAGGAGGGAGAGGC	10612
rs776674591	snp	C/G	1.79622e-05	0.00299679	intron-variant	TRIM3	GRCh38.p7	11:6457074	GCAGACTGGCACAGG[C/G]GGAGTCTCTGTGATT	10612
rs776675454	snp	C/T			intron-variant	TRIM3	GRCh38.p7	11:6462608	GAGACTGCATCTCAC[C/T]ATGTTGTTTCCCAAG	10612
rs776803574	snp	A/C			intron-variant	TRIM3	GRCh38.p7	11:6463362	TAGCCAGTCCCTGGC[A/C]AACAGTAAGCAATCA	10612
rs776936169	snp	C/T			intron-variant	TRIM3	GRCh38.p7	11:6451157	GGGCTGGGGAAAGAA[C/T]AGGGAGTAGGAGGAG	10612
rs776953599	snp	A/G	1.65138e-05	0.00287343	intron-variant	TRIM3	GRCh38.p7	11:6456196	GGAAGGGACAGGAGG[A/G]AAAACAAAATAATTC	10612
rs776957988	snp	A/G	1.65081e-05	0.00287293	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6457400	CACTGATCTGGGCCA[A/G]GGCCTCTGCCTTGCG	10612
rs777026708	snp	G/T	6.6921e-05	0.00578412	intron-variant	TRIM3	GRCh38.p7	11:6457484	GTGGCAATCTGGAGG[G/T]GGAATATCTCATTCC	10612
rs777060904	snp	A/G			intron-variant	TRIM3	GRCh38.p7	11:6452170	TACAAGAATTAGTCC[A/G]TTCAGGCTATGGGGC	10612
rs777114687	snp	C/T	1.82297e-05	0.00301903	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456351	TTCGTTTGCCGCCTG[C/T]GCTGTACATGGAGCT	10612
rs777231519	snp	C/T	1.70702e-05	0.00292144	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456837	CCTCAAGGACCAGTT[C/T]CAGCTGTGCATTCTC	10612
rs777319242	snp	C/T	4.99929e-05	0.0049994	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456937	CAACACCTCCGGGGC[C/T]GAGCCCAGGCGCAGT	10612
rs777352650	snp	C/T	1.6617e-05	0.00288239	missense, utr-variant-5-prime, nc-transcript-variant	TRIM3	GRCh38.p7	11:6458211	TCTGCAGTGCCGAGA[C/T]GCCCTGCTCTGGGAG	10612
rs777409068	snp	C/T			intron-variant	TRIM3	GRCh38.p7	11:6453769	CTGATGCTGGTTCCA[C/T]TCAGTGAGGTCTGCC	10612
rs777460030	snp	A/G			utr-variant-3-prime, upstream-variant-2KB	ARFIP2, TRIM3	GRCh38.p7	11:6474976	TGCAGGCTGATCAAA[A/G]CCCAGAAGACTGTCT	10612
rs777528137	snp	A/T	1.64966e-05	0.00287194	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6457379	GCTCCAGGTCCTCGA[A/T]CGCTGCACTGATCTG	10612
rs777600054	snp	C/T	0.000115839	0.00760962	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6457442	GCTGGCTGATGCCCC[C/T]GACTAAGGCAATTGC	10612
rs777684374	snp	A/G	9.88403e-05	0.00702925	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456114	TACCACGATGCGGCC[A/G]CTGCTGGCTGCGGAC	10612
rs777787585	snp	G/T	1.65381e-05	0.00287555	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6449372	CACAGCTACTCCTGT[G/T]GGGGCATTGAACTGC	10612
rs777805026	snp	A/G			intron-variant	TRIM3	GRCh38.p7	11:6465014	AAAAAAAAAAAAAGA[A/G]TAAGGATCTTATCTG	10612
rs778056320	snp	A/G	9.20429e-05	0.00678329	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456538	CGAGAGGAGCAGCTC[A/G]CCTTCCGTGCGCGCT	10612
