Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 5361 |
|---|---|
| ensemblid | ENSG00000114554.12 |
| hgncid | 9099 |
| symbol | PLXNA1 |
| name | plexin A1 |
| refseq_nuc | NM_032242.4 |
| refseq_prot | NP_115618.3 |
| ensembl_nuc | ENST00000393409.3 |
| ensembl_prot | ENSP00000377061.2 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 126983115 |
| end | 127037389 |
| strand | + |
| ver | v1.2 |
| region | chr3:126983115-127037389 |
| region5000 | chr3:126978115-127042389 |
| regionname0 | PLXNA1_chr3_126983115_127037389 |
| regionname5000 | PLXNA1_chr3_126978115_127042389 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0000 | 0/0 | 0 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001 | 1/1 | 1896 | 336 | 88 | 56 | 144 | 12 | 34 | 108 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0002 | 0/0 | 1896 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0003 | 0/0 | 1896 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0004 | 0/0 | 1896 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0005 | 0/0 | 1896 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0006 | 0/0 | 1896 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0007 | 0/0 | 1896 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0008 | 0/0 | 1896 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0009 | 0/0 | 1896 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 5691 | 116 | 13 | 26 | 60 | 5 | 12 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| c0002 | 0/0 | 5691 | 53 | 0 | 5 | 37 | 1 | 10 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| c0003 | 1/1 | 5691 | 31 | 9 | 6 | 12 | 0 | 2 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| c0004 | 0/0 | 5691 | 24 | 7 | 2 | 10 | 2 | 3 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| c0005 | 0/0 | 5691 | 23 | 1 | 2 | 16 | 2 | 2 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| c0006 | 0/0 | 5691 | 18 | 17 | 1 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| c0007 | 0/0 | 5691 | 12 | 10 | 2 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| c0008 | 0/0 | 5691 | 12 | 5 | 7 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| c0009 | 0/0 | 5691 | 5 | 5 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| c0010 | 0/0 | 5691 | 4 | 4 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| c0011 | 0/0 | 5691 | 4 | 0 | 1 | 2 | 0 | 1 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| c0012 | 0/0 | 5691 | 3 | 3 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| c0013 | 0/0 | 5691 | 3 | 0 | 2 | 0 | 1 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| c0014 | 0/0 | 5691 | 3 | 3 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| c0015 | 0/0 | 5691 | 2 | 1 | 1 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| c0016 | 0/0 | 5691 | 2 | 0 | 0 | 1 | 0 | 1 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| c0017 | 0/0 | 5691 | 2 | 2 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| c0018 | 0/0 | 5691 | 2 | 0 | 0 | 2 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| c0019 | 0/0 | 5691 | 2 | 0 | 0 | 2 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| c0020 | 0/0 | 5691 | 2 | 0 | 1 | 0 | 1 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| c0021 | 0/0 | 5691 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| c0022 | 0/0 | 5691 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| c0023 | 0/0 | 5691 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| c0024 | 0/0 | 5691 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| c0025 | 0/0 | 5691 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| c0026 | 0/0 | 5691 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| c0027 | 0/0 | 5691 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| c0028 | 0/0 | 5680 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| c0029 | 0/0 | 5691 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| c0030 | 0/0 | 5691 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| c0031 | 0/0 | 5691 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| c0032 | 0/0 | 5691 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| c0033 | 0/0 | 5691 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| c0034 | 0/0 | 5691 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| c0035 | 0/0 | 5691 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| c0036 | 0/0 | 5691 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| c0037 | 0/0 | 5691 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| c0038 | 0/0 | 5691 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| c0039 | 0/0 | 5691 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| c0040 | 0/0 | 5691 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| c0041 | 0/0 | 5691 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| c0042 | 0/0 | 5691 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| c0043 | 0/0 | 5691 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 3619 | 140 | 21 | 34 | 62 | 6 | 15 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| t0002 | 0/0 | 3619 | 40 | 3 | 0 | 30 | 1 | 6 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| t0003 | 0/0 | 3619 | 24 | 22 | 2 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| t0004 | 0/0 | 3619 | 23 | 5 | 1 | 11 | 1 | 5 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| t0005 | 0/0 | 3619 | 21 | 1 | 2 | 16 | 2 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| t0006 | 0/0 | 3619 | 9 | 0 | 5 | 1 | 0 | 3 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| t0007 | 0/0 | 3620 | 6 | 0 | 5 | 0 | 1 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| t0008 | 0/0 | 3619 | 6 | 0 | 0 | 6 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| t0009 | 0/0 | 3619 | 6 | 4 | 0 | 2 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| t0010 | 0/0 | 3619 | 6 | 0 | 0 | 6 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| t0011 | 0/0 | 3619 | 5 | 1 | 2 | 0 | 1 | 1 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| t0012 | 0/0 | 3619 | 5 | 3 | 1 | 0 | 0 | 1 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| t0013 | 0/0 | 3619 | 4 | 2 | 2 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| t0014 | 0/0 | 3619 | 4 | 4 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| t0015 | 0/0 | 3619 | 4 | 4 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| t0016 | 0/0 | 3619 | 4 | 0 | 0 | 4 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| t0017 | 0/0 | 3619 | 2 | 2 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| t0018 | 0/0 | 3620 | 2 | 0 | 2 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| t0019 | 0/0 | 3619 | 2 | 2 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| t0020 | 0/0 | 3619 | 2 | 2 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| t0021 | 0/0 | 3619 | 2 | 0 | 0 | 2 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| t0022 | 0/0 | 3619 | 2 | 0 | 0 | 1 | 0 | 1 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| t0023 | 0/0 | 3619 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| t0024 | 0/0 | 3619 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| t0025 | 0/0 | 3619 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| t0026 | 0/0 | 3619 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| t0027 | 0/0 | 3619 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| t0028 | 0/0 | 3619 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| t0029 | 0/0 | 3619 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| t0030 | 0/0 | 3619 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| t0031 | 0/0 | 3619 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| t0032 | 0/0 | 3619 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| t0033 | 0/0 | 3619 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| t0034 | 0/0 | 3619 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| t0035 | 0/0 | 3619 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| t0036 | 0/0 | 3619 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| t0037 | 0/0 | 3619 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| t0038 | 0/0 | 3619 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| t0039 | 0/0 | 3619 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| t0040 | 0/0 | 3619 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| t0041 | 0/0 | 3619 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| t0042 | 0/0 | 3619 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| t0043 | 0/0 | 3619 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| t0044 | 0/0 | 3619 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| t0045 | 0/0 | 3619 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| t0046 | 0/0 | 3619 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| t0047 | 0/0 | 3619 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| t0048 | 0/0 | 3619 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| t0049 | 0/0 | 3619 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 25 | 1 | 7 | 8 | 3 | 6 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0002 | 0/0 | 22 | 0 | 0 | 18 | 1 | 3 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0003 | 0/0 | 13 | 3 | 3 | 5 | 0 | 2 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0004 | 0/0 | 10 | 1 | 2 | 4 | 2 | 1 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0005 | 0/0 | 8 | 7 | 1 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0006 | 0/0 | 8 | 0 | 1 | 7 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0007 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0008 | 0/0 | 7 | 0 | 3 | 4 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0009 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0010 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0011 | 0/0 | 5 | 1 | 2 | 0 | 1 | 1 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0012 | 0/0 | 5 | 1 | 4 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0014 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0016 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0017 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0020 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0022 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0023 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0039 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0042 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0146 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0184 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0000c0028 | 0/0 | 5680 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0001 | 0/0 | 5691 | 116 | 13 | 26 | 60 | 5 | 12 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0002 | 0/0 | 5691 | 53 | 0 | 5 | 37 | 1 | 10 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0003 | 1/1 | 5691 | 31 | 9 | 6 | 12 | 0 | 2 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0004 | 0/0 | 5691 | 24 | 7 | 2 | 10 | 2 | 3 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0005 | 0/0 | 5691 | 23 | 1 | 2 | 16 | 2 | 2 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0006 | 0/0 | 5691 | 18 | 17 | 1 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0007 | 0/0 | 5691 | 12 | 10 | 2 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0008 | 0/0 | 5691 | 12 | 5 | 7 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0009 | 0/0 | 5691 | 5 | 5 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0010 | 0/0 | 5691 | 4 | 4 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0011 | 0/0 | 5691 | 4 | 0 | 1 | 2 | 0 | 1 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0012 | 0/0 | 5691 | 3 | 3 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0013 | 0/0 | 5691 | 3 | 0 | 2 | 0 | 1 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0014 | 0/0 | 5691 | 3 | 3 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0015 | 0/0 | 5691 | 2 | 1 | 1 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0016 | 0/0 | 5691 | 2 | 0 | 0 | 1 | 0 | 1 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0017 | 0/0 | 5691 | 2 | 2 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0018 | 0/0 | 5691 | 2 | 0 | 0 | 2 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0020 | 0/0 | 5691 | 2 | 0 | 1 | 0 | 1 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0021 | 0/0 | 5691 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0023 | 0/0 | 5691 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0024 | 0/0 | 5691 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0026 | 0/0 | 5691 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0027 | 0/0 | 5691 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0029 | 0/0 | 5691 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0030 | 0/0 | 5691 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0032 | 0/0 | 5691 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0033 | 0/0 | 5691 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0036 | 0/0 | 5691 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0037 | 0/0 | 5691 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0038 | 0/0 | 5691 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0039 | 0/0 | 5691 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0040 | 0/0 | 5691 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0041 | 0/0 | 5691 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0002c0019 | 0/0 | 5691 | 2 | 0 | 0 | 2 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0003c0043 | 0/0 | 5691 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0004c0042 | 0/0 | 5691 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0005c0022 | 0/0 | 5691 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0006c0035 | 0/0 | 5691 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0007c0025 | 0/0 | 5691 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0008c0034 | 0/0 | 5691 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0009c0031 | 0/0 | 5691 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0000c0028t0034 | 0/0 | 9298 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0001t0001 | 0/0 | 9309 | 97 | 10 | 26 | 45 | 5 | 11 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0001t0010 | 0/0 | 9309 | 6 | 0 | 0 | 6 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0001t0016 | 0/0 | 9309 | 4 | 0 | 0 | 4 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0001t0022 | 0/0 | 9309 | 2 | 0 | 0 | 1 | 0 | 1 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0001t0039 | 0/0 | 9309 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0001t0041 | 0/0 | 9309 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0001t0042 | 0/0 | 9309 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0001t0043 | 0/0 | 9309 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0001t0044 | 0/0 | 9309 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0001t0046 | 0/0 | 9309 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0001t0047 | 0/0 | 9309 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0002t0002 | 0/0 | 9309 | 34 | 0 | 0 | 28 | 1 | 5 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0002t0004 | 0/0 | 9309 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0002t0006 | 0/0 | 9309 | 7 | 0 | 4 | 0 | 0 | 3 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0002t0008 | 0/0 | 9309 | 5 | 0 | 0 | 5 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0002t0012 | 0/0 | 9309 | 2 | 0 | 1 | 0 | 0 | 1 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0002t0021 | 0/0 | 9309 | 2 | 0 | 0 | 2 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0002t0024 | 0/0 | 9309 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0002t0035 | 0/0 | 9309 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0003t0001 | 1/1 | 9309 | 29 | 8 | 6 | 11 | 0 | 2 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0003t0040 | 0/0 | 9309 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0003t0048 | 0/0 | 9309 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0004t0004 | 0/0 | 9309 | 17 | 4 | 0 | 9 | 1 | 3 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0004t0006 | 0/0 | 9309 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0004t0011 | 0/0 | 9309 | 4 | 1 | 2 | 0 | 1 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0004t0019 | 0/0 | 9309 | 2 | 2 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0005t0005 | 0/0 | 9309 | 20 | 1 | 2 | 15 | 2 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0005t0025 | 0/0 | 9309 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0005t0030 | 0/0 | 9309 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0005t0032 | 0/0 | 9309 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0006t0001 | 0/0 | 9309 | 3 | 2 | 1 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0006t0003 | 0/0 | 9309 | 10 | 10 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0006t0014 | 0/0 | 9309 | 4 | 4 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0006t0029 | 0/0 | 9309 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0007t0003 | 0/0 | 9309 | 10 | 8 | 2 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0007t0020 | 0/0 | 9309 | 2 | 2 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0008t0007 | 0/0 | 9310 | 3 | 0 | 3 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0008t0013 | 0/0 | 9309 | 4 | 2 | 2 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0008t0017 | 0/0 | 9309 | 2 | 2 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0008t0018 | 0/0 | 9310 | 2 | 0 | 2 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0008t0023 | 0/0 | 9309 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0009t0002 | 0/0 | 9309 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0009t0012 | 0/0 | 9309 | 2 | 2 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0009t0027 | 0/0 | 9309 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0009t0028 | 0/0 | 9309 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0010t0009 | 0/0 | 9309 | 4 | 4 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0011t0004 | 0/0 | 9309 | 4 | 0 | 1 | 2 | 0 | 1 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0012t0015 | 0/0 | 9309 | 3 | 3 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0013t0007 | 0/0 | 9310 | 3 | 0 | 2 | 0 | 1 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0014t0002 | 0/0 | 9309 | 2 | 2 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0014t0026 | 0/0 | 9309 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0015t0003 | 0/0 | 9309 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0015t0006 | 0/0 | 9309 | 1 | 0 | 1 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0016t0005 | 0/0 | 9309 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0016t0031 | 0/0 | 9309 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0017t0012 | 0/0 | 9309 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0017t0037 | 0/0 | 9309 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0018t0002 | 0/0 | 9309 | 2 | 0 | 0 | 2 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0020t0001 | 0/0 | 9309 | 2 | 0 | 1 | 0 | 1 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0021t0015 | 0/0 | 9309 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0023t0003 | 0/0 | 9309 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0024t0036 | 0/0 | 9309 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0026t0004 | 0/0 | 9309 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0027t0002 | 0/0 | 9309 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0029t0008 | 0/0 | 9309 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0030t0001 | 0/0 | 9309 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0032t0049 | 0/0 | 9309 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0033t0009 | 0/0 | 9309 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0036t0001 | 0/0 | 9309 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0037t0045 | 0/0 | 9309 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0038t0038 | 0/0 | 9309 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0039t0001 | 0/0 | 9309 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0040t0009 | 0/0 | 9309 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0001c0041t0003 | 0/0 | 9309 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0002c0019t0001 | 0/0 | 9309 | 2 | 0 | 0 | 2 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0003c0043t0033 | 0/0 | 9309 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0004c0042t0001 | 0/0 | 9309 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0005c0022t0003 | 0/0 | 9309 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0006c0035t0001 | 0/0 | 9309 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0007c0025t0011 | 0/0 | 9309 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0008c0034t0001 | 0/0 | 9309 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| a0009c0031t0001 | 0/0 | 9309 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | copy fasta | chr3 | 126978115 | 127042389 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0000c0028t0034g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0001t0001g0001 | 0/0 | 19 | 0 | 6 | 6 | 2 | 5 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0001t0001g0003 | 0/0 | 10 | 3 | 3 | 2 | 0 | 2 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0001t0001g0007 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0001t0001g0008 | 0/0 | 5 | 0 | 3 | 2 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0001t0001g0012 | 0/0 | 5 | 1 | 4 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0001t0001g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0001t0001g0022 