| geneid | 2596 |
|---|---|
| ensemblid | ENSG00000172020.13 |
| hgncid | 4140 |
| symbol | GAP43 |
| name | growth associated protein 43 |
| refseq_nuc | NM_002045.4 |
| refseq_prot | NP_002036.1 |
| ensembl_nuc | ENST00000305124.11 |
| ensembl_prot | ENSP00000305010.7 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 115623510 |
| end | 115721483 |
| strand | + |
| ver | v1.2 |
| region | chr3:115623510-115721483 |
| region5000 | chr3:115618510-115726483 |
| regionname0 | GAP43_chr3_115623510_115721483 |
| regionname5000 | GAP43_chr3_115618510_115726483 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 238 | 352 | 92 | 72 | 132 | 10 | 44 | 106 | GAP43_chr3_115618510_115726483 | GAP43 | copy fasta | chr3 | 115618510 | 115726483 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 717 | 338 | 84 | 70 | 128 | 10 | 44 | GAP43_chr3_115618510_115726483 | GAP43 | copy fasta | chr3 | 115618510 | 115726483 |
| c0002 | 0/0 | 717 | 14 | 8 | 2 | 4 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | copy fasta | chr3 | 115618510 | 115726483 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 782 | 138 | 57 | 23 | 32 | 5 | 19 | GAP43_chr3_115618510_115726483 | GAP43 | copy fasta | chr3 | 115618510 | 115726483 |
| t0002 | 0/0 | 784 | 102 | 7 | 18 | 66 | 2 | 9 | GAP43_chr3_115618510_115726483 | GAP43 | copy fasta | chr3 | 115618510 | 115726483 |
| t0003 | 0/0 | 782 | 43 | 8 | 12 | 6 | 3 | 14 | GAP43_chr3_115618510_115726483 | GAP43 | copy fasta | chr3 | 115618510 | 115726483 |
| t0004 | 0/0 | 782 | 31 | 0 | 11 | 20 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | copy fasta | chr3 | 115618510 | 115726483 |
| t0005 | 0/0 | 783 | 17 | 15 | 2 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | copy fasta | chr3 | 115618510 | 115726483 |
| t0006 | 0/0 | 785 | 3 | 0 | 0 | 3 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | copy fasta | chr3 | 115618510 | 115726483 |
| t0007 | 0/0 | 783 | 3 | 0 | 0 | 2 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | copy fasta | chr3 | 115618510 | 115726483 |
| t0008 | 0/0 | 783 | 2 | 0 | 2 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | copy fasta | chr3 | 115618510 | 115726483 |
| t0009 | 0/0 | 781 | 2 | 0 | 2 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | copy fasta | chr3 | 115618510 | 115726483 |
| t0010 | 0/0 | 782 | 2 | 2 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | copy fasta | chr3 | 115618510 | 115726483 |
| t0011 | 0/0 | 782 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | copy fasta | chr3 | 115618510 | 115726483 |
| t0012 | 0/0 | 782 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | copy fasta | chr3 | 115618510 | 115726483 |
| t0013 | 0/0 | 783 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | copy fasta | chr3 | 115618510 | 115726483 |
| t0014 | 0/0 | 784 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | copy fasta | chr3 | 115618510 | 115726483 |
| t0015 | 0/0 | 784 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | copy fasta | chr3 | 115618510 | 115726483 |
| t0016 | 0/0 | 784 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | copy fasta | chr3 | 115618510 | 115726483 |
| t0017 | 0/0 | 782 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | copy fasta | chr3 | 115618510 | 115726483 |
| t0018 | 0/0 | 781 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | copy fasta | chr3 | 115618510 | 115726483 |
| t0019 | 0/0 | 783 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | copy fasta | chr3 | 115618510 | 115726483 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0050 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0084 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0311 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 717 | 338 | 84 | 70 | 128 | 10 | 44 | GAP43_chr3_115618510_115726483 | GAP43 | copy fasta | chr3 | 115618510 | 115726483 |
| a0001c0002 | 0/0 | 717 | 14 | 8 | 2 | 4 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | copy fasta | chr3 | 115618510 | 115726483 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1498 | 128 | 52 | 22 | 28 | 5 | 19 | GAP43_chr3_115618510_115726483 | GAP43 | copy fasta | chr3 | 115618510 | 115726483 |
| a0001c0001t0002 | 0/0 | 1500 | 99 | 5 | 17 | 66 | 2 | 9 | GAP43_chr3_115618510_115726483 | GAP43 | copy fasta | chr3 | 115618510 | 115726483 |
| a0001c0001t0003 | 0/0 | 1498 | 43 | 8 | 12 | 6 | 3 | 14 | GAP43_chr3_115618510_115726483 | GAP43 | copy fasta | chr3 | 115618510 | 115726483 |
| a0001c0001t0004 | 0/0 | 1498 | 31 | 0 | 11 | 20 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | copy fasta | chr3 | 115618510 | 115726483 |
| a0001c0001t0005 | 0/0 | 1499 | 17 | 15 | 2 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | copy fasta | chr3 | 115618510 | 115726483 |
| a0001c0001t0006 | 0/0 | 1501 | 3 | 0 | 0 | 3 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | copy fasta | chr3 | 115618510 | 115726483 |
| a0001c0001t0007 | 0/0 | 1499 | 3 | 0 | 0 | 2 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | copy fasta | chr3 | 115618510 | 115726483 |
| a0001c0001t0008 | 0/0 | 1499 | 2 | 0 | 2 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | copy fasta | chr3 | 115618510 | 115726483 |
| a0001c0001t0009 | 0/0 | 1497 | 2 | 0 | 2 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | copy fasta | chr3 | 115618510 | 115726483 |
| a0001c0001t0010 | 0/0 | 1498 | 2 | 2 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | copy fasta | chr3 | 115618510 | 115726483 |
| a0001c0001t0011 | 0/0 | 1498 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | copy fasta | chr3 | 115618510 | 115726483 |
| a0001c0001t0012 | 0/0 | 1498 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | copy fasta | chr3 | 115618510 | 115726483 |
| a0001c0001t0013 | 0/0 | 1499 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | copy fasta | chr3 | 115618510 | 115726483 |
| a0001c0001t0014 | 0/0 | 1500 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | copy fasta | chr3 | 115618510 | 115726483 |
| a0001c0001t0015 | 0/0 | 1500 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | copy fasta | chr3 | 115618510 | 115726483 |
| a0001c0001t0016 | 0/0 | 1500 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | copy fasta | chr3 | 115618510 | 115726483 |
| a0001c0001t0018 | 0/0 | 1497 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | copy fasta | chr3 | 115618510 | 115726483 |
| a0001c0001t0019 | 0/0 | 1499 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | copy fasta | chr3 | 115618510 | 115726483 |
| a0001c0002t0001 | 0/0 | 1498 | 10 | 5 | 1 | 4 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | copy fasta | chr3 | 115618510 | 115726483 |
| a0001c0002t0002 | 0/0 | 1500 | 3 | 2 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | copy fasta | chr3 | 115618510 | 115726483 |
| a0001c0002t0017 | 0/0 | 1498 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | copy fasta | chr3 | 115618510 | 115726483 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0050 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0084 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0001g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0002g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0003g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0003g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0003g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0003g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0003g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0003g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0003g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0003g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0003g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0003g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0003g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0003g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0003g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0003g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0003g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0003g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0003g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0003g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0003g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0003g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0003g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0003g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0003g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0003g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0003g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0003g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0003g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0003g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0003g0311 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0003g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0003g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0003g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0004g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0004g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0004g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0004g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0004g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0004g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0004g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0004g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0004g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0004g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0004g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0004g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0004g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0004g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0004g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0004g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0004g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0004g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0004g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0004g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0004g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0004g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0004g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0004g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0004g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0004g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0004g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0004g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0004g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0004g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0004g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0005g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0005g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0005g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0005g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0005g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0005g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0005g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0005g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0005g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0005g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0005g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0005g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0005g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0005g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0005g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0005g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0005g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0006g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0006g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0006g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0007g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0007g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0007g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0008g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0008g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0009g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0009g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0010g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0010g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0011g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0012g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0013g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0014g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0015g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0016g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0018g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0001t0019g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0002t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0002t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0002t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0002t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0002t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0002t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0002t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0002t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0002t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| a0001c0002t0017g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0046 | EUR | GBR | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG00140 | hp2 | a0001 | c0001 | t0003 | g0196 | EUR | GBR | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0304 | EUR | FIN | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0264 | EUR | FIN | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG00408 | hp1 | a0001 | c0001 | t0004 | g0280 | EAS | CHS | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0111 | EAS | CHS | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG00438 | hp1 | a0001 | c0001 | t0014 | g0250 | EAS | CHS | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG00438 | hp2 | a0001 | c0001 | t0004 | g0059 | EAS | CHS | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG00544 | hp1 | a0001 | c0001 | t0004 | g0130 | EAS | CHS | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0260 | EAS | CHS | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | CHS | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0211 | EAS | CHS | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | CHS | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG00609 | hp2 | a0001 | c0001 | t0004 | g0333 | EAS | CHS | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0142 | EAS | CHS | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0107 | EAS | CHS | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0117 | AMR | PUR | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0155 | AMR | PUR | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0203 | EAS | CHS | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG00673 | hp2 | a0001 | c0001 | t0004 | g0248 | EAS | CHS | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG00735 | hp2 | a0001 | c0001 | t0012 | g0300 | AMR | PUR | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG00738 | hp2 | a0001 | c0001 | t0003 | g0125 | AMR | PUR | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0076 | AMR | PUR | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0178 | AMR | PUR | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01069 | hp2 | a0001 | c0001 | t0008 | g0235 | AMR | PUR | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0184 | AMR | PUR | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | PUR | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0156 | AMR | PUR | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0290 | AMR | PUR | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01081 | hp1 | a0001 | c0001 | t0008 | g0236 | AMR | PUR | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01081 | hp2 | a0001 | c0001 | t0005 | g0348 | AMR | PUR | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0289 | AMR | PUR | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0118 | AMR | PUR | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01106 | hp1 | a0001 | c0002 | t0002 | g0039 | AMR | PUR | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0267 | AMR | PUR | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0349 | AMR | PUR | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0279 | AMR | PUR | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01169 | hp1 | a0001 | c0001 | t0009 | g0077 | AMR | PUR | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01169 | hp2 | a0001 | c0001 | t0009 | g0187 | AMR | PUR | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0351 | AMR | PUR | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0231 | AMR | PUR | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0237 | AMR | PUR | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01255 | hp1 | a0001 | c0001 | t0003 | g0162 | AMR | CLM | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | CLM | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0292 | AMR | CLM | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | CLM | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01257 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | CLM | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0239 | AMR | CLM | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0291 | AMR | CLM | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01258 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | CLM | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01261 | hp2 | a0001 | c0001 | t0011 | g0075 | AMR | CLM | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | CLM | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0161 | AMR | CLM | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01361 | hp1 | a0001 | c0001 | t0005 | g0344 | AMR | CLM | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01361 | hp2 | a0001 | c0001 | t0003 | g0113 | AMR | CLM | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01433 | hp2 | a0001 | c0001 | t0003 | g0190 | AMR | CLM | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01496 | hp1 | a0001 | c0001 | t0004 | g0144 | AMR | CLM | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0326 | AMR | CLM | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01517 | hp1 | a0001 | c0001 | t0003 | g0126 | EUR | IBS | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01517 | hp2 | a0001 | c0001 | t0003 | g0311 | EUR | IBS | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0296 | AFR | ACB | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0009 | AFR | ACB | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | ACB | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0346 | AFR | ACB | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0138 | AMR | PEL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01928 | hp2 | a0001 | c0001 | t0004 | g0181 | AMR | PEL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0302 | AMR | PEL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01934 | hp2 | a0001 | c0001 | t0004 | g0182 | AMR | PEL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01943 | hp1 | a0001 | c0001 | t0004 | g0176 | AMR | PEL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0198 | AMR | PEL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01952 | hp1 | a0001 | c0001 | t0004 | g0183 | AMR | PEL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01952 | hp2 | a0001 | c0001 | t0004 | g0256 | AMR | PEL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | PEL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01975 | hp2 | a0001 | c0001 | t0004 | g0030 | AMR | PEL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0158 | AMR | PEL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01981 | hp2 | a0001 | c0001 | t0003 | g0312 | AMR | PEL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01993 | hp1 | a0001 | c0001 | t0004 | g0177 | AMR | PEL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG01993 | hp2 | a0001 | c0001 | t0003 | g0062 | AMR | PEL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | PEL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02004 | hp2 | a0001 | c0001 | t0004 | g0143 | AMR | PEL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02055 | hp2 | a0001 | c0001 | t0005 | g0340 | AFR | ACB | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02071 | hp1 | a0001 | c0001 | t0004 | g0139 | EAS | KHV | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0324 | EAS | KHV | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | KHV | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0131 | EAS | KHV | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0129 | EAS | KHV | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02083 | hp2 | a0001 | c0001 | t0004 | g0054 | EAS | KHV | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02129 | hp1 | a0001 | c0001 | t0004 | g0137 | EAS | KHV | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02129 | hp2 | a0001 | c0001 | t0004 | g0109 | EAS | KHV | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0244 | AFR | ACB | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02148 | hp1 | a0001 | c0001 | t0004 | g0180 | AMR | PEL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0230 | AMR | PEL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | ACB | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02257 | hp2 | a0001 | c0001 | t0005 | g0278 | AFR | ACB | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | ACB | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | ACB | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0308 | AFR | ACB | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0243 | AFR | ACB | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02293 | hp1 | a0001 | c0001 | t0004 | g0189 | AMR | PEL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02293 | hp2 | a0001 | c0002 | t0001 | g0150 | AMR | PEL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0255 | AMR | PEL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0045 | AMR | PEL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | ACB | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0307 | AFR | ACB | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02523 | hp1 | a0001 | c0001 | t0004 | g0257 | EAS | KHV | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0323 | EAS | KHV | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0157 | SAS | PJL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0214 | SAS | PJL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0021 | AFR | GWD | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02615 | hp2 | a0001 | c0002 | t0001 | g0035 | AFR | GWD | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02622 | hp2 | a0001 | c0002 | t0002 | g0223 | AFR | GWD | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | GWD | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | GWD | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | GWD | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0083 | AFR | GWD | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0170 | SAS | PJL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | GWD | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02723 | hp2 | a0001 | c0001 | t0005 | g0011 | AFR | GWD | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0102 | SAS | PJL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02735 | hp2 | a0001 | c0001 | t0003 | g0195 | SAS | PJL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02738 | hp1 | a0001 | c0001 | t0003 | g0316 | SAS | PJL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02738 | hp2 | a0001 | c0001 | t0003 | g0303 | SAS | PJL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02809 | hp2 | a0001 | c0001 | t0005 | g0341 | AFR | GWD | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0342 | AFR | GWD | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0301 | AFR | GWD | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0020 | AFR | GWD | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | GWD | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02895 | hp1 | a0001 | c0001 | t0010 | g0246 | AFR | GWD | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02895 | hp2 | a0001 | c0001 | t0005 | g0204 | AFR | GWD | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | GWD | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | GWD | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02897 | hp1 | a0001 | c0001 | t0010 | g0245 | AFR | GWD | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | ESN | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0259 | AFR | ESN | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | ESN | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | ESN | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0265 | AFR | ESN | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0347 | AFR | ESN | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0350 | AFR | ESN | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0188 | AFR | ESN | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG03017 | hp1 | a0001 | c0001 | t0007 | g0275 | SAS | PJL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0208 | SAS | PJL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG03041 | hp1 | a0001 | c0001 | t0005 | g0097 | AFR | GWD | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0332 | AFR | GWD | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | ESN | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0298 | AFR | ESN | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG03195 | hp1 | a0001 | c0001 | t0005 | g0003 | AFR | ESN | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG03195 | hp2 | a0001 | c0001 | t0005 | g0096 | AFR | ESN | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG03225 | hp1 | a0001 | c0002 | t0002 | g0192 | AFR | MSL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG03225 | hp2 | a0001 | c0001 | t0005 | g0343 | AFR | MSL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0191 | SAS | PJL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0218 | SAS | PJL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0345 | AFR | MSL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0242 | AFR | MSL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0339 | AFR | MSL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | MSL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0145 | SAS | PJL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG03491 | hp1 | a0001 | c0001 | t0003 | g0266 | SAS | PJL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0063 | SAS | PJL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0070 | SAS | PJL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG03516 | hp1 | a0001 | c0001 | t0005 | g0233 | AFR | ESN | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | ESN | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0313 | AFR | GWD | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG03579 | hp1 | a0001 | c0002 | t0001 | g0285 | AFR | MSL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | MSL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG03654 | hp1 | a0001 | c0001 | t0003 | g0241 | SAS | PJL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0319 | SAS | PJL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0051 | SAS | PJL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG03688 | hp1 | a0001 | c0001 | t0003 | g0283 | SAS | STU | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0207 | SAS | STU | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0293 | SAS | PJL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG03704 | hp2 | a0001 | c0001 | t0003 | g0074 | SAS | PJL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0071 | SAS | PJL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG03710 | hp2 | a0001 | c0001 | t0003 | g0284 | SAS | PJL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG03834 | hp1 | a0001 | c0001 | t0003 | g0014 | SAS | BEB | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0305 | SAS | BEB | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0057 | SAS | BEB | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0320 | SAS | BEB | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG03942 | hp1 | a0001 | c0001 | t0003 | g0078 | SAS | BEB | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0042 | SAS | BEB | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0337 | SAS | BEB | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG04184 | hp2 | a0001 | c0001 | t0003 | g0274 | SAS | BEB | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0327 | SAS | STU | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | STU | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0094 | SAS | STU | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0240 | SAS | STU | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0079 | SAS | STU | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG04228 | hp2 | a0001 | c0001 | t0019 | g0013 | SAS | STU | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | YRI | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | YRI | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | CHB | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0294 | EAS | CHB | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0325 | AFR | YRI | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18906 | hp2 | a0001 | c0001 | t0003 | g0023 | AFR | YRI | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18939 | hp2 | a0001 | c0002 | t0001 | g0254 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0277 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18945 | hp2 | a0001 | c0002 | t0001 | g0132 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18948 | hp1 | a0001 | c0001 | t0007 | g0029 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18948 | hp2 | a0001 | c0001 | t0007 | g0175 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0261 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0321 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18962 | hp2 | a0001 | c0001 | t0016 | g0269 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0258 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0331 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18968 | hp2 | a0001 | c0001 | t0004 | g0159 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0334 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18970 | hp1 | a0001 | c0001 | t0003 | g0288 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18971 | hp1 | a0001 | c0001 | t0004 | g0309 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18974 | hp1 | a0001 | c0001 | t0006 | g0034 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0318 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0263 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18980 | hp2 | a0001 | c0001 | t0003 | g0027 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0329 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18983 | hp1 | a0001 | c0001 | t0004 | g0200 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18984 | hp2 | a0001 | c0001 | t0006 | g0114 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18986 | hp1 | a0001 | c0001 | t0003 | g0206 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18986 | hp2 | a0001 | c0001 | t0004 | g0287 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18995 | hp1 | a0001 | c0001 | t0003 | g0272 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0281 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0276 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18999 | hp2 | a0001 | c0002 | t0001 | g0253 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0336 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA19002 | hp2 | a0001 | c0001 | t0003 | g0273 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0322 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA19010 | hp1 | a0001 | c0001 | t0004 | g0160 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA19011 | hp1 | a0001 | c0001 | t0004 | g0141 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0317 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0315 | AFR | LWK | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0297 | AFR | LWK | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA19043 | hp1 | a0001 | c0002 | t0001 | g0006 | AFR | LWK | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0306 | AFR | LWK | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0330 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0295 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0328 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA19066 | hp1 | a0001 | c0001 | t0004 | g0025 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA19072 | hp1 | a0001 | c0001 | t0004 | g0282 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA19072 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA19077 | hp1 | a0001 | c0001 | t0004 | g0249 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA19080 | hp2 | a0001 | c0001 | t0006 | g0149 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA19081 | hp1 | a0001 | c0001 | t0018 | g0335 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA19082 | hp1 | a0001 | c0002 | t0001 | g0133 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA19084 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0286 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA19090 | hp1 | a0001 | c0001 | t0004 | g0247 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0338 | AFR | YRI | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA19240 | hp2 | a0001 | c0001 | t0005 | g0005 | AFR | YRI | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ASW | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA20129 | hp2 | a0001 | c0002 | t0001 | g0098 | AFR | ASW | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0058 | EUR | TSI | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0056 | EUR | TSI | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0104 | EUR | TSI | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0053 | EUR | TSI | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0217 | SAS | GIH | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0043 | SAS | GIH | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | ACB | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | ACB | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02486 | hp1 | a0001 | c0001 | t0005 | g0012 | AFR | ACB | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02486 | hp2 | a0001 | c0002 | t0017 | g0314 | AFR | ACB | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02559 | hp1 | a0001 | c0001 | t0005 | g0101 | AFR | ACB | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG02559 | hp2 | a0001 | c0001 | t0005 | g0299 | AFR | ACB | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0164 | AFR | MSL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG03471 | hp2 | a0001 | c0001 | t0005 | g0310 | AFR | MSL | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0016 | AFR | USA | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | USA | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA20300 | hp1 | a0001 | c0001 | t0013 | g0219 | AFR | USA | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | USA | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA21309 | hp1 | a0001 | c0001 | t0015 | g0154 | AFR | LWK | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| NA21309 | hp2 | a0001 | c0002 | t0001 | g0095 | AFR | LWK | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0050 | REF | REF | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0084 | REF | REF | GAP43_chr3_115618510_115726483 | GAP43 | chr3 | 115618510 | 115726483 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:115676474
|
G | A | 1 | a0001c0002 | 14 | HG01106.hp1 HG02293.hp2 HG02486.hp2 others(11): Show |
synonymous_variant | LOW | c.492G>A | p.Glu164Glu | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/3 | 672/1498 | 492/717 | 164/238 | chr3 | 115676474 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:115623548
|
G | C | 1 | a0001c0001t0011 | 1 | HG01261.hp2 | 5_prime_UTR_variant | MODIFIER | c.-142G>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/3 | 142 | chr3 | 115623548 | |||||
| chr3:115623556
|
G | C | 1 | a0001c0001t0012 | 1 | HG00735.hp2 | 5_prime_UTR_variant | MODIFIER | c.-134G>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/3 | 134 | chr3 | 115623556 | |||||
| chr3:115623673
|
C | T | 1 | a0001c0001t0019 | 1 | HG04228.hp2 | 5_prime_UTR_variant | MODIFIER | c.-17C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/3 | 17 | chr3 | 115623673 | |||||
| chr3:115720905
|
A | G | 1 | a0001c0001t0010 | 2 | HG02895.hp1 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*23A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 3/3 | 23 | chr3 | 115720905 | |||||
| chr3:115721047
|
T | TA | 5 | a0001c0001t0005a0001c0001t0006a0001c0001t0008others(2): Show | 24 | HG01069.hp2 HG01081.hp1 HG01081.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*182dupA | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 3/3 | 183 | INFO_REALIGN_3_PRIME | chr3 | 115721047 | ||||
| chr3:115721047
|
TA | T | 3 | a0001c0001t0007a0001c0001t0009a0001c0001t0018 | 6 | HG01169.hp1 HG01169.hp2 HG03017.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*182delA | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 3/3 | 182 | INFO_REALIGN_3_PRIME | chr3 | 115721047 | ||||
| chr3:115721071
|
A | G | 1 | a0001c0002t0017 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*189A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 3/3 | 189 | chr3 | 115721071 | |||||
| chr3:115721119
|
G | A | 1 | a0001c0001t0014 | 1 | HG00438.hp1 | 3_prime_UTR_variant | MODIFIER | c.*237G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 3/3 | 237 | chr3 | 115721119 | |||||
| chr3:115721160
|
T | G | 6 | a0001c0001t0003a0001c0001t0004a0001c0001t0008others(3): Show | 80 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*278T>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 3/3 | 278 | chr3 | 115721160 | |||||
| chr3:115721185
|
G | C | 1 | a0001c0001t0016 | 1 | NA18962.hp2 | 3_prime_UTR_variant | MODIFIER | c.*303G>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 3/3 | 303 | chr3 | 115721185 | |||||
| chr3:115721227
|
C | CCT | 7 | a0001c0001t0002a0001c0001t0006a0001c0001t0007others(4): Show | 111 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(108): Show |
3_prime_UTR_variant | MODIFIER | c.*362_*363dupCT | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 3/3 | 364 | INFO_REALIGN_3_PRIME | chr3 | 115721227 | ||||
| chr3:115721295
|
C | T | 1 | a0001c0001t0005 | 17 | HG01081.hp2 HG01361.hp1 HG02055.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*413C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 3/3 | 413 | chr3 | 115721295 | |||||
| chr3:115721324
|
C | T | 1 | a0001c0001t0004 | 31 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*442C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 3/3 | 442 | chr3 | 115721324 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:115623781
|
G | A | 5 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0005g0003others(2): Show | 5 | HG01433.hp1 HG03195.hp1 NA19043.hp1 others(2): Show |
intron_variant | MODIFIER | c.30+62G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115623781 | ||||||
| chr3:115623929
|
G | A | 1 | a0001c0001t0003g0007 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.30+210G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115623929 | ||||||
| chr3:115623963
|
AT | A | 17 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0019others(14): Show | 17 | HG01255.hp2 HG01261.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.30+255delT | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115623963 | |||||
| chr3:115624098
|
CA | C | 283 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0015others(280): Show | 283 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(280): Show |
intron_variant | MODIFIER | c.30+385delA | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115624098 | |||||
| chr3:115624201
|
A | C | 1 | a0001c0001t0002g0351 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.30+482A>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115624201 | ||||||
| chr3:115624300
|
AT | A | 14 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0033others(11): Show | 14 | HG01255.hp2 HG01975.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.30+595delT | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115624300 | |||||
| chr3:115624300
|
ATT | A | 148 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0017others(145): Show | 148 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.30+594_30+595delTT | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115624300 | |||||
| chr3:115624300
|
ATTT | A | 125 | a0001c0001t0001g0002a0001c0001t0001g0090a0001c0001t0001g0091others(122): Show | 125 | HG00140.hp2 HG00408.hp2 HG00544.hp1 others(122): Show |
intron_variant | MODIFIER | c.30+593_30+595delTT others(1): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115624300 | |||||
| chr3:115624366
|
A | G | 276 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0015others(273): Show | 276 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.30+647A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115624366 | ||||||
| chr3:115624443
|
G | C | 3 | a0001c0001t0001g0210a0001c0001t0002g0211a0001c0001t0002g0212 | 3 | HG00558.hp2 NA18965.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.30+724G>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115624443 | ||||||
| chr3:115624548
|
A | G | 36 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0207others(33): Show | 36 | HG00609.hp1 HG00609.hp2 HG01496.hp2 others(33): Show |
intron_variant | MODIFIER | c.30+829A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115624548 | ||||||
| chr3:115624853
|
G | T | 1 | a0001c0001t0002g0205 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.30+1134G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115624853 | ||||||
| chr3:115625051
|
G | A | 11 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0213others(8): Show | 11 | HG01261.hp1 HG01975.hp1 HG02004.hp1 others(8): Show |
intron_variant | MODIFIER | c.30+1332G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115625051 | ||||||
| chr3:115625132
|
G | C | 1 | a0001c0001t0002g0218 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.30+1413G>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115625132 | ||||||
| chr3:115625206
|
C | CATAA | 96 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0022others(93): Show | 96 | HG00408.hp2 HG00544.hp1 HG00621.hp1 others(93): Show |
intron_variant | MODIFIER | c.30+1508_30+1511dup others(4): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115625206 | |||||
| chr3:115625206
|
C | CATAAATA others(1): Show |
44 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0033others(41): Show | 44 | HG00609.hp1 HG00609.hp2 HG01255.hp2 others(41): Show |
intron_variant | MODIFIER | c.30+1504_30+1511dup others(8): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115625206 | |||||
| chr3:115625206
|
C | CATAAATA others(5): Show |
16 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0036others(13): Show | 16 | HG01261.hp1 HG01517.hp2 HG01975.hp1 others(13): Show |
intron_variant | MODIFIER | c.30+1500_30+1511dup others(12): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115625206 | |||||
| chr3:115625206
|
C | CATAAATA others(13): Show |
4 | a0001c0001t0001g0339a0001c0001t0001g0342a0001c0001t0005g0340others(1): Show | 4 | HG02055.hp2 HG02809.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.30+1492_30+1511dup others(20): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115625206 | |||||
| chr3:115625250
|
T | C | 8 | a0001c0001t0001g0345a0001c0001t0001g0346a0001c0001t0001g0347others(5): Show | 8 | HG01081.hp2 HG01109.hp1 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.30+1531T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115625250 | ||||||
| chr3:115625272
|
T | A | 109 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0022others(106): Show | 109 | HG00408.hp2 HG00544.hp1 HG00621.hp1 others(106): Show |
intron_variant | MODIFIER | c.30+1553T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115625272 | ||||||
| chr3:115625361
|
C | T | 1 | a0001c0001t0005g0233 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.30+1642C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115625361 | ||||||
| chr3:115625494
|
A | G | 1 | a0001c0001t0002g0163 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.30+1775A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115625494 | ||||||
| chr3:115625596
|
C | T | 4 | a0001c0001t0001g0339a0001c0001t0001g0342a0001c0001t0005g0340others(1): Show | 4 | HG02055.hp2 HG02809.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.30+1877C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115625596 | ||||||
| chr3:115625663
|
A | G | 1 | a0001c0001t0004g0309 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.30+1944A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115625663 | ||||||
| chr3:115625761
|
G | T | 1 | a0001c0001t0001g0350 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.30+2042G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115625761 | ||||||
| chr3:115625840
|
T | C | 1 | a0001c0001t0002g0164 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.30+2121T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115625840 | ||||||
| chr3:115626093
|
C | T | 1 | a0001c0001t0002g0163 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.30+2374C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115626093 | ||||||
| chr3:115626140
|
C | T | 4 | a0001c0001t0001g0215a0001c0001t0001g0216a0001c0001t0002g0217others(1): Show | 4 | HG01975.hp1 HG02004.hp1 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.30+2421C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115626140 | ||||||
| chr3:115626202
|
T | C | 1 | a0001c0001t0001g0038 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.30+2483T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115626202 | ||||||
| chr3:115626219
|
C | G | 11 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0228others(8): Show | 11 | HG00733.hp1 HG00735.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.30+2500C>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115626219 | ||||||
| chr3:115626478
|
G | C | 1 | a0001c0001t0001g0234 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.30+2759G>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115626478 | ||||||
| chr3:115626481
|
T | G | 11 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0228others(8): Show | 11 | HG00733.hp1 HG00735.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.30+2762T>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115626481 | ||||||