rs778075390	snp	A/G	1.90551e-05	0.00308661	intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6449495	GGCCTCAGGCAGAGG[A/G]TAGGGCTTTGGAGGA	10612
rs778191486	snp	C/T			intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6450367	TACATTTGCTTTGTG[C/T]ATCACTGTATCTCCA	10612
rs778196798	snp	A/G	1.64898e-05	0.00287135	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6451369	CCACACCTGTGGGGC[A/G]CTGCAGCTGCCCAGG	10612
rs778199589	snp	C/G			intron-variant	TRIM3	GRCh38.p7	11:6470361	GAGCAGTTTGGATGA[C/G]AGGGTGATAAGTTTG	10612
rs778245109	snp	C/T			missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6450597	ACAATTTCATTCTTG[C/T]TGTTCACAGCCACAA	10612
rs778262801	snp	A/G	0.000192984	0.00982114	intron-variant	TRIM3	GRCh38.p7	11:6457051	AGGGGTAGGGGAGGA[A/G]TGGGTGAGCAGACTG	10612
rs778275520	snp	A/G			intron-variant	TRIM3	GRCh38.p7	11:6469057	GTAATGGGTTCTGGA[A/G]TCTGAAGACTTAATA	10612
rs778339380	snp	C/T	1.974e-05	0.0031416	intron-variant	TRIM3	GRCh38.p7	11:6458028	CCTCCTCCTCCCACC[C/T]CAAGTCCCGGCCTCA	10612
rs778368657	snp	C/T	3.29728e-05	0.00406021	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6451015	GTCCATTCCGGTCTA[C/T]GGCCACTCCCTTGGG	10612
rs778458675	snp	C/T	1.66073e-05	0.00288156	intron-variant	TRIM3	GRCh38.p7	11:6451223	AGGCACTAGACTGGT[C/T]AGTTCAGCTGGACAC	10612
rs778463704	snp	C/T			intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6451879	GAATTATGTTTTATC[C/T]TGGGTGTAATGAGGA	10612
rs778497296	snp	C/G	1.66297e-05	0.0028835	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456949	GGCCGAGCCCAGGCG[C/G]AGTGCCTGCTCTGCA	10612
rs778599774	in-del	-/G	1.67587e-05	0.00289466	intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6451461	AGAGGAGCAAGGGGA[-/G]GGAGCAGGTAGGAGG	10612
rs778651050	snp	A/G/T	3.63169e-05	0.00426115	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456310	ACCAACACGGAAGAC[A/G/T]AGCTCATCCTCAATT	10612
rs778780532	snp	C/G	4.95037e-05	0.00497488	intron-variant	TRIM3	GRCh38.p7	11:6465528	CTCATCCTCCCCACA[C/G]GGTCCTCATCCCTCC	10612
rs778812981	snp	C/T	1.64781e-05	0.00287033	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6449174	AGGAGCCAGAGCTGT[C/T]GAATACCTGGGGAAG	10612
rs778933636	snp	A/G	0.000110855	0.00744412	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456405	GCACATGGCTGCCGG[A/G]GCCGCCAGGGGACTT	10612
rs778942917	snp	G/T			intron-variant	TRIM3	GRCh38.p7	11:6468812	GACCAGGTCACCATT[G/T]TCTGTGCTGTTGGAT	10612
rs779057521	snp	A/G			intron-variant	TRIM3	GRCh38.p7	11:6455215	TGTCAAGTATAGTAC[A/G]TCATTTAACACTCCC	10612
rs779110679	snp	G/T	1.82061e-05	0.00301708	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456331	ATCCTCAATTGGGTT[G/T]TCCTTTCGTTTGCCG	10612