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0001t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0001t0010g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0001t0010g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0001t0010g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0001t0010g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0001t0010g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0001t0010g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0001t0016g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0001t0016g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0001t0016g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0001t0022g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0001t0022g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0001t0039g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0001t0041g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0001t0042g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0001t0043g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0001t0044g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0001t0046g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0001t0047g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0002t0002g0002 | 0/0 | 15 | 0 | 0 | 11 | 1 | 3 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0002t0002g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0002t0002g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0002t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0002t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0002t0004g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0002t0006g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0002t0006g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0002t0006g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0002t0006g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0002t0006g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0002t0006g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0002t0008g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0002t0008g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0002t0012g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0002t0012g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0002t0021g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0002t0021g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0002t0024g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0002t0035g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0003t0001g0006 | 0/0 | 8 | 0 | 1 | 7 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0003t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0003t0001g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0003t0001g0017 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0003t0001g0023 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0003t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0003t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0003t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0003t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0003t0001g0146 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0003t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0003t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0003t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0003t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0003t0001g0184 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0003t0040g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0003t0048g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0004t0004g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0004t0004g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0004t0004g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0004t0004g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0004t0004g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0004t0004g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0004t0004g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0004t0004g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0004t0004g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0004t0004g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0004t0004g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0004t0004g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0004t0006g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0004t0011g0011 | 0/0 | 4 | 1 | 2 | 0 | 1 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0004t0019g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0004t0019g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0005t0005g0004 | 0/0 | 8 | 1 | 2 | 3 | 2 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0005t0005g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0005t0005g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0005t0005g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0005t0005g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0005t0005g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0005t0005g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0005t0005g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0005t0005g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0005t0005g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0005t0025g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0005t0030g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0005t0032g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0006t0001g0020 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0006t0003g0009 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0006t0003g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0006t0003g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0006t0003g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0006t0003g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0006t0003g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0006t0014g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0006t0014g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0006t0029g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0007t0003g0005 | 0/0 | 8 | 7 | 1 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0007t0003g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0007t0003g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0007t0020g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0007t0020g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0008t0007g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0008t0007g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0008t0013g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0008t0013g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0008t0013g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0008t0017g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0008t0017g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0008t0018g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0008t0023g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0009t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0009t0012g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0009t0027g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0009t0028g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0010t0009g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0010t0009g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0010t0009g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0011t0004g0010 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0011t0004g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0011t0004g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0012t0015g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0013t0007g0014 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0013t0007g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0014t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0014t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0014t0026g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0015t0003g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0015t0006g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0016t0005g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0016t0031g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0017t0012g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0017t0037g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0018t0002g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0018t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0020t0001g0001 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0021t0015g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0023t0003g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0024t0036g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0026t0004g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0027t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0029t0008g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0030t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0032t0049g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0033t0009g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0036t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0037t0045g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0038t0038g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0039t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0040t0009g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0001c0041t0003g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0002c0019t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0002c0019t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0003c0043t0033g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0004c0042t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0005c0022t0003g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0006c0035t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0007c0025t0011g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0008c0034t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| a0009c0031t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0002 | g0002 | EUR | GBR | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0157 | EUR | GBR | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG00140 | hp2 | a0001 | c0013 | t0007 | g0014 | EUR | GBR | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0102 | EUR | FIN | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG00280 | hp2 | a0001 | c0004 | t0004 | g0177 | EUR | FIN | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG00323 | hp2 | a0001 | c0005 | t0005 | g0004 | EUR | FIN | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG00408 | hp2 | a0001 | c0011 | t0004 | g0173 | EAS | CHS | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG00438 | hp1 | a0001 | c0004 | t0004 | g0174 | EAS | CHS | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG00544 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | CHS | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG00544 | hp2 | a0001 | c0004 | t0004 | g0010 | EAS | CHS | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | CHS | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG00597 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | CHS | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG00609 | hp1 | a0001 | c0002 | t0002 | g0070 | EAS | CHS | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG00609 | hp2 | a0001 | c0036 | t0001 | g0140 | EAS | CHS | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG00639 | hp1 | a0001 | c0007 | t0003 | g0005 | AMR | PUR | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG00735 | hp1 | a0001 | c0020 | t0001 | g0001 | AMR | PUR | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG01069 | hp1 | a0001 | c0008 | t0007 | g0029 | AMR | PUR | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG01070 | hp1 | a0001 | c0008 | t0007 | g0061 | AMR | PUR | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG01071 | hp2 | a0001 | c0008 | t0007 | g0029 | AMR | PUR | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG01099 | hp1 | a0001 | c0015 | t0006 | g0062 | AMR | PUR | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG01099 | hp2 | a0001 | c0002 | t0012 | g0072 | AMR | PUR | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG01109 | hp1 | a0001 | c0007 | t0003 | g0090 | AMR | PUR | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG01167 | hp2 | a0001 | c0008 | t0013 | g0030 | AMR | PUR | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG01168 | hp2 | a0001 | c0005 | t0005 | g0004 | AMR | PUR | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG01169 | hp1 | a0001 | c0008 | t0013 | g0030 | AMR | PUR | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG01169 | hp2 | a0001 | c0005 | t0005 | g0004 | AMR | PUR | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG01175 | hp1 | a0001 | c0003 | t0001 | g0023 | AMR | PUR | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG01243 | hp1 | a0001 | c0003 | t0001 | g0017 | AMR | PUR | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG01255 | hp1 | a0001 | c0006 | t0001 | g0020 | AMR | CLM | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG01256 | hp1 | a0001 | c0002 | t0006 | g0077 | AMR | CLM | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG01256 | hp2 | a0001 | c0008 | t0018 | g0014 | AMR | CLM | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG01258 | hp2 | a0001 | c0008 | t0018 | g0014 | AMR | CLM | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | CLM | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | CLM | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG01346 | hp1 | a0001 | c0011 | t0004 | g0042 | AMR | CLM | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG01346 | hp2 | a0001 | c0003 | t0001 | g0162 | AMR | CLM | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG01496 | hp1 | a0001 | c0004 | t0011 | g0011 | AMR | CLM | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG01515 | hp1 | a0001 | c0005 | t0005 | g0004 | EUR | IBS | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG01515 | hp2 | a0001 | c0020 | t0001 | g0001 | EUR | IBS | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG01884 | hp1 | a0001 | c0001 | t0041 | g0122 | AFR | ACB | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG01884 | hp2 | a0001 | c0004 | t0004 | g0045 | AFR | ACB | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG01891 | hp1 | a0001 | c0017 | t0037 | g0081 | AFR | ACB | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG01891 | hp2 | a0001 | c0007 | t0003 | g0005 | AFR | ACB | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG01928 | hp1 | a0001 | c0003 | t0001 | g0154 | AMR | PEL | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG01928 | hp2 | a0001 | c0002 | t0006 | g0076 | AMR | PEL | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG01975 | hp2 | a0001 | c0003 | t0001 | g0153 | AMR | PEL | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG01978 | hp1 | a0001 | c0002 | t0006 | g0080 | AMR | PEL | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG01978 | hp2 | a0001 | c0013 | t0007 | g0060 | AMR | PEL | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG01981 | hp1 | a0001 | c0004 | t0011 | g0011 | AMR | PEL | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG01981 | hp2 | a0001 | c0003 | t0001 | g0006 | AMR | PEL | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PEL | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG02004 | hp2 | a0001 | c0002 | t0006 | g0079 | AMR | PEL | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | KHV | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG02027 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | KHV | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | KHV | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG02040 | hp2 | a0001 | c0005 | t0005 | g0169 | EAS | KHV | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG02055 | hp1 | a0001 | c0004 | t0004 | g0045 | AFR | ACB | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG02055 | hp2 | a0001 | c0012 | t0015 | g0024 | AFR | ACB | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG02071 | hp1 | a0001 | c0001 | t0042 | g0003 | EAS | KHV | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG02071 | hp2 | a0001 | c0003 | t0001 | g0130 | EAS | KHV | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | KHV | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG02074 | hp2 | a0001 | c0011 | t0004 | g0010 | EAS | KHV | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | KHV | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG02080 | hp2 | a0001 | c0004 | t0004 | g0010 | EAS | KHV | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG02129 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | KHV | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG02132 | hp1 | a0001 | c0016 | t0005 | g0180 | EAS | KHV | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | KHV | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG02135 | hp2 | a0001 | c0005 | t0005 | g0168 | EAS | KHV | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG02145 | hp1 | a0001 | c0005 | t0005 | g0004 | AFR | ACB | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG02145 | hp2 | a0001 | c0023 | t0003 | g0009 | AFR | ACB | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG02155 | hp1 | a0001 | c0004 | t0004 | g0010 | EAS | CDX | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG02155 | hp2 | a0001 | c0040 | t0009 | g0147 | EAS | CDX | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG02165 | hp2 | a0001 | c0002 | t0002 | g0075 | EAS | CDX | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG02257 | hp1 | a0001 | c0001 | t0039 | g0132 | AFR | ACB | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG02257 | hp2 | a0001 | c0012 | t0015 | g0024 | AFR | ACB | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG02258 | hp1 | a0005 | c0022 | t0003 | g0100 | AFR | ACB | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG02258 | hp2 | a0001 | c0008 | t0017 | g0064 | AFR | ACB | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG02280 | hp1 | a0001 | c0010 | t0009 | g0105 | AFR | ACB | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG02280 | hp2 | a0001 | c0006 | t0003 | g0009 | AFR | ACB | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG02300 | hp1 | a0001 | c0013 | t0007 | g0014 | AMR | PEL | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG02451 | hp1 | a0001 | c0006 | t0014 | g0019 | AFR | ACB | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG02451 | hp2 | a0001 | c0014 | t0026 | g0073 | AFR | ACB | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG02572 | hp1 | a0001 | c0041 | t0003 | g0087 | AFR | GWD | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG02572 | hp2 | a0001 | c0024 | t0036 | g0086 | AFR | GWD | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG02602 | hp1 | a0001 | c0003 | t0001 | g0039 | SAS | PJL | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0145 | SAS | PJL | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG02615 | hp2 | a0001 | c0010 | t0009 | g0033 | AFR | GWD | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG02622 | hp1 | a0001 | c0030 | t0001 | g0016 | AFR | GWD | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG02622 | hp2 | a0001 | c0006 | t0003 | g0096 | AFR | GWD | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG02630 | hp1 | a0001 | c0006 | t0003 | g0097 | AFR | GWD | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG02630 | hp2 | a0001 | c0001 | t0044 | g0101 | AFR | GWD | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG02647 | hp1 | a0001 | c0007 | t0003 | g0005 | AFR | GWD | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG02647 | hp2 | a0001 | c0006 | t0014 | g0098 | AFR | GWD | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG02698 | hp1 | a0001 | c0002 | t0012 | g0078 | SAS | PJL | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG02698 | hp2 | a0001 | c0005 | t0032 | g0172 | SAS | PJL | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG02717 | hp2 | a0001 | c0021 | t0015 | g0107 | AFR | GWD | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG02735 | hp2 | a0001 | c0027 | t0002 | g0057 | SAS | PJL | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG02809 | hp1 | a0001 | c0037 | t0045 | g0001 | AFR | GWD | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG02809 | hp2 | a0001 | c0006 | t0001 | g0020 | AFR | GWD | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG02886 | hp1 | a0001 | c0008 | t0023 | g0085 | AFR | GWD | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG02886 | hp2 | a0001 | c0006 | t0029 | g0009 | AFR | GWD | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG02895 | hp1 | a0001 | c0010 | t0009 | g0033 | AFR | GWD | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG02895 | hp2 | a0001 | c0006 | t0003 | g0032 | AFR | GWD | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG02896 | hp1 | a0001 | c0006 | t0003 | g0009 | AFR | GWD | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG02896 | hp2 | a0001 | c0003 | t0001 | g0016 | AFR | GWD | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG02897 | hp1 | a0001 | c0003 | t0001 | g0016 | AFR | GWD | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG02897 | hp2 | a0001 | c0006 | t0003 | g0032 | AFR | GWD | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG02965 | hp1 | a0001 | c0009 | t0012 | g0018 | AFR | ESN | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG02965 | hp2 | a0001 | c0003 | t0048 | g0160 | AFR | ESN | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | ESN | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG02970 | hp2 | a0001 | c0003 | t0001 | g0017 | AFR | ESN | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG02976 | hp1 | a0001 | c0006 | t0003 | g0009 | AFR | ESN | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG02976 | hp2 | a0001 | c0007 | t0003 | g0005 | AFR | ESN | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | GWD | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG03041 | hp2 | a0001 | c0006 | t0003 | g0095 | AFR | GWD | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG03098 | hp1 | a0001 | c0007 | t0003 | g0005 | AFR | MSL | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG03098 | hp2 | a0001 | c0006 | t0014 | g0019 | AFR | MSL | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG03139 | hp2 | a0001 | c0009 | t0012 | g0018 | AFR | ESN | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG03195 | hp1 | a0001 | c0009 | t0028 | g0093 | AFR | ESN | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG03195 | hp2 | a0001 | c0007 | t0003 | g0005 | AFR | ESN | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG03209 | hp1 | a0001 | c0015 | t0003 | g0094 | AFR | MSL | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG03209 | hp2 | a0001 | c0004 | t0019 | g0044 | AFR | MSL | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG03225 | hp1 | a0001 | c0006 | t0003 | g0099 | AFR | MSL | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG03225 | hp2 | a0001 | c0012 | t0015 | g0024 | AFR | MSL | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG03239 | hp1 | a0007 | c0025 | t0011 | g0011 | SAS | PJL | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG03453 | hp2 | a0001 | c0003 | t0001 | g0017 | AFR | MSL | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG03486 | hp1 | a0001 | c0017 | t0012 | g0074 | AFR | MSL | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG03486 | hp2 | a0001 | c0014 | t0002 | g0092 | AFR | MSL | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG03491 | hp1 | a0001 | c0002 | t0006 | g0031 | SAS | PJL | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG03492 | hp1 | a0001 | c0002 | t0006 | g0031 | SAS | PJL | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG03516 | hp1 | a0001 | c0003 | t0001 | g0023 | AFR | ESN | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG03516 | hp2 | a0001 | c0004 | t0004 | g0167 | AFR | ESN | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG03540 | hp1 | a0001 | c0008 | t0013 | g0053 | AFR | GWD | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG03540 | hp2 | a0001 | c0004 | t0019 | g0170 | AFR | GWD | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG03579 | hp1 | a0001 | c0007 | t0003 | g0005 | AFR | MSL | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG03579 | hp2 | a0001 | c0010 | t0009 | g0106 | AFR | MSL | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG03654 | hp1 | a0001 | c0032 | t0049 | g0001 | SAS | PJL | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG03654 | hp2 | a0001 | c0002 | t0006 | g0068 | SAS | PJL | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG03669 | hp1 | a0001 | c0002 | t0002 | g0083 | SAS | PJL | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0133 | SAS | PJL | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG03688 | hp1 | a0001 | c0004 | t0004 | g0178 | SAS | STU | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG03704 | hp1 | a0001 | c0003 | t0001 | g0143 | SAS | PJL | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG03704 | hp2 | a0001 | c0039 | t0001 | g0120 | SAS | PJL | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG03710 | hp1 | a0001 | c0002 | t0002 | g0002 | SAS | PJL | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG03942 | hp1 | a0001 | c0002 | t0004 | g0069 | SAS | BEB | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG03942 | hp2 | a0004 | c0042 | t0001 | g0150 | SAS | BEB | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG04115 | hp1 | a0001 | c0011 | t0004 | g0010 | SAS | STU | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG04115 | hp2 | a0001 | c0005 | t0025 | g0181 | SAS | STU | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG04184 | hp1 | a0001 | c0002 | t0002 | g0054 | SAS | BEB | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG04184 | hp2 | a0001 | c0001 | t0022 | g0139 | SAS | BEB | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG04199 | hp2 | a0001 | c0002 | t0002 | g0002 | SAS | STU | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG04204 | hp1 | a0001 | c0002 | t0002 | g0002 | SAS | STU | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG04204 | hp2 | a0001 | c0004 | t0004 | g0164 | SAS | STU | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG04228 | hp2 | a0001 | c0004 | t0004 | g0166 | SAS | STU | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA18522 | hp1 | a0001 | c0006 | t0003 | g0009 | AFR | YRI | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA18522 | hp2 | a0001 | c0007 | t0020 | g0091 | AFR | YRI | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA18612 | hp1 | a0001 | c0002 | t0035 | g0002 | EAS | CHB | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA18612 | hp2 | a0001 | c0005 | t0005 | g0165 | EAS | CHB | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA18747 | hp1 | a0001 | c0002 | t0002 | g0051 | EAS | CHB | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | CHB | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA18906 | hp1 | a0001 | c0014 | t0002 | g0018 | AFR | YRI | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA18906 | hp2 | a0001 | c0003 | t0001 | g0017 | AFR | YRI | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA18939 | hp1 | a0001 | c0004 | t0004 | g0043 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA18939 | hp2 | a0002 | c0019 | t0001 | g0115 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA18940 | hp1 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA18940 | hp2 | a0001 | c0002 | t0002 | g0055 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA18944 | hp1 | a0001 | c0002 | t0002 | g0084 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA18945 | hp2 | a0001 | c0002 | t0002 | g0013 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA18947 | hp2 | a0001 | c0005 | t0005 | g0026 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA18950 | hp1 | a0001 | c0001 | t0043 | g0008 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA18954 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA18956 | hp2 | a0001 | c0002 | t0002 | g0082 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA18960 | hp2 | a0001 | c0005 | t0005 | g0004 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA18962 | hp1 | a0009 | c0031 | t0001 | g0001 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA18962 | hp2 | a0001 | c0002 | t0021 | g0015 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA18964 | hp1 | a0001 | c0033 | t0009 | g0129 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA18964 | hp2 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA18967 | hp1 | a0001 | c0002 | t0002 | g0013 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA18969 | hp1 | a0001 | c0004 | t0004 | g0171 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA18970 | hp1 | a0001 | c0018 | t0002 | g0059 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA18970 | hp2 | a0001 | c0001 | t0016 | g0034 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA18971 | hp1 | a0001 | c0004 | t0004 | g0043 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA18971 | hp2 | a0001 | c0003 | t0001 | g0035 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA18974 | hp1 | a0008 | c0034 | t0001 | g0003 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA18974 | hp2 | a0001 | c0002 | t0002 | g0067 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA18977 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA18979 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA18979 | hp2 | a0001 | c0001 | t0010 | g0124 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA18980 | hp1 | a0001 | c0004 | t0006 | g0175 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA18980 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA18983 | hp1 | a0006 | c0035 | t0001 | g0003 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA18983 | hp2 | a0001 | c0003 | t0040 | g0007 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA18984 | hp1 | a0001 | c0001 | t0010 | g0128 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA18984 | hp2 | a0001 | c0002 | t0002 | g0013 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA18986 | hp1 | a0001 | c0002 | t0008 | g0015 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA18989 | hp1 | a0001 | c0001 | t0016 | g0117 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA18992 | hp2 | a0001 | c0004 | t0004 | g0010 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA18994 | hp1 | a0001 | c0002 | t0008 | g0002 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA18995 | hp1 | a0001 | c0001 | t0016 | g0036 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA18995 | hp2 | a0001 | c0005 | t0005 | g0182 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA18997 | hp2 | a0001 | c0002 | t0008 | g0015 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA18998 | hp1 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA18998 | hp2 | a0001 | c0005 | t0005 | g0179 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA18999 | hp1 | a0001 | c0002 | t0002 | g0013 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA18999 | hp2 | a0001 | c0005 | t0005 | g0026 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA19000 | hp1 | a0001 | c0002 | t0024 | g0002 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA19000 | hp2 | a0001 | c0001 | t0016 | g0036 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA19007 | hp1 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA19007 | hp2 | a0001 | c0002 | t0002 | g0071 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA19009 | hp1 | a0001 | c0005 | t0005 | g0025 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA19009 | hp2 | a0001 | c0003 | t0001 | g0035 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA19010 | hp2 | a0001 | c0005 | t0005 | g0025 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA19011 | hp1 | a0002 | c0019 | t0001 | g0008 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA19011 | hp2 | a0001 | c0005 | t0005 | g0004 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA19030 | hp1 | a0001 | c0009 | t0002 | g0065 | AFR | LWK | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA19030 | hp2 | a0001 | c0006 | t0001 | g0020 | AFR | LWK | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA19043 | hp1 | a0001 | c0003 | t0001 | g0016 | AFR | LWK | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | LWK | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA19055 | hp1 | a0001 | c0001 | t0047 | g0001 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA19057 | hp2 | a0000 | c0028 | t0034 | g0052 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA19060 | hp2 | a0001 | c0002 | t0021 | g0002 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA19063 | hp1 | a0001 | c0001 | t0010 | g0127 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA19063 | hp2 | a0001 | c0002 | t0002 | g0058 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA19064 | hp1 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA19064 | hp2 | a0001 | c0005 | t0005 | g0046 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA19066 | hp2 | a0001 | c0002 | t0002 | g0028 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA19067 | hp2 | a0001 | c0005 | t0005 | g0025 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA19068 | hp2 | a0001 | c0005 | t0005 | g0176 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA19070 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA19074 | hp1 | a0001 | c0001 | t0010 | g0125 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA19074 | hp2 | a0001 | c0002 | t0002 | g0028 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA19077 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA19077 | hp2 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA19079 | hp2 | a0001 | c0002 | t0008 | g0002 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA19080 | hp2 | a0001 | c0018 | t0002 | g0002 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA19082 | hp1 | a0001 | c0002 | t0002 | g0056 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA19082 | hp2 | a0001 | c0001 | t0046 | g0119 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA19084 | hp2 | a0001 | c0005 | t0005 | g0004 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA19085 | hp1 | a0001 | c0003 | t0001 | g0007 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA19085 | hp2 | a0001 | c0002 | t0002 | g0047 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA19087 | hp1 | a0001 | c0029 | t0008 | g0002 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA19087 | hp2 | a0001 | c0001 | t0010 | g0126 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA19088 | hp1 | a0001 | c0005 | t0030 | g0004 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA19088 | hp2 | a0001 | c0001 | t0010 | g0185 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA19089 | hp1 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA19089 | hp2 | a0001 | c0004 | t0004 | g0183 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA19090 | hp2 | a0001 | c0002 | t0008 | g0015 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA19091 | hp1 | a0001 | c0001 | t0022 | g0048 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA19091 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA19240 | hp1 | a0003 | c0043 | t0033 | g0050 | AFR | YRI | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | YRI | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA20129 | hp1 | a0001 | c0026 | t0004 | g0042 | AFR | ASW | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA20129 | hp2 | a0001 | c0007 | t0003 | g0005 | AFR | ASW | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA20752 | hp1 | a0001 | c0004 | t0011 | g0011 | EUR | TSI | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0022 | EUR | TSI | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | GIH | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA20905 | hp2 | a0001 | c0016 | t0031 | g0004 | SAS | GIH | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG02109 | hp1 | a0001 | c0038 | t0038 | g0158 | AFR | ACB | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG02109 | hp2 | a0001 | c0008 | t0013 | g0063 | AFR | ACB | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG02559 | hp1 | a0001 | c0004 | t0004 | g0044 | AFR | ACB | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG02559 | hp2 | a0001 | c0009 | t0027 | g0066 | AFR | ACB | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG03471 | hp1 | a0001 | c0007 | t0020 | g0088 | AFR | MSL | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | MSL | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG06807 | hp1 | a0001 | c0007 | t0003 | g0089 | AFR | USA | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| HG06807 | hp2 | a0001 | c0006 | t0014 | g0019 | AFR | USA | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA20300 | hp1 | a0001 | c0003 | t0001 | g0152 | AFR | USA | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA20300 | hp2 | a0001 | c0008 | t0017 | g0049 | AFR | USA | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA21309 | hp1 | a0001 | c0004 | t0011 | g0011 | AFR | LWK | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | LWK | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0003 | t0001 | g0146 | REF | REF | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| homoSapiens_grch38 | hp1 | a0001 | c0003 | t0001 | g0184 | REF | REF | PLXNA1_chr3_126978115_127042389 | PLXNA1 | chr3 | 126978115 | 127042389 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:126988607
|
C | T | 1 | a0003 | 1 | NA19240.hp1 | missense_variant | MODERATE | c.14C>T | p.Pro5Leu | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 2/32 | 260/9309 | 14/5691 | 5/1896 | chr3 | 126988607 | ||
| chr3:126988711
|
C | G | 1 | a0004 | 1 | HG03942.hp2 | missense_variant | MODERATE | c.118C>G | p.Pro40Ala | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 2/32 | 364/9309 | 118/5691 | 40/1896 | chr3 | 126988711 | ||
| chr3:127006088
|
G | A | 1 | a0005 | 1 | HG02258.hp1 | missense_variant | MODERATE | c.1907G>A | p.Arg636Gln | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 8/32 | 2153/9309 | 1907/5691 | 636/1896 | chr3 | 127006088 | ||
| chr3:127014238
|
G | C | 1 | a0009 | 1 | NA18962.hp1 | missense_variant | MODERATE | c.2467G>C | p.Asp823His | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 12/32 | 2713/9309 | 2467/5691 | 823/1896 | chr3 | 127014238 | ||
| chr3:127014242
|
C | T | 1 | a0006 | 1 | NA18983.hp1 | missense_variant | MODERATE | c.2471C>T | p.Pro824Leu | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 12/32 | 2717/9309 | 2471/5691 | 824/1896 | chr3 | 127014242 | ||
| chr3:127015301
|
C | T | 1 | a0008 | 1 | NA18974.hp1 | missense_variant | MODERATE | c.2995C>T | p.Arg999Trp | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 15/32 | 3241/9309 | 2995/5691 | 999/1896 | chr3 | 127015301 | ||
| chr3:127017485
|
G | C | 1 | a0002 | 2 | NA18939.hp2 NA19011.hp1 |
missense_variant | MODERATE | c.3337G>C | p.Val1113Leu | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 18/32 | 3583/9309 | 3337/5691 | 1113/1896 | chr3 | 127017485 | ||
| chr3:127017763
|
G | C | 1 | a0007 | 1 | HG03239.hp1 | missense_variant | MODERATE | c.3531G>C | p.Leu1177Phe | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 19/32 | 3777/9309 | 3531/5691 | 1177/1896 | chr3 | 127017763 | ||
| chr3:127033974
|
GCAAGCTG others(4): Show |
G | 1 | a0000 | 1 | NA19057.hp2 | frameshift_variant | HIGH | c.5649_5659delCAAGCT others(5): Show |
p.Ser1883fs | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 32/32 | 5895/9309 | 5649/5691 | 1883/1896 | chr3 | 127033974 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:126988962
|
C | T | 1 | a0001c0041 | 1 | HG02572.hp1 | synonymous_variant | LOW | c.369C>T | p.Ala123Ala | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 2/32 | 615/9309 | 369/5691 | 123/1896 | chr3 | 126988962 | ||
| chr3:126989499
|
C | T | 1 | a0001c0040 | 1 | HG02155.hp2 | synonymous_variant | LOW | c.906C>T | p.Cys302Cys | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 2/32 | 1152/9309 | 906/5691 | 302/1896 | chr3 | 126989499 | ||
| chr3:126989532
|
G | A | 3 | a0001c0010a0001c0012a0001c0021 | 8 | HG02055.hp2 HG02257.hp2 HG02280.hp1 others(5): Show |
synonymous_variant | LOW | c.939G>A | p.Gln313Gln | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 2/32 | 1185/9309 | 939/5691 | 313/1896 | chr3 | 126989532 | ||
| chr3:126989610
|
T | C | 27 | a0000c0028a0001c0002a0001c0004others(24): Show | 183 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(180): Show |
synonymous_variant | LOW | c.1017T>C | p.Thr339Thr | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 2/32 | 1263/9309 | 1017/5691 | 339/1896 | chr3 | 126989610 | ||
| chr3:126989616
|
C | T | 5 | a0000c0028a0001c0002a0001c0018others(2): Show | 58 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(55): Show |
synonymous_variant | LOW | c.1023C>T | p.Phe341Phe | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 2/32 | 1269/9309 | 1023/5691 | 341/1896 | chr3 | 126989616 | ||
| chr3:126991494
|
C | T | 1 | a0001c0039 | 1 | HG03704.hp2 | synonymous_variant | LOW | c.1305C>T | p.Thr435Thr | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/32 | 1551/9309 | 1305/5691 | 435/1896 | chr3 | 126991494 | ||
| chr3:127003461
|
C | T | 8 | a0000c0028a0001c0002a0001c0009others(5): Show | 68 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(65): Show |
synonymous_variant | LOW | c.1509C>T | p.Thr503Thr | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 4/32 | 1755/9309 | 1509/5691 | 503/1896 | chr3 | 127003461 | ||
| chr3:127004706
|
C | T | 6 | a0001c0004a0001c0005a0001c0011others(3): Show | 55 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(52): Show |
synonymous_variant | LOW | c.1614C>T | p.His538His | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 5/32 | 1860/9309 | 1614/5691 | 538/1896 | chr3 | 127004706 | ||
| chr3:127006170
|
C | T | 1 | a0001c0017 | 2 | HG01891.hp1 HG03486.hp1 |
synonymous_variant | LOW | c.1989C>T | p.Val663Val | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 8/32 | 2235/9309 | 1989/5691 | 663/1896 | chr3 | 127006170 | ||
| chr3:127007862
|
A | G | 8 | a0001c0004a0001c0005a0001c0011others(5): Show | 57 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(54): Show |
synonymous_variant | LOW | c.2061A>G | p.Thr687Thr | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 9/32 | 2307/9309 | 2061/5691 | 687/1896 | chr3 | 127007862 | ||
| chr3:127012017
|
C | T | 1 | a0001c0037 | 1 | HG02809.hp1 | synonymous_variant | LOW | c.2172C>T | p.Pro724Pro | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 10/32 | 2418/9309 | 2172/5691 | 724/1896 | chr3 | 127012017 | ||
| chr3:127012023
|
C | A | 1 | a0001c0030 | 1 | HG02622.hp1 | synonymous_variant | LOW | c.2178C>A | p.Thr726Thr | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 10/32 | 2424/9309 | 2178/5691 | 726/1896 | chr3 | 127012023 | ||
| chr3:127014210
|
C | T | 3 | a0001c0008a0001c0013a0003c0043 | 16 | HG00140.hp2 HG01069.hp1 HG01070.hp1 others(13): Show |
synonymous_variant | LOW | c.2439C>T | p.Arg813Arg | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 12/32 | 2685/9309 | 2439/5691 | 813/1896 | chr3 | 127014210 | ||
| chr3:127014231
|
C | T | 1 | a0001c0036 | 1 | HG00609.hp2 | synonymous_variant | LOW | c.2460C>T | p.Leu820Leu | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 12/32 | 2706/9309 | 2460/5691 | 820/1896 | chr3 | 127014231 | ||
| chr3:127014237
|
C | T | 1 | a0001c0029 | 1 | NA19087.hp1 | synonymous_variant | LOW | c.2466C>T | p.Ala822Ala | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 12/32 | 2712/9309 | 2466/5691 | 822/1896 | chr3 | 127014237 | ||
| chr3:127014333
|
G | A | 2 | a0001c0012a0001c0021 | 4 | HG02055.hp2 HG02257.hp2 HG02717.hp2 others(1): Show |
synonymous_variant | LOW | c.2562G>A | p.Ala854Ala | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 12/32 | 2808/9309 | 2562/5691 | 854/1896 | chr3 | 127014333 | ||
| chr3:127014486
|
C | T | 2 | a0001c0007a0001c0041 | 13 | HG00639.hp1 HG01109.hp1 HG01891.hp2 others(10): Show |