| chr3:115626553
|
T | C | 1 | a0001c0002t0002g0039 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.30+2834T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115626553 | ||||||
| chr3:115626610
|
G | T | 1 | a0001c0001t0001g0085 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.30+2891G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115626610 | ||||||
| chr3:115626710
|
G | T | 1 | a0001c0001t0001g0234 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.30+2991G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115626710 | ||||||
| chr3:115626721
|
G | A | 1 | a0001c0001t0001g0094 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.30+3002G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115626721 | ||||||
| chr3:115626817
|
C | T | 1 | a0001c0001t0001g0234 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.30+3098C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115626817 | ||||||
| chr3:115627045
|
T | C | 3 | a0001c0001t0001g0313a0001c0001t0005g0343a0001c0001t0005g0344 | 3 | HG01361.hp1 HG03225.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.30+3326T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115627045 | ||||||
| chr3:115627105
|
T | G | 1 | a0001c0001t0001g0345 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.30+3386T>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115627105 | ||||||
| chr3:115627122
|
CTTTTTTC others(5): Show |
C | 4 | a0001c0001t0001g0339a0001c0001t0001g0342a0001c0001t0005g0340others(1): Show | 4 | HG02055.hp2 HG02809.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.30+3410_30+3421del others(12): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115627122 | |||||
| chr3:115627133
|
CT | C | 192 | a0001c0001t0001g0004a0001c0001t0001g0028a0001c0001t0001g0031others(189): Show | 192 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(189): Show |
intron_variant | MODIFIER | c.30+3430delT | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115627133 | |||||
| chr3:115627133
|
CTT | C | 134 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0017others(131): Show | 135 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.30+3429_30+3430del others(2): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115627133 | |||||
| chr3:115627133
|
CTTT | C | 13 | a0001c0001t0001g0040a0001c0001t0001g0086a0001c0001t0001g0087others(10): Show | 13 | HG00639.hp2 HG01069.hp2 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.30+3428_30+3430del others(3): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115627133 | |||||
| chr3:115627286
|
CAG | C | 6 | a0001c0001t0001g0004a0001c0001t0001g0307a0001c0001t0002g0308others(3): Show | 6 | HG02280.hp1 HG02451.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.30+3570_30+3571del others(2): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115627286 | |||||
| chr3:115627349
|
T | C | 2 | a0001c0001t0001g0209a0001c0002t0001g0035 | 2 | HG02615.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.30+3630T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115627349 | ||||||
| chr3:115627571
|
T | G | 81 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0017others(78): Show | 82 | HG00140.hp1 HG00438.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.30+3852T>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115627571 | ||||||
| chr3:115627646
|
A | G | 6 | a0001c0001t0001g0339a0001c0001t0001g0342a0001c0001t0005g0340others(3): Show | 6 | HG02055.hp2 HG02809.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.30+3927A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115627646 | ||||||
| chr3:115627901
|
T | C | 1 | a0001c0001t0001g0002 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.30+4182T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115627901 | ||||||
| chr3:115627987
|
C | A | 1 | a0001c0001t0002g0163 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.30+4268C>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115627987 | ||||||
| chr3:115627989
|
A | C | 1 | a0001c0001t0002g0163 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.30+4270A>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115627989 | ||||||
| chr3:115628002
|
A | G | 2 | a0001c0001t0001g0306a0001c0001t0001g0307 | 2 | HG02451.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.30+4283A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115628002 | ||||||
| chr3:115628018
|
T | G | 4 | a0001c0001t0001g0242a0001c0001t0002g0243a0001c0001t0002g0244others(1): Show | 4 | HG02145.hp1 HG02280.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.30+4299T>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115628018 | ||||||
| chr3:115628028
|
A | C | 6 | a0001c0001t0001g0339a0001c0001t0001g0342a0001c0001t0005g0340others(3): Show | 6 | HG02055.hp2 HG02809.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.30+4309A>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115628028 | ||||||
| chr3:115628029
|
T | C | 2 | a0001c0001t0001g0224a0001c0001t0001g0225 | 2 | HG02630.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.30+4310T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115628029 | ||||||
| chr3:115628237
|
C | T | 1 | a0001c0001t0012g0300 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.30+4518C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115628237 | ||||||
| chr3:115628302
|
T | C | 92 | a0001c0001t0001g0024a0001c0001t0001g0036a0001c0001t0001g0037others(89): Show | 92 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.30+4583T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115628302 | ||||||
| chr3:115628337
|
C | T | 1 | a0001c0001t0002g0203 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.30+4618C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115628337 | ||||||
| chr3:115628367
|
T | C | 6 | a0001c0001t0001g0339a0001c0001t0001g0342a0001c0001t0005g0340others(3): Show | 6 | HG02055.hp2 HG02809.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.30+4648T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115628367 | ||||||
| chr3:115628382
|
C | T | 1 | a0001c0001t0005g0233 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.30+4663C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115628382 | ||||||
| chr3:115628709
|
G | T | 81 | a0001c0001t0001g0024a0001c0001t0001g0040a0001c0001t0001g0061others(78): Show | 81 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.30+4990G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115628709 | ||||||
| chr3:115628745
|
A | G | 1 | a0001c0001t0001g0234 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.30+5026A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115628745 | ||||||
| chr3:115628778
|
A | G | 1 | a0001c0001t0002g0334 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.30+5059A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115628778 | ||||||
| chr3:115628793
|
C | G | 6 | a0001c0001t0001g0339a0001c0001t0001g0342a0001c0001t0005g0340others(3): Show | 6 | HG02055.hp2 HG02809.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.30+5074C>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115628793 | ||||||
| chr3:115628829
|
A | G | 75 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0017others(72): Show | 76 | HG00140.hp1 HG00438.hp2 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.30+5110A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115628829 | ||||||
| chr3:115628972
|
G | A | 1 | a0001c0001t0013g0219 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.30+5253G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115628972 | ||||||
| chr3:115629104
|
C | T | 1 | a0001c0001t0005g0233 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.30+5385C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115629104 | ||||||
| chr3:115629162
|
T | G | 11 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0228others(8): Show | 11 | HG00733.hp1 HG00735.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.30+5443T>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115629162 | ||||||
| chr3:115629323
|
T | C | 17 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0228others(14): Show | 17 | HG00733.hp1 HG00735.hp1 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.30+5604T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115629323 | ||||||
| chr3:115629408
|
C | CT | 138 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0024others(135): Show | 139 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.30+5703dupT | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115629408 | |||||
| chr3:115629408
|
C | CTT | 10 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0298others(7): Show | 10 | HG01884.hp1 HG02055.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.30+5702_30+5703dup others(2): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115629408 | |||||
| chr3:115629540
|
G | C | 1 | a0001c0001t0003g0316 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.30+5821G>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115629540 | ||||||
| chr3:115629691
|
G | A | 1 | a0001c0001t0013g0219 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.30+5972G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115629691 | ||||||
| chr3:115629862
|
A | T | 2 | a0001c0001t0001g0202a0001c0001t0002g0201 | 2 | NA18998.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.30+6143A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115629862 | ||||||
| chr3:115629959
|
G | A | 11 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0228others(8): Show | 11 | HG00733.hp1 HG00735.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.30+6240G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115629959 | ||||||
| chr3:115630067
|
C | G | 11 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0213others(8): Show | 11 | HG01261.hp1 HG01975.hp1 HG02004.hp1 others(8): Show |
intron_variant | MODIFIER | c.30+6348C>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115630067 | ||||||
| chr3:115630309
|
G | A | 2 | a0001c0001t0001g0210a0001c0001t0002g0211 | 2 | HG00558.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.30+6590G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115630309 | ||||||
| chr3:115630309
|
G | C | 51 | a0001c0001t0001g0002a0001c0001t0001g0038a0001c0001t0001g0041others(48): Show | 52 | HG00140.hp1 HG00438.hp2 HG00558.hp1 others(49): Show |
intron_variant | MODIFIER | c.30+6590G>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115630309 | ||||||
| chr3:115630417
|
A | G | 6 | a0001c0001t0001g0234a0001c0001t0001g0242a0001c0001t0002g0243others(3): Show | 6 | HG02109.hp2 HG02145.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.30+6698A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115630417 | ||||||
| chr3:115630479
|
T | G | 6 | a0001c0001t0001g0234a0001c0001t0001g0242a0001c0001t0002g0243others(3): Show | 6 | HG02109.hp2 HG02145.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.30+6760T>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115630479 | ||||||
| chr3:115630543
|
C | T | 3 | a0001c0001t0001g0017a0001c0001t0001g0213a0001c0001t0002g0018 | 3 | NA18939.hp1 NA18943.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.30+6824C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115630543 | ||||||
| chr3:115630621
|
G | A | 5 | a0001c0001t0001g0004a0001c0001t0002g0308a0001c0001t0005g0003others(2): Show | 5 | HG02280.hp1 HG03195.hp1 NA19043.hp1 others(2): Show |
intron_variant | MODIFIER | c.30+6902G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115630621 | ||||||
| chr3:115630949
|
A | G | 321 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0015others(318): Show | 322 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.30+7230A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115630949 | ||||||
| chr3:115630995
|
A | G | 3 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0001g0234 | 3 | HG02109.hp2 HG02630.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.30+7276A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115630995 | ||||||
| chr3:115631084
|
T | C | 7 | a0001c0001t0001g0002a0001c0001t0001g0221a0001c0001t0001g0222others(4): Show | 7 | HG01433.hp1 HG02922.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.30+7365T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115631084 | ||||||
| chr3:115631156
|
A | C | 1 | a0001c0001t0003g0241 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.30+7437A>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115631156 | ||||||
| chr3:115631279
|
C | T | 1 | a0001c0001t0001g0081 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.30+7560C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115631279 | ||||||
| chr3:115631335
|
G | T | 1 | a0001c0001t0004g0333 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.30+7616G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115631335 | ||||||
| chr3:115631359
|
G | A | 70 | a0001c0001t0001g0094a0001c0001t0001g0104a0001c0001t0001g0110others(67): Show | 70 | HG00408.hp2 HG00544.hp1 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.30+7640G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115631359 | ||||||
| chr3:115631400
|
T | G | 42 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0033others(39): Show | 42 | HG00609.hp1 HG00609.hp2 HG01255.hp2 others(39): Show |
intron_variant | MODIFIER | c.30+7681T>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115631400 | ||||||
| chr3:115631435
|
G | C | 1 | a0001c0001t0001g0306 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.30+7716G>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115631435 | ||||||
| chr3:115631516
|
A | G | 2 | a0001c0001t0004g0159a0001c0001t0004g0160 | 2 | NA18968.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.30+7797A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115631516 | ||||||
| chr3:115631826
|
G | A | 4 | a0001c0001t0002g0317a0001c0001t0002g0318a0001c0001t0003g0206others(1): Show | 4 | NA18975.hp2 NA18986.hp1 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.30+8107G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115631826 | ||||||
| chr3:115632661
|
G | A | 12 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0213others(9): Show | 12 | HG01261.hp1 HG01975.hp1 HG02004.hp1 others(9): Show |
intron_variant | MODIFIER | c.30+8942G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115632661 | ||||||
| chr3:115632954
|
G | A | 1 | a0001c0002t0001g0095 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.30+9235G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115632954 | ||||||
| chr3:115632969
|
G | A | 1 | a0001c0001t0001g0019 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.30+9250G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115632969 | ||||||
| chr3:115632977
|
A | G | 5 | a0001c0001t0001g0339a0001c0001t0001g0342a0001c0001t0005g0340others(2): Show | 5 | HG02055.hp2 HG02809.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.30+9258A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115632977 | ||||||
| chr3:115633002
|
T | G | 1 | a0001c0001t0002g0164 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.30+9283T>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115633002 | ||||||
| chr3:115633023
|
AG | A | 82 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0040others(79): Show | 82 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.30+9305delG | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115633023 | ||||||
| chr3:115633024
|
G | A | 1 | a0001c0001t0002g0163 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.30+9305G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115633024 | ||||||
| chr3:115633037
|
G | A | 5 | a0001c0001t0001g0004a0001c0001t0002g0308a0001c0001t0005g0003others(2): Show | 5 | HG02280.hp1 HG03195.hp1 NA19043.hp1 others(2): Show |
intron_variant | MODIFIER | c.30+9318G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115633037 | ||||||
| chr3:115633037
|
G | C | 1 | a0001c0001t0013g0219 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.30+9318G>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115633037 | ||||||
| chr3:115633128
|
C | T | 5 | a0001c0001t0001g0004a0001c0001t0002g0308a0001c0001t0005g0003others(2): Show | 5 | HG02280.hp1 HG03195.hp1 NA19043.hp1 others(2): Show |
intron_variant | MODIFIER | c.30+9409C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115633128 | ||||||
| chr3:115633132
|
A | G | 1 | a0001c0001t0005g0233 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.30+9413A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115633132 | ||||||
| chr3:115633242
|
G | C | 1 | a0001c0001t0002g0164 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.30+9523G>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115633242 | ||||||
| chr3:115633338
|
A | C | 1 | a0001c0001t0002g0164 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.30+9619A>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115633338 | ||||||
| chr3:115633480
|
G | A | 2 | a0001c0001t0001g0224a0001c0001t0001g0225 | 2 | HG02630.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.30+9761G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115633480 | ||||||
| chr3:115633511
|
G | A | 4 | a0001c0001t0002g0317a0001c0001t0002g0318a0001c0001t0003g0206others(1): Show | 4 | NA18975.hp2 NA18986.hp1 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.30+9792G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115633511 | ||||||
| chr3:115633591
|
C | T | 1 | a0001c0001t0001g0234 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.30+9872C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115633591 | ||||||
| chr3:115633625
|
C | T | 1 | a0001c0001t0013g0219 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.30+9906C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115633625 | ||||||
| chr3:115634071
|
C | T | 1 | a0001c0001t0013g0219 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.30+10352C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115634071 | ||||||
| chr3:115634185
|
T | C | 89 | a0001c0001t0001g0024a0001c0001t0001g0036a0001c0001t0001g0037others(86): Show | 89 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.30+10466T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115634185 | ||||||
| chr3:115634500
|
A | C | 7 | a0001c0001t0001g0339a0001c0001t0001g0342a0001c0001t0005g0340others(4): Show | 7 | HG02055.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.30+10781A>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115634500 | ||||||
| chr3:115634567
|
C | T | 2 | a0001c0001t0001g0015a0001c0001t0003g0016 | 2 | HG01261.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.30+10848C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115634567 | ||||||
| chr3:115634663
|
T | C | 1 | a0001c0001t0001g0224 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.30+10944T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115634663 | ||||||
| chr3:115634668
|
G | T | 2 | a0001c0001t0001g0224a0001c0001t0001g0225 | 2 | HG02630.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.30+10949G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115634668 | ||||||
| chr3:115634693
|
C | T | 1 | a0001c0001t0012g0300 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.30+10974C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115634693 | ||||||
| chr3:115634723
|
T | C | 2 | a0001c0001t0001g0224a0001c0001t0001g0225 | 2 | HG02630.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.30+11004T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115634723 | ||||||
| chr3:115634770
|
AAAATAAA others(1): Show |
A | 4 | a0001c0001t0001g0242a0001c0001t0002g0243a0001c0001t0002g0244others(1): Show | 4 | HG02145.hp1 HG02280.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.30+11070_30+11077d others(10): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115634770 | |||||
| chr3:115634826
|
C | T | 12 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0213others(9): Show | 12 | HG01261.hp1 HG01975.hp1 HG02004.hp1 others(9): Show |
intron_variant | MODIFIER | c.30+11107C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115634826 | ||||||
| chr3:115634916
|
T | C | 1 | a0001c0001t0001g0173 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.30+11197T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115634916 | ||||||
| chr3:115634972
|
A | G | 127 | a0001c0001t0001g0004a0001c0001t0001g0028a0001c0001t0001g0031others(124): Show | 127 | HG00408.hp2 HG00544.hp1 HG00609.hp1 others(124): Show |
intron_variant | MODIFIER | c.30+11253A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115634972 | ||||||
| chr3:115635062
|
T | C | 1 | a0001c0001t0013g0219 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.30+11343T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115635062 | ||||||
| chr3:115635358
|
A | T | 41 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0185others(38): Show | 41 | HG00140.hp2 HG00673.hp1 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.30+11639A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115635358 | ||||||
| chr3:115635392
|
A | G | 6 | a0001c0001t0001g0002a0001c0001t0001g0234a0001c0001t0005g0096others(3): Show | 6 | HG01433.hp1 HG02109.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.30+11673A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115635392 | ||||||
| chr3:115635408
|
C | T | 1 | a0001c0001t0002g0158 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.30+11689C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115635408 | ||||||
| chr3:115635440
|
A | G | 1 | a0001c0001t0001g0019 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.30+11721A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115635440 | ||||||
| chr3:115635701
|
C | G | 3 | a0001c0001t0003g0155a0001c0001t0003g0156a0001c0001t0003g0157 | 3 | HG00642.hp2 HG01074.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.30+11982C>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115635701 | ||||||
| chr3:115635703
|
G | T | 1 | a0001c0001t0002g0171 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.30+11984G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115635703 | ||||||
| chr3:115635761
|
A | C | 2 | a0001c0001t0002g0293a0001c0001t0002g0294 | 2 | HG03704.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.30+12042A>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115635761 | ||||||
| chr3:115635864
|
T | C | 5 | a0001c0001t0001g0242a0001c0001t0002g0243a0001c0001t0002g0244others(2): Show | 5 | HG02145.hp1 HG02280.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.30+12145T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115635864 | ||||||
| chr3:115635933
|
G | A | 2 | a0001c0001t0001g0224a0001c0001t0001g0225 | 2 | HG02630.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.30+12214G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115635933 | ||||||
| chr3:115635948
|
C | A | 1 | a0001c0001t0001g0041 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.30+12229C>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115635948 | ||||||
| chr3:115635968
|
C | G | 1 | a0001c0001t0003g0001 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.30+12249C>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115635968 | ||||||
| chr3:115635988
|
C | T | 4 | a0001c0001t0001g0242a0001c0001t0002g0243a0001c0001t0002g0244others(1): Show | 4 | HG02145.hp1 HG02280.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.30+12269C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115635988 | ||||||
| chr3:115636099
|
C | T | 2 | a0001c0001t0001g0153a0001c0001t0015g0154 | 2 | HG01192.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.30+12380C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115636099 | ||||||
| chr3:115636282
|
T | A | 2 | a0001c0001t0001g0224a0001c0001t0001g0225 | 2 | HG02630.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.30+12563T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115636282 | ||||||
| chr3:115636358
|
T | C | 2 | a0001c0001t0001g0224a0001c0001t0001g0225 | 2 | HG02630.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.30+12639T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115636358 | ||||||
| chr3:115636369
|
T | G | 1 | a0001c0001t0005g0343 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.30+12650T>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115636369 | ||||||
| chr3:115636414
|
A | C | 2 | a0001c0001t0001g0224a0001c0001t0001g0225 | 2 | HG02630.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.30+12695A>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115636414 | ||||||
| chr3:115636571
|
T | G | 197 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0015others(194): Show | 198 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.30+12852T>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115636571 | ||||||
| chr3:115636682
|
G | A | 2 | a0001c0001t0004g0247a0001c0001t0004g0248 | 2 | HG00673.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.30+12963G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115636682 | ||||||
| chr3:115636739
|
G | A | 2 | a0001c0001t0001g0224a0001c0001t0001g0225 | 2 | HG02630.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.30+13020G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115636739 | ||||||
| chr3:115637031
|
T | C | 1 | a0001c0001t0005g0204 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.30+13312T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115637031 | ||||||
| chr3:115637114
|
A | G | 1 | a0001c0001t0013g0219 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.30+13395A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115637114 | ||||||
| chr3:115637117
|
A | G | 45 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0047others(42): Show | 46 | HG00558.hp1 HG00738.hp1 HG00741.hp2 others(43): Show |
intron_variant | MODIFIER | c.30+13398A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115637117 | ||||||
| chr3:115637126
|
C | T | 2 | a0001c0001t0001g0152a0001c0001t0002g0151 | 2 | NA18968.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.30+13407C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115637126 | ||||||
| chr3:115637160
|
A | T | 4 | a0001c0001t0001g0290a0001c0001t0001g0291a0001c0001t0001g0292others(1): Show | 4 | HG01074.hp2 HG01099.hp1 HG01256.hp1 others(1): Show |
intron_variant | MODIFIER | c.30+13441A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115637160 | ||||||
| chr3:115637162
|
A | C | 1 | a0001c0001t0005g0233 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.30+13443A>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115637162 | ||||||
| chr3:115637329
|
C | G | 49 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(46): Show | 49 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(46): Show |
intron_variant | MODIFIER | c.30+13610C>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115637329 | ||||||
| chr3:115637755
|
C | T | 2 | a0001c0001t0003g0288a0001c0001t0004g0287 | 2 | NA18970.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.30+14036C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115637755 | ||||||
| chr3:115637813
|
T | C | 22 | a0001c0001t0001g0104a0001c0001t0001g0110a0001c0001t0001g0112others(19): Show | 22 | HG00408.hp2 HG00621.hp2 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.30+14094T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115637813 | ||||||
| chr3:115638167
|
G | A | 1 | a0001c0001t0013g0219 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.30+14448G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115638167 | ||||||
| chr3:115638511
|
CT | C | 126 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0017others(123): Show | 126 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(123): Show |
intron_variant | MODIFIER | c.30+14806delT | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115638511 | |||||
| chr3:115638559
|
T | A | 2 | a0001c0001t0005g0204a0001c0001t0005g0233 | 2 | HG02895.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.30+14840T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115638559 | ||||||
| chr3:115638773
|
C | T | 1 | a0001c0001t0005g0233 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.30+15054C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115638773 | ||||||
| chr3:115638851
|
A | G | 2 | a0001c0001t0001g0298a0001c0001t0005g0299 | 2 | HG02559.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.30+15132A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115638851 | ||||||
| chr3:115638958
|
G | A | 1 | a0001c0001t0005g0233 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.30+15239G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115638958 | ||||||
| chr3:115638995
|
T | A | 2 | a0001c0001t0001g0015a0001c0001t0003g0016 | 2 | HG01261.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.30+15276T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115638995 | ||||||
| chr3:115639004
|
A | G | 3 | a0001c0001t0001g0242a0001c0001t0002g0243a0001c0001t0002g0244 | 3 | HG02145.hp1 HG02280.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.30+15285A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115639004 | ||||||
| chr3:115639308
|
G | A | 183 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0015others(180): Show | 184 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(181): Show |
intron_variant | MODIFIER | c.30+15589G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115639308 | ||||||
| chr3:115639326
|
G | A | 1 | a0001c0001t0012g0300 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.30+15607G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115639326 | ||||||
| chr3:115639376
|
C | T | 1 | a0001c0001t0002g0208 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.30+15657C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115639376 | ||||||
| chr3:115639471
|
C | T | 1 | a0001c0001t0002g0286 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.30+15752C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115639471 | ||||||
| chr3:115639511
|
G | C | 1 | a0001c0001t0001g0224 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.30+15792G>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115639511 | ||||||
| chr3:115639600
|
T | C | 2 | a0001c0001t0001g0224a0001c0001t0001g0225 | 2 | HG02630.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.30+15881T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115639600 | ||||||
| chr3:115639820
|
A | T | 1 | a0001c0001t0001g0060 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.30+16101A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115639820 | ||||||
| chr3:115639977
|
A | C | 143 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0028others(140): Show | 143 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(140): Show |
intron_variant | MODIFIER | c.30+16258A>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115639977 | ||||||
| chr3:115640034
|
T | G | 1 | a0001c0002t0002g0039 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.30+16315T>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115640034 | ||||||
| chr3:115640263
|
T | G | 1 | a0001c0001t0003g0214 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.30+16544T>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115640263 | ||||||
| chr3:115640418
|
C | T | 43 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(40): Show | 43 | HG00140.hp1 HG00140.hp2 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.30+16699C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115640418 | ||||||
| chr3:115640534
|
G | T | 9 | a0001c0001t0001g0313a0001c0001t0001g0346a0001c0001t0001g0347others(6): Show | 9 | HG01081.hp2 HG01109.hp1 HG01361.hp1 others(6): Show |
intron_variant | MODIFIER | c.30+16815G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115640534 | ||||||
| chr3:115640586
|
C | T | 1 | a0001c0001t0005g0204 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.30+16867C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115640586 | ||||||
| chr3:115640708
|
G | C | 3 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0230 | 3 | HG00733.hp1 HG00735.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.30+16989G>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115640708 | ||||||
| chr3:115640759
|
G | T | 4 | a0001c0001t0002g0317a0001c0001t0002g0318a0001c0001t0003g0206others(1): Show | 4 | NA18975.hp2 NA18986.hp1 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.30+17040G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115640759 | ||||||
| chr3:115640880
|
G | A | 1 | a0001c0001t0005g0011 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.30+17161G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115640880 | ||||||
| chr3:115640925
|
C | CT | 94 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0060others(91): Show | 94 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.30+17213dupT | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115640925 | |||||
| chr3:115640925
|
C | T | 1 | a0001c0001t0002g0103 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.30+17206C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115640925 | ||||||
| chr3:115640965
|
C | CCCTT | 97 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0060others(94): Show | 97 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.30+17260_30+17263d others(6): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115640965 | |||||
| chr3:115641035
|
T | C | 93 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0060others(90): Show | 93 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.30+17316T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115641035 | ||||||
| chr3:115641036
|
T | C | 1 | a0001c0001t0015g0154 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.30+17317T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115641036 | ||||||
| chr3:115641036
|
TC | T | 93 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0060others(90): Show | 93 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.30+17318delC | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115641036 | ||||||
| chr3:115641037
|
C | T | 1 | a0001c0001t0015g0154 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.30+17318C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115641037 | ||||||
| chr3:115641130
|
G | A | 87 | a0001c0001t0001g0017a0001c0001t0001g0060a0001c0001t0001g0064others(84): Show | 87 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.30+17411G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115641130 | ||||||
| chr3:115641241
|
A | G | 1 | a0001c0001t0013g0219 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.30+17522A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115641241 | ||||||
| chr3:115641332
|
G | T | 6 | a0001c0001t0001g0004a0001c0001t0001g0306a0001c0001t0001g0307others(3): Show | 6 | HG02451.hp2 HG03195.hp1 NA19043.hp1 others(3): Show |
intron_variant | MODIFIER | c.30+17613G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115641332 | ||||||
| chr3:115641345
|
C | T | 40 | a0001c0001t0001g0002a0001c0001t0001g0088a0001c0001t0001g0089others(37): Show | 40 | HG00609.hp1 HG00609.hp2 HG01433.hp1 others(37): Show |
intron_variant | MODIFIER | c.30+17626C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115641345 | ||||||
| chr3:115641365
|
C | T | 1 | a0001c0001t0001g0172 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.30+17646C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115641365 | ||||||
| chr3:115641382
|
TTG | T | 3 | a0001c0001t0001g0346a0001c0001t0001g0347a0001c0001t0001g0350 | 3 | HG01891.hp2 HG02970.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.30+17677_30+17678d others(4): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115641382 | |||||
| chr3:115641401
|
C | A | 3 | a0001c0001t0002g0252a0001c0002t0001g0253a0001c0002t0001g0254 | 3 | NA18939.hp2 NA18999.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.30+17682C>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115641401 | ||||||
| chr3:115641450
|
T | G | 1 | a0001c0001t0002g0199 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.30+17731T>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115641450 | ||||||
| chr3:115641452
|
T | G | 106 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0038others(103): Show | 107 | HG00140.hp2 HG00558.hp1 HG00673.hp1 others(104): Show |
intron_variant | MODIFIER | c.30+17733T>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115641452 | ||||||
| chr3:115641454
|
T | G | 241 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0017others(238): Show | 242 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.30+17735T>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115641454 | ||||||
| chr3:115641456
|
G | T | 2 | a0001c0001t0002g0317a0001c0001t0002g0318 | 2 | NA18975.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.30+17737G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115641456 | ||||||
| chr3:115641510
|
T | TCA | 8 | a0001c0001t0001g0040a0001c0001t0001g0061a0001c0001t0001g0210others(5): Show | 8 | HG00544.hp2 HG00558.hp2 HG00639.hp2 others(5): Show |
intron_variant | MODIFIER | c.30+17823_30+17824d others(4): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115641510 | |||||
| chr3:115641510
|
T | TCACACAC others(1): Show |
18 | a0001c0001t0001g0079a0001c0001t0001g0091a0001c0001t0001g0092others(15): Show | 18 | HG01106.hp1 HG02109.hp2 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.30+17817_30+17824d others(10): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115641510 | |||||
| chr3:115641510
|
T | TCACACAC others(3): Show |
54 | a0001c0001t0001g0056a0001c0001t0001g0060a0001c0001t0001g0072others(51): Show | 55 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.30+17815_30+17824d others(12): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115641510 | |||||
| chr3:115641510
|
T | TCACACAC others(5): Show |
45 | a0001c0001t0001g0017a0001c0001t0001g0028a0001c0001t0001g0031others(42): Show | 45 | HG00408.hp2 HG00558.hp1 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.30+17813_30+17824d others(14): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115641510 | |||||
| chr3:115641510
|
T | TCACACAC others(7): Show |
13 | a0001c0001t0001g0004a0001c0001t0001g0019a0001c0001t0001g0119others(10): Show | 13 | HG00642.hp1 HG00642.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.30+17811_30+17824d others(16): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115641510 | |||||
| chr3:115641510
|
T | TCACACAC others(9): Show |
1 | a0001c0001t0001g0306 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.30+17809_30+17824d others(18): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115641510 | |||||
| chr3:115641510
|
T | TCACACAC others(11): Show |
1 | a0001c0001t0001g0069 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.30+17807_30+17824d others(20): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115641510 | |||||
| chr3:115641510
|
T | TCACACAC others(15): Show |
1 | a0001c0001t0001g0172 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.30+17803_30+17824d others(24): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115641510 | |||||
| chr3:115641539
|
C | CACACACA others(3): Show |
2 | a0001c0001t0010g0245a0001c0001t0010g0246 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.30+17824_30+17825i others(12): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115641539 | |||||
| chr3:115641543
|
C | CACACACA others(9): Show |
3 | a0001c0001t0003g0016a0001c0001t0008g0235a0001c0001t0008g0236 | 3 | HG01069.hp2 HG01081.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.30+17824_30+17825i others(18): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115641543 | ||||||
| chr3:115641543
|
C | CACACACA others(7): Show |
2 | a0001c0001t0002g0237a0001c0001t0002g0337 | 2 | HG01192.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.30+17824_30+17825i others(16): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115641543 | ||||||
| chr3:115641543
|
C | CACACACA others(5): Show |
25 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0050others(22): Show | 25 | HG00738.hp1 HG00741.hp2 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.30+17824_30+17825i others(14): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115641543 | ||||||
| chr3:115641543
|
C | CACACACA others(3): Show |
3 | a0001c0001t0001g0207a0001c0001t0002g0208a0001c0001t0005g0233 | 3 | HG03017.hp2 HG03516.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.30+17824_30+17825i others(12): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115641543 | ||||||
| chr3:115641543
|
C | CACACACA others(1): Show |
5 | a0001c0001t0001g0058a0001c0001t0001g0332a0001c0001t0002g0320others(2): Show | 5 | HG00609.hp2 HG02622.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.30+17824_30+17825i others(10): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115641543 | ||||||
| chr3:115641543
|
C | CACACAGA others(3): Show |
16 | a0001c0001t0001g0174a0001c0001t0001g0339a0001c0001t0001g0342others(13): Show | 16 | HG00673.hp1 HG01069.hp1 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.30+17824_30+17825i others(12): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115641543 | ||||||
| chr3:115641543
|
C | CACACAT | 35 | a0001c0001t0001g0002a0001c0001t0001g0088a0001c0001t0001g0089others(32): Show | 35 | HG00609.hp1 HG01433.hp1 HG01496.hp2 others(32): Show |
intron_variant | MODIFIER | c.30+17824_30+17825i others(8): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115641543 | ||||||
| chr3:115641543
|
C | CACAGACA others(1): Show |
28 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(25): Show | 28 | HG00140.hp1 HG00140.hp2 HG01169.hp2 others(25): Show |
intron_variant | MODIFIER | c.30+17824_30+17825i others(10): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115641543 | ||||||
| chr3:115641543
|
C | CAGACAT | 5 | a0001c0001t0001g0173a0001c0001t0001g0197a0001c0001t0001g0302others(2): Show | 5 | HG00280.hp1 HG01934.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.30+17824_30+17825i others(8): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115641543 | ||||||
| chr3:115641543
|
C | CAT | 11 | a0001c0001t0001g0313a0001c0001t0001g0346a0001c0001t0001g0347others(8): Show | 11 | HG00735.hp2 HG01081.hp2 HG01109.hp1 others(8): Show |
intron_variant | MODIFIER | c.30+17824_30+17825i others(4): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115641543 | ||||||
| chr3:115641555
|
G | C | 1 | a0001c0001t0002g0164 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.30+17836G>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115641555 | ||||||
| chr3:115641582
|
A | C | 51 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(48): Show | 51 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(48): Show |
intron_variant | MODIFIER | c.30+17863A>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115641582 | ||||||
| chr3:115641753
|
G | A | 1 | a0001c0001t0012g0300 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.30+18034G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115641753 | ||||||
| chr3:115641861
|
C | T | 1 | a0001c0001t0013g0219 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.30+18142C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115641861 | ||||||
| chr3:115641981
|
A | G | 1 | a0001c0001t0013g0219 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.30+18262A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115641981 | ||||||
| chr3:115642160
|
A | G | 3 | a0001c0001t0001g0215a0001c0001t0001g0216a0001c0001t0002g0217 | 3 | HG01975.hp1 HG02004.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.30+18441A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115642160 | ||||||
| chr3:115642289
|
C | G | 6 | a0001c0001t0001g0336a0001c0001t0002g0147a0001c0001t0002g0148others(3): Show | 6 | NA18970.hp2 NA19000.hp2 NA19063.hp1 others(3): Show |
intron_variant | MODIFIER | c.30+18570C>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115642289 | ||||||
| chr3:115642304
|
A | G | 1 | a0001c0001t0002g0337 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.30+18585A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115642304 | ||||||
| chr3:115642406
|
A | AT | 54 | a0001c0001t0001g0002a0001c0001t0001g0028a0001c0001t0001g0031others(51): Show | 54 | HG00609.hp1 HG00609.hp2 HG01255.hp2 others(51): Show |
intron_variant | MODIFIER | c.30+18702dupT | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115642406 | |||||
| chr3:115642406
|
AT | A | 7 | a0001c0001t0001g0262a0001c0001t0001g0307a0001c0001t0002g0178others(4): Show | 7 | HG01069.hp1 HG01069.hp2 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.30+18702delT | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115642406 | |||||
| chr3:115642482
|
G | A | 1 | a0001c0001t0003g0214 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.30+18763G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115642482 | ||||||
| chr3:115642703
|
A | T | 2 | a0001c0001t0002g0178a0001c0001t0002g0184 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.30+18984A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115642703 | ||||||
| chr3:115642773
|
A | C | 50 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(47): Show | 50 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(47): Show |
intron_variant | MODIFIER | c.30+19054A>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115642773 | ||||||
| chr3:115642890
|
A | C | 57 | a0001c0001t0001g0002a0001c0001t0001g0028a0001c0001t0001g0031others(54): Show | 57 | HG00609.hp1 HG00609.hp2 HG01255.hp2 others(54): Show |
intron_variant | MODIFIER | c.30+19171A>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115642890 | ||||||
| chr3:115642989
|
G | A | 348 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0015others(345): Show | 349 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(346): Show |
intron_variant | MODIFIER | c.30+19270G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115642989 | ||||||
| chr3:115643031
|
T | C | 1 | a0001c0001t0003g0027 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.30+19312T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115643031 | ||||||
| chr3:115643170
|
T | C | 5 | a0001c0001t0001g0004a0001c0001t0001g0307a0001c0001t0005g0003others(2): Show | 5 | HG02451.hp2 HG03195.hp1 NA19043.hp1 others(2): Show |
intron_variant | MODIFIER | c.30+19451T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115643170 | ||||||
| chr3:115643179
|
C | G | 1 | a0001c0001t0013g0219 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.30+19460C>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115643179 | ||||||
| chr3:115643514
|
A | G | 1 | a0001c0001t0013g0219 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.30+19795A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115643514 | ||||||
| chr3:115643534
|
C | A | 3 | a0001c0001t0001g0038a0001c0001t0001g0050a0001c0001t0001g0051 | 3 | HG00741.hp2 HG03669.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.30+19815C>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115643534 | ||||||
| chr3:115643586
|