rs779123246	snp	C/T			downstream-variant-500B	TRIM3	GRCh38.p7	11:6448273	GAACTTCAAAGATTG[C/T]TTTCATAGCCTGACA	10612
rs779125524	snp	C/T	1.68043e-05	0.0028986	missense, utr-variant-5-prime, nc-transcript-variant	TRIM3	GRCh38.p7	11:6458148	GGTCGTGGGCCCCAT[C/T]AGGTGCCTGCTGCAT	10612
rs779155712	snp	A/G			intron-variant	TRIM3	GRCh38.p7	11:6470182	TTAAAGGGCAAGGAC[A/G]GAAAATTAAGAAACT	10612
rs779224265	snp	A/G	1.65776e-05	0.00287898	intron-variant	TRIM3	GRCh38.p7	11:6450662	GCAGTAAGCTGGGAT[A/G]CTGAGTGGGATGGGG	10612
rs779315014	snp	C/G			intron-variant	TRIM3	GRCh38.p7	11:6461748	TTGTCAAGTGTACCT[C/G]GCTCACGATAGCTTC	10612
rs779400339	snp	G/T	6.89691e-05	0.00587195	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456669	CTGTGCGCACCAACC[G/T]CCCGTCCTTGTCTTT	10612
rs779436566	snp	C/T	1.89439e-05	0.00307759	intron-variant	TRIM3	GRCh38.p7	11:6458045	AAGTCCCGGCCTCAC[C/T]GGGCCTCGCTTGGGC	10612
rs779436617	snp	A/C/G	1.65132e-05	0.00287339	utr-variant-3-prime, nc-transcript-variant	TRIM3	GRCh38.p7	11:6449015	CCACAAGCCAGGCAG[A/C/G]GCCTCTGTACAGCTA	10612
rs779487127	snp	A/C	8.56553e-05	0.00654372	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456799	TGCGCCCAGATTGAG[A/C]ACCGATCGCCGCAGA	10612
rs779489394	snp	A/G	1.64838e-05	0.00287083	intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6450518	AGGAAAGGATGTTGG[A/G]ACAGTGGTCACGGAG	10612
rs779506735	snp	A/C	1.66902e-05	0.00288874	intron-variant	TRIM3	GRCh38.p7	11:6457285	TAGGAAAGGGTGAAC[A/C]CAAGACACACCTTCT	10612
rs779594654	snp	A/G	1.65031e-05	0.00287251	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6451390	GCTGCCCAGGTGAGC[A/G]TCCTCGGACCCCAAA	10612
rs779629769	snp	A/G			intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6450510	TGTGGAAGAGGAAAG[A/G]ATGTTGGGACAGTGG	10612
rs779688912	snp	A/G			intron-variant	TRIM3	GRCh38.p7	11:6454955	GAAGAAGTAAAGTGC[A/G]TGGTAGTTAGAAACA	10612
rs779694463	snp	A/C	1.65842e-05	0.00287955	intron-variant	TRIM3	GRCh38.p7	11:6451238	CAGTTCAGCTGGACA[A/C]CAGGGTAAGTAAAGT	10612
rs779751530	snp	A/C			intron-variant	TRIM3	GRCh38.p7	11:6454055	GAGAGTGGAGCTATA[A/C]CAGGTGTTCCCTCTC	10612
rs779797530	snp	A/G	1.64773e-05	0.00287026	intron-variant	TRIM3	GRCh38.p7	11:6449186	TGTCGAATACCTGGG[A/G]AAGGAGTGCAGAAAG	10612
rs779958037	snp	A/C	5.34012e-05	0.00516699	intron-variant	TRIM3	GRCh38.p7	11:6457064	GAGTGGGTGAGCAGA[A/C]TGGCACAGGGGGAGT	10612
rs779965761	snp	G/T	9.133e-05	0.00675697	utr-variant-5-prime, intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6465710	TGGCGCCCACAGATG[G/T]CTCCCGCCACTCACA	10612
rs780025601	in-del	-/A	1.68616e-05	0.00290353	intron-variant	TRIM3	GRCh38.p7	11:6450859	CTCTGGAACAGGGGT[-/A]TCAGCATAGATCTTG	10612