synonymous_variant | LOW | c.2613C>T | p.Pro871Pro | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 13/32 | 2859/9309 | 2613/5691 | 871/1896 | chr3 | 127014486 | ||
| chr3:127014756
|
C | T | 1 | a0001c0021 | 1 | HG02717.hp2 | synonymous_variant | LOW | c.2802C>T | p.Asp934Asp | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 14/32 | 3048/9309 | 2802/5691 | 934/1896 | chr3 | 127014756 | ||
| chr3:127015312
|
C | T | 1 | a0001c0024 | 1 | HG02572.hp2 | synonymous_variant | LOW | c.3006C>T | p.Ser1002Ser | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 15/32 | 3252/9309 | 3006/5691 | 1002/1896 | chr3 | 127015312 | ||
| chr3:127016610
|
C | T | 7 | a0001c0004a0001c0005a0001c0011others(4): Show | 56 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(53): Show |
synonymous_variant | LOW | c.3108C>T | p.Thr1036Thr | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 16/32 | 3354/9309 | 3108/5691 | 1036/1896 | chr3 | 127016610 | ||
| chr3:127018299
|
G | A | 1 | a0001c0032 | 1 | HG03654.hp1 | synonymous_variant | LOW | c.3666G>A | p.Arg1222Arg | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 20/32 | 3912/9309 | 3666/5691 | 1222/1896 | chr3 | 127018299 | ||
| chr3:127018320
|
G | T | 1 | a0001c0023 | 1 | HG02145.hp2 | synonymous_variant | LOW | c.3687G>T | p.Ser1229Ser | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 20/32 | 3933/9309 | 3687/5691 | 1229/1896 | chr3 | 127018320 | ||
| chr3:127018425
|
C | A | 15 | a0001c0001a0001c0005a0001c0009others(12): Show | 168 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(165): Show |
synonymous_variant | LOW | c.3792C>A | p.Leu1264Leu | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 20/32 | 4038/9309 | 3792/5691 | 1264/1896 | chr3 | 127018425 | ||
| chr3:127022168
|
G | A | 5 | a0001c0005a0001c0010a0001c0016others(2): Show | 31 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(28): Show |
synonymous_variant | LOW | c.4122G>A | p.Thr1374Thr | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 22/32 | 4368/9309 | 4122/5691 | 1374/1896 | chr3 | 127022168 | ||
| chr3:127022198
|
C | T | 1 | a0001c0020 | 2 | HG00735.hp1 HG01515.hp2 |
synonymous_variant | LOW | c.4152C>T | p.Arg1384Arg | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 22/32 | 4398/9309 | 4152/5691 | 1384/1896 | chr3 | 127022198 | ||
| chr3:127029448
|
C | T | 2 | a0001c0007a0001c0041 | 13 | HG00639.hp1 HG01109.hp1 HG01891.hp2 others(10): Show |
synonymous_variant | LOW | c.4782C>T | p.Asp1594Asp | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 27/32 | 5028/9309 | 4782/5691 | 1594/1896 | chr3 | 127029448 | ||
| chr3:127032570
|
C | T | 1 | a0001c0026 | 1 | NA20129.hp1 | synonymous_variant | LOW | c.5415C>T | p.Asp1805Asp | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 30/32 | 5661/9309 | 5415/5691 | 1805/1896 | chr3 | 127032570 | ||
| chr3:127032740
|
G | A | 1 | a0001c0027 | 1 | HG02735.hp2 | synonymous_variant | LOW | c.5499G>A | p.Ala1833Ala | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 31/32 | 5745/9309 | 5499/5691 | 1833/1896 | chr3 | 127032740 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:126988533
|
T | C | 51 | a0000c0028t0034a0001c0002t0002a0001c0002t0004others(48): Show | 172 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(169): Show |
5_prime_UTR_variant | MODIFIER | c.-61T>C | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 2/32 | 61 | chr3 | 126988533 | |||||
| chr3:127034066
|
A | T | 3 | a0001c0002t0008a0001c0002t0021a0001c0029t0008 | 8 | NA18962.hp2 NA18986.hp1 NA18994.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*49A>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 32/32 | 49 | chr3 | 127034066 | |||||
| chr3:127034116
|
C | T | 1 | a0001c0017t0037 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*99C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 32/32 | 99 | chr3 | 127034116 | |||||
| chr3:127034126
|
C | A | 6 | a0001c0008t0007a0001c0008t0013a0001c0008t0017others(3): Show | 15 | HG00140.hp2 HG01069.hp1 HG01070.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*109C>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 32/32 | 109 | chr3 | 127034126 | |||||
| chr3:127034134
|
C | T | 1 | a0001c0007t0020 | 2 | HG03471.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*117C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 32/32 | 117 | chr3 | 127034134 | |||||
| chr3:127034502
|
G | A | 1 | a0001c0038t0038 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*485G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 32/32 | 485 | chr3 | 127034502 | |||||
| chr3:127034527
|
C | T | 1 | a0001c0024t0036 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*510C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 32/32 | 510 | chr3 | 127034527 | |||||
| chr3:127034564
|
C | T | 1 | a0001c0032t0049 | 1 | HG03654.hp1 | 3_prime_UTR_variant | MODIFIER | c.*547C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 32/32 | 547 | chr3 | 127034564 | |||||
| chr3:127034639
|
C | T | 1 | a0001c0002t0035 | 1 | NA18612.hp1 | 3_prime_UTR_variant | MODIFIER | c.*622C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 32/32 | 622 | chr3 | 127034639 | |||||
| chr3:127034665
|
G | GC | 3 | a0001c0008t0007a0001c0008t0018a0001c0013t0007 | 8 | HG00140.hp2 HG01069.hp1 HG01070.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*652dupC | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 32/32 | 653 | INFO_REALIGN_3_PRIME | chr3 | 127034665 | ||||
| chr3:127034723
|
C | T | 6 | a0001c0008t0007a0001c0008t0013a0001c0008t0017others(3): Show | 15 | HG00140.hp2 HG01069.hp1 HG01070.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*706C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 32/32 | 706 | chr3 | 127034723 | |||||
| chr3:127034794
|
C | T | 1 | a0001c0003t0048 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*777C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 32/32 | 777 | chr3 | 127034794 | |||||
| chr3:127034803
|
C | T | 1 | a0001c0003t0048 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*786C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 32/32 | 786 | chr3 | 127034803 | |||||
| chr3:127034810
|
G | A | 9 | a0001c0001t0039a0001c0002t0004a0001c0004t0004others(6): Show | 32 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*793G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 32/32 | 793 | chr3 | 127034810 | |||||
| chr3:127035003
|
T | G | 1 | a0001c0002t0024 | 1 | NA19000.hp1 | 3_prime_UTR_variant | MODIFIER | c.*986T>G | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 32/32 | 986 | chr3 | 127035003 | |||||
| chr3:127035054
|
T | G | 1 | a0001c0003t0040 | 1 | NA18983.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1037T>G | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 32/32 | 1037 | chr3 | 127035054 | |||||
| chr3:127035095
|
T | G | 1 | a0001c0006t0014 | 4 | HG02451.hp1 HG02647.hp2 HG03098.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1078T>G | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 32/32 | 1078 | chr3 | 127035095 | |||||
| chr3:127035096
|
C | G | 1 | a0001c0006t0014 | 4 | HG02451.hp1 HG02647.hp2 HG03098.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1079C>G | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 32/32 | 1079 | chr3 | 127035096 | |||||
| chr3:127035432
|
C | T | 1 | a0001c0001t0047 | 1 | NA19055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1415C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 32/32 | 1415 | chr3 | 127035432 | |||||
| chr3:127035504
|
G | A | 1 | a0001c0005t0025 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1487G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 32/32 | 1487 | chr3 | 127035504 | |||||
| chr3:127035592
|
A | C | 1 | a0000c0028t0034 | 1 | NA19057.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1575A>C | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 32/32 | 1575 | chr3 | 127035592 | |||||
| chr3:127035696
|
C | T | 1 | a0001c0024t0036 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1679C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 32/32 | 1679 | chr3 | 127035696 | |||||
| chr3:127035761
|
C | G | 1 | a0001c0001t0046 | 1 | NA19082.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1744C>G | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 32/32 | 1744 | chr3 | 127035761 | |||||
| chr3:127035801
|
G | C | 56 | a0000c0028t0034a0001c0001t0039a0001c0002t0002others(53): Show | 176 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(173): Show |
3_prime_UTR_variant | MODIFIER | c.*1784G>C | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 32/32 | 1784 | chr3 | 127035801 | |||||
| chr3:127035810
|
C | T | 2 | a0001c0004t0011a0007c0025t0011 | 5 | HG01496.hp1 HG01981.hp1 HG03239.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1793C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 32/32 | 1793 | chr3 | 127035810 | |||||
| chr3:127035852
|
C | T | 1 | a0001c0037t0045 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1835C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 32/32 | 1835 | chr3 | 127035852 | |||||
| chr3:127035868
|
G | A | 18 | a0000c0028t0034a0001c0002t0002a0001c0002t0008others(15): Show | 60 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*1851G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 32/32 | 1851 | chr3 | 127035868 | |||||
| chr3:127035903
|
C | T | 5 | a0001c0008t0007a0001c0008t0013a0001c0008t0018others(2): Show | 13 | HG00140.hp2 HG01069.hp1 HG01070.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1886C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 32/32 | 1886 | chr3 | 127035903 | |||||
| chr3:127035970
|
C | T | 9 | a0001c0005t0005a0001c0005t0025a0001c0005t0030others(6): Show | 31 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*1953C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 32/32 | 1953 | chr3 | 127035970 | |||||
| chr3:127035971
|
T | G | 1 | a0001c0024t0036 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1954T>G | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 32/32 | 1954 | chr3 | 127035971 | |||||
| chr3:127036275
|
C | G | 1 | a0001c0009t0028 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2258C>G | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 32/32 | 2258 | chr3 | 127036275 | |||||
| chr3:127036291
|
C | T | 26 | a0000c0028t0034a0001c0001t0022a0001c0002t0002others(23): Show | 92 | HG00099.hp1 HG00323.hp2 HG00544.hp1 others(89): Show |
3_prime_UTR_variant | MODIFIER | c.*2274C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 32/32 | 2274 | chr3 | 127036291 | |||||
| chr3:127036350
|
G | C | 1 | a0001c0001t0016 | 4 | NA18970.hp2 NA18989.hp1 NA18995.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2333G>C | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 32/32 | 2333 | chr3 | 127036350 | |||||
| chr3:127036352
|
T | C | 2 | a0001c0001t0041a0001c0014t0026 | 2 | HG01884.hp1 HG02451.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2335T>C | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 32/32 | 2335 | chr3 | 127036352 | |||||
| chr3:127036508
|
G | A | 1 | a0001c0009t0027 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2491G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 32/32 | 2491 | chr3 | 127036508 | |||||
| chr3:127036542
|
C | T | 1 | a0001c0001t0041 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2525C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 32/32 | 2525 | chr3 | 127036542 | |||||
| chr3:127036571
|
T | C | 2 | a0001c0004t0011a0007c0025t0011 | 5 | HG01496.hp1 HG01981.hp1 HG03239.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2554T>C | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 32/32 | 2554 | chr3 | 127036571 | |||||
| chr3:127036617
|
G | A | 1 | a0001c0001t0042 | 1 | HG02071.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2600G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 32/32 | 2600 | chr3 | 127036617 | |||||
| chr3:127036650
|
C | G | 2 | a0001c0001t0010a0001c0001t0046 | 7 | NA18979.hp2 NA18984.hp1 NA19063.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2633C>G | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 32/32 | 2633 | chr3 | 127036650 | |||||
| chr3:127036690
|
G | A | 1 | a0001c0001t0043 | 1 | NA18950.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2673G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 32/32 | 2673 | chr3 | 127036690 | |||||
| chr3:127036706
|
C | T | 1 | a0001c0009t0028 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2689C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 32/32 | 2689 | chr3 | 127036706 | |||||
| chr3:127036713
|
C | T | 5 | a0001c0008t0007a0001c0008t0013a0001c0008t0017others(2): Show | 13 | HG00140.hp2 HG01069.hp1 HG01070.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2696C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 32/32 | 2696 | chr3 | 127036713 | |||||
| chr3:127036760
|
T | C | 1 | a0001c0016t0031 | 1 | NA20905.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2743T>C | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 32/32 | 2743 | chr3 | 127036760 | |||||
| chr3:127036888
|
C | T | 1 | a0003c0043t0033 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2871C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 32/32 | 2871 | chr3 | 127036888 | |||||
| chr3:127037036
|
G | A | 1 | a0001c0024t0036 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3019G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 32/32 | 3019 | chr3 | 127037036 | |||||
| chr3:127037090
|
G | A | 1 | a0001c0005t0032 | 1 | HG02698.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3073G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 32/32 | 3073 | chr3 | 127037090 | |||||
| chr3:127037208
|
G | A | 1 | a0001c0001t0044 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3191G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 32/32 | 3191 | chr3 | 127037208 | |||||
| chr3:127037272
|
T | C | 1 | a0001c0024t0036 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3255T>C | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 32/32 | 3255 | chr3 | 127037272 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:126983299
|
C | T | 1 | a0001c0001t0001g0012 | 5 | HG00735.hp2 HG01074.hp1 HG01109.hp2 others(2): Show |
intron_variant | MODIFIER | c.-74+12C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 1/31 | chr3 | 126983299 | ||||||
| chr3:126983345
|
G | T | 2 | a0001c0004t0011g0011a0007c0025t0011g0011 | 5 | HG01496.hp1 HG01981.hp1 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.-74+58G>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 1/31 | chr3 | 126983345 | ||||||
| chr3:126983347
|
T | C | 2 | a0001c0005t0005g0026a0001c0005t0005g0046 | 3 | NA18947.hp2 NA18999.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.-74+60T>C | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 1/31 | chr3 | 126983347 | ||||||
| chr3:126983546
|
C | T | 1 | a0001c0001t0010g0185 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-74+259C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 1/31 | chr3 | 126983546 | ||||||
| chr3:126983550
|
G | C | 1 | a0001c0002t0002g0047 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.-74+263G>C | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 1/31 | chr3 | 126983550 | ||||||
| chr3:126983643
|
C | T | 2 | a0001c0004t0011g0011a0007c0025t0011g0011 | 5 | HG01496.hp1 HG01981.hp1 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.-74+356C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 1/31 | chr3 | 126983643 | ||||||
| chr3:126983665
|
G | C | 2 | a0001c0005t0005g0026a0001c0005t0005g0046 | 3 | NA18947.hp2 NA18999.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.-74+378G>C | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 1/31 | chr3 | 126983665 | ||||||
| chr3:126983746
|
T | G | 217 | a0000c0028t0034g0052a0001c0001t0001g0001a0001c0001t0001g0003others(214): Show | 345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.-74+459T>G | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 1/31 | chr3 | 126983746 | ||||||
| chr3:126983807
|
C | T | 34 | a0001c0004t0004g0010a0001c0004t0004g0043a0001c0004t0004g0044others(31): Show | 50 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(47): Show |
intron_variant | MODIFIER | c.-74+520C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 1/31 | chr3 | 126983807 | ||||||
| chr3:126983915
|
C | G | 1 | a0001c0001t0001g0163 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-74+628C>G | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 1/31 | chr3 | 126983915 | ||||||
| chr3:126984022
|
G | A | 1 | a0001c0004t0004g0164 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-74+735G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 1/31 | chr3 | 126984022 | ||||||
| chr3:126984115
|
C | T | 2 | a0001c0004t0011g0011a0007c0025t0011g0011 | 5 | HG01496.hp1 HG01981.hp1 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.-74+828C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 1/31 | chr3 | 126984115 | ||||||
| chr3:126984116
|
C | T | 1 | a0001c0003t0001g0162 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-74+829C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 1/31 | chr3 | 126984116 | ||||||
| chr3:126984174
|
C | T | 2 | a0001c0004t0011g0011a0007c0025t0011g0011 | 5 | HG01496.hp1 HG01981.hp1 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.-74+887C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 1/31 | chr3 | 126984174 | ||||||
| chr3:126984208
|
G | A | 1 | a0001c0001t0001g0027 | 2 | HG01255.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.-74+921G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 1/31 | chr3 | 126984208 | ||||||
| chr3:126984326
|
C | T | 2 | a0001c0001t0001g0041a0001c0001t0001g0161 | 3 | NA18960.hp1 NA18994.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.-74+1039C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 1/31 | chr3 | 126984326 | ||||||
| chr3:126984391
|
G | A | 2 | a0001c0004t0011g0011a0007c0025t0011g0011 | 5 | HG01496.hp1 HG01981.hp1 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.-74+1104G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 1/31 | chr3 | 126984391 | ||||||
| chr3:126984411
|
T | G | 1 | a0001c0001t0022g0048 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-74+1124T>G | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 1/31 | chr3 | 126984411 | ||||||
| chr3:126984631
|
A | G | 36 | a0001c0004t0004g0010a0001c0004t0004g0043a0001c0004t0004g0044others(33): Show | 55 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(52): Show |
intron_variant | MODIFIER | c.-74+1344A>G | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 1/31 | chr3 | 126984631 | ||||||
| chr3:126984658
|
C | CAG | 113 | a0000c0028t0034g0052a0001c0002t0002g0002a0001c0002t0002g0013others(110): Show | 172 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.-74+1374_-74+1375d others(4): Show |
PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr3 | 126984658 | |||||
| chr3:126984732
|
C | T | 12 | a0001c0006t0003g0009a0001c0006t0003g0032a0001c0006t0003g0095others(9): Show | 18 | HG02145.hp2 HG02258.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.-74+1445C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 1/31 | chr3 | 126984732 | ||||||
| chr3:126984911
|
T | C | 1 | a0001c0001t0044g0101 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-74+1624T>C | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 1/31 | chr3 | 126984911 | ||||||
| chr3:126984938
|
A | G | 34 | a0001c0004t0004g0010a0001c0004t0004g0043a0001c0004t0004g0044others(31): Show | 50 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(47): Show |
intron_variant | MODIFIER | c.-74+1651A>G | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 1/31 | chr3 | 126984938 | ||||||
| chr3:126985069
|
A | G | 1 | a0001c0012t0015g0024 | 3 | HG02055.hp2 HG02257.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-74+1782A>G | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 1/31 | chr3 | 126985069 | ||||||
| chr3:126985116
|
G | C | 1 | a0001c0001t0001g0102 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-74+1829G>C | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 1/31 | chr3 | 126985116 | ||||||
| chr3:126985198
|
C | A | 1 | a0001c0001t0001g0103 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-74+1911C>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 1/31 | chr3 | 126985198 | ||||||
| chr3:126985242
|
C | T | 2 | a0001c0009t0028g0093a0001c0014t0002g0092 | 2 | HG03195.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-74+1955C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 1/31 | chr3 | 126985242 | ||||||
| chr3:126985265
|
G | A | 1 | a0001c0001t0001g0104 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-74+1978G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 1/31 | chr3 | 126985265 | ||||||
| chr3:126985293
|
C | T | 1 | a0001c0003t0048g0160 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-74+2006C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 1/31 | chr3 | 126985293 | ||||||
| chr3:126985415
|
T | C | 1 | a0001c0008t0017g0049 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-74+2128T>C | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 1/31 | chr3 | 126985415 | ||||||
| chr3:126985440
|
C | G | 1 | a0001c0001t0001g0159 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-74+2153C>G | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 1/31 | chr3 | 126985440 | ||||||
| chr3:126985489
|
G | A | 119 | a0000c0028t0034g0052a0001c0002t0002g0002a0001c0002t0002g0013others(116): Show | 183 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.-74+2202G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 1/31 | chr3 | 126985489 | ||||||
| chr3:126985492
|