T | G | 1 | a0001c0001t0001g0197 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.30+19867T>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115643586 | ||||||
| chr3:115643689
|
C | T | 2 | a0001c0001t0001g0088a0001c0001t0001g0089 | 2 | HG00609.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.30+19970C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115643689 | ||||||
| chr3:115643690
|
A | G | 104 | a0001c0001t0001g0002a0001c0001t0001g0028a0001c0001t0001g0031others(101): Show | 104 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.30+19971A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115643690 | ||||||
| chr3:115643706
|
C | T | 1 | a0001c0001t0001g0240 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.30+19987C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115643706 | ||||||
| chr3:115643752
|
C | G | 50 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(47): Show | 50 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(47): Show |
intron_variant | MODIFIER | c.30+20033C>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115643752 | ||||||
| chr3:115643770
|
A | G | 1 | a0001c0001t0013g0219 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.30+20051A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115643770 | ||||||
| chr3:115643774
|
A | C | 50 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(47): Show | 50 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(47): Show |
intron_variant | MODIFIER | c.30+20055A>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115643774 | ||||||
| chr3:115643800
|
C | T | 126 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0017others(123): Show | 127 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.30+20081C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115643800 | ||||||
| chr3:115644190
|
T | C | 47 | a0001c0001t0001g0002a0001c0001t0001g0085a0001c0001t0001g0088others(44): Show | 47 | HG00609.hp1 HG00609.hp2 HG01433.hp1 others(44): Show |
intron_variant | MODIFIER | c.30+20471T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115644190 | ||||||
| chr3:115644561
|
A | G | 44 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(41): Show | 44 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(41): Show |
intron_variant | MODIFIER | c.30+20842A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115644561 | ||||||
| chr3:115644668
|
C | A | 1 | a0001c0001t0002g0263 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.30+20949C>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115644668 | ||||||
| chr3:115644722
|
C | T | 37 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0047others(34): Show | 38 | HG00558.hp1 HG00738.hp1 HG00741.hp2 others(35): Show |
intron_variant | MODIFIER | c.30+21003C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115644722 | ||||||
| chr3:115644824
|
A | C | 2 | a0001c0001t0003g0195a0001c0001t0003g0196 | 2 | HG00140.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.30+21105A>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115644824 | ||||||
| chr3:115645189
|
G | T | 34 | a0001c0001t0001g0002a0001c0001t0001g0085a0001c0001t0001g0088others(31): Show | 34 | HG00609.hp1 HG00609.hp2 HG01433.hp1 others(31): Show |
intron_variant | MODIFIER | c.30+21470G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115645189 | ||||||
| chr3:115645209
|
T | G | 1 | a0001c0001t0001g0240 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.30+21490T>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115645209 | ||||||
| chr3:115645297
|
T | C | 46 | a0001c0001t0001g0002a0001c0001t0001g0085a0001c0001t0001g0088others(43): Show | 46 | HG00609.hp1 HG00609.hp2 HG01433.hp1 others(43): Show |
intron_variant | MODIFIER | c.30+21578T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115645297 | ||||||
| chr3:115645366
|
T | C | 1 | a0001c0001t0002g0321 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.30+21647T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115645366 | ||||||
| chr3:115645611
|
GA | G | 174 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0017others(171): Show | 175 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.30+21900delA | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115645611 | |||||
| chr3:115645980
|
G | A | 37 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0047others(34): Show | 38 | HG00558.hp1 HG00738.hp1 HG00741.hp2 others(35): Show |
intron_variant | MODIFIER | c.30+22261G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115645980 | ||||||
| chr3:115646165
|
A | G | 49 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(46): Show | 49 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(46): Show |
intron_variant | MODIFIER | c.30+22446A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115646165 | ||||||
| chr3:115646189
|
T | C | 57 | a0001c0001t0001g0002a0001c0001t0001g0028a0001c0001t0001g0031others(54): Show | 57 | HG00609.hp1 HG00609.hp2 HG01255.hp2 others(54): Show |
intron_variant | MODIFIER | c.30+22470T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115646189 | ||||||
| chr3:115646437
|
T | C | 1 | a0001c0001t0005g0310 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.30+22718T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115646437 | ||||||
| chr3:115646608
|
A | C | 13 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0092others(10): Show | 13 | HG01081.hp2 HG01109.hp1 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.30+22889A>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115646608 | ||||||
| chr3:115646646
|
C | T | 4 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0002g0244others(1): Show | 4 | HG00735.hp2 HG02145.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.30+22927C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115646646 | ||||||
| chr3:115646780
|
G | T | 1 | a0001c0001t0003g0316 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.30+23061G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115646780 | ||||||
| chr3:115646798
|
G | A | 83 | a0001c0001t0001g0017a0001c0001t0001g0060a0001c0001t0001g0064others(80): Show | 83 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.30+23079G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115646798 | ||||||
| chr3:115646812
|
A | C | 1 | a0001c0001t0002g0194 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.30+23093A>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115646812 | ||||||
| chr3:115647136
|
T | C | 345 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0015others(342): Show | 346 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(343): Show |
intron_variant | MODIFIER | c.30+23417T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115647136 | ||||||
| chr3:115647174
|
G | A | 41 | a0001c0001t0001g0002a0001c0001t0001g0088a0001c0001t0001g0089others(38): Show | 41 | HG00609.hp1 HG00609.hp2 HG01433.hp1 others(38): Show |
intron_variant | MODIFIER | c.30+23455G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115647174 | ||||||
| chr3:115647180
|
CCTTG | C | 233 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0015others(230): Show | 234 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(231): Show |
intron_variant | MODIFIER | c.30+23466_30+23469d others(6): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115647180 | |||||
| chr3:115647221
|
C | T | 7 | a0001c0001t0001g0173a0001c0001t0001g0193a0001c0001t0001g0197others(4): Show | 7 | HG02109.hp1 HG02258.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.30+23502C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115647221 | ||||||
| chr3:115647503
|
C | T | 38 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0047others(35): Show | 39 | HG00558.hp1 HG00738.hp1 HG00741.hp2 others(36): Show |
intron_variant | MODIFIER | c.30+23784C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115647503 | ||||||
| chr3:115647517
|
C | T | 1 | a0001c0001t0001g0307 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.30+23798C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115647517 | ||||||
| chr3:115647739
|
A | C | 43 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(40): Show | 43 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(40): Show |
intron_variant | MODIFIER | c.30+24020A>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115647739 | ||||||
| chr3:115647754
|
A | AAAAC | 7 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0092others(4): Show | 7 | HG01934.hp1 HG02647.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.30+24039_30+24042d others(6): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115647754 | |||||
| chr3:115647754
|
A | C | 1 | a0001c0001t0001g0041 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.30+24035A>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115647754 | ||||||
| chr3:115647758
|
C | A | 1 | a0001c0001t0019g0013 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.30+24039C>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115647758 | ||||||
| chr3:115647758
|
C | CA | 58 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0028others(55): Show | 58 | HG00280.hp2 HG00609.hp1 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.30+24051dupA | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115647758 | |||||
| chr3:115647758
|
C | CAA | 89 | a0001c0001t0001g0017a0001c0001t0001g0060a0001c0001t0001g0064others(86): Show | 89 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.30+24050_30+24051d others(4): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115647758 | |||||
| chr3:115647758
|
C | CAAA | 31 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0038others(28): Show | 32 | HG00558.hp1 HG00738.hp1 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.30+24049_30+24051d others(5): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115647758 | |||||
| chr3:115647759
|
A | AAAC | 49 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(46): Show | 49 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(46): Show |
intron_variant | MODIFIER | c.30+24042_30+24043i others(5): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115647759 | |||||
| chr3:115647925
|
T | C | 1 | a0001c0001t0001g0060 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.30+24206T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115647925 | ||||||
| chr3:115648102
|
T | C | 1 | a0001c0001t0001g0265 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.30+24383T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115648102 | ||||||
| chr3:115648119
|
C | T | 178 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0017others(175): Show | 179 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(176): Show |
intron_variant | MODIFIER | c.30+24400C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115648119 | ||||||
| chr3:115648139
|
T | C | 5 | a0001c0001t0001g0004a0001c0001t0001g0307a0001c0001t0005g0003others(2): Show | 5 | HG02451.hp2 HG03195.hp1 NA19043.hp1 others(2): Show |
intron_variant | MODIFIER | c.30+24420T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115648139 | ||||||
| chr3:115648168
|
G | C | 3 | a0001c0001t0002g0255a0001c0001t0003g0266a0001c0001t0004g0256 | 3 | HG01952.hp2 HG02300.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.30+24449G>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115648168 | ||||||
| chr3:115648274
|
G | A | 1 | a0001c0001t0002g0107 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.30+24555G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115648274 | ||||||
| chr3:115648287
|
A | G | 58 | a0001c0001t0001g0002a0001c0001t0001g0028a0001c0001t0001g0031others(55): Show | 58 | HG00609.hp1 HG00609.hp2 HG00735.hp2 others(55): Show |
intron_variant | MODIFIER | c.30+24568A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115648287 | ||||||
| chr3:115648367
|
A | G | 2 | a0001c0001t0001g0224a0001c0001t0001g0225 | 2 | HG02630.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.30+24648A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115648367 | ||||||
| chr3:115648370
|
T | C | 1 | a0001c0001t0005g0233 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.30+24651T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115648370 | ||||||
| chr3:115648382
|
C | T | 1 | a0001c0001t0005g0343 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.30+24663C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115648382 | ||||||
| chr3:115648731
|
A | G | 1 | a0001c0001t0002g0163 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.30+25012A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115648731 | ||||||
| chr3:115648755
|
G | A | 177 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0017others(174): Show | 178 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.30+25036G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115648755 | ||||||
| chr3:115648936
|
A | G | 1 | a0001c0001t0001g0213 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.30+25217A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115648936 | ||||||
| chr3:115648954
|
T | C | 57 | a0001c0001t0001g0002a0001c0001t0001g0028a0001c0001t0001g0031others(54): Show | 57 | HG00609.hp1 HG00609.hp2 HG01255.hp2 others(54): Show |
intron_variant | MODIFIER | c.30+25235T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115648954 | ||||||
| chr3:115649143
|
T | C | 188 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0017others(185): Show | 189 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.30+25424T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115649143 | ||||||
| chr3:115649221
|
T | G | 1 | a0001c0001t0005g0233 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.30+25502T>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115649221 | ||||||
| chr3:115649297
|
C | G | 9 | a0001c0001t0001g0313a0001c0001t0001g0346a0001c0001t0001g0347others(6): Show | 9 | HG01081.hp2 HG01109.hp1 HG01361.hp1 others(6): Show |
intron_variant | MODIFIER | c.30+25578C>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115649297 | ||||||
| chr3:115649359
|
C | G | 1 | a0001c0001t0013g0219 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.30+25640C>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115649359 | ||||||
| chr3:115649822
|
A | AAAAAG | 158 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0028others(155): Show | 158 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(155): Show |
intron_variant | MODIFIER | c.30+26106_30+26107i others(7): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115649822 | |||||
| chr3:115649822
|
A | AAAAG | 97 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0041others(94): Show | 98 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(95): Show |
intron_variant | MODIFIER | c.30+26119_30+26122d others(6): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115649822 | |||||
| chr3:115650221
|
T | G | 1 | a0001c0001t0012g0300 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.31-25792T>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115650221 | ||||||
| chr3:115650256
|
A | G | 1 | a0001c0001t0001g0307 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.31-25757A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115650256 | ||||||
| chr3:115650289
|
C | T | 2 | a0001c0001t0001g0221a0001c0001t0001g0222 | 2 | HG02922.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.31-25724C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115650289 | ||||||
| chr3:115650324
|
G | A | 1 | a0001c0001t0001g0185 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.31-25689G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115650324 | ||||||
| chr3:115650351
|
A | C | 1 | a0001c0001t0002g0212 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.31-25662A>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115650351 | ||||||
| chr3:115650386
|
G | T | 1 | a0001c0001t0001g0191 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.31-25627G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115650386 | ||||||
| chr3:115650731
|
TTTTTAAA others(14): Show |
T | 1 | a0001c0001t0013g0219 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.31-25256_31-25236d others(23): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115650731 | |||||
| chr3:115650782
|
C | T | 1 | a0001c0001t0005g0233 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.31-25231C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115650782 | ||||||
| chr3:115650834
|
G | A | 2 | a0001c0001t0002g0166a0001c0001t0002g0167 | 2 | NA18982.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.31-25179G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115650834 | ||||||
| chr3:115650859
|
T | C | 8 | a0001c0001t0001g0313a0001c0001t0001g0346a0001c0001t0001g0347others(5): Show | 8 | HG01081.hp2 HG01109.hp1 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.31-25154T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115650859 | ||||||
| chr3:115650893
|
C | T | 1 | a0001c0001t0001g0307 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.31-25120C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115650893 | ||||||
| chr3:115650907
|
T | C | 4 | a0001c0001t0001g0002a0001c0001t0005g0096a0001c0001t0005g0097others(1): Show | 4 | HG01433.hp1 HG03041.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.31-25106T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115650907 | ||||||
| chr3:115650945
|
C | T | 6 | a0001c0001t0001g0022a0001c0001t0001g0315a0001c0001t0003g0020others(3): Show | 6 | HG02486.hp2 HG02615.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.31-25068C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115650945 | ||||||
| chr3:115651413
|
A | T | 5 | a0001c0001t0002g0161a0001c0001t0002g0198a0001c0001t0004g0143others(2): Show | 5 | HG01358.hp2 HG01496.hp1 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.31-24600A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115651413 | ||||||
| chr3:115651768
|
G | T | 1 | a0001c0001t0003g0078 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.31-24245G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115651768 | ||||||
| chr3:115651771
|
G | T | 1 | a0001c0001t0002g0308 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.31-24242G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115651771 | ||||||
| chr3:115652050
|
A | G | 1 | a0001c0001t0001g0193 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.31-23963A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115652050 | ||||||
| chr3:115652233
|
G | T | 141 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0033others(138): Show | 141 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.31-23780G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115652233 | ||||||
| chr3:115652356
|
C | CT | 29 | a0001c0001t0001g0024a0001c0001t0001g0073a0001c0001t0001g0152others(26): Show | 29 | HG01106.hp1 HG01257.hp2 HG01358.hp1 others(26): Show |
intron_variant | MODIFIER | c.31-23628dupT | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115652356 | |||||
| chr3:115652356
|
C | CTT | 69 | a0001c0001t0001g0017a0001c0001t0001g0031a0001c0001t0001g0036others(66): Show | 69 | HG00280.hp1 HG00544.hp2 HG00621.hp2 others(66): Show |
intron_variant | MODIFIER | c.31-23629_31-23628d others(4): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115652356 | |||||
| chr3:115652356
|
C | CTTT | 54 | a0001c0001t0001g0033a0001c0001t0001g0037a0001c0001t0001g0051others(51): Show | 54 | HG00280.hp2 HG00408.hp1 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.31-23630_31-23628d others(5): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115652356 | |||||
| chr3:115652356
|
C | CTTTT | 18 | a0001c0001t0001g0191a0001c0001t0001g0202a0001c0001t0002g0142others(15): Show | 18 | HG00438.hp2 HG00621.hp1 HG00673.hp1 others(15): Show |
intron_variant | MODIFIER | c.31-23631_31-23628d others(6): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115652356 | |||||
| chr3:115652356
|
CT | C | 62 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0040others(59): Show | 62 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.31-23628delT | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115652356 | |||||
| chr3:115652356
|
CTT | C | 9 | a0001c0001t0001g0022a0001c0001t0001g0168a0001c0001t0001g0169others(6): Show | 10 | HG00733.hp1 HG01257.hp1 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.31-23629_31-23628d others(4): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115652356 | |||||
| chr3:115652356
|
CTTT | C | 12 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0170others(9): Show | 12 | HG01106.hp2 HG01496.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.31-23630_31-23628d others(5): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115652356 | |||||
| chr3:115652356
|
CTTTTTTT others(1): Show |
C | 6 | a0001c0001t0001g0072a0001c0001t0001g0085a0001c0001t0001g0313others(3): Show | 6 | HG01109.hp1 HG01361.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.31-23635_31-23628d others(10): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115652356 | |||||
| chr3:115652356
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0001g0112 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.31-23638_31-23628d others(13): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115652356 | |||||
| chr3:115652356
|
CTTTTTTT others(7): Show |
C | 1 | a0001c0001t0001g0342 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.31-23641_31-23628d others(16): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115652356 | |||||
| chr3:115652356
|
CTTTTTTT others(8): Show |
C | 6 | a0001c0001t0001g0135a0001c0001t0001g0296a0001c0001t0001g0339others(3): Show | 6 | HG01884.hp1 HG02055.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.31-23642_31-23628d others(17): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115652356 | |||||
| chr3:115652356
|
CTTTTTTT others(12): Show |
C | 2 | a0001c0001t0002g0231a0001c0001t0003g0162 | 2 | HG01175.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.31-23646_31-23628d others(21): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115652356 | |||||
| chr3:115652386
|
G | T | 9 | a0001c0001t0001g0019a0001c0001t0001g0099a0001c0001t0001g0100others(6): Show | 9 | HG01081.hp2 HG02559.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.31-23627G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115652386 | ||||||
| chr3:115652388
|
G | T | 10 | a0001c0001t0001g0019a0001c0001t0001g0061a0001c0001t0001g0099others(7): Show | 10 | HG01081.hp2 HG02559.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.31-23625G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115652388 | ||||||
| chr3:115652389
|
A | T | 10 | a0001c0001t0001g0019a0001c0001t0001g0061a0001c0001t0001g0099others(7): Show | 10 | HG01081.hp2 HG02559.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.31-23624A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115652389 | ||||||
| chr3:115652391
|
A | T | 10 | a0001c0001t0001g0019a0001c0001t0001g0061a0001c0001t0001g0099others(7): Show | 10 | HG01081.hp2 HG02559.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.31-23622A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115652391 | ||||||
| chr3:115652413
|
T | C | 111 | a0001c0001t0001g0017a0001c0001t0001g0028a0001c0001t0001g0031others(108): Show | 111 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(108): Show |
intron_variant | MODIFIER | c.31-23600T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115652413 | ||||||
| chr3:115652565
|
T | C | 110 | a0001c0001t0001g0017a0001c0001t0001g0028a0001c0001t0001g0031others(107): Show | 110 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.31-23448T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115652565 | ||||||
| chr3:115652584
|
T | C | 264 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0017others(261): Show | 264 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(261): Show |
intron_variant | MODIFIER | c.31-23429T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115652584 | ||||||
| chr3:115652585
|
G | A | 47 | a0001c0001t0001g0051a0001c0001t0001g0060a0001c0001t0001g0088others(44): Show | 47 | HG00280.hp2 HG00438.hp2 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.31-23428G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115652585 | ||||||
| chr3:115652636
|
C | G | 113 | a0001c0001t0001g0017a0001c0001t0001g0028a0001c0001t0001g0031others(110): Show | 113 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(110): Show |
intron_variant | MODIFIER | c.31-23377C>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115652636 | ||||||
| chr3:115652686
|
G | T | 265 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0017others(262): Show | 265 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(262): Show |
intron_variant | MODIFIER | c.31-23327G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115652686 | ||||||
| chr3:115652722
|
C | T | 34 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0040others(31): Show | 34 | HG00140.hp2 HG00438.hp1 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.31-23291C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115652722 | ||||||
| chr3:115652773
|
T | A | 17 | a0001c0001t0001g0002a0001c0001t0001g0090a0001c0001t0001g0091others(14): Show | 17 | HG01433.hp1 HG01891.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.31-23240T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115652773 | ||||||
| chr3:115652836
|
C | T | 12 | a0001c0001t0001g0022a0001c0001t0001g0086a0001c0001t0001g0087others(9): Show | 12 | HG01106.hp2 HG02615.hp1 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.31-23177C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115652836 | ||||||
| chr3:115653167
|
C | T | 1 | a0001c0001t0016g0269 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.31-22846C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115653167 | ||||||
| chr3:115653313
|
A | G | 260 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0015others(257): Show | 260 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(257): Show |
intron_variant | MODIFIER | c.31-22700A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115653313 | ||||||
| chr3:115653319
|
G | A | 10 | a0001c0001t0001g0019a0001c0001t0001g0061a0001c0001t0001g0099others(7): Show | 10 | HG01081.hp2 HG02559.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.31-22694G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115653319 | ||||||
| chr3:115653328
|
C | G | 138 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0019others(135): Show | 138 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.31-22685C>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115653328 | ||||||
| chr3:115653329
|
C | T | 86 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0040others(83): Show | 86 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.31-22684C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115653329 | ||||||
| chr3:115653427
|
G | A | 1 | a0001c0001t0012g0300 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.31-22586G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115653427 | ||||||
| chr3:115653576
|
C | T | 1 | a0001c0001t0005g0005 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.31-22437C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115653576 | ||||||
| chr3:115653607
|
T | A | 6 | a0001c0001t0001g0072a0001c0001t0001g0085a0001c0001t0001g0313others(3): Show | 6 | HG01109.hp1 HG01361.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.31-22406T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115653607 | ||||||
| chr3:115653674
|
C | T | 24 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0061others(21): Show | 24 | HG01081.hp2 HG01106.hp2 HG02559.hp1 others(21): Show |
intron_variant | MODIFIER | c.31-22339C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115653674 | ||||||
| chr3:115653805
|
T | C | 1 | a0001c0001t0001g0110 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.31-22208T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115653805 | ||||||
| chr3:115653943
|
C | T | 2 | a0001c0001t0001g0173a0001c0001t0001g0197 | 2 | HG02258.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.31-22070C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115653943 | ||||||
| chr3:115654476
|
T | C | 1 | a0001c0001t0001g0072 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.31-21537T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115654476 | ||||||
| chr3:115654480
|
A | T | 7 | a0001c0001t0001g0024a0001c0001t0001g0242a0001c0001t0001g0259others(4): Show | 7 | HG02145.hp1 HG02280.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.31-21533A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115654480 | ||||||
| chr3:115654588
|
C | T | 50 | a0001c0001t0001g0051a0001c0001t0001g0060a0001c0001t0001g0073others(47): Show | 50 | HG00280.hp2 HG00438.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.31-21425C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115654588 | ||||||
| chr3:115654743
|
A | C | 2 | a0001c0001t0001g0066a0001c0001t0001g0067 | 2 | NA18747.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.31-21270A>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115654743 | ||||||
| chr3:115654882
|
C | G | 268 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0017others(265): Show | 268 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(265): Show |
intron_variant | MODIFIER | c.31-21131C>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115654882 | ||||||
| chr3:115654948
|
A | G | 90 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0040others(87): Show | 90 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.31-21065A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115654948 | ||||||
| chr3:115655238
|
T | G | 2 | a0001c0001t0003g0020a0001c0001t0003g0021 | 2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.31-20775T>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115655238 | ||||||
| chr3:115655260
|
G | C | 1 | a0001c0001t0001g0224 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.31-20753G>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115655260 | ||||||
| chr3:115655525
|
C | T | 1 | a0001c0001t0004g0109 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.31-20488C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115655525 | ||||||
| chr3:115655704
|
A | G | 16 | a0001c0001t0001g0022a0001c0001t0001g0086a0001c0001t0001g0087others(13): Show | 16 | HG01106.hp2 HG01884.hp2 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.31-20309A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115655704 | ||||||
| chr3:115655741
|
A | G | 1 | a0001c0001t0002g0304 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.31-20272A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115655741 | ||||||
| chr3:115655819
|
A | C | 3 | a0001c0001t0002g0271a0001c0001t0003g0272a0001c0001t0003g0273 | 3 | NA18995.hp1 NA19002.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.31-20194A>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115655819 | ||||||
| chr3:115655850
|
G | C | 1 | a0001c0001t0001g0091 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.31-20163G>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115655850 | ||||||
| chr3:115655950
|
C | G | 1 | a0001c0001t0001g0262 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.31-20063C>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115655950 | ||||||
| chr3:115656028
|
C | T | 2 | a0001c0001t0001g0215a0001c0001t0001g0216 | 2 | HG01975.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.31-19985C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115656028 | ||||||
| chr3:115656231
|
T | C | 2 | a0001c0001t0001g0224a0001c0001t0001g0225 | 2 | HG02630.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.31-19782T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115656231 | ||||||
| chr3:115656252
|
C | A | 2 | a0001c0001t0002g0317a0001c0001t0002g0318 | 2 | NA18975.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.31-19761C>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115656252 | ||||||
| chr3:115656393
|
A | G | 23 | a0001c0001t0001g0022a0001c0001t0001g0072a0001c0001t0001g0085others(20): Show | 23 | HG01106.hp2 HG01109.hp1 HG01361.hp1 others(20): Show |
intron_variant | MODIFIER | c.31-19620A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115656393 | ||||||
| chr3:115656788
|
C | A | 17 | a0001c0001t0001g0002a0001c0001t0001g0090a0001c0001t0001g0091others(14): Show | 17 | HG01433.hp1 HG01891.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.31-19225C>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115656788 | ||||||
| chr3:115656848
|
A | T | 1 | a0001c0001t0004g0183 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.31-19165A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115656848 | ||||||
| chr3:115656852
|
G | A | 2 | a0001c0001t0005g0003a0001c0002t0001g0006 | 2 | HG03195.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.31-19161G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115656852 | ||||||
| chr3:115656909
|
C | T | 1 | a0001c0001t0003g0283 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.31-19104C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115656909 | ||||||
| chr3:115656922
|
T | C | 1 | a0001c0001t0005g0344 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.31-19091T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115656922 | ||||||
| chr3:115657035
|
G | C | 33 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0040others(30): Show | 33 | HG00140.hp2 HG00438.hp1 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.31-18978G>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115657035 | ||||||
| chr3:115657125
|
T | C | 86 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0040others(83): Show | 86 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.31-18888T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115657125 | ||||||
| chr3:115657199
|
G | T | 16 | a0001c0001t0001g0056a0001c0001t0001g0104a0001c0001t0001g0302others(13): Show | 16 | HG00280.hp1 HG00642.hp1 HG01099.hp2 others(13): Show |
intron_variant | MODIFIER | c.31-18814G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115657199 | ||||||
| chr3:115657263
|
G | A | 109 | a0001c0001t0001g0017a0001c0001t0001g0028a0001c0001t0001g0031others(106): Show | 109 | HG00280.hp1 HG00408.hp1 HG00621.hp2 others(106): Show |
intron_variant | MODIFIER | c.31-18750G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115657263 | ||||||
| chr3:115657347
|
T | C | 27 | a0001c0001t0001g0019a0001c0001t0001g0024a0001c0001t0001g0036others(24): Show | 27 | HG01081.hp2 HG01884.hp1 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.31-18666T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115657347 | ||||||
| chr3:115657363
|
G | C | 8 | a0001c0001t0001g0058a0001c0001t0001g0290a0001c0001t0001g0291others(5): Show | 8 | HG01074.hp2 HG01099.hp1 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.31-18650G>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115657363 | ||||||
| chr3:115657445
|
A | G | 7 | a0001c0001t0001g0296a0001c0001t0001g0339a0001c0001t0001g0342others(4): Show | 7 | HG01884.hp1 HG02055.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.31-18568A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115657445 | ||||||
| chr3:115657465
|
C | A | 1 | a0001c0001t0002g0147 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.31-18548C>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115657465 | ||||||
| chr3:115657476
|
A | AT | 13 | a0001c0001t0001g0019a0001c0001t0001g0036a0001c0001t0001g0037others(10): Show | 13 | HG01081.hp2 HG02055.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.31-18531dupT | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115657476 | |||||
| chr3:115657502
|
C | T | 84 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0040others(81): Show | 84 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.31-18511C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115657502 | ||||||
| chr3:115657590
|
G | A | 51 | a0001c0001t0001g0051a0001c0001t0001g0060a0001c0001t0001g0064others(48): Show | 51 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.31-18423G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115657590 | ||||||
| chr3:115657703
|
G | A | 23 | a0001c0001t0001g0022a0001c0001t0001g0072a0001c0001t0001g0085others(20): Show | 23 | HG01106.hp2 HG01109.hp1 HG01361.hp1 others(20): Show |
intron_variant | MODIFIER | c.31-18310G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115657703 | ||||||
| chr3:115657834
|
A | G | 3 | a0001c0001t0001g0024a0001c0001t0001g0259a0001c0001t0001g0332 | 3 | HG02717.hp1 HG02922.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.31-18179A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115657834 | ||||||
| chr3:115657838
|
G | A | 17 | a0001c0001t0001g0002a0001c0001t0001g0090a0001c0001t0001g0091others(14): Show | 17 | HG01433.hp1 HG01891.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.31-18175G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115657838 | ||||||
| chr3:115657844
|
C | T | 2 | a0001c0001t0005g0003a0001c0002t0001g0006 | 2 | HG03195.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.31-18169C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115657844 | ||||||
| chr3:115658022
|
G | C | 246 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0017others(243): Show | 246 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.31-17991G>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115658022 | ||||||
| chr3:115658187
|
A | G | 246 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0017others(243): Show | 246 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.31-17826A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115658187 | ||||||
| chr3:115658280
|
G | A | 108 | a0001c0001t0001g0017a0001c0001t0001g0028a0001c0001t0001g0031others(105): Show | 108 | HG00280.hp1 HG00408.hp1 HG00621.hp2 others(105): Show |
intron_variant | MODIFIER | c.31-17733G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115658280 | ||||||
| chr3:115658305
|
C | T | 1 | a0001c0001t0001g0350 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.31-17708C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115658305 | ||||||
| chr3:115658407
|
C | A | 240 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0017others(237): Show | 240 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(237): Show |
intron_variant | MODIFIER | c.31-17606C>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115658407 | ||||||
| chr3:115658535
|
C | T | 2 | a0001c0001t0001g0051a0001c0001t0003g0062 | 2 | HG01993.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.31-17478C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115658535 | ||||||
| chr3:115658697
|
G | A | 8 | a0001c0001t0001g0296a0001c0001t0001g0339a0001c0001t0001g0342others(5): Show | 8 | HG00544.hp2 HG01884.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.31-17316G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115658697 | ||||||
| chr3:115658968
|
G | C | 9 | a0001c0001t0001g0072a0001c0001t0001g0085a0001c0001t0001g0265others(6): Show | 9 | HG01109.hp1 HG01361.hp1 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.31-17045G>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115658968 | ||||||
| chr3:115659005
|
G | A | 88 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0040others(85): Show | 88 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.31-17008G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115659005 | ||||||
| chr3:115659010
|
T | C | 80 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0033others(77): Show | 80 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.31-17003T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115659010 | ||||||
| chr3:115659103
|
C | G | 2 | a0001c0001t0001g0051a0001c0001t0003g0062 | 2 | HG01993.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.31-16910C>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115659103 | ||||||
| chr3:115659270
|
T | C | 38 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0040others(35): Show | 38 | HG00140.hp2 HG00438.hp1 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.31-16743T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115659270 | ||||||
| chr3:115659345
|
C | A | 17 | a0001c0001t0001g0002a0001c0001t0001g0090a0001c0001t0001g0091others(14): Show | 17 | HG01433.hp1 HG01891.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.31-16668C>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115659345 | ||||||
| chr3:115659618
|
TAGAG | T | 36 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0040others(33): Show | 36 | HG00140.hp2 HG00438.hp1 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.31-16387_31-16384d others(6): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115659618 | |||||
| chr3:115659623
|
A | G | 1 | a0001c0001t0005g0233 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.31-16390A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115659623 | ||||||
| chr3:115659770
|
G | T | 3 | a0001c0001t0001g0038a0001c0001t0001g0040a0001c0001t0001g0050 | 3 | HG00639.hp2 HG00741.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.31-16243G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115659770 | ||||||
| chr3:115659846
|
A | C | 1 | a0001c0001t0005g0310 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.31-16167A>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115659846 | ||||||
| chr3:115659900
|
C | G | 1 | a0001c0002t0001g0095 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.31-16113C>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115659900 | ||||||
| chr3:115659914
|
A | G | 2 | a0001c0001t0001g0051a0001c0001t0003g0062 | 2 | HG01993.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.31-16099A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115659914 | ||||||
| chr3:115660109
|
G | T | 17 | a0001c0001t0001g0002a0001c0001t0001g0090a0001c0001t0001g0091others(14): Show | 17 | HG01433.hp1 HG01891.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.31-15904G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115660109 | ||||||
| chr3:115660536
|
A | G | 14 | a0001c0001t0001g0022a0001c0001t0001g0086a0001c0001t0001g0087others(11): Show | 14 | HG01106.hp2 HG01884.hp2 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.31-15477A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115660536 | ||||||
| chr3:115660555
|
T | A | 17 | a0001c0001t0001g0019a0001c0001t0001g0024a0001c0001t0001g0061others(14): Show | 17 | HG01081.hp2 HG02451.hp2 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.31-15458T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115660555 | ||||||
| chr3:115660893
|
A | G | 1 | a0001c0001t0001g0225 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.31-15120A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115660893 | ||||||
| chr3:115661088
|
C | A | 1 | a0001c0001t0002g0227 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.31-14925C>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115661088 | ||||||
| chr3:115661124
|
T | TA | 8 | a0001c0001t0001g0072a0001c0001t0001g0085a0001c0001t0001g0170others(5): Show | 8 | HG01109.hp1 HG01361.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.31-14879dupA | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115661124 | |||||
| chr3:115661134
|
ACT | A | 22 | a0001c0001t0001g0209a0001c0001t0001g0306a0001c0001t0001g0324others(19): Show | 22 | HG00609.hp2 HG01106.hp1 HG01496.hp1 others(19): Show |
intron_variant | MODIFIER | c.31-14878_31-14877d others(4): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115661134 | ||||||
| chr3:115661248
|
A | G | 26 | a0001c0001t0001g0019a0001c0001t0001g0209a0001c0001t0001g0306others(23): Show | 26 | HG00609.hp2 HG01106.hp1 HG01496.hp1 others(23): Show |
intron_variant | MODIFIER | c.31-14765A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115661248 | ||||||
| chr3:115661258
|
C | T | 288 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0017others(285): Show | 288 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(285): Show |
intron_variant | MODIFIER | c.31-14755C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115661258 | ||||||
| chr3:115661422
|
G | A | 1 | a0001c0001t0003g0023 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.31-14591G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115661422 | ||||||
| chr3:115661512
|
G | A | 1 | a0001c0001t0001g0234 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.31-14501G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115661512 | ||||||
| chr3:115661527
|
C | T | 2 | a0001c0001t0001g0265a0001c0001t0002g0164 | 2 | HG02970.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.31-14486C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115661527 | ||||||
| chr3:115661539
|
A | G | 1 | a0001c0001t0002g0142 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.31-14474A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115661539 | ||||||
| chr3:115661673
|
A | G | 17 | a0001c0001t0001g0002a0001c0001t0001g0090a0001c0001t0001g0091others(14): Show | 17 | HG01433.hp1 HG01891.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.31-14340A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115661673 | ||||||
| chr3:115661710
|
G | A | 49 | a0001c0001t0001g0051a0001c0001t0001g0060a0001c0001t0001g0073others(46): Show | 49 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.31-14303G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115661710 | ||||||
| chr3:115661778
|
G | A | 1 | a0001c0001t0005g0233 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.31-14235G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115661778 | ||||||
| chr3:115661802
|
C | T | 6 | a0001c0001t0001g0072a0001c0001t0001g0085a0001c0001t0001g0313others(3): Show | 6 | HG01109.hp1 HG01361.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.31-14211C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115661802 | ||||||
| chr3:115661812
|
G | A | 1 | a0001c0001t0002g0328 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.31-14201G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115661812 | ||||||
| chr3:115661831
|
C | CTTTTTTT others(3): Show |
35 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0040others(32): Show | 35 | HG00140.hp2 HG00438.hp1 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.31-14177_31-14168d others(12): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115661831 | |||||
| chr3:115661831
|
C | CTTTTTTT others(4): Show |
49 | a0001c0001t0001g0051a0001c0001t0001g0060a0001c0001t0001g0064others(46): Show | 49 | HG00438.hp2 HG00609.hp1 HG00642.hp2 others(46): Show |
intron_variant | MODIFIER | c.31-14178_31-14168d others(13): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115661831 | |||||
| chr3:115661831
|
C | CTTTTTTT others(5): Show |
45 | a0001c0001t0001g0019a0001c0001t0001g0024a0001c0001t0001g0061others(42): Show | 45 | HG00408.hp1 HG00609.hp2 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.31-14179_31-14168d others(14): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115661831 | |||||
| chr3:115661831
|
C | CTTTTTTT others(6): Show |
