Item | Value |
---|---|
geneid | 5154 |
ensemblid | ENSG00000197461.13 |
hgncid | 8799 |
symbol | PDGFA |
name | platelet derived growth factor subunit A |
refseq_nuc | NM_033023.5 |
refseq_prot | NP_148983.1 |
ensembl_nuc | ENST00000402802.8 |
ensembl_prot | ENSP00000383889.3 |
mane_status | MANE Select |
chr | chr7 |
start | 497258 |
end | 519846 |
strand | - |
ver | v1.2 |
region | chr7:497258-519846 |
region5000 | chr7:492258-524846 |
regionname0 | PDGFA_chr7_497258_519846 |
regionname5000 | PDGFA_chr7_492258_524846 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 196 | 298 | 73 | 62 | 117 | 16 | 28 | 83 | PDGFA_chr7_492258_524846 | PDGFA | MRTLA others(191): Show |
chr7 | 492258 | 524846 |
a0002 | 0/0 | 196 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | MRTLA others(191): Show |
chr7 | 492258 | 524846 |
a0003 | 0/0 | 196 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PDGFA_chr7_492258_524846 | PDGFA | MRTLA others(191): Show |
chr7 | 492258 | 524846 |
a0004 | 0/0 | 196 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PDGFA_chr7_492258_524846 | PDGFA | MRTLA others(191): Show |
chr7 | 492258 | 524846 |
a0005 | 0/0 | 196 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PDGFA_chr7_492258_524846 | PDGFA | MRTLA others(191): Show |
chr7 | 492258 | 524846 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 588 | 201 | 63 | 42 | 66 | 11 | 17 | PDGFA_chr7_492258_524846 | PDGFA | ATGAG others(583): Show |
chr7 | 492258 | 524846 | ||
a0001c0002 | 0/0 | 588 | 91 | 8 | 16 | 51 | 5 | 11 | PDGFA_chr7_492258_524846 | PDGFA | ATGAG others(583): Show |
chr7 | 492258 | 524846 | ||
a0001c0003 | 0/0 | 588 | 5 | 1 | 4 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ATGAG others(583): Show |
chr7 | 492258 | 524846 | ||
a0001c0007 | 0/0 | 588 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ATGAG others(583): Show |
chr7 | 492258 | 524846 | ||
a0002c0008 | 0/0 | 588 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ATGAG others(583): Show |
chr7 | 492258 | 524846 | ||
a0003c0004 | 0/0 | 588 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ATGAG others(583): Show |
chr7 | 492258 | 524846 | ||
a0004c0006 | 0/0 | 588 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ATGAG others(583): Show |
chr7 | 492258 | 524846 | ||
a0005c0005 | 0/0 | 588 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ATGAG others(583): Show |
chr7 | 492258 | 524846 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 2738 | 22 | 2 | 4 | 10 | 2 | 4 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2733): Show |
chr7 | 492258 | 524846 |
a0001c0001t0002 | 1/0 | 2742 | 14 | 0 | 0 | 10 | 3 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2737): Show |
chr7 | 492258 | 524846 |
a0001c0001t0003 | 0/0 | 2746 | 2 | 0 | 1 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2741): Show |
chr7 | 492258 | 524846 |
a0001c0001t0004 | 0/0 | 2748 | 13 | 6 | 3 | 0 | 1 | 3 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2743): Show |
chr7 | 492258 | 524846 |
a0001c0001t0005 | 0/0 | 2748 | 4 | 0 | 1 | 2 | 0 | 1 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2743): Show |
chr7 | 492258 | 524846 |
a0001c0001t0007 | 0/0 | 2747 | 2 | 0 | 1 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2742): Show |
chr7 | 492258 | 524846 |
a0001c0001t0008 | 0/0 | 2739 | 10 | 1 | 6 | 2 | 1 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2734): Show |
chr7 | 492258 | 524846 |
a0001c0001t0009 | 0/0 | 2739 | 8 | 0 | 1 | 7 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2734): Show |
chr7 | 492258 | 524846 |
a0001c0001t0010 | 0/0 | 2742 | 6 | 5 | 1 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2737): Show |
chr7 | 492258 | 524846 |
a0001c0001t0011 | 0/0 | 2747 | 4 | 3 | 0 | 0 | 0 | 1 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2742): Show |
chr7 | 492258 | 524846 |
a0001c0001t0013 | 0/0 | 2743 | 5 | 5 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2738): Show |
chr7 | 492258 | 524846 |
a0001c0001t0014 | 0/0 | 2748 | 2 | 2 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2743): Show |
chr7 | 492258 | 524846 |
a0001c0001t0015 | 0/0 | 2740 | 4 | 2 | 2 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2735): Show |
chr7 | 492258 | 524846 |
a0001c0001t0016 | 0/0 | 2747 | 3 | 0 | 0 | 3 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2742): Show |
chr7 | 492258 | 524846 |
a0001c0001t0017 | 0/0 | 2740 | 4 | 0 | 0 | 3 | 0 | 1 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2735): Show |
chr7 | 492258 | 524846 |
a0001c0001t0018 | 0/0 | 2738 | 2 | 2 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2733): Show |
chr7 | 492258 | 524846 |
a0001c0001t0019 | 0/0 | 2746 | 3 | 2 | 0 | 0 | 0 | 1 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2741): Show |
chr7 | 492258 | 524846 |
a0001c0001t0020 | 0/0 | 2743 | 2 | 0 | 0 | 2 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2738): Show |
chr7 | 492258 | 524846 |
a0001c0001t0021 | 0/0 | 2748 | 3 | 1 | 2 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2743): Show |
chr7 | 492258 | 524846 |
a0001c0001t0023 | 0/0 | 2746 | 3 | 0 | 0 | 3 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2741): Show |
chr7 | 492258 | 524846 |
a0001c0001t0024 | 0/0 | 2749 | 3 | 0 | 2 | 0 | 0 | 1 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2744): Show |
chr7 | 492258 | 524846 |
a0001c0001t0025 | 0/0 | 2747 | 3 | 2 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2742): Show |
chr7 | 492258 | 524846 |
a0001c0001t0026 | 0/0 | 2748 | 3 | 0 | 1 | 2 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2743): Show |
chr7 | 492258 | 524846 |
a0001c0001t0027 | 0/0 | 2743 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2738): Show |
chr7 | 492258 | 524846 |
a0001c0001t0028 | 0/0 | 2739 | 2 | 0 | 2 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2734): Show |
chr7 | 492258 | 524846 |
a0001c0001t0029 | 0/0 | 2748 | 2 | 0 | 0 | 0 | 1 | 1 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2743): Show |
chr7 | 492258 | 524846 |
a0001c0001t0031 | 0/0 | 2745 | 1 | 0 | 1 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2740): Show |
chr7 | 492258 | 524846 |
a0001c0001t0032 | 0/0 | 2745 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2740): Show |
chr7 | 492258 | 524846 |
a0001c0001t0033 | 0/0 | 2737 | 2 | 1 | 1 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2732): Show |
chr7 | 492258 | 524846 |
a0001c0001t0034 | 0/0 | 2742 | 2 | 0 | 0 | 1 | 0 | 1 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2737): Show |
chr7 | 492258 | 524846 |
a0001c0001t0035 | 0/0 | 2740 | 2 | 2 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2735): Show |
chr7 | 492258 | 524846 |
a0001c0001t0036 | 0/0 | 2744 | 2 | 2 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2739): Show |
chr7 | 492258 | 524846 |
a0001c0001t0037 | 0/0 | 2741 | 2 | 0 | 2 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2736): Show |
chr7 | 492258 | 524846 |
a0001c0001t0038 | 0/0 | 2742 | 2 | 0 | 2 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2737): Show |
chr7 | 492258 | 524846 |
a0001c0001t0039 | 0/0 | 2745 | 2 | 0 | 0 | 2 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2740): Show |
chr7 | 492258 | 524846 |
a0001c0001t0040 | 0/0 | 2747 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2742): Show |
chr7 | 492258 | 524846 |
a0001c0001t0041 | 0/0 | 2749 | 2 | 2 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2744): Show |
chr7 | 492258 | 524846 |
a0001c0001t0042 | 0/0 | 2748 | 1 | 0 | 0 | 0 | 0 | 1 | PDGFA_chr7_492258_524846 | PDGFA | ACACC others(2743): Show |
chr7 | 492258 | 524846 |
a0001c0001t0045 | 0/0 | 2746 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2741): Show |
chr7 | 492258 | 524846 |
a0001c0001t0046 | 0/0 | 2742 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2737): Show |
chr7 | 492258 | 524846 |
a0001c0001t0047 | 0/0 | 2739 | 1 | 0 | 1 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2734): Show |
chr7 | 492258 | 524846 |
a0001c0001t0048 | 0/0 | 2748 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2743): Show |
chr7 | 492258 | 524846 |
a0001c0001t0049 | 0/0 | 2739 | 1 | 0 | 1 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2734): Show |
chr7 | 492258 | 524846 |
a0001c0001t0051 | 0/0 | 2745 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2740): Show |
chr7 | 492258 | 524846 |
a0001c0001t0052 | 0/0 | 2746 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2741): Show |
chr7 | 492258 | 524846 |
a0001c0001t0053 | 0/0 | 2739 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2734): Show |
chr7 | 492258 | 524846 |
a0001c0001t0054 | 0/0 | 2745 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2740): Show |
chr7 | 492258 | 524846 |
a0001c0001t0057 | 0/0 | 2741 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2736): Show |
chr7 | 492258 | 524846 |
a0001c0001t0059 | 0/0 | 2741 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2736): Show |
chr7 | 492258 | 524846 |
a0001c0001t0061 | 0/0 | 2742 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2737): Show |
chr7 | 492258 | 524846 |
a0001c0001t0062 | 0/0 | 2745 | 1 | 0 | 0 | 0 | 0 | 1 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2740): Show |
chr7 | 492258 | 524846 |
a0001c0001t0063 | 0/0 | 2747 | 1 | 0 | 1 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2742): Show |
chr7 | 492258 | 524846 |
a0001c0001t0065 | 0/0 | 2741 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2736): Show |
chr7 | 492258 | 524846 |
a0001c0001t0066 | 0/0 | 2747 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2742): Show |
chr7 | 492258 | 524846 |
a0001c0001t0067 | 0/0 | 2749 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2744): Show |
chr7 | 492258 | 524846 |
a0001c0001t0068 | 0/0 | 2747 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2742): Show |
chr7 | 492258 | 524846 |
a0001c0001t0071 | 0/0 | 2748 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2743): Show |
chr7 | 492258 | 524846 |
a0001c0001t0074 | 0/0 | 2727 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2722): Show |
chr7 | 492258 | 524846 |
a0001c0001t0075 | 0/0 | 2748 | 1 | 0 | 1 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2743): Show |
chr7 | 492258 | 524846 |
a0001c0001t0076 | 0/0 | 2751 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2746): Show |
chr7 | 492258 | 524846 |
a0001c0001t0079 | 0/0 | 2746 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2741): Show |
chr7 | 492258 | 524846 |
a0001c0001t0080 | 0/0 | 2747 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2742): Show |
chr7 | 492258 | 524846 |
a0001c0001t0081 | 0/0 | 2748 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2743): Show |
chr7 | 492258 | 524846 |
a0001c0001t0082 | 0/0 | 2739 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2734): Show |
chr7 | 492258 | 524846 |
a0001c0001t0084 | 0/0 | 2742 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2737): Show |
chr7 | 492258 | 524846 |
a0001c0001t0086 | 0/0 | 2748 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2743): Show |
chr7 | 492258 | 524846 |
a0001c0001t0087 | 0/0 | 2739 | 1 | 0 | 0 | 0 | 1 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2734): Show |
chr7 | 492258 | 524846 |
a0001c0001t0088 | 0/0 | 2737 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2732): Show |
chr7 | 492258 | 524846 |
a0001c0001t0089 | 0/0 | 2738 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2733): Show |
chr7 | 492258 | 524846 |
a0001c0001t0090 | 0/0 | 2747 | 1 | 0 | 0 | 0 | 1 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2742): Show |
chr7 | 492258 | 524846 |
a0001c0001t0091 | 0/0 | 2738 | 1 | 0 | 1 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2733): Show |
chr7 | 492258 | 524846 |
a0001c0001t0092 | 0/0 | 2737 | 1 | 0 | 0 | 0 | 0 | 1 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2732): Show |
chr7 | 492258 | 524846 |
a0001c0001t0093 | 0/0 | 2738 | 1 | 0 | 1 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2733): Show |
chr7 | 492258 | 524846 |
a0001c0001t0094 | 0/0 | 2741 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2736): Show |
chr7 | 492258 | 524846 |
a0001c0001t0095 | 0/0 | 2742 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2737): Show |
chr7 | 492258 | 524846 |
a0001c0001t0097 | 0/0 | 2749 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2744): Show |
chr7 | 492258 | 524846 |
a0001c0001t0098 | 0/0 | 2744 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2739): Show |
chr7 | 492258 | 524846 |
a0001c0001t0100 | 0/0 | 2750 | 1 | 0 | 0 | 0 | 1 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2745): Show |
chr7 | 492258 | 524846 |
a0001c0001t0101 | 0/0 | 2745 | 1 | 0 | 1 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2740): Show |
chr7 | 492258 | 524846 |
a0001c0001t0102 | 0/0 | 2748 | 1 | 0 | 1 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2743): Show |
chr7 | 492258 | 524846 |
a0001c0001t0105 | 0/0 | 2744 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2739): Show |
chr7 | 492258 | 524846 |
a0001c0001t0106 | 0/0 | 2746 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2741): Show |
chr7 | 492258 | 524846 |
a0001c0001t0107 | 0/0 | 2747 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2742): Show |
chr7 | 492258 | 524846 |
a0001c0001t0108 | 0/0 | 2749 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2744): Show |
chr7 | 492258 | 524846 |
a0001c0001t0109 | 0/0 | 2747 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2742): Show |
chr7 | 492258 | 524846 |
a0001c0001t0110 | 0/0 | 2750 | 1 | 0 | 1 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2745): Show |
chr7 | 492258 | 524846 |
a0001c0001t0111 | 0/0 | 2748 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2743): Show |
chr7 | 492258 | 524846 |
a0001c0001t0112 | 0/1 | 2749 | 1 | 0 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2744): Show |
chr7 | 492258 | 524846 |
a0001c0001t0114 | 0/0 | 2748 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2743): Show |
chr7 | 492258 | 524846 |
a0001c0002t0001 | 0/0 | 2738 | 2 | 0 | 1 | 0 | 1 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2733): Show |
chr7 | 492258 | 524846 |
a0001c0002t0002 | 0/0 | 2742 | 3 | 0 | 0 | 3 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2737): Show |
chr7 | 492258 | 524846 |
a0001c0002t0003 | 0/0 | 2746 | 18 | 0 | 2 | 14 | 0 | 2 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2741): Show |
chr7 | 492258 | 524846 |
a0001c0002t0005 | 0/0 | 2748 | 7 | 0 | 1 | 6 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2743): Show |
chr7 | 492258 | 524846 |
a0001c0002t0006 | 0/0 | 2745 | 10 | 0 | 1 | 7 | 0 | 2 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2740): Show |
chr7 | 492258 | 524846 |
a0001c0002t0007 | 0/0 | 2747 | 8 | 0 | 1 | 5 | 1 | 1 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2742): Show |
chr7 | 492258 | 524846 |
a0001c0002t0009 | 0/0 | 2739 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2734): Show |
chr7 | 492258 | 524846 |
a0001c0002t0010 | 0/0 | 2742 | 2 | 1 | 0 | 0 | 1 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2737): Show |
chr7 | 492258 | 524846 |
a0001c0002t0011 | 0/0 | 2747 | 3 | 1 | 1 | 0 | 0 | 1 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2742): Show |
chr7 | 492258 | 524846 |
a0001c0002t0012 | 0/0 | 2749 | 5 | 0 | 0 | 5 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2744): Show |
chr7 | 492258 | 524846 |
a0001c0002t0013 | 0/0 | 2743 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2738): Show |
chr7 | 492258 | 524846 |
a0001c0002t0014 | 0/0 | 2748 | 3 | 0 | 2 | 0 | 1 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2743): Show |
chr7 | 492258 | 524846 |
a0001c0002t0016 | 0/0 | 2747 | 1 | 0 | 1 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2742): Show |
chr7 | 492258 | 524846 |
a0001c0002t0018 | 0/0 | 2738 | 1 | 0 | 0 | 0 | 0 | 1 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2733): Show |
chr7 | 492258 | 524846 |
a0001c0002t0022 | 0/0 | 2747 | 3 | 0 | 1 | 0 | 0 | 2 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2742): Show |
chr7 | 492258 | 524846 |
a0001c0002t0027 | 0/0 | 2743 | 1 | 0 | 0 | 0 | 1 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2738): Show |
chr7 | 492258 | 524846 |
a0001c0002t0030 | 0/0 | 2746 | 2 | 0 | 0 | 2 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2741): Show |
chr7 | 492258 | 524846 |
a0001c0002t0031 | 0/0 | 2745 | 1 | 0 | 1 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2740): Show |
chr7 | 492258 | 524846 |
a0001c0002t0032 | 0/0 | 2745 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2740): Show |
chr7 | 492258 | 524846 |
a0001c0002t0040 | 0/0 | 2747 | 1 | 0 | 1 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2742): Show |
chr7 | 492258 | 524846 |
a0001c0002t0043 | 0/0 | 2752 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2747): Show |
chr7 | 492258 | 524846 |
a0001c0002t0044 | 0/0 | 2749 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2744): Show |
chr7 | 492258 | 524846 |
a0001c0002t0050 | 0/0 | 2746 | 1 | 0 | 1 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2741): Show |
chr7 | 492258 | 524846 |
a0001c0002t0055 | 0/0 | 2746 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2741): Show |
chr7 | 492258 | 524846 |
a0001c0002t0056 | 0/0 | 2738 | 1 | 0 | 1 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2733): Show |
chr7 | 492258 | 524846 |
a0001c0002t0058 | 0/0 | 2750 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2745): Show |
chr7 | 492258 | 524846 |
a0001c0002t0064 | 0/0 | 2746 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2741): Show |
chr7 | 492258 | 524846 |
a0001c0002t0069 | 0/0 | 2746 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2741): Show |
chr7 | 492258 | 524846 |
a0001c0002t0070 | 0/0 | 2747 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2742): Show |
chr7 | 492258 | 524846 |
a0001c0002t0072 | 0/0 | 2747 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2742): Show |
chr7 | 492258 | 524846 |
a0001c0002t0073 | 0/0 | 2746 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2741): Show |
chr7 | 492258 | 524846 |
a0001c0002t0077 | 0/0 | 2749 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2744): Show |
chr7 | 492258 | 524846 |
a0001c0002t0078 | 0/0 | 2750 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2745): Show |
chr7 | 492258 | 524846 |
a0001c0002t0085 | 0/0 | 2745 | 1 | 0 | 0 | 0 | 0 | 1 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2740): Show |
chr7 | 492258 | 524846 |
a0001c0002t0099 | 0/0 | 2748 | 1 | 0 | 1 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2743): Show |
chr7 | 492258 | 524846 |
a0001c0002t0103 | 0/0 | 2747 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2742): Show |
chr7 | 492258 | 524846 |
a0001c0002t0113 | 0/0 | 2738 | 1 | 0 | 0 | 0 | 0 | 1 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2733): Show |
chr7 | 492258 | 524846 |
a0001c0003t0002 | 0/0 | 2742 | 3 | 0 | 3 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2737): Show |
chr7 | 492258 | 524846 |
a0001c0003t0020 | 0/0 | 2743 | 1 | 0 | 1 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2738): Show |
chr7 | 492258 | 524846 |
a0001c0003t0083 | 0/0 | 2747 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2742): Show |
chr7 | 492258 | 524846 |
a0001c0007t0096 | 0/0 | 2746 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2741): Show |
chr7 | 492258 | 524846 |
a0002c0008t0104 | 0/0 | 2743 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2738): Show |
chr7 | 492258 | 524846 |
a0003c0004t0012 | 0/0 | 2749 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2744): Show |
chr7 | 492258 | 524846 |
a0004c0006t0060 | 0/0 | 2741 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2736): Show |
chr7 | 492258 | 524846 |
a0005c0005t0002 | 0/0 | 2742 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | ACACG others(2737): Show |
chr7 | 492258 | 524846 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0002g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0002g0003 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0002g0113 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0003g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0004g0006 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0004g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0004g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0004g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0004g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0004g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0004g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0004g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0004g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0004g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0004g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0004g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0005g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0005g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0005g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0005g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0007g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0007g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0008g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0008g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0008g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0008g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0008g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0008g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0008g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0008g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0008g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0008g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0009g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0009g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0009g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0009g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0009g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0009g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0009g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0009g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0010g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0010g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0010g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0010g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0010g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0010g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0011g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0011g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0011g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0011g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0013g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0013g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0013g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0013g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0013g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0014g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0014g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0015g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0015g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0015g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0015g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0016g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0016g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0016g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0017g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0017g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0017g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0017g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0018g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0018g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0019g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0019g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0019g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0020g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0020g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0021g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0021g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0021g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0023g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0023g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0023g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0024g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0024g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0024g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0025g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0025g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0025g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0026g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0026g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0026g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0027g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0028g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0028g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0029g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0029g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0031g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0032g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0033g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0033g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0034g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0034g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0035g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0035g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0036g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0036g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0037g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0037g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0038g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0038g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0039g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0039g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0040g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0041g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0041g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0042g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0045g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0046g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0047g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0048g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0049g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0051g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0052g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0053g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0054g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0057g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0059g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0061g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0062g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0063g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0065g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0066g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0067g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0068g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0071g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0074g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0075g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0076g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0079g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0080g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0081g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0082g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0084g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0086g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0087g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0088g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0089g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0090g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0091g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0092g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0093g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0094g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0095g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0097g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0098g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0100g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0101g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0102g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0105g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0106g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0107g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0108g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0109g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0110g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0111g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0112g0269 