C | G | 1 | a0001c0004t0004g0045 | 2 | HG01884.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.-74+2205C>G | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 1/31 | chr3 | 126985492 | ||||||
| chr3:126985855
|
C | T | 2 | a0001c0004t0011g0011a0007c0025t0011g0011 | 5 | HG01496.hp1 HG01981.hp1 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.-74+2568C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 1/31 | chr3 | 126985855 | ||||||
| chr3:126985941
|
C | G | 7 | a0001c0007t0003g0005a0001c0007t0003g0089a0001c0007t0003g0090others(4): Show | 14 | HG00639.hp1 HG01109.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.-73-2580C>G | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 1/31 | chr3 | 126985941 | ||||||
| chr3:126985958
|
TCCCTTC | T | 43 | a0001c0004t0004g0010a0001c0004t0004g0043a0001c0004t0004g0044others(40): Show | 69 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(66): Show |
intron_variant | MODIFIER | c.-73-2560_-73-2555d others(8): Show |
PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr3 | 126985958 | |||||
| chr3:126986021
|
A | G | 217 | a0000c0028t0034g0052a0001c0001t0001g0001a0001c0001t0001g0003others(214): Show | 345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.-73-2500A>G | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 1/31 | chr3 | 126986021 | ||||||
| chr3:126986106
|
C | T | 1 | a0001c0003t0048g0160 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-73-2415C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 1/31 | chr3 | 126986106 | ||||||
| chr3:126986128
|
G | A | 2 | a0001c0001t0001g0034a0001c0001t0016g0034 | 2 | NA18970.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.-73-2393G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 1/31 | chr3 | 126986128 | ||||||
| chr3:126986231
|
G | A | 2 | a0001c0001t0001g0108a0001c0001t0001g0109 | 2 | HG02040.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.-73-2290G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 1/31 | chr3 | 126986231 | ||||||
| chr3:126986426
|
T | A | 1 | a0001c0003t0048g0160 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-73-2095T>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 1/31 | chr3 | 126986426 | ||||||
| chr3:126986427
|
C | T | 1 | a0001c0003t0048g0160 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-73-2094C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 1/31 | chr3 | 126986427 | ||||||
| chr3:126986498
|
G | A | 1 | a0001c0004t0004g0045 | 2 | HG01884.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.-73-2023G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 1/31 | chr3 | 126986498 | ||||||
| chr3:126986566
|
C | T | 2 | a0001c0012t0015g0024a0001c0021t0015g0107 | 4 | HG02055.hp2 HG02257.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.-73-1955C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 1/31 | chr3 | 126986566 | ||||||
| chr3:126986590
|
G | A | 1 | a0003c0043t0033g0050 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-73-1931G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 1/31 | chr3 | 126986590 | ||||||
| chr3:126986678
|
G | C | 6 | a0001c0001t0001g0041a0001c0001t0001g0110a0001c0001t0001g0111others(3): Show | 8 | HG02015.hp1 NA18960.hp1 NA18971.hp2 others(5): Show |
intron_variant | MODIFIER | c.-73-1843G>C | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 1/31 | chr3 | 126986678 | ||||||
| chr3:126986920
|
C | A | 96 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(93): Show | 160 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.-73-1601C>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 1/31 | chr3 | 126986920 | ||||||
| chr3:126986974
|
T | C | 1 | a0001c0008t0017g0049 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-73-1547T>C | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 1/31 | chr3 | 126986974 | ||||||
| chr3:126987354
|
G | A | 1 | a0001c0002t0002g0051 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-73-1167G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 1/31 | chr3 | 126987354 | ||||||
| chr3:126987538
|
C | G | 1 | a0001c0001t0001g0157 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-73-983C>G | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 1/31 | chr3 | 126987538 | ||||||
| chr3:126987547
|
G | A | 1 | a0000c0028t0034g0052 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-73-974G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 1/31 | chr3 | 126987547 | ||||||
| chr3:126987666
|
C | T | 1 | a0001c0004t0004g0183 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-73-855C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 1/31 | chr3 | 126987666 | ||||||
| chr3:126987682
|
G | A | 2 | a0001c0004t0011g0011a0007c0025t0011g0011 | 5 | HG01496.hp1 HG01981.hp1 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.-73-839G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 1/31 | chr3 | 126987682 | ||||||
| chr3:126987708
|
T | C | 217 | a0000c0028t0034g0052a0001c0001t0001g0001a0001c0001t0001g0003others(214): Show | 345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.-73-813T>C | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 1/31 | chr3 | 126987708 | ||||||
| chr3:126987932
|
G | A | 1 | a0001c0008t0013g0053 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-73-589G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 1/31 | chr3 | 126987932 | ||||||
| chr3:126987944
|
C | T | 6 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0003t0001g0006others(3): Show | 13 | HG00597.hp1 HG01346.hp2 HG01928.hp1 others(10): Show |
intron_variant | MODIFIER | c.-73-577C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 1/31 | chr3 | 126987944 | ||||||
| chr3:126987957
|
C | G | 119 | a0000c0028t0034g0052a0001c0002t0002g0002a0001c0002t0002g0013others(116): Show | 183 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.-73-564C>G | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 1/31 | chr3 | 126987957 | ||||||
| chr3:126988072
|
C | T | 7 | a0001c0007t0003g0005a0001c0007t0003g0089a0001c0007t0003g0090others(4): Show | 14 | HG00639.hp1 HG01109.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.-73-449C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 1/31 | chr3 | 126988072 | ||||||
| chr3:126988179
|
G | C | 1 | a0001c0001t0001g0113 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-73-342G>C | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 1/31 | chr3 | 126988179 | ||||||
| chr3:126989804
|
C | T | 7 | a0001c0007t0003g0005a0001c0007t0003g0089a0001c0007t0003g0090others(4): Show | 14 | HG00639.hp1 HG01109.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.1194+17C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 2/31 | chr3 | 126989804 | ||||||
| chr3:126990056
|
T | A | 2 | a0001c0004t0011g0011a0007c0025t0011g0011 | 5 | HG01496.hp1 HG01981.hp1 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.1194+269T>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 2/31 | chr3 | 126990056 | ||||||
| chr3:126990149
|
A | G | 2 | a0001c0004t0011g0011a0007c0025t0011g0011 | 5 | HG01496.hp1 HG01981.hp1 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.1194+362A>G | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 2/31 | chr3 | 126990149 | ||||||
| chr3:126990258
|
C | T | 12 | a0001c0006t0003g0009a0001c0006t0003g0032a0001c0006t0003g0095others(9): Show | 18 | HG02145.hp2 HG02258.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.1194+471C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 2/31 | chr3 | 126990258 | ||||||
| chr3:126990359
|
C | T | 113 | a0000c0028t0034g0052a0001c0002t0002g0002a0001c0002t0002g0013others(110): Show | 172 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.1194+572C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 2/31 | chr3 | 126990359 | ||||||
| chr3:126990447
|
G | A | 1 | a0001c0003t0048g0160 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1194+660G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 2/31 | chr3 | 126990447 | ||||||
| chr3:126990609
|
G | A | 1 | a0001c0002t0002g0054 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1195-775G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 2/31 | chr3 | 126990609 | ||||||
| chr3:126990659
|
T | A | 216 | a0000c0028t0034g0052a0001c0001t0001g0001a0001c0001t0001g0003others(213): Show | 344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.1195-725T>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 2/31 | chr3 | 126990659 | ||||||
| chr3:126990692
|
G | A | 1 | a0001c0002t0002g0054 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1195-692G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 2/31 | chr3 | 126990692 | ||||||
| chr3:126990707
|
T | C | 216 | a0000c0028t0034g0052a0001c0001t0001g0001a0001c0001t0001g0003others(213): Show | 344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.1195-677T>C | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 2/31 | chr3 | 126990707 | ||||||
| chr3:126991020
|
T | C | 215 | a0000c0028t0034g0052a0001c0001t0001g0001a0001c0001t0001g0003others(212): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.1195-364T>C | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 2/31 | chr3 | 126991020 | ||||||
| chr3:126991048
|
C | T | 5 | a0001c0010t0009g0033a0001c0010t0009g0105a0001c0010t0009g0106others(2): Show | 8 | HG02055.hp2 HG02257.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1195-336C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 2/31 | chr3 | 126991048 | ||||||
| chr3:126991151
|
G | A | 7 | a0001c0007t0003g0005a0001c0007t0003g0089a0001c0007t0003g0090others(4): Show | 14 | HG00639.hp1 HG01109.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.1195-233G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 2/31 | chr3 | 126991151 | ||||||
| chr3:126991178
|
C | T | 1 | a0001c0007t0020g0091 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1195-206C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 2/31 | chr3 | 126991178 | ||||||
| chr3:126991194
|
A | G | 1 | a0001c0005t0025g0181 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1195-190A>G | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 2/31 | chr3 | 126991194 | ||||||
| chr3:126991278
|
C | G | 1 | a0001c0008t0017g0049 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1195-106C>G | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 2/31 | chr3 | 126991278 | ||||||
| chr3:126991318
|
C | G | 1 | a0001c0008t0023g0085 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1195-66C>G | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 2/31 | chr3 | 126991318 | ||||||
| chr3:126991347
|
G | GC | 12 | a0001c0006t0003g0009a0001c0006t0003g0032a0001c0006t0003g0095others(9): Show | 18 | HG02145.hp2 HG02258.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.1195-34dupC | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr3 | 126991347 | |||||
| chr3:126991627
|
C | T | 2 | a0001c0004t0011g0011a0007c0025t0011g0011 | 5 | HG01496.hp1 HG01981.hp1 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.1377+61C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 126991627 | ||||||
| chr3:126991628
|
G | A | 2 | a0001c0001t0001g0114a0001c0001t0016g0036 | 3 | NA18995.hp1 NA19000.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.1377+62G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 126991628 | ||||||
| chr3:126991730
|
A | C | 1 | a0001c0003t0048g0160 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1377+164A>C | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 126991730 | ||||||
| chr3:126991805
|
G | A | 1 | a0001c0006t0001g0020 | 3 | HG01255.hp1 HG02809.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1377+239G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 126991805 | ||||||
| chr3:126991933
|
C | A | 8 | a0000c0028t0034g0052a0001c0002t0002g0013a0001c0002t0002g0028others(5): Show | 12 | HG02735.hp2 NA18940.hp2 NA18945.hp2 others(9): Show |
intron_variant | MODIFIER | c.1377+367C>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 126991933 | ||||||
| chr3:126992113
|
G | A | 13 | a0001c0008t0007g0029a0001c0008t0007g0061a0001c0008t0013g0030others(10): Show | 17 | HG00140.hp2 HG01069.hp1 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.1377+547G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 126992113 | ||||||
| chr3:126992122
|
G | A | 13 | a0001c0008t0007g0029a0001c0008t0007g0061a0001c0008t0013g0030others(10): Show | 17 | HG00140.hp2 HG01069.hp1 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.1377+556G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 126992122 | ||||||
| chr3:126992227
|
G | A | 97 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(94): Show | 161 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.1377+661G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 126992227 | ||||||
| chr3:126992250
|
G | T | 2 | a0001c0003t0001g0017a0001c0003t0001g0152 | 5 | HG01243.hp1 HG02970.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1377+684G>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 126992250 | ||||||
| chr3:126992292
|
C | T | 7 | a0001c0007t0003g0005a0001c0007t0003g0089a0001c0007t0003g0090others(4): Show | 14 | HG00639.hp1 HG01109.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.1377+726C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 126992292 | ||||||
| chr3:126992661
|
G | A | 1 | a0001c0009t0002g0065 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1377+1095G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 126992661 | ||||||
| chr3:126992682
|
G | A | 1 | a0001c0009t0027g0066 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1377+1116G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 126992682 | ||||||
| chr3:126992702
|
G | T | 1 | a0001c0001t0010g0185 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1377+1136G>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 126992702 | ||||||
| chr3:126992783
|
G | T | 1 | a0001c0005t0005g0046 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1377+1217G>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 126992783 | ||||||
| chr3:126992862
|
C | T | 96 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(93): Show | 160 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.1377+1296C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 126992862 | ||||||
| chr3:126992896
|
C | A | 1 | a0001c0015t0003g0094 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1377+1330C>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 126992896 | ||||||
| chr3:126992956
|
C | T | 2 | a0001c0001t0001g0156a0001c0003t0048g0160 | 2 | HG00597.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1377+1390C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 126992956 | ||||||
| chr3:126993035
|
C | T | 34 | a0001c0004t0004g0010a0001c0004t0004g0043a0001c0004t0004g0044others(31): Show | 50 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(47): Show |
intron_variant | MODIFIER | c.1377+1469C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 126993035 | ||||||
| chr3:126993070
|
A | G | 43 | a0001c0004t0004g0010a0001c0004t0004g0043a0001c0004t0004g0044others(40): Show | 69 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(66): Show |
intron_variant | MODIFIER | c.1377+1504A>G | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 126993070 | ||||||
| chr3:126993596
|
A | T | 113 | a0000c0028t0034g0052a0001c0002t0002g0002a0001c0002t0002g0013others(110): Show | 172 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.1377+2030A>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 126993596 | ||||||
| chr3:126993613
|
C | T | 1 | a0001c0002t0002g0084 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1377+2047C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 126993613 | ||||||
| chr3:126993653
|
T | C | 216 | a0000c0028t0034g0052a0001c0001t0001g0001a0001c0001t0001g0003others(213): Show | 344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.1377+2087T>C | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 126993653 | ||||||
| chr3:126993656
|
G | T | 1 | a0001c0001t0044g0101 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1377+2090G>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 126993656 | ||||||
| chr3:126993755
|
G | C | 1 | a0001c0002t0002g0054 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1377+2189G>C | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 126993755 | ||||||
| chr3:126993786
|
T | G | 1 | a0003c0043t0033g0050 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1377+2220T>G | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 126993786 | ||||||
| chr3:126993808
|
G | A | 1 | a0002c0019t0001g0115 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1377+2242G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 126993808 | ||||||
| chr3:126993915
|
C | T | 41 | a0001c0004t0004g0010a0001c0004t0004g0043a0001c0004t0004g0044others(38): Show | 64 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(61): Show |
intron_variant | MODIFIER | c.1377+2349C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 126993915 | ||||||
| chr3:126994027
|
G | A | 1 | a0001c0002t0002g0047 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1377+2461G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 126994027 | ||||||
| chr3:126994216
|
C | G | 1 | a0003c0043t0033g0050 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1377+2650C>G | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 126994216 | ||||||
| chr3:126994294
|
T | C | 2 | a0001c0009t0028g0093a0001c0014t0002g0092 | 2 | HG03195.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1377+2728T>C | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 126994294 | ||||||
| chr3:126994480
|
C | T | 1 | a0001c0001t0001g0151 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1377+2914C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 126994480 | ||||||
| chr3:126994723
|
C | T | 1 | a0004c0042t0001g0150 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1377+3157C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 126994723 | ||||||
| chr3:126994788
|
G | A | 1 | a0001c0005t0005g0165 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1377+3222G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 126994788 | ||||||
| chr3:126994847
|
G | A | 1 | a0001c0008t0017g0049 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1377+3281G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 126994847 | ||||||
| chr3:126994929
|
C | T | 1 | a0001c0001t0001g0103 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1377+3363C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 126994929 | ||||||
| chr3:126995051
|
C | T | 9 | a0001c0001t0001g0012a0001c0001t0001g0023a0001c0001t0001g0149others(6): Show | 19 | HG00735.hp2 HG01074.hp1 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.1377+3485C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 126995051 | ||||||
| chr3:126995066
|
G | T | 1 | a0001c0001t0001g0148 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1377+3500G>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 126995066 | ||||||
| chr3:126995122
|
G | T | 43 | a0001c0004t0004g0010a0001c0004t0004g0043a0001c0004t0004g0044others(40): Show | 69 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(66): Show |
intron_variant | MODIFIER | c.1377+3556G>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 126995122 | ||||||
| chr3:126995156
|
G | A | 6 | a0001c0008t0007g0029a0001c0008t0007g0061a0001c0008t0018g0014others(3): Show | 9 | HG00140.hp2 HG01069.hp1 HG01070.hp1 others(6): Show |
intron_variant | MODIFIER | c.1377+3590G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 126995156 | ||||||
| chr3:126995164
|
C | G | 1 | a0001c0016t0005g0180 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1377+3598C>G | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 126995164 | ||||||
| chr3:126995360
|
C | T | 2 | a0001c0012t0015g0024a0001c0021t0015g0107 | 4 | HG02055.hp2 HG02257.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1377+3794C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 126995360 | ||||||
| chr3:126995536
|
G | T | 1 | a0001c0001t0001g0114 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1377+3970G>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 126995536 | ||||||
| chr3:126995613
|
G | A | 1 | a0001c0001t0001g0116 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1377+4047G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 126995613 | ||||||
| chr3:126995627
|
C | T | 1 | a0001c0005t0005g0179 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1377+4061C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 126995627 | ||||||
| chr3:126995894
|
C | T | 1 | a0001c0003t0048g0160 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1377+4328C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 126995894 | ||||||
| chr3:126996010
|
A | G | 1 | a0001c0040t0009g0147 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1377+4444A>G | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 126996010 | ||||||
| chr3:126996200
|
C | T | 2 | a0001c0012t0015g0024a0001c0021t0015g0107 | 4 | HG02055.hp2 HG02257.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1377+4634C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 126996200 | ||||||
| chr3:126996244
|
C | T | 6 | a0001c0008t0013g0030a0001c0008t0013g0053a0001c0008t0013g0063others(3): Show | 7 | HG01167.hp2 HG01169.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.1377+4678C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 126996244 | ||||||
| chr3:126996259
|
C | T | 6 | a0001c0007t0003g0005a0001c0007t0003g0089a0001c0007t0003g0090others(3): Show | 13 | HG00639.hp1 HG01109.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.1377+4693C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 126996259 | ||||||
| chr3:126996348
|
T | C | 216 | a0000c0028t0034g0052a0001c0001t0001g0001a0001c0001t0001g0003others(213): Show | 344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.1377+4782T>C | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 126996348 | ||||||