75 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0033others(72): Show | 75 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.31-14180_31-14168d others(15): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115661831 | |||||
| chr3:115661831
|
C | CTTTTTTT others(7): Show |
33 | a0001c0001t0001g0036a0001c0001t0001g0069a0001c0001t0001g0082others(30): Show | 33 | HG00673.hp2 HG01069.hp1 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.31-14181_31-14168d others(16): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115661831 | |||||
| chr3:115661831
|
C | CTTTTTTT others(8): Show |
15 | a0001c0001t0001g0017a0001c0001t0001g0037a0001c0001t0001g0072others(12): Show | 15 | HG00735.hp2 HG01109.hp1 HG01361.hp1 others(12): Show |
intron_variant | MODIFIER | c.31-14168_31-14167i others(17): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115661831 | |||||
| chr3:115661831
|
C | CTTTTTTT others(12): Show |
1 | a0001c0001t0005g0204 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.31-14168_31-14167i others(21): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115661831 | |||||
| chr3:115661831
|
C | CTTTTTTT others(15): Show |
3 | a0001c0001t0001g0242a0001c0001t0001g0346a0001c0001t0002g0243 | 3 | HG01891.hp2 HG02280.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.31-14168_31-14167i others(24): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115661831 | |||||
| chr3:115661831
|
C | CTTTTTTT others(16): Show |
8 | a0001c0001t0001g0002a0001c0001t0001g0173a0001c0001t0001g0197others(5): Show | 8 | HG01433.hp1 HG02145.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.31-14168_31-14167i others(25): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115661831 | |||||
| chr3:115661831
|
C | CTTTTTTT others(17): Show |
7 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093others(4): Show | 7 | HG02109.hp1 HG02723.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.31-14168_31-14167i others(26): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115661831 | |||||
| chr3:115661831
|
C | CTTTTTTT others(18): Show |
2 | a0001c0001t0001g0090a0001c0001t0005g0011 | 2 | HG02647.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.31-14168_31-14167i others(27): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115661831 | |||||
| chr3:115662016
|
G | A | 4 | a0001c0001t0001g0242a0001c0001t0002g0243a0001c0001t0002g0244others(1): Show | 4 | HG02145.hp1 HG02280.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.31-13997G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115662016 | ||||||
| chr3:115662043
|
G | T | 268 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0017others(265): Show | 268 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(265): Show |
intron_variant | MODIFIER | c.31-13970G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115662043 | ||||||
| chr3:115662057
|
G | C | 268 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0017others(265): Show | 268 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(265): Show |
intron_variant | MODIFIER | c.31-13956G>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115662057 | ||||||
| chr3:115662085
|
G | A | 1 | a0001c0001t0001g0080 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.31-13928G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115662085 | ||||||
| chr3:115662123
|
T | C | 1 | a0001c0001t0001g0209 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.31-13890T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115662123 | ||||||
| chr3:115662185
|
G | A | 273 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0017others(270): Show | 273 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(270): Show |
intron_variant | MODIFIER | c.31-13828G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115662185 | ||||||
| chr3:115662462
|
G | T | 36 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0040others(33): Show | 36 | HG00140.hp2 HG00438.hp1 HG00609.hp2 others(33): Show |
intron_variant | MODIFIER | c.31-13551G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115662462 | ||||||
| chr3:115662579
|
C | T | 1 | a0001c0001t0001g0234 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.31-13434C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115662579 | ||||||
| chr3:115662692
|
T | A | 1 | a0001c0001t0003g0074 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.31-13321T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115662692 | ||||||
| chr3:115662955
|
G | A | 15 | a0001c0001t0001g0306a0001c0001t0002g0198a0001c0001t0004g0143others(12): Show | 15 | HG01106.hp1 HG01496.hp1 HG01943.hp2 others(12): Show |
intron_variant | MODIFIER | c.31-13058G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115662955 | ||||||
| chr3:115663116
|
C | T | 1 | a0001c0001t0001g0336 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.31-12897C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115663116 | ||||||
| chr3:115663188
|
C | T | 1 | a0001c0001t0001g0173 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.31-12825C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115663188 | ||||||
| chr3:115663252
|
G | A | 2 | a0001c0001t0001g0135a0001c0001t0002g0136 | 2 | NA18951.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.31-12761G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115663252 | ||||||
| chr3:115663274
|
G | A | 80 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0051others(77): Show | 80 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.31-12739G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115663274 | ||||||
| chr3:115663449
|
G | T | 12 | a0001c0001t0001g0019a0001c0001t0001g0061a0001c0001t0001g0086others(9): Show | 12 | HG02683.hp2 HG02886.hp2 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.31-12564G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115663449 | ||||||
| chr3:115663627
|
G | A | 1 | a0001c0001t0002g0212 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.31-12386G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115663627 | ||||||
| chr3:115663734
|
A | G | 3 | a0001c0001t0001g0242a0001c0001t0002g0243a0001c0001t0002g0244 | 3 | HG02145.hp1 HG02280.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.31-12279A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115663734 | ||||||
| chr3:115663790
|
C | T | 5 | a0001c0001t0001g0234a0001c0001t0001g0242a0001c0001t0001g0307others(2): Show | 5 | HG02109.hp2 HG02145.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.31-12223C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115663790 | ||||||
| chr3:115663808
|
C | T | 23 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0306others(20): Show | 23 | HG01106.hp1 HG01496.hp1 HG01943.hp2 others(20): Show |
intron_variant | MODIFIER | c.31-12205C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115663808 | ||||||
| chr3:115663938
|
C | T | 1 | a0001c0001t0004g0247 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.31-12075C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115663938 | ||||||
| chr3:115663963
|
C | A | 2 | a0001c0001t0003g0272a0001c0001t0003g0273 | 2 | NA18995.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.31-12050C>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115663963 | ||||||
| chr3:115663975
|
C | G | 3 | a0001c0001t0001g0242a0001c0001t0002g0243a0001c0001t0002g0244 | 3 | HG02145.hp1 HG02280.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.31-12038C>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115663975 | ||||||
| chr3:115663997
|
G | A | 1 | a0001c0001t0001g0224 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.31-12016G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115663997 | ||||||
| chr3:115664061
|
G | A | 1 | a0001c0001t0001g0345 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.31-11952G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115664061 | ||||||
| chr3:115664067
|
AT | A | 9 | a0001c0001t0001g0022a0001c0001t0001g0172a0001c0001t0001g0173others(6): Show | 9 | HG01081.hp2 HG02258.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.31-11944delT | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115664067 | |||||
| chr3:115664204
|
T | C | 1 | a0001c0001t0002g0267 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.31-11809T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115664204 | ||||||
| chr3:115664221
|
AG | A | 71 | a0001c0001t0001g0056a0001c0001t0001g0068a0001c0001t0001g0072others(68): Show | 72 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.31-11789delG | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115664221 | |||||
| chr3:115664230
|
T | TATGTCAT others(328): Show |
11 | a0001c0001t0002g0122a0001c0001t0002g0194a0001c0001t0002g0201others(8): Show | 11 | HG01928.hp2 HG01943.hp1 HG01993.hp1 others(8): Show |
intron_variant | MODIFIER | c.31-11769_31-11768i others(337): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115664230 | |||||
| chr3:115664230
|
T | TATGTCAT others(328): Show |
1 | a0001c0001t0001g0268 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.31-11769_31-11768i others(337): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115664230 | |||||
| chr3:115664230
|
T | TATGTCAT others(329): Show |
1 | a0001c0001t0001g0060 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.31-11769_31-11768i others(338): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115664230 | |||||
| chr3:115664230
|
T | TATGTCAT others(329): Show |
29 | a0001c0001t0001g0049a0001c0001t0001g0051a0001c0001t0001g0073others(26): Show | 29 | HG00609.hp1 HG00621.hp1 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.31-11769_31-11768i others(338): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115664230 | |||||
| chr3:115664230
|
T | TATGTCAT others(330): Show |
1 | a0001c0001t0004g0059 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.31-11769_31-11768i others(339): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115664230 | |||||
| chr3:115664230
|
T | TATGTCAT others(330): Show |
16 | a0001c0001t0001g0326a0001c0001t0002g0199a0001c0001t0002g0260others(13): Show | 16 | HG00544.hp2 HG00642.hp2 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.31-11769_31-11768i others(339): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115664230 | |||||
| chr3:115664230
|
T | TATGTCAT others(330): Show |
1 | a0001c0001t0002g0203 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.31-11769_31-11768i others(339): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115664230 | |||||
| chr3:115664230
|
T | TATGTCAT others(331): Show |
4 | a0001c0001t0002g0108a0001c0001t0003g0009a0001c0001t0003g0301others(1): Show | 4 | HG01884.hp2 HG02738.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.31-11769_31-11768i others(340): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115664230 | |||||
| chr3:115664230
|
T | TATGTCAT others(332): Show |
2 | a0001c0001t0004g0159a0001c0001t0004g0160 | 2 | NA18968.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.31-11769_31-11768i others(341): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115664230 | |||||
| chr3:115664378
|
A | G | 2 | a0001c0001t0001g0347a0001c0001t0005g0003 | 2 | HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.31-11635A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115664378 | ||||||
| chr3:115664532
|
G | A | 2 | a0001c0001t0001g0347a0001c0001t0005g0003 | 2 | HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.31-11481G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115664532 | ||||||
| chr3:115665188
|
T | C | 77 | a0001c0001t0001g0002a0001c0001t0001g0049a0001c0001t0001g0051others(74): Show | 77 | HG00438.hp2 HG00544.hp2 HG00609.hp1 others(74): Show |
intron_variant | MODIFIER | c.31-10825T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115665188 | ||||||
| chr3:115665251
|
C | A | 1 | a0001c0001t0003g0113 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.31-10762C>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115665251 | ||||||
| chr3:115665254
|
C | G | 1 | a0001c0001t0012g0300 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.31-10759C>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115665254 | ||||||
| chr3:115665507
|
G | T | 20 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0042others(17): Show | 20 | HG01106.hp2 HG01891.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.31-10506G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115665507 | ||||||
| chr3:115665512
|
G | A | 1 | a0001c0001t0002g0277 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.31-10501G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115665512 | ||||||
| chr3:115665568
|
C | T | 32 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0040others(29): Show | 32 | HG00140.hp2 HG00609.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.31-10445C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115665568 | ||||||
| chr3:115665686
|
G | A | 5 | a0001c0001t0001g0173a0001c0001t0001g0197a0001c0001t0001g0338others(2): Show | 5 | HG01081.hp2 HG02258.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.31-10327G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115665686 | ||||||
| chr3:115665733
|
A | G | 1 | a0001c0001t0005g0204 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.31-10280A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115665733 | ||||||
| chr3:115665852
|
T | C | 1 | a0001c0001t0003g0312 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.31-10161T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115665852 | ||||||
| chr3:115665989
|
A | AGT | 9 | a0001c0001t0001g0112a0001c0001t0001g0315a0001c0001t0002g0171others(6): Show | 9 | HG02257.hp2 HG04199.hp2 NA18966.hp2 others(6): Show |
intron_variant | MODIFIER | c.31-9982_31-9981dup others(2): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115665989 | |||||
| chr3:115665989
|
A | AGTGT | 5 | a0001c0001t0001g0015a0001c0001t0001g0185a0001c0001t0001g0186others(2): Show | 5 | HG01261.hp1 HG02451.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.31-9984_31-9981dup others(4): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115665989 | |||||
| chr3:115665989
|
A | AGTTT | 5 | a0001c0001t0001g0224a0001c0001t0003g0274a0001c0002t0001g0006others(2): Show | 5 | HG02486.hp2 HG02630.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.31-10022_31-10021i others(6): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115665989 | |||||
| chr3:115665989
|
A | AGTTTGT | 13 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0002g0198others(10): Show | 13 | HG01106.hp1 HG01496.hp1 HG01943.hp2 others(10): Show |
intron_variant | MODIFIER | c.31-10022_31-10021i others(8): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115665989 | |||||
| chr3:115665989
|
A | AGTTTGTG others(1): Show |
6 | a0001c0001t0001g0242a0001c0001t0001g0306a0001c0001t0002g0243others(3): Show | 6 | HG02280.hp2 HG02622.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.31-10022_31-10021i others(10): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115665989 | |||||
| chr3:115665989
|
A | AGTTTGTG others(9): Show |
2 | a0001c0001t0001g0234a0001c0001t0001g0307 | 2 | HG02109.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.31-10022_31-10021i others(18): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115665989 | |||||
| chr3:115665989
|
AGT | A | 26 | a0001c0001t0001g0017a0001c0001t0001g0036a0001c0001t0001g0037others(23): Show | 26 | HG00738.hp1 HG01071.hp2 HG01175.hp1 others(23): Show |
intron_variant | MODIFIER | c.31-9982_31-9981del others(2): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115665989 | |||||
| chr3:115665989
|
AGTGT | A | 167 | a0001c0001t0001g0004a0001c0001t0001g0022a0001c0001t0001g0024others(164): Show | 168 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.31-9984_31-9981del others(4): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115665989 | |||||
| chr3:115665989
|
AGTGTGT | A | 57 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0033others(54): Show | 57 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.31-9986_31-9981del others(6): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115665989 | |||||
| chr3:115665989
|
AGTGTGTG others(1): Show |
A | 6 | a0001c0001t0001g0072a0001c0001t0001g0085a0001c0001t0002g0203others(3): Show | 6 | HG00673.hp1 HG02257.hp1 NA18986.hp1 others(3): Show |
intron_variant | MODIFIER | c.31-9988_31-9981del others(8): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115665989 | |||||
| chr3:115665989
|
AGTGTGTG others(3): Show |
A | 2 | a0001c0001t0002g0166a0001c0001t0009g0187 | 2 | HG01169.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.31-9990_31-9981del others(10): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115665989 | |||||
| chr3:115665989
|
AGTGTGTG others(9): Show |
A | 11 | a0001c0001t0001g0002a0001c0001t0001g0090a0001c0001t0001g0091others(8): Show | 11 | HG01433.hp1 HG01891.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.31-9996_31-9981del others(16): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115665989 | |||||
| chr3:115665990
|
G | GTT | 5 | a0001c0001t0001g0172a0001c0001t0001g0240a0001c0001t0002g0115others(2): Show | 5 | HG02895.hp2 HG02896.hp1 HG04204.hp2 others(2): Show |
intron_variant | MODIFIER | c.31-10022_31-10021i others(4): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115665990 | |||||
| chr3:115665992
|
G | T | 9 | a0001c0001t0001g0061a0001c0001t0001g0086a0001c0001t0001g0087others(6): Show | 9 | HG01884.hp1 HG02683.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.31-10021G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115665992 | ||||||
| chr3:115665994
|
G | T | 14 | a0001c0001t0001g0049a0001c0001t0001g0110a0001c0001t0001g0168others(11): Show | 14 | HG01175.hp1 HG02074.hp1 HG02602.hp2 others(11): Show |
intron_variant | MODIFIER | c.31-10019G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115665994 | ||||||
| chr3:115665996
|
G | T | 146 | a0001c0001t0001g0004a0001c0001t0001g0022a0001c0001t0001g0024others(143): Show | 147 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.31-10017G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115665996 | ||||||
| chr3:115665998
|
G | T | 57 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0033others(54): Show | 57 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.31-10015G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115665998 | ||||||
| chr3:115666000
|
G | T | 4 | a0001c0001t0002g0203a0001c0001t0002g0271a0001c0001t0003g0206others(1): Show | 4 | HG00673.hp1 NA18986.hp1 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.31-10013G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115666000 | ||||||
| chr3:115666002
|
G | T | 1 | a0001c0001t0002g0166 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.31-10011G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115666002 | ||||||
| chr3:115666003
|
T | A | 2 | a0001c0001t0001g0168a0001c0001t0001g0169 | 2 | HG02965.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.31-10010T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115666003 | ||||||
| chr3:115666008
|
G | T | 11 | a0001c0001t0001g0002a0001c0001t0001g0090a0001c0001t0001g0091others(8): Show | 11 | HG01433.hp1 HG01891.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.31-10005G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115666008 | ||||||
| chr3:115666168
|
CAGTT | C | 8 | a0001c0001t0001g0072a0001c0001t0001g0085a0001c0001t0001g0313others(5): Show | 8 | HG01109.hp1 HG01361.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.31-9844_31-9841del others(4): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115666168 | ||||||
| chr3:115666404
|
C | T | 2 | a0001c0001t0001g0347a0001c0001t0005g0003 | 2 | HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.31-9609C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115666404 | ||||||
| chr3:115666465
|
C | T | 1 | a0001c0001t0001g0046 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.31-9548C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115666465 | ||||||
| chr3:115666472
|
C | G | 9 | a0001c0001t0001g0022a0001c0001t0001g0172a0001c0001t0001g0173others(6): Show | 9 | HG01081.hp2 HG02258.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.31-9541C>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115666472 | ||||||
| chr3:115666486
|
G | A | 1 | a0001c0001t0001g0112 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.31-9527G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115666486 | ||||||
| chr3:115666622
|
A | G | 1 | a0001c0001t0003g0214 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.31-9391A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115666622 | ||||||
| chr3:115666731
|
A | G | 1 | a0001c0001t0003g0007 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.31-9282A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115666731 | ||||||
| chr3:115666743
|
G | A | 1 | a0001c0001t0005g0003 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.31-9270G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115666743 | ||||||
| chr3:115666835
|
A | G | 224 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0019others(221): Show | 224 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(221): Show |
intron_variant | MODIFIER | c.31-9178A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115666835 | ||||||
| chr3:115666852
|
C | A | 1 | a0001c0001t0001g0296 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.31-9161C>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115666852 | ||||||
| chr3:115666867
|
T | C | 2 | a0001c0001t0002g0317a0001c0001t0002g0318 | 2 | NA18975.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.31-9146T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115666867 | ||||||
| chr3:115666991
|
G | A | 1 | a0001c0001t0001g0225 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.31-9022G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115666991 | ||||||
| chr3:115667031
|
C | T | 3 | a0001c0001t0001g0242a0001c0001t0002g0243a0001c0001t0002g0244 | 3 | HG02145.hp1 HG02280.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.31-8982C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115667031 | ||||||
| chr3:115667117
|
C | G | 73 | a0001c0001t0001g0056a0001c0001t0001g0068a0001c0001t0001g0072others(70): Show | 74 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.31-8896C>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115667117 | ||||||
| chr3:115667128
|
A | T | 1 | a0001c0001t0001g0079 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.31-8885A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115667128 | ||||||
| chr3:115667139
|
G | C | 1 | a0001c0001t0009g0187 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.31-8874G>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115667139 | ||||||
| chr3:115667186
|
T | C | 2 | a0001c0001t0001g0347a0001c0001t0005g0003 | 2 | HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.31-8827T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115667186 | ||||||
| chr3:115667199
|
G | T | 1 | a0001c0001t0003g0157 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.31-8814G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115667199 | ||||||
| chr3:115667317
|
G | A | 2 | a0001c0001t0001g0234a0001c0001t0001g0307 | 2 | HG02109.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.31-8696G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115667317 | ||||||
| chr3:115667724
|
G | T | 85 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0049others(82): Show | 85 | HG00438.hp2 HG00544.hp2 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.31-8289G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115667724 | ||||||
| chr3:115667763
|
A | G | 1 | a0001c0001t0001g0066 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.31-8250A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115667763 | ||||||
| chr3:115667777
|
G | A | 1 | a0001c0001t0001g0224 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.31-8236G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115667777 | ||||||
| chr3:115667816
|
A | T | 2 | a0001c0001t0001g0347a0001c0001t0005g0003 | 2 | HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.31-8197A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115667816 | ||||||
| chr3:115668013
|
G | A | 56 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0033others(53): Show | 56 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.31-8000G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115668013 | ||||||
| chr3:115668163
|
T | C | 183 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0028others(180): Show | 184 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.31-7850T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115668163 | ||||||
| chr3:115668240
|
G | A | 1 | a0001c0001t0001g0024 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.31-7773G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115668240 | ||||||
| chr3:115668278
|
T | G | 2 | a0001c0001t0001g0234a0001c0001t0001g0307 | 2 | HG02109.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.31-7735T>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115668278 | ||||||
| chr3:115668725
|
C | T | 213 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0019others(210): Show | 213 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(210): Show |
intron_variant | MODIFIER | c.31-7288C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115668725 | ||||||
| chr3:115669044
|
TA | T | 21 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0042others(18): Show | 21 | HG01106.hp2 HG01891.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.31-6956delA | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115669044 | |||||
| chr3:115669069
|
T | TAC | 96 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0033others(93): Show | 96 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.31-6922_31-6921dup others(2): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115669069 | |||||
| chr3:115669069
|
T | TACAC | 21 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0042others(18): Show | 21 | HG01106.hp2 HG02055.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.31-6924_31-6921dup others(4): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115669069 | |||||
| chr3:115669104
|
T | G | 10 | a0001c0001t0001g0019a0001c0001t0001g0061a0001c0001t0001g0086others(7): Show | 10 | HG02683.hp2 HG02886.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.31-6909T>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115669104 | ||||||
| chr3:115669151
|
T | C | 1 | a0001c0001t0001g0242 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.31-6862T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115669151 | ||||||
| chr3:115669480
|
G | A | 1 | a0001c0001t0002g0103 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.31-6533G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115669480 | ||||||
| chr3:115669497
|
A | C | 1 | a0001c0002t0002g0192 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.31-6516A>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115669497 | ||||||
| chr3:115669551
|
T | A | 9 | a0001c0001t0001g0022a0001c0001t0001g0172a0001c0001t0001g0173others(6): Show | 9 | HG01081.hp2 HG02258.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.31-6462T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115669551 | ||||||
| chr3:115669711
|
G | A | 12 | a0001c0001t0001g0019a0001c0001t0001g0061a0001c0001t0001g0086others(9): Show | 12 | HG02683.hp2 HG02886.hp2 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.31-6302G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115669711 | ||||||
| chr3:115669869
|
G | A | 1 | a0001c0001t0013g0219 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.31-6144G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115669869 | ||||||
| chr3:115669873
|
C | A | 1 | a0001c0001t0001g0225 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.31-6140C>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115669873 | ||||||
| chr3:115669912
|
A | G | 2 | a0001c0001t0003g0288a0001c0001t0004g0287 | 2 | NA18970.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.31-6101A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115669912 | ||||||
| chr3:115669922
|
T | C | 4 | a0001c0001t0001g0242a0001c0001t0001g0265a0001c0001t0002g0243others(1): Show | 4 | HG02145.hp1 HG02280.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.31-6091T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115669922 | ||||||
| chr3:115669932
|
C | T | 1 | a0001c0001t0001g0209 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.31-6081C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115669932 | ||||||
| chr3:115669965
|
A | AT | 3 | a0001c0001t0001g0326a0001c0001t0003g0009a0001c0001t0003g0301 | 3 | HG01496.hp2 HG01884.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.31-6043dupT | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115669965 | |||||
| chr3:115669969
|
TTA | T | 7 | a0001c0001t0001g0135a0001c0001t0002g0108a0001c0001t0002g0136others(4): Show | 7 | HG01169.hp1 NA18951.hp1 NA18974.hp2 others(4): Show |
intron_variant | MODIFIER | c.31-6042_31-6041del others(2): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115669969 | |||||
| chr3:115669970
|
TA | T | 53 | a0001c0001t0001g0049a0001c0001t0001g0051a0001c0001t0001g0060others(50): Show | 53 | HG00438.hp2 HG00544.hp2 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.31-6042delA | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115669970 | ||||||
| chr3:115669971
|
A | T | 5 | a0001c0001t0001g0326a0001c0001t0003g0009a0001c0001t0003g0188others(2): Show | 5 | HG01496.hp2 HG01884.hp2 HG02602.hp2 others(2): Show |
intron_variant | MODIFIER | c.31-6042A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115669971 | ||||||
| chr3:115669971
|
AT | A | 12 | a0001c0001t0001g0022a0001c0001t0001g0165a0001c0001t0001g0172others(9): Show | 12 | HG01081.hp2 HG01943.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.31-6030delT | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115669971 | |||||
| chr3:115669973
|
TTTTTTTT others(5): Show |
T | 1 | a0001c0001t0005g0278 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.31-6017_31-6006del others(12): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115669973 | |||||
| chr3:115669977
|
T | A | 4 | a0001c0001t0001g0234a0001c0001t0001g0307a0001c0001t0005g0011others(1): Show | 4 | HG01361.hp1 HG02109.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.31-6036T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115669977 | ||||||
| chr3:115669982
|
TTA | T | 20 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0042others(17): Show | 20 | HG01106.hp2 HG01891.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.31-6030_31-6029del others(2): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115669982 | ||||||
| chr3:115669983
|
T | A | 3 | a0001c0001t0001g0242a0001c0001t0002g0243a0001c0001t0002g0244 | 3 | HG02145.hp1 HG02280.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.31-6030T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115669983 | ||||||
| chr3:115669985
|
A | AT | 9 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0002g0171others(6): Show | 9 | HG02451.hp1 HG02630.hp2 NA18966.hp2 others(6): Show |
intron_variant | MODIFIER | c.31-6018dupT | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115669985 | |||||
| chr3:115669985
|
A | T | 1 | a0001c0001t0002g0116 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.31-6028A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115669985 | ||||||
| chr3:115669986
|
T | A | 20 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0042others(17): Show | 20 | HG01106.hp2 HG01891.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.31-6027T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115669986 | ||||||
| chr3:115669995
|
T | A | 8 | a0001c0001t0001g0061a0001c0001t0001g0086a0001c0001t0001g0087others(5): Show | 8 | HG02683.hp2 HG02886.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.31-6018T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115669995 | ||||||
| chr3:115669997
|
A | AT | 178 | a0001c0001t0001g0022a0001c0001t0001g0028a0001c0001t0001g0031others(175): Show | 178 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(175): Show |
intron_variant | MODIFIER | c.31-6005dupT | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115669997 | |||||
| chr3:115669997
|
A | T | 8 | a0001c0001t0001g0061a0001c0001t0001g0086a0001c0001t0001g0087others(5): Show | 8 | HG02683.hp2 HG02886.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.31-6016A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115669997 | ||||||
| chr3:115670013
|
T | C | 1 | a0001c0001t0001g0170 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.31-6000T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115670013 | ||||||
| chr3:115670072
|
TG | T | 20 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0042others(17): Show | 20 | HG01106.hp2 HG01891.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.31-5940delG | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115670072 | ||||||
| chr3:115670085
|
C | T | 1 | a0001c0001t0001g0094 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.31-5928C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115670085 | ||||||
| chr3:115670101
|
G | A | 1 | a0001c0001t0005g0204 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.31-5912G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115670101 | ||||||
| chr3:115670144
|
C | T | 9 | a0001c0001t0001g0022a0001c0001t0001g0172a0001c0001t0001g0173others(6): Show | 9 | HG01081.hp2 HG02258.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.31-5869C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115670144 | ||||||
| chr3:115670274
|
A | G | 2 | a0001c0001t0003g0288a0001c0001t0004g0287 | 2 | NA18970.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.31-5739A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115670274 | ||||||
| chr3:115670294
|
A | G | 2 | a0001c0001t0002g0264a0001c0001t0007g0275 | 2 | HG00280.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.31-5719A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115670294 | ||||||
| chr3:115670362
|
T | C | 22 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0042others(19): Show | 22 | HG01106.hp2 HG01891.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.31-5651T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115670362 | ||||||
| chr3:115670437
|
A | T | 1 | a0001c0001t0003g0023 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.31-5576A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115670437 | ||||||
| chr3:115670510
|
C | T | 1 | a0001c0001t0001g0336 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.31-5503C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115670510 | ||||||
| chr3:115670539
|
G | T | 1 | a0001c0001t0001g0079 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.31-5474G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115670539 | ||||||
| chr3:115670707
|
G | A | 216 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0019others(213): Show | 216 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(213): Show |
intron_variant | MODIFIER | c.31-5306G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115670707 | ||||||
| chr3:115670720
|
T | A | 1 | a0001c0001t0001g0191 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.31-5293T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115670720 | ||||||
| chr3:115670842
|
G | A | 2 | a0001c0001t0001g0234a0001c0001t0001g0307 | 2 | HG02109.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.31-5171G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115670842 | ||||||
| chr3:115670949
|
G | A | 131 | a0001c0001t0001g0004a0001c0001t0001g0019a0001c0001t0001g0022others(128): Show | 131 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.31-5064G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115670949 | ||||||
| chr3:115670972
|
T | C | 20 | a0001c0001t0001g0262a0001c0001t0001g0336a0001c0001t0002g0105others(17): Show | 20 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(17): Show |
intron_variant | MODIFIER | c.31-5041T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115670972 | ||||||
| chr3:115671002
|
T | A | 1 | a0001c0001t0001g0265 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.31-5011T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115671002 | ||||||
| chr3:115671284
|
C | T | 277 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0019others(274): Show | 278 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(275): Show |
intron_variant | MODIFIER | c.31-4729C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115671284 | ||||||
| chr3:115671450
|
G | A | 1 | a0001c0001t0005g0310 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.31-4563G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115671450 | ||||||
| chr3:115671989
|
G | A | 2 | a0001c0001t0001g0347a0001c0001t0005g0003 | 2 | HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.31-4024G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115671989 | ||||||
| chr3:115672020
|
G | C | 1 | a0001c0001t0002g0120 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.31-3993G>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115672020 | ||||||
| chr3:115672048
|
C | G | 275 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0022others(272): Show | 276 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.31-3965C>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115672048 | ||||||
| chr3:115672389
|
T | C | 1 | a0001c0001t0002g0148 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.31-3624T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115672389 | ||||||
| chr3:115672732
|
C | CCCTCT | 25 | a0001c0001t0001g0042a0001c0001t0001g0047a0001c0001t0001g0049others(22): Show | 25 | HG00558.hp1 HG01106.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.31-3247_31-3243dup others(5): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115672732 | |||||
| chr3:115672732
|
C | CCCTCTCC others(3): Show |
98 | a0001c0001t0001g0004a0001c0001t0001g0022a0001c0001t0001g0024others(95): Show | 98 | HG00280.hp1 HG00408.hp2 HG00621.hp2 others(95): Show |
intron_variant | MODIFIER | c.31-3252_31-3243dup others(10): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115672732 | |||||
| chr3:115672732
|
C | CCCTCTCC others(8): Show |
102 | a0001c0001t0001g0019a0001c0001t0001g0041a0001c0001t0001g0043others(99): Show | 102 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.31-3257_31-3243dup others(15): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115672732 | |||||
| chr3:115672732
|
C | CCCTCTCC others(13): Show |
46 | a0001c0001t0001g0051a0001c0001t0001g0060a0001c0001t0001g0068others(43): Show | 47 | HG00438.hp1 HG00544.hp2 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.31-3262_31-3243dup others(20): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115672732 | |||||
| chr3:115672732
|
C | CCCTCTCC others(18): Show |
9 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0193others(6): Show | 9 | HG01175.hp1 HG01891.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.31-3267_31-3243dup others(25): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115672732 | |||||
| chr3:115672732
|
C | CCCTCTCC others(23): Show |
3 | a0001c0001t0001g0002a0001c0001t0002g0243a0001c0001t0002g0244 | 3 | HG01433.hp1 HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.31-3272_31-3243dup others(30): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115672732 | |||||
| chr3:115672732
|
C | CCCTCTCC others(28): Show |
1 | a0001c0001t0001g0319 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.31-3277_31-3243dup others(35): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115672732 | |||||
| chr3:115672732
|
C | CCTCTCCT others(12): Show |
1 | a0001c0001t0002g0118 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.31-3280_31-3279ins others(19): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115672732 | |||||
| chr3:115672732
|
CCCTCTCC others(3): Show |
C | 1 | a0001c0001t0001g0112 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.31-3252_31-3243del others(10): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115672732 | |||||
| chr3:115672761
|
CTCCTCTC others(3): Show |
C | 1 | a0001c0001t0001g0215 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.31-3247_31-3238del others(10): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115672761 | |||||
| chr3:115672771
|
T | C | 9 | a0001c0001t0001g0022a0001c0001t0001g0172a0001c0001t0001g0173others(6): Show | 9 | HG01081.hp2 HG02258.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.31-3242T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115672771 | ||||||
| chr3:115672784
|
A | C | 1 | a0001c0001t0001g0215 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.31-3229A>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115672784 | ||||||
| chr3:115672794
|
G | A | 1 | a0001c0001t0001g0296 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.31-3219G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115672794 | ||||||
| chr3:115672845
|
T | C | 9 | a0001c0001t0001g0061a0001c0001t0001g0086a0001c0001t0001g0087others(6): Show | 9 | HG02683.hp2 HG02886.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.31-3168T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115672845 | ||||||
| chr3:115672899
|
C | T | 1 | a0001c0001t0001g0296 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.31-3114C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115672899 | ||||||
| chr3:115672942
|
C | T | 1 | a0001c0001t0004g0282 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.31-3071C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115672942 | ||||||
| chr3:115673167
|
G | A | 11 | a0001c0001t0001g0051a0001c0001t0002g0239a0001c0001t0003g0062others(8): Show | 11 | HG00642.hp2 HG00741.hp1 HG01074.hp1 others(8): Show |
intron_variant | MODIFIER | c.31-2846G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115673167 | ||||||
| chr3:115673184
|
C | T | 1 | a0001c0001t0003g0214 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.31-2829C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115673184 | ||||||
| chr3:115673253
|
G | A | 62 | a0001c0001t0001g0056a0001c0001t0001g0068a0001c0001t0001g0104others(59): Show | 63 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.31-2760G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115673253 | ||||||
| chr3:115673317
|
C | T | 1 | a0001c0001t0001g0031 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.31-2696C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115673317 | ||||||
| chr3:115673475
|
A | G | 1 | a0001c0001t0005g0003 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.31-2538A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115673475 | ||||||
| chr3:115673616
|
T | A | 66 | a0001c0001t0001g0049a0001c0001t0001g0051a0001c0001t0001g0060others(63): Show | 66 | HG00438.hp2 HG00544.hp2 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.31-2397T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115673616 | ||||||
| chr3:115673617
|
C | T | 66 | a0001c0001t0001g0049a0001c0001t0001g0051a0001c0001t0001g0060others(63): Show | 66 | HG00438.hp2 HG00544.hp2 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.31-2396C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115673617 | ||||||
| chr3:115673712
|
T | A | 148 | a0001c0001t0001g0002a0001c0001t0001g0049a0001c0001t0001g0051others(145): Show | 149 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(146): Show |
intron_variant | MODIFIER | c.31-2301T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115673712 | ||||||
| chr3:115673720
|
C | T | 3 | a0001c0001t0002g0163a0001c0001t0004g0248a0001c0001t0004g0282 | 3 | HG00673.hp2 NA18985.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.31-2293C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115673720 | ||||||
| chr3:115673833
|
C | T | 1 | a0001c0001t0013g0219 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.31-2180C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115673833 | ||||||
| chr3:115673916
|
G | A | 265 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0022others(262): Show | 266 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(263): Show |
intron_variant | MODIFIER | c.31-2097G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115673916 | ||||||
| chr3:115674009
|
C | T | 6 | a0001c0001t0002g0140a0001c0001t0002g0147a0001c0001t0002g0148others(3): Show | 6 | HG00558.hp2 NA18970.hp2 NA18995.hp2 others(3): Show |
intron_variant | MODIFIER | c.31-2004C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115674009 | ||||||
| chr3:115674031
|
C | T | 1 | a0001c0001t0001g0224 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.31-1982C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115674031 | ||||||
| chr3:115674170
|
G | C | 154 | a0001c0001t0001g0002a0001c0001t0001g0049a0001c0001t0001g0051others(151): Show | 155 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(152): Show |
intron_variant | MODIFIER | c.31-1843G>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115674170 | ||||||
| chr3:115674286
|
A | G | 7 | a0001c0001t0002g0161a0001c0001t0002g0178a0001c0001t0002g0184others(4): Show | 7 | HG01069.hp1 HG01071.hp1 HG01358.hp2 others(4): Show |
intron_variant | MODIFIER | c.31-1727A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115674286 | ||||||
| chr3:115674390
|
C | T | 107 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0028others(104): Show | 107 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.31-1623C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115674390 | ||||||
| chr3:115674391
|
C | T | 77 | a0001c0001t0001g0002a0001c0001t0001g0049a0001c0001t0001g0051others(74): Show | 77 | HG00438.hp2 HG00544.hp2 HG00609.hp1 others(74): Show |
intron_variant | MODIFIER | c.31-1622C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115674391 | ||||||
| chr3:115674445
|
T | C | 3 | a0001c0002t0001g0095a0001c0002t0001g0098a0001c0002t0001g0285 | 3 | HG03579.hp1 NA20129.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.31-1568T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115674445 | ||||||
| chr3:115674489
|
G | A | 76 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0033others(73): Show | 76 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.31-1524G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115674489 | ||||||
| chr3:115674496
|
T | G | 1 | a0001c0001t0001g0043 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.31-1517T>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115674496 | ||||||
| chr3:115674585
|
A | G | 1 | a0001c0001t0001g0224 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.31-1428A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115674585 | ||||||
| chr3:115674624
|
A | T | 286 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0019others(283): Show | 287 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(284): Show |
intron_variant | MODIFIER | c.31-1389A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115674624 | ||||||