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0001t0114g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0002t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0002t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0002t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0002t0003g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0002t0003g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0002t0003g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0002t0003g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0002t0003g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0002t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0002t0003g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0002t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0002t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0002t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0002t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0002t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0002t0003g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0002t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0002t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0002t0003g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0002t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0002t0005g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0002t0005g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0002t0005g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0002t0005g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0002t0005g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0002t0005g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0002t0005g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0002t0006g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0002t0006g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0002t0006g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0002t0006g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0002t0006g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0002t0006g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0002t0006g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0002t0006g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0002t0006g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0002t0006g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0002t0007g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0002t0007g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0002t0007g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0002t0007g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0002t0007g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0002t0007g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0002t0007g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0002t0007g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0002t0009g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0002t0010g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0002t0010g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0002t0011g0004 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0002t0011g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0002t0012g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0002t0012g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0002t0012g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0002t0012g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0002t0012g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0002t0013g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0002t0014g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0002t0014g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0002t0014g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0002t0016g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0002t0018g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0002t0022g0005 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0002t0022g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0002t0027g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0002t0030g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0002t0030g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0002t0031g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0002t0032g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0002t0040g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0002t0043g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0002t0044g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0002t0050g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0002t0055g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0002t0056g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0002t0058g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0002t0064g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0002t0069g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0002t0070g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0002t0072g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0002t0073g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0002t0077g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0002t0078g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0002t0085g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0002t0099g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0002t0103g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0002t0113g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0003t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0003t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0003t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0003t0020g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0003t0083g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0001c0007t0096g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0002c0008t0104g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0003c0004t0012g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0004c0006t0060g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
a0005c0005t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0002 | t0007 | g0050 | EUR | GBR | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG00099 | hp2 | a0001 | c0001 | t0090 | g0180 | EUR | GBR | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG00280 | hp1 | a0001 | c0001 | t0100 | g0190 | EUR | FIN | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG00280 | hp2 | a0001 | c0001 | t0004 | g0188 | EUR | FIN | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG00323 | hp1 | a0001 | c0002 | t0027 | g0044 | EUR | FIN | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG00323 | hp2 | a0001 | c0001 | t0002 | g0003 | EUR | FIN | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG00408 | hp1 | a0001 | c0001 | t0016 | g0160 | EAS | CHS | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG00408 | hp2 | a0001 | c0002 | t0012 | g0034 | EAS | CHS | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG00423 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | CHS | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | CHS | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | CHS | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG00544 | hp2 | a0001 | c0002 | t0007 | g0098 | EAS | CHS | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG00558 | hp1 | a0001 | c0001 | t0074 | g0024 | EAS | CHS | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG00558 | hp2 | a0001 | c0002 | t0012 | g0043 | EAS | CHS | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | CHS | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG00609 | hp2 | a0001 | c0001 | t0020 | g0109 | EAS | CHS | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG00621 | hp2 | a0001 | c0001 | t0026 | g0272 | EAS | CHS | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG00639 | hp1 | a0001 | c0001 | t0075 | g0082 | AMR | PUR | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG00639 | hp2 | a0001 | c0001 | t0033 | g0280 | AMR | PUR | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG00642 | hp1 | a0001 | c0001 | t0028 | g0084 | AMR | PUR | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG00642 | hp2 | a0001 | c0002 | t0014 | g0168 | AMR | PUR | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0118 | EAS | CHS | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG00673 | hp2 | a0001 | c0002 | t0012 | g0079 | EAS | CHS | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG00733 | hp1 | a0001 | c0001 | t0008 | g0236 | AMR | PUR | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG00733 | hp2 | a0001 | c0001 | t0091 | g0239 | AMR | PUR | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG00738 | hp1 | a0001 | c0002 | t0006 | g0089 | AMR | PUR | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG00738 | hp2 | a0001 | c0002 | t0056 | g0088 | AMR | PUR | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG00741 | hp1 | a0001 | c0001 | t0008 | g0144 | AMR | PUR | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG00741 | hp2 | a0001 | c0001 | t0008 | g0161 | AMR | PUR | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG01069 | hp1 | a0001 | c0001 | t0031 | g0059 | AMR | PUR | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG01069 | hp2 | a0001 | c0001 | t0063 | g0086 | AMR | PUR | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG01071 | hp1 | a0001 | c0001 | t0021 | g0087 | AMR | PUR | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG01071 | hp2 | a0001 | c0001 | t0004 | g0181 | AMR | PUR | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG01074 | hp1 | a0001 | c0002 | t0011 | g0004 | AMR | PUR | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG01074 | hp2 | a0001 | c0001 | t0024 | g0184 | AMR | PUR | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG01081 | hp1 | a0001 | c0001 | t0015 | g0135 | AMR | PUR | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG01081 | hp2 | a0001 | c0001 | t0101 | g0207 | AMR | PUR | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG01099 | hp1 | a0001 | c0001 | t0093 | g0281 | AMR | PUR | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0244 | AMR | PUR | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG01106 | hp1 | a0001 | c0001 | t0008 | g0245 | AMR | PUR | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG01106 | hp2 | a0001 | c0001 | t0009 | g0200 | AMR | PUR | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG01109 | hp1 | a0001 | c0001 | t0102 | g0235 | AMR | PUR | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG01109 | hp2 | a0001 | c0001 | t0008 | g0217 | AMR | PUR | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG01167 | hp1 | a0001 | c0001 | t0004 | g0006 | AMR | PUR | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG01167 | hp2 | a0001 | c0002 | t0050 | g0023 | AMR | PUR | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG01168 | hp1 | a0001 | c0001 | t0110 | g0183 | AMR | PUR | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG01169 | hp1 | a0001 | c0001 | t0047 | g0012 | AMR | PUR | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG01169 | hp2 | a0001 | c0001 | t0004 | g0153 | AMR | PUR | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG01175 | hp2 | a0001 | c0001 | t0049 | g0015 | AMR | PUR | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG01192 | hp1 | a0001 | c0001 | t0008 | g0246 | AMR | PUR | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG01192 | hp2 | a0001 | c0001 | t0037 | g0176 | AMR | PUR | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG01243 | hp1 | a0001 | c0001 | t0015 | g0017 | AMR | PUR | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG01243 | hp2 | a0001 | c0001 | t0010 | g0204 | AMR | PUR | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG01256 | hp1 | a0001 | c0002 | t0016 | g0163 | AMR | CLM | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG01257 | hp1 | a0001 | c0001 | t0024 | g0182 | AMR | CLM | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG01257 | hp2 | a0001 | c0001 | t0038 | g0234 | AMR | CLM | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG01258 | hp1 | a0001 | c0002 | t0099 | g0164 | AMR | CLM | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG01258 | hp2 | a0001 | c0001 | t0038 | g0233 | AMR | CLM | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG01261 | hp1 | a0001 | c0002 | t0040 | g0165 | AMR | CLM | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG01261 | hp2 | a0001 | c0002 | t0005 | g0100 | AMR | CLM | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG01346 | hp1 | a0001 | c0001 | t0007 | g0062 | AMR | CLM | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG01346 | hp2 | a0001 | c0001 | t0028 | g0125 | AMR | CLM | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG01358 | hp1 | a0001 | c0002 | t0014 | g0169 | AMR | CLM | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG01358 | hp2 | a0001 | c0002 | t0001 | g0232 | AMR | CLM | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG01361 | hp1 | a0001 | c0001 | t0026 | g0198 | AMR | CLM | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG01361 | hp2 | a0001 | c0002 | t0022 | g0005 | AMR | CLM | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG01496 | hp1 | a0001 | c0002 | t0031 | g0048 | AMR | CLM | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG01496 | hp2 | a0001 | c0001 | t0021 | g0065 | AMR | CLM | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG01515 | hp1 | a0001 | c0002 | t0014 | g0166 | EUR | IBS | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG01515 | hp2 | a0001 | c0001 | t0087 | g0157 | EUR | IBS | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0003 | EUR | IBS | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG01516 | hp2 | a0001 | c0001 | t0029 | g0064 | EUR | IBS | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG01517 | hp1 | a0001 | c0002 | t0010 | g0267 | EUR | IBS | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG01517 | hp2 | a0001 | c0001 | t0002 | g0112 | EUR | IBS | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG01884 | hp1 | a0001 | c0001 | t0004 | g0006 | AFR | ACB | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG01884 | hp2 | a0001 | c0001 | t0010 | g0259 | AFR | ACB | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG01891 | hp1 | a0001 | c0002 | t0077 | g0020 | AFR | ACB | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG01891 | hp2 | a0001 | c0001 | t0089 | g0248 | AFR | ACB | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG01934 | hp1 | a0001 | c0001 | t0037 | g0254 | AMR | PEL | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG01934 | hp2 | a0001 | c0001 | t0005 | g0072 | AMR | PEL | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG01981 | hp1 | a0001 | c0003 | t0020 | g0120 | AMR | PEL | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG01981 | hp2 | a0001 | c0002 | t0007 | g0039 | AMR | PEL | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG02004 | hp1 | a0001 | c0001 | t0003 | g0060 | AMR | PEL | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG02004 | hp2 | a0001 | c0003 | t0002 | g0107 | AMR | PEL | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG02015 | hp1 | a0001 | c0001 | t0066 | g0101 | EAS | KHV | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG02015 | hp2 | a0001 | c0002 | t0005 | g0029 | EAS | KHV | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG02027 | hp1 | a0001 | c0002 | t0005 | g0030 | EAS | KHV | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG02027 | hp2 | a0001 | c0001 | t0023 | g0271 | EAS | KHV | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG02040 | hp1 | a0001 | c0001 | t0039 | g0210 | EAS | KHV | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0106 | EAS | KHV | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG02055 | hp1 | a0001 | c0002 | t0078 | g0078 | AFR | ACB | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG02055 | hp2 | a0001 | c0001 | t0053 | g0132 | AFR | ACB | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | KHV | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG02129 | hp2 | a0001 | c0001 | t0016 | g0196 | EAS | KHV | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG02132 | hp1 | a0001 | c0001 | t0114 | g0295 | EAS | KHV | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG02132 | hp2 | a0001 | c0001 | t0017 | g0242 | EAS | KHV | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG02135 | hp1 | a0001 | c0002 | t0002 | g0071 | EAS | KHV | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0117 | EAS | KHV | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG02145 | hp1 | a0001 | c0001 | t0094 | g0288 | AFR | ACB | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG02145 | hp2 | a0001 | c0001 | t0004 | g0293 | AFR | ACB | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG02165 | hp1 | a0001 | c0001 | t0106 | g0228 | EAS | CDX | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG02165 | hp2 | a0001 | c0002 | t0007 | g0097 | EAS | CDX | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG02257 | hp1 | a0001 | c0001 | t0095 | g0192 | AFR | ACB | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG02257 | hp2 | a0001 | c0001 | t0097 | g0177 | AFR | ACB | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG02258 | hp1 | a0001 | c0001 | t0013 | g0260 | AFR | ACB | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG02258 | hp2 | a0001 | c0002 | t0043 | g0010 | AFR | ACB | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG02273 | hp1 | a0001 | c0002 | t0003 | g0037 | AMR | PEL | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG02273 | hp2 | a0001 | c0003 | t0002 | g0108 | AMR | PEL | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG02280 | hp1 | a0001 | c0001 | t0025 | g0273 | AFR | ACB | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG02280 | hp2 | a0001 | c0001 | t0025 | g0277 | AFR | ACB | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG02293 | hp1 | a0001 | c0002 | t0003 | g0049 | AMR | PEL | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG02293 | hp2 | a0001 | c0003 | t0002 | g0119 | AMR | PEL | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG02451 | hp1 | a0001 | c0001 | t0068 | g0133 | AFR | ACB | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG02451 | hp2 | a0001 | c0007 | t0096 | g0202 | AFR | ACB | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG02523 | hp1 | a0001 | c0002 | t0073 | g0067 | EAS | KHV | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG02523 | hp2 | a0001 | c0002 | t0064 | g0077 | EAS | KHV | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG02572 | hp1 | a0001 | c0001 | t0046 | g0013 | AFR | GWD | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG02572 | hp2 | a0001 | c0001 | t0010 | g0189 | AFR | GWD | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0187 | SAS | PJL | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG02602 | hp2 | a0001 | c0001 | t0062 | g0099 | SAS | PJL | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG02622 | hp1 | a0001 | c0001 | t0041 | g0276 | AFR | GWD | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG02622 | hp2 | a0001 | c0001 | t0084 | g0283 | AFR | GWD | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG02630 | hp1 | a0001 | c0001 | t0018 | g0083 | AFR | GWD | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG02630 | hp2 | a0001 | c0001 | t0011 | g0257 | AFR | GWD | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG02647 | hp1 | a0001 | c0002 | t0010 | g0173 | AFR | GWD | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG02647 | hp2 | a0001 | c0001 | t0035 | g0174 | AFR | GWD | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG02717 | hp1 | a0001 | c0001 | t0041 | g0275 | AFR | GWD | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG02717 | hp2 | a0001 | c0001 | t0111 | g0262 | AFR | GWD | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG02723 | hp1 | a0001 | c0001 | t0013 | g0294 | AFR | GWD | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG02723 | hp2 | a0001 | c0001 | t0004 | g0162 | AFR | GWD | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG02738 | hp1 | a0001 | c0001 | t0029 | g0139 | SAS | PJL | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG02738 | hp2 | a0001 | c0002 | t0006 | g0025 | SAS | PJL | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG02809 | hp1 | a0001 | c0001 | t0011 | g0287 | AFR | GWD | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG02809 | hp2 | a0001 | c0003 | t0083 | g0291 | AFR | GWD | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG02818 | hp1 | a0001 | c0001 | t0015 | g0134 | AFR | GWD | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG02818 | hp2 | a0001 | c0001 | t0004 | g0279 | AFR | GWD | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG02886 | hp1 | a0001 | c0001 | t0098 | g0208 | AFR | GWD | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG02886 | hp2 | a0001 | c0001 | t0008 | g0175 | AFR | GWD | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG02922 | hp1 | a0001 | c0001 | t0109 | g0274 | AFR | ESN | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG02922 | hp2 | a0001 | c0001 | t0018 | g0085 | AFR | ESN | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG02965 | hp1 | a0001 | c0001 | t0052 | g0140 | AFR | ESN | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0270 | AFR | ESN | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG02970 | hp1 | a0001 | c0001 | t0015 | g0136 | AFR | ESN | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG02970 | hp2 | a0001 | c0001 | t0010 | g0290 | AFR | ESN | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG03098 | hp1 | a0001 | c0002 | t0055 | g0018 | AFR | MSL | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG03098 | hp2 | a0001 | c0001 | t0057 | g0111 | AFR | MSL | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG03130 | hp1 | a0001 | c0001 | t0013 | g0261 | AFR | ESN | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG03130 | hp2 | a0001 | c0001 | t0019 | g0093 | AFR | ESN | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG03225 | hp1 | a0001 | c0001 | t0051 | g0141 | AFR | MSL | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG03225 | hp2 | a0001 | c0001 | t0045 | g0011 | AFR | MSL | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG03239 | hp1 | a0001 | c0001 | t0004 | g0193 | SAS | PJL | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG03239 | hp2 | a0001 | c0002 | t0011 | g0004 | SAS | PJL | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG03453 | hp1 | a0001 | c0001 | t0048 | g0014 | AFR | MSL | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG03453 | hp2 | a0001 | c0002 | t0032 | g0171 | AFR | MSL | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG03486 | hp1 | a0001 | c0001 | t0014 | g0256 | AFR | MSL | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG03486 | hp2 | a0001 | c0001 | t0021 | g0138 | AFR | MSL | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG03492 | hp1 | a0001 | c0002 | t0022 | g0178 | SAS | PJL | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG03492 | hp2 | a0001 | c0001 | t0042 | g0008 | SAS | PJL | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG03516 | hp1 | a0001 | c0001 | t0036 | g0258 | AFR | ESN | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG03516 | hp2 | a0001 | c0001 | t0004 | g0289 | AFR | ESN | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG03540 | hp1 | a0001 | c0001 | t0054 | g0022 | AFR | GWD | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG03540 | hp2 | a0001 | c0001 | t0061 | g0021 | AFR | GWD | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG03579 | hp1 | a0001 | c0001 | t0088 | g0263 | AFR | MSL | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG03579 | hp2 | a0001 | c0001 | t0011 | g0186 | AFR | MSL | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG03688 | hp1 | a0001 | c0001 | t0004 | g0185 | SAS | STU | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG03688 | hp2 | a0001 | c0001 | t0019 | g0063 | SAS | STU | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG03704 | hp1 | a0001 | c0001 | t0092 | g0215 | SAS | PJL | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0265 | SAS | PJL | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG03710 | hp1 | a0001 | c0002 | t0085 | g0148 | SAS | PJL | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG03710 | hp2 | a0001 | c0002 | t0022 | g0005 | SAS | PJL | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG03927 | hp1 | a0001 | c0001 | t0005 | g0130 | SAS | BEB | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG03927 | hp2 | a0001 | c0001 | t0017 | g0219 | SAS | BEB | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG03942 | hp1 | a0001 | c0002 | t0113 | g0264 | SAS | BEB | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG03942 | hp2 | a0001 | c0001 | t0011 | g0206 | SAS | BEB | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG04115 | hp1 | a0001 | c0001 | t0034 | g0211 | SAS | STU | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG04115 | hp2 | a0001 | c0002 | t0003 | g0091 | SAS | STU | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG04184 | hp1 | a0001 | c0001 | t0004 | g0191 | SAS | BEB | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG04184 | hp2 | a0001 | c0002 | t0003 | g0129 | SAS | BEB | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG04204 | hp1 | a0001 | c0001 | t0024 | g0222 | SAS | STU | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG04204 | hp2 | a0001 | c0002 | t0018 | g0122 | SAS | STU | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG04228 | hp1 | a0001 | c0002 | t0007 | g0040 | SAS | STU | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0147 | SAS | STU | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
NA18612 | hp1 | a0001 | c0001 | t0016 | g0159 | EAS | CHB | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
NA18612 | hp2 | a0001 | c0002 | t0002 | g0038 | EAS | CHB | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | CHB | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
NA18747 | hp2 | a0001 | c0002 | t0003 | g0001 | EAS | CHB | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
NA18906 | hp1 | a0001 | c0001 | t0010 | g0282 | AFR | YRI | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