rs780054313	snp	A/G			intron-variant	TRIM3	GRCh38.p7	11:6462245	AGCTCTCGTTTTCTT[A/G]ATTGCTTACTGTCAG	10612
rs780074606	snp	C/T	1.65214e-05	0.0028741	intron-variant	TRIM3	GRCh38.p7	11:6449301	CATTCCCAGGCCTTA[C/T]TCACCTGGATGCGGC	10612
rs780085513	snp	C/T	1.82144e-05	0.00301776	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456336	CAATTGGGTTGTCCT[C/T]TCGTTTGCCGCCTGT	10612
rs780179383	snp	C/T	3.73267e-05	0.00431995	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456425	CCAGGGGACTTGACA[C/T]GGCGCTTCACATCGT	10612
rs780211545	snp	G/T	3.31956e-05	0.0040739	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6457459	ACTAAGGCAATTGCT[G/T]CGGACAGCTGTGGCA	10612
rs780270350	snp	A/G			intron-variant	TRIM3	GRCh38.p7	11:6471640	AGTTTTTAGACTAAT[A/G]TGAGAAACAGAAATG	10612
rs780324727	snp	C/T	3.29973e-05	0.00406172	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6450967	GCTGGAAGGTAAAGA[C/T]GCAGCAAGACTTGTT	10612
rs780451218	snp	C/G	1.67044e-05	0.00288997	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456930	GCACCAGCAACACCT[C/G]CGGGGCCGAGCCCAG	10612
rs780505279	snp	C/T			intron-variant	TRIM3	GRCh38.p7	11:6467719	GCAGTGAGCCATAAT[C/T]GTGCCACTGCACTCT	10612
rs780532629	snp	C/T			splice-acceptor-variant	TRIM3	GRCh38.p7	11:6458297	TAGTTTTGGAGACAT[C/T]TGTCCAGGAAGGAGA	10612
rs780547892	snp	A/C/T	3.42057e-05	0.00413545	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456816	CCGATCGCCGCAGAC[A/C/T]GTCCACCTCAAGGAC	10612
rs780656833	snp	A/T			utr-variant-3-prime, upstream-variant-2KB	ARFIP2, TRIM3	GRCh38.p7	11:6475115	GGAAAATCCTGAAAA[A/T]TTCTGGTTTCCTTGG	10612
rs780710506	snp	C/T			downstream-variant-500B	TRIM3	GRCh38.p7	11:6448214	ATGGAGTCTCCCACA[C/T]GTAGCTACCACCTGG	10612
rs780717048	snp	C/T			missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6449440	ACTCTCCATCGGCAC[C/T]GTACACCTGGCGGGG	10612
rs780730822	snp	A/G	3.37149e-05	0.00410564	intron-variant	TRIM3	GRCh38.p7	11:6450856	GTTCTCTGGAACAGG[A/G]GTATCAGCATAGATC	10612
rs780777299	snp	G/T			intron-variant	TRIM3	GRCh38.p7	11:6462140	CACCTCCTCAGGGAA[G/T]CCTTCCTTGATGACT	10612
rs780922940	snp	A/T	3.29832e-05	0.00406085	intron-variant	TRIM3	GRCh38.p7	11:6456062	GGAGGAGAGCGGTAA[A/T]GGTGCTTACCTGAAT	10612
rs781049359	snp	A/G	1.86232e-05	0.00305143	intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6449490	GACCTGGCCTCAGGC[A/G]GAGGGTAGGGCTTTG	10612
rs781117013	snp	C/G			intron-variant	TRIM3	GRCh38.p7	11:6452794	CCAGTTTGAGCAGCT[C/G]AGGTTCTGGCTCAAT	10612
rs781127684	snp	C/G			intron-variant	TRIM3	GRCh38.p7	11:6467424	AAGAGGTGAGTTTGG[C/G]AAGATAGGTAGAGAT	10612
rs781133893	in-del	-/A			intron-variant	TRIM3	GRCh38.p7	11:6464700	TGTGTATCAGTTTTT[-/A]AAAAGAGTAAGCACG	10612