| chr3:115674685
|
G | A | 2 | a0001c0001t0001g0099a0001c0001t0001g0100 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.31-1328G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115674685 | ||||||
| chr3:115674779
|
T | C | 86 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0033others(83): Show | 86 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.31-1234T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115674779 | ||||||
| chr3:115674939
|
C | T | 1 | a0001c0001t0002g0134 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.31-1074C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115674939 | ||||||
| chr3:115675027
|
A | G | 288 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0019others(285): Show | 289 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(286): Show |
intron_variant | MODIFIER | c.31-986A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115675027 | ||||||
| chr3:115675162
|
C | T | 7 | a0001c0001t0002g0198a0001c0001t0004g0143a0001c0001t0004g0144others(4): Show | 7 | HG01496.hp1 HG01943.hp2 HG02004.hp2 others(4): Show |
intron_variant | MODIFIER | c.31-851C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115675162 | ||||||
| chr3:115675291
|
C | T | 33 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0040others(30): Show | 33 | HG00140.hp2 HG00609.hp2 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.31-722C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115675291 | ||||||
| chr3:115675355
|
C | T | 1 | a0001c0001t0001g0265 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.31-658C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115675355 | ||||||
| chr3:115675412
|
G | T | 2 | a0001c0001t0001g0234a0001c0001t0001g0307 | 2 | HG02109.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.31-601G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115675412 | ||||||
| chr3:115675446
|
C | T | 202 | a0001c0001t0001g0004a0001c0001t0001g0019a0001c0001t0001g0022others(199): Show | 203 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.31-567C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115675446 | ||||||
| chr3:115675463
|
T | C | 1 | a0001c0001t0001g0307 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.31-550T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115675463 | ||||||
| chr3:115675536
|
C | T | 126 | a0001c0001t0001g0004a0001c0001t0001g0019a0001c0001t0001g0022others(123): Show | 126 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.31-477C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115675536 | ||||||
| chr3:115675589
|
C | T | 1 | a0001c0001t0003g0214 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.31-424C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115675589 | ||||||
| chr3:115675716
|
G | C | 118 | a0001c0001t0001g0004a0001c0001t0001g0019a0001c0001t0001g0024others(115): Show | 118 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.31-297G>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115675716 | ||||||
| chr3:115675758
|
C | CA | 45 | a0001c0001t0001g0015a0001c0001t0001g0040a0001c0001t0001g0050others(42): Show | 45 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.31-225dupA | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115675758 | |||||
| chr3:115675758
|
C | CAA | 11 | a0001c0001t0001g0017a0001c0001t0001g0036a0001c0001t0001g0037others(8): Show | 11 | HG00609.hp2 HG00741.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.31-226_31-225dupAA | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115675758 | |||||
| chr3:115675758
|
CA | C | 47 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0028others(44): Show | 47 | HG00673.hp2 HG01106.hp2 HG01109.hp1 others(44): Show |
intron_variant | MODIFIER | c.31-225delA | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115675758 | |||||
| chr3:115675758
|
CAA | C | 131 | a0001c0001t0001g0031a0001c0001t0001g0033a0001c0001t0001g0041others(128): Show | 132 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.31-226_31-225delAA | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115675758 | |||||
| chr3:115675758
|
CAAA | C | 78 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0051others(75): Show | 78 | HG00544.hp2 HG00609.hp1 HG00642.hp2 others(75): Show |
intron_variant | MODIFIER | c.31-227_31-225delAA others(1): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115675758 | |||||
| chr3:115675758
|
CAAAA | C | 10 | a0001c0001t0001g0049a0001c0001t0001g0100a0001c0001t0001g0221others(7): Show | 10 | HG00621.hp1 HG01884.hp1 HG01934.hp2 others(7): Show |
intron_variant | MODIFIER | c.31-228_31-225delAA others(2): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115675758 | |||||
| chr3:115675758
|
CAAAAAAA | C | 9 | a0001c0001t0001g0022a0001c0001t0001g0172a0001c0001t0001g0173others(6): Show | 9 | HG01081.hp2 HG02258.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.31-231_31-225delAA others(5): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 115675758 | |||||
| chr3:115675858
|
T | C | 299 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0019others(296): Show | 300 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.31-155T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 1/2 | chr3 | 115675858 | ||||||
| chr3:115676700
|
G | C | 3 | a0001c0001t0001g0242a0001c0001t0002g0243a0001c0001t0002g0244 | 3 | HG02145.hp1 HG02280.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.628+90G>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115676700 | ||||||
| chr3:115676799
|
CCA | C | 18 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0306others(15): Show | 18 | HG01106.hp1 HG02293.hp2 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.628+190_628+191del others(2): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115676799 | ||||||
| chr3:115676871
|
C | T | 24 | a0001c0001t0001g0042a0001c0001t0001g0063a0001c0001t0001g0070others(21): Show | 24 | HG01106.hp2 HG01891.hp1 HG02258.hp1 others(21): Show |
intron_variant | MODIFIER | c.628+261C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115676871 | ||||||
| chr3:115676973
|
T | C | 21 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0069others(18): Show | 21 | HG01081.hp2 HG01433.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.628+363T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115676973 | ||||||
| chr3:115677154
|
C | T | 1 | a0001c0001t0001g0085 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.628+544C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115677154 | ||||||
| chr3:115677335
|
C | T | 3 | a0001c0001t0001g0242a0001c0001t0002g0243a0001c0001t0002g0244 | 3 | HG02145.hp1 HG02280.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.628+725C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115677335 | ||||||
| chr3:115677404
|
T | G | 323 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0015others(320): Show | 324 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(321): Show |
intron_variant | MODIFIER | c.628+794T>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115677404 | ||||||
| chr3:115677422
|
A | C | 103 | a0001c0001t0001g0015a0001c0001t0001g0024a0001c0001t0001g0028others(100): Show | 103 | HG00140.hp2 HG00544.hp2 HG00609.hp2 others(100): Show |
intron_variant | MODIFIER | c.628+812A>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115677422 | ||||||
| chr3:115677508
|
C | T | 1 | a0001c0001t0004g0054 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.628+898C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115677508 | ||||||
| chr3:115677625
|
A | G | 3 | a0001c0001t0001g0242a0001c0001t0002g0243a0001c0001t0002g0244 | 3 | HG02145.hp1 HG02280.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.628+1015A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115677625 | ||||||
| chr3:115677681
|
T | C | 27 | a0001c0001t0001g0042a0001c0001t0001g0058a0001c0001t0001g0063others(24): Show | 27 | HG00280.hp1 HG00733.hp1 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.628+1071T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115677681 | ||||||
| chr3:115677734
|
C | T | 73 | a0001c0001t0001g0019a0001c0001t0001g0037a0001c0001t0001g0056others(70): Show | 74 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.628+1124C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115677734 | ||||||
| chr3:115677747
|
C | T | 1 | a0001c0001t0001g0251 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.628+1137C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115677747 | ||||||
| chr3:115677781
|
A | T | 3 | a0001c0001t0001g0019a0001c0001t0001g0037a0001c0002t0001g0098 | 3 | HG03516.hp2 NA18522.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.628+1171A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115677781 | ||||||
| chr3:115678353
|
G | A | 8 | a0001c0001t0001g0004a0001c0001t0001g0082a0001c0001t0001g0170others(5): Show | 8 | HG02683.hp2 HG02970.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.628+1743G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115678353 | ||||||
| chr3:115678452
|
A | G | 60 | a0001c0001t0001g0031a0001c0001t0001g0033a0001c0001t0001g0041others(57): Show | 60 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(57): Show |
intron_variant | MODIFIER | c.628+1842A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115678452 | ||||||
| chr3:115678575
|
GATA | G | 19 | a0001c0001t0001g0042a0001c0001t0001g0063a0001c0001t0001g0070others(16): Show | 19 | HG01106.hp2 HG01934.hp1 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.628+1971_628+1973d others(5): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115678575 | |||||
| chr3:115678767
|
A | G | 1 | a0001c0001t0001g0265 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.628+2157A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115678767 | ||||||
| chr3:115678938
|
G | A | 201 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0024others(198): Show | 202 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.628+2328G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115678938 | ||||||
| chr3:115679099
|
G | C | 2 | a0001c0001t0002g0211a0001c0001t0006g0149 | 2 | HG00558.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.628+2489G>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115679099 | ||||||
| chr3:115679184
|
G | A | 1 | a0001c0001t0003g0311 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.628+2574G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115679184 | ||||||
| chr3:115679272
|
T | C | 8 | a0001c0001t0001g0022a0001c0001t0001g0172a0001c0001t0001g0173others(5): Show | 8 | HG02258.hp2 HG02615.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.628+2662T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115679272 | ||||||
| chr3:115679277
|
A | G | 3 | a0001c0001t0001g0042a0001c0001t0001g0063a0001c0001t0001g0070 | 3 | HG03491.hp2 HG03492.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.628+2667A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115679277 | ||||||
| chr3:115679866
|
A | G | 1 | a0001c0001t0013g0219 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.628+3256A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115679866 | ||||||
| chr3:115679910
|
A | G | 1 | a0001c0002t0001g0285 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.628+3300A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115679910 | ||||||
| chr3:115679993
|
T | A | 208 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0019others(205): Show | 209 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.628+3383T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115679993 | ||||||
| chr3:115680179
|
T | G | 209 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0019others(206): Show | 210 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.628+3569T>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115680179 | ||||||
| chr3:115680188
|
G | A | 5 | a0001c0001t0001g0022a0001c0001t0001g0172a0001c0001t0003g0020others(2): Show | 5 | HG02615.hp1 HG02622.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.628+3578G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115680188 | ||||||
| chr3:115680381
|
G | A | 17 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0319others(14): Show | 17 | HG01106.hp1 HG02293.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.628+3771G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115680381 | ||||||
| chr3:115680557
|
A | G | 1 | a0001c0001t0005g0204 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.628+3947A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115680557 | ||||||
| chr3:115680656
|
G | A | 67 | a0001c0001t0001g0056a0001c0001t0001g0061a0001c0001t0001g0068others(64): Show | 68 | HG00280.hp2 HG00544.hp1 HG00642.hp1 others(65): Show |
intron_variant | MODIFIER | c.628+4046G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115680656 | ||||||
| chr3:115680666
|
G | A | 1 | a0001c0001t0003g0214 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.628+4056G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115680666 | ||||||
| chr3:115680980
|
G | T | 1 | a0001c0001t0007g0275 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.628+4370G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115680980 | ||||||
| chr3:115681211
|
C | T | 58 | a0001c0001t0001g0051a0001c0001t0001g0121a0001c0001t0001g0168others(55): Show | 58 | HG00544.hp2 HG00621.hp1 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.628+4601C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115681211 | ||||||
| chr3:115681356
|
C | T | 12 | a0001c0001t0001g0042a0001c0001t0001g0063a0001c0001t0001g0070others(9): Show | 12 | HG01106.hp2 HG01934.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.628+4746C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115681356 | ||||||
| chr3:115681435
|
G | A | 74 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0031others(71): Show | 74 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.628+4825G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115681435 | ||||||
| chr3:115681745
|
T | C | 1 | a0001c0001t0002g0277 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.628+5135T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115681745 | ||||||
| chr3:115681997
|
C | A | 1 | a0001c0001t0004g0280 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.628+5387C>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115681997 | ||||||
| chr3:115682201
|
A | G | 7 | a0001c0001t0001g0072a0001c0001t0001g0085a0001c0001t0001g0099others(4): Show | 7 | HG01361.hp1 HG02257.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.628+5591A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115682201 | ||||||
| chr3:115682451
|
C | A | 27 | a0001c0001t0001g0004a0001c0001t0001g0066a0001c0001t0001g0067others(24): Show | 27 | HG01106.hp1 HG02293.hp2 HG02486.hp2 others(24): Show |
intron_variant | MODIFIER | c.628+5841C>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115682451 | ||||||
| chr3:115682599
|
T | C | 313 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0015others(310): Show | 314 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(311): Show |
intron_variant | MODIFIER | c.628+5989T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115682599 | ||||||
| chr3:115682729
|
A | G | 312 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0019others(309): Show | 313 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(310): Show |
intron_variant | MODIFIER | c.628+6119A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115682729 | ||||||
| chr3:115682780
|
G | T | 2 | a0001c0001t0001g0082a0001c0001t0001g0350 | 2 | HG02976.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.628+6170G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115682780 | ||||||
| chr3:115682834
|
T | C | 1 | a0001c0001t0002g0120 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.628+6224T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115682834 | ||||||
| chr3:115682896
|
G | A | 2 | a0001c0001t0003g0155a0001c0001t0003g0156 | 2 | HG00642.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.628+6286G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115682896 | ||||||
| chr3:115682952
|
A | G | 1 | a0001c0001t0005g0011 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.628+6342A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115682952 | ||||||
| chr3:115683032
|
G | A | 77 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0031others(74): Show | 77 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.628+6422G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115683032 | ||||||
| chr3:115683113
|
CTACA | C | 22 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0082others(19): Show | 22 | HG01106.hp1 HG02293.hp2 HG02486.hp2 others(19): Show |
intron_variant | MODIFIER | c.628+6509_628+6512d others(6): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115683113 | |||||
| chr3:115683118
|
TACATGTG others(7): Show |
T | 2 | a0001c0001t0001g0207a0001c0002t0001g0095 | 2 | HG03688.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.628+6509_628+6522d others(16): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115683118 | ||||||
| chr3:115683121
|
A | G | 1 | a0001c0001t0001g0240 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.628+6511A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115683121 | ||||||
| chr3:115683122
|
TGTGCGCG others(7): Show |
T | 1 | a0001c0001t0005g0344 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.628+6514_628+6527d others(16): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115683122 | |||||
| chr3:115683122
|
TGTGCGCG others(9): Show |
T | 4 | a0001c0001t0001g0072a0001c0001t0001g0085a0001c0001t0001g0313others(1): Show | 4 | HG02257.hp1 HG03041.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.628+6514_628+6529d others(18): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115683122 | |||||
| chr3:115683124
|
T | C | 3 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0240 | 3 | HG02896.hp2 HG02897.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.628+6514T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115683124 | ||||||
| chr3:115683124
|
T | TGCGCGCG others(3): Show |
1 | a0001c0001t0001g0019 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.628+6521_628+6522i others(12): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115683124 | |||||
| chr3:115683124
|
T | TGCGCGCG others(5): Show |
1 | a0001c0001t0001g0349 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.628+6521_628+6522i others(14): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115683124 | |||||
| chr3:115683124
|
TGC | T | 86 | a0001c0001t0001g0033a0001c0001t0001g0041a0001c0001t0001g0043others(83): Show | 87 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.628+6522_628+6523d others(4): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115683124 | |||||
| chr3:115683124
|
TGCGCGCG others(5): Show |
T | 1 | a0001c0001t0005g0204 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.628+6524_628+6535d others(14): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115683124 | |||||
| chr3:115683126
|
C | T | 1 | a0001c0001t0003g0014 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.628+6516C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115683126 | ||||||
| chr3:115683126
|
CGCGCGCG others(1): Show |
C | 12 | a0001c0001t0001g0038a0001c0001t0001g0040a0001c0001t0001g0050others(9): Show | 12 | HG00639.hp1 HG00639.hp2 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.628+6524_628+6531d others(10): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115683126 | |||||
| chr3:115683128
|
C | CGCGT | 3 | a0001c0001t0001g0081a0001c0001t0005g0011a0001c0001t0005g0348 | 3 | HG01081.hp2 HG02258.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.628+6521_628+6522i others(6): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115683128 | |||||
| chr3:115683128
|
CGCGCGT | C | 21 | a0001c0001t0001g0015a0001c0001t0001g0052a0001c0001t0001g0067others(18): Show | 21 | HG00140.hp2 HG00738.hp1 HG01258.hp1 others(18): Show |
intron_variant | MODIFIER | c.628+6524_628+6529d others(8): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115683128 | |||||
| chr3:115683129
|
G | GTGTGCGC others(7): Show |
1 | a0001c0001t0001g0225 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.628+6519_628+6520i others(16): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115683129 | ||||||
| chr3:115683130
|
C | A | 1 | a0001c0001t0001g0225 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.628+6520C>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115683130 | ||||||
| chr3:115683130
|
C | CGT | 9 | a0001c0001t0001g0002a0001c0001t0001g0173a0001c0001t0001g0197others(6): Show | 9 | HG01433.hp1 HG02258.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.628+6521_628+6522i others(4): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115683130 | |||||
| chr3:115683130
|
CGCGT | C | 47 | a0001c0001t0001g0024a0001c0001t0001g0028a0001c0001t0001g0051others(44): Show | 47 | HG00544.hp2 HG00621.hp1 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.628+6524_628+6527d others(6): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115683130 | |||||
| chr3:115683132
|
C | A | 1 | a0001c0001t0001g0342 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.628+6522C>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115683132 | ||||||
| chr3:115683132
|
C | T | 56 | a0001c0001t0001g0022a0001c0001t0001g0031a0001c0001t0001g0042others(53): Show | 56 | HG00280.hp1 HG00280.hp2 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.628+6522C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115683132 | ||||||
| chr3:115683132
|
CGT | C | 27 | a0001c0001t0001g0079a0001c0001t0001g0168a0001c0001t0001g0169others(24): Show | 27 | HG00408.hp1 HG01261.hp2 HG01496.hp1 others(24): Show |
intron_variant | MODIFIER | c.628+6524_628+6525d others(4): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115683132 | |||||
| chr3:115683133
|
GTGCGCGC others(11): Show |
G | 2 | a0001c0001t0001g0099a0001c0001t0001g0100 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.628+6524_628+6541d others(20): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115683133 | ||||||
| chr3:115683134
|
T | C | 108 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0019others(105): Show | 108 | HG00280.hp1 HG00280.hp2 HG00609.hp2 others(105): Show |
intron_variant | MODIFIER | c.628+6524T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115683134 | ||||||
| chr3:115683134
|
T | TGC | 3 | a0001c0001t0001g0089a0001c0001t0001g0315a0001c0001t0002g0331 | 3 | HG00609.hp1 NA18966.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.628+6537_628+6538d others(4): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115683134 | |||||
| chr3:115683136
|
C | T | 13 | a0001c0001t0002g0008a0001c0001t0002g0045a0001c0001t0002g0115others(10): Show | 13 | HG00673.hp2 HG01255.hp2 HG02083.hp1 others(10): Show |
intron_variant | MODIFIER | c.628+6526C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115683136 | ||||||
| chr3:115683137
|
GCGCGCGC others(21): Show |
G | 2 | a0001c0001t0001g0082a0001c0001t0001g0350 | 2 | HG02976.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.628+6529_628+6556d others(30): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115683137 | |||||
| chr3:115683138
|
C | T | 1 | a0001c0002t0001g0098 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.628+6528C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115683138 | ||||||
| chr3:115683139
|
G | A | 1 | a0001c0001t0001g0224 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.628+6529G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115683139 | ||||||
| chr3:115683141
|
G | A | 9 | a0001c0001t0001g0224a0001c0001t0001g0240a0001c0001t0001g0319others(6): Show | 9 | HG02293.hp2 HG02486.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.628+6531G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115683141 | ||||||
| chr3:115683141
|
G | GCACACAC others(3): Show |
1 | a0001c0001t0003g0190 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.628+6532_628+6533i others(12): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115683141 | |||||
| chr3:115683141
|
GCGCGCGC others(3): Show |
G | 2 | a0001c0001t0001g0153a0001c0001t0002g0218 | 2 | HG01192.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.628+6533_628+6542d others(12): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115683141 | |||||
| chr3:115683141
|
GCGCGCGC others(5): Show |
G | 2 | a0001c0001t0001g0064a0001c0001t0004g0333 | 2 | HG00609.hp2 HG00733.hp2 |
intron_variant | MODIFIER | c.628+6533_628+6544d others(14): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115683141 | |||||
| chr3:115683143
|
G | A | 28 | a0001c0001t0001g0002a0001c0001t0001g0066a0001c0001t0001g0170others(25): Show | 28 | HG00673.hp1 HG00738.hp2 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.628+6533G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115683143 | ||||||
| chr3:115683143
|
G | GCA | 3 | a0001c0001t0002g0337a0001c0001t0003g0155a0001c0001t0003g0157 | 3 | HG00642.hp2 HG02602.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.628+6534_628+6535i others(4): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115683143 | |||||
| chr3:115683143
|
G | GCACA | 5 | a0001c0001t0002g0026a0001c0001t0002g0226a0001c0001t0002g0323others(2): Show | 5 | HG00741.hp1 HG02523.hp2 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.628+6534_628+6535i others(6): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115683143 | |||||
| chr3:115683143
|
G | GCACACAC others(3): Show |
1 | a0001c0001t0003g0284 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.628+6534_628+6535i others(12): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115683143 | |||||
| chr3:115683143
|
G | T | 1 | a0001c0001t0001g0232 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.628+6533G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115683143 | ||||||
| chr3:115683144
|
C | A | 1 | a0001c0001t0001g0232 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.628+6534C>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115683144 | ||||||
| chr3:115683145
|
G | A | 79 | a0001c0001t0001g0002a0001c0001t0001g0055a0001c0001t0001g0066others(76): Show | 79 | HG00408.hp1 HG00621.hp2 HG00642.hp2 others(76): Show |
intron_variant | MODIFIER | c.628+6535G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115683145 | ||||||
| chr3:115683145
|
G | GCA | 3 | a0001c0001t0008g0235a0001c0001t0008g0236a0001c0001t0009g0077 | 3 | HG01069.hp2 HG01081.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.628+6536_628+6537i others(4): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115683145 | |||||
| chr3:115683145
|
G | GCACA | 3 | a0001c0001t0001g0037a0001c0001t0002g0179a0001c0001t0002g0201 | 3 | HG03516.hp2 NA18985.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.628+6536_628+6537i others(6): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115683145 | |||||
| chr3:115683145
|
GCGCA | G | 11 | a0001c0001t0002g0102a0001c0001t0002g0120a0001c0001t0002g0294others(8): Show | 11 | HG01517.hp2 HG01952.hp2 HG01975.hp2 others(8): Show |
intron_variant | MODIFIER | c.628+6537_628+6540d others(6): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115683145 | |||||
| chr3:115683146
|
C | T | 6 | a0001c0001t0001g0056a0001c0001t0001g0290a0001c0001t0002g0117others(3): Show | 6 | HG00642.hp1 HG01074.hp2 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.628+6536C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115683146 | ||||||
| chr3:115683147
|
G | A | 166 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0024others(163): Show | 166 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.628+6537G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115683147 | ||||||
| chr3:115683147
|
G | GCA | 4 | a0001c0001t0001g0049a0001c0001t0001g0060a0001c0001t0004g0059others(1): Show | 4 | HG00438.hp2 HG03225.hp2 NA18955.hp1 others(1): Show |
intron_variant | MODIFIER | c.628+6577_628+6578d others(4): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115683147 | |||||
| chr3:115683147
|
G | GCACA | 3 | a0001c0001t0001g0073a0001c0001t0004g0249a0001c0001t0010g0246 | 3 | HG02683.hp1 HG02895.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.628+6575_628+6578d others(6): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115683147 | |||||
| chr3:115683147
|
G | GCACACA | 4 | a0001c0001t0001g0088a0001c0001t0001g0302a0001c0001t0002g0127others(1): Show | 4 | HG01934.hp1 HG02897.hp1 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.628+6573_628+6578d others(8): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115683147 | |||||
| chr3:115683147
|
G | GCGCGCGC others(3): Show |
1 | a0001c0001t0005g0341 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.628+6538_628+6539i others(12): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115683147 | |||||
| chr3:115683147
|
G | GCGCGCGC others(5): Show |
1 | a0001c0001t0005g0310 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.628+6538_628+6539i others(14): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115683147 | |||||
| chr3:115683147
|
G | GCGCGCGC others(7): Show |
4 | a0001c0001t0001g0042a0001c0001t0001g0070a0001c0001t0002g0164others(1): Show | 4 | HG02280.hp1 HG03471.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.628+6538_628+6539i others(16): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115683147 | |||||
| chr3:115683147
|
G | GCGCGCGC others(7): Show |
1 | a0001c0001t0002g0267 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.628+6538_628+6539i others(16): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115683147 | |||||
| chr3:115683147
|
G | GCGCGCGC others(5): Show |
1 | a0001c0001t0003g0241 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.628+6538_628+6539i others(14): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115683147 | |||||
| chr3:115683147
|
G | GCGCGCGC others(7): Show |
1 | a0001c0001t0001g0087 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.628+6538_628+6539i others(16): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115683147 | |||||
| chr3:115683147
|
GCA | G | 18 | a0001c0001t0001g0036a0001c0001t0001g0047a0001c0001t0001g0119others(15): Show | 18 | HG00558.hp1 HG02055.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.628+6577_628+6578d others(4): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115683147 | |||||
| chr3:115683147
|
GCACA | G | 29 | a0001c0001t0001g0056a0001c0001t0001g0068a0001c0001t0001g0145others(26): Show | 30 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.628+6575_628+6578d others(6): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115683147 | |||||
| chr3:115683147
|
GCACACA | G | 8 | a0001c0001t0001g0004a0001c0001t0001g0104a0001c0001t0001g0228others(5): Show | 8 | HG00733.hp1 HG00735.hp1 HG02148.hp2 others(5): Show |
intron_variant | MODIFIER | c.628+6573_628+6578d others(8): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115683147 | |||||
| chr3:115683147
|
GCACACAC others(3): Show |
G | 1 | a0001c0001t0002g0304 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.628+6569_628+6578d others(12): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115683147 | |||||
| chr3:115683148
|
C | T | 2 | a0001c0001t0002g0057a0001c0001t0002g0118 | 2 | HG01099.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.628+6538C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115683148 | ||||||
| chr3:115683149
|
A | G | 32 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0040others(29): Show | 32 | HG00639.hp1 HG00639.hp2 HG00735.hp2 others(29): Show |
intron_variant | MODIFIER | c.628+6539A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115683149 | ||||||
| chr3:115683151
|
A | G | 6 | a0001c0001t0001g0081a0001c0001t0001g0119a0001c0001t0002g0171others(3): Show | 6 | HG02145.hp1 HG02258.hp1 HG03669.hp2 others(3): Show |
intron_variant | MODIFIER | c.628+6541A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115683151 | ||||||
| chr3:115683153
|
A | G | 1 | a0001c0001t0002g0231 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.628+6543A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115683153 | ||||||
| chr3:115683155
|
A | G | 6 | a0001c0001t0001g0004a0001c0001t0001g0228a0001c0001t0001g0229others(3): Show | 6 | HG00733.hp1 HG00735.hp1 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.628+6545A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115683155 | ||||||
| chr3:115683157
|
A | G | 6 | a0001c0001t0001g0058a0001c0001t0001g0228a0001c0001t0001g0229others(3): Show | 6 | HG00733.hp1 HG00735.hp1 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.628+6547A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115683157 | ||||||
| chr3:115683159
|
A | G | 5 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0230others(2): Show | 5 | HG00280.hp1 HG00733.hp1 HG00735.hp1 others(2): Show |
intron_variant | MODIFIER | c.628+6549A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115683159 | ||||||
| chr3:115683161
|
A | G | 1 | a0001c0001t0002g0304 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.628+6551A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115683161 | ||||||
| chr3:115683360
|
G | C | 1 | a0001c0001t0004g0139 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.628+6750G>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115683360 | ||||||
| chr3:115683375
|
A | G | 2 | a0001c0001t0001g0290a0001c0001t0002g0289 | 2 | HG01074.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.628+6765A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115683375 | ||||||
| chr3:115683399
|
G | A | 2 | a0001c0001t0001g0066a0001c0001t0001g0067 | 2 | NA18747.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.628+6789G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115683399 | ||||||
| chr3:115683604
|
A | AG | 290 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0015others(287): Show | 291 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.628+6994_628+6995i others(3): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115683604 | ||||||
| chr3:115683609
|
A | G | 1 | a0001c0001t0002g0239 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.628+6999A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115683609 | ||||||
| chr3:115683688
|
G | T | 2 | a0001c0001t0002g0140a0001c0001t0002g0147 | 2 | NA18970.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.628+7078G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115683688 | ||||||
| chr3:115683766
|
C | T | 4 | a0001c0001t0001g0080a0001c0001t0001g0209a0001c0001t0001g0306others(1): Show | 4 | HG01891.hp1 HG02055.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.628+7156C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115683766 | ||||||
| chr3:115683838
|
A | T | 81 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0031others(78): Show | 81 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.628+7228A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115683838 | ||||||
| chr3:115683895
|
T | C | 291 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0015others(288): Show | 292 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.628+7285T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115683895 | ||||||
| chr3:115683928
|
G | A | 2 | a0001c0002t0002g0192a0001c0002t0002g0223 | 2 | HG02622.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.628+7318G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115683928 | ||||||
| chr3:115684208
|
C | T | 208 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0019others(205): Show | 209 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.628+7598C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115684208 | ||||||
| chr3:115684368
|
A | G | 1 | a0001c0001t0001g0349 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.628+7758A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115684368 | ||||||
| chr3:115684495
|
C | T | 1 | a0001c0001t0002g0295 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.628+7885C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115684495 | ||||||
| chr3:115684563
|
G | A | 2 | a0001c0001t0008g0235a0001c0001t0008g0236 | 2 | HG01069.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.628+7953G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115684563 | ||||||
| chr3:115684564
|
G | GT | 8 | a0001c0001t0001g0022a0001c0001t0001g0172a0001c0001t0001g0173others(5): Show | 8 | HG02258.hp2 HG02615.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.628+7955dupT | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115684564 | |||||
| chr3:115684744
|
G | A | 5 | a0001c0001t0001g0019a0001c0001t0001g0037a0001c0001t0001g0081others(2): Show | 5 | HG01109.hp1 HG02258.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.628+8134G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115684744 | ||||||
| chr3:115684886
|
C | T | 9 | a0001c0001t0001g0004a0001c0001t0001g0082a0001c0001t0001g0170others(6): Show | 9 | HG02683.hp2 HG02970.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.628+8276C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115684886 | ||||||
| chr3:115684968
|
C | A | 1 | a0001c0001t0005g0204 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.628+8358C>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115684968 | ||||||
| chr3:115684971
|
C | T | 82 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0031others(79): Show | 82 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.628+8361C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115684971 | ||||||
| chr3:115685022
|
T | C | 1 | a0001c0001t0009g0187 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.628+8412T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115685022 | ||||||
| chr3:115685081
|
T | G | 286 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0015others(283): Show | 287 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(284): Show |
intron_variant | MODIFIER | c.628+8471T>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115685081 | ||||||
| chr3:115685746
|
T | C | 209 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0019others(206): Show | 210 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.628+9136T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115685746 | ||||||
| chr3:115685799
|
G | A | 8 | a0001c0001t0001g0061a0001c0001t0001g0297a0001c0001t0001g0345others(5): Show | 8 | HG01081.hp2 HG02559.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.628+9189G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115685799 | ||||||
| chr3:115685830
|
C | T | 1 | a0001c0001t0004g0280 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.628+9220C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115685830 | ||||||
| chr3:115685866
|
C | T | 33 | a0001c0001t0001g0004a0001c0001t0001g0066a0001c0001t0001g0067others(30): Show | 33 | HG01106.hp1 HG01361.hp1 HG02257.hp1 others(30): Show |
intron_variant | MODIFIER | c.628+9256C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115685866 | ||||||
| chr3:115686144
|
C | T | 312 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0015others(309): Show | 313 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(310): Show |
intron_variant | MODIFIER | c.628+9534C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115686144 | ||||||
| chr3:115686321
|
C | G | 312 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0015others(309): Show | 313 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(310): Show |
intron_variant | MODIFIER | c.628+9711C>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115686321 | ||||||
| chr3:115686344
|
C | T | 105 | a0001c0001t0001g0019a0001c0001t0001g0037a0001c0001t0001g0056others(102): Show | 106 | HG00280.hp2 HG00544.hp1 HG00642.hp1 others(103): Show |
intron_variant | MODIFIER | c.628+9734C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115686344 | ||||||
| chr3:115686550
|
A | G | 4 | a0001c0001t0001g0080a0001c0001t0001g0209a0001c0001t0001g0306others(1): Show | 4 | HG01891.hp1 HG02055.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.628+9940A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115686550 | ||||||
| chr3:115686658
|
T | C | 83 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0031others(80): Show | 83 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.628+10048T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115686658 | ||||||
| chr3:115686940
|
G | A | 2 | a0001c0001t0003g0020a0001c0001t0003g0021 | 2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.628+10330G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115686940 | ||||||
| chr3:115687108
|
C | G | 3 | a0001c0001t0002g0179a0001c0001t0002g0194a0001c0001t0002g0201 | 3 | NA18974.hp2 NA18985.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.628+10498C>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115687108 | ||||||
| chr3:115687114
|
TC | T | 89 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0031others(86): Show | 89 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.628+10505delC | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115687114 | ||||||
| chr3:115687115
|
C | CT | 240 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0019others(237): Show | 241 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(238): Show |
intron_variant | MODIFIER | c.628+10518dupT | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115687115 | |||||
| chr3:115687115
|
C | CTT | 14 | a0001c0001t0001g0004a0001c0001t0001g0051a0001c0001t0001g0082others(11): Show | 14 | HG01069.hp2 HG01081.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.628+10517_628+1051 others(6): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115687115 | |||||
| chr3:115687209
|
A | T | 1 | a0001c0001t0002g0321 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.628+10599A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115687209 | ||||||
| chr3:115687239
|
T | C | 318 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0015others(315): Show | 319 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(316): Show |
intron_variant | MODIFIER | c.628+10629T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115687239 | ||||||
| chr3:115687380
|
C | T | 1 | a0001c0001t0005g0005 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.628+10770C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115687380 | ||||||
| chr3:115687421
|
A | G | 1 | a0001c0001t0001g0297 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.628+10811A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115687421 | ||||||
| chr3:115687438
|
A | G | 2 | a0001c0001t0002g0106a0001c0001t0002g0295 | 2 | NA18969.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.628+10828A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115687438 | ||||||
| chr3:115687631
|
T | C | 202 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0022others(199): Show | 202 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.628+11021T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115687631 | ||||||
| chr3:115687634
|
C | T | 74 | a0001c0001t0001g0019a0001c0001t0001g0037a0001c0001t0001g0052others(71): Show | 75 | HG00280.hp2 HG00544.hp1 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.628+11024C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115687634 | ||||||
| chr3:115687706
|
C | T | 11 | a0001c0001t0001g0052a0001c0001t0001g0056a0001c0001t0001g0290others(8): Show | 11 | HG00642.hp1 HG00738.hp1 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.628+11096C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115687706 | ||||||
| chr3:115687729
|
A | G | 1 | a0001c0001t0002g0158 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.628+11119A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115687729 | ||||||
| chr3:115687750
|
C | G | 343 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0015others(340): Show | 344 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(341): Show |
intron_variant | MODIFIER | c.628+11140C>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115687750 | ||||||
| chr3:115687960
|
A | C | 98 | a0001c0001t0001g0015a0001c0001t0001g0024a0001c0001t0001g0028others(95): Show | 98 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.628+11350A>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115687960 | ||||||
| chr3:115687995
|
G | A | 1 | a0001c0001t0004g0141 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.628+11385G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115687995 | ||||||
| chr3:115688006
|
A | ATTAT | 138 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0019others(135): Show | 139 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(136): Show |
intron_variant | MODIFIER | c.628+11417_628+1142 others(8): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115688006 | |||||
| chr3:115688006
|
A | T | 2 | a0001c0001t0001g0342a0001c0001t0005g0341 | 2 | HG02809.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.628+11396A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115688006 | ||||||
| chr3:115688051
|
C | G | 1 | a0001c0001t0002g0220 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.628+11441C>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115688051 | ||||||
| chr3:115688137
|
C | T | 19 | a0001c0001t0001g0042a0001c0001t0001g0063a0001c0001t0001g0070others(16): Show | 19 | HG01106.hp2 HG01934.hp1 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.628+11527C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115688137 | ||||||
| chr3:115688152
|
G | A | 81 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0031others(78): Show | 81 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.628+11542G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115688152 | ||||||
| chr3:115688187
|
T | A | 3 | a0001c0001t0003g0071a0001c0001t0003g0078a0001c0001t0011g0075 | 3 | HG01261.hp2 HG03710.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.628+11577T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115688187 | ||||||
| chr3:115688215
|
G | A | 17 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0319others(14): Show | 17 | HG01106.hp1 HG02293.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.628+11605G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115688215 | ||||||
| chr3:115688307
|
G | C | 343 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0015others(340): Show | 344 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(341): Show |
intron_variant | MODIFIER | c.628+11697G>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115688307 | ||||||
| chr3:115688406
|
T | C | 62 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0036others(59): Show | 62 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.628+11796T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115688406 | ||||||
| chr3:115688462
|
CTCTA | C | 82 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0024others(79): Show | 82 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.628+11858_628+1186 others(8): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115688462 | |||||
| chr3:115688463
|