NA18906 | hp2 | a0001 | c0001 | t0067 | g0137 | AFR | YRI | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
NA18940 | hp1 | a0001 | c0002 | t0069 | g0126 | EAS | JPT | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
NA18940 | hp2 | a0001 | c0001 | t0007 | g0128 | EAS | JPT | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
NA18944 | hp1 | a0001 | c0001 | t0009 | g0240 | EAS | JPT | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
NA18944 | hp2 | a0001 | c0002 | t0012 | g0033 | EAS | JPT | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
NA18945 | hp1 | a0001 | c0002 | t0005 | g0080 | EAS | JPT | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
NA18945 | hp2 | a0001 | c0001 | t0023 | g0155 | EAS | JPT | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
NA18947 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
NA18947 | hp2 | a0001 | c0002 | t0006 | g0076 | EAS | JPT | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
NA18948 | hp1 | a0001 | c0002 | t0003 | g0032 | EAS | JPT | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
NA18948 | hp2 | a0001 | c0001 | t0034 | g0209 | EAS | JPT | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
NA18950 | hp1 | a0001 | c0002 | t0012 | g0036 | EAS | JPT | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
NA18952 | hp1 | a0001 | c0001 | t0020 | g0105 | EAS | JPT | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
NA18952 | hp2 | a0001 | c0002 | t0007 | g0031 | EAS | JPT | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
NA18953 | hp1 | a0001 | c0001 | t0040 | g0221 | EAS | JPT | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
NA18959 | hp1 | a0001 | c0001 | t0105 | g0229 | EAS | JPT | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
NA18959 | hp2 | a0001 | c0001 | t0009 | g0238 | EAS | JPT | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
NA18963 | hp1 | a0001 | c0002 | t0044 | g0009 | EAS | JPT | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
NA18963 | hp2 | a0001 | c0001 | t0023 | g0146 | EAS | JPT | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
NA18964 | hp1 | a0003 | c0004 | t0012 | g0094 | EAS | JPT | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
NA18966 | hp1 | a0001 | c0001 | t0009 | g0195 | EAS | JPT | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
NA18967 | hp1 | a0001 | c0002 | t0007 | g0090 | EAS | JPT | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
NA18967 | hp2 | a0001 | c0001 | t0082 | g0226 | EAS | JPT | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
NA18970 | hp1 | a0001 | c0002 | t0003 | g0051 | EAS | JPT | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
NA18970 | hp2 | a0001 | c0002 | t0003 | g0124 | EAS | JPT | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
NA18971 | hp1 | a0001 | c0001 | t0005 | g0058 | EAS | JPT | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
NA18975 | hp1 | a0001 | c0001 | t0026 | g0268 | EAS | JPT | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
NA18975 | hp2 | a0001 | c0001 | t0065 | g0131 | EAS | JPT | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
NA18979 | hp1 | a0001 | c0001 | t0025 | g0156 | EAS | JPT | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
NA18979 | hp2 | a0001 | c0002 | t0003 | g0055 | EAS | JPT | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
NA18980 | hp2 | a0001 | c0001 | t0027 | g0104 | EAS | JPT | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
NA18981 | hp1 | a0001 | c0001 | t0017 | g0225 | EAS | JPT | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
NA18981 | hp2 | a0001 | c0002 | t0030 | g0035 | EAS | JPT | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
NA18983 | hp1 | a0001 | c0001 | t0003 | g0061 | EAS | JPT | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
NA18983 | hp2 | a0001 | c0002 | t0006 | g0054 | EAS | JPT | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
NA18994 | hp1 | a0001 | c0002 | t0030 | g0052 | EAS | JPT | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
NA18994 | hp2 | a0001 | c0002 | t0006 | g0047 | EAS | JPT | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
NA18995 | hp1 | a0001 | c0002 | t0003 | g0070 | EAS | JPT | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
NA18995 | hp2 | a0001 | c0001 | t0008 | g0194 | EAS | JPT | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
NA18997 | hp1 | a0001 | c0002 | t0013 | g0172 | EAS | JPT | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
NA18997 | hp2 | a0004 | c0006 | t0060 | g0057 | EAS | JPT | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
NA18999 | hp1 | a0001 | c0002 | t0005 | g0127 | EAS | JPT | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
NA18999 | hp2 | a0001 | c0001 | t0008 | g0224 | EAS | JPT | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
NA19003 | hp1 | a0001 | c0002 | t0002 | g0056 | EAS | JPT | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
NA19003 | hp2 | a0001 | c0002 | t0072 | g0042 | EAS | JPT | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
NA19004 | hp2 | a0001 | c0002 | t0003 | g0045 | EAS | JPT | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
NA19007 | hp1 | a0001 | c0002 | t0009 | g0249 | EAS | JPT | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
NA19007 | hp2 | a0001 | c0002 | t0007 | g0046 | EAS | JPT | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
NA19009 | hp1 | a0001 | c0002 | t0006 | g0096 | EAS | JPT | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
NA19009 | hp2 | a0001 | c0001 | t0108 | g0158 | EAS | JPT | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
NA19010 | hp1 | a0001 | c0002 | t0003 | g0142 | EAS | JPT | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
NA19010 | hp2 | a0001 | c0002 | t0003 | g0016 | EAS | JPT | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
NA19012 | hp1 | a0001 | c0001 | t0107 | g0201 | EAS | JPT | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
NA19012 | hp2 | a0001 | c0002 | t0005 | g0066 | EAS | JPT | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
NA19043 | hp1 | a0001 | c0001 | t0019 | g0092 | AFR | LWK | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
NA19043 | hp2 | a0001 | c0002 | t0011 | g0152 | AFR | LWK | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
NA19057 | hp1 | a0001 | c0002 | t0006 | g0028 | EAS | JPT | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
NA19057 | hp2 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
NA19062 | hp1 | a0001 | c0002 | t0006 | g0075 | EAS | JPT | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
NA19062 | hp2 | a0001 | c0001 | t0079 | g0149 | EAS | JPT | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
NA19064 | hp1 | a0001 | c0002 | t0070 | g0041 | EAS | JPT | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
NA19064 | hp2 | a0001 | c0001 | t0009 | g0255 | EAS | JPT | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
NA19065 | hp1 | a0001 | c0001 | t0076 | g0115 | EAS | JPT | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
NA19065 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
NA19070 | hp1 | a0001 | c0001 | t0017 | g0241 | EAS | JPT | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
NA19070 | hp2 | a0001 | c0002 | t0003 | g0053 | EAS | JPT | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
NA19074 | hp1 | a0001 | c0001 | t0009 | g0197 | EAS | JPT | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
NA19074 | hp2 | a0001 | c0001 | t0039 | g0213 | EAS | JPT | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
NA19079 | hp1 | a0001 | c0001 | t0080 | g0151 | EAS | JPT | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
NA19079 | hp2 | a0001 | c0002 | t0003 | g0068 | EAS | JPT | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
NA19081 | hp1 | a0001 | c0001 | t0081 | g0150 | EAS | JPT | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
NA19081 | hp2 | a0001 | c0001 | t0005 | g0081 | EAS | JPT | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
NA19082 | hp1 | a0001 | c0002 | t0003 | g0095 | EAS | JPT | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
NA19082 | hp2 | a0001 | c0001 | t0009 | g0243 | EAS | JPT | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
NA19084 | hp1 | a0001 | c0002 | t0003 | g0027 | EAS | JPT | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
NA19084 | hp2 | a0001 | c0001 | t0009 | g0247 | EAS | JPT | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
NA19085 | hp1 | a0005 | c0005 | t0002 | g0073 | EAS | JPT | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
NA19085 | hp2 | a0001 | c0002 | t0103 | g0203 | EAS | JPT | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
NA19088 | hp1 | a0001 | c0002 | t0005 | g0123 | EAS | JPT | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
NA19088 | hp2 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
NA19090 | hp1 | a0001 | c0001 | t0086 | g0266 | EAS | JPT | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
NA19090 | hp2 | a0001 | c0002 | t0006 | g0069 | EAS | JPT | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
NA19240 | hp1 | a0001 | c0001 | t0036 | g0285 | AFR | YRI | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
NA19240 | hp2 | a0001 | c0001 | t0033 | g0278 | AFR | YRI | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
NA20129 | hp1 | a0001 | c0001 | t0071 | g0116 | AFR | ASW | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
NA20129 | hp2 | a0001 | c0001 | t0013 | g0284 | AFR | ASW | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0218 | EUR | TSI | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0199 | EUR | TSI | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
NA20805 | hp1 | a0001 | c0001 | t0008 | g0170 | EUR | TSI | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
NA20805 | hp2 | a0001 | c0002 | t0001 | g0223 | EUR | TSI | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
NA20905 | hp1 | a0001 | c0002 | t0006 | g0121 | SAS | GIH | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0214 | SAS | GIH | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG02109 | hp1 | a0002 | c0008 | t0104 | g0143 | AFR | ACB | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG02109 | hp2 | a0001 | c0001 | t0014 | g0237 | AFR | ACB | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | ACB | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG02486 | hp2 | a0001 | c0001 | t0010 | g0292 | AFR | ACB | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG02559 | hp1 | a0001 | c0002 | t0058 | g0026 | AFR | ACB | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG02559 | hp2 | a0001 | c0001 | t0035 | g0145 | AFR | ACB | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG03471 | hp1 | a0001 | c0001 | t0013 | g0286 | AFR | MSL | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG03471 | hp2 | a0001 | c0001 | t0032 | g0154 | AFR | MSL | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG06807 | hp1 | a0001 | c0001 | t0059 | g0019 | AFR | USA | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
HG06807 | hp2 | a0001 | c0001 | t0004 | g0179 | AFR | USA | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
homoSapiens | chm13v2 | a0001 | c0001 | t0112 | g0269 | REF | REF | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0113 | REF | REF | PDGFA_chr7_492258_524846 | PDGFA | chr7 | 492258 | 524846 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:501236 | T | G | 1 | a0004 | 1 | NA18997.hp2 | missense_variant | MODERATE | c.460A>C | p.Lys154Gln | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 5/6 | 1305/2742 | 460/591 | 154/196 | chr7 | 501236 | |||
chr7:510835 | A | G | 1 | a0005 | 1 | NA19085.hp1 | missense_variant | MODERATE | c.427T>C | p.Ser143Pro | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/6 | 1272/2742 | 427/591 | 143/196 | chr7 | 510835 | |||
chr7:510873 | G | T | 1 | a0003 | 1 | NA18964.hp1 | missense_variant | MODERATE | c.389C>A | p.Thr130Asn | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/6 | 1234/2742 | 389/591 | 130/196 | chr7 | 510873 | |||
chr7:512435 | T | G | 1 | a0002 | 1 | HG02109.hp1 | missense_variant | MODERATE | c.181A>C | p.Thr61Pro | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 3/6 | 1026/2742 | 181/591 | 61/196 | chr7 | 512435 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:501186 | C | T | 1 | a0001c0007 | 1 | HG02451.hp2 | synonymous_variant | LOW | c.510G>A | p.Arg170Arg | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 5/6 | 1355/2742 | 510/591 | 170/196 | chr7 | 501186 | |||
chr7:510830 | G | A | 2 | a0001c0003 a0001c0007 |
6 | HG01981.hp1 HG02004.hp2 HG02273.hp2 others(3): Show |
synonymous_variant | LOW | c.432C>T | p.Arg144Arg | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/6 | 1277/2742 | 432/591 | 144/196 | chr7 | 510830 | |||
chr7:512409 | A | G | 5 | a0001c0002 a0002c0008 a0003c0004 others(2): Show |
95 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(92): Show |
synonymous_variant | LOW | c.207T>C | p.His69His | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 3/6 | 1052/2742 | 207/591 | 69/196 | chr7 | 512409 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:497281 | T | C | 1 | a0004c0006t0060 | 1 | NA18997.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1283A>G | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 6/6 | 1283 | chr7 | 497281 | ||||||
chr7:497294 | A | C | 2 | a0001c0001t0033 a0001c0001t0093 |
3 | HG00639.hp2 HG01099.hp1 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1270T>G | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 6/6 | 1270 | chr7 | 497294 | ||||||
chr7:497345 | G | A | 27 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0009 others(24): Show |
75 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*1219C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 6/6 | 1219 | chr7 | 497345 | ||||||
chr7:497490 | G | A | 1 | a0001c0002t0069 | 1 | NA18940.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1074C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 6/6 | 1074 | chr7 | 497490 | ||||||
chr7:497606 | G | T | 1 | a0001c0001t0061 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*958C>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 6/6 | 958 | chr7 | 497606 | ||||||
chr7:497616 | G | A | 1 | a0001c0002t0056 | 1 | HG00738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*948C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 6/6 | 948 | chr7 | 497616 | ||||||
chr7:497758 | A | T | 1 | a0004c0006t0060 | 1 | NA18997.hp2 | 3_prime_UTR_variant | MODIFIER | c.*806T>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 6/6 | 806 | chr7 | 497758 | ||||||
chr7:497759 | T | A | 1 | a0004c0006t0060 | 1 | NA18997.hp2 | 3_prime_UTR_variant | MODIFIER | c.*805A>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 6/6 | 805 | chr7 | 497759 | ||||||
chr7:497840 | A | T | 1 | a0001c0001t0095 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*724T>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 6/6 | 724 | chr7 | 497840 | ||||||
chr7:497841 | T | A | 1 | a0001c0001t0095 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*723A>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 6/6 | 723 | chr7 | 497841 | ||||||
chr7:497842 | C | T | 1 | a0001c0001t0095 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*722G>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 6/6 | 722 | chr7 | 497842 | ||||||
chr7:497869 | T | TA | 10 | a0001c0001t0027 a0001c0001t0031 a0001c0001t0036 others(7): Show |
12 | HG00323.hp1 HG01069.hp1 HG01496.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*694dupT | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 6/6 | 694 | chr7 | 497869 | ||||||
chr7:497869 | T | TAA | 18 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0007 others(15): Show |
68 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*693_*694dupTT | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 6/6 | 694 | chr7 | 497869 | ||||||
chr7:497869 | T | TAAA | 11 | a0001c0001t0042 a0001c0001t0051 a0001c0001t0053 others(8): Show |
12 | HG02015.hp1 HG02055.hp2 HG02451.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*692_*694dupTTT | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 6/6 | 694 | chr7 | 497869 | ||||||
chr7:497869 | T | TAAAA | 23 | a0001c0001t0015 a0001c0001t0016 a0001c0001t0019 others(20): Show |
35 | HG00099.hp2 HG00408.hp1 HG01081.hp1 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*691_*694dupTTTT | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 6/6 | 694 | chr7 | 497869 | ||||||
chr7:497869 | T | TAAAAA | 14 | a0001c0001t0004 a0001c0001t0011 a0001c0001t0021 others(11): Show |
38 | HG00280.hp2 HG01069.hp2 HG01071.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*690_*694dupTTTTT | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 6/6 | 694 | chr7 | 497869 | ||||||
chr7:497869 | T | TAAAAAA | 9 | a0001c0001t0014 a0001c0001t0097 a0001c0001t0100 others(6): Show |
12 | HG00280.hp1 HG00642.hp2 HG01109.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*689_*694dupTTTTTT | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 6/6 | 694 | chr7 | 497869 | ||||||
chr7:497869 | TAAA | T | 8 | a0001c0001t0008 a0001c0001t0035 a0001c0001t0037 others(5): Show |
20 | HG00733.hp1 HG00741.hp1 HG00741.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*692_*694delTTT | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 6/6 | 692 | chr7 | 497869 | ||||||
chr7:497869 | TAAAA | T | 17 | a0001c0001t0001 a0001c0001t0009 a0001c0001t0017 others(14): Show |
52 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*691_*694delTTTT | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 6/6 | 691 | chr7 | 497869 | ||||||
chr7:497913 | G | A | 1 | a0001c0002t0073 | 1 | HG02523.hp1 | 3_prime_UTR_variant | MODIFIER | c.*651C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 6/6 | 651 | chr7 | 497913 | ||||||
chr7:497939 | T | TA | 35 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0009 others(32): Show |
85 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(82): Show |
3_prime_UTR_variant | MODIFIER | c.*624dupT | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 6/6 | 624 | chr7 | 497939 | ||||||
chr7:497939 | T | TAA | 20 | a0001c0001t0007 a0001c0001t0017 a0001c0001t0024 others(17): Show |
35 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*623_*624dupTT | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 6/6 | 624 | chr7 | 497939 | ||||||
chr7:497939 | T | TAAA | 9 | a0001c0001t0005 a0001c0001t0026 a0001c0001t0038 others(6): Show |
21 | HG00621.hp2 HG01081.hp2 HG01257.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*622_*624dupTTT | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 6/6 | 624 | chr7 | 497939 | ||||||
chr7:497939 | T | TAAAA | 4 | a0001c0001t0076 a0001c0001t0108 a0001c0002t0012 others(1): Show |
8 | HG00408.hp2 HG00558.hp2 HG00673.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*621_*624dupTTTT | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 6/6 | 624 | chr7 | 497939 | ||||||
chr7:497939 | TA | T | 9 | a0001c0001t0033 a0001c0001t0057 a0001c0001t0059 others(6): Show |
10 | HG00639.hp2 HG01099.hp1 HG01891.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*624delT | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 6/6 | 624 | chr7 | 497939 | ||||||
chr7:497941 | AAAAAAAA others(11): Show |
A | 1 | a0001c0001t0074 | 1 | HG00558.hp1 | 3_prime_UTR_variant | MODIFIER | c.*605_*622delGTTTTT others(12): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 6/6 | 605 | chr7 | 497941 | ||||||
chr7:497943 | AAAAAAAA others(9): Show |
A | 1 | a0001c0002t0006 | 2 | HG02738.hp2 NA20905.hp1 |
3_prime_UTR_variant | MODIFIER | c.*605_*620delGTTTTT others(10): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 6/6 | 605 | chr7 | 497943 | ||||||
chr7:497945 | AAAAAAAA others(7): Show |
A | 2 | a0001c0001t0008 a0001c0001t0011 |
7 | HG00733.hp1 HG00741.hp1 HG00741.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*605_*618delGTTTTT others(8): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 6/6 | 605 | chr7 | 497945 | ||||||
chr7:497948 | A | C | 1 | a0001c0003t0083 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*616T>G | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 6/6 | 616 | chr7 | 497948 | ||||||
chr7:497948 | AAAAAAAA others(4): Show |
A | 4 | a0001c0001t0015 a0001c0001t0051 a0001c0001t0052 others(1): Show |
8 | HG01081.hp1 HG01243.hp1 HG02818.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*605_*615delGTTTTT others(5): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 6/6 | 605 | chr7 | 497948 | ||||||
chr7:497949 | AAAAAAAA others(3): Show |
A | 2 | a0001c0001t0053 a0001c0002t0022 |
2 | HG01361.hp2 HG02055.hp2 |
3_prime_UTR_variant | MODIFIER | c.*605_*614delGTTTTT others(4): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 6/6 | 605 | chr7 | 497949 | ||||||
chr7:497951 | AAAAAAAA others(16): Show |
A | 1 | a0001c0002t0050 | 1 | HG01167.hp2 | 3_prime_UTR_variant | MODIFIER | c.*590_*612delGTTTTT others(17): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 6/6 | 590 | chr7 | 497951 | ||||||
chr7:497952 | A | C | 1 | a0001c0001t0057 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*612T>G | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 6/6 | 612 | chr7 | 497952 | ||||||
chr7:497955 | A | C | 2 | a0001c0001t0102 a0001c0002t0085 |
2 | HG01109.hp1 HG03710.hp1 |
3_prime_UTR_variant | MODIFIER | c.*609T>G | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 6/6 | 609 | chr7 | 497955 | ||||||
chr7:497957 | A | C | 2 | a0001c0001t0011 a0001c0001t0019 |
3 | HG03130.hp2 HG03579.hp2 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*607T>G | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 6/6 | 607 | chr7 | 497957 | ||||||
chr7:497958 | A | AAAAAC | 4 | a0001c0001t0008 a0001c0002t0010 a0001c0002t0011 others(1): Show |
7 | HG00642.hp2 HG01074.hp1 HG01109.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*605_*606insGTTTT | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 6/6 | 605 | chr7 | 497958 | ||||||
chr7:497958 | A | AAC | 6 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0011 others(3): Show |
8 | HG01099.hp2 HG02027.hp2 HG02135.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*605_*606insGT | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 6/6 | 605 | chr7 | 497958 | ||||||
chr7:497958 | A | C | 3 | a0001c0001t0014 a0001c0001t0041 a0001c0001t0109 |
4 | HG02109.hp2 HG02622.hp1 HG02717.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*606T>G | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 6/6 | 606 | chr7 | 497958 | ||||||
chr7:497958 | AC | A | 3 | a0001c0001t0011 a0001c0001t0019 a0001c0001t0034 |
4 | HG03130.hp2 HG03579.hp2 NA18948.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*605delG | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 6/6 | 605 | chr7 | 497958 | ||||||
chr7:497959 | C | A | 57 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(54): Show |
119 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(116): Show |
3_prime_UTR_variant | MODIFIER | c.*605G>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 6/6 | 605 | chr7 | 497959 | ||||||
chr7:497960 | A | C | 3 | a0001c0001t0091 a0001c0002t0103 a0001c0003t0083 |
3 | HG00733.hp2 HG02809.hp2 NA19085.hp2 |
3_prime_UTR_variant | MODIFIER | c.*604T>G | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 6/6 | 604 | chr7 | 497960 | ||||||
chr7:497963 | A | C | 9 | a0001c0001t0032 a0001c0001t0045 a0001c0001t0054 others(6): Show |
9 | HG00099.hp2 HG01891.hp1 HG02559.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*601T>G | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 6/6 | 601 | chr7 | 497963 | ||||||
chr7:497964 | A | C | 2 | a0001c0001t0088 a0001c0001t0089 |
2 | HG01891.hp2 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*600T>G | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 6/6 | 600 | chr7 | 497964 | ||||||
chr7:497965 | A | C | 1 | a0001c0001t0087 | 1 | HG01515.hp2 | 3_prime_UTR_variant | MODIFIER | c.*599T>G | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 6/6 | 599 | chr7 | 497965 | ||||||
chr7:497967 | A | C | 1 | a0001c0001t0086 | 1 | NA19090.hp1 | 3_prime_UTR_variant | MODIFIER | c.*597T>G | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 6/6 | 597 | chr7 | 497967 | ||||||
chr7:497968 | A | C | 5 | a0001c0001t0032 a0001c0001t0045 a0001c0001t0054 others(2): Show |
5 | HG03098.hp1 HG03225.hp2 HG03453.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*596T>G | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 6/6 | 596 | chr7 | 497968 | ||||||
chr7:497972 | A | C | 1 | a0001c0001t0057 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*592T>G | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 6/6 | 592 | chr7 | 497972 | ||||||
chr7:497973 | A | C | 1 | a0001c0002t0077 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*591T>G | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 6/6 | 591 | chr7 | 497973 | ||||||
chr7:497974 | C | A | 8 | a0001c0001t0015 a0001c0001t0051 a0001c0001t0052 others(5): Show |
13 | HG01081.hp1 HG01109.hp1 HG01243.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*590G>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 6/6 | 590 | chr7 | 497974 | ||||||
chr7:497985 | C | CA | 37 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0007 others(34): Show |
91 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(88): Show |
3_prime_UTR_variant | MODIFIER | c.*578dupT | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 6/6 | 578 | chr7 | 497985 | ||||||
chr7:497985 | CA | C | 10 | a0001c0001t0032 a0001c0001t0045 a0001c0001t0046 others(7): Show |
10 | HG00738.hp2 HG02572.hp1 HG02622.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*578delT | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 6/6 | 578 | chr7 | 497985 | ||||||
chr7:498256 | C | T | 1 | a0001c0001t0082 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*308G>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 6/6 | 308 | chr7 | 498256 | ||||||
chr7:498310 | T | TTC | 7 | a0001c0001t0041 a0001c0001t0075 a0001c0001t0076 others(4): Show |
8 | HG00639.hp1 HG01168.hp1 HG01891.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*252_*253dupGA | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 6/6 | 253 | chr7 | 498310 | ||||||
chr7:498312 | C | G | 1 | a0001c0001t0048 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*252G>C | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 6/6 | 252 | chr7 | 498312 | ||||||
chr7:498312 | C | T | 3 | a0001c0001t0079 a0001c0001t0080 a0001c0001t0081 |
3 | NA19062.hp2 NA19079.hp1 NA19081.hp1 |
3_prime_UTR_variant | MODIFIER | c.*252G>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 6/6 | 252 | chr7 | 498312 | ||||||
chr7:498316 | CTCTCTT | C | 2 | a0001c0001t0015 a0001c0001t0053 |
5 | HG01081.hp1 HG01243.hp1 HG02055.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*242_*247delAAGAGA | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 6/6 | 242 | chr7 | 498316 | ||||||
chr7:498322 | T | C | 109 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(106): Show |
244 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(241): Show |
3_prime_UTR_variant | MODIFIER | c.*242A>G | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 6/6 | 242 | chr7 | 498322 | ||||||
chr7:498367 | G | A | 1 | a0001c0002t0113 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*197C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 6/6 | 197 | chr7 | 498367 | ||||||
chr7:498522 | G | A | 1 | a0001c0002t0078 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*42C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 6/6 | 42 | chr7 | 498522 | ||||||
chr7:498554 | C | T | 6 | a0001c0001t0015 a0001c0001t0051 a0001c0001t0052 others(3): Show |