| chr3:126996427
|
G | A | 2 | a0001c0008t0013g0030a0001c0008t0013g0053 | 3 | HG01167.hp2 HG01169.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1377+4861G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 126996427 | ||||||
| chr3:126996458
|
G | C | 5 | a0001c0008t0013g0030a0001c0008t0013g0053a0001c0008t0013g0063others(2): Show | 6 | HG01167.hp2 HG01169.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.1377+4892G>C | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 126996458 | ||||||
| chr3:126996479
|
G | T | 2 | a0001c0004t0011g0011a0007c0025t0011g0011 | 5 | HG01496.hp1 HG01981.hp1 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.1377+4913G>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 126996479 | ||||||
| chr3:126996534
|
T | A | 1 | a0001c0001t0016g0117 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1377+4968T>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 126996534 | ||||||
| chr3:126996687
|
G | C | 2 | a0001c0004t0011g0011a0007c0025t0011g0011 | 5 | HG01496.hp1 HG01981.hp1 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.1377+5121G>C | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 126996687 | ||||||
| chr3:126996699
|
T | G | 1 | a0001c0006t0001g0020 | 3 | HG01255.hp1 HG02809.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1377+5133T>G | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 126996699 | ||||||
| chr3:126997012
|
T | G | 1 | a0001c0001t0016g0117 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1377+5446T>G | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 126997012 | ||||||
| chr3:126997037
|
C | T | 1 | a0001c0001t0001g0103 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1377+5471C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 126997037 | ||||||
| chr3:126997298
|
G | A | 1 | a0001c0024t0036g0086 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1377+5732G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 126997298 | ||||||
| chr3:126997320
|
A | AACTCTCT others(3): Show |
1 | a0001c0001t0001g0114 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1377+5757_1377+576 others(14): Show |
PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr3 | 126997320 | |||||
| chr3:126997436
|
T | C | 1 | a0001c0002t0002g0067 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1377+5870T>C | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 126997436 | ||||||
| chr3:126997577
|
C | G | 2 | a0001c0004t0011g0011a0007c0025t0011g0011 | 5 | HG01496.hp1 HG01981.hp1 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.1378-5753C>G | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 126997577 | ||||||
| chr3:126997611
|
G | A | 1 | a0001c0004t0004g0166 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1378-5719G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 126997611 | ||||||
| chr3:126997625
|
G | A | 1 | a0001c0004t0004g0045 | 2 | HG01884.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.1378-5705G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 126997625 | ||||||
| chr3:126997651
|
A | C | 1 | a0001c0008t0017g0049 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1378-5679A>C | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 126997651 | ||||||
| chr3:126997714
|
A | G | 1 | a0003c0043t0033g0050 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1378-5616A>G | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 126997714 | ||||||
| chr3:126997898
|
C | T | 2 | a0001c0001t0001g0022a0001c0001t0001g0040 | 5 | HG01070.hp2 HG01071.hp1 NA18944.hp2 others(2): Show |
intron_variant | MODIFIER | c.1378-5432C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 126997898 | ||||||
| chr3:126998042
|
C | T | 12 | a0001c0006t0003g0009a0001c0006t0003g0032a0001c0006t0003g0095others(9): Show | 18 | HG02145.hp2 HG02258.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.1378-5288C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 126998042 | ||||||
| chr3:126998074
|
G | T | 2 | a0001c0004t0004g0166a0001c0004t0004g0178 | 2 | HG03688.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.1378-5256G>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 126998074 | ||||||
| chr3:126998111
|
C | T | 6 | a0001c0007t0003g0005a0001c0007t0003g0089a0001c0007t0003g0090others(3): Show | 13 | HG00639.hp1 HG01109.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.1378-5219C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 126998111 | ||||||
| chr3:126998409
|
C | T | 3 | a0001c0010t0009g0033a0001c0010t0009g0105a0001c0010t0009g0106 | 4 | HG02280.hp1 HG02615.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1378-4921C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 126998409 | ||||||
| chr3:126998416
|
G | A | 35 | a0001c0004t0004g0010a0001c0004t0004g0043a0001c0004t0004g0044others(32): Show | 51 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(48): Show |
intron_variant | MODIFIER | c.1378-4914G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 126998416 | ||||||
| chr3:126998567
|
C | T | 2 | a0001c0001t0001g0039a0001c0003t0001g0039 | 2 | HG02602.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1378-4763C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 126998567 | ||||||
| chr3:126998582
|
A | G | 1 | a0001c0001t0001g0012 | 5 | HG00735.hp2 HG01074.hp1 HG01109.hp2 others(2): Show |
intron_variant | MODIFIER | c.1378-4748A>G | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 126998582 | ||||||
| chr3:126998603
|
A | C | 34 | a0001c0004t0004g0010a0001c0004t0004g0043a0001c0004t0004g0044others(31): Show | 50 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(47): Show |
intron_variant | MODIFIER | c.1378-4727A>C | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 126998603 | ||||||
| chr3:126998837
|
G | C | 12 | a0001c0006t0003g0009a0001c0006t0003g0032a0001c0006t0003g0095others(9): Show | 18 | HG02145.hp2 HG02258.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.1378-4493G>C | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 126998837 | ||||||
| chr3:126998877
|
G | A | 2 | a0001c0004t0011g0011a0007c0025t0011g0011 | 5 | HG01496.hp1 HG01981.hp1 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.1378-4453G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 126998877 | ||||||
| chr3:126998940
|
A | G | 1 | a0001c0010t0009g0106 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1378-4390A>G | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 126998940 | ||||||
| chr3:126998947
|
C | T | 2 | a0001c0006t0003g0032a0001c0006t0003g0099 | 3 | HG02895.hp2 HG02897.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1378-4383C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 126998947 | ||||||
| chr3:126998982
|
A | G | 2 | a0001c0001t0016g0036a0001c0001t0016g0117 | 3 | NA18989.hp1 NA18995.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.1378-4348A>G | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 126998982 | ||||||
| chr3:126999018
|
A | G | 1 | a0001c0001t0001g0116 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1378-4312A>G | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 126999018 | ||||||
| chr3:126999121
|
A | G | 97 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(94): Show | 161 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.1378-4209A>G | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 126999121 | ||||||
| chr3:126999196
|
C | T | 1 | a0001c0003t0001g0146 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1378-4134C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 126999196 | ||||||
| chr3:126999207
|
C | T | 34 | a0001c0004t0004g0010a0001c0004t0004g0043a0001c0004t0004g0044others(31): Show | 50 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(47): Show |
intron_variant | MODIFIER | c.1378-4123C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 126999207 | ||||||
| chr3:126999232
|
C | T | 1 | a0001c0001t0001g0145 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1378-4098C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 126999232 | ||||||
| chr3:126999244
|
G | A | 1 | a0001c0004t0004g0183 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1378-4086G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 126999244 | ||||||
| chr3:126999279
|
G | T | 1 | a0004c0042t0001g0150 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1378-4051G>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 126999279 | ||||||
| chr3:126999296
|
G | A | 2 | a0001c0004t0011g0011a0007c0025t0011g0011 | 5 | HG01496.hp1 HG01981.hp1 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.1378-4034G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 126999296 | ||||||
| chr3:126999510
|
C | T | 1 | a0001c0008t0017g0064 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1378-3820C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 126999510 | ||||||
| chr3:126999593
|
G | A | 1 | a0001c0001t0001g0108 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1378-3737G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 126999593 | ||||||
| chr3:126999630
|
C | T | 1 | a0001c0001t0001g0144 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1378-3700C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 126999630 | ||||||
| chr3:126999688
|
G | A | 1 | a0001c0001t0001g0114 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1378-3642G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 126999688 | ||||||
| chr3:126999904
|
C | T | 1 | a0001c0008t0013g0063 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1378-3426C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 126999904 | ||||||
| chr3:126999911
|
G | A | 2 | a0001c0012t0015g0024a0001c0021t0015g0107 | 4 | HG02055.hp2 HG02257.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1378-3419G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 126999911 | ||||||
| chr3:126999974
|
C | A | 1 | a0001c0001t0001g0037 | 2 | HG03471.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1378-3356C>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 126999974 | ||||||
| chr3:127000305
|
G | A | 1 | a0001c0001t0001g0156 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1378-3025G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 127000305 | ||||||
| chr3:127000351
|
C | T | 1 | a0001c0002t0002g0083 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1378-2979C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 127000351 | ||||||
| chr3:127000437
|
G | A | 45 | a0000c0028t0034g0052a0001c0002t0002g0002a0001c0002t0002g0013others(42): Show | 68 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.1378-2893G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 127000437 | ||||||
| chr3:127000440
|
C | T | 1 | a0001c0008t0017g0064 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1378-2890C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 127000440 | ||||||
| chr3:127000491
|
C | T | 1 | a0001c0038t0038g0158 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1378-2839C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 127000491 | ||||||
| chr3:127000622
|
G | A | 2 | a0001c0001t0001g0118a0001c0015t0006g0062 | 2 | HG01099.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.1378-2708G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 127000622 | ||||||
| chr3:127000675
|
C | T | 1 | a0001c0004t0004g0177 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1378-2655C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 127000675 | ||||||
| chr3:127000743
|
T | C | 1 | a0001c0004t0004g0167 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1378-2587T>C | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 127000743 | ||||||
| chr3:127001009
|
G | A | 1 | a0001c0006t0001g0020 | 3 | HG01255.hp1 HG02809.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1378-2321G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 127001009 | ||||||
| chr3:127001105
|
G | C | 1 | a0001c0024t0036g0086 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1378-2225G>C | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 127001105 | ||||||
| chr3:127001217
|
C | A | 1 | a0001c0001t0046g0119 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1378-2113C>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 127001217 | ||||||
| chr3:127001275
|
G | A | 1 | a0001c0008t0017g0049 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1378-2055G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 127001275 | ||||||
| chr3:127001307
|
G | C | 2 | a0001c0004t0011g0011a0007c0025t0011g0011 | 5 | HG01496.hp1 HG01981.hp1 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.1378-2023G>C | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 127001307 | ||||||
| chr3:127001312
|
G | A | 44 | a0000c0028t0034g0052a0001c0002t0002g0002a0001c0002t0002g0013others(41): Show | 67 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(64): Show |
intron_variant | MODIFIER | c.1378-2018G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 127001312 | ||||||
| chr3:127001484
|
G | A | 1 | a0001c0008t0007g0029 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1378-1846G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 127001484 | ||||||
| chr3:127001513
|
G | A | 1 | a0001c0006t0001g0020 | 3 | HG01255.hp1 HG02809.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1378-1817G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 127001513 | ||||||
| chr3:127001519
|
G | A | 2 | a0001c0002t0004g0069a0001c0002t0006g0068 | 2 | HG03654.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.1378-1811G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 127001519 | ||||||
| chr3:127001543
|
G | A | 1 | a0001c0005t0025g0181 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1378-1787G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 127001543 | ||||||
| chr3:127001560
|
CG | C | 2 | a0001c0004t0011g0011a0007c0025t0011g0011 | 5 | HG01496.hp1 HG01981.hp1 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.1378-1769delG | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 127001560 | ||||||
| chr3:127001604
|
C | T | 2 | a0001c0012t0015g0024a0001c0021t0015g0107 | 4 | HG02055.hp2 HG02257.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1378-1726C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 127001604 | ||||||
| chr3:127001694
|
C | T | 1 | a0001c0002t0002g0028 | 2 | NA19066.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.1378-1636C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 127001694 | ||||||
| chr3:127001721
|
G | T | 38 | a0001c0002t0002g0082a0001c0004t0004g0010a0001c0004t0004g0043others(35): Show | 57 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.1378-1609G>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 127001721 | ||||||
| chr3:127001728
|
C | T | 1 | a0001c0006t0001g0020 | 3 | HG01255.hp1 HG02809.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1378-1602C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 127001728 | ||||||
| chr3:127001738
|
T | C | 1 | a0001c0002t0006g0031 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1378-1592T>C | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 127001738 | ||||||
| chr3:127001762
|
C | T | 1 | a0001c0001t0001g0112 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1378-1568C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 127001762 | ||||||
| chr3:127001888
|
G | A | 1 | a0001c0006t0001g0020 | 3 | HG01255.hp1 HG02809.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1378-1442G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 127001888 | ||||||
| chr3:127002051
|
C | G | 1 | a0003c0043t0033g0050 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1378-1279C>G | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 127002051 | ||||||
| chr3:127002058
|
C | T | 2 | a0001c0002t0002g0013a0001c0002t0002g0058 | 5 | NA18945.hp2 NA18967.hp1 NA18984.hp2 others(2): Show |
intron_variant | MODIFIER | c.1378-1272C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 127002058 | ||||||
| chr3:127002227
|
T | C | 1 | a0001c0008t0017g0049 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1378-1103T>C | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 127002227 | ||||||
| chr3:127002230
|
G | T | 1 | a0001c0006t0014g0098 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1378-1100G>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 127002230 | ||||||
| chr3:127002306
|
G | A | 1 | a0001c0008t0017g0049 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1378-1024G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 127002306 | ||||||
| chr3:127002358
|
G | T | 1 | a0001c0001t0001g0116 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1378-972G>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 127002358 | ||||||
| chr3:127002575
|
G | C | 12 | a0001c0001t0001g0003a0001c0001t0001g0037a0001c0001t0001g0116others(9): Show | 22 | HG01069.hp2 HG01074.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.1378-755G>C | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 127002575 | ||||||
| chr3:127002812
|
G | A | 1 | a0001c0001t0001g0104 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1378-518G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 127002812 | ||||||
| chr3:127003138
|
A | ACTGGGGC others(5): Show |
33 | a0001c0004t0004g0010a0001c0004t0004g0043a0001c0004t0004g0044others(30): Show | 49 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(46): Show |
intron_variant | MODIFIER | c.1378-167_1378-156d others(14): Show |
PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr3 | 127003138 | |||||
| chr3:127003138
|
ACTGGGGC others(5): Show |
A | 7 | a0001c0004t0011g0011a0001c0008t0013g0030a0001c0008t0013g0053others(4): Show | 11 | HG01167.hp2 HG01169.hp1 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.1378-167_1378-156d others(14): Show |
PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr3 | 127003138 | |||||
| chr3:127003266
|
G | C | 5 | a0001c0009t0002g0065a0001c0009t0012g0018a0001c0009t0028g0093others(2): Show | 6 | HG02965.hp1 HG03139.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.1378-64G>C | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 3/31 | chr3 | 127003266 | ||||||
| chr3:127003566
|
A | G | 1 | a0001c0006t0001g0020 | 3 | HG01255.hp1 HG02809.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1518+96A>G | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 4/31 | chr3 | 127003566 | ||||||
| chr3:127003573
|
C | T | 1 | a0001c0004t0004g0164 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1518+103C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 4/31 | chr3 | 127003573 | ||||||
| chr3:127003617
|
C | T | 6 | a0001c0001t0001g0008a0001c0001t0001g0040a0001c0001t0022g0048others(3): Show | 11 | HG01081.hp2 HG01975.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.1518+147C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 4/31 | chr3 | 127003617 | ||||||
| chr3:127003809
|
G | A | 1 | a0003c0043t0033g0050 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1518+339G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 4/31 | chr3 | 127003809 | ||||||
| chr3:127003821
|
G | A | 12 | a0001c0006t0003g0009a0001c0006t0003g0032a0001c0006t0003g0095others(9): Show | 18 | HG02145.hp2 HG02258.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.1518+351G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 4/31 | chr3 | 127003821 | ||||||
| chr3:127003881
|
C | T | 1 | a0001c0002t0002g0058 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1518+411C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 4/31 | chr3 | 127003881 | ||||||
| chr3:127004128
|
A | G | 12 | a0001c0006t0003g0009a0001c0006t0003g0032a0001c0006t0003g0095others(9): Show | 18 | HG02145.hp2 HG02258.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.1519-483A>G | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 4/31 | chr3 | 127004128 | ||||||
| chr3:127004470
|
A | T | 1 | a0001c0005t0005g0179 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1519-141A>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 4/31 | chr3 | 127004470 | ||||||
| chr3:127004765
|
A | C | 1 | a0001c0027t0002g0057 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1619+54A>C | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 5/31 | chr3 | 127004765 | ||||||
| chr3:127005039
|
G | T | 2 | a0001c0003t0001g0143a0004c0042t0001g0150 | 2 | HG03704.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1743+31G>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 6/31 | chr3 | 127005039 | ||||||
| chr3:127005289
|
G | A | 1 | a0001c0010t0009g0105 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1897+46G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 7/31 | chr3 | 127005289 | ||||||
| chr3:127005308
|
G | A | 5 | a0001c0008t0007g0029a0001c0008t0007g0061a0001c0008t0018g0014others(2): Show | 8 | HG00140.hp2 HG01069.hp1 HG01070.hp1 others(5): Show |
intron_variant | MODIFIER | c.1897+65G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 7/31 | chr3 | 127005308 | ||||||
| chr3:127005315
|
TAGCGCCT others(9): Show |
T | 1 | a0001c0001t0001g0142 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1897+75_1897+90del others(16): Show |
PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 7/31 | INFO_REALIGN_3_PRIME | chr3 | 127005315 | |||||
| chr3:127005495
|
T | C | 3 | a0001c0010t0009g0033a0001c0010t0009g0105a0001c0010t0009g0106 | 4 | HG02280.hp1 HG02615.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1897+252T>C | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 7/31 | chr3 | 127005495 | ||||||
| chr3:127005526
|
C | A | 34 | a0001c0004t0004g0010a0001c0004t0004g0043a0001c0004t0004g0045others(31): Show | 53 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(50): Show |
intron_variant | MODIFIER | c.1897+283C>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 7/31 | chr3 | 127005526 | ||||||
| chr3:127005735