T | C | 62 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0036others(59): Show | 62 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.628+11853T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115688463 | ||||||
| chr3:115688655
|
A | G | 8 | a0001c0001t0001g0022a0001c0001t0001g0172a0001c0001t0001g0173others(5): Show | 8 | HG02258.hp2 HG02615.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.628+12045A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115688655 | ||||||
| chr3:115688715
|
C | T | 1 | a0001c0001t0001g0053 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.628+12105C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115688715 | ||||||
| chr3:115688877
|
T | C | 1 | a0001c0001t0001g0306 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.628+12267T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115688877 | ||||||
| chr3:115688937
|
G | A | 19 | a0001c0001t0001g0042a0001c0001t0001g0063a0001c0001t0001g0070others(16): Show | 19 | HG01074.hp2 HG01099.hp1 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.628+12327G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115688937 | ||||||
| chr3:115689149
|
T | C | 1 | a0001c0001t0004g0249 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.628+12539T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115689149 | ||||||
| chr3:115689258
|
G | T | 3 | a0001c0001t0002g0108a0001c0001t0002g0122a0001c0001t0002g0123 | 3 | NA18955.hp2 NA19003.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.628+12648G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115689258 | ||||||
| chr3:115689355
|
A | G | 11 | a0001c0001t0001g0019a0001c0001t0001g0024a0001c0001t0001g0037others(8): Show | 11 | HG01109.hp1 HG02109.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.628+12745A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115689355 | ||||||
| chr3:115689445
|
GA | G | 4 | a0001c0002t0001g0035a0001c0002t0002g0039a0001c0002t0002g0192others(1): Show | 4 | HG01106.hp1 HG02615.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.628+12838delA | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115689445 | |||||
| chr3:115689465
|
A | G | 1 | a0001c0001t0005g0204 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.628+12855A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115689465 | ||||||
| chr3:115689506
|
T | C | 42 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0036others(39): Show | 42 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.628+12896T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115689506 | ||||||
| chr3:115689814
|
A | T | 1 | a0001c0001t0004g0141 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.628+13204A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115689814 | ||||||
| chr3:115690061
|
T | C | 1 | a0001c0001t0004g0287 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.628+13451T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115690061 | ||||||
| chr3:115690197
|
C | T | 1 | a0001c0001t0001g0207 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.628+13587C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115690197 | ||||||
| chr3:115690223
|
C | G | 1 | a0001c0001t0001g0332 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.628+13613C>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115690223 | ||||||
| chr3:115690237
|
C | T | 2 | a0001c0001t0001g0015a0001c0001t0002g0239 | 2 | HG01257.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.628+13627C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115690237 | ||||||
| chr3:115690549
|
G | C | 3 | a0001c0001t0001g0019a0001c0001t0001g0224a0001c0001t0001g0265 | 3 | HG02630.hp1 HG02970.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.628+13939G>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115690549 | ||||||
| chr3:115690602
|
T | C | 4 | a0001c0001t0010g0245a0001c0001t0010g0246a0001c0002t0002g0192others(1): Show | 4 | HG02622.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.628+13992T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115690602 | ||||||
| chr3:115690620
|
T | C | 1 | a0001c0001t0002g0271 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.628+14010T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115690620 | ||||||
| chr3:115690711
|
A | G | 1 | a0001c0001t0001g0104 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.628+14101A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115690711 | ||||||
| chr3:115690746
|
T | C | 1 | a0001c0001t0014g0250 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.628+14136T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115690746 | ||||||
| chr3:115690757
|
C | CT | 26 | a0001c0001t0001g0002a0001c0001t0001g0052a0001c0001t0001g0170others(23): Show | 26 | HG00438.hp2 HG00609.hp2 HG00733.hp1 others(23): Show |
intron_variant | MODIFIER | c.628+14163dupT | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115690757 | |||||
| chr3:115690778
|
C | T | 18 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0088others(15): Show | 18 | HG02071.hp2 HG02293.hp2 HG02630.hp2 others(15): Show |
intron_variant | MODIFIER | c.628+14168C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115690778 | ||||||
| chr3:115690792
|
G | A | 1 | a0001c0001t0019g0013 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.628+14182G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115690792 | ||||||
| chr3:115690807
|
G | A | 1 | a0001c0001t0003g0113 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.628+14197G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115690807 | ||||||
| chr3:115690842
|
G | A | 1 | a0001c0001t0005g0204 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.628+14232G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115690842 | ||||||
| chr3:115691307
|
T | A | 1 | a0001c0001t0003g0279 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.628+14697T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115691307 | ||||||
| chr3:115691469
|
C | T | 1 | a0001c0001t0001g0225 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.628+14859C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115691469 | ||||||
| chr3:115691470
|
G | A | 1 | a0001c0001t0002g0108 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.628+14860G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115691470 | ||||||
| chr3:115692016
|
G | A | 2 | a0001c0001t0001g0174a0001c0001t0018g0335 | 2 | NA18982.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.628+15406G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115692016 | ||||||
| chr3:115692083
|
C | T | 3 | a0001c0001t0001g0173a0001c0001t0001g0197a0001c0001t0001g0338 | 3 | HG02258.hp2 HG06807.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.628+15473C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115692083 | ||||||
| chr3:115692144
|
A | G | 36 | a0001c0001t0001g0017a0001c0001t0001g0024a0001c0001t0001g0031others(33): Show | 36 | HG00733.hp1 HG00735.hp1 HG01361.hp1 others(33): Show |
intron_variant | MODIFIER | c.628+15534A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115692144 | ||||||
| chr3:115692386
|
G | T | 82 | a0001c0001t0001g0004a0001c0001t0001g0022a0001c0001t0001g0037others(79): Show | 82 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.628+15776G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115692386 | ||||||
| chr3:115692568
|
C | T | 1 | a0001c0001t0001g0225 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.628+15958C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115692568 | ||||||
| chr3:115692631
|
G | A | 1 | a0001c0001t0001g0209 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.628+16021G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115692631 | ||||||
| chr3:115692691
|
G | C | 1 | a0001c0001t0001g0306 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.628+16081G>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115692691 | ||||||
| chr3:115692702
|
T | G | 1 | a0001c0001t0001g0225 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.628+16092T>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115692702 | ||||||
| chr3:115692728
|
G | A | 1 | a0001c0001t0002g0218 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.628+16118G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115692728 | ||||||
| chr3:115692818
|
T | A | 1 | a0001c0001t0001g0345 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.628+16208T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115692818 | ||||||
| chr3:115692818
|
T | C | 2 | a0001c0001t0001g0024a0001c0002t0001g0035 | 2 | HG02615.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.628+16208T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115692818 | ||||||
| chr3:115692837
|
T | C | 1 | a0001c0001t0001g0259 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.628+16227T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115692837 | ||||||
| chr3:115692908
|
C | T | 1 | a0001c0001t0004g0030 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.628+16298C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115692908 | ||||||
| chr3:115692986
|
T | C | 1 | a0001c0001t0013g0219 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.628+16376T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115692986 | ||||||
| chr3:115693000
|
C | T | 37 | a0001c0001t0001g0017a0001c0001t0001g0024a0001c0001t0001g0031others(34): Show | 37 | HG00733.hp1 HG00735.hp1 HG01361.hp1 others(34): Show |
intron_variant | MODIFIER | c.628+16390C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115693000 | ||||||
| chr3:115693267
|
A | G | 1 | a0001c0002t0001g0133 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.628+16657A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115693267 | ||||||
| chr3:115693339
|
C | G | 8 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0092others(5): Show | 8 | HG02451.hp1 HG02622.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.628+16729C>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115693339 | ||||||
| chr3:115693485
|
TAA | T | 8 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0092others(5): Show | 8 | HG02451.hp1 HG02622.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.628+16877_628+1687 others(6): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115693485 | |||||
| chr3:115693487
|
AATTATT | A | 55 | a0001c0001t0001g0015a0001c0001t0001g0165a0001c0001t0001g0349others(52): Show | 55 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.628+16893_628+1689 others(10): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115693487 | |||||
| chr3:115693716
|
G | A | 54 | a0001c0001t0001g0015a0001c0001t0001g0165a0001c0001t0002g0010others(51): Show | 54 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.628+17106G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115693716 | ||||||
| chr3:115694215
|
T | G | 1 | a0001c0001t0001g0225 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.628+17605T>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115694215 | ||||||
| chr3:115694232
|
C | T | 24 | a0001c0001t0001g0165a0001c0001t0001g0349a0001c0001t0002g0270others(21): Show | 24 | HG00544.hp1 HG00673.hp2 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.628+17622C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115694232 | ||||||
| chr3:115694578
|
A | T | 39 | a0001c0001t0001g0017a0001c0001t0001g0024a0001c0001t0001g0031others(36): Show | 39 | HG00733.hp1 HG00735.hp1 HG01361.hp1 others(36): Show |
intron_variant | MODIFIER | c.628+17968A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115694578 | ||||||
| chr3:115694812
|
C | G | 1 | a0001c0001t0002g0123 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.628+18202C>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115694812 | ||||||
| chr3:115694869
|
A | G | 1 | a0001c0001t0001g0225 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.628+18259A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115694869 | ||||||
| chr3:115694960
|
C | T | 21 | a0001c0001t0001g0165a0001c0001t0002g0270a0001c0001t0002g0294others(18): Show | 21 | HG00544.hp1 HG00673.hp2 HG01928.hp2 others(18): Show |
intron_variant | MODIFIER | c.628+18350C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115694960 | ||||||
| chr3:115694963
|
C | A | 343 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0015others(340): Show | 344 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(341): Show |
intron_variant | MODIFIER | c.628+18353C>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115694963 | ||||||
| chr3:115695005
|
G | A | 1 | a0001c0001t0005g0341 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.628+18395G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115695005 | ||||||
| chr3:115695026
|
A | T | 218 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0015others(215): Show | 219 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.628+18416A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115695026 | ||||||
| chr3:115695134
|
A | G | 1 | a0001c0001t0012g0300 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.628+18524A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115695134 | ||||||
| chr3:115695341
|
C | G | 218 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0015others(215): Show | 219 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.628+18731C>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115695341 | ||||||
| chr3:115695730
|
C | T | 1 | a0001c0001t0001g0119 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.628+19120C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115695730 | ||||||
| chr3:115695899
|
G | T | 343 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0015others(340): Show | 344 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(341): Show |
intron_variant | MODIFIER | c.628+19289G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115695899 | ||||||
| chr3:115696104
|
T | C | 38 | a0001c0001t0001g0019a0001c0001t0001g0165a0001c0001t0001g0224others(35): Show | 38 | HG00438.hp2 HG00544.hp1 HG00609.hp2 others(35): Show |
intron_variant | MODIFIER | c.628+19494T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115696104 | ||||||
| chr3:115696174
|
A | G | 2 | a0001c0001t0010g0245a0001c0001t0010g0246 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.628+19564A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115696174 | ||||||
| chr3:115696211
|
A | G | 38 | a0001c0001t0001g0019a0001c0001t0001g0165a0001c0001t0001g0224others(35): Show | 38 | HG00438.hp2 HG00544.hp1 HG00609.hp2 others(35): Show |
intron_variant | MODIFIER | c.628+19601A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115696211 | ||||||
| chr3:115696294
|
C | T | 1 | a0001c0001t0001g0225 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.628+19684C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115696294 | ||||||
| chr3:115696575
|
A | C | 1 | a0001c0001t0001g0302 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.628+19965A>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115696575 | ||||||
| chr3:115696576
|
C | A | 1 | a0001c0001t0001g0302 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.628+19966C>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115696576 | ||||||
| chr3:115696576
|
C | CCA | 8 | a0001c0001t0001g0169a0001c0001t0002g0010a0001c0001t0002g0032others(5): Show | 8 | HG03486.hp2 NA18944.hp1 NA18970.hp2 others(5): Show |
intron_variant | MODIFIER | c.628+19967_628+1996 others(6): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115696576 | |||||
| chr3:115696577
|
C | CA | 60 | a0001c0001t0001g0015a0001c0001t0001g0044a0001c0001t0001g0080others(57): Show | 60 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.628+19967_628+1996 others(5): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115696577 | ||||||
| chr3:115696577
|
CG | C | 16 | a0001c0001t0001g0052a0001c0001t0001g0056a0001c0001t0001g0063others(13): Show | 16 | HG00738.hp1 HG01071.hp2 HG01074.hp2 others(13): Show |
intron_variant | MODIFIER | c.628+19968delG | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115696577 | ||||||
| chr3:115696578
|
G | A | 128 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0028others(125): Show | 129 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.628+19968G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115696578 | ||||||
| chr3:115696578
|
G | C | 72 | a0001c0001t0001g0015a0001c0001t0001g0044a0001c0001t0001g0080others(69): Show | 72 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.628+19968G>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115696578 | ||||||
| chr3:115696578
|
G | GC | 16 | a0001c0001t0001g0061a0001c0001t0001g0068a0001c0001t0001g0073others(13): Show | 16 | HG02148.hp2 HG02258.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.628+19980dupC | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115696578 | |||||
| chr3:115696578
|
G | GCC | 24 | a0001c0001t0001g0017a0001c0001t0001g0087a0001c0001t0001g0091others(21): Show | 24 | HG01361.hp1 HG01884.hp1 HG02083.hp2 others(21): Show |
intron_variant | MODIFIER | c.628+19979_628+1998 others(6): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115696578 | |||||
| chr3:115696578
|
G | GCCC | 25 | a0001c0001t0001g0031a0001c0001t0001g0033a0001c0001t0001g0037others(22): Show | 25 | HG00673.hp2 HG01081.hp2 HG01943.hp1 others(22): Show |
intron_variant | MODIFIER | c.628+19978_628+1998 others(7): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115696578 | |||||
| chr3:115696578
|
G | GCCCC | 15 | a0001c0001t0001g0262a0001c0001t0001g0349a0001c0001t0004g0130others(12): Show | 15 | HG00544.hp1 HG01109.hp1 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.628+19977_628+1998 others(8): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115696578 | |||||
| chr3:115696579
|
C | A | 17 | a0001c0001t0001g0052a0001c0001t0001g0056a0001c0001t0001g0063others(14): Show | 17 | HG00738.hp1 HG01071.hp2 HG01074.hp2 others(14): Show |
intron_variant | MODIFIER | c.628+19969C>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115696579 | ||||||
| chr3:115696584
|
C | A | 21 | a0001c0001t0001g0036a0001c0001t0001g0066a0001c0001t0001g0067others(18): Show | 21 | HG02055.hp1 HG02071.hp2 HG02293.hp2 others(18): Show |
intron_variant | MODIFIER | c.628+19974C>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115696584 | ||||||
| chr3:115696808
|
T | G | 38 | a0001c0001t0001g0019a0001c0001t0001g0165a0001c0001t0001g0224others(35): Show | 38 | HG00438.hp2 HG00544.hp1 HG00609.hp2 others(35): Show |
intron_variant | MODIFIER | c.628+20198T>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115696808 | ||||||
| chr3:115696852
|
G | GACAGAGT others(277): Show |
1 | a0001c0001t0001g0209 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.628+20255_628+2025 others(288): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115696852 | |||||
| chr3:115696862
|
C | T | 2 | a0001c0001t0001g0222a0001c0001t0001g0307 | 2 | HG02451.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.628+20252C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115696862 | ||||||
| chr3:115696902
|
A | G | 343 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0015others(340): Show | 344 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(341): Show |
intron_variant | MODIFIER | c.628+20292A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115696902 | ||||||
| chr3:115696987
|
A | G | 44 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0024others(41): Show | 44 | HG00733.hp1 HG00735.hp1 HG01361.hp1 others(41): Show |
intron_variant | MODIFIER | c.628+20377A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115696987 | ||||||
| chr3:115696991
|
G | A | 12 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0092others(9): Show | 12 | HG02145.hp1 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.628+20381G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115696991 | ||||||
| chr3:115696994
|
TA | T | 4 | a0001c0001t0001g0242a0001c0001t0001g0306a0001c0001t0002g0243others(1): Show | 4 | HG02145.hp1 HG02280.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.628+20387delA | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115696994 | |||||
| chr3:115697057
|
T | C | 4 | a0001c0001t0001g0242a0001c0001t0001g0306a0001c0001t0002g0243others(1): Show | 4 | HG02145.hp1 HG02280.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.628+20447T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115697057 | ||||||
| chr3:115697187
|
T | G | 3 | a0001c0001t0001g0019a0001c0001t0001g0224a0001c0001t0001g0265 | 3 | HG02630.hp1 HG02970.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.628+20577T>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115697187 | ||||||
| chr3:115697207
|
A | AATAAT | 347 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0015others(344): Show | 348 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(345): Show |
intron_variant | MODIFIER | c.628+20601_628+2060 others(9): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115697207 | |||||
| chr3:115697284
|
A | G | 38 | a0001c0001t0001g0019a0001c0001t0001g0165a0001c0001t0001g0224others(35): Show | 38 | HG00438.hp2 HG00544.hp1 HG00609.hp2 others(35): Show |
intron_variant | MODIFIER | c.628+20674A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115697284 | ||||||
| chr3:115697379
|
C | T | 1 | a0001c0001t0001g0297 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.628+20769C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115697379 | ||||||
| chr3:115697466
|
C | A | 25 | a0001c0001t0001g0165a0001c0001t0001g0349a0001c0001t0002g0270others(22): Show | 25 | HG00544.hp1 HG00673.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.628+20856C>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115697466 | ||||||
| chr3:115697489
|
C | T | 8 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0092others(5): Show | 8 | HG02451.hp1 HG02622.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.628+20879C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115697489 | ||||||
| chr3:115697668
|
A | G | 3 | a0001c0001t0001g0061a0001c0001t0001g0345a0001c0001t0003g0325 | 3 | HG02886.hp2 HG03453.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.628+21058A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115697668 | ||||||
| chr3:115697701
|
G | C | 3 | a0001c0001t0001g0242a0001c0001t0002g0243a0001c0001t0002g0244 | 3 | HG02145.hp1 HG02280.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.628+21091G>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115697701 | ||||||
| chr3:115697815
|
T | C | 4 | a0001c0001t0001g0242a0001c0001t0001g0306a0001c0001t0002g0243others(1): Show | 4 | HG02145.hp1 HG02280.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.628+21205T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115697815 | ||||||
| chr3:115697831
|
A | G | 1 | a0001c0001t0005g0204 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.628+21221A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115697831 | ||||||
| chr3:115697896
|
A | T | 1 | a0001c0001t0003g0157 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.628+21286A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115697896 | ||||||
| chr3:115697908
|
T | C | 1 | a0001c0001t0001g0326 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.628+21298T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115697908 | ||||||
| chr3:115697950
|
G | A | 2 | a0001c0002t0001g0095a0001c0002t0001g0098 | 2 | NA20129.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.628+21340G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115697950 | ||||||
| chr3:115697982
|
T | TGC | 194 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0022others(191): Show | 195 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.628+21374_628+2137 others(6): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115697982 | |||||
| chr3:115697984
|
C | CGCGT | 14 | a0001c0001t0001g0046a0001c0001t0001g0064a0001c0001t0001g0082others(11): Show | 14 | HG00140.hp1 HG00140.hp2 HG00733.hp2 others(11): Show |
intron_variant | MODIFIER | c.628+21375_628+2137 others(8): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115697984 | |||||
| chr3:115697984
|
CGT | C | 127 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0019others(124): Show | 127 | HG00438.hp2 HG00544.hp1 HG00609.hp2 others(124): Show |
intron_variant | MODIFIER | c.628+21399_628+2140 others(6): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115697984 | |||||
| chr3:115697986
|
T | C | 8 | a0001c0001t0002g0010a0001c0001t0002g0032a0001c0001t0002g0134others(5): Show | 8 | HG01943.hp2 HG02523.hp2 NA18970.hp2 others(5): Show |
intron_variant | MODIFIER | c.628+21376T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115697986 | ||||||
| chr3:115698000
|
T | C | 127 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0019others(124): Show | 127 | HG00438.hp2 HG00544.hp1 HG00609.hp2 others(124): Show |
intron_variant | MODIFIER | c.628+21390T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698000 | ||||||
| chr3:115698021
|
T | C | 21 | a0001c0001t0001g0037a0001c0001t0002g0164a0001c0001t0002g0308others(18): Show | 21 | HG00438.hp2 HG00609.hp2 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.628+21411T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698021 | ||||||
| chr3:115698024
|
C | T | 25 | a0001c0001t0001g0165a0001c0001t0001g0349a0001c0001t0002g0270others(22): Show | 25 | HG00544.hp1 HG00673.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.628+21414C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698024 | ||||||
| chr3:115698027
|
GTATATAA others(16): Show |
G | 1 | a0001c0001t0001g0019 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.628+21441_628+2146 others(27): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698027 | |||||
| chr3:115698035
|
A | AATATATA others(66): Show |
1 | a0001c0001t0003g0279 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.628+21477_628+2147 others(77): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698035 | |||||
| chr3:115698043
|
TTATATAT others(9): Show |
T | 4 | a0001c0001t0001g0242a0001c0001t0001g0265a0001c0001t0001g0306others(1): Show | 4 | HG02280.hp2 HG02970.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.628+21447_628+2146 others(20): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698043 | |||||
| chr3:115698044
|
TATATATT others(7): Show |
T | 2 | a0001c0001t0001g0225a0001c0001t0005g0005 | 2 | HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.628+21441_628+2145 others(18): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698044 | |||||
| chr3:115698050
|
T | TAA | 23 | a0001c0001t0001g0165a0001c0001t0002g0270a0001c0001t0002g0294others(20): Show | 23 | HG00544.hp1 HG00673.hp2 HG01928.hp2 others(20): Show |
intron_variant | MODIFIER | c.628+21440_628+2144 others(6): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698050 | ||||||
| chr3:115698050
|
T | TAATATAT others(4): Show |
1 | a0001c0001t0004g0137 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.628+21440_628+2144 others(15): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698050 | ||||||
| chr3:115698050
|
T | TAATATAT others(258): Show |
1 | a0001c0001t0001g0349 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.628+21440_628+2144 others(269): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698050 | ||||||
| chr3:115698050
|
T | TAATATAT others(4): Show |
31 | a0001c0001t0001g0037a0001c0001t0001g0090a0001c0001t0001g0091others(28): Show | 31 | HG00438.hp2 HG00609.hp2 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.628+21440_628+2144 others(15): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698050 | ||||||
| chr3:115698050
|
T | TAATATAT others(8): Show |
21 | a0001c0001t0001g0015a0001c0001t0001g0066a0001c0001t0001g0067others(18): Show | 21 | HG01261.hp1 HG02071.hp2 HG02293.hp2 others(18): Show |
intron_variant | MODIFIER | c.628+21440_628+2144 others(19): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698050 | ||||||
| chr3:115698050
|
T | TAATATAT others(29): Show |
2 | a0001c0001t0001g0036a0001c0001t0001g0315 | 2 | HG02055.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.628+21440_628+2144 others(40): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698050 | ||||||
| chr3:115698050
|
TTATATAA | T | 37 | a0001c0001t0001g0017a0001c0001t0001g0024a0001c0001t0001g0031others(34): Show | 37 | HG00733.hp1 HG00735.hp1 HG01361.hp1 others(34): Show |
intron_variant | MODIFIER | c.628+21441_628+2144 others(11): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698050 | ||||||
| chr3:115698051
|
T | A | 2 | a0001c0001t0002g0244a0001c0001t0003g0007 | 2 | HG02145.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.628+21441T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698051 | ||||||
| chr3:115698057
|
A | T | 10 | a0001c0001t0002g0244a0001c0001t0004g0025a0001c0001t0004g0059others(7): Show | 10 | HG00438.hp2 HG00609.hp2 HG01496.hp1 others(7): Show |
intron_variant | MODIFIER | c.628+21447A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698057 | ||||||
| chr3:115698058
|
A | T | 1 | a0001c0001t0004g0137 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.628+21448A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698058 | ||||||
| chr3:115698058
|
AATATATA others(68): Show |
A | 1 | a0001c0001t0002g0244 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.628+21456_628+2153 others(79): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698058 | |||||
| chr3:115698066
|
T | A | 26 | a0001c0001t0001g0165a0001c0001t0001g0225a0001c0001t0002g0270others(23): Show | 26 | HG00544.hp1 HG00673.hp2 HG01928.hp2 others(23): Show |
intron_variant | MODIFIER | c.628+21456T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698066 | ||||||
| chr3:115698067
|
T | A | 42 | a0001c0001t0001g0017a0001c0001t0001g0024a0001c0001t0001g0031others(39): Show | 42 | HG00733.hp1 HG00735.hp1 HG01361.hp1 others(39): Show |
intron_variant | MODIFIER | c.628+21457T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698067 | ||||||
| chr3:115698070
|
ATAT | A | 37 | a0001c0001t0001g0017a0001c0001t0001g0024a0001c0001t0001g0031others(34): Show | 37 | HG00733.hp1 HG00735.hp1 HG01361.hp1 others(34): Show |
intron_variant | MODIFIER | c.628+21461_628+2146 others(7): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698070 | ||||||
| chr3:115698074
|
A | ATTATATA others(197): Show |
1 | a0001c0001t0004g0249 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.628+21464_628+2146 others(208): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698074 | ||||||
| chr3:115698074
|
A | ATTATATA others(231): Show |
13 | a0001c0001t0001g0165a0001c0001t0002g0294a0001c0001t0004g0130others(10): Show | 13 | HG00544.hp1 HG01928.hp2 HG01934.hp2 others(10): Show |
intron_variant | MODIFIER | c.628+21464_628+2146 others(242): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698074 | ||||||
| chr3:115698074
|
A | ATTATATA others(299): Show |
1 | a0001c0001t0004g0200 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.628+21464_628+2146 others(310): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698074 | ||||||
| chr3:115698074
|
A | ATTATATA others(265): Show |
2 | a0001c0001t0004g0054a0001c0001t0004g0309 | 2 | HG02083.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.628+21464_628+2146 others(276): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698074 | ||||||
| chr3:115698074
|
A | ATTATATA others(265): Show |
1 | a0001c0001t0003g0023 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.628+21464_628+2146 others(276): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698074 | ||||||
| chr3:115698074
|
A | ATTATATA others(299): Show |
1 | a0001c0001t0015g0154 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.628+21464_628+2146 others(310): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698074 | ||||||
| chr3:115698074
|
A | ATTATATA others(299): Show |
1 | a0001c0001t0013g0219 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.628+21464_628+2146 others(310): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698074 | ||||||
| chr3:115698074
|
A | ATTATATA others(197): Show |
3 | a0001c0001t0002g0270a0001c0001t0004g0248a0001c0001t0004g0282 | 3 | HG00673.hp2 NA18990.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.628+21464_628+2146 others(208): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698074 | ||||||
| chr3:115698076
|
T | A | 1 | a0001c0001t0001g0238 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.628+21466T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698076 | ||||||
| chr3:115698082
|
A | AAATATAT | 17 | a0001c0001t0001g0015a0001c0001t0001g0066a0001c0001t0001g0067others(14): Show | 17 | HG01261.hp1 HG02071.hp2 HG02293.hp2 others(14): Show |
intron_variant | MODIFIER | c.628+21477_628+2147 others(11): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698082 | |||||
| chr3:115698082
|
A | T | 1 | a0001c0001t0003g0007 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.628+21472A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698082 | ||||||
| chr3:115698083
|
A | AATATATA others(9): Show |
1 | a0001c0001t0005g0341 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.628+21477_628+2147 others(20): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698083 | |||||
| chr3:115698083
|
A | T | 1 | a0001c0001t0003g0007 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.628+21473A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698083 | ||||||
| chr3:115698088
|
G | A | 342 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0015others(339): Show | 343 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(340): Show |
intron_variant | MODIFIER | c.628+21478G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698088 | ||||||
| chr3:115698091
|
T | A | 16 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0002g0083others(13): Show | 16 | HG00438.hp2 HG00609.hp2 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.628+21481T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698091 | ||||||
| chr3:115698099
|
A | T | 4 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0002g0083others(1): Show | 4 | HG02647.hp2 HG03490.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.628+21489A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698099 | ||||||
| chr3:115698107
|
A | T | 17 | a0001c0001t0001g0015a0001c0001t0001g0066a0001c0001t0001g0067others(14): Show | 17 | HG01261.hp1 HG02071.hp2 HG02293.hp2 others(14): Show |
intron_variant | MODIFIER | c.628+21497A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698107 | ||||||
| chr3:115698108
|
A | G | 2 | a0001c0001t0001g0019a0001c0001t0001g0265 | 2 | HG02970.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.628+21498A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698108 | ||||||
| chr3:115698108
|
A | T | 28 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0165others(25): Show | 28 | HG00544.hp1 HG00673.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.628+21498A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698108 | ||||||
| chr3:115698109
|
ATATATAA others(7): Show |
A | 3 | a0001c0001t0001g0242a0001c0001t0001g0306a0001c0001t0002g0243 | 3 | HG02280.hp2 HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.628+21506_628+2151 others(18): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698109 | |||||
| chr3:115698114
|
T | TAA | 24 | a0001c0001t0001g0165a0001c0001t0001g0349a0001c0001t0002g0270others(21): Show | 24 | HG00544.hp1 HG00673.hp2 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.628+21505_628+2150 others(6): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698114 | |||||
| chr3:115698114
|
T | TCTTATAT others(215): Show |
1 | a0001c0001t0004g0180 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.628+21504_628+2150 others(226): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698114 | ||||||
| chr3:115698114
|
T | TCTTATAT others(224): Show |
6 | a0001c0001t0004g0025a0001c0001t0004g0059a0001c0001t0004g0159others(3): Show | 6 | HG00438.hp2 HG00609.hp2 NA18968.hp2 others(3): Show |
intron_variant | MODIFIER | c.628+21504_628+2150 others(235): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698114 | ||||||
| chr3:115698114
|
T | TCTTATAT others(249): Show |
1 | a0001c0001t0004g0143 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.628+21504_628+2150 others(260): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698114 | ||||||
| chr3:115698114
|
T | TCTTATAT others(283): Show |
1 | a0001c0001t0004g0144 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.628+21504_628+2150 others(294): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698114 | ||||||
| chr3:115698115
|
A | C | 1 | a0001c0001t0004g0137 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.628+21505A>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698115 | ||||||
| chr3:115698115
|
A | T | 1 | a0001c0001t0003g0007 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.628+21505A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698115 | ||||||
| chr3:115698116
|
A | T | 2 | a0001c0001t0001g0225a0001c0001t0004g0137 | 2 | HG02129.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.628+21506A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698116 | ||||||
| chr3:115698117
|
T | A | 18 | a0001c0001t0001g0015a0001c0001t0001g0066a0001c0001t0001g0067others(15): Show | 18 | HG01261.hp1 HG02071.hp2 HG02293.hp2 others(15): Show |
intron_variant | MODIFIER | c.628+21507T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698117 | ||||||
| chr3:115698121
|
T | A | 1 | a0001c0001t0003g0007 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.628+21511T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698121 | ||||||
| chr3:115698122
|
A | T | 1 | a0001c0001t0003g0007 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.628+21512A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698122 | ||||||
| chr3:115698123
|
T | A | 3 | a0001c0001t0002g0083a0001c0001t0003g0007a0001c0001t0005g0233 | 3 | HG02647.hp2 HG03516.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.628+21513T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698123 | ||||||
| chr3:115698124
|
T | A | 6 | a0001c0001t0001g0225a0001c0001t0002g0083a0001c0001t0004g0137others(3): Show | 6 | HG02129.hp1 HG02647.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.628+21514T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698124 | ||||||
| chr3:115698126
|
T | A | 17 | a0001c0001t0001g0015a0001c0001t0001g0066a0001c0001t0001g0067others(14): Show | 17 | HG01261.hp1 HG02071.hp2 HG02293.hp2 others(14): Show |
intron_variant | MODIFIER | c.628+21516T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698126 | ||||||
| chr3:115698130
|
T | A | 17 | a0001c0001t0001g0015a0001c0001t0001g0066a0001c0001t0001g0067others(14): Show | 17 | HG01261.hp1 HG02071.hp2 HG02293.hp2 others(14): Show |
intron_variant | MODIFIER | c.628+21520T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698130 | ||||||
| chr3:115698130
|
TAA | T | 52 | a0001c0001t0001g0046a0001c0001t0001g0051a0001c0001t0001g0297others(49): Show | 53 | HG00140.hp1 HG00140.hp2 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.628+21521_628+2152 others(6): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698130 | ||||||
| chr3:115698131
|
A | T | 180 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0015others(177): Show | 180 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.628+21521A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698131 | ||||||
| chr3:115698131
|
AAT | A | 3 | a0001c0001t0001g0242a0001c0001t0001g0306a0001c0001t0002g0243 | 3 | HG02280.hp2 HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.628+21529_628+2153 others(6): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698131 | |||||
| chr3:115698131
|
AATATATA others(10): Show |
A | 1 | a0001c0001t0001g0240 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.628+21522_628+2153 others(21): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698131 | ||||||
| chr3:115698132
|
ATATATAT others(9): Show |
A | 32 | a0001c0001t0001g0017a0001c0001t0001g0024a0001c0001t0001g0031others(29): Show | 32 | HG01361.hp1 HG01884.hp1 HG02109.hp2 others(29): Show |
intron_variant | MODIFIER | c.628+21538_628+2155 others(20): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698132 | |||||
| chr3:115698133
|
T | A | 3 | a0001c0001t0003g0007a0001c0002t0001g0095a0001c0002t0001g0098 | 3 | NA19084.hp1 NA20129.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.628+21523T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698133 | ||||||
| chr3:115698134
|
A | ATATATTA others(32): Show |
2 | a0001c0002t0001g0095a0001c0002t0001g0098 | 2 | NA20129.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.628+21529_628+2153 others(43): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698134 | |||||
| chr3:115698139
|
T | A | 34 | a0001c0001t0001g0165a0001c0001t0001g0349a0001c0001t0002g0212others(31): Show | 34 | HG00438.hp2 HG00544.hp1 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.628+21529T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698139 | ||||||
| chr3:115698139
|
T | TAAAATAT others(272): Show |
1 | a0001c0001t0004g0137 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.628+21531_628+2153 others(283): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698139 | |||||
| chr3:115698139
|
T | TTA | 17 | a0001c0001t0001g0015a0001c0001t0001g0066a0001c0001t0001g0067others(14): Show | 17 | HG01261.hp1 HG02071.hp2 HG02293.hp2 others(14): Show |
intron_variant | MODIFIER | c.628+21529_628+2153 others(6): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698139 | ||||||
| chr3:115698140
|
A | AATATATA others(18): Show |
2 | a0001c0001t0010g0245a0001c0001t0010g0246 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.628+21537_628+2153 others(29): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698140 | |||||
| chr3:115698140
|
A | T | 54 | a0001c0001t0001g0046a0001c0001t0001g0051a0001c0001t0001g0297others(51): Show | 55 | HG00140.hp1 HG00140.hp2 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.628+21530A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698140 | ||||||
| chr3:115698140
|
AATATATA others(2): Show |
A | 159 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0028others(156): Show | 159 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.628+21538_628+2154 others(13): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698140 | |||||
| chr3:115698141
|
A | T | 1 | a0001c0001t0003g0007 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.628+21531A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698141 | ||||||
| chr3:115698142
|
T | A | 2 | a0001c0002t0001g0095a0001c0002t0001g0098 | 2 | NA20129.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.628+21532T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698142 | ||||||
| chr3:115698147
|
A | AAAATATA others(34): Show |
10 | a0001c0001t0002g0164a0001c0001t0002g0308a0001c0001t0005g0003others(7): Show | 10 | HG01081.hp2 HG01106.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.628+21537_628+2153 others(45): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698147 | ||||||
| chr3:115698147
|
A | C | 3 | a0001c0001t0001g0019a0001c0001t0001g0224a0001c0001t0001g0265 | 3 | HG02630.hp1 HG02970.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.628+21537A>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698147 | ||||||
| chr3:115698147
|
A | T | 2 | a0001c0001t0001g0037a0001c0001t0005g0341 | 2 | HG02809.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.628+21537A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698147 | ||||||
| chr3:115698148
|
T | A | 13 | a0001c0001t0001g0073a0001c0001t0001g0170a0001c0001t0001g0228others(10): Show | 13 | HG00733.hp1 HG00735.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.628+21538T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698148 | ||||||
| chr3:115698149
|
T | A | 63 | a0001c0001t0001g0046a0001c0001t0001g0051a0001c0001t0001g0073others(60): Show | 64 | HG00140.hp1 HG00140.hp2 HG00642.hp2 others(61): Show |
intron_variant | MODIFIER | c.628+21539T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698149 | ||||||
| chr3:115698149
|
T | TATATATA others(41): Show |
1 | a0001c0001t0002g0212 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.628+21561_628+2156 others(52): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698149 | |||||
| chr3:115698155
|
T | A | 1 | a0001c0001t0003g0007 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.628+21545T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698155 | ||||||
| chr3:115698156
|
A | T | 22 | a0001c0001t0001g0015a0001c0001t0001g0066a0001c0001t0001g0067others(19): Show | 22 | HG00733.hp1 HG00735.hp1 HG01261.hp1 others(19): Show |
intron_variant | MODIFIER | c.628+21546A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698156 | ||||||
| chr3:115698158
|
T | A | 5 | a0001c0001t0001g0073a0001c0001t0001g0170a0001c0001t0001g0228others(2): Show | 5 | HG00733.hp1 HG00735.hp1 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.628+21548T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698158 | ||||||
| chr3:115698162
|
T | A | 22 | a0001c0001t0001g0015a0001c0001t0001g0066a0001c0001t0001g0067others(19): Show | 22 | HG00733.hp1 HG00735.hp1 HG01261.hp1 others(19): Show |
intron_variant | MODIFIER | c.628+21552T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698162 | ||||||
| chr3:115698163
|
A | T | 5 | a0001c0001t0001g0073a0001c0001t0001g0170a0001c0001t0001g0228others(2): Show | 5 | HG00733.hp1 HG00735.hp1 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.628+21553A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698163 | ||||||
| chr3:115698165
|
A | T | 25 | a0001c0001t0001g0015a0001c0001t0001g0066a0001c0001t0001g0067others(22): Show | 25 | HG00733.hp1 HG00735.hp1 HG01261.hp1 others(22): Show |
intron_variant | MODIFIER | c.628+21555A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698165 | ||||||
| chr3:115698169
|
TA | T | 3 | a0001c0001t0001g0222a0001c0001t0001g0234a0001c0001t0001g0307 | 3 | HG02109.hp2 HG02451.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.628+21560delA | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698169 | ||||||
| chr3:115698171
|
T | A | 18 | a0001c0001t0001g0015a0001c0001t0001g0066a0001c0001t0001g0067others(15): Show | 18 | HG01261.hp1 HG02071.hp2 HG02293.hp2 others(15): Show |
intron_variant | MODIFIER | c.628+21561T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698171 | ||||||
| chr3:115698172
|
T | A | 2 | a0001c0002t0001g0095a0001c0002t0001g0098 | 2 | NA20129.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.628+21562T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698172 | ||||||
| chr3:115698172
|
TAAA | T | 34 | a0001c0001t0001g0165a0001c0001t0001g0349a0001c0001t0002g0270others(31): Show | 34 | HG00438.hp2 HG00544.hp1 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.628+21563_628+2156 others(7): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698172 | ||||||
| chr3:115698174
|
A | T | 18 | a0001c0001t0001g0015a0001c0001t0001g0066a0001c0001t0001g0067others(15): Show | 18 | HG01261.hp1 HG02071.hp2 HG02293.hp2 others(15): Show |
intron_variant | MODIFIER | c.628+21564A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698174 | ||||||