11 | HG01081.hp1 HG01167.hp2 HG01243.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*10G>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 6/6 | 10 | chr7 | 498554 | ||||||
chr7:519050 | G | A | 1 | a0001c0001t0114 | 1 | HG02132.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-49C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 1/6 | chr7 | 519050 | |||||||
chr7:519243 | C | G | 1 | a0001c0001t0049 | 1 | HG01175.hp2 | 5_prime_UTR_variant | MODIFIER | c.-242G>C | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 1/6 | 242 | chr7 | 519243 | ||||||
chr7:519470 | G | A | 74 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0008 others(71): Show |
165 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(162): Show |
5_prime_UTR_variant | MODIFIER | c.-469C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 1/6 | 469 | chr7 | 519470 | ||||||
chr7:519581 | C | T | 1 | a0001c0001t0048 | 1 | HG03453.hp1 | 5_prime_UTR_variant | MODIFIER | c.-580G>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 1/6 | 580 | chr7 | 519581 | ||||||
chr7:519590 | A | AC | 5 | a0001c0001t0045 a0001c0001t0046 a0001c0001t0047 others(2): Show |
5 | HG01169.hp1 HG02258.hp2 HG02572.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-590dupG | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 1/6 | 590 | chr7 | 519590 | ||||||
chr7:519594 | C | G | 1 | a0001c0001t0042 | 1 | HG03492.hp2 | 5_prime_UTR_variant | MODIFIER | c.-593G>C | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 1/6 | 593 | chr7 | 519594 | ||||||
chr7:519842 | C | G | 1 | a0001c0001t0042 | 1 | HG03492.hp2 | 5_prime_UTR_variant | MODIFIER | c.-841G>C | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 1/6 | 841 | chr7 | 519842 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:498640 | G | C | 75 | a0001c0001t0001g0007 a0001c0001t0001g0147 a0001c0001t0001g0167 others(72): Show |
76 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(73): Show |
intron_variant | MODIFIER | c.581-66C>G | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 5/5 | chr7 | 498640 | |||||||
chr7:498647 | T | C | 73 | a0001c0001t0001g0007 a0001c0001t0001g0147 a0001c0001t0001g0167 others(70): Show |
74 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.581-73A>G | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 5/5 | chr7 | 498647 | |||||||
chr7:498711 | A | T | 73 | a0001c0001t0001g0007 a0001c0001t0001g0147 a0001c0001t0001g0167 others(70): Show |
74 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.581-137T>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 5/5 | chr7 | 498711 | |||||||
chr7:498761 | A | ACAGGAAT others(4): Show |
1 | a0001c0001t0009g0197 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.581-198_581-188dup others(11): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 5/5 | chr7 | 498761 | |||||||
chr7:498768 | T | C | 1 | a0001c0003t0083g0291 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.581-194A>G | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 5/5 | chr7 | 498768 | |||||||
chr7:498786 | C | T | 1 | a0001c0002t0030g0052 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.581-212G>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 5/5 | chr7 | 498786 | |||||||
chr7:498998 | C | T | 105 | a0001c0001t0003g0060 a0001c0001t0003g0061 a0001c0001t0005g0058 others(102): Show |
108 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.581-424G>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 5/5 | chr7 | 498998 | |||||||
chr7:499019 | T | C | 81 | a0001c0001t0001g0007 a0001c0001t0001g0147 a0001c0001t0001g0167 others(78): Show |
83 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(80): Show |
intron_variant | MODIFIER | c.581-445A>G | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 5/5 | chr7 | 499019 | |||||||
chr7:499072 | A | G | 2 | a0001c0001t0018g0083 a0001c0001t0028g0084 |
2 | HG00642.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.581-498T>C | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 5/5 | chr7 | 499072 | |||||||
chr7:499073 | C | T | 1 | a0001c0002t0005g0123 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.581-499G>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 5/5 | chr7 | 499073 | |||||||
chr7:499103 | C | T | 1 | a0001c0001t0057g0111 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.581-529G>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 5/5 | chr7 | 499103 | |||||||
chr7:499228 | A | C | 28 | a0001c0001t0001g0007 a0001c0001t0001g0147 a0001c0001t0001g0167 others(25): Show |
29 | HG00423.hp2 HG00609.hp1 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.581-654T>G | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 5/5 | chr7 | 499228 | |||||||
chr7:499244 | A | G | 73 | a0001c0001t0001g0007 a0001c0001t0001g0147 a0001c0001t0001g0167 others(70): Show |
74 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.581-670T>C | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 5/5 | chr7 | 499244 | |||||||
chr7:499281 | G | A | 1 | a0001c0001t0048g0014 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.581-707C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 5/5 | chr7 | 499281 | |||||||
chr7:499482 | G | C | 1 | a0001c0001t0014g0237 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.581-908C>G | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 5/5 | chr7 | 499482 | |||||||
chr7:499719 | T | TCCCCCCC others(3): Show |
1 | a0001c0001t0028g0125 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.581-1146_581-1145i others(12): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 5/5 | chr7 | 499719 | |||||||
chr7:499719 | T | TCCCCCCC others(9): Show |
1 | a0001c0001t0034g0211 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.581-1146_581-1145i others(18): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 5/5 | chr7 | 499719 | |||||||
chr7:499720 | T | C | 5 | a0001c0001t0011g0257 a0001c0001t0028g0125 a0001c0001t0034g0211 others(2): Show |
5 | HG01346.hp2 HG01891.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.581-1146A>G | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 5/5 | chr7 | 499720 | |||||||
chr7:499720 | T | TACCCCCC others(4): Show |
1 | a0001c0001t0001g0214 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.581-1147_581-1146i others(13): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 5/5 | chr7 | 499720 | |||||||
chr7:499720 | T | TCCCCACC others(15): Show |
1 | a0001c0001t0004g0289 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.581-1147_581-1146i others(24): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 5/5 | chr7 | 499720 | |||||||
chr7:499720 | T | TCCCCCCA others(10): Show |
1 | a0001c0003t0002g0108 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.581-1147_581-1146i others(19): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 5/5 | chr7 | 499720 | |||||||
chr7:499720 | T | TCCCCCCC | 15 | a0001c0001t0001g0007 a0001c0001t0001g0205 a0001c0001t0001g0230 others(12): Show |
16 | HG00609.hp1 HG01081.hp2 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.581-1153_581-1147d others(9): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 5/5 | chr7 | 499720 | |||||||
chr7:499720 | T | TCCCCCCC others(1): Show |
30 | a0001c0001t0001g0187 a0001c0001t0001g0212 a0001c0001t0001g0231 others(27): Show |
30 | HG00423.hp2 HG00609.hp2 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.581-1154_581-1147d others(10): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 5/5 | chr7 | 499720 | |||||||
chr7:499720 | T | TCCCCCCC others(13): Show |
1 | a0001c0001t0001g0216 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.581-1147_581-1146i others(22): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 5/5 | chr7 | 499720 | |||||||
chr7:499720 | T | TCCCCCCC others(15): Show |
1 | a0004c0006t0060g0057 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.581-1147_581-1146i others(24): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 5/5 | chr7 | 499720 | |||||||
chr7:499720 | T | TCCCCCCC others(2): Show |
32 | a0001c0001t0001g0199 a0001c0001t0001g0218 a0001c0001t0001g0253 others(29): Show |
32 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(29): Show |
intron_variant | MODIFIER | c.581-1155_581-1147d others(11): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 5/5 | chr7 | 499720 | |||||||
chr7:499720 | T | TCCCCCCC others(3): Show |
33 | a0001c0001t0001g0147 a0001c0001t0001g0244 a0001c0001t0001g0250 others(30): Show |
35 | HG00280.hp2 HG00408.hp1 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.581-1156_581-1147d others(12): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 5/5 | chr7 | 499720 | |||||||
chr7:499720 | T | TCCCCCCC others(4): Show |
17 | a0001c0001t0002g0114 a0001c0001t0002g0117 a0001c0001t0002g0118 others(14): Show |
17 | HG00673.hp1 HG01169.hp2 HG01934.hp1 others(14): Show |
intron_variant | MODIFIER | c.581-1157_581-1147d others(13): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 5/5 | chr7 | 499720 | |||||||
chr7:499720 | T | TCCCCCCC others(5): Show |
16 | a0001c0001t0002g0074 a0001c0001t0010g0259 a0001c0001t0016g0196 others(13): Show |
16 | HG01515.hp2 HG01884.hp2 HG02027.hp2 others(13): Show |
intron_variant | MODIFIER | c.581-1158_581-1147d others(14): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 5/5 | chr7 | 499720 | |||||||
chr7:499720 | T | TCCCCCCC others(6): Show |
7 | a0001c0001t0001g0167 a0001c0001t0004g0293 a0001c0001t0017g0242 others(4): Show |
7 | HG01099.hp1 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.581-1159_581-1147d others(15): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 5/5 | chr7 | 499720 | |||||||
chr7:499720 | T | TCCCCCCC others(7): Show |
5 | a0001c0001t0008g0170 a0001c0001t0009g0195 a0001c0001t0009g0200 others(2): Show |
5 | HG01106.hp2 HG01257.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.581-1147_581-1146i others(16): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 5/5 | chr7 | 499720 | |||||||
chr7:499720 | T | TCCCCCCC others(8): Show |
2 | a0001c0001t0008g0245 a0001c0002t0010g0173 |
2 | HG01106.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.581-1147_581-1146i others(17): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 5/5 | chr7 | 499720 | |||||||
chr7:499720 | T | TCCCCCCC others(9): Show |
1 | a0001c0001t0001g0227 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.581-1147_581-1146i others(18): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 5/5 | chr7 | 499720 | |||||||
chr7:499720 | T | TCCCCCCC others(10): Show |
2 | a0001c0001t0008g0194 a0001c0001t0009g0247 |
2 | NA18995.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.581-1147_581-1146i others(19): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 5/5 | chr7 | 499720 | |||||||
chr7:499720 | T | TCCCCCCC others(14): Show |
1 | a0001c0001t0018g0083 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.581-1147_581-1146i others(23): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 5/5 | chr7 | 499720 | |||||||
chr7:499720 | T | TCCCCCCC others(15): Show |
1 | a0001c0002t0002g0038 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.581-1147_581-1146i others(24): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 5/5 | chr7 | 499720 | |||||||
chr7:499720 | T | TCCCCCCC others(16): Show |
1 | a0001c0003t0002g0119 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.581-1147_581-1146i others(25): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 5/5 | chr7 | 499720 | |||||||
chr7:499720 | T | TCCCCCCC others(17): Show |
1 | a0001c0001t0047g0012 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.581-1147_581-1146i others(26): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 5/5 | chr7 | 499720 | |||||||
chr7:499720 | T | TCCCCCCC others(18): Show |
1 | a0001c0001t0019g0093 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.581-1147_581-1146i others(27): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 5/5 | chr7 | 499720 | |||||||
chr7:499720 | T | TCCCCCCC others(47): Show |
1 | a0001c0002t0064g0077 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.581-1147_581-1146i others(56): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 5/5 | chr7 | 499720 | |||||||
chr7:499720 | T | TCCCCCCC others(32): Show |
1 | a0001c0001t0079g0149 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.581-1147_581-1146i others(41): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 5/5 | chr7 | 499720 | |||||||
chr7:499720 | T | TCCCCCCC others(73): Show |
1 | a0001c0002t0013g0172 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.581-1147_581-1146i others(82): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 5/5 | chr7 | 499720 | |||||||
chr7:499727 | C | A | 94 | a0001c0001t0003g0060 a0001c0001t0003g0061 a0001c0001t0005g0058 others(91): Show |
97 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.581-1153G>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 5/5 | chr7 | 499727 | |||||||
chr7:499793 | T | C | 73 | a0001c0001t0001g0007 a0001c0001t0001g0147 a0001c0001t0001g0167 others(70): Show |
74 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.581-1219A>G | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 5/5 | chr7 | 499793 | |||||||
chr7:499842 | G | A | 1 | a0001c0001t0029g0064 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.581-1268C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 5/5 | chr7 | 499842 | |||||||
chr7:499873 | C | G | 4 | a0001c0001t0004g0279 a0001c0001t0014g0256 a0001c0001t0021g0138 others(1): Show |
4 | HG02818.hp2 HG03486.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.580+1243G>C | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 5/5 | chr7 | 499873 | |||||||
chr7:500128 | G | A | 1 | a0001c0001t0001g0187 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.580+988C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 5/5 | chr7 | 500128 | |||||||
chr7:500163 | C | T | 7 | a0001c0001t0010g0290 a0001c0001t0013g0284 a0001c0001t0013g0286 others(4): Show |
7 | HG02559.hp2 HG02572.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.580+953G>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 5/5 | chr7 | 500163 | |||||||
chr7:500182 | A | G | 1 | a0001c0001t0015g0135 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.580+934T>C | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 5/5 | chr7 | 500182 | |||||||
chr7:500187 | C | T | 1 | a0001c0001t0005g0081 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.580+929G>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 5/5 | chr7 | 500187 | |||||||
chr7:500222 | C | A | 1 | a0004c0006t0060g0057 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.580+894G>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 5/5 | chr7 | 500222 | |||||||
chr7:500239 | C | G | 1 | a0001c0002t0085g0148 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.580+877G>C | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 5/5 | chr7 | 500239 | |||||||
chr7:500521 | G | A | 10 | a0001c0001t0015g0017 a0001c0001t0015g0134 a0001c0001t0015g0135 others(7): Show |
11 | HG01081.hp1 HG01167.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.580+595C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 5/5 | chr7 | 500521 | |||||||
chr7:500629 | A | ACTCAGCC others(3): Show |
1 | a0001c0001t0001g0251 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.580+486_580+487ins others(10): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 5/5 | chr7 | 500629 | |||||||
chr7:500638 | T | C | 1 | a0001c0001t0001g0251 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.580+478A>G | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 5/5 | chr7 | 500638 | |||||||
chr7:500640 | C | A | 1 | a0001c0001t0001g0251 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.580+476G>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 5/5 | chr7 | 500640 | |||||||
chr7:500641 | C | A | 1 | a0001c0001t0001g0251 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.580+475G>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 5/5 | chr7 | 500641 | |||||||
chr7:500645 | A | G | 3 | a0001c0001t0025g0273 a0001c0001t0025g0277 a0001c0001t0071g0116 |
3 | HG02280.hp1 HG02280.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.580+471T>C | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 5/5 | chr7 | 500645 | |||||||
chr7:500646 | T | TTTGCTCT others(13): Show |
1 | a0001c0001t0001g0251 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.580+469_580+470ins others(20): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 5/5 | chr7 | 500646 | |||||||
chr7:500647 | G | T | 1 | a0001c0001t0001g0251 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.580+469C>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 5/5 | chr7 | 500647 | |||||||
chr7:500664 | A | T | 1 | a0001c0001t0001g0251 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.580+452T>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 5/5 | chr7 | 500664 | |||||||
chr7:500665 | T | G | 1 | a0001c0001t0001g0251 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.580+451A>C | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 5/5 | chr7 | 500665 | |||||||
chr7:500705 | G | A | 20 | a0001c0001t0002g0002 a0001c0001t0002g0074 a0001c0001t0002g0102 others(17): Show |
21 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(18): Show |
intron_variant | MODIFIER | c.580+411C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 5/5 | chr7 | 500705 | |||||||
chr7:500748 | G | A | 1 | a0001c0001t0008g0161 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.580+368C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 5/5 | chr7 | 500748 | |||||||
chr7:500757 | G | A | 1 | a0001c0001t0009g0243 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.580+359C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 5/5 | chr7 | 500757 | |||||||
chr7:500771 | C | T | 1 | a0001c0001t0076g0115 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.580+345G>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 5/5 | chr7 | 500771 | |||||||
chr7:500820 | C | T | 1 | a0001c0002t0085g0148 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.580+296G>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 5/5 | chr7 | 500820 | |||||||
chr7:500881 | T | C | 124 | a0001c0001t0001g0007 a0001c0001t0001g0147 a0001c0001t0001g0167 others(121): Show |
126 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(123): Show |
intron_variant | MODIFIER | c.580+235A>G | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 5/5 | chr7 | 500881 | |||||||
chr7:500905 | C | T | 1 | a0001c0001t0004g0191 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.580+211G>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 5/5 | chr7 | 500905 | |||||||
chr7:500917 | T | C | 1 | a0001c0001t0081g0150 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.580+199A>G | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 5/5 | chr7 | 500917 | |||||||
chr7:500918 | C | T | 1 | a0001c0001t0081g0150 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.580+198G>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 5/5 | chr7 | 500918 | |||||||
chr7:500924 | C | T | 3 | a0001c0001t0041g0275 a0001c0001t0041g0276 a0001c0001t0109g0274 |
3 | HG02622.hp1 HG02717.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.580+192G>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 5/5 | chr7 | 500924 | |||||||
chr7:500986 | G | A | 1 | a0001c0001t0002g0114 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.580+130C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 5/5 | chr7 | 500986 | |||||||
chr7:501016 | A | T | 1 | a0001c0001t0081g0150 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.580+100T>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 5/5 | chr7 | 501016 | |||||||
chr7:501031 | G | A | 1 | a0001c0001t0082g0226 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.580+85C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 5/5 | chr7 | 501031 | |||||||
chr7:501104 | G | A | 163 | a0001c0001t0001g0270 a0001c0001t0003g0060 a0001c0001t0003g0061 others(160): Show |
166 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.580+12C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 5/5 | chr7 | 501104 | |||||||
chr7:501260 | G | C | 1 | a0001c0001t0074g0024 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.454-18C>G | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 501260 | |||||||
chr7:501309 | G | A | 2 | a0001c0001t0111g0262 a0001c0002t0077g0020 |
2 | HG01891.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.454-67C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 501309 | |||||||
chr7:501341 | C | T | 1 | a0001c0001t0018g0083 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.454-99G>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 501341 | |||||||
chr7:501395 | C | G | 167 | a0001c0001t0001g0270 a0001c0001t0003g0060 a0001c0001t0003g0061 others(164): Show |
170 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.454-153G>C | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 501395 | |||||||
chr7:501438 | T | G | 1 | a0001c0002t0078g0078 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.454-196A>C | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 501438 | |||||||
chr7:501439 | G | T | 1 | a0001c0002t0078g0078 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.454-197C>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 501439 | |||||||
chr7:501440 | T | G | 1 | a0001c0002t0078g0078 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.454-198A>C | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 501440 | |||||||
chr7:501513 | C | A | 1 | a0001c0001t0014g0237 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.454-271G>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 501513 | |||||||
chr7:501597 | T | G | 1 | a0001c0007t0096g0202 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.454-355A>C | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 501597 | |||||||
chr7:501687 | T | TGCTGGAA others(23): Show |
1 | a0001c0001t0110g0183 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.454-475_454-446dup others(30): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 501687 | |||||||
chr7:501705 | G | C | 3 | a0001c0001t0025g0273 a0001c0001t0025g0277 a0001c0001t0071g0116 |
3 | HG02280.hp1 HG02280.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.454-463C>G | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 501705 | |||||||
chr7:501710 | G | A | 2 | a0001c0002t0085g0148 a0001c0003t0083g0291 |
2 | HG02809.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.454-468C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 501710 | |||||||
chr7:501794 | G | A | 70 | a0001c0001t0004g0006 a0001c0001t0004g0153 a0001c0001t0004g0162 others(67): Show |
71 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.454-552C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 501794 | |||||||
chr7:501827 | A | G | 176 | a0001c0001t0001g0270 a0001c0001t0003g0060 a0001c0001t0003g0061 others(173): Show |
180 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.454-585T>C | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 501827 | |||||||
chr7:501860 | G | A | 6 | a0001c0002t0010g0267 a0001c0002t0011g0004 a0001c0002t0014g0166 others(3): Show |
7 | HG00642.hp2 HG01074.hp1 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.454-618C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 501860 | |||||||
chr7:501962 | C | A | 1 | a0001c0001t0004g0188 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.454-720G>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 501962 | |||||||
chr7:502077 | T | G | 1 | a0001c0001t0014g0237 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.454-835A>C | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 502077 | |||||||
chr7:502099 | T | G | 1 | a0001c0002t0013g0172 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.454-857A>C | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 502099 | |||||||
chr7:502137 | G | A | 1 | a0001c0001t0090g0180 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.454-895C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 502137 | |||||||
chr7:502193 | G | A | 67 | a0001c0001t0004g0006 a0001c0001t0004g0153 a0001c0001t0004g0162 others(64): Show |
68 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.454-951C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 502193 | |||||||
chr7:502197 | G | A | 3 | a0001c0001t0025g0273 a0001c0001t0025g0277 a0001c0001t0071g0116 |
3 | HG02280.hp1 HG02280.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.454-955C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 502197 | |||||||
chr7:502204 | A | T | 171 | a0001c0001t0001g0270 a0001c0001t0003g0060 a0001c0001t0003g0061 others(168): Show |
175 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.454-962T>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 502204 | |||||||
chr7:502271 | C | T | 1 | a0001c0007t0096g0202 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.454-1029G>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 502271 | |||||||
chr7:502291 | AG | A | 68 | a0001c0001t0004g0006 a0001c0001t0004g0153 a0001c0001t0004g0162 others(65): Show |
69 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(66): Show |
intron_variant | MODIFIER | c.454-1050delC | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 502291 | |||||||
chr7:502313 | C | G | 95 | a0001c0001t0003g0060 a0001c0001t0003g0061 a0001c0001t0005g0058 others(92): Show |
98 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.454-1071G>C | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 502313 | |||||||
chr7:502345 | GGGCCCCA others(10): Show |
G | 5 | a0001c0001t0001g0270 a0001c0001t0041g0275 a0001c0001t0041g0276 others(2): Show |
5 | HG01109.hp1 HG02622.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.454-1120_454-1104d others(19): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 502345 | |||||||
chr7:502360 | G | A | 9 | a0001c0001t0004g0006 a0001c0001t0004g0153 a0001c0001t0004g0191 others(6): Show |
10 | HG00280.hp1 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.454-1118C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 502360 | |||||||
chr7:502362 | C | CG | 163 | a0001c0001t0003g0060 a0001c0001t0003g0061 a0001c0001t0004g0006 others(160): Show |
167 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.454-1121dupC | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 502362 | |||||||
chr7:502403 | C | T | 5 | a0001c0001t0001g0270 a0001c0001t0041g0275 a0001c0001t0041g0276 others(2): Show |
5 | HG01109.hp1 HG02622.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.454-1161G>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 502403 | |||||||
chr7:502477 | T | C | 173 | a0001c0001t0001g0270 a0001c0001t0003g0060 a0001c0001t0003g0061 others(170): Show |
177 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.454-1235A>G | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 502477 | |||||||
chr7:502565 | C | T | 1 | a0001c0002t0064g0077 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.454-1323G>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 502565 | |||||||
chr7:502611 | T | C | 3 | a0001c0001t0025g0273 a0001c0001t0025g0277 a0001c0001t0071g0116 |
3 | HG02280.hp1 HG02280.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.454-1369A>G | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 502611 | |||||||
chr7:502617 | C | T | 1 | a0001c0001t0010g0204 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.454-1375G>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 502617 | |||||||
chr7:502653 | C | T | 95 | a0001c0001t0003g0060 a0001c0001t0003g0061 a0001c0001t0005g0058 others(92): Show |
98 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.454-1411G>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 502653 | |||||||
chr7:502716 | C | T | 2 | a0001c0001t0111g0262 a0001c0002t0077g0020 |