|
C | T | 1 | a0001c0024t0036g0086 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1898-344C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 7/31 | chr3 | 127005735 | ||||||
| chr3:127005802
|
G | A | 45 | a0000c0028t0034g0052a0001c0002t0002g0002a0001c0002t0002g0013others(42): Show | 68 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.1898-277G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 7/31 | chr3 | 127005802 | ||||||
| chr3:127005811
|
T | C | 9 | a0001c0001t0001g0021a0001c0001t0001g0163a0001c0001t0010g0124others(6): Show | 11 | NA18979.hp2 NA18984.hp1 NA18992.hp1 others(8): Show |
intron_variant | MODIFIER | c.1898-268T>C | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 7/31 | chr3 | 127005811 | ||||||
| chr3:127005993
|
G | A | 1 | a0001c0005t0005g0169 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1898-86G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 7/31 | chr3 | 127005993 | ||||||
| chr3:127006038
|
G | C | 97 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(94): Show | 161 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.1898-41G>C | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 7/31 | chr3 | 127006038 | ||||||
| chr3:127006200
|
C | T | 1 | a0001c0001t0001g0141 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1997+22C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 8/31 | chr3 | 127006200 | ||||||
| chr3:127006228
|
C | G | 1 | a0001c0004t0004g0043 | 2 | NA18939.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.1997+50C>G | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 8/31 | chr3 | 127006228 | ||||||
| chr3:127006235
|
G | A | 4 | a0001c0003t0001g0016a0001c0003t0001g0017a0001c0003t0001g0152others(1): Show | 9 | HG01243.hp1 HG02622.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.1997+57G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 8/31 | chr3 | 127006235 | ||||||
| chr3:127006329
|
G | A | 1 | a0001c0033t0009g0129 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1997+151G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 8/31 | chr3 | 127006329 | ||||||
| chr3:127006332
|
G | A | 45 | a0000c0028t0034g0052a0001c0002t0002g0002a0001c0002t0002g0013others(42): Show | 68 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.1997+154G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 8/31 | chr3 | 127006332 | ||||||
| chr3:127006545
|
G | A | 1 | a0001c0002t0002g0070 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1997+367G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 8/31 | chr3 | 127006545 | ||||||
| chr3:127006625
|
A | G | 1 | a0003c0043t0033g0050 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1997+447A>G | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 8/31 | chr3 | 127006625 | ||||||
| chr3:127006724
|
G | A | 1 | a0001c0002t0002g0071 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1997+546G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 8/31 | chr3 | 127006724 | ||||||
| chr3:127006770
|
C | T | 1 | a0001c0036t0001g0140 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1997+592C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 8/31 | chr3 | 127006770 | ||||||
| chr3:127006989
|
C | T | 6 | a0001c0007t0003g0005a0001c0007t0003g0089a0001c0007t0003g0090others(3): Show | 13 | HG00639.hp1 HG01109.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.1998-810C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 8/31 | chr3 | 127006989 | ||||||
| chr3:127007070
|
C | T | 1 | a0001c0002t0002g0028 | 2 | NA19066.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.1998-729C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 8/31 | chr3 | 127007070 | ||||||
| chr3:127007127
|
C | T | 45 | a0000c0028t0034g0052a0001c0002t0002g0002a0001c0002t0002g0013others(42): Show | 68 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.1998-672C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 8/31 | chr3 | 127007127 | ||||||
| chr3:127007185
|
A | G | 12 | a0001c0006t0003g0009a0001c0006t0003g0032a0001c0006t0003g0095others(9): Show | 18 | HG02145.hp2 HG02258.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.1998-614A>G | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 8/31 | chr3 | 127007185 | ||||||
| chr3:127007221
|
G | C | 1 | a0001c0008t0017g0064 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1998-578G>C | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 8/31 | chr3 | 127007221 | ||||||
| chr3:127007257
|
C | T | 1 | a0001c0024t0036g0086 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1998-542C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 8/31 | chr3 | 127007257 | ||||||
| chr3:127007476
|
C | T | 6 | a0001c0001t0010g0124a0001c0001t0010g0125a0001c0001t0010g0126others(3): Show | 6 | NA18979.hp2 NA18984.hp1 NA19063.hp1 others(3): Show |
intron_variant | MODIFIER | c.1998-323C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 8/31 | chr3 | 127007476 | ||||||
| chr3:127007526
|
C | T | 1 | a0001c0024t0036g0086 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1998-273C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 8/31 | chr3 | 127007526 | ||||||
| chr3:127007960
|
A | G | 34 | a0001c0004t0004g0010a0001c0004t0004g0043a0001c0004t0004g0044others(31): Show | 50 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(47): Show |
intron_variant | MODIFIER | c.2112+47A>G | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 9/31 | chr3 | 127007960 | ||||||
| chr3:127008080
|
T | G | 1 | a0001c0038t0038g0158 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2112+167T>G | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 9/31 | chr3 | 127008080 | ||||||
| chr3:127008166
|
C | T | 1 | a0001c0017t0037g0081 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2112+253C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 9/31 | chr3 | 127008166 | ||||||
| chr3:127008307
|
G | A | 1 | a0001c0024t0036g0086 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2112+394G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 9/31 | chr3 | 127008307 | ||||||
| chr3:127008338
|
T | C | 1 | a0001c0024t0036g0086 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2112+425T>C | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 9/31 | chr3 | 127008338 | ||||||
| chr3:127008366
|
C | T | 2 | a0001c0006t0003g0097a0002c0019t0001g0115 | 2 | HG02630.hp1 NA18939.hp2 |
intron_variant | MODIFIER | c.2112+453C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 9/31 | chr3 | 127008366 | ||||||
| chr3:127008396
|
A | G | 217 | a0000c0028t0034g0052a0001c0001t0001g0001a0001c0001t0001g0003others(214): Show | 345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.2112+483A>G | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 9/31 | chr3 | 127008396 | ||||||
| chr3:127008453
|
A | G | 32 | a0001c0004t0004g0010a0001c0004t0004g0043a0001c0004t0004g0044others(29): Show | 47 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(44): Show |
intron_variant | MODIFIER | c.2112+540A>G | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 9/31 | chr3 | 127008453 | ||||||
| chr3:127008475
|
A | G | 217 | a0000c0028t0034g0052a0001c0001t0001g0001a0001c0001t0001g0003others(214): Show | 345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.2112+562A>G | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 9/31 | chr3 | 127008475 | ||||||
| chr3:127008479
|
T | C | 1 | a0001c0002t0012g0072 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2112+566T>C | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 9/31 | chr3 | 127008479 | ||||||
| chr3:127008580
|
C | T | 1 | a0001c0001t0001g0149 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2112+667C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 9/31 | chr3 | 127008580 | ||||||
| chr3:127008661
|
C | T | 1 | a0001c0005t0005g0176 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.2112+748C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 9/31 | chr3 | 127008661 | ||||||
| chr3:127008720
|
G | A | 12 | a0001c0006t0003g0009a0001c0006t0003g0032a0001c0006t0003g0095others(9): Show | 18 | HG02145.hp2 HG02258.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.2112+807G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 9/31 | chr3 | 127008720 | ||||||
| chr3:127009111
|
CT | C | 6 | a0001c0007t0003g0005a0001c0007t0003g0089a0001c0007t0003g0090others(3): Show | 13 | HG00639.hp1 HG01109.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.2112+1199delT | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 9/31 | chr3 | 127009111 | ||||||
| chr3:127009146
|
G | A | 2 | a0001c0004t0011g0011a0007c0025t0011g0011 | 5 | HG01496.hp1 HG01981.hp1 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.2112+1233G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 9/31 | chr3 | 127009146 | ||||||
| chr3:127009146
|
G | T | 1 | a0001c0001t0001g0123 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.2112+1233G>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 9/31 | chr3 | 127009146 | ||||||
| chr3:127009195
|
CAG | C | 2 | a0001c0004t0011g0011a0007c0025t0011g0011 | 5 | HG01496.hp1 HG01981.hp1 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.2112+1283_2112+128 others(6): Show |
PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 9/31 | chr3 | 127009195 | ||||||
| chr3:127009353
|
A | G | 119 | a0000c0028t0034g0052a0001c0002t0002g0002a0001c0002t0002g0013others(116): Show | 183 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.2112+1440A>G | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 9/31 | chr3 | 127009353 | ||||||
| chr3:127009364
|
T | G | 3 | a0001c0008t0013g0063a0001c0008t0017g0064a0001c0008t0023g0085 | 3 | HG02109.hp2 HG02258.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.2112+1451T>G | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 9/31 | chr3 | 127009364 | ||||||
| chr3:127009421
|
T | C | 1 | a0001c0024t0036g0086 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2112+1508T>C | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 9/31 | chr3 | 127009421 | ||||||
| chr3:127009505
|
G | A | 2 | a0001c0004t0011g0011a0007c0025t0011g0011 | 5 | HG01496.hp1 HG01981.hp1 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.2112+1592G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 9/31 | chr3 | 127009505 | ||||||
| chr3:127009506
|
T | G | 2 | a0001c0004t0011g0011a0007c0025t0011g0011 | 5 | HG01496.hp1 HG01981.hp1 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.2112+1593T>G | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 9/31 | chr3 | 127009506 | ||||||
| chr3:127009583
|
G | A | 1 | a0001c0002t0006g0068 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2112+1670G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 9/31 | chr3 | 127009583 | ||||||
| chr3:127009609
|
G | T | 1 | a0001c0001t0010g0128 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.2112+1696G>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 9/31 | chr3 | 127009609 | ||||||
| chr3:127009649
|
G | A | 3 | a0001c0010t0009g0033a0001c0010t0009g0105a0001c0010t0009g0106 | 4 | HG02280.hp1 HG02615.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.2112+1736G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 9/31 | chr3 | 127009649 | ||||||
| chr3:127009865
|
G | C | 5 | a0001c0002t0002g0013a0001c0002t0002g0028a0001c0002t0002g0055others(2): Show | 9 | NA18940.hp2 NA18945.hp2 NA18967.hp1 others(6): Show |
intron_variant | MODIFIER | c.2112+1952G>C | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 9/31 | chr3 | 127009865 | ||||||
| chr3:127009879
|
G | A | 1 | a0001c0006t0001g0020 | 3 | HG01255.hp1 HG02809.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2112+1966G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 9/31 | chr3 | 127009879 | ||||||
| chr3:127009970
|
G | A | 1 | a0001c0004t0004g0171 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.2113-1988G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 9/31 | chr3 | 127009970 | ||||||
| chr3:127010035
|
C | G | 12 | a0001c0006t0003g0009a0001c0006t0003g0032a0001c0006t0003g0095others(9): Show | 18 | HG02145.hp2 HG02258.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.2113-1923C>G | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 9/31 | chr3 | 127010035 | ||||||
| chr3:127010095
|
C | T | 10 | a0001c0008t0007g0029a0001c0008t0007g0061a0001c0008t0013g0030others(7): Show | 14 | HG00140.hp2 HG01069.hp1 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.2113-1863C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 9/31 | chr3 | 127010095 | ||||||
| chr3:127010213
|
G | A | 1 | a0001c0008t0023g0085 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2113-1745G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 9/31 | chr3 | 127010213 | ||||||
| chr3:127010237
|
C | T | 1 | a0001c0024t0036g0086 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2113-1721C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 9/31 | chr3 | 127010237 | ||||||
| chr3:127010253
|
T | G | 2 | a0001c0012t0015g0024a0001c0021t0015g0107 | 4 | HG02055.hp2 HG02257.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.2113-1705T>G | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 9/31 | chr3 | 127010253 | ||||||
| chr3:127010330
|
C | T | 1 | a0001c0038t0038g0158 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2113-1628C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 9/31 | chr3 | 127010330 | ||||||
| chr3:127010400
|
C | G | 1 | a0001c0024t0036g0086 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2113-1558C>G | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 9/31 | chr3 | 127010400 | ||||||
| chr3:127010403
|
A | G | 37 | a0001c0004t0004g0010a0001c0004t0004g0043a0001c0004t0004g0044others(34): Show | 56 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(53): Show |
intron_variant | MODIFIER | c.2113-1555A>G | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 9/31 | chr3 | 127010403 | ||||||
| chr3:127010404
|
T | G | 37 | a0001c0004t0004g0010a0001c0004t0004g0043a0001c0004t0004g0044others(34): Show | 56 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(53): Show |
intron_variant | MODIFIER | c.2113-1554T>G | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 9/31 | chr3 | 127010404 | ||||||
| chr3:127010420
|
C | T | 12 | a0001c0008t0007g0029a0001c0008t0007g0061a0001c0008t0013g0030others(9): Show | 16 | HG00140.hp2 HG01069.hp1 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.2113-1538C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 9/31 | chr3 | 127010420 | ||||||
| chr3:127010575
|
C | A | 1 | a0001c0005t0032g0172 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2113-1383C>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 9/31 | chr3 | 127010575 | ||||||
| chr3:127010631
|
G | A | 1 | a0001c0004t0004g0177 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2113-1327G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 9/31 | chr3 | 127010631 | ||||||
| chr3:127010645
|
C | T | 37 | a0001c0004t0004g0010a0001c0004t0004g0043a0001c0004t0004g0044others(34): Show | 56 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(53): Show |
intron_variant | MODIFIER | c.2113-1313C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 9/31 | chr3 | 127010645 | ||||||
| chr3:127010701
|
G | A | 2 | a0001c0004t0011g0011a0007c0025t0011g0011 | 5 | HG01496.hp1 HG01981.hp1 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.2113-1257G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 9/31 | chr3 | 127010701 | ||||||
| chr3:127010776
|
T | A | 2 | a0001c0012t0015g0024a0001c0021t0015g0107 | 4 | HG02055.hp2 HG02257.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.2113-1182T>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 9/31 | chr3 | 127010776 | ||||||
| chr3:127010846
|
C | T | 14 | a0001c0008t0007g0029a0001c0008t0007g0061a0001c0008t0013g0030others(11): Show | 20 | HG00140.hp2 HG01069.hp1 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.2113-1112C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 9/31 | chr3 | 127010846 | ||||||
| chr3:127011024
|
G | A | 2 | a0001c0011t0004g0042a0001c0026t0004g0042 | 2 | HG01346.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2113-934G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 9/31 | chr3 | 127011024 | ||||||
| chr3:127011109
|
T | C | 1 | a0001c0004t0019g0170 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2113-849T>C | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 9/31 | chr3 | 127011109 | ||||||
| chr3:127011198
|
C | G | 1 | a0001c0001t0022g0139 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2113-760C>G | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 9/31 | chr3 | 127011198 | ||||||
| chr3:127011514
|
T | C | 9 | a0001c0009t0002g0065a0001c0009t0012g0018a0001c0009t0027g0066others(6): Show | 10 | HG01891.hp1 HG02451.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.2113-444T>C | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 9/31 | chr3 | 127011514 | ||||||
| chr3:127011938
|
C | G | 1 | a0001c0001t0010g0185 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.2113-20C>G | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 9/31 | chr3 | 127011938 | ||||||
| chr3:127012234
|
G | A | 1 | a0001c0012t0015g0024 | 3 | HG02055.hp2 HG02257.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2313+76G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 10/31 | chr3 | 127012234 | ||||||
| chr3:127012264
|
G | C | 1 | a0001c0003t0048g0160 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2313+106G>C | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 10/31 | chr3 | 127012264 | ||||||
| chr3:127012405
|
T | A | 38 | a0001c0004t0004g0010a0001c0004t0004g0043a0001c0004t0004g0044others(35): Show | 57 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.2313+247T>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 10/31 | chr3 | 127012405 | ||||||
| chr3:127012478
|
C | T | 1 | a0001c0038t0038g0158 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2313+320C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 10/31 | chr3 | 127012478 | ||||||
| chr3:127012663
|
G | A | 5 | a0001c0008t0007g0029a0001c0008t0007g0061a0001c0008t0018g0014others(2): Show | 8 | HG00140.hp2 HG01069.hp1 HG01070.hp1 others(5): Show |
intron_variant | MODIFIER | c.2313+505G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 10/31 | chr3 | 127012663 | ||||||
| chr3:127012883
|
G | A | 35 | a0001c0004t0004g0010a0001c0004t0004g0043a0001c0004t0004g0044others(32): Show | 51 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(48): Show |
intron_variant | MODIFIER | c.2313+725G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 10/31 | chr3 | 127012883 | ||||||
| chr3:127012885
|
G | T | 1 | a0003c0043t0033g0050 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2313+727G>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 10/31 | chr3 | 127012885 | ||||||
| chr3:127013041
|
C | T | 1 | a0001c0001t0041g0122 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2313+883C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 10/31 | chr3 | 127013041 | ||||||
| chr3:127013183
|
C | T | 2 | a0001c0012t0015g0024a0001c0021t0015g0107 | 4 | HG02055.hp2 HG02257.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.2314-837C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 10/31 | chr3 | 127013183 | ||||||
| chr3:127013193
|
A | G | 1 | a0001c0008t0023g0085 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2314-827A>G | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 10/31 | chr3 | 127013193 | ||||||
| chr3:127013204
|
T | C | 118 | a0000c0028t0034g0052a0001c0002t0002g0002a0001c0002t0002g0013others(115): Show | 182 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(179): Show |
intron_variant | MODIFIER | c.2314-816T>C | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 10/31 | chr3 | 127013204 | ||||||
| chr3:127013316
|
C | A | 38 | a0001c0004t0004g0010a0001c0004t0004g0043a0001c0004t0004g0044others(35): Show | 57 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.2314-704C>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 10/31 | chr3 | 127013316 | ||||||
| chr3:127013581
|
C | G | 37 | a0001c0004t0004g0010a0001c0004t0004g0043a0001c0004t0004g0044others(34): Show | 56 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(53): Show |
intron_variant | MODIFIER | c.2314-439C>G | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 10/31 | chr3 | 127013581 | ||||||
| chr3:127013908
|
T | TGGCTGCA others(14): Show |
1 | a0001c0001t0010g0185 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.2314-93_2314-92ins others(21): Show |
PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 10/31 | INFO_REALIGN_3_PRIME | chr3 | 127013908 | |||||
| chr3:127014131
|
C | T | 2 | a0001c0003t0048g0160a0001c0024t0036g0086 | 2 | HG02572.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.2410+15C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 11/31 | chr3 | 127014131 | ||||||
| chr3:127015324
|
C | T | 1 | a0001c0001t0001g0103 | 1 | HG01081.hp1 | splice_region_variant&intron_variant | LOW | c.3014+4C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 15/31 | chr3 | 127015324 | ||||||
| chr3:127015345
|
G | A | 1 | a0001c0024t0036g0086 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.3014+25G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 15/31 | chr3 | 127015345 | ||||||
| chr3:127015394
|
T | C | 1 | a0001c0003t0048g0160 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.3014+74T>C | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 15/31 | chr3 | 127015394 | ||||||
| chr3:127015608
|
G | A | 1 | a0001c0003t0001g0130 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.3014+288G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 15/31 | chr3 | 127015608 | ||||||
| chr3:127015724
|
A | G | 1 | a0001c0001t0001g0155 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.3014+404A>G | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 15/31 | chr3 | 127015724 | ||||||