| chr3:115698177
|
A | ATATATT | 5 | a0001c0001t0001g0073a0001c0001t0001g0170a0001c0001t0001g0228others(2): Show | 5 | HG00733.hp1 HG00735.hp1 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.628+21567_628+2156 others(10): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698177 | ||||||
| chr3:115698177
|
AAT | A | 3 | a0001c0001t0001g0019a0001c0001t0001g0224a0001c0001t0001g0265 | 3 | HG02630.hp1 HG02970.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.628+21576_628+2157 others(6): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698177 | |||||
| chr3:115698179
|
T | C | 27 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0090others(24): Show | 27 | HG01081.hp2 HG01106.hp1 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.628+21569T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698179 | ||||||
| chr3:115698179
|
T | TATATA | 17 | a0001c0001t0001g0015a0001c0001t0001g0066a0001c0001t0001g0067others(14): Show | 17 | HG01261.hp1 HG02071.hp2 HG02293.hp2 others(14): Show |
intron_variant | MODIFIER | c.628+21570_628+2157 others(9): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698179 | |||||
| chr3:115698182
|
A | AT | 5 | a0001c0001t0001g0073a0001c0001t0001g0170a0001c0001t0001g0228others(2): Show | 5 | HG00733.hp1 HG00735.hp1 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.628+21573dupT | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698182 | |||||
| chr3:115698188
|
T | A | 58 | a0001c0001t0001g0015a0001c0001t0001g0066a0001c0001t0001g0067others(55): Show | 58 | HG00438.hp2 HG00544.hp1 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.628+21578T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698188 | ||||||
| chr3:115698189
|
A | T | 2 | a0001c0002t0001g0095a0001c0002t0001g0098 | 2 | NA20129.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.628+21579A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698189 | ||||||
| chr3:115698198
|
T | A | 7 | a0001c0001t0001g0073a0001c0001t0001g0170a0001c0001t0001g0228others(4): Show | 7 | HG00733.hp1 HG00735.hp1 HG02148.hp2 others(4): Show |
intron_variant | MODIFIER | c.628+21588T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698198 | ||||||
| chr3:115698199
|
T | A | 18 | a0001c0001t0001g0015a0001c0001t0001g0066a0001c0001t0001g0067others(15): Show | 18 | HG01261.hp1 HG02071.hp2 HG02293.hp2 others(15): Show |
intron_variant | MODIFIER | c.628+21589T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698199 | ||||||
| chr3:115698205
|
T | A | 5 | a0001c0001t0001g0073a0001c0001t0001g0170a0001c0001t0001g0228others(2): Show | 5 | HG00733.hp1 HG00735.hp1 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.628+21595T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698205 | ||||||
| chr3:115698205
|
T | TAATA | 18 | a0001c0001t0001g0015a0001c0001t0001g0066a0001c0001t0001g0067others(15): Show | 18 | HG01261.hp1 HG02071.hp2 HG02293.hp2 others(15): Show |
intron_variant | MODIFIER | c.628+21595_628+2159 others(8): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698205 | ||||||
| chr3:115698205
|
TTATATAA others(2): Show |
T | 8 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0092others(5): Show | 8 | HG02451.hp1 HG02622.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.628+21603_628+2161 others(13): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698205 | |||||
| chr3:115698210
|
T | TAATATAT others(18): Show |
1 | a0001c0001t0001g0037 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.628+21602_628+2160 others(29): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698210 | |||||
| chr3:115698210
|
T | TAATATAT others(4): Show |
5 | a0001c0001t0001g0073a0001c0001t0001g0170a0001c0001t0001g0228others(2): Show | 5 | HG00733.hp1 HG00735.hp1 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.628+21602_628+2160 others(15): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698210 | |||||
| chr3:115698210
|
TAA | T | 15 | a0001c0001t0001g0242a0001c0001t0001g0306a0001c0001t0002g0164others(12): Show | 15 | HG01081.hp2 HG01106.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.628+21603_628+2160 others(6): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698210 | |||||
| chr3:115698212
|
A | AAATATAT | 44 | a0001c0001t0001g0017a0001c0001t0001g0024a0001c0001t0001g0031others(41): Show | 44 | HG01361.hp1 HG01884.hp1 HG01943.hp2 others(41): Show |
intron_variant | MODIFIER | c.628+21618_628+2162 others(11): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698212 | |||||
| chr3:115698212
|
A | AAATATAT others(41): Show |
1 | a0001c0001t0001g0042 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.628+21624_628+2162 others(52): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698212 | |||||
| chr3:115698212
|
A | AAATATAT others(34): Show |
110 | a0001c0001t0001g0004a0001c0001t0001g0022a0001c0001t0001g0028others(107): Show | 110 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.628+21624_628+2162 others(45): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698212 | |||||
| chr3:115698212
|
A | AAATATAT others(68): Show |
75 | a0001c0001t0001g0002a0001c0001t0001g0038a0001c0001t0001g0040others(72): Show | 76 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(73): Show |
intron_variant | MODIFIER | c.628+21624_628+2162 others(79): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698212 | |||||
| chr3:115698212
|
A | AAATATAT others(102): Show |
6 | a0001c0001t0001g0046a0001c0001t0002g0131a0001c0001t0003g0078others(3): Show | 6 | HG00140.hp1 HG00140.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.628+21624_628+2162 others(113): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698212 | |||||
| chr3:115698212
|
A | AAATATAT others(170): Show |
9 | a0001c0001t0001g0051a0001c0001t0003g0062a0001c0001t0003g0125others(6): Show | 9 | HG00642.hp2 HG00738.hp2 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.628+21624_628+2162 others(181): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698212 | |||||
| chr3:115698212
|
A | AAATATAT others(204): Show |
1 | a0001c0001t0003g0303 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.628+21624_628+2162 others(215): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698212 | |||||
| chr3:115698212
|
A | AAATATAT others(105): Show |
3 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0346 | 3 | HG01891.hp2 HG02965.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.628+21624_628+2162 others(116): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698212 | |||||
| chr3:115698212
|
A | AAATATAT others(32): Show |
1 | a0001c0001t0002g0305 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.628+21623_628+2162 others(43): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698212 | |||||
| chr3:115698212
|
A | T | 2 | a0001c0002t0001g0095a0001c0002t0001g0098 | 2 | NA20129.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.628+21602A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698212 | ||||||
| chr3:115698213
|
A | AAT | 19 | a0001c0001t0001g0015a0001c0001t0001g0066a0001c0001t0001g0067others(16): Show | 19 | HG01261.hp1 HG02071.hp2 HG02293.hp2 others(16): Show |
intron_variant | MODIFIER | c.628+21609_628+2161 others(6): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698213 | |||||
| chr3:115698213
|
A | AATATATA others(27): Show |
1 | a0001c0001t0001g0240 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.628+21624_628+2162 others(38): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698213 | |||||
| chr3:115698213
|
A | T | 6 | a0001c0001t0001g0037a0001c0001t0001g0073a0001c0001t0001g0170others(3): Show | 6 | HG00733.hp1 HG00735.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.628+21603A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698213 | ||||||
| chr3:115698214
|
A | ATATATAA others(66): Show |
5 | a0001c0001t0002g0127a0001c0001t0002g0128a0001c0001t0002g0179others(2): Show | 5 | NA18974.hp2 NA18983.hp2 NA18985.hp1 others(2): Show |
intron_variant | MODIFIER | c.628+21624_628+2162 others(77): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698214 | |||||
| chr3:115698229
|
T | TATATAAT others(32): Show |
1 | a0001c0001t0002g0129 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.628+21624_628+2162 others(43): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698229 | |||||
| chr3:115698231
|
T | C | 5 | a0001c0001t0001g0185a0001c0001t0001g0221a0001c0001t0001g0339others(2): Show | 5 | HG02630.hp2 HG02922.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.628+21621T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698231 | ||||||
| chr3:115698237
|
A | T | 1 | a0001c0001t0002g0129 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.628+21627A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698237 | ||||||
| chr3:115698240
|
T | A | 1 | a0001c0001t0002g0129 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.628+21630T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698240 | ||||||
| chr3:115698247
|
A | ATTATATA others(28): Show |
31 | a0001c0001t0001g0165a0001c0001t0002g0270a0001c0001t0002g0294others(28): Show | 31 | HG00438.hp2 HG00544.hp1 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.628+21637_628+2163 others(39): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698247 | ||||||
| chr3:115698247
|
A | ATTATATA others(30): Show |
2 | a0001c0001t0001g0349a0001c0001t0013g0219 | 2 | HG01109.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.628+21637_628+2163 others(41): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698247 | ||||||
| chr3:115698247
|
A | T | 20 | a0001c0001t0001g0015a0001c0001t0001g0066a0001c0001t0001g0067others(17): Show | 20 | HG01261.hp1 HG02071.hp2 HG02293.hp2 others(17): Show |
intron_variant | MODIFIER | c.628+21637A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698247 | ||||||
| chr3:115698249
|
T | A | 33 | a0001c0001t0001g0165a0001c0001t0001g0349a0001c0001t0002g0270others(30): Show | 33 | HG00438.hp2 HG00544.hp1 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.628+21639T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698249 | ||||||
| chr3:115698255
|
AT | A | 18 | a0001c0001t0001g0015a0001c0001t0001g0066a0001c0001t0001g0067others(15): Show | 18 | HG01261.hp1 HG02071.hp2 HG02293.hp2 others(15): Show |
intron_variant | MODIFIER | c.628+21646delT | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698255 | ||||||
| chr3:115698262
|
T | A | 18 | a0001c0001t0001g0015a0001c0001t0001g0066a0001c0001t0001g0067others(15): Show | 18 | HG01261.hp1 HG02071.hp2 HG02293.hp2 others(15): Show |
intron_variant | MODIFIER | c.628+21652T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698262 | ||||||
| chr3:115698263
|
A | T | 18 | a0001c0001t0001g0015a0001c0001t0001g0066a0001c0001t0001g0067others(15): Show | 18 | HG01261.hp1 HG02071.hp2 HG02293.hp2 others(15): Show |
intron_variant | MODIFIER | c.628+21653A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698263 | ||||||
| chr3:115698265
|
A | AATATATA others(72): Show |
1 | a0001c0001t0001g0319 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.628+21663_628+2166 others(83): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698265 | |||||
| chr3:115698265
|
A | T | 19 | a0001c0001t0001g0015a0001c0001t0001g0066a0001c0001t0001g0067others(16): Show | 19 | HG01261.hp1 HG01943.hp2 HG02071.hp2 others(16): Show |
intron_variant | MODIFIER | c.628+21655A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698265 | ||||||
| chr3:115698282
|
A | AATATAAT others(24): Show |
1 | a0001c0001t0002g0212 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.628+21687_628+2168 others(35): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698282 | |||||
| chr3:115698282
|
A | T | 1 | a0001c0001t0002g0198 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.628+21672A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698282 | ||||||
| chr3:115698287
|
A | AAT | 121 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0019others(118): Show | 121 | HG00438.hp2 HG00544.hp1 HG00609.hp2 others(118): Show |
intron_variant | MODIFIER | c.628+21686_628+2168 others(6): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698287 | |||||
| chr3:115698287
|
A | AATAT | 3 | a0001c0001t0001g0037a0001c0001t0005g0003a0001c0001t0005g0005 | 3 | HG03195.hp1 HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.628+21684_628+2168 others(8): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698287 | |||||
| chr3:115698287
|
A | AATATATA others(26): Show |
1 | a0001c0001t0001g0073 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.628+21687_628+2168 others(37): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698287 | |||||
| chr3:115698287
|
A | AATATATA others(26): Show |
11 | a0001c0001t0001g0004a0001c0001t0001g0038a0001c0001t0001g0043others(8): Show | 11 | HG00140.hp2 HG00741.hp2 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.628+21687_628+2168 others(37): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698287 | |||||
| chr3:115698287
|
A | AATATATA others(28): Show |
186 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0041others(183): Show | 187 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.628+21687_628+2168 others(39): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698287 | |||||
| chr3:115698287
|
A | AATATATA others(30): Show |
1 | a0001c0001t0002g0295 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.628+21687_628+2168 others(41): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698287 | |||||
| chr3:115698287
|
A | AATATATA others(59): Show |
1 | a0001c0001t0002g0201 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.628+21687_628+2168 others(70): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698287 | |||||
| chr3:115698287
|
A | AATATATA others(61): Show |
7 | a0001c0001t0001g0028a0001c0001t0002g0127a0001c0001t0002g0128others(4): Show | 7 | HG01433.hp2 NA18944.hp1 NA18974.hp2 others(4): Show |
intron_variant | MODIFIER | c.628+21687_628+2168 others(72): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698287 | |||||
| chr3:115698287
|
A | AATATATA others(24): Show |
1 | a0001c0001t0001g0040 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.628+21687_628+2168 others(35): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698287 | |||||
| chr3:115698287
|
A | AATATATA others(26): Show |
1 | a0001c0001t0002g0267 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.628+21687_628+2168 others(37): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698287 | |||||
| chr3:115698287
|
A | AATATATA others(54): Show |
1 | a0001c0001t0001g0302 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.628+21687_628+2168 others(65): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698287 | |||||
| chr3:115698287
|
A | AATATATA others(30): Show |
1 | a0001c0001t0002g0199 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.628+21687_628+2168 others(41): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698287 | |||||
| chr3:115698287
|
A | AATATATA others(26): Show |
3 | a0001c0001t0001g0082a0001c0001t0001g0268a0001c0001t0002g0171 | 3 | NA18522.hp1 NA18943.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.628+21687_628+2171 others(37): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698287 | |||||
| chr3:115698287
|
A | ATATATAT others(60): Show |
1 | a0001c0001t0002g0198 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.628+21677_628+2167 others(71): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698287 | ||||||
| chr3:115698287
|
A | ATATATAT others(23): Show |
1 | a0001c0001t0003g0316 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.628+21677_628+2167 others(34): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698287 | ||||||
| chr3:115698298
|
T | A | 1 | a0001c0001t0001g0225 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.628+21688T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698298 | ||||||
| chr3:115698299
|
A | T | 1 | a0001c0001t0001g0225 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.628+21689A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698299 | ||||||
| chr3:115698312
|
A | G | 1 | a0001c0001t0002g0226 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.628+21702A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698312 | ||||||
| chr3:115698316
|
A | AAT | 34 | a0001c0001t0001g0165a0001c0001t0001g0349a0001c0001t0002g0270others(31): Show | 34 | HG00438.hp2 HG00544.hp1 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.628+21718_628+2171 others(6): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698316 | |||||
| chr3:115698316
|
A | T | 2 | a0001c0001t0002g0105a0001c0001t0002g0146 | 2 | NA19012.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.628+21706A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698316 | ||||||
| chr3:115698326
|
T | C | 4 | a0001c0001t0001g0242a0001c0001t0001g0306a0001c0001t0002g0243others(1): Show | 4 | HG02145.hp1 HG02280.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.628+21716T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698326 | ||||||
| chr3:115698343
|
C | T | 1 | a0001c0001t0001g0081 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.628+21733C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698343 | ||||||
| chr3:115698473
|
G | C | 6 | a0001c0001t0001g0019a0001c0001t0001g0036a0001c0001t0001g0224others(3): Show | 6 | HG02055.hp1 HG02630.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.628+21863G>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698473 | ||||||
| chr3:115698925
|
C | T | 12 | a0001c0001t0001g0037a0001c0001t0002g0164a0001c0001t0002g0308others(9): Show | 12 | HG01081.hp2 HG01106.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.629-21869C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698925 | ||||||
| chr3:115698926
|
G | A | 85 | a0001c0001t0001g0046a0001c0001t0001g0051a0001c0001t0001g0165others(82): Show | 86 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.629-21868G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698926 | ||||||
| chr3:115698968
|
T | A | 1 | a0001c0001t0005g0005 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.629-21826T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115698968 | ||||||
| chr3:115698982
|
CTG | C | 3 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0088 | 3 | NA18747.hp1 NA19065.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.629-21808_629-2180 others(6): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115698982 | |||||
| chr3:115699018
|
C | T | 86 | a0001c0001t0001g0015a0001c0001t0001g0046a0001c0001t0001g0051others(83): Show | 87 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.629-21776C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115699018 | ||||||
| chr3:115699070
|
A | G | 85 | a0001c0001t0001g0046a0001c0001t0001g0051a0001c0001t0001g0165others(82): Show | 86 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.629-21724A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115699070 | ||||||
| chr3:115699119
|
G | A | 3 | a0001c0001t0001g0209a0001c0001t0010g0245a0001c0001t0010g0246 | 3 | HG02895.hp1 HG02897.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.629-21675G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115699119 | ||||||
| chr3:115699199
|
C | T | 8 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0092others(5): Show | 8 | HG02451.hp1 HG02622.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.629-21595C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115699199 | ||||||
| chr3:115699201
|
C | G | 1 | a0001c0001t0001g0349 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.629-21593C>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115699201 | ||||||
| chr3:115699201
|
C | T | 8 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0092others(5): Show | 8 | HG02451.hp1 HG02622.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.629-21593C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115699201 | ||||||
| chr3:115699333
|
C | T | 1 | a0001c0001t0002g0277 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.629-21461C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115699333 | ||||||
| chr3:115699531
|
C | T | 1 | a0001c0001t0001g0037 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.629-21263C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115699531 | ||||||
| chr3:115699646
|
G | C | 1 | a0001c0001t0001g0089 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.629-21148G>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115699646 | ||||||
| chr3:115699687
|
T | C | 1 | a0001c0001t0004g0141 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.629-21107T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115699687 | ||||||
| chr3:115699871
|
G | T | 1 | a0001c0001t0002g0205 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.629-20923G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115699871 | ||||||
| chr3:115700234
|
G | T | 1 | a0001c0001t0001g0234 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.629-20560G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115700234 | ||||||
| chr3:115700494
|
A | C | 2 | a0001c0001t0001g0019a0001c0001t0001g0265 | 2 | HG02970.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.629-20300A>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115700494 | ||||||
| chr3:115700520
|
G | T | 1 | a0001c0001t0002g0163 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.629-20274G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115700520 | ||||||
| chr3:115700533
|
A | C | 1 | a0001c0001t0002g0208 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.629-20261A>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115700533 | ||||||
| chr3:115700556
|
A | G | 8 | a0001c0001t0005g0003a0001c0001t0005g0011a0001c0001t0005g0012others(5): Show | 8 | HG01081.hp2 HG02055.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.629-20238A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115700556 | ||||||
| chr3:115700889
|
T | C | 1 | a0001c0001t0004g0189 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.629-19905T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115700889 | ||||||
| chr3:115700895
|
A | C | 11 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0092others(8): Show | 11 | HG01106.hp1 HG02280.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.629-19899A>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115700895 | ||||||
| chr3:115700948
|
G | A | 176 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0028others(173): Show | 176 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.629-19846G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115700948 | ||||||
| chr3:115701065
|
T | A | 1 | a0001c0001t0004g0200 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.629-19729T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115701065 | ||||||
| chr3:115701257
|
C | T | 166 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0022others(163): Show | 166 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.629-19537C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115701257 | ||||||
| chr3:115701345
|
T | G | 11 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0092others(8): Show | 11 | HG01106.hp1 HG02280.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.629-19449T>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115701345 | ||||||
| chr3:115701671
|
T | A | 3 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0088 | 3 | NA18747.hp1 NA19065.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.629-19123T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115701671 | ||||||
| chr3:115701747
|
A | G | 1 | a0001c0001t0001g0037 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.629-19047A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115701747 | ||||||
| chr3:115701790
|
C | T | 4 | a0001c0001t0001g0242a0001c0001t0001g0306a0001c0001t0002g0243others(1): Show | 4 | HG02145.hp1 HG02280.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.629-19004C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115701790 | ||||||
| chr3:115702463
|
C | T | 1 | a0001c0001t0005g0299 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.629-18331C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115702463 | ||||||
| chr3:115702738
|
C | T | 1 | a0001c0002t0001g0098 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.629-18056C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115702738 | ||||||
| chr3:115702769
|
C | T | 4 | a0001c0001t0001g0242a0001c0001t0001g0306a0001c0001t0002g0243others(1): Show | 4 | HG02145.hp1 HG02280.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.629-18025C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115702769 | ||||||
| chr3:115702843
|
G | C | 1 | a0001c0001t0001g0302 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.629-17951G>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115702843 | ||||||
| chr3:115702844
|
G | A | 1 | a0001c0001t0001g0302 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.629-17950G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115702844 | ||||||
| chr3:115702845
|
G | C | 1 | a0001c0001t0001g0302 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.629-17949G>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115702845 | ||||||
| chr3:115702848
|
A | C | 1 | a0001c0001t0001g0302 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.629-17946A>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115702848 | ||||||
| chr3:115702850
|
G | C | 1 | a0001c0001t0001g0302 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.629-17944G>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115702850 | ||||||
| chr3:115702852
|
T | A | 1 | a0001c0001t0001g0302 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.629-17942T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115702852 | ||||||
| chr3:115702854
|
T | G | 1 | a0001c0001t0001g0302 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.629-17940T>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115702854 | ||||||
| chr3:115702857
|
A | G | 1 | a0001c0001t0001g0302 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.629-17937A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115702857 | ||||||
| chr3:115702946
|
G | A | 30 | a0001c0001t0001g0165a0001c0001t0002g0270a0001c0001t0002g0294others(27): Show | 30 | HG00438.hp2 HG00544.hp1 HG00609.hp2 others(27): Show |
intron_variant | MODIFIER | c.629-17848G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115702946 | ||||||
| chr3:115702966
|
T | A | 1 | a0001c0001t0001g0302 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.629-17828T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115702966 | ||||||
| chr3:115703023
|
T | A | 3 | a0001c0001t0001g0036a0001c0001t0001g0315a0001c0001t0001g0342 | 3 | HG02055.hp1 HG02818.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.629-17771T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115703023 | ||||||
| chr3:115703085
|
A | G | 1 | a0001c0001t0001g0037 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.629-17709A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115703085 | ||||||
| chr3:115703092
|
A | G | 2 | a0001c0001t0010g0245a0001c0001t0010g0246 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.629-17702A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115703092 | ||||||
| chr3:115703218
|
A | G | 11 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0092others(8): Show | 11 | HG01106.hp1 HG02280.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.629-17576A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115703218 | ||||||
| chr3:115703457
|
A | G | 1 | a0001c0001t0002g0330 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.629-17337A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115703457 | ||||||
| chr3:115703494
|
C | A | 177 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0019others(174): Show | 178 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(175): Show |
intron_variant | MODIFIER | c.629-17300C>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115703494 | ||||||
| chr3:115703700
|
A | G | 3 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0346 | 3 | HG01891.hp2 HG02965.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.629-17094A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115703700 | ||||||
| chr3:115703701
|
T | C | 166 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0019others(163): Show | 167 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(164): Show |
intron_variant | MODIFIER | c.629-17093T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115703701 | ||||||
| chr3:115703760
|
C | T | 4 | a0001c0001t0001g0242a0001c0001t0001g0306a0001c0001t0002g0243others(1): Show | 4 | HG02145.hp1 HG02280.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.629-17034C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115703760 | ||||||
| chr3:115703777
|
A | T | 166 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0019others(163): Show | 167 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(164): Show |
intron_variant | MODIFIER | c.629-17017A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115703777 | ||||||
| chr3:115703805
|
G | A | 2 | a0001c0001t0003g0311a0001c0001t0003g0312 | 2 | HG01517.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.629-16989G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115703805 | ||||||
| chr3:115703912
|
G | A | 166 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0019others(163): Show | 167 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(164): Show |
intron_variant | MODIFIER | c.629-16882G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115703912 | ||||||
| chr3:115703986
|
T | G | 1 | a0001c0001t0001g0061 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.629-16808T>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115703986 | ||||||
| chr3:115704007
|
T | C | 2 | a0001c0001t0001g0228a0001c0001t0001g0229 | 2 | HG00733.hp1 HG00735.hp1 |
intron_variant | MODIFIER | c.629-16787T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115704007 | ||||||
| chr3:115704079
|
C | A | 2 | a0001c0001t0010g0245a0001c0001t0010g0246 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.629-16715C>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115704079 | ||||||
| chr3:115704257
|
T | C | 2 | a0001c0001t0001g0191a0001c0001t0001g0238 | 2 | HG01071.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.629-16537T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115704257 | ||||||
| chr3:115704279
|
C | T | 1 | a0001c0001t0002g0026 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.629-16515C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115704279 | ||||||
| chr3:115704292
|
C | T | 1 | a0001c0001t0001g0037 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.629-16502C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115704292 | ||||||
| chr3:115704382
|
C | T | 167 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0019others(164): Show | 168 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(165): Show |
intron_variant | MODIFIER | c.629-16412C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115704382 | ||||||
| chr3:115704481
|
C | T | 1 | a0001c0001t0002g0199 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.629-16313C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115704481 | ||||||
| chr3:115704498
|
A | G | 1 | a0001c0001t0003g0027 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.629-16296A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115704498 | ||||||
| chr3:115704551
|
C | T | 1 | a0001c0001t0019g0013 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.629-16243C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115704551 | ||||||
| chr3:115704662
|
G | A | 1 | a0001c0001t0001g0225 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.629-16132G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115704662 | ||||||
| chr3:115704669
|
A | G | 350 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0015others(347): Show | 351 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(348): Show |
intron_variant | MODIFIER | c.629-16125A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115704669 | ||||||
| chr3:115704753
|
G | A | 1 | a0001c0001t0001g0015 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.629-16041G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115704753 | ||||||
| chr3:115704871
|
A | T | 2 | a0001c0001t0001g0082a0001c0001t0001g0350 | 2 | HG02976.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.629-15923A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115704871 | ||||||
| chr3:115704957
|
T | C | 8 | a0001c0001t0001g0056a0001c0001t0001g0191a0001c0001t0001g0232others(5): Show | 8 | HG01071.hp2 HG01074.hp2 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.629-15837T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115704957 | ||||||
| chr3:115704964
|
G | T | 82 | a0001c0001t0001g0046a0001c0001t0001g0051a0001c0001t0001g0165others(79): Show | 83 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.629-15830G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115704964 | ||||||
| chr3:115704966
|
C | A | 3 | a0001c0001t0001g0036a0001c0001t0001g0315a0001c0001t0001g0342 | 3 | HG02055.hp1 HG02818.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.629-15828C>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115704966 | ||||||
| chr3:115705129
|
C | T | 9 | a0001c0001t0005g0003a0001c0001t0005g0011a0001c0001t0005g0012others(6): Show | 9 | HG01081.hp2 HG02055.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.629-15665C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115705129 | ||||||
| chr3:115705200
|
G | A | 8 | a0001c0001t0001g0004a0001c0001t0001g0172a0001c0001t0001g0173others(5): Show | 8 | HG02258.hp2 HG02486.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.629-15594G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115705200 | ||||||
| chr3:115705212
|
G | A | 167 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0019others(164): Show | 168 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(165): Show |
intron_variant | MODIFIER | c.629-15582G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115705212 | ||||||
| chr3:115705226
|
G | A | 1 | a0001c0001t0001g0040 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.629-15568G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115705226 | ||||||
| chr3:115705302
|
G | T | 167 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0019others(164): Show | 168 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(165): Show |
intron_variant | MODIFIER | c.629-15492G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115705302 | ||||||
| chr3:115705376
|
CT | C | 3 | a0001c0001t0001g0019a0001c0001t0001g0224a0001c0001t0001g0265 | 3 | HG02630.hp1 HG02970.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.629-15417delT | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115705376 | ||||||
| chr3:115705473
|
T | G | 2 | a0001c0001t0003g0284a0001c0001t0003g0316 | 2 | HG02738.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.629-15321T>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115705473 | ||||||
| chr3:115705659
|
C | T | 3 | a0001c0001t0002g0271a0001c0001t0002g0317a0001c0001t0002g0318 | 3 | NA18975.hp2 NA19009.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.629-15135C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115705659 | ||||||
| chr3:115706127
|
A | G | 167 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0019others(164): Show | 168 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(165): Show |
intron_variant | MODIFIER | c.629-14667A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115706127 | ||||||
| chr3:115706180
|
CA | C | 167 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0019others(164): Show | 168 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(165): Show |
intron_variant | MODIFIER | c.629-14607delA | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115706180 | |||||
| chr3:115706298
|
C | G | 61 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0024others(58): Show | 61 | HG00733.hp1 HG00735.hp1 HG01261.hp1 others(58): Show |
intron_variant | MODIFIER | c.629-14496C>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115706298 | ||||||
| chr3:115706341
|
G | C | 146 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0024others(143): Show | 147 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(144): Show |
intron_variant | MODIFIER | c.629-14453G>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115706341 | ||||||
| chr3:115706383
|
A | G | 177 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0022others(174): Show | 177 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.629-14411A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115706383 | ||||||
| chr3:115706397
|
TG | T | 177 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0022others(174): Show | 177 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.629-14391delG | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115706397 | |||||
| chr3:115706496
|
A | C | 3 | a0001c0001t0001g0019a0001c0001t0001g0224a0001c0001t0001g0265 | 3 | HG02630.hp1 HG02970.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.629-14298A>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115706496 | ||||||
| chr3:115706664
|
C | T | 5 | a0001c0001t0001g0046a0001c0001t0002g0131a0001c0001t0003g0195others(2): Show | 5 | HG00140.hp1 HG00140.hp2 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.629-14130C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115706664 | ||||||
| chr3:115706758
|
C | G | 1 | a0001c0001t0002g0108 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.629-14036C>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115706758 | ||||||
| chr3:115706863
|
A | T | 61 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0024others(58): Show | 61 | HG00733.hp1 HG00735.hp1 HG01261.hp1 others(58): Show |
intron_variant | MODIFIER | c.629-13931A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115706863 | ||||||
| chr3:115707178
|
T | G | 1 | a0001c0001t0001g0019 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.629-13616T>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115707178 | ||||||
| chr3:115707332
|
G | A | 1 | a0001c0001t0003g0157 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.629-13462G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115707332 | ||||||
| chr3:115707427
|
T | C | 344 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0015others(341): Show | 345 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(342): Show |
intron_variant | MODIFIER | c.629-13367T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115707427 | ||||||
| chr3:115707463
|
T | A | 1 | a0001c0001t0001g0081 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.629-13331T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115707463 | ||||||
| chr3:115707532
|
C | T | 1 | a0001c0001t0002g0337 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.629-13262C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115707532 | ||||||
| chr3:115707762
|
C | G | 83 | a0001c0001t0001g0046a0001c0001t0001g0051a0001c0001t0001g0165others(80): Show | 84 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.629-13032C>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115707762 | ||||||
| chr3:115707781
|
G | A | 3 | a0001c0001t0001g0019a0001c0001t0001g0224a0001c0001t0001g0265 | 3 | HG02630.hp1 HG02970.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.629-13013G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115707781 | ||||||
| chr3:115707886
|
A | G | 3 | a0001c0001t0001g0242a0001c0001t0002g0243a0001c0001t0002g0244 | 3 | HG02145.hp1 HG02280.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.629-12908A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115707886 | ||||||
| chr3:115707972
|
A | G | 1 | a0001c0001t0001g0296 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.629-12822A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115707972 | ||||||
| chr3:115707985
|
C | T | 177 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0022others(174): Show | 177 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.629-12809C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115707985 | ||||||
| chr3:115707990
|
T | TAC | 5 | a0001c0001t0001g0037a0001c0001t0001g0225a0001c0001t0001g0306others(2): Show | 5 | HG01069.hp2 HG01081.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.629-12780_629-1277 others(6): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115707990 | |||||
| chr3:115707990
|
T | TACAC | 12 | a0001c0001t0001g0242a0001c0001t0002g0243a0001c0001t0002g0244others(9): Show | 12 | HG01081.hp2 HG02055.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.629-12782_629-1277 others(8): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115707990 | |||||
| chr3:115707990
|
TAC | T | 130 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0031others(127): Show | 130 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.629-12780_629-1277 others(6): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115707990 | |||||
| chr3:115708000
|
CACACACA others(9): Show |
C | 177 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0022others(174): Show | 177 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.629-12792_629-1277 others(20): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115708000 | |||||
| chr3:115708014
|
C | T | 6 | a0001c0001t0001g0024a0001c0001t0003g0001a0001c0001t0003g0071others(3): Show | 7 | HG01257.hp1 HG01258.hp2 HG01261.hp2 others(4): Show |
intron_variant | MODIFIER | c.629-12780C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115708014 | ||||||
| chr3:115708016
|
T | C | 1 | a0001c0001t0001g0225 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.629-12778T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115708016 | ||||||
| chr3:115708024
|
T | C | 4 | a0001c0001t0003g0001a0001c0001t0003g0071a0001c0001t0003g0113others(1): Show | 5 | HG01257.hp1 HG01258.hp2 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.629-12770T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115708024 | ||||||
| chr3:115708050
|
A | T | 1 | a0001c0001t0001g0104 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.629-12744A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115708050 | ||||||
| chr3:115708157
|
A | G | 146 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0024others(143): Show | 147 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(144): Show |
intron_variant | MODIFIER | c.629-12637A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115708157 | ||||||
| chr3:115708234
|
G | A | 1 | a0001c0001t0001g0225 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.629-12560G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115708234 | ||||||
| chr3:115708265
|
G | T | 1 | a0001c0001t0002g0277 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.629-12529G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115708265 | ||||||
| chr3:115708460
|
A | T | 3 | a0001c0001t0001g0036a0001c0001t0001g0315a0001c0001t0001g0342 | 3 | HG02055.hp1 HG02818.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.629-12334A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115708460 | ||||||
| chr3:115708528
|
G | C | 3 | a0001c0001t0001g0036a0001c0001t0001g0315a0001c0001t0001g0342 | 3 | HG02055.hp1 HG02818.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.629-12266G>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115708528 | ||||||
| chr3:115708726
|
A | G | 1 | a0001c0002t0002g0223 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.629-12068A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115708726 | ||||||
| chr3:115708903
|
G | A | 1 | a0001c0001t0004g0280 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.629-11891G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115708903 | ||||||
| chr3:115708940
|
G | GT | 39 | a0001c0001t0001g0061a0001c0001t0001g0072a0001c0001t0001g0085others(36): Show | 39 | HG00438.hp2 HG00738.hp2 HG01074.hp1 others(36): Show |
intron_variant | MODIFIER | c.629-11830dupT | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115708940 | |||||
| chr3:115708940
|
GT | G | 13 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0099others(10): Show | 13 | HG00733.hp1 HG01069.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.629-11830delT | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115708940 | |||||
| chr3:115708940
|
GTTT | G | 25 | a0001c0001t0001g0019a0001c0001t0001g0041a0001c0001t0001g0069others(22): Show | 25 | HG00280.hp1 HG00621.hp1 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.629-11832_629-1183 others(7): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115708940 | |||||
| chr3:115708940
|
GTTTT | G | 147 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0022others(144): Show | 147 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.629-11833_629-1183 others(8): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115708940 | |||||
| chr3:115709251
|
G | A | 3 | a0001c0001t0001g0036a0001c0001t0001g0315a0001c0001t0001g0342 | 3 | HG02055.hp1 HG02818.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.629-11543G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115709251 | ||||||
| chr3:115709391
|
A | G | 344 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0015others(341): Show | 345 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(342): Show |
intron_variant | MODIFIER | c.629-11403A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115709391 | ||||||
| chr3:115709582
|
G | A | 1 | a0001c0001t0002g0264 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.629-11212G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115709582 | ||||||
| chr3:115709661
|
A | G | 1 | a0001c0001t0004g0183 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.629-11133A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115709661 | ||||||
| chr3:115709762
|
T | C | 178 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0022others(175): Show | 178 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(175): Show |
intron_variant | MODIFIER | c.629-11032T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115709762 | ||||||
| chr3:115709844
|
C | CAT | 72 | a0001c0001t0001g0046a0001c0001t0001g0051a0001c0001t0001g0165others(69): Show | 73 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.629-10930_629-1092 others(6): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115709844 | |||||
| chr3:115709844
|
C | CATAT | 20 | a0001c0001t0001g0015a0001c0001t0001g0037a0001c0001t0001g0066others(17): Show | 20 | HG01109.hp1 HG01261.hp1 HG01981.hp2 others(17): Show |
intron_variant | MODIFIER | c.629-10932_629-1092 others(8): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115709844 | |||||
| chr3:115709844
|
C | CATATAT | 7 | a0001c0001t0001g0067a0001c0001t0001g0345a0001c0001t0003g0007others(4): Show | 7 | HG02293.hp2 HG03453.hp1 NA18939.hp2 others(4): Show |
intron_variant | MODIFIER | c.629-10934_629-1092 others(10): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115709844 | |||||