rs781172203	snp	A/G			intron-variant, utr-variant-5-prime, upstream-variant-2KB, downstream-variant-500B	ARFIP2, TRIM3	GRCh38.p7	11:6474229	GGTGTAGTCGGTCTC[A/G]GGGATTGAGATGAGA	10612
rs781187322	snp	C/G	1.6498e-05	0.00287206	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6457376	CTTGCTCCAGGTCCT[C/G]GAACGCTGCACTGAT	10612
rs781203376	snp	A/C/G	3.30508e-05	0.00406501	missense, synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6451409	TCGGACCCCAAAACG[A/C/G]AACTTGAACTGGCCC	10612
rs781307595	snp	C/T	1.88375e-05	0.00306894	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456523	TCCGTAGAGCAGCAC[C/T]GAGAGGAGCAGCTCG	10612
rs781314460	snp	G/T	1.65086e-05	0.00287298	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6449321	CTGGATGCGGCTGTT[G/T]CCCCAGTCAGCCACA	10612
rs781432453	snp	C/T	4.96792e-05	0.00498368	missense, nc-transcript-variant	TRIM3	GRCh38.p7	11:6457790	GCTCACGATGCTCCC[C/T]GGCGCGGCACTCACC	10612
rs781472169	snp	A/G	1.72184e-05	0.00293409	stop-gained, nc-transcript-variant	TRIM3	GRCh38.p7	11:6457697	TGCCCAGTGCCTACC[A/G]GCCACGCACAGCCTC	10612
rs781551235	snp	C/T			intron-variant	TRIM3	GRCh38.p7	11:6453418	TCCTAGTTTGGTCCT[C/T]AACATCTCTCTCCTA	10612
rs781568380	snp	C/T	1.68207e-05	0.00290001	intron-variant	TRIM3	GRCh38.p7	11:6451102	GCTTTATTCTGACAG[C/T]GGGGAAAGTAGTCCT	10612
rs781671401	snp	C/T			intron-variant	TRIM3	GRCh38.p7	11:6470533	CTTGGCCTGCCAAAG[C/T]GTGGGGGTTGCAGGC	10612
rs781675146	snp	A/G	8.24219e-05	0.00641905	synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6451004	CACAATGATATGTCC[A/G]TTCCGGTCTACGGCC	10612
rs781747990	snp	C/T			intron-variant	TRIM3	GRCh38.p7	11:6471684	ACAATGTGATAAGTA[C/T]CATGATATTGACATG	10612
rs781766734	snp	A/G			intron-variant	TRIM3	GRCh38.p7	11:6458005	ACTCGGCACCCCCCA[A/G]TGCCTCTCCTCCTCC	10612
rs796296745	snp	A/C			intron-variant	TRIM3	GRCh38.p7	11:6468486	AGGGCCTGGCACAAG[A/C]GAGGGGAGCCAGCAA	10612
rs796409415	multinucleotide-polymorphism	CC/TG			intron-variant	TRIM3	GRCh38.p7	11:6460332	GGAGCTTGAAAGTTC[CC/TG]ATGAGGAGCTGGTTG	10612
rs796495799	snp	C/T			synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6457015	GCGCAGTGTGTCCAG[C/T]TGGCTTTGCAACACC	10612
rs796625961	snp	A/C			intron-variant, nc-transcript-variant	TRIM3	GRCh38.p7	11:6451531	GAGGGAGGAGACCCC[A/C]CCACCACCATTTATT	10612
rs796717938	snp	A/C			synonymous-codon, nc-transcript-variant	TRIM3	GRCh38.p7	11:6456763	CACCGTTTCGTGTGC[A/C]GTGGCGCTCGTGGTG	10612
rs796718960	in-del	-/TGCTGGGTCA			intron-variant	TRIM3	GRCh38.p7	11:6469193	AGAGTGGGAGTGGTC[-/TGCTGGGTCA]TGCTGGGTCCTGCTG	10612
rs796958082	snp	C/T			intron-variant	TRIM3	GRCh38.p7	11:6460875	ATTTAATTGTGTTTT[C/T]TTTGTTTTTGTTTTT	10612

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