2 | HG01891.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.454-1474G>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 502716 | |||||||
chr7:502768 | T | TCA | 55 | a0001c0001t0001g0007 a0001c0001t0001g0205 a0001c0001t0001g0220 others(52): Show |
56 | HG00408.hp1 HG00423.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.454-1528_454-1527d others(4): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 502768 | |||||||
chr7:502768 | T | TCACA | 21 | a0001c0001t0001g0244 a0001c0001t0004g0181 a0001c0001t0011g0186 others(18): Show |
21 | HG00280.hp1 HG00639.hp2 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.454-1530_454-1527d others(6): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 502768 | |||||||
chr7:502768 | T | TCACACA | 9 | a0001c0001t0004g0185 a0001c0001t0004g0188 a0001c0001t0004g0289 others(6): Show |
9 | HG00280.hp2 HG01074.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.454-1532_454-1527d others(8): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 502768 | |||||||
chr7:502768 | T | TCACACAC others(1): Show |
10 | a0001c0001t0004g0006 a0001c0001t0004g0153 a0001c0001t0011g0206 others(7): Show |
11 | HG00099.hp2 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.454-1534_454-1527d others(10): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 502768 | |||||||
chr7:502768 | T | TCACACAC others(3): Show |
5 | a0001c0001t0004g0179 a0001c0001t0004g0193 a0001c0001t0024g0222 others(2): Show |
5 | HG02257.hp2 HG03098.hp2 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.454-1536_454-1527d others(12): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 502768 | |||||||
chr7:502768 | T | TCACACAC others(5): Show |
1 | a0001c0001t0011g0287 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.454-1538_454-1527d others(14): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 502768 | |||||||
chr7:502768 | TCA | T | 15 | a0001c0001t0002g0102 a0001c0001t0010g0282 a0001c0001t0010g0290 others(12): Show |
15 | HG01358.hp2 HG01891.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.454-1528_454-1527d others(4): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 502768 | |||||||
chr7:502768 | TCACACA | T | 4 | a0001c0001t0001g0147 a0001c0001t0041g0275 a0001c0001t0041g0276 others(1): Show |
4 | HG02622.hp1 HG02717.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.454-1532_454-1527d others(8): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 502768 | |||||||
chr7:502768 | TCACACAC others(9): Show |
T | 2 | a0001c0001t0025g0273 a0001c0001t0025g0277 |
2 | HG02280.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.454-1542_454-1527d others(18): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 502768 | |||||||
chr7:502768 | TCACACAC others(11): Show |
T | 1 | a0001c0002t0085g0148 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.454-1544_454-1527d others(20): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 502768 | |||||||
chr7:502768 | TCACACAC others(13): Show |
T | 1 | a0001c0001t0071g0116 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.454-1546_454-1527d others(22): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 502768 | |||||||
chr7:502783 | CACACACA others(21): Show |
C | 2 | a0001c0002t0006g0025 a0001c0002t0006g0121 |
2 | HG02738.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.454-1569_454-1542d others(30): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 502783 | |||||||
chr7:502805 | CACACAT | C | 7 | a0001c0001t0076g0115 a0001c0001t0111g0262 a0001c0002t0003g0051 others(4): Show |
8 | HG01361.hp2 HG02717.hp2 HG03492.hp1 others(5): Show |
intron_variant | MODIFIER | c.454-1569_454-1564d others(8): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 502805 | |||||||
chr7:502807 | CACAT | C | 14 | a0001c0001t0015g0017 a0001c0001t0015g0134 a0001c0001t0015g0135 others(11): Show |
14 | HG01081.hp1 HG01167.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.454-1569_454-1566d others(6): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 502807 | |||||||
chr7:502809 | C | CACACACA others(3): Show |
1 | a0001c0003t0083g0291 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.454-1568_454-1567i others(12): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 502809 | |||||||
chr7:502809 | CAT | C | 48 | a0001c0001t0003g0060 a0001c0001t0003g0061 a0001c0001t0005g0072 others(45): Show |
49 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(46): Show |
intron_variant | MODIFIER | c.454-1569_454-1568d others(4): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 502809 | |||||||
chr7:502811 | T | C | 93 | a0001c0001t0004g0006 a0001c0001t0004g0153 a0001c0001t0004g0162 others(90): Show |
94 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.454-1569A>G | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 502811 | |||||||
chr7:502850 | C | A | 10 | a0001c0001t0015g0017 a0001c0001t0015g0134 a0001c0001t0015g0135 others(7): Show |
11 | HG01081.hp1 HG01167.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.454-1608G>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 502850 | |||||||
chr7:502913 | C | G | 162 | a0001c0001t0003g0060 a0001c0001t0003g0061 a0001c0001t0004g0006 others(159): Show |
166 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.454-1671G>C | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 502913 | |||||||
chr7:502914 | A | C | 162 | a0001c0001t0003g0060 a0001c0001t0003g0061 a0001c0001t0004g0006 others(159): Show |
166 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.454-1672T>G | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 502914 | |||||||
chr7:502914 | A | G | 1 | a0001c0001t0110g0183 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.454-1672T>C | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 502914 | |||||||
chr7:502918 | G | A | 1 | a0001c0001t0111g0262 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.454-1676C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 502918 | |||||||
chr7:502928 | T | C | 166 | a0001c0001t0003g0060 a0001c0001t0003g0061 a0001c0001t0004g0006 others(163): Show |
170 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.454-1686A>G | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 502928 | |||||||
chr7:502929 | G | A | 9 | a0001c0001t0004g0289 a0001c0001t0004g0293 a0001c0001t0011g0186 others(6): Show |
9 | HG02055.hp1 HG02145.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.454-1687C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 502929 | |||||||
chr7:502934 | G | A | 3 | a0001c0001t0016g0196 a0001c0001t0023g0271 a0001c0002t0064g0077 |
3 | HG02027.hp2 HG02129.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.454-1692C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 502934 | |||||||
chr7:502945 | C | G | 162 | a0001c0001t0003g0060 a0001c0001t0003g0061 a0001c0001t0004g0006 others(159): Show |
166 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.454-1703G>C | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 502945 | |||||||
chr7:502946 | C | G | 1 | a0001c0001t0081g0150 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.454-1704G>C | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 502946 | |||||||
chr7:503046 | T | A | 1 | a0001c0001t0025g0273 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.454-1804A>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 503046 | |||||||
chr7:503061 | C | T | 2 | a0001c0001t0111g0262 a0001c0002t0077g0020 |
2 | HG01891.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.454-1819G>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 503061 | |||||||
chr7:503086 | C | T | 1 | a0001c0001t0057g0111 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.454-1844G>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 503086 | |||||||
chr7:503093 | A | G | 1 | a0001c0002t0001g0223 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.454-1851T>C | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 503093 | |||||||
chr7:503099 | C | T | 164 | a0001c0001t0003g0060 a0001c0001t0003g0061 a0001c0001t0004g0006 others(161): Show |
168 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.454-1857G>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 503099 | |||||||
chr7:503149 | C | T | 165 | a0001c0001t0003g0060 a0001c0001t0003g0061 a0001c0001t0004g0006 others(162): Show |
169 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.454-1907G>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 503149 | |||||||
chr7:503154 | T | C | 165 | a0001c0001t0003g0060 a0001c0001t0003g0061 a0001c0001t0004g0006 others(162): Show |
169 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.454-1912A>G | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 503154 | |||||||
chr7:503191 | C | T | 163 | a0001c0001t0003g0060 a0001c0001t0003g0061 a0001c0001t0004g0006 others(160): Show |
167 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.454-1949G>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 503191 | |||||||
chr7:503233 | C | T | 5 | a0001c0001t0001g0270 a0001c0001t0041g0275 a0001c0001t0041g0276 others(2): Show |
5 | HG01109.hp1 HG02622.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.454-1991G>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 503233 | |||||||
chr7:503338 | T | C | 166 | a0001c0001t0001g0214 a0001c0001t0003g0060 a0001c0001t0003g0061 others(163): Show |
170 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.454-2096A>G | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 503338 | |||||||
chr7:503371 | G | C | 9 | a0001c0001t0004g0289 a0001c0001t0004g0293 a0001c0001t0011g0186 others(6): Show |
9 | HG02055.hp1 HG02145.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.454-2129C>G | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 503371 | |||||||
chr7:503439 | C | T | 3 | a0001c0001t0041g0275 a0001c0001t0041g0276 a0001c0001t0109g0274 |
3 | HG02622.hp1 HG02717.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.454-2197G>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 503439 | |||||||
chr7:503472 | G | A | 1 | a0001c0002t0003g0068 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.454-2230C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 503472 | |||||||
chr7:503524 | A | C | 1 | a0001c0002t0013g0172 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.454-2282T>G | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 503524 | |||||||
chr7:503533 | G | T | 2 | a0001c0001t0025g0277 a0001c0001t0071g0116 |
2 | HG02280.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.454-2291C>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 503533 | |||||||
chr7:503538 | G | T | 1 | a0001c0001t0014g0237 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.454-2296C>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 503538 | |||||||
chr7:503557 | T | C | 2 | a0001c0001t0025g0277 a0001c0001t0071g0116 |
2 | HG02280.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.454-2315A>G | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 503557 | |||||||
chr7:503653 | G | A | 1 | a0001c0002t0006g0089 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.454-2411C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 503653 | |||||||
chr7:503690 | T | C | 69 | a0001c0001t0004g0006 a0001c0001t0004g0153 a0001c0001t0004g0162 others(66): Show |
70 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(67): Show |
intron_variant | MODIFIER | c.454-2448A>G | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 503690 | |||||||
chr7:503771 | G | A | 1 | a0001c0001t0019g0063 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.454-2529C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 503771 | |||||||
chr7:503890 | A | G | 1 | a0001c0001t0109g0274 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.454-2648T>C | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 503890 | |||||||
chr7:503911 | C | A | 1 | a0001c0001t0021g0138 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.454-2669G>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 503911 | |||||||
chr7:503970 | G | A | 3 | a0001c0001t0041g0275 a0001c0001t0041g0276 a0001c0001t0109g0274 |
3 | HG02622.hp1 HG02717.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.454-2728C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 503970 | |||||||
chr7:504136 | G | A | 3 | a0001c0001t0026g0198 a0001c0002t0006g0089 a0001c0002t0027g0044 |
3 | HG00323.hp1 HG00738.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.454-2894C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 504136 | |||||||
chr7:504186 | C | T | 1 | a0001c0002t0085g0148 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.454-2944G>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 504186 | |||||||
chr7:504233 | A | C | 17 | a0001c0001t0001g0270 a0001c0001t0015g0017 a0001c0001t0015g0134 others(14): Show |
18 | HG01081.hp1 HG01109.hp1 HG01167.hp2 others(15): Show |
intron_variant | MODIFIER | c.454-2991T>G | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 504233 | |||||||
chr7:504293 | C | G | 245 | a0001c0001t0001g0007 a0001c0001t0001g0147 a0001c0001t0001g0167 others(242): Show |
250 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.454-3051G>C | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 504293 | |||||||
chr7:504294 | GGAGAGGC others(16): Show |
G | 1 | a0001c0001t0025g0273 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.454-3075_454-3053d others(25): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 504294 | |||||||
chr7:504309 | G | A | 1 | a0001c0001t0019g0093 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.454-3067C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 504309 | |||||||
chr7:504379 | G | C | 172 | a0001c0001t0001g0270 a0001c0001t0003g0060 a0001c0001t0003g0061 others(169): Show |
176 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.454-3137C>G | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 504379 | |||||||
chr7:504424 | G | A | 1 | a0001c0001t0109g0274 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.454-3182C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 504424 | |||||||
chr7:504485 | A | G | 19 | a0001c0001t0001g0270 a0001c0001t0025g0277 a0001c0001t0041g0275 others(16): Show |
20 | HG00642.hp2 HG01074.hp1 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.454-3243T>C | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 504485 | |||||||
chr7:504487 | C | T | 1 | a0001c0001t0107g0201 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.454-3245G>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 504487 | |||||||
chr7:504514 | G | T | 2 | a0001c0001t0001g0270 a0001c0001t0102g0235 |
2 | HG01109.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.454-3272C>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 504514 | |||||||
chr7:504557 | C | T | 1 | a0001c0001t0071g0116 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.454-3315G>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 504557 | |||||||
chr7:504566 | A | G | 2 | a0001c0001t0001g0270 a0001c0001t0102g0235 |
2 | HG01109.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.454-3324T>C | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 504566 | |||||||
chr7:504622 | C | T | 3 | a0001c0001t0010g0204 a0001c0001t0010g0282 a0001c0001t0036g0285 |
3 | HG01243.hp2 NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.454-3380G>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 504622 | |||||||
chr7:504628 | T | C | 1 | a0001c0007t0096g0202 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.454-3386A>G | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 504628 | |||||||
chr7:504709 | CCCGGCCC others(30): Show |
C | 1 | a0001c0002t0043g0010 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.454-3504_454-3468d others(39): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 504709 | |||||||
chr7:504714 | C | T | 1 | a0001c0001t0020g0109 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.454-3472G>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 504714 | |||||||
chr7:504725 | C | T | 8 | a0001c0001t0025g0277 a0001c0001t0041g0275 a0001c0001t0041g0276 others(5): Show |
8 | HG01891.hp2 HG02280.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.454-3483G>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 504725 | |||||||
chr7:504801 | G | A | 1 | a0001c0001t0003g0061 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.454-3559C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 504801 | |||||||
chr7:504840 | C | G | 2 | a0001c0001t0088g0263 a0001c0001t0089g0248 |
2 | HG01891.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.454-3598G>C | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 504840 | |||||||
chr7:504903 | T | C | 165 | a0001c0001t0001g0007 a0001c0001t0001g0212 a0001c0001t0001g0227 others(162): Show |
170 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.454-3661A>G | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 504903 | |||||||
chr7:504917 | A | T | 1 | a0001c0001t0025g0273 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.454-3675T>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 504917 | |||||||
chr7:504923 | G | A | 1 | a0001c0001t0014g0237 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.454-3681C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 504923 | |||||||
chr7:504927 | C | A | 4 | a0001c0002t0002g0038 a0001c0002t0002g0071 a0004c0006t0060g0057 others(1): Show |
4 | HG02135.hp1 NA18612.hp2 NA18997.hp2 others(1): Show |
intron_variant | MODIFIER | c.454-3685G>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 504927 | |||||||
chr7:504968 | C | T | 1 | a0001c0001t0007g0128 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.454-3726G>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 504968 | |||||||
chr7:504969 | G | A | 1 | a0001c0001t0046g0013 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.454-3727C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 504969 | |||||||
chr7:504975 | G | T | 2 | a0001c0001t0088g0263 a0001c0001t0089g0248 |
2 | HG01891.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.454-3733C>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 504975 | |||||||
chr7:505064 | G | A | 1 | a0001c0001t0009g0200 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.454-3822C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 505064 | |||||||
chr7:505130 | A | C | 1 | a0001c0001t0091g0239 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.454-3888T>G | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 505130 | |||||||
chr7:505163 | A | C | 1 | a0001c0001t0025g0273 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.454-3921T>G | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 505163 | |||||||
chr7:505193 | T | C | 3 | a0001c0001t0054g0022 a0001c0002t0032g0171 a0001c0002t0055g0018 |
3 | HG03098.hp1 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.454-3951A>G | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 505193 | |||||||
chr7:505212 | G | T | 3 | a0001c0001t0041g0275 a0001c0001t0041g0276 a0001c0001t0109g0274 |
3 | HG02622.hp1 HG02717.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.454-3970C>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 505212 | |||||||
chr7:505242 | G | A | 1 | a0001c0001t0017g0219 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.454-4000C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 505242 | |||||||
chr7:505248 | C | T | 1 | a0001c0001t0008g0224 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.454-4006G>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 505248 | |||||||
chr7:505278 | C | T | 1 | a0001c0001t0110g0183 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.454-4036G>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 505278 | |||||||
chr7:505347 | T | C | 31 | a0001c0001t0004g0006 a0001c0001t0004g0153 a0001c0001t0004g0162 others(28): Show |
32 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(29): Show |
intron_variant | MODIFIER | c.454-4105A>G | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 505347 | |||||||
chr7:505365 | C | T | 4 | a0001c0001t0066g0101 a0001c0001t0079g0149 a0001c0001t0080g0151 others(1): Show |
4 | HG02015.hp1 NA19062.hp2 NA19079.hp1 others(1): Show |
intron_variant | MODIFIER | c.454-4123G>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 505365 | |||||||
chr7:505446 | C | T | 85 | a0001c0001t0003g0060 a0001c0001t0003g0061 a0001c0001t0005g0058 others(82): Show |
88 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.454-4204G>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 505446 | |||||||
chr7:505447 | G | A | 1 | a0001c0002t0018g0122 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.454-4205C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 505447 | |||||||
chr7:505563 | G | T | 1 | a0001c0001t0010g0292 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.454-4321C>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 505563 | |||||||
chr7:505611 | C | T | 3 | a0001c0001t0041g0275 a0001c0001t0041g0276 a0001c0001t0109g0274 |
3 | HG02622.hp1 HG02717.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.454-4369G>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 505611 | |||||||
chr7:505697 | G | A | 2 | a0001c0001t0088g0263 a0001c0001t0089g0248 |
2 | HG01891.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.454-4455C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 505697 | |||||||
chr7:505725 | C | A | 3 | a0001c0001t0041g0275 a0001c0001t0041g0276 a0001c0001t0109g0274 |
3 | HG02622.hp1 HG02717.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.454-4483G>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 505725 | |||||||
chr7:505807 | C | T | 1 | a0001c0001t0036g0258 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.454-4565G>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 505807 | |||||||
chr7:505832 | T | C | 1 | a0001c0001t0010g0292 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.454-4590A>G | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 505832 | |||||||
chr7:505912 | G | C | 1 | a0001c0002t0056g0088 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.454-4670C>G | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 505912 | |||||||
chr7:505925 | G | A | 11 | a0001c0001t0025g0277 a0001c0001t0033g0280 a0001c0001t0041g0275 others(8): Show |
11 | HG00639.hp2 HG01099.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.454-4683C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 505925 | |||||||
chr7:505939 | C | T | 2 | a0001c0001t0088g0263 a0001c0001t0089g0248 |
2 | HG01891.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.454-4697G>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 505939 | |||||||
chr7:505947 | G | A | 6 | a0001c0002t0010g0267 a0001c0002t0011g0004 a0001c0002t0014g0166 others(3): Show |
7 | HG00642.hp2 HG01074.hp1 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.454-4705C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 505947 | |||||||
chr7:505960 | G | C | 3 | a0001c0001t0015g0017 a0001c0001t0015g0136 a0001c0001t0053g0132 |
3 | HG01243.hp1 HG02055.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.454-4718C>G | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 505960 | |||||||
chr7:505972 | A | C | 7 | a0001c0001t0010g0204 a0001c0001t0010g0282 a0001c0001t0025g0277 others(4): Show |
7 | HG00639.hp2 HG01099.hp1 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.454-4730T>G | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 505972 | |||||||
chr7:506037 | G | A | 2 | a0001c0001t0076g0115 a0001c0002t0012g0036 |
2 | NA18950.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.453+4772C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 506037 | |||||||
chr7:506112 | G | A | 1 | a0001c0001t0026g0268 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.453+4697C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 506112 | |||||||
chr7:506127 | T | G | 131 | a0001c0001t0001g0270 a0001c0001t0003g0060 a0001c0001t0003g0061 others(128): Show |
134 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.453+4682A>C | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 506127 | |||||||
chr7:506159 | G | C | 125 | a0001c0001t0003g0060 a0001c0001t0003g0061 a0001c0001t0004g0006 others(122): Show |
128 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.453+4650C>G | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 506159 | |||||||
chr7:506175 | C | CA | 14 | a0001c0001t0001g0212 a0001c0001t0001g0250 a0001c0001t0004g0179 others(11): Show |
14 | HG00741.hp1 HG02027.hp2 HG02132.hp2 others(11): Show |
intron_variant | MODIFIER | c.453+4633dupT | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 506175 | |||||||
chr7:506175 | C | CAA | 27 | a0001c0001t0004g0006 a0001c0001t0004g0153 a0001c0001t0004g0162 others(24): Show |
28 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(25): Show |
intron_variant | MODIFIER | c.453+4632_453+4633d others(4): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 506175 | |||||||
chr7:506175 | C | CAAA | 6 | a0001c0001t0011g0186 a0001c0001t0011g0257 a0001c0001t0032g0154 others(3): Show |
6 | HG02451.hp2 HG02630.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.453+4631_453+4633d others(5): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 506175 | |||||||
chr7:506175 | C | CAAAAAAA others(2): Show |
62 | a0001c0001t0003g0060 a0001c0001t0003g0061 a0001c0001t0005g0058 others(59): Show |
64 | HG00099.hp1 HG00323.hp1 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.453+4625_453+4633d others(11): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 506175 | |||||||
chr7:506175 | C | CAAAAAAA others(3): Show |
18 | a0001c0001t0005g0072 a0001c0001t0026g0272 a0001c0001t0076g0115 others(15): Show |
18 | HG00408.hp2 HG00621.hp2 HG01358.hp1 others(15): Show |
intron_variant | MODIFIER | c.453+4624_453+4633d others(12): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 506175 | |||||||
chr7:506175 | C | CAAAAAAA others(4): Show |
1 | a0001c0002t0044g0009 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.453+4623_453+4633d others(13): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 506175 | |||||||
chr7:506175 | C | CAAAAAAA others(5): Show |
3 | a0001c0001t0025g0273 a0001c0001t0025g0277 a0001c0002t0085g0148 |
3 | HG02280.hp1 HG02280.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.453+4622_453+4633d others(14): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 506175 | |||||||
chr7:506175 | C | CAAAAAAA others(6): Show |
6 | a0001c0001t0001g0270 a0001c0001t0071g0116 a0001c0001t0102g0235 others(3): Show |
7 | HG01109.hp1 HG01361.hp2 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.453+4621_453+4633d others(15): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 506175 | |||||||
chr7:506175 | C | CAAAAAAA others(7): Show |
1 | a0001c0001t0057g0111 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.453+4620_453+4633d others(16): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 506175 | |||||||
chr7:506175 | C | CAAAAAAA others(8): Show |
2 | a0001c0001t0088g0263 a0001c0001t0089g0248 |
2 | HG01891.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.453+4619_453+4633d others(17): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 506175 | |||||||
chr7:506175 | CA | C | 7 | a0001c0001t0010g0259 a0001c0001t0053g0132 a0001c0001t0059g0019 others(4): Show |
7 | HG01256.hp1 HG01884.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.453+4633delT | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 506175 | |||||||
chr7:506287 | GA | G | 9 | a0001c0001t0016g0196 a0001c0001t0023g0271 a0001c0001t0059g0019 others(6): Show |
9 | HG02015.hp1 HG02027.hp2 HG02129.hp2 others(6): Show |
intron_variant | MODIFIER | c.453+4521delT | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 506287 | |||||||
chr7:506288 | A | G | 1 | a0001c0001t0002g0102 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.453+4521T>C | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 506288 | |||||||