| chr3:115709844
|
C | CATATATA others(3): Show |
9 | a0001c0001t0001g0202a0001c0001t0005g0003a0001c0001t0005g0011others(6): Show | 9 | HG01081.hp2 HG02055.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.629-10938_629-1092 others(14): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115709844 | |||||
| chr3:115709844
|
CAT | C | 176 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0022others(173): Show | 176 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.629-10930_629-1092 others(6): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115709844 | |||||
| chr3:115709848
|
T | C | 1 | a0001c0001t0001g0207 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.629-10946T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115709848 | ||||||
| chr3:115709856
|
T | C | 4 | a0001c0001t0002g0107a0001c0001t0002g0151a0001c0001t0002g0227others(1): Show | 4 | HG00621.hp2 NA18979.hp2 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.629-10938T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115709856 | ||||||
| chr3:115709864
|
T | C | 1 | a0001c0001t0002g0122 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.629-10930T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115709864 | ||||||
| chr3:115709864
|
T | TATATATA others(5): Show |
1 | a0001c0001t0005g0341 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.629-10929_629-1092 others(16): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115709864 | |||||
| chr3:115709938
|
A | G | 1 | a0001c0001t0003g0016 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.629-10856A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115709938 | ||||||
| chr3:115710256
|
CT | C | 167 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0019others(164): Show | 168 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(165): Show |
intron_variant | MODIFIER | c.629-10527delT | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115710256 | |||||
| chr3:115710405
|
C | T | 6 | a0001c0001t0004g0176a0001c0001t0004g0177a0001c0001t0004g0181others(3): Show | 6 | HG01928.hp2 HG01934.hp2 HG01943.hp1 others(3): Show |
intron_variant | MODIFIER | c.629-10389C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115710405 | ||||||
| chr3:115710633
|
T | A | 177 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0022others(174): Show | 177 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.629-10161T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115710633 | ||||||
| chr3:115710700
|
A | T | 341 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0015others(338): Show | 342 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(339): Show |
intron_variant | MODIFIER | c.629-10094A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115710700 | ||||||
| chr3:115710795
|
T | G | 1 | a0001c0001t0004g0200 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.629-9999T>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115710795 | ||||||
| chr3:115710858
|
T | C | 1 | a0001c0001t0002g0277 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.629-9936T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115710858 | ||||||
| chr3:115710890
|
C | T | 1 | a0001c0001t0001g0037 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.629-9904C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115710890 | ||||||
| chr3:115711253
|
C | T | 8 | a0001c0001t0001g0038a0001c0001t0001g0040a0001c0001t0001g0043others(5): Show | 8 | HG00639.hp2 HG00741.hp2 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.629-9541C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115711253 | ||||||
| chr3:115711494
|
TAC | T | 169 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0022others(166): Show | 169 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.629-9283_629-9282d others(4): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115711494 | |||||
| chr3:115711498
|
C | T | 10 | a0001c0001t0001g0037a0001c0001t0005g0003a0001c0001t0005g0011others(7): Show | 10 | HG01081.hp2 HG02055.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.629-9296C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115711498 | ||||||
| chr3:115711506
|
C | T | 1 | a0001c0001t0001g0049 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.629-9288C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115711506 | ||||||
| chr3:115711511
|
A | C | 141 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0024others(138): Show | 141 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(138): Show |
intron_variant | MODIFIER | c.629-9283A>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115711511 | ||||||
| chr3:115711511
|
ACC | A | 8 | a0001c0001t0001g0064a0001c0001t0002g0057a0001c0001t0002g0117others(5): Show | 8 | HG00642.hp1 HG00733.hp2 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.629-9278_629-9277d others(4): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115711511 | |||||
| chr3:115711513
|
C | A | 3 | a0001c0001t0001g0019a0001c0001t0001g0224a0001c0001t0001g0265 | 3 | HG02630.hp1 HG02970.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.629-9281C>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115711513 | ||||||
| chr3:115711516
|
C | A | 2 | a0001c0001t0010g0245a0001c0001t0010g0246 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.629-9278C>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115711516 | ||||||
| chr3:115711561
|
T | C | 1 | a0001c0001t0001g0207 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.629-9233T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115711561 | ||||||
| chr3:115711595
|
G | A | 2 | a0001c0001t0010g0245a0001c0001t0010g0246 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.629-9199G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115711595 | ||||||
| chr3:115711658
|
G | A | 3 | a0001c0001t0001g0019a0001c0001t0001g0224a0001c0001t0001g0265 | 3 | HG02630.hp1 HG02970.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.629-9136G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115711658 | ||||||
| chr3:115711736
|
C | T | 1 | a0001c0001t0001g0306 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.629-9058C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115711736 | ||||||
| chr3:115711763
|
T | A | 4 | a0001c0001t0001g0242a0001c0001t0001g0306a0001c0001t0002g0243others(1): Show | 4 | HG02145.hp1 HG02280.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.629-9031T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115711763 | ||||||
| chr3:115711807
|
CTGTT | C | 177 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0022others(174): Show | 177 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.629-8982_629-8979d others(6): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115711807 | |||||
| chr3:115711948
|
A | G | 1 | a0001c0001t0004g0130 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.629-8846A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115711948 | ||||||
| chr3:115711958
|
A | G | 177 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0022others(174): Show | 177 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.629-8836A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115711958 | ||||||
| chr3:115712033
|
C | T | 177 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0022others(174): Show | 177 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.629-8761C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115712033 | ||||||
| chr3:115712183
|
C | A | 177 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0022others(174): Show | 177 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.629-8611C>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115712183 | ||||||
| chr3:115712193
|
A | G | 1 | a0001c0001t0001g0324 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.629-8601A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115712193 | ||||||
| chr3:115712321
|
A | C | 55 | a0001c0001t0001g0002a0001c0001t0001g0028a0001c0001t0001g0038others(52): Show | 55 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.629-8473A>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115712321 | ||||||
| chr3:115712360
|
G | A | 167 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0019others(164): Show | 168 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(165): Show |
intron_variant | MODIFIER | c.629-8434G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115712360 | ||||||
| chr3:115712437
|
TA | T | 167 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0019others(164): Show | 168 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(165): Show |
intron_variant | MODIFIER | c.629-8353delA | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115712437 | |||||
| chr3:115712621
|
C | T | 1 | a0001c0001t0005g0096 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.629-8173C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115712621 | ||||||
| chr3:115712636
|
C | G | 168 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0017others(165): Show | 169 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(166): Show |
intron_variant | MODIFIER | c.629-8158C>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115712636 | ||||||
| chr3:115712637
|
G | A | 1 | a0001c0001t0002g0337 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.629-8157G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115712637 | ||||||
| chr3:115712661
|
T | C | 177 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0028others(174): Show | 177 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.629-8133T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115712661 | ||||||
| chr3:115712960
|
A | G | 1 | a0001c0001t0001g0094 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.629-7834A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115712960 | ||||||
| chr3:115712982
|
GA | G | 4 | a0001c0001t0001g0242a0001c0001t0001g0306a0001c0001t0002g0243others(1): Show | 4 | HG02145.hp1 HG02280.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.629-7809delA | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115712982 | |||||
| chr3:115713026
|
A | T | 1 | a0001c0001t0002g0351 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.629-7768A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115713026 | ||||||
| chr3:115713040
|
C | T | 178 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0022others(175): Show | 178 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(175): Show |
intron_variant | MODIFIER | c.629-7754C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115713040 | ||||||
| chr3:115713041
|
G | A | 143 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0024others(140): Show | 144 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(141): Show |
intron_variant | MODIFIER | c.629-7753G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115713041 | ||||||
| chr3:115713174
|
A | T | 178 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0022others(175): Show | 178 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(175): Show |
intron_variant | MODIFIER | c.629-7620A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115713174 | ||||||
| chr3:115713389
|
G | A | 4 | a0001c0001t0001g0110a0001c0001t0001g0152a0001c0001t0001g0174others(1): Show | 4 | HG02074.hp1 NA18968.hp1 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.629-7405G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115713389 | ||||||
| chr3:115713637
|
A | G | 1 | a0001c0002t0001g0150 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.629-7157A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115713637 | ||||||
| chr3:115713709
|
T | C | 4 | a0001c0001t0001g0242a0001c0001t0001g0306a0001c0001t0002g0243others(1): Show | 4 | HG02145.hp1 HG02280.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.629-7085T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115713709 | ||||||
| chr3:115713724
|
A | T | 1 | a0001c0001t0001g0240 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.629-7070A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115713724 | ||||||
| chr3:115713800
|
T | A | 1 | a0001c0001t0002g0201 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.629-6994T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115713800 | ||||||
| chr3:115713977
|
T | A | 1 | a0001c0001t0001g0225 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.629-6817T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115713977 | ||||||
| chr3:115714097
|
G | A | 1 | a0001c0001t0001g0324 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.629-6697G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115714097 | ||||||
| chr3:115714197
|
A | T | 1 | a0001c0001t0001g0265 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.629-6597A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115714197 | ||||||
| chr3:115714248
|
A | G | 19 | a0001c0001t0001g0037a0001c0001t0005g0003a0001c0001t0005g0005others(16): Show | 19 | HG01081.hp2 HG01361.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.629-6546A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115714248 | ||||||
| chr3:115714403
|
A | G | 1 | a0001c0001t0001g0345 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.629-6391A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115714403 | ||||||
| chr3:115714407
|
GCAGGTTA | G | 5 | a0001c0001t0001g0222a0001c0001t0001g0234a0001c0001t0001g0242others(2): Show | 5 | HG02109.hp2 HG02451.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.629-6383_629-6377d others(9): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115714407 | |||||
| chr3:115714708
|
GT | G | 344 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0015others(341): Show | 345 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(342): Show |
intron_variant | MODIFIER | c.629-6074delT | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115714708 | |||||
| chr3:115714827
|
T | C | 1 | a0001c0001t0001g0172 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.629-5967T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115714827 | ||||||
| chr3:115714869
|
G | A | 2 | a0001c0001t0001g0017a0001c0001t0001g0213 | 2 | NA18939.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.629-5925G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115714869 | ||||||
| chr3:115714873
|
G | GCA | 117 | a0001c0001t0001g0017a0001c0001t0001g0022a0001c0001t0001g0024others(114): Show | 118 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(115): Show |
intron_variant | MODIFIER | c.629-5898_629-5897d others(4): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115714873 | |||||
| chr3:115714873
|
G | GCACACAC others(1): Show |
18 | a0001c0001t0005g0003a0001c0001t0005g0005a0001c0001t0005g0011others(15): Show | 18 | HG01081.hp2 HG01361.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.629-5904_629-5897d others(10): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115714873 | |||||
| chr3:115714873
|
GCA | G | 6 | a0001c0001t0001g0209a0001c0001t0001g0222a0001c0001t0001g0234others(3): Show | 6 | HG02109.hp2 HG02451.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.629-5898_629-5897d others(4): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115714873 | |||||
| chr3:115714890
|
C | T | 172 | a0001c0001t0001g0002a0001c0001t0001g0028a0001c0001t0001g0038others(169): Show | 172 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.629-5904C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115714890 | ||||||
| chr3:115714964
|
C | A | 84 | a0001c0001t0001g0165a0001c0001t0002g0127a0001c0001t0002g0128others(81): Show | 85 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.629-5830C>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115714964 | ||||||
| chr3:115715019
|
A | G | 19 | a0001c0001t0001g0037a0001c0001t0005g0003a0001c0001t0005g0005others(16): Show | 19 | HG01081.hp2 HG01361.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.629-5775A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115715019 | ||||||
| chr3:115715079
|
C | G | 1 | a0001c0001t0001g0209 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.629-5715C>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115715079 | ||||||
| chr3:115715129
|
G | A | 1 | a0001c0001t0003g0027 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.629-5665G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115715129 | ||||||
| chr3:115715273
|
A | T | 1 | a0001c0001t0002g0147 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.629-5521A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115715273 | ||||||
| chr3:115715323
|
C | T | 25 | a0001c0001t0001g0017a0001c0001t0001g0022a0001c0001t0001g0024others(22): Show | 25 | HG01884.hp1 HG02109.hp1 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.629-5471C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115715323 | ||||||
| chr3:115715466
|
C | T | 297 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0028others(294): Show | 298 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.629-5328C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115715466 | ||||||
| chr3:115715477
|
A | G | 4 | a0001c0001t0002g0083a0001c0001t0002g0164a0001c0001t0002g0308others(1): Show | 4 | HG01106.hp1 HG02280.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.629-5317A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115715477 | ||||||
| chr3:115715604
|
G | T | 1 | a0001c0001t0001g0336 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.629-5190G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115715604 | ||||||
| chr3:115715912
|
A | G | 1 | a0001c0001t0009g0187 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.629-4882A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115715912 | ||||||
| chr3:115715914
|
G | A | 1 | a0001c0001t0005g0005 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.629-4880G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115715914 | ||||||
| chr3:115715933
|
C | G | 19 | a0001c0001t0001g0037a0001c0001t0005g0003a0001c0001t0005g0005others(16): Show | 19 | HG01081.hp2 HG01361.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.629-4861C>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115715933 | ||||||
| chr3:115716158
|
A | G | 1 | a0001c0001t0002g0083 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.629-4636A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115716158 | ||||||
| chr3:115716195
|
G | A | 1 | a0001c0001t0001g0193 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.629-4599G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115716195 | ||||||
| chr3:115716510
|
T | C | 4 | a0001c0001t0002g0008a0001c0001t0002g0102a0001c0001t0002g0120others(1): Show | 4 | HG01255.hp2 HG02735.hp1 NA18950.hp1 others(1): Show |
intron_variant | MODIFIER | c.629-4284T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115716510 | ||||||
| chr3:115716710
|
TCAGA | T | 12 | a0001c0001t0001g0051a0001c0001t0001g0079a0001c0001t0001g0172others(9): Show | 12 | HG00621.hp1 HG01099.hp1 HG01358.hp2 others(9): Show |
intron_variant | MODIFIER | c.629-4081_629-4078d others(6): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115716710 | |||||
| chr3:115716711
|
C | CAA | 3 | a0001c0001t0002g0205a0001c0001t0002g0264a0001c0001t0002g0304 | 3 | HG00280.hp1 HG00280.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.629-4082_629-4081i others(4): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115716711 | |||||
| chr3:115716711
|
CAG | C | 16 | a0001c0001t0001g0002a0001c0001t0001g0042a0001c0001t0001g0053others(13): Show | 16 | HG00621.hp2 HG01074.hp2 HG01433.hp1 others(13): Show |
intron_variant | MODIFIER | c.629-4081_629-4080d others(4): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115716711 | |||||
| chr3:115716711
|
CAGACAA | C | 26 | a0001c0001t0001g0043a0001c0001t0001g0049a0001c0001t0001g0055others(23): Show | 26 | HG00438.hp1 HG01175.hp1 HG01175.hp2 others(23): Show |
intron_variant | MODIFIER | c.629-4081_629-4076d others(8): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115716711 | |||||
| chr3:115716711
|
CAGACAAA others(1): Show |
C | 49 | a0001c0001t0001g0038a0001c0001t0001g0040a0001c0001t0001g0047others(46): Show | 49 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.629-4081_629-4074d others(10): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115716711 | |||||
| chr3:115716711
|
CAGACAAA others(3): Show |
C | 14 | a0001c0001t0001g0028a0001c0001t0001g0044a0001c0001t0001g0046others(11): Show | 14 | HG00140.hp1 HG01256.hp1 HG02074.hp2 others(11): Show |
intron_variant | MODIFIER | c.629-4081_629-4072d others(12): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115716711 | |||||
| chr3:115716711
|
CAGACAAA others(5): Show |
C | 18 | a0001c0001t0001g0058a0001c0001t0001g0069a0001c0001t0001g0089others(15): Show | 18 | HG00609.hp1 HG01106.hp1 HG01257.hp2 others(15): Show |
intron_variant | MODIFIER | c.629-4081_629-4070d others(14): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115716711 | |||||
| chr3:115716711
|
CAGACAAA others(7): Show |
C | 6 | a0001c0001t0001g0041a0001c0001t0001g0064a0001c0001t0001g0092others(3): Show | 6 | HG00733.hp2 HG01192.hp1 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.629-4081_629-4068d others(16): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115716711 | |||||
| chr3:115716711
|
CAGACAAA others(9): Show |
C | 4 | a0001c0001t0001g0090a0001c0001t0001g0186a0001c0001t0001g0238others(1): Show | 4 | HG01071.hp2 HG02451.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.629-4081_629-4066d others(18): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115716711 | |||||
| chr3:115716711
|
CAGACAAA others(11): Show |
C | 1 | a0001c0001t0001g0093 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.629-4081_629-4064d others(20): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115716711 | |||||
| chr3:115716711
|
CAGACAAA others(13): Show |
C | 5 | a0001c0001t0001g0050a0001c0001t0002g0212a0001c0001t0002g0226others(2): Show | 5 | HG03927.hp2 NA18965.hp1 NA18998.hp2 others(2): Show |
intron_variant | MODIFIER | c.629-4081_629-4062d others(22): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115716711 | |||||
| chr3:115716711
|
CAGACAAA others(15): Show |
C | 4 | a0001c0001t0001g0173a0001c0001t0001g0197a0001c0001t0002g0140others(1): Show | 4 | HG02258.hp2 HG06807.hp2 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.629-4081_629-4060d others(24): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115716711 | |||||
| chr3:115716711
|
CAGACAAA others(17): Show |
C | 2 | a0001c0001t0001g0082a0001c0001t0001g0350 | 2 | HG02976.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.629-4081_629-4058d others(26): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115716711 | |||||
| chr3:115716711
|
CAGACAAA others(23): Show |
C | 1 | a0001c0001t0016g0269 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.629-4081_629-4052d others(32): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115716711 | |||||
| chr3:115716713
|
G | A | 8 | a0001c0001t0001g0052a0001c0001t0001g0145a0001c0001t0002g0129others(5): Show | 8 | HG00738.hp1 HG01943.hp2 HG02083.hp1 others(5): Show |
intron_variant | MODIFIER | c.629-4081G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115716713 | ||||||
| chr3:115716713
|
G | T | 5 | a0001c0001t0001g0302a0001c0001t0002g0205a0001c0001t0002g0264others(2): Show | 5 | HG00280.hp1 HG00280.hp2 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.629-4081G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115716713 | ||||||
| chr3:115716715
|
C | A | 16 | a0001c0001t0001g0002a0001c0001t0001g0042a0001c0001t0001g0053others(13): Show | 16 | HG00621.hp2 HG01074.hp2 HG01433.hp1 others(13): Show |
intron_variant | MODIFIER | c.629-4079C>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115716715 | ||||||
| chr3:115716715
|
C | T | 14 | a0001c0001t0001g0052a0001c0001t0001g0145a0001c0001t0001g0302others(11): Show | 14 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(11): Show |
intron_variant | MODIFIER | c.629-4079C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115716715 | ||||||
| chr3:115716716
|
AAATATAT others(6): Show |
A | 1 | a0001c0001t0003g0279 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.629-4076_629-4064d others(15): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115716716 | |||||
| chr3:115716717
|
A | AAT | 4 | a0001c0001t0001g0088a0001c0001t0001g0265a0001c0001t0003g0155others(1): Show | 4 | HG00642.hp2 HG02970.hp1 NA19072.hp1 others(1): Show |
intron_variant | MODIFIER | c.629-4027_629-4026d others(4): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115716717 | |||||
| chr3:115716717
|
A | AATATATA others(5): Show |
1 | a0001c0001t0003g0288 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.629-4037_629-4026d others(14): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115716717 | |||||
| chr3:115716717
|
A | T | 31 | a0001c0001t0001g0002a0001c0001t0001g0042a0001c0001t0001g0052others(28): Show | 31 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.629-4077A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115716717 | ||||||
| chr3:115716717
|
AAT | A | 18 | a0001c0001t0001g0037a0001c0001t0001g0086a0001c0001t0001g0087others(15): Show | 18 | HG01433.hp2 HG02071.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.629-4027_629-4026d others(4): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115716717 | |||||
| chr3:115716717
|
AATAT | A | 17 | a0001c0001t0001g0031a0001c0001t0001g0033a0001c0001t0001g0104others(14): Show | 18 | HG00738.hp2 HG01169.hp2 HG01255.hp1 others(15): Show |
intron_variant | MODIFIER | c.629-4029_629-4026d others(6): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115716717 | |||||
| chr3:115716717
|
AATATAT | A | 18 | a0001c0001t0001g0024a0001c0001t0001g0068a0001c0001t0001g0193others(15): Show | 18 | HG00544.hp1 HG01069.hp2 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.629-4031_629-4026d others(8): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115716717 | |||||
| chr3:115716717
|
AATATATA others(1): Show |
A | 33 | a0001c0001t0001g0017a0001c0001t0001g0165a0001c0001t0001g0228others(30): Show | 33 | HG00609.hp2 HG00673.hp2 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.629-4033_629-4026d others(10): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115716717 | |||||
| chr3:115716717
|
AATATATA others(3): Show |
A | 3 | a0001c0001t0001g0170a0001c0001t0003g0078a0001c0001t0004g0160 | 3 | HG02683.hp2 HG03942.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.629-4035_629-4026d others(12): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115716717 | |||||
| chr3:115716717
|
AATATATA others(5): Show |
A | 13 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0003g0241others(10): Show | 13 | HG00438.hp2 HG01361.hp1 HG02004.hp2 others(10): Show |
intron_variant | MODIFIER | c.629-4037_629-4026d others(14): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115716717 | |||||
| chr3:115716717
|
AATATATA others(7): Show |
A | 6 | a0001c0001t0001g0349a0001c0001t0005g0012a0001c0001t0005g0278others(3): Show | 6 | HG01081.hp2 HG01109.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.629-4039_629-4026d others(16): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115716717 | |||||
| chr3:115716717
|
AATATATA others(9): Show |
A | 4 | a0001c0001t0004g0054a0001c0001t0005g0101a0001c0001t0005g0233others(1): Show | 4 | HG02083.hp2 HG02559.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.629-4041_629-4026d others(18): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115716717 | |||||
| chr3:115716717
|
AATATATA others(11): Show |
A | 2 | a0001c0001t0001g0224a0001c0001t0005g0204 | 2 | HG02630.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.629-4043_629-4026d others(20): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115716717 | |||||
| chr3:115716717
|
AATATATA others(13): Show |
A | 2 | a0001c0001t0002g0128a0001c0001t0013g0219 | 2 | NA19066.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.629-4045_629-4026d others(22): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115716717 | |||||
| chr3:115716717
|
AATATATA others(15): Show |
A | 1 | a0001c0001t0004g0309 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.629-4047_629-4026d others(24): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115716717 | |||||
| chr3:115716717
|
AATATATA others(19): Show |
A | 4 | a0001c0001t0001g0004a0001c0001t0001g0036a0001c0001t0001g0298others(1): Show | 4 | HG02055.hp1 HG03139.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.629-4051_629-4026d others(28): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115716717 | |||||
| chr3:115716717
|
AATATATA others(25): Show |
A | 1 | a0001c0001t0001g0185 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.629-4057_629-4026d others(34): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115716717 | |||||
| chr3:115716719
|
T | A | 26 | a0001c0001t0001g0043a0001c0001t0001g0049a0001c0001t0001g0055others(23): Show | 26 | HG00438.hp1 HG01175.hp1 HG01175.hp2 others(23): Show |
intron_variant | MODIFIER | c.629-4075T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115716719 | ||||||
| chr3:115716721
|
T | A | 49 | a0001c0001t0001g0038a0001c0001t0001g0040a0001c0001t0001g0047others(46): Show | 49 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.629-4073T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115716721 | ||||||
| chr3:115716723
|
T | A | 14 | a0001c0001t0001g0028a0001c0001t0001g0044a0001c0001t0001g0046others(11): Show | 14 | HG00140.hp1 HG01256.hp1 HG02074.hp2 others(11): Show |
intron_variant | MODIFIER | c.629-4071T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115716723 | ||||||
| chr3:115716725
|
T | A | 18 | a0001c0001t0001g0058a0001c0001t0001g0069a0001c0001t0001g0089others(15): Show | 18 | HG00609.hp1 HG01106.hp1 HG01257.hp2 others(15): Show |
intron_variant | MODIFIER | c.629-4069T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115716725 | ||||||
| chr3:115716727
|
T | A | 6 | a0001c0001t0001g0041a0001c0001t0001g0064a0001c0001t0001g0092others(3): Show | 6 | HG00733.hp2 HG01192.hp1 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.629-4067T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115716727 | ||||||
| chr3:115716729
|
T | A | 4 | a0001c0001t0001g0090a0001c0001t0001g0186a0001c0001t0001g0238others(1): Show | 4 | HG01071.hp2 HG02451.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.629-4065T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115716729 | ||||||
| chr3:115716729
|
T | TATATATA others(12): Show |
1 | a0001c0001t0003g0027 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.629-4064_629-4046d others(21): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115716729 | |||||
| chr3:115716731
|
T | A | 1 | a0001c0001t0001g0093 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.629-4063T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115716731 | ||||||
| chr3:115716733
|
T | A | 5 | a0001c0001t0001g0050a0001c0001t0002g0212a0001c0001t0002g0226others(2): Show | 5 | HG03927.hp2 NA18965.hp1 NA18998.hp2 others(2): Show |
intron_variant | MODIFIER | c.629-4061T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115716733 | ||||||
| chr3:115716735
|
T | A | 4 | a0001c0001t0001g0173a0001c0001t0001g0197a0001c0001t0002g0140others(1): Show | 4 | HG02258.hp2 HG06807.hp2 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.629-4059T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115716735 | ||||||
| chr3:115716736
|
A | T | 1 | a0001c0001t0001g0172 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.629-4058A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115716736 | ||||||
| chr3:115716737
|
T | A | 2 | a0001c0001t0001g0082a0001c0001t0001g0350 | 2 | HG02976.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.629-4057T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115716737 | ||||||
| chr3:115716737
|
T | G | 1 | a0001c0001t0001g0172 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.629-4057T>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115716737 | ||||||
| chr3:115716739
|
T | G | 1 | a0001c0001t0001g0172 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.629-4055T>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115716739 | ||||||
| chr3:115716743
|
T | A | 1 | a0001c0001t0016g0269 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.629-4051T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115716743 | ||||||
| chr3:115716749
|
TATATATA others(19): Show |
T | 1 | a0001c0001t0001g0339 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.629-4043_629-4018d others(28): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115716749 | |||||
| chr3:115716754
|
A | G | 1 | a0001c0002t0017g0314 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.629-4040A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115716754 | ||||||
| chr3:115716757
|
TATATATA others(9): Show |
T | 1 | a0001c0001t0001g0112 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.629-4035_629-4020d others(18): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115716757 | |||||
| chr3:115716759
|
T | C | 24 | a0001c0001t0001g0017a0001c0001t0001g0024a0001c0001t0001g0031others(21): Show | 24 | HG00733.hp1 HG00735.hp1 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.629-4035T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115716759 | ||||||
| chr3:115716759
|
TATATATA others(7): Show |
T | 1 | a0001c0001t0001g0225 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.629-4033_629-4020d others(16): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115716759 | |||||
| chr3:115716761
|
TATATATA others(7): Show |
T | 1 | a0001c0001t0001g0019 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.629-4031_629-4018d others(16): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115716761 | |||||
| chr3:115716763
|
TATATACA others(5): Show |
T | 2 | a0001c0001t0001g0319a0001c0002t0001g0253 | 2 | HG03654.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.629-4029_629-4018d others(14): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115716763 | |||||
| chr3:115716765
|
T | C | 18 | a0001c0001t0001g0037a0001c0001t0001g0216a0001c0001t0005g0003others(15): Show | 18 | HG01081.hp2 HG01361.hp1 HG02004.hp1 others(15): Show |
intron_variant | MODIFIER | c.629-4029T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115716765 | ||||||
| chr3:115716765
|
TATACAGA others(3): Show |
T | 2 | a0001c0001t0001g0015a0001c0001t0001g0073 | 2 | HG01261.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.629-4027_629-4018d others(12): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115716765 | |||||
| chr3:115716767
|
T | C | 14 | a0001c0001t0001g0042a0001c0001t0001g0051a0001c0001t0001g0052others(11): Show | 14 | HG00639.hp1 HG00738.hp1 HG02004.hp1 others(11): Show |
intron_variant | MODIFIER | c.629-4027T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115716767 | ||||||
| chr3:115716767
|
T | G | 16 | a0001c0001t0001g0037a0001c0001t0001g0342a0001c0001t0005g0003others(13): Show | 16 | HG01081.hp2 HG01361.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.629-4027T>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115716767 | ||||||
| chr3:115716767
|
TACAG | T | 3 | a0001c0001t0001g0066a0001c0001t0001g0202a0001c0002t0001g0150 | 3 | HG02293.hp2 NA18747.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.629-4025_629-4022d others(6): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115716767 | |||||
| chr3:115716769
|
C | CAGAG | 4 | a0001c0001t0005g0101a0001c0001t0005g0204a0001c0001t0005g0233others(1): Show | 4 | HG02559.hp1 HG02895.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.629-4006_629-4003d others(6): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115716769 | |||||
| chr3:115716769
|
C | G | 19 | a0001c0001t0001g0037a0001c0001t0001g0259a0001c0001t0001g0342others(16): Show | 19 | HG01081.hp2 HG01361.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.629-4025C>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115716769 | ||||||
| chr3:115716769
|
C | T | 1 | a0001c0001t0001g0088 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.629-4025C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115716769 | ||||||
| chr3:115716769
|
CAGAGAGA others(1): Show |
C | 4 | a0001c0001t0001g0067a0001c0001t0001g0221a0001c0001t0001g0347others(1): Show | 4 | HG02922.hp1 HG02970.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.629-4010_629-4003d others(10): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115716769 | |||||
| chr3:115716771
|
G | T | 3 | a0001c0001t0001g0088a0001c0001t0019g0013a0001c0002t0001g0132 | 3 | HG04228.hp2 NA18945.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.629-4023G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115716771 | ||||||
| chr3:115716773
|
G | T | 6 | a0001c0001t0001g0066a0001c0001t0001g0088a0001c0001t0001g0202others(3): Show | 6 | HG02293.hp2 HG04228.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.629-4021G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115716773 | ||||||
| chr3:115716775
|
G | C | 3 | a0001c0001t0001g0112a0001c0001t0001g0225a0001c0001t0019g0013 | 3 | HG02717.hp2 HG04199.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.629-4019G>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115716775 | ||||||
| chr3:115716775
|
G | T | 6 | a0001c0001t0001g0066a0001c0001t0001g0088a0001c0001t0001g0202others(3): Show | 6 | HG02293.hp2 NA18747.hp1 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.629-4019G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115716775 | ||||||
| chr3:115716777
|
G | C | 14 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0066others(11): Show | 14 | HG01261.hp1 HG02293.hp2 HG02683.hp1 others(11): Show |
intron_variant | MODIFIER | c.629-4017G>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115716777 | ||||||
| chr3:115716841
|
A | C | 1 | a0001c0001t0003g0014 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.629-3953A>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115716841 | ||||||
| chr3:115716847
|
T | C | 343 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0015others(340): Show | 344 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(341): Show |
intron_variant | MODIFIER | c.629-3947T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115716847 | ||||||
| chr3:115716964
|
C | A | 7 | a0001c0001t0001g0061a0001c0001t0001g0222a0001c0001t0001g0234others(4): Show | 7 | HG02109.hp2 HG02451.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.629-3830C>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115716964 | ||||||
| chr3:115716985
|
G | A | 3 | a0001c0001t0001g0209a0001c0001t0010g0245a0001c0001t0010g0246 | 3 | HG02895.hp1 HG02897.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.629-3809G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115716985 | ||||||
| chr3:115717001
|
C | T | 1 | a0001c0001t0003g0009 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.629-3793C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115717001 | ||||||
| chr3:115717043
|
G | T | 17 | a0001c0001t0005g0003a0001c0001t0005g0005a0001c0001t0005g0011others(14): Show | 17 | HG01081.hp2 HG01361.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.629-3751G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115717043 | ||||||
| chr3:115717159
|
G | C | 6 | a0001c0001t0001g0004a0001c0001t0001g0036a0001c0001t0001g0224others(3): Show | 6 | HG01109.hp1 HG02055.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.629-3635G>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115717159 | ||||||
| chr3:115717214
|
G | A | 2 | a0001c0001t0001g0037a0001c0001t0001g0342 | 2 | HG02818.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.629-3580G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115717214 | ||||||
| chr3:115717315
|
C | CT | 195 | a0001c0001t0001g0002a0001c0001t0001g0028a0001c0001t0001g0038others(192): Show | 195 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(192): Show |
intron_variant | MODIFIER | c.629-3466dupT | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115717315 | |||||
| chr3:115717315
|
C | CTT | 94 | a0001c0001t0001g0037a0001c0001t0001g0165a0001c0001t0001g0259others(91): Show | 95 | HG00140.hp2 HG00438.hp2 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.629-3467_629-3466d others(4): Show |
GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115717315 | |||||
| chr3:115717358
|
G | A | 5 | a0001c0001t0001g0209a0001c0001t0002g0243a0001c0001t0002g0244others(2): Show | 5 | HG02145.hp1 HG02280.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.629-3436G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115717358 | ||||||
| chr3:115717497
|
C | T | 2 | a0001c0001t0002g0018a0001c0001t0002g0258 | 2 | NA18943.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.629-3297C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115717497 | ||||||
| chr3:115717498
|
G | A | 1 | a0001c0001t0001g0306 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.629-3296G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115717498 | ||||||
| chr3:115717669
|
C | CT | 13 | a0001c0001t0003g0062a0001c0001t0003g0074a0001c0001t0003g0076others(10): Show | 13 | HG00642.hp2 HG00738.hp2 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.629-3109dupT | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115717669 | |||||
| chr3:115717669
|
CT | C | 24 | a0001c0001t0001g0037a0001c0001t0001g0197a0001c0001t0001g0259others(21): Show | 24 | HG01069.hp1 HG01071.hp1 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.629-3109delT | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115717669 | |||||
| chr3:115717797
|
G | A | 6 | a0001c0001t0001g0004a0001c0001t0001g0036a0001c0001t0001g0224others(3): Show | 6 | HG01109.hp1 HG02055.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.629-2997G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115717797 | ||||||
| chr3:115718277
|
G | T | 1 | a0001c0001t0012g0300 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.629-2517G>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115718277 | ||||||
| chr3:115718328
|
T | C | 181 | a0001c0001t0001g0002a0001c0001t0001g0028a0001c0001t0001g0038others(178): Show | 181 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(178): Show |
intron_variant | MODIFIER | c.629-2466T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115718328 | ||||||
| chr3:115718358
|
T | A | 1 | a0001c0001t0004g0247 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.629-2436T>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115718358 | ||||||
| chr3:115718427
|
C | A | 2 | a0001c0001t0001g0037a0001c0001t0001g0342 | 2 | HG02818.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.629-2367C>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115718427 | ||||||
| chr3:115718460
|
G | A | 6 | a0001c0001t0001g0004a0001c0001t0001g0036a0001c0001t0001g0224others(3): Show | 6 | HG01109.hp1 HG02055.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.629-2334G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115718460 | ||||||
| chr3:115718552
|
A | T | 2 | a0001c0001t0002g0178a0001c0001t0002g0184 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.629-2242A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115718552 | ||||||
| chr3:115718595
|
A | G | 2 | a0001c0001t0001g0037a0001c0001t0001g0342 | 2 | HG02818.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.629-2199A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115718595 | ||||||
| chr3:115718728
|
G | A | 1 | a0001c0001t0001g0209 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.629-2066G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115718728 | ||||||
| chr3:115718757
|
T | C | 5 | a0001c0001t0001g0209a0001c0001t0002g0243a0001c0001t0002g0244others(2): Show | 5 | HG02145.hp1 HG02280.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.629-2037T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115718757 | ||||||
| chr3:115718852
|
A | G | 2 | a0001c0001t0002g0243a0001c0001t0002g0244 | 2 | HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.629-1942A>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115718852 | ||||||
| chr3:115718912
|
T | C | 1 | a0001c0001t0001g0037 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.629-1882T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115718912 | ||||||
| chr3:115719078
|
C | G | 2 | a0001c0001t0010g0245a0001c0001t0010g0246 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.629-1716C>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115719078 | ||||||
| chr3:115719268
|
GA | G | 180 | a0001c0001t0001g0002a0001c0001t0001g0028a0001c0001t0001g0038others(177): Show | 180 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(177): Show |
intron_variant | MODIFIER | c.629-1515delA | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 115719268 | |||||
| chr3:115719295
|
G | A | 1 | a0001c0001t0001g0222 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.629-1499G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115719295 | ||||||
| chr3:115719416
|
C | G | 1 | a0001c0002t0001g0035 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.629-1378C>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115719416 | ||||||
| chr3:115719441
|
G | C | 1 | a0001c0001t0001g0259 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.629-1353G>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115719441 | ||||||
| chr3:115719448
|
C | A | 47 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0017others(44): Show | 47 | HG01109.hp1 HG01261.hp1 HG01884.hp1 others(44): Show |
intron_variant | MODIFIER | c.629-1346C>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115719448 | ||||||
| chr3:115719456
|
C | G | 3 | a0001c0001t0002g0271a0001c0001t0002g0317a0001c0001t0002g0318 | 3 | NA18975.hp2 NA19009.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.629-1338C>G | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115719456 | ||||||
| chr3:115719811
|
G | A | 78 | a0001c0001t0002g0294a0001c0001t0003g0001a0001c0001t0003g0007others(75): Show | 79 | HG00140.hp2 HG00408.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.629-983G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115719811 | ||||||
| chr3:115719907
|
A | T | 2 | a0001c0001t0001g0031a0001c0001t0001g0033 | 2 | NA18950.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.629-887A>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115719907 | ||||||
| chr3:115720003
|
G | A | 343 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0015others(340): Show | 344 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(341): Show |
intron_variant | MODIFIER | c.629-791G>A | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115720003 | ||||||
| chr3:115720405
|
C | T | 2 | a0001c0001t0001g0037a0001c0001t0001g0342 | 2 | HG02818.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.629-389C>T | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115720405 | ||||||
| chr3:115720529
|
T | C | 2 | a0001c0001t0001g0037a0001c0001t0001g0342 | 2 | HG02818.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.629-265T>C | GAP43 | ENSG00000172020.13 | transcript | ENST00000305124.11 | protein_coding | 2/2 | chr3 | 115720529 |