chr7:506334 | T | C | 90 | a0001c0001t0003g0060 a0001c0001t0003g0061 a0001c0001t0004g0193 others(87): Show |
92 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.453+4475A>G | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 506334 | |||||||
chr7:506406 | T | C | 147 | a0001c0001t0001g0251 a0001c0001t0001g0270 a0001c0001t0003g0060 others(144): Show |
151 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.453+4403A>G | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 506406 | |||||||
chr7:506407 | C | T | 147 | a0001c0001t0001g0251 a0001c0001t0001g0270 a0001c0001t0003g0060 others(144): Show |
151 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.453+4402G>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 506407 | |||||||
chr7:506413 | C | T | 3 | a0001c0001t0010g0189 a0001c0001t0095g0192 a0001c0002t0050g0023 |
3 | HG01167.hp2 HG02257.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.453+4396G>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 506413 | |||||||
chr7:506460 | C | T | 1 | a0001c0001t0097g0177 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.453+4349G>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 506460 | |||||||
chr7:506462 | T | C | 37 | a0001c0001t0001g0199 a0001c0001t0004g0006 a0001c0001t0004g0153 others(34): Show |
38 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(35): Show |
intron_variant | MODIFIER | c.453+4347A>G | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 506462 | |||||||
chr7:506500 | T | G | 37 | a0001c0001t0004g0006 a0001c0001t0004g0153 a0001c0001t0004g0162 others(34): Show |
38 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(35): Show |
intron_variant | MODIFIER | c.453+4309A>C | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 506500 | |||||||
chr7:506542 | C | T | 2 | a0001c0002t0005g0030 a0001c0002t0007g0097 |
2 | HG02027.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.453+4267G>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 506542 | |||||||
chr7:506557 | C | T | 2 | a0001c0001t0002g0102 a0001c0001t0002g0103 |
2 | NA18971.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.453+4252G>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 506557 | |||||||
chr7:506675 | C | T | 1 | a0001c0001t0089g0248 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.453+4134G>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 506675 | |||||||
chr7:506680 | C | T | 1 | a0001c0002t0058g0026 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.453+4129G>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 506680 | |||||||
chr7:506877 | A | C | 37 | a0001c0001t0004g0006 a0001c0001t0004g0153 a0001c0001t0004g0162 others(34): Show |
38 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(35): Show |
intron_variant | MODIFIER | c.453+3932T>G | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 506877 | |||||||
chr7:506905 | G | T | 1 | a0001c0001t0010g0290 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.453+3904C>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 506905 | |||||||
chr7:507017 | C | T | 2 | a0001c0001t0032g0154 a0001c0001t0045g0011 |
2 | HG03225.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.453+3792G>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 507017 | |||||||
chr7:507073 | G | A | 7 | a0001c0002t0010g0267 a0001c0002t0011g0004 a0001c0002t0014g0166 others(4): Show |
8 | HG00642.hp2 HG01074.hp1 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.453+3736C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 507073 | |||||||
chr7:507109 | G | C | 15 | a0001c0001t0039g0210 a0001c0001t0039g0213 a0001c0001t0057g0111 others(12): Show |
17 | HG00642.hp2 HG01074.hp1 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.453+3700C>G | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 507109 | |||||||
chr7:507248 | A | G | 20 | a0001c0001t0039g0210 a0001c0001t0039g0213 a0001c0001t0041g0275 others(17): Show |
22 | HG00642.hp2 HG01074.hp1 HG01358.hp1 others(19): Show |
intron_variant | MODIFIER | c.453+3561T>C | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 507248 | |||||||
chr7:507315 | C | A | 26 | a0001c0001t0004g0006 a0001c0001t0004g0153 a0001c0001t0004g0162 others(23): Show |
27 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(24): Show |
intron_variant | MODIFIER | c.453+3494G>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 507315 | |||||||
chr7:507346 | C | T | 5 | a0001c0001t0039g0210 a0001c0001t0039g0213 a0001c0001t0105g0229 others(2): Show |
5 | HG02040.hp1 HG02165.hp1 NA18959.hp1 others(2): Show |
intron_variant | MODIFIER | c.453+3463G>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 507346 | |||||||
chr7:507493 | C | A | 1 | a0001c0003t0083g0291 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.453+3316G>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 507493 | |||||||
chr7:507520 | A | C | 10 | a0001c0001t0019g0063 a0001c0001t0029g0064 a0001c0001t0029g0139 others(7): Show |
11 | HG01256.hp1 HG01258.hp1 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.453+3289T>G | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 507520 | |||||||
chr7:507525 | C | A | 1 | a0001c0001t0110g0183 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.453+3284G>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 507525 | |||||||
chr7:507613 | C | T | 5 | a0001c0001t0015g0017 a0001c0001t0015g0134 a0001c0001t0015g0136 others(2): Show |
5 | HG01243.hp1 HG02055.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.453+3196G>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 507613 | |||||||
chr7:507687 | G | A | 3 | a0001c0001t0057g0111 a0001c0002t0022g0005 a0001c0002t0022g0178 |
4 | HG01361.hp2 HG03098.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.453+3122C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 507687 | |||||||
chr7:507706 | G | T | 1 | a0001c0007t0096g0202 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.453+3103C>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 507706 | |||||||
chr7:507710 | C | T | 1 | a0001c0001t0025g0273 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.453+3099G>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 507710 | |||||||
chr7:507743 | C | T | 1 | a0001c0001t0004g0179 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.453+3066G>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 507743 | |||||||
chr7:507797 | TGGGCTCA others(8): Show |
T | 1 | a0001c0002t0006g0025 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.453+2997_453+3011d others(17): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 507797 | |||||||
chr7:507821 | G | T | 1 | a0001c0001t0009g0238 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.453+2988C>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 507821 | |||||||
chr7:507920 | A | G | 1 | a0001c0001t0025g0273 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.453+2889T>C | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 507920 | |||||||
chr7:507928 | G | A | 6 | a0001c0002t0010g0267 a0001c0002t0011g0004 a0001c0002t0014g0166 others(3): Show |
7 | HG00642.hp2 HG01074.hp1 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.453+2881C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 507928 | |||||||
chr7:507950 | C | G | 5 | a0001c0001t0039g0210 a0001c0001t0039g0213 a0001c0001t0105g0229 others(2): Show |
5 | HG02040.hp1 HG02165.hp1 NA18959.hp1 others(2): Show |
intron_variant | MODIFIER | c.453+2859G>C | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 507950 | |||||||
chr7:508034 | C | A | 1 | a0001c0001t0088g0263 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.453+2775G>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 508034 | |||||||
chr7:508112 | G | A | 1 | a0001c0001t0026g0268 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.453+2697C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 508112 | |||||||
chr7:508113 | A | AG | 4 | a0001c0001t0001g0187 a0001c0001t0002g0112 a0001c0001t0046g0013 others(1): Show |
4 | HG01517.hp2 HG02572.hp1 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.453+2695dupC | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 508113 | |||||||
chr7:508163 | G | C | 141 | a0001c0001t0001g0270 a0001c0001t0003g0060 a0001c0001t0003g0061 others(138): Show |
145 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.453+2646C>G | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 508163 | |||||||
chr7:508174 | T | A | 1 | a0001c0001t0025g0273 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.453+2635A>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 508174 | |||||||
chr7:508209 | C | CG | 6 | a0001c0001t0001g0231 a0001c0001t0017g0219 a0001c0001t0025g0273 others(3): Show |
6 | HG00423.hp2 HG02145.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.453+2599dupC | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 508209 | |||||||
chr7:508352 | G | A | 1 | a0001c0002t0058g0026 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.453+2457C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 508352 | |||||||
chr7:508429 | T | G | 111 | a0001c0001t0003g0060 a0001c0001t0003g0061 a0001c0001t0004g0006 others(108): Show |
113 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.453+2380A>C | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 508429 | |||||||
chr7:508534 | T | C | 13 | a0001c0001t0001g0270 a0001c0001t0019g0063 a0001c0001t0025g0273 others(10): Show |
14 | HG01109.hp1 HG01256.hp1 HG01258.hp1 others(11): Show |
intron_variant | MODIFIER | c.453+2275A>G | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 508534 | |||||||
chr7:508559 | C | A | 1 | a0001c0001t0110g0183 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.453+2250G>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 508559 | |||||||
chr7:508559 | C | CA | 49 | a0001c0001t0001g0167 a0001c0001t0001g0212 a0001c0001t0001g0227 others(46): Show |
50 | HG00323.hp2 HG00423.hp2 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.453+2249dupT | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 508559 | |||||||
chr7:508559 | C | CAA | 15 | a0001c0001t0001g0147 a0001c0001t0004g0289 a0001c0001t0008g0175 others(12): Show |
15 | HG01081.hp1 HG01192.hp1 HG02015.hp1 others(12): Show |
intron_variant | MODIFIER | c.453+2248_453+2249d others(4): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 508559 | |||||||
chr7:508559 | C | CAAAAA | 16 | a0001c0001t0004g0006 a0001c0001t0004g0162 a0001c0001t0004g0185 others(13): Show |
17 | HG00099.hp2 HG00280.hp2 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.453+2245_453+2249d others(7): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 508559 | |||||||
chr7:508559 | C | CAAAAAA | 19 | a0001c0001t0001g0270 a0001c0001t0002g0118 a0001c0001t0004g0153 others(16): Show |
20 | HG00280.hp1 HG00673.hp1 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.453+2244_453+2249d others(8): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 508559 | |||||||
chr7:508559 | C | CAAAAAAA others(2): Show |
20 | a0001c0001t0005g0058 a0001c0002t0003g0032 a0001c0002t0003g0068 others(17): Show |
21 | HG00099.hp1 HG00673.hp2 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.453+2241_453+2249d others(11): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 508559 | |||||||
chr7:508559 | C | CAAAAAAA others(3): Show |
31 | a0001c0001t0003g0060 a0001c0001t0003g0061 a0001c0001t0005g0081 others(28): Show |
32 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(29): Show |
intron_variant | MODIFIER | c.453+2240_453+2249d others(12): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 508559 | |||||||
chr7:508559 | C | CAAAAAAA others(4): Show |
19 | a0001c0001t0005g0130 a0001c0001t0007g0062 a0001c0001t0007g0128 others(16): Show |
19 | HG00558.hp1 HG00621.hp2 HG01346.hp1 others(16): Show |
intron_variant | MODIFIER | c.453+2239_453+2249d others(13): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 508559 | |||||||
chr7:508559 | C | CAAAAAAA others(5): Show |
2 | a0001c0001t0005g0072 a0001c0002t0003g0070 |
2 | HG01934.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.453+2238_453+2249d others(14): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 508559 | |||||||
chr7:508559 | C | CAAAAAAA others(7): Show |
4 | a0001c0001t0011g0257 a0001c0001t0076g0115 a0001c0002t0012g0036 others(1): Show |
4 | HG02630.hp2 HG04204.hp2 NA18950.hp1 others(1): Show |
intron_variant | MODIFIER | c.453+2236_453+2249d others(16): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 508559 | |||||||
chr7:508559 | C | CAAAAAAA others(8): Show |
1 | a0001c0002t0043g0010 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.453+2235_453+2249d others(17): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 508559 | |||||||
chr7:508559 | C | CAAAAAAA others(9): Show |
1 | a0001c0001t0111g0262 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.453+2234_453+2249d others(18): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 508559 | |||||||
chr7:508559 | C | CAAAAAAA others(11): Show |
1 | a0001c0002t0078g0078 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.453+2232_453+2249d others(20): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 508559 | |||||||
chr7:508559 | CAAAAAAA others(4): Show |
C | 1 | a0001c0002t0113g0264 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.453+2239_453+2249d others(13): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 508559 | |||||||
chr7:508590 | T | C | 291 | a0001c0001t0001g0007 a0001c0001t0001g0147 a0001c0001t0001g0167 others(288): Show |
297 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.453+2219A>G | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 508590 | |||||||
chr7:508678 | C | G | 1 | a0001c0002t0058g0026 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.453+2131G>C | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 508678 | |||||||
chr7:508763 | A | T | 13 | a0001c0001t0001g0270 a0001c0001t0019g0063 a0001c0001t0025g0273 others(10): Show |
14 | HG01109.hp1 HG01256.hp1 HG01258.hp1 others(11): Show |
intron_variant | MODIFIER | c.453+2046T>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 508763 | |||||||
chr7:508774 | C | T | 1 | a0001c0002t0001g0232 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.453+2035G>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 508774 | |||||||
chr7:508858 | C | A | 3 | a0001c0001t0001g0270 a0001c0001t0025g0273 a0001c0001t0102g0235 |
3 | HG01109.hp1 HG02280.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.453+1951G>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 508858 | |||||||
chr7:508889 | C | A | 1 | a0001c0001t0088g0263 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.453+1920G>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 508889 | |||||||
chr7:508900 | C | T | 40 | a0001c0001t0004g0006 a0001c0001t0004g0153 a0001c0001t0004g0162 others(37): Show |
41 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(38): Show |
intron_variant | MODIFIER | c.453+1909G>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 508900 | |||||||
chr7:508930 | C | G | 1 | a0001c0001t0001g0250 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.453+1879G>C | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 508930 | |||||||
chr7:509033 | C | T | 1 | a0001c0001t0017g0219 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.453+1776G>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 509033 | |||||||
chr7:509094 | T | C | 1 | a0001c0002t0058g0026 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.453+1715A>G | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 509094 | |||||||
chr7:509116 | G | A | 73 | a0001c0001t0003g0060 a0001c0001t0003g0061 a0001c0001t0005g0058 others(70): Show |
74 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.453+1693C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 509116 | |||||||
chr7:509124 | A | C | 1 | a0001c0001t0004g0191 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.453+1685T>G | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 509124 | |||||||
chr7:509164 | G | A | 2 | a0001c0001t0014g0256 a0001c0001t0039g0213 |
2 | HG03486.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.453+1645C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 509164 | |||||||
chr7:509171 | C | T | 1 | a0001c0001t0009g0240 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.453+1638G>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 509171 | |||||||
chr7:509330 | T | C | 1 | a0001c0007t0096g0202 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.453+1479A>G | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 509330 | |||||||
chr7:509348 | GTGATGCC others(8): Show |
G | 1 | a0001c0001t0040g0221 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.453+1446_453+1460d others(17): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 509348 | |||||||
chr7:509437 | C | G | 1 | a0001c0002t0058g0026 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.453+1372G>C | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 509437 | |||||||
chr7:509454 | C | T | 3 | a0001c0001t0001g0270 a0001c0001t0025g0273 a0001c0001t0102g0235 |
3 | HG01109.hp1 HG02280.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.453+1355G>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 509454 | |||||||
chr7:509472 | G | A | 5 | a0001c0001t0032g0154 a0001c0001t0045g0011 a0001c0001t0054g0022 others(2): Show |
5 | HG03098.hp1 HG03225.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.453+1337C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 509472 | |||||||
chr7:509560 | G | A | 3 | a0001c0001t0041g0275 a0001c0001t0041g0276 a0001c0001t0109g0274 |
3 | HG02622.hp1 HG02717.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.453+1249C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 509560 | |||||||
chr7:509575 | G | A | 1 | a0001c0003t0083g0291 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.453+1234C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 509575 | |||||||
chr7:509583 | G | A | 4 | a0001c0001t0001g0218 a0001c0001t0015g0017 a0001c0001t0015g0136 others(1): Show |
4 | HG01243.hp1 HG02055.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.453+1226C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 509583 | |||||||
chr7:509598 | T | C | 5 | a0001c0001t0001g0270 a0001c0001t0025g0273 a0001c0001t0025g0277 others(2): Show |
5 | HG01109.hp1 HG02280.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.453+1211A>G | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 509598 | |||||||
chr7:509693 | G | A | 1 | a0001c0001t0026g0268 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.453+1116C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 509693 | |||||||
chr7:509708 | A | G | 45 | a0001c0001t0001g0265 a0001c0001t0001g0270 a0001c0001t0004g0006 others(42): Show |
46 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(43): Show |
intron_variant | MODIFIER | c.453+1101T>C | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 509708 | |||||||
chr7:509822 | A | G | 2 | a0001c0001t0004g0185 a0001c0001t0004g0188 |
2 | HG00280.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.453+987T>C | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 509822 | |||||||
chr7:509881 | G | T | 33 | a0001c0001t0001g0265 a0001c0001t0004g0006 a0001c0001t0004g0153 others(30): Show |
34 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(31): Show |
intron_variant | MODIFIER | c.453+928C>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 509881 | |||||||
chr7:509888 | A | G | 89 | a0001c0001t0001g0253 a0001c0001t0003g0060 a0001c0001t0003g0061 others(86): Show |
91 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.453+921T>C | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 509888 | |||||||
chr7:509898 | T | C | 1 | a0001c0001t0111g0262 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.453+911A>G | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 509898 | |||||||
chr7:509902 | T | C | 247 | a0001c0001t0001g0007 a0001c0001t0001g0147 a0001c0001t0001g0167 others(244): Show |
252 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.453+907A>G | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 509902 | |||||||
chr7:509928 | G | C | 1 | a0001c0001t0001g0252 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.453+881C>G | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 509928 | |||||||
chr7:509956 | C | T | 1 | a0001c0002t0058g0026 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.453+853G>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 509956 | |||||||
chr7:509973 | G | T | 1 | a0001c0002t0003g0037 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.453+836C>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 509973 | |||||||
chr7:510039 | AC | A | 118 | a0001c0001t0001g0265 a0001c0001t0002g0106 a0001c0001t0003g0060 others(115): Show |
121 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(118): Show |
intron_variant | MODIFIER | c.453+769delG | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 510039 | |||||||
chr7:510101 | G | C | 1 | a0001c0002t0005g0029 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.453+708C>G | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 510101 | |||||||
chr7:510106 | C | T | 2 | a0001c0002t0043g0010 a0001c0002t0078g0078 |
2 | HG02055.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.453+703G>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 510106 | |||||||
chr7:510181 | A | G | 1 | a0001c0001t0002g0102 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.453+628T>C | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 510181 | |||||||
chr7:510206 | G | A | 1 | a0001c0002t0085g0148 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.453+603C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 510206 | |||||||
chr7:510307 | T | TG | 3 | a0001c0001t0007g0128 a0001c0001t0086g0266 a0001c0002t0002g0056 |
3 | NA18940.hp2 NA19003.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.453+501dupC | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 510307 | |||||||
chr7:510320 | G | A | 29 | a0001c0001t0004g0162 a0001c0001t0004g0179 a0001c0001t0004g0181 others(26): Show |
29 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(26): Show |
intron_variant | MODIFIER | c.453+489C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 510320 | |||||||
chr7:510351 | T | C | 1 | a0001c0002t0085g0148 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.453+458A>G | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 510351 | |||||||
chr7:510510 | C | CAGGGCTC others(282): Show |
2 | a0001c0001t0001g0270 a0001c0001t0102g0235 |
2 | HG01109.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.453+298_453+299ins others(289): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 510510 | |||||||
chr7:510530 | C | T | 2 | a0001c0001t0025g0277 a0001c0001t0071g0116 |
2 | HG02280.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.453+279G>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 510530 | |||||||
chr7:510588 | TGGGGAGG others(3): Show |
T | 1 | a0001c0001t0049g0015 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.453+211_453+220del others(10): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 510588 | |||||||
chr7:510592 | G | A | 1 | a0001c0001t0010g0290 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.453+217C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 510592 | |||||||
chr7:510628 | C | CAGGGCTC others(164): Show |
1 | a0001c0001t0068g0133 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.453+180_453+181ins others(171): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 510628 | |||||||
chr7:510628 | CAGGGCTC others(164): Show |
C | 2 | a0001c0002t0003g0049 a0001c0002t0031g0048 |
2 | HG01496.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.453+10_453+180del | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 510628 | |||||||
chr7:510661 | A | AGGAGGGA others(90): Show |
1 | a0001c0001t0008g0161 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.453+147_453+148ins others(97): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 510661 | |||||||
chr7:510663 | G | C | 1 | a0001c0001t0002g0114 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.453+146C>G | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 510663 | |||||||
chr7:510695 | C | T | 2 | a0001c0001t0010g0282 a0001c0002t0058g0026 |
2 | HG02559.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.453+114G>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 510695 | |||||||
chr7:510699 | C | T | 2 | a0001c0001t0025g0277 a0001c0001t0071g0116 |
2 | HG02280.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.453+110G>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 510699 | |||||||
chr7:510707 | G | GGGGAGGG others(15): Show |
1 | a0001c0001t0002g0117 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.453+101_453+102ins others(22): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 510707 | |||||||
chr7:510715 | A | AG | 5 | a0001c0001t0054g0022 a0001c0001t0107g0201 a0001c0002t0006g0028 others(2): Show |
5 | HG02109.hp1 HG03540.hp1 NA18940.hp1 others(2): Show |
intron_variant | MODIFIER | c.453+93dupC | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 510715 | |||||||
chr7:510716 | G | A | 1 | a0001c0001t0009g0247 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.453+93C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 510716 | |||||||
chr7:510720 | A | AGGGGAGA others(296): Show |
1 | a0001c0001t0025g0273 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.453+88_453+89insCT others(301): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 510720 | |||||||
chr7:510722 | G | A | 1 | a0001c0001t0002g0117 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.453+87C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 510722 | |||||||
chr7:510722 | G | GGGAGAGG others(13): Show |
11 | a0001c0001t0002g0002 a0001c0001t0002g0102 a0001c0001t0002g0103 others(8): Show |
12 | HG00423.hp1 HG00621.hp1 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.453+67_453+86dupTC others(18): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 510722 | |||||||
chr7:510722 | G | GGGAGAGG others(33): Show |
1 | a0001c0001t0020g0105 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.453+47_453+86dupTC others(38): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 510722 | |||||||
chr7:510722 | GGGAGAGG others(38): Show |
G | 2 | a0001c0001t0025g0277 a0001c0001t0071g0116 |
2 | HG02280.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.453+42_453+86delTC others(43): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 510722 | |||||||
chr7:510732 | G | A | 2 | a0001c0001t0004g0279 a0001c0001t0021g0138 |
2 | HG02818.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.453+77C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 510732 | |||||||
chr7:510747 | A | AGGAGG | 20 | a0001c0001t0004g0006 a0001c0001t0004g0153 a0001c0001t0004g0181 others(17): Show |
20 | HG00280.hp1 HG00280.hp2 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.453+57_453+61dupCC others(3): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 510747 | |||||||
chr7:510747 | A | AGGAGGGG others(18): Show |
4 | a0001c0001t0032g0154 a0001c0001t0045g0011 a0001c0001t0054g0022 others(1): Show |
4 | HG03098.hp1 HG03225.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.453+37_453+61dupCC others(23): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 510747 | |||||||
chr7:510747 | A | G | 1 | a0001c0007t0096g0202 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.453+62T>C | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 510747 | |||||||
chr7:510747 | AGGAGGGG others(18): Show |
A | 2 | a0001c0001t0004g0279 a0001c0001t0021g0138 |
2 | HG02818.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.453+37_453+61delCC others(23): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 510747 | |||||||
chr7:510757 | G | A | 1 | a0001c0001t0089g0248 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.453+52C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 510757 | |||||||
chr7:510757 | GGGAGAGG others(3): Show |
G | 10 | a0001c0001t0016g0160 a0001c0001t0019g0063 a0001c0001t0023g0271 others(7): Show |
10 | HG00408.hp1 HG01258.hp1 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.453+42_453+51delTC others(8): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 510757 | |||||||
chr7:510762 | A | G | 98 | a0001c0001t0001g0007 a0001c0001t0001g0147 a0001c0001t0001g0167 others(95): Show |
99 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.453+47T>C | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 510762 | |||||||
chr7:510767 | A | AGGAGG | 3 | a0001c0001t0010g0204 a0001c0002t0022g0005 a0001c0002t0022g0178 |
4 | HG01243.hp2 HG01361.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.453+37_453+41dupCC others(3): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 510767 | |||||||
chr7:510767 | A | AGGAGGGG others(3): Show |
1 | a0001c0001t0014g0256 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.453+32_453+41dupCC others(8): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 510767 | |||||||
chr7:510767 | A | AGGAGGGG others(33): Show |
1 | a0001c0007t0096g0202 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.453+41_453+42insCC others(38): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 510767 | |||||||
chr7:510767 | AGGAGG | A | 16 | a0001c0001t0004g0006 a0001c0001t0004g0162 a0001c0001t0004g0181 others(13): Show |
16 | HG00280.hp1 HG00280.hp2 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.453+37_453+41delCC others(3): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 510767 | |||||||
chr7:510767 | AGGAGGGG others(3): Show |
A | 1 | a0001c0001t0097g0177 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.453+32_453+41delCC others(8): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 510767 | |||||||
chr7:510767 | AGGAGGGG others(8): Show |
A | 7 | a0001c0001t0023g0146 a0001c0001t0023g0155 a0001c0001t0025g0156 others(4): Show |
7 | HG01256.hp1 HG02602.hp2 NA18945.hp2 others(4): Show |
intron_variant | MODIFIER | c.453+27_453+41delCC others(13): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 510767 | |||||||
chr7:510772 | G | A | 102 | a0001c0001t0001g0007 a0001c0001t0001g0147 a0001c0001t0001g0167 others(99): Show |
103 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.453+37C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 510772 | |||||||
chr7:510772 | G | GGGAGGGG others(13): Show |
7 | a0001c0001t0019g0092 a0001c0001t0019g0093 a0001c0001t0059g0019 others(4): Show |
7 | HG01891.hp1 HG02055.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.453+36_453+37insTC others(18): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 510772 | |||||||
chr7:510772 | G | GGGAGGGG others(184): Show |
1 | a0001c0001t0020g0109 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.453+36_453+37insTC others(189): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 510772 | |||||||
chr7:510777 | G | A | 10 | a0001c0001t0016g0160 a0001c0001t0019g0063 a0001c0001t0023g0271 others(7): Show |
10 | HG00408.hp1 HG01258.hp1 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.453+32C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 510777 | |||||||
chr7:510780 | A | AG | 4 | a0001c0001t0008g0144 a0001c0001t0025g0273 a0001c0002t0005g0030 others(1): Show |
4 | HG00741.hp1 HG02027.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.453+28dupC | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 510780 | |||||||
chr7:510780 | A | G | 1 | a0005c0005t0002g0073 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.453+29T>C | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 510780 | |||||||
chr7:510781 | G | A | 1 | a0005c0005t0002g0073 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.453+28C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 510781 | |||||||
chr7:510782 | G | A | 12 | a0001c0001t0016g0160 a0001c0001t0019g0063 a0001c0001t0023g0271 others(9): Show |
12 | HG00408.hp1 HG01258.hp1 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.453+27C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 4/5 | chr7 | 510782 | |||||||
chr7:511006 | C | CG | 8 | a0001c0001t0004g0179 a0001c0001t0004g0191 a0001c0001t0004g0293 others(5): Show |
8 | HG01358.hp2 HG02145.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.266-11dupC | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 3/5 | chr7 | 511006 | |||||||
chr7:511007 | G | A | 1 | a0001c0001t0089g0248 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.266-11C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 3/5 | chr7 | 511007 | |||||||
chr7:511100 | G | C | 129 | a0001c0001t0001g0007 a0001c0001t0001g0147 a0001c0001t0001g0167 others(126): Show |
132 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.266-104C>G | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 3/5 | chr7 | 511100 | |||||||
chr7:511154 | T | C | 249 | a0001c0001t0001g0007 a0001c0001t0001g0147 a0001c0001t0001g0167 others(246): Show |
254 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.266-158A>G | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 3/5 | chr7 | 511154 | |||||||
chr7:511253 | GGAGGGGA others(81): Show |
G | 1 | a0001c0002t0085g0148 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.266-345_266-258del others(88): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 3/5 | chr7 | 511253 | |||||||
chr7:511274 | GGGGCCAG others(36): Show |
G | 1 | a0001c0001t0076g0115 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.266-321_266-279del others(43): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 3/5 | chr7 | 511274 | |||||||
chr7:511275 | G | C | 2 | a0001c0001t0028g0125 a0001c0001t0101g0207 |
2 | HG01081.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.266-279C>G | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 3/5 | chr7 | 511275 | |||||||
chr7:511284 | GCTGGGGG others(37): Show |
G | 47 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0074 others(44): Show |
49 | HG00323.hp2 HG00621.hp1 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.266-332_266-289del others(44): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 3/5 | chr7 | 511284 | |||||||
chr7:511289 | G | A | 6 | a0001c0001t0028g0125 a0001c0001t0101g0207 a0001c0001t0111g0262 others(3): Show |
6 | HG01081.hp2 HG01346.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.266-293C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 3/5 | chr7 | 511289 | |||||||
chr7:511290 | GGTGGGGA others(39): Show |
G | 1 | a0001c0001t0111g0262 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.266-340_266-295del others(46): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 3/5 | chr7 | 511290 | |||||||
chr7:511292 | TGGGGAGA others(38): Show |
T | 1 | a0001c0001t0002g0102 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.266-341_266-297del others(45): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 3/5 | chr7 | 511292 | |||||||
chr7:511296 | G | C | 5 | a0001c0001t0028g0125 a0001c0001t0101g0207 a0001c0002t0010g0173 others(2): Show |
5 | HG01081.hp2 HG01346.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.266-300C>G | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 3/5 | chr7 | 511296 | |||||||
chr7:511307 | T | C | 18 | a0001c0001t0001g0147 a0001c0001t0001g0270 a0001c0001t0002g0110 others(15): Show |
19 | HG00423.hp1 HG00609.hp2 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.266-311A>G | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 3/5 | chr7 | 511307 | |||||||
chr7:511307 | TTAGTCCA others(37): Show |
T | 22 | a0001c0001t0004g0279 a0001c0001t0005g0072 a0001c0001t0015g0017 others(19): Show |
22 | HG00639.hp2 HG01081.hp1 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.266-355_266-312del others(44): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 3/5 | chr7 | 511307 | |||||||
chr7:511319 | G | GGGCCAGT others(37): Show |
3 | a0001c0001t0041g0275 a0001c0001t0041g0276 a0001c0001t0109g0274 |
3 | HG02622.hp1 HG02717.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.266-324_266-323ins others(44): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 3/5 | chr7 | 511319 | |||||||
chr7:511326 | A | T | 5 | a0001c0001t0025g0277 a0001c0001t0041g0275 a0001c0001t0041g0276 others(2): Show |
5 | HG02280.hp2 HG02622.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.266-330T>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 3/5 | chr7 | 511326 | |||||||
chr7:511328 | A | ACTGGGGG others(176): Show |
1 | a0001c0001t0014g0256 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.266-333_266-332ins others(183): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 3/5 | chr7 | 511328 | |||||||
chr7:511328 | A | ACTGGGGG others(132): Show |
1 | a0001c0001t0088g0263 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.266-333_266-332ins others(139): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 3/5 | chr7 | 511328 | |||||||
chr7:511328 | A | ACTGGGGG others(84): Show |
3 | a0001c0002t0003g0049 a0001c0002t0006g0096 a0001c0002t0031g0048 |
3 | HG01496.hp1 HG02293.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.266-333_266-332ins others(91): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 3/5 | chr7 | 511328 | |||||||
chr7:511328 | A | G | 10 | a0001c0001t0001g0270 a0001c0001t0025g0277 a0001c0001t0028g0125 others(7): Show |
10 | HG01346.hp2 HG02109.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.266-332T>C | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 3/5 | chr7 | 511328 | |||||||
chr7:511331 | GGGGGTGG others(36): Show |
G | 1 | a0001c0001t0010g0282 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.266-378_266-336del others(43): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 3/5 | chr7 | 511331 | |||||||
chr7:511332 | GGGGTGGG others(44): Show |
G | 1 | a0001c0001t0025g0277 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.266-387_266-337del others(51): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 3/5 | chr7 | 511332 | |||||||
chr7:511336 | T | G | 5 | a0001c0002t0001g0232 a0001c0002t0006g0089 a0001c0002t0030g0052 others(2): Show |
5 | HG00738.hp1 HG01358.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.266-340A>C | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 3/5 | chr7 | 511336 | |||||||
chr7:511336 | T | TGGCAG | 137 | a0001c0001t0001g0214 a0001c0001t0001g0216 a0001c0001t0001g0218 others(134): Show |
140 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.266-341_266-340ins others(5): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 3/5 | chr7 | 511336 | |||||||
chr7:511336 | T | TGGCAGGG others(40): Show |
48 | a0001c0001t0001g0007 a0001c0001t0001g0167 a0001c0001t0001g0187 others(45): Show |
49 | HG00099.hp1 HG00544.hp1 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.266-341_266-340ins others(47): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 3/5 | chr7 | 511336 | |||||||
chr7:511336 | T | TGGCAGGG others(40): Show |
4 | a0001c0001t0032g0154 a0001c0001t0045g0011 a0001c0001t0054g0022 others(1): Show |
4 | HG03225.hp2 HG03453.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.266-341_266-340ins others(47): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 3/5 | chr7 | 511336 | |||||||
chr7:511336 | T | TGGCAGGG others(42): Show |
1 | a0001c0001t0107g0201 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.266-341_266-340ins others(49): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 3/5 | chr7 | 511336 | |||||||
chr7:511336 | T | TGGCGG | 5 | a0001c0001t0001g0270 a0001c0001t0057g0111 a0001c0001t0101g0207 others(2): Show |
5 | HG01081.hp2 HG02451.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.266-341_266-340ins others(5): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 3/5 | chr7 | 511336 | |||||||
chr7:511336 | T | TGGCGGGG others(40): Show |
6 | a0001c0002t0011g0152 a0001c0002t0022g0005 a0001c0002t0022g0178 others(3): Show |
7 | HG00738.hp2 HG01361.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.266-341_266-340ins others(47): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 3/5 | chr7 | 511336 | |||||||
chr7:511336 | T | TGGCGGGG others(82): Show |
1 | a0001c0002t0010g0173 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.266-341_266-340ins others(89): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 3/5 | chr7 | 511336 | |||||||
chr7:511336 | T | TGGCGGGG others(133): Show |
1 | a0001c0001t0001g0147 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.266-341_266-340ins others(140): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 3/5 | chr7 | 511336 | |||||||
chr7:511336 | T | TGGCGGGG others(40): Show |
1 | a0001c0001t0011g0257 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.266-341_266-340ins others(47): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 3/5 | chr7 | 511336 | |||||||
chr7:511340 | G | C | 210 | a0001c0001t0001g0007 a0001c0001t0001g0147 a0001c0001t0001g0167 others(207): Show |
215 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.266-344C>G | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 3/5 | chr7 | 511340 | |||||||
chr7:511341 | A | G | 1 | a0001c0001t0028g0125 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.266-345T>C | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 3/5 | chr7 | 511341 | |||||||
chr7:511342 | G | A | 1 | a0001c0001t0028g0125 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.266-346C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 3/5 | chr7 | 511342 | |||||||
chr7:511348 | A | G | 1 | a0001c0001t0028g0125 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.266-352T>C | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 3/5 | chr7 | 511348 | |||||||
chr7:511351 | C | T | 146 | a0001c0001t0001g0214 a0001c0001t0001g0216 a0001c0001t0001g0218 others(143): Show |
149 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.266-355G>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 3/5 | chr7 | 511351 | |||||||
chr7:511363 | G | C | 142 | a0001c0001t0001g0214 a0001c0001t0001g0216 a0001c0001t0001g0218 others(139): Show |
145 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.266-367C>G | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 3/5 | chr7 | 511363 | |||||||
chr7:511368 | A | G | 1 | a0001c0001t0014g0237 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.266-372T>C | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 3/5 | chr7 | 511368 | |||||||
chr7:511370 | A | T | 145 | a0001c0001t0001g0216 a0001c0001t0001g0218 a0001c0001t0001g0230 others(142): Show |
148 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.266-374T>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 3/5 | chr7 | 511370 | |||||||
chr7:511372 | A | G | 173 | a0001c0001t0001g0216 a0001c0001t0001g0218 a0001c0001t0001g0227 others(170): Show |
176 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.266-376T>C | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 3/5 | chr7 | 511372 | |||||||
chr7:511376 | GGGGTGGC | G | 139 | a0001c0001t0001g0216 a0001c0001t0001g0218 a0001c0001t0001g0230 others(136): Show |
142 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.266-387_266-381del others(7): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 3/5 | chr7 | 511376 | |||||||
chr7:511380 | T | A | 5 | a0001c0001t0002g0110 a0001c0001t0004g0191 a0001c0001t0020g0109 others(2): Show |
5 | HG00423.hp1 HG00609.hp2 HG01346.hp2 others(2): Show |
intron_variant | MODIFIER | c.266-384A>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 3/5 | chr7 | 511380 | |||||||
chr7:511382 | GC | G | 4 | a0001c0001t0002g0110 a0001c0001t0004g0191 a0001c0001t0020g0109 others(1): Show |
4 | HG00423.hp1 HG00609.hp2 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.266-387delG | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 3/5 | chr7 | 511382 | |||||||
chr7:511383 | C | A | 1 | a0001c0001t0086g0266 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.266-387G>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 3/5 | chr7 | 511383 | |||||||
chr7:511383 | C | CAGGGGCA others(35): Show |
3 | a0001c0002t0003g0049 a0001c0002t0006g0096 a0001c0002t0031g0048 |
3 | HG01496.hp1 HG02293.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.266-388_266-387ins others(42): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 3/5 | chr7 | 511383 | |||||||
chr7:511383 | C | CGGGGGCA others(168): Show |
1 | a0001c0001t0101g0207 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.266-388_266-387ins others(175): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 3/5 | chr7 | 511383 | |||||||
chr7:511383 | C | CGGGGGCA others(35): Show |
1 | a0001c0002t0012g0036 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.266-388_266-387ins others(42): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 3/5 | chr7 | 511383 | |||||||
chr7:511383 | C | CGGGGGGA others(40): Show |
10 | a0001c0001t0001g0227 a0001c0001t0008g0194 a0001c0001t0009g0195 others(7): Show |
10 | HG00099.hp1 HG00544.hp1 HG02129.hp2 others(7): Show |
intron_variant | MODIFIER | c.266-388_266-387ins others(47): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 3/5 | chr7 | 511383 | |||||||
chr7:511384 | A | G | 64 | a0001c0001t0001g0007 a0001c0001t0001g0147 a0001c0001t0001g0167 others(61): Show |
66 | HG00609.hp1 HG00738.hp2 HG01106.hp2 others(63): Show |
intron_variant | MODIFIER | c.266-388T>C | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 3/5 | chr7 | 511384 | |||||||
chr7:511389 | C | G | 29 | a0001c0001t0001g0227 a0001c0001t0002g0110 a0001c0001t0004g0191 others(26): Show |
29 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(26): Show |
intron_variant | MODIFIER | c.266-393G>C | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 3/5 | chr7 | 511389 | |||||||
chr7:511389 | C | T | 10 | a0001c0001t0004g0179 a0001c0001t0004g0181 a0001c0001t0004g0185 others(7): Show |
10 | HG00099.hp2 HG00280.hp2 HG01069.hp2 others(7): Show |
intron_variant | MODIFIER | c.266-393G>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 3/5 | chr7 | 511389 | |||||||
chr7:511390 | A | AAGGGGGA others(41): Show |
1 | a0001c0001t0008g0224 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.266-395_266-394ins others(48): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 3/5 | chr7 | 511390 | |||||||
chr7:511390 | A | G | 16 | a0001c0001t0001g0227 a0001c0001t0002g0110 a0001c0001t0004g0191 others(13): Show |
16 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(13): Show |
intron_variant | MODIFIER | c.266-394T>C | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 3/5 | chr7 | 511390 | |||||||
chr7:511390 | AG | A | 12 | a0001c0001t0011g0257 a0001c0001t0032g0154 a0001c0001t0033g0278 others(9): Show |
12 | HG01891.hp2 HG02451.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.266-395delC | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 3/5 | chr7 | 511390 | |||||||
chr7:511391 | G | A | 17 | a0001c0001t0001g0227 a0001c0001t0002g0110 a0001c0001t0004g0191 others(14): Show |
17 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(14): Show |
intron_variant | MODIFIER | c.266-395C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 3/5 | chr7 | 511391 | |||||||
chr7:511397 | A | G | 14 | a0001c0001t0011g0257 a0001c0001t0032g0154 a0001c0001t0033g0278 others(11): Show |
14 | HG01891.hp2 HG02451.hp2 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.266-401T>C | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 3/5 | chr7 | 511397 | |||||||
chr7:511400 | C | CTAGTCCA others(41): Show |
2 | a0001c0002t0055g0018 a0002c0008t0104g0143 |
2 | HG02109.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.266-405_266-404ins others(48): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 3/5 | chr7 | 511400 | |||||||
chr7:511400 | C | T | 32 | a0001c0001t0010g0282 a0001c0001t0011g0257 a0001c0001t0014g0256 others(29): Show |
33 | HG00738.hp2 HG01256.hp1 HG01258.hp1 others(30): Show |
intron_variant | MODIFIER | c.266-404G>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 3/5 | chr7 | 511400 | |||||||
chr7:511412 | G | C | 16 | a0001c0001t0014g0256 a0001c0001t0019g0092 a0001c0001t0019g0093 others(13): Show |
17 | HG01256.hp1 HG01258.hp1 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.266-416C>G | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 3/5 | chr7 | 511412 | |||||||
chr7:511459 | C | G | 4 | a0001c0001t0004g0185 a0001c0001t0004g0188 a0001c0001t0024g0184 others(1): Show |
4 | HG00280.hp2 HG01074.hp2 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.266-463G>C | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 3/5 | chr7 | 511459 | |||||||
chr7:511484 | A | AGAGTGGT others(3): Show |
1 | a0001c0002t0006g0028 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.266-489_266-488ins others(10): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 3/5 | chr7 | 511484 | |||||||
chr7:511485 | A | G | 135 | a0001c0001t0001g0007 a0001c0001t0001g0147 a0001c0001t0001g0167 others(132): Show |
137 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.266-489T>C | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 3/5 | chr7 | 511485 | |||||||
chr7:511488 | T | A | 1 | a0005c0005t0002g0073 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.266-492A>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 3/5 | chr7 | 511488 | |||||||
chr7:511488 | T | G | 1 | a0001c0002t0006g0028 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.266-492A>C | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 3/5 | chr7 | 511488 | |||||||
chr7:511619 | A | T | 7 | a0001c0001t0025g0277 a0001c0001t0033g0278 a0001c0001t0041g0275 others(4): Show |
7 | HG01891.hp1 HG02280.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.266-623T>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 3/5 | chr7 | 511619 | |||||||
chr7:511713 | C | T | 2 | a0001c0002t0005g0030 a0001c0002t0007g0097 |
2 | HG02027.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.265+638G>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 3/5 | chr7 | 511713 | |||||||
chr7:511715 | C | A | 1 | a0001c0002t0007g0097 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.265+636G>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 3/5 | chr7 | 511715 | |||||||
chr7:511716 | G | A | 15 | a0001c0001t0004g0279 a0001c0001t0014g0237 a0001c0001t0015g0017 others(12): Show |
15 | HG00639.hp2 HG01081.hp1 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.265+635C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 3/5 | chr7 | 511716 | |||||||
chr7:511756 | C | A | 3 | a0001c0001t0001g0270 a0001c0001t0025g0273 a0001c0001t0102g0235 |
3 | HG01109.hp1 HG02280.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.265+595G>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 3/5 | chr7 | 511756 | |||||||
chr7:511772 | T | C | 1 | a0001c0001t0046g0013 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.265+579A>G | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 3/5 | chr7 | 511772 | |||||||
chr7:511781 | G | T | 1 | a0001c0001t0089g0248 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.265+570C>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 3/5 | chr7 | 511781 | |||||||
chr7:511839 | C | G | 1 | a0001c0001t0107g0201 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.265+512G>C | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 3/5 | chr7 | 511839 | |||||||
chr7:511879 | C | A | 1 | a0005c0005t0002g0073 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.265+472G>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 3/5 | chr7 | 511879 | |||||||
chr7:511879 | C | T | 105 | a0001c0001t0003g0060 a0001c0001t0003g0061 a0001c0001t0004g0006 others(102): Show |
108 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.265+472G>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 3/5 | chr7 | 511879 | |||||||
chr7:511884 | G | A | 2 | a0001c0002t0001g0223 a0001c0002t0056g0088 |
2 | HG00738.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.265+467C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 3/5 | chr7 | 511884 | |||||||
chr7:511900 | T | C | 107 | a0001c0001t0001g0007 a0001c0001t0001g0147 a0001c0001t0001g0167 others(104): Show |
109 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(106): Show |
intron_variant | MODIFIER | c.265+451A>G | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 3/5 | chr7 | 511900 | |||||||
chr7:511900 | T | TC | 4 | a0001c0002t0016g0163 a0001c0002t0040g0165 a0001c0002t0085g0148 others(1): Show |
4 | HG01256.hp1 HG01258.hp1 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.265+450dupG | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 3/5 | chr7 | 511900 | |||||||
chr7:511902 | G | A | 4 | a0001c0002t0016g0163 a0001c0002t0040g0165 a0001c0002t0085g0148 others(1): Show |
4 | HG01256.hp1 HG01258.hp1 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.265+449C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 3/5 | chr7 | 511902 | |||||||
chr7:511903 | G | A | 5 | a0001c0002t0003g0053 a0001c0002t0003g0055 a0001c0002t0006g0028 others(2): Show |
5 | NA18979.hp2 NA18983.hp2 NA18997.hp1 others(2): Show |
intron_variant | MODIFIER | c.265+448C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 3/5 | chr7 | 511903 | |||||||
chr7:511921 | C | G | 1 | a0001c0001t0014g0256 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.265+430G>C | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 3/5 | chr7 | 511921 | |||||||
chr7:511975 | C | G | 4 | a0001c0002t0016g0163 a0001c0002t0040g0165 a0001c0002t0085g0148 others(1): Show |
4 | HG01256.hp1 HG01258.hp1 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.265+376G>C | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 3/5 | chr7 | 511975 | |||||||
chr7:511978 | C | A | 5 | a0001c0001t0025g0277 a0001c0001t0033g0278 a0001c0001t0041g0275 others(2): Show |
5 | HG02280.hp2 HG02622.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.265+373G>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 3/5 | chr7 | 511978 | |||||||
chr7:511978 | C | T | 1 | a0001c0002t0043g0010 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.265+373G>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 3/5 | chr7 | 511978 | |||||||
chr7:511997 | G | A | 1 | a0001c0001t0014g0237 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.265+354C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 3/5 | chr7 | 511997 | |||||||
chr7:512009 | G | A | 38 | a0001c0001t0001g0227 a0001c0001t0001g0270 a0001c0001t0004g0006 others(35): Show |
39 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(36): Show |
intron_variant | MODIFIER | c.265+342C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 3/5 | chr7 | 512009 | |||||||
chr7:512038 | A | C | 1 | a0001c0002t0085g0148 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.265+313T>G | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 3/5 | chr7 | 512038 | |||||||
chr7:512121 | C | CG | 4 | a0001c0002t0002g0056 a0001c0002t0018g0122 a0002c0008t0104g0143 others(1): Show |
4 | HG02109.hp1 HG04204.hp2 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.265+229dupC | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 3/5 | chr7 | 512121 | |||||||
chr7:512129 | G | C | 99 | a0001c0001t0001g0007 a0001c0001t0001g0147 a0001c0001t0001g0167 others(96): Show |
100 | HG00408.hp1 HG00423.hp2 HG00621.hp2 others(97): Show |
intron_variant | MODIFIER | c.265+222C>G | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 3/5 | chr7 | 512129 | |||||||
chr7:512240 | C | T | 1 | a0001c0002t0078g0078 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.265+111G>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 3/5 | chr7 | 512240 | |||||||
chr7:512266 | C | CACCCGGC others(37): Show |
1 | a0001c0002t0006g0075 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.265+84_265+85insCG others(42): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 3/5 | chr7 | 512266 | |||||||
chr7:512266 | CACCCGGC others(37): Show |
C | 1 | a0001c0001t0010g0204 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.265+41_265+84delCA others(42): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 3/5 | chr7 | 512266 | |||||||
chr7:512290 | C | T | 3 | a0001c0001t0001g0270 a0001c0001t0025g0273 a0001c0001t0102g0235 |
3 | HG01109.hp1 HG02280.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.265+61G>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 3/5 | chr7 | 512290 | |||||||
chr7:512291 | G | A | 3 | a0001c0002t0016g0163 a0001c0002t0040g0165 a0001c0002t0099g0164 |
3 | HG01256.hp1 HG01258.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.265+60C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 3/5 | chr7 | 512291 | |||||||
chr7:512291 | G | C | 1 | a0001c0001t0001g0187 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.265+60C>G | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 3/5 | chr7 | 512291 | |||||||
chr7:512309 | T | C | 243 | a0001c0001t0001g0007 a0001c0001t0001g0147 a0001c0001t0001g0167 others(240): Show |
248 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.265+42A>G | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 3/5 | chr7 | 512309 | |||||||
chr7:512321 | G | GC | 3 | a0001c0001t0049g0015 a0001c0002t0002g0056 a0004c0006t0060g0057 |
3 | HG01175.hp2 NA18997.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.265+29dupG | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 3/5 | chr7 | 512321 | |||||||
chr7:512509 | G | T | 5 | a0001c0001t0001g0270 a0001c0001t0025g0273 a0001c0001t0088g0263 others(2): Show |
5 | HG01109.hp1 HG01891.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.161-54C>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 2/5 | chr7 | 512509 | |||||||
chr7:512666 | G | A | 1 | a0001c0001t0059g0019 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.161-211C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 2/5 | chr7 | 512666 | |||||||
chr7:512704 | C | T | 1 | a0001c0002t0069g0126 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.161-249G>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 2/5 | chr7 | 512704 | |||||||
chr7:512706 | C | A | 4 | a0001c0002t0005g0066 a0001c0002t0016g0163 a0001c0002t0040g0165 others(1): Show |
4 | HG01256.hp1 HG01258.hp1 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.161-251G>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 2/5 | chr7 | 512706 | |||||||
chr7:512719 | G | A | 2 | a0001c0002t0001g0223 a0001c0002t0056g0088 |
2 | HG00738.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.161-264C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 2/5 | chr7 | 512719 | |||||||
chr7:512808 | C | T | 1 | a0001c0001t0011g0257 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.161-353G>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 2/5 | chr7 | 512808 | |||||||
chr7:512831 | G | C | 4 | a0001c0001t0004g0185 a0001c0001t0004g0188 a0001c0001t0024g0184 others(1): Show |
4 | HG00280.hp2 HG01074.hp2 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.161-376C>G | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 2/5 | chr7 | 512831 | |||||||
chr7:512848 | T | C | 1 | a0005c0005t0002g0073 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.161-393A>G | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 2/5 | chr7 | 512848 | |||||||
chr7:512853 | G | A | 3 | a0001c0001t0004g0279 a0001c0001t0021g0138 a0001c0001t0067g0137 |
3 | HG02818.hp2 HG03486.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.161-398C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 2/5 | chr7 | 512853 | |||||||
chr7:512910 | A | T | 1 | a0001c0001t0061g0021 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.161-455T>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 2/5 | chr7 | 512910 | |||||||
chr7:512978 | T | A | 1 | a0001c0002t0006g0075 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.161-523A>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 2/5 | chr7 | 512978 | |||||||
chr7:513016 | C | T | 2 | a0001c0001t0054g0022 a0001c0002t0055g0018 |
2 | HG03098.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.161-561G>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 2/5 | chr7 | 513016 | |||||||
chr7:513115 | G | A | 1 | a0001c0003t0020g0120 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.161-660C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 2/5 | chr7 | 513115 | |||||||
chr7:513166 | C | A | 1 | a0001c0002t0073g0067 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.161-711G>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 2/5 | chr7 | 513166 | |||||||
chr7:513206 | TTACAGCC others(17): Show |
T | 1 | a0001c0001t0047g0012 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.161-775_161-752del others(24): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 2/5 | chr7 | 513206 | |||||||
chr7:513246 | G | C | 1 | a0001c0002t0085g0148 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.161-791C>G | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 2/5 | chr7 | 513246 | |||||||
chr7:513282 | G | A | 7 | a0001c0001t0001g0270 a0001c0001t0025g0273 a0001c0001t0059g0019 others(4): Show |
7 | HG01109.hp1 HG01891.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.161-827C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 2/5 | chr7 | 513282 | |||||||
chr7:513310 | G | T | 1 | a0001c0001t0008g0194 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.161-855C>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 2/5 | chr7 | 513310 | |||||||
chr7:513313 | C | T | 1 | a0001c0001t0011g0206 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.161-858G>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 2/5 | chr7 | 513313 | |||||||
chr7:513332 | C | T | 7 | a0001c0001t0001g0270 a0001c0001t0025g0273 a0001c0001t0059g0019 others(4): Show |
7 | HG01109.hp1 HG01891.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.161-877G>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 2/5 | chr7 | 513332 | |||||||
chr7:513356 | T | A | 1 | a0001c0001t0004g0162 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.161-901A>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 2/5 | chr7 | 513356 | |||||||
chr7:513385 | G | A | 2 | a0001c0001t0009g0240 a0001c0001t0017g0241 |
2 | NA18944.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.161-930C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 2/5 | chr7 | 513385 | |||||||
chr7:513418 | GAC | G | 245 | a0001c0001t0001g0007 a0001c0001t0001g0147 a0001c0001t0001g0167 others(242): Show |
250 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.161-965_161-964del others(2): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 2/5 | chr7 | 513418 | |||||||
chr7:513420 | C | G | 1 | a0003c0004t0012g0094 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.161-965G>C | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 2/5 | chr7 | 513420 | |||||||
chr7:513445 | G | A | 1 | a0001c0001t0016g0196 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.161-990C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 2/5 | chr7 | 513445 | |||||||
chr7:513492 | A | G | 218 | a0001c0001t0001g0007 a0001c0001t0001g0147 a0001c0001t0001g0167 others(215): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.161-1037T>C | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 2/5 | chr7 | 513492 | |||||||
chr7:513518 | G | GCC | 169 | a0001c0001t0001g0007 a0001c0001t0001g0167 a0001c0001t0001g0187 others(166): Show |
173 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.161-1065_161-1064d others(4): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 2/5 | chr7 | 513518 | |||||||
chr7:513518 | G | GCCC | 31 | a0001c0001t0001g0147 a0001c0001t0001g0244 a0001c0001t0004g0185 others(28): Show |
31 | HG00621.hp2 HG00738.hp1 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.161-1066_161-1064d others(5): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 2/5 | chr7 | 513518 | |||||||
chr7:513524 | C | A | 1 | a0001c0001t0010g0292 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.161-1069G>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 2/5 | chr7 | 513524 | |||||||
chr7:513565 | G | C | 1 | a0003c0004t0012g0094 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.161-1110C>G | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 2/5 | chr7 | 513565 | |||||||
chr7:513566 | C | G | 1 | a0003c0004t0012g0094 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.161-1111G>C | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 2/5 | chr7 | 513566 | |||||||
chr7:513643 | A | G | 204 | a0001c0001t0001g0007 a0001c0001t0001g0147 a0001c0001t0001g0167 others(201): Show |
208 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.161-1188T>C | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 2/5 | chr7 | 513643 | |||||||
chr7:513644 | T | C | 203 | a0001c0001t0001g0007 a0001c0001t0001g0147 a0001c0001t0001g0167 others(200): Show |
207 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.161-1189A>G | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 2/5 | chr7 | 513644 | |||||||
chr7:513715 | T | C | 138 | a0001c0001t0001g0270 a0001c0001t0003g0060 a0001c0001t0003g0061 others(135): Show |
141 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.161-1260A>G | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 2/5 | chr7 | 513715 | |||||||
chr7:513770 | A | C | 1 | a0001c0002t0077g0020 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.161-1315T>G | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 2/5 | chr7 | 513770 | |||||||
chr7:513776 | G | C | 1 | a0001c0002t0077g0020 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.161-1321C>G | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 2/5 | chr7 | 513776 | |||||||
chr7:513804 | C | T | 1 | a0001c0002t0005g0029 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.161-1349G>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 2/5 | chr7 | 513804 | |||||||
chr7:514111 | G | A | 1 | a0001c0002t0003g0091 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.161-1656C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 2/5 | chr7 | 514111 | |||||||
chr7:514134 | G | C | 1 | a0001c0001t0026g0268 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.161-1679C>G | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 2/5 | chr7 | 514134 | |||||||
chr7:514173 | C | T | 7 | a0001c0001t0001g0270 a0001c0001t0025g0273 a0001c0001t0059g0019 others(4): Show |
7 | HG01109.hp1 HG01891.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.161-1718G>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 2/5 | chr7 | 514173 | |||||||
chr7:514174 | G | A | 1 | a0001c0001t0009g0247 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.161-1719C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 2/5 | chr7 | 514174 | |||||||
chr7:514247 | G | A | 23 | a0001c0001t0001g0227 a0001c0001t0001g0250 a0001c0001t0001g0251 others(20): Show |
23 | HG00544.hp1 HG02109.hp2 HG02129.hp1 others(20): Show |
intron_variant | MODIFIER | c.161-1792C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 2/5 | chr7 | 514247 | |||||||
chr7:514288 | C | T | 10 | a0001c0001t0004g0006 a0001c0001t0004g0153 a0001c0001t0004g0162 others(7): Show |
11 | HG00280.hp1 HG01081.hp2 HG01167.hp1 others(8): Show |
intron_variant | MODIFIER | c.161-1833G>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 2/5 | chr7 | 514288 | |||||||
chr7:514333 | G | A | 60 | a0001c0001t0001g0007 a0001c0001t0001g0147 a0001c0001t0001g0187 others(57): Show |
61 | HG00408.hp1 HG00423.hp2 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.161-1878C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 2/5 | chr7 | 514333 | |||||||
chr7:514347 | C | T | 67 | a0001c0001t0001g0007 a0001c0001t0001g0147 a0001c0001t0001g0187 others(64): Show |
68 | HG00408.hp1 HG00423.hp2 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.161-1892G>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 2/5 | chr7 | 514347 | |||||||
chr7:514396 | A | G | 1 | a0001c0002t0006g0075 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.161-1941T>C | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 2/5 | chr7 | 514396 | |||||||
chr7:514397 | C | A | 1 | a0001c0002t0006g0075 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.161-1942G>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 2/5 | chr7 | 514397 | |||||||
chr7:514455 | C | T | 1 | a0001c0001t0034g0209 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.161-2000G>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 2/5 | chr7 | 514455 | |||||||
chr7:514544 | T | C | 59 | a0001c0001t0001g0007 a0001c0001t0001g0147 a0001c0001t0001g0187 others(56): Show |
60 | HG00408.hp1 HG00423.hp2 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.161-2089A>G | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 2/5 | chr7 | 514544 | |||||||
chr7:514655 | G | T | 1 | a0001c0002t0006g0028 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.161-2200C>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 2/5 | chr7 | 514655 | |||||||
chr7:514695 | C | T | 245 | a0001c0001t0001g0007 a0001c0001t0001g0147 a0001c0001t0001g0167 others(242): Show |
250 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.161-2240G>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 2/5 | chr7 | 514695 | |||||||
chr7:514804 | C | T | 1 | a0001c0001t0033g0278 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.161-2349G>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 2/5 | chr7 | 514804 | |||||||
chr7:514887 | C | T | 1 | a0001c0002t0032g0171 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.161-2432G>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 2/5 | chr7 | 514887 | |||||||
chr7:514908 | G | C | 1 | a0001c0001t0004g0193 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.161-2453C>G | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 2/5 | chr7 | 514908 | |||||||
chr7:514918 | T | G | 1 | a0001c0002t0006g0075 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.161-2463A>C | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 2/5 | chr7 | 514918 | |||||||
chr7:514967 | AAGACCCC | A | 27 | a0001c0001t0001g0167 a0001c0001t0001g0227 a0001c0001t0008g0194 others(24): Show |
28 | HG00544.hp1 HG00642.hp2 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.160+2420_160+2426d others(9): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 2/5 | chr7 | 514967 | |||||||
chr7:515078 | G | A | 1 | a0001c0001t0088g0263 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.160+2316C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 2/5 | chr7 | 515078 | |||||||
chr7:515151 | G | A | 2 | a0001c0001t0019g0092 a0001c0001t0019g0093 |
2 | HG03130.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.160+2243C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 2/5 | chr7 | 515151 | |||||||
chr7:515157 | T | A | 1 | a0001c0001t0009g0197 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.160+2237A>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 2/5 | chr7 | 515157 | |||||||
chr7:515211 | C | T | 17 | a0001c0001t0004g0006 a0001c0001t0004g0153 a0001c0001t0004g0162 others(14): Show |
18 | HG00280.hp1 HG01081.hp2 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.160+2183G>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 2/5 | chr7 | 515211 | |||||||
chr7:515212 | G | A | 1 | a0001c0001t0029g0139 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.160+2182C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 2/5 | chr7 | 515212 | |||||||
chr7:515220 | G | A | 2 | a0001c0001t0054g0022 a0001c0002t0055g0018 |
2 | HG03098.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.160+2174C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 2/5 | chr7 | 515220 | |||||||
chr7:515294 | C | T | 7 | a0001c0001t0001g0270 a0001c0001t0025g0273 a0001c0001t0059g0019 others(4): Show |
7 | HG01109.hp1 HG01891.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.160+2100G>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 2/5 | chr7 | 515294 | |||||||
chr7:515312 | G | A | 103 | a0001c0001t0001g0007 a0001c0001t0001g0147 a0001c0001t0001g0187 others(100): Show |
105 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.160+2082C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 2/5 | chr7 | 515312 | |||||||
chr7:515314 | C | G | 5 | a0001c0001t0001g0270 a0001c0001t0025g0273 a0001c0001t0088g0263 others(2): Show |
5 | HG01109.hp1 HG01891.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.160+2080G>C | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 2/5 | chr7 | 515314 | |||||||
chr7:515322 | C | T | 1 | a0001c0001t0065g0131 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.160+2072G>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 2/5 | chr7 | 515322 | |||||||
chr7:515384 | G | A | 1 | a0001c0001t0011g0257 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.160+2010C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 2/5 | chr7 | 515384 | |||||||
chr7:515424 | G | A | 8 | a0001c0001t0001g0270 a0001c0001t0025g0273 a0001c0001t0059g0019 others(5): Show |
8 | HG01109.hp1 HG01891.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.160+1970C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 2/5 | chr7 | 515424 | |||||||
chr7:515499 | G | A | 99 | a0001c0001t0001g0007 a0001c0001t0001g0147 a0001c0001t0001g0187 others(96): Show |
101 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.160+1895C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 2/5 | chr7 | 515499 | |||||||
chr7:515545 | TC | T | 4 | a0001c0001t0025g0277 a0001c0001t0033g0278 a0001c0001t0048g0014 others(1): Show |
4 | HG02280.hp2 HG02559.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.160+1848delG | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 2/5 | chr7 | 515545 | |||||||
chr7:515563 | A | G | 23 | a0001c0001t0001g0227 a0001c0001t0004g0006 a0001c0001t0004g0153 others(20): Show |
24 | HG00280.hp1 HG00544.hp1 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.160+1831T>C | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 2/5 | chr7 | 515563 | |||||||
chr7:515712 | C | T | 1 | a0001c0001t0014g0256 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.160+1682G>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 2/5 | chr7 | 515712 | |||||||
chr7:515765 | G | GT | 150 | a0001c0001t0001g0187 a0001c0001t0001g0227 a0001c0001t0001g0270 others(147): Show |
153 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.160+1628dupA | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 2/5 | chr7 | 515765 | |||||||
chr7:515881 | C | T | 2 | a0001c0001t0054g0022 a0001c0002t0055g0018 |
2 | HG03098.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.160+1513G>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 2/5 | chr7 | 515881 | |||||||
chr7:515998 | A | AC | 126 | a0001c0001t0001g0167 a0001c0001t0001g0187 a0001c0001t0001g0244 others(123): Show |
128 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.160+1395dupG | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 2/5 | chr7 | 515998 | |||||||
chr7:516003 | C | G | 53 | a0001c0001t0001g0007 a0001c0001t0001g0147 a0001c0001t0001g0199 others(50): Show |
55 | HG00280.hp1 HG00423.hp2 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.160+1391G>C | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 2/5 | chr7 | 516003 | |||||||
chr7:516004 | C | G | 1 | a0001c0001t0004g0153 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.160+1390G>C | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 2/5 | chr7 | 516004 | |||||||
chr7:516008 | A | G | 1 | a0001c0002t0003g0027 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.160+1386T>C | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 2/5 | chr7 | 516008 | |||||||
chr7:516040 | G | GC | 46 | a0001c0001t0001g0007 a0001c0001t0001g0167 a0001c0001t0001g0212 others(43): Show |
49 | HG00642.hp2 HG00673.hp1 HG01074.hp1 others(46): Show |
intron_variant | MODIFIER | c.160+1353dupG | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 2/5 | chr7 | 516040 | |||||||
chr7:516040 | G | GCC | 19 | a0001c0001t0001g0147 a0001c0001t0001g0227 a0001c0001t0001g0230 others(16): Show |
19 | HG00423.hp2 HG00544.hp1 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.160+1352_160+1353d others(4): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 2/5 | chr7 | 516040 | |||||||
chr7:516046 | C | T | 1 | a0001c0001t0010g0189 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.160+1348G>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 2/5 | chr7 | 516046 | |||||||
chr7:516049 | C | CCCG | 17 | a0001c0001t0001g0187 a0001c0001t0004g0188 a0001c0001t0008g0161 others(14): Show |
17 | HG00280.hp2 HG00408.hp1 HG00544.hp2 others(14): Show |
intron_variant | MODIFIER | c.160+1344_160+1345i others(5): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 2/5 | chr7 | 516049 | |||||||
chr7:516049 | C | CCG | 138 | a0001c0001t0001g0244 a0001c0001t0001g0250 a0001c0001t0001g0251 others(135): Show |
140 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.160+1344_160+1345i others(4): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 2/5 | chr7 | 516049 | |||||||
chr7:516053 | A | C | 1 | a0001c0001t0004g0153 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.160+1341T>G | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 2/5 | chr7 | 516053 | |||||||
chr7:516054 | C | A | 1 | a0001c0001t0004g0153 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.160+1340G>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 2/5 | chr7 | 516054 | |||||||
chr7:516055 | T | C | 1 | a0001c0001t0004g0153 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.160+1339A>G | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 2/5 | chr7 | 516055 | |||||||
chr7:516140 | T | C | 2 | a0001c0002t0003g0124 a0001c0002t0005g0123 |
2 | NA18970.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.160+1254A>G | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 2/5 | chr7 | 516140 | |||||||
chr7:516185 | G | A | 5 | a0001c0001t0008g0217 a0001c0001t0017g0219 a0001c0001t0038g0233 others(2): Show |
5 | HG01109.hp2 HG01175.hp2 HG01257.hp2 others(2): Show |
intron_variant | MODIFIER | c.160+1209C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 2/5 | chr7 | 516185 | |||||||
chr7:516281 | G | A | 1 | a0001c0001t0111g0262 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.160+1113C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 2/5 | chr7 | 516281 | |||||||
chr7:516484 | A | G | 24 | a0001c0001t0001g0167 a0001c0001t0004g0162 a0001c0001t0008g0161 others(21): Show |
25 | HG00408.hp1 HG00642.hp2 HG00741.hp2 others(22): Show |
intron_variant | MODIFIER | c.160+910T>C | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 2/5 | chr7 | 516484 | |||||||
chr7:516491 | C | T | 24 | a0001c0001t0001g0167 a0001c0001t0004g0162 a0001c0001t0008g0161 others(21): Show |
25 | HG00408.hp1 HG00642.hp2 HG00741.hp2 others(22): Show |
intron_variant | MODIFIER | c.160+903G>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 2/5 | chr7 | 516491 | |||||||
chr7:516540 | C | A | 1 | a0001c0002t0043g0010 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.160+854G>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 2/5 | chr7 | 516540 | |||||||
chr7:516558 | T | C | 1 | a0001c0001t0088g0263 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.160+836A>G | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 2/5 | chr7 | 516558 | |||||||
chr7:516610 | G | A | 2 | a0001c0001t0038g0233 a0001c0001t0038g0234 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.160+784C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 2/5 | chr7 | 516610 | |||||||
chr7:517074 | C | A | 32 | a0001c0001t0001g0244 a0001c0001t0001g0250 a0001c0001t0001g0251 others(29): Show |
32 | HG00733.hp1 HG00733.hp2 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.160+320G>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 2/5 | chr7 | 517074 | |||||||
chr7:517222 | G | A | 1 | a0001c0001t0004g0153 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.160+172C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 2/5 | chr7 | 517222 | |||||||
chr7:517223 | T | G | 1 | a0001c0001t0004g0153 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.160+171A>C | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 2/5 | chr7 | 517223 | |||||||
chr7:517224 | G | T | 1 | a0001c0001t0004g0153 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.160+170C>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 2/5 | chr7 | 517224 | |||||||
chr7:517225 | GAGACTGG others(7): Show |
G | 1 | a0001c0001t0023g0146 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.160+155_160+168del others(14): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 2/5 | chr7 | 517225 | |||||||
chr7:517372 | G | A | 1 | a0001c0001t0088g0263 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.160+22C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 2/5 | chr7 | 517372 | |||||||
chr7:517550 | C | G | 1 | a0001c0002t0011g0152 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.64-60G>C | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 1/5 | chr7 | 517550 | |||||||
chr7:517674 | G | A | 2 | a0001c0001t0001g0265 a0001c0002t0113g0264 |
2 | HG03704.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.64-184C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 1/5 | chr7 | 517674 | |||||||
chr7:517729 | G | GC | 22 | a0001c0001t0005g0130 a0001c0001t0007g0128 a0001c0001t0015g0017 others(19): Show |
22 | HG01081.hp1 HG01243.hp1 HG01517.hp1 others(19): Show |
intron_variant | MODIFIER | c.64-240dupG | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 1/5 | chr7 | 517729 | |||||||
chr7:517812 | G | T | 1 | a0001c0001t0023g0146 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.64-322C>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 1/5 | chr7 | 517812 | |||||||
chr7:517939 | A | G | 1 | a0001c0002t0006g0025 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.64-449T>C | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 1/5 | chr7 | 517939 | |||||||
chr7:518141 | G | A | 1 | a0001c0002t0003g0142 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.64-651C>T | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 1/5 | chr7 | 518141 | |||||||
chr7:518584 | G | T | 4 | a0001c0001t0079g0149 a0001c0001t0080g0151 a0001c0001t0081g0150 others(1): Show |
4 | HG03710.hp1 NA19062.hp2 NA19079.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+355C>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 1/5 | chr7 | 518584 | |||||||
chr7:518683 | C | T | 1 | a0001c0001t0074g0024 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.63+256G>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 1/5 | chr7 | 518683 | |||||||
chr7:518687 | C | G | 1 | a0001c0001t0001g0147 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.63+252G>C | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 1/5 | chr7 | 518687 | |||||||
chr7:518715 | GCTGCTCC others(13): Show |
G | 1 | a0001c0001t0023g0146 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.63+204_63+223delTC others(18): Show |
PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 1/5 | chr7 | 518715 | |||||||
chr7:518746 | C | G | 134 | a0001c0001t0001g0007 a0001c0001t0001g0147 a0001c0001t0001g0167 others(131): Show |
138 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.63+193G>C | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 1/5 | chr7 | 518746 | |||||||
chr7:518773 | C | T | 5 | a0001c0001t0054g0022 a0001c0001t0059g0019 a0001c0001t0061g0021 others(2): Show |
5 | HG01891.hp1 HG03098.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+166G>A | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 1/5 | chr7 | 518773 | |||||||
chr7:518923 | C | CG | 5 | a0001c0001t0008g0144 a0001c0001t0015g0017 a0001c0001t0035g0145 others(2): Show |
5 | HG00741.hp1 HG01243.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+15dupC | PDGFA | ENSG00000197461.13 | transcript | ENST00000402802.8 | protein_coding | 1/5 | chr7 | 518923 |