| chr3:127015821
|
C | T | 1 | a0001c0001t0001g0104 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.3014+501C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 15/31 | chr3 | 127015821 | ||||||
| chr3:127015833
|
T | C | 217 | a0000c0028t0034g0052a0001c0001t0001g0001a0001c0001t0001g0003others(214): Show | 345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.3014+513T>C | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 15/31 | chr3 | 127015833 | ||||||
| chr3:127015899
|
G | C | 1 | a0001c0001t0001g0103 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.3014+579G>C | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 15/31 | chr3 | 127015899 | ||||||
| chr3:127016021
|
C | G | 2 | a0001c0006t0003g0096a0001c0006t0003g0097 | 2 | HG02622.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.3015-496C>G | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 15/31 | chr3 | 127016021 | ||||||
| chr3:127016027
|
C | A | 1 | a0001c0024t0036g0086 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.3015-490C>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 15/31 | chr3 | 127016027 | ||||||
| chr3:127016172
|
C | T | 5 | a0001c0008t0007g0029a0001c0008t0007g0061a0001c0008t0018g0014others(2): Show | 8 | HG00140.hp2 HG01069.hp1 HG01070.hp1 others(5): Show |
intron_variant | MODIFIER | c.3015-345C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 15/31 | chr3 | 127016172 | ||||||
| chr3:127016210
|
G | A | 2 | a0001c0012t0015g0024a0001c0021t0015g0107 | 4 | HG02055.hp2 HG02257.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.3015-307G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 15/31 | chr3 | 127016210 | ||||||
| chr3:127016326
|
G | A | 1 | a0001c0001t0001g0131 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.3015-191G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 15/31 | chr3 | 127016326 | ||||||
| chr3:127016353
|
G | A | 1 | a0001c0001t0010g0124 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.3015-164G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 15/31 | chr3 | 127016353 | ||||||
| chr3:127016436
|
C | T | 1 | a0003c0043t0033g0050 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3015-81C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 15/31 | chr3 | 127016436 | ||||||
| chr3:127016504
|
C | T | 6 | a0001c0007t0003g0005a0001c0007t0003g0089a0001c0007t0003g0090others(3): Show | 13 | HG00639.hp1 HG01109.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.3015-13C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 15/31 | chr3 | 127016504 | ||||||
| chr3:127016732
|
C | T | 1 | a0001c0004t0004g0171 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.3182+48C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 16/31 | chr3 | 127016732 | ||||||
| chr3:127017206
|
C | T | 6 | a0001c0007t0003g0005a0001c0007t0003g0089a0001c0007t0003g0090others(3): Show | 13 | HG00639.hp1 HG01109.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.3276+169C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 17/31 | chr3 | 127017206 | ||||||
| chr3:127017215
|
G | A | 1 | a0001c0001t0001g0142 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.3276+178G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 17/31 | chr3 | 127017215 | ||||||
| chr3:127017382
|
A | G | 1 | a0001c0003t0048g0160 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.3277-43A>G | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 17/31 | chr3 | 127017382 | ||||||
| chr3:127017978
|
C | T | 41 | a0000c0028t0034g0052a0001c0002t0002g0002a0001c0002t0002g0013others(38): Show | 64 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.3660+86C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 19/31 | chr3 | 127017978 | ||||||
| chr3:127018127
|
C | A | 1 | a0001c0006t0003g0096 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3661-167C>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 19/31 | chr3 | 127018127 | ||||||
| chr3:127018188
|
C | G | 21 | a0001c0004t0004g0010a0001c0004t0004g0043a0001c0004t0004g0044others(18): Show | 30 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(27): Show |
intron_variant | MODIFIER | c.3661-106C>G | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 19/31 | chr3 | 127018188 | ||||||
| chr3:127018623
|
G | A | 48 | a0000c0028t0034g0052a0001c0002t0002g0002a0001c0002t0002g0013others(45): Show | 78 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.3895+95G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 20/31 | chr3 | 127018623 | ||||||
| chr3:127018645
|
T | C | 2 | a0001c0001t0001g0012a0001c0009t0002g0065 | 6 | HG00735.hp2 HG01074.hp1 HG01109.hp2 others(3): Show |
intron_variant | MODIFIER | c.3895+117T>C | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 20/31 | chr3 | 127018645 | ||||||
| chr3:127018690
|
G | A | 1 | a0001c0004t0004g0166 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.3895+162G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 20/31 | chr3 | 127018690 | ||||||
| chr3:127018818
|
T | C | 1 | a0001c0038t0038g0158 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3895+290T>C | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 20/31 | chr3 | 127018818 | ||||||
| chr3:127019104
|
G | A | 2 | a0001c0012t0015g0024a0001c0021t0015g0107 | 4 | HG02055.hp2 HG02257.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.3895+576G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 20/31 | chr3 | 127019104 | ||||||
| chr3:127019108
|
G | A | 1 | a0001c0003t0001g0035 | 2 | NA18971.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.3895+580G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 20/31 | chr3 | 127019108 | ||||||
| chr3:127019173
|
AGTGTTCC others(59): Show |
A | 1 | a0001c0001t0001g0116 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.3895+647_3895+712d others(68): Show |
PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 20/31 | INFO_REALIGN_3_PRIME | chr3 | 127019173 | |||||
| chr3:127019205
|
T | C | 1 | a0001c0024t0036g0086 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.3895+677T>C | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 20/31 | chr3 | 127019205 | ||||||
| chr3:127019477
|
G | A | 24 | a0001c0001t0039g0132a0001c0002t0004g0069a0001c0004t0004g0010others(21): Show | 33 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(30): Show |
intron_variant | MODIFIER | c.3896-725G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 20/31 | chr3 | 127019477 | ||||||
| chr3:127019602
|
T | G | 1 | a0001c0041t0003g0087 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3896-600T>G | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 20/31 | chr3 | 127019602 | ||||||
| chr3:127019606
|
A | G | 3 | a0001c0001t0001g0022a0001c0012t0015g0024a0001c0021t0015g0107 | 7 | HG01070.hp2 HG01071.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.3896-596A>G | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 20/31 | chr3 | 127019606 | ||||||
| chr3:127019611
|
C | T | 5 | a0001c0008t0007g0029a0001c0008t0007g0061a0001c0008t0018g0014others(2): Show | 8 | HG00140.hp2 HG01069.hp1 HG01070.hp1 others(5): Show |
intron_variant | MODIFIER | c.3896-591C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 20/31 | chr3 | 127019611 | ||||||
| chr3:127019622
|
G | A | 1 | a0001c0024t0036g0086 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.3896-580G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 20/31 | chr3 | 127019622 | ||||||
| chr3:127019654
|
C | T | 12 | a0001c0006t0003g0009a0001c0006t0003g0032a0001c0006t0003g0095others(9): Show | 18 | HG02145.hp2 HG02258.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.3896-548C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 20/31 | chr3 | 127019654 | ||||||
| chr3:127019953
|
T | G | 1 | a0001c0001t0001g0133 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.3896-249T>G | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 20/31 | chr3 | 127019953 | ||||||
| chr3:127020067
|
A | G | 1 | a0001c0003t0001g0152 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.3896-135A>G | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 20/31 | chr3 | 127020067 | ||||||
| chr3:127020089
|
G | A | 1 | a0001c0006t0001g0020 | 3 | HG01255.hp1 HG02809.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.3896-113G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 20/31 | chr3 | 127020089 | ||||||
| chr3:127020169
|
G | T | 72 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(69): Show | 124 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.3896-33G>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 20/31 | chr3 | 127020169 | ||||||
| chr3:127020187
|
C | T | 3 | a0001c0014t0026g0073a0001c0017t0012g0074a0001c0017t0037g0081 | 3 | HG01891.hp1 HG02451.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.3896-15C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 20/31 | chr3 | 127020187 | ||||||
| chr3:127020448
|
T | C | 214 | a0000c0028t0034g0052a0001c0001t0001g0001a0001c0001t0001g0003others(211): Show | 339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.4038+104T>C | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 21/31 | chr3 | 127020448 | ||||||
| chr3:127020457
|
G | A | 2 | a0001c0005t0005g0025a0001c0005t0005g0165 | 4 | NA18612.hp2 NA19009.hp1 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.4038+113G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 21/31 | chr3 | 127020457 | ||||||
| chr3:127020744
|
G | A | 1 | a0001c0005t0032g0172 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.4038+400G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 21/31 | chr3 | 127020744 | ||||||
| chr3:127020801
|
G | A | 20 | a0001c0005t0005g0004a0001c0005t0005g0025a0001c0005t0005g0026others(17): Show | 31 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(28): Show |
intron_variant | MODIFIER | c.4038+457G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 21/31 | chr3 | 127020801 | ||||||
| chr3:127020959
|
C | G | 1 | a0001c0024t0036g0086 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.4038+615C>G | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 21/31 | chr3 | 127020959 | ||||||
| chr3:127020989
|
G | C | 1 | a0001c0024t0036g0086 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.4038+645G>C | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 21/31 | chr3 | 127020989 | ||||||
| chr3:127021031
|
C | T | 1 | a0001c0002t0006g0077 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.4038+687C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 21/31 | chr3 | 127021031 | ||||||
| chr3:127021076
|
A | G | 12 | a0001c0008t0007g0029a0001c0008t0007g0061a0001c0008t0013g0030others(9): Show | 16 | HG00140.hp2 HG01069.hp1 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.4038+732A>G | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 21/31 | chr3 | 127021076 | ||||||
| chr3:127021286
|
G | A | 2 | a0001c0012t0015g0024a0001c0021t0015g0107 | 4 | HG02055.hp2 HG02257.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.4039-799G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 21/31 | chr3 | 127021286 | ||||||
| chr3:127021410
|
C | T | 6 | a0001c0007t0003g0005a0001c0007t0003g0089a0001c0007t0003g0090others(3): Show | 13 | HG00639.hp1 HG01109.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.4039-675C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 21/31 | chr3 | 127021410 | ||||||
| chr3:127021412
|
A | G | 1 | a0001c0007t0003g0090 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.4039-673A>G | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 21/31 | chr3 | 127021412 | ||||||
| chr3:127021497
|
A | G | 14 | a0001c0008t0007g0029a0001c0008t0007g0061a0001c0008t0013g0030others(11): Show | 20 | HG00140.hp2 HG01069.hp1 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.4039-588A>G | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 21/31 | chr3 | 127021497 | ||||||
| chr3:127021554
|
T | TGTGTCCT others(5): Show |
1 | a0001c0001t0010g0127 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.4039-530_4039-519d others(14): Show |
PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 21/31 | INFO_REALIGN_3_PRIME | chr3 | 127021554 | |||||
| chr3:127021594
|
G | A | 1 | a0001c0001t0010g0125 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.4039-491G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 21/31 | chr3 | 127021594 | ||||||
| chr3:127021598
|
A | G | 1 | a0001c0001t0001g0151 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.4039-487A>G | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 21/31 | chr3 | 127021598 | ||||||
| chr3:127021655
|
G | T | 1 | a0001c0008t0013g0063 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.4039-430G>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 21/31 | chr3 | 127021655 | ||||||
| chr3:127021701
|
G | A | 12 | a0001c0006t0003g0009a0001c0006t0003g0032a0001c0006t0003g0095others(9): Show | 18 | HG02145.hp2 HG02258.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.4039-384G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 21/31 | chr3 | 127021701 | ||||||
| chr3:127022015
|
C | T | 2 | a0001c0017t0012g0074a0001c0017t0037g0081 | 2 | HG01891.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.4039-70C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 21/31 | chr3 | 127022015 | ||||||
| chr3:127022046
|
G | A | 1 | a0001c0001t0001g0108 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.4039-39G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 21/31 | chr3 | 127022046 | ||||||
| chr3:127022351
|
G | C | 1 | a0001c0001t0001g0145 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.4295+10G>C | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 22/31 | chr3 | 127022351 | ||||||
| chr3:127022352
|
G | A | 1 | a0001c0001t0022g0048 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.4295+11G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 22/31 | chr3 | 127022352 | ||||||
| chr3:127022394
|
T | A | 1 | a0000c0028t0034g0052 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.4295+53T>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 22/31 | chr3 | 127022394 | ||||||
| chr3:127022424
|
G | A | 23 | a0001c0001t0039g0132a0001c0002t0004g0069a0001c0002t0008g0015others(20): Show | 31 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(28): Show |
intron_variant | MODIFIER | c.4295+83G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 22/31 | chr3 | 127022424 | ||||||
| chr3:127022513
|
G | T | 1 | a0000c0028t0034g0052 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.4295+172G>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 22/31 | chr3 | 127022513 | ||||||
| chr3:127022584
|
C | A | 1 | a0001c0038t0038g0158 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.4296-168C>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 22/31 | chr3 | 127022584 | ||||||
| chr3:127022592
|
G | T | 1 | a0001c0001t0001g0138 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.4296-160G>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 22/31 | chr3 | 127022592 | ||||||
| chr3:127022635
|
C | T | 12 | a0001c0001t0001g0003a0001c0001t0001g0116a0001c0001t0001g0118others(9): Show | 21 | HG01069.hp2 HG01074.hp2 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.4296-117C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 22/31 | chr3 | 127022635 | ||||||
| chr3:127022831
|
G | A | 37 | a0000c0028t0034g0052a0001c0002t0002g0002a0001c0002t0002g0013others(34): Show | 59 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.4362+13G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 23/31 | chr3 | 127022831 | ||||||
| chr3:127022856
|
G | T | 1 | a0001c0008t0007g0061 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.4362+38G>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 23/31 | chr3 | 127022856 | ||||||
| chr3:127022897
|
T | C | 37 | a0000c0028t0034g0052a0001c0002t0002g0002a0001c0002t0002g0013others(34): Show | 59 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.4362+79T>C | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 23/31 | chr3 | 127022897 | ||||||
| chr3:127022936
|
C | T | 1 | a0001c0003t0001g0146 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.4362+118C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 23/31 | chr3 | 127022936 | ||||||
| chr3:127023581
|
C | T | 20 | a0001c0001t0039g0132a0001c0002t0004g0069a0001c0004t0004g0010others(17): Show | 26 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(23): Show |
intron_variant | MODIFIER | c.4362+763C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 23/31 | chr3 | 127023581 | ||||||
| chr3:127023737
|
C | T | 2 | a0001c0004t0011g0011a0007c0025t0011g0011 | 5 | HG01496.hp1 HG01981.hp1 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.4362+919C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 23/31 | chr3 | 127023737 | ||||||
| chr3:127023738
|
A | G | 217 | a0000c0028t0034g0052a0001c0001t0001g0001a0001c0001t0001g0003others(214): Show | 345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.4362+920A>G | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 23/31 | chr3 | 127023738 | ||||||
| chr3:127023753
|
C | G | 1 | a0000c0028t0034g0052 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.4362+935C>G | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 23/31 | chr3 | 127023753 | ||||||
| chr3:127023848
|
G | A | 38 | a0000c0028t0034g0052a0001c0002t0002g0002a0001c0002t0002g0013others(35): Show | 60 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.4362+1030G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 23/31 | chr3 | 127023848 | ||||||
| chr3:127023939
|
G | A | 1 | a0001c0004t0004g0043 | 2 | NA18939.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.4362+1121G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 23/31 | chr3 | 127023939 | ||||||
| chr3:127024052
|
G | A | 7 | a0001c0001t0010g0127a0001c0007t0003g0005a0001c0007t0003g0089others(4): Show | 14 | HG00639.hp1 HG01109.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.4362+1234G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 23/31 | chr3 | 127024052 | ||||||
| chr3:127024067
|
T | C | 38 | a0000c0028t0034g0052a0001c0002t0002g0002a0001c0002t0002g0013others(35): Show | 60 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.4362+1249T>C | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 23/31 | chr3 | 127024067 | ||||||
| chr3:127024380
|
G | A | 1 | a0001c0001t0001g0142 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.4362+1562G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 23/31 | chr3 | 127024380 | ||||||
| chr3:127024386
|
G | C | 12 | a0001c0006t0003g0009a0001c0006t0003g0032a0001c0006t0003g0095others(9): Show | 18 | HG02145.hp2 HG02258.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.4362+1568G>C | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 23/31 | chr3 | 127024386 | ||||||
| chr3:127024556
|
G | A | 1 | a0001c0039t0001g0120 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.4362+1738G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 23/31 | chr3 | 127024556 | ||||||
| chr3:127024766
|
C | T | 1 | a0001c0008t0013g0063 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.4362+1948C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 23/31 | chr3 | 127024766 | ||||||
| chr3:127024791
|
C | T | 1 | a0001c0024t0036g0086 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.4362+1973C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 23/31 | chr3 | 127024791 | ||||||
| chr3:127024819
|
T | C | 24 | a0001c0001t0039g0132a0001c0002t0004g0069a0001c0004t0004g0010others(21): Show | 33 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(30): Show |
intron_variant | MODIFIER | c.4362+2001T>C | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 23/31 | chr3 | 127024819 | ||||||
| chr3:127024867
|
C | T | 1 | a0001c0007t0003g0089 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.4362+2049C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 23/31 | chr3 | 127024867 | ||||||
| chr3:127024921
|
T | G | 1 | a0001c0001t0001g0134 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.4362+2103T>G | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 23/31 | chr3 | 127024921 | ||||||
| chr3:127025145
|
C | T | 23 | a0001c0001t0039g0132a0001c0002t0004g0069a0001c0004t0004g0010others(20): Show | 32 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(29): Show |
intron_variant | MODIFIER | c.4362+2327C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 23/31 | chr3 | 127025145 | ||||||
| chr3:127025149
|
G | C | 23 | a0001c0001t0039g0132a0001c0002t0004g0069a0001c0004t0004g0010others(20): Show | 32 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(29): Show |
intron_variant | MODIFIER | c.4362+2331G>C | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 23/31 | chr3 | 127025149 | ||||||
| chr3:127025324
|
C | T | 23 | a0001c0001t0039g0132a0001c0002t0004g0069a0001c0004t0004g0010others(20): Show | 32 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(29): Show |
intron_variant | MODIFIER | c.4362+2506C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 23/31 | chr3 | 127025324 | ||||||
| chr3:127025364
|
T | C | 115 | a0000c0028t0034g0052a0001c0001t0039g0132a0001c0002t0002g0002others(112): Show | 178 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(175): Show |
intron_variant | MODIFIER | c.4362+2546T>C | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 23/31 | chr3 | 127025364 | ||||||
| chr3:127025436
|
A | G | 1 | a0001c0005t0032g0172 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.4363-2504A>G | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 23/31 | chr3 | 127025436 | ||||||
| chr3:127025590
|
T | G | 1 | a0001c0001t0001g0141 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.4363-2350T>G | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 23/31 | chr3 | 127025590 | ||||||
| chr3:127025633
|
A | G | 2 | a0001c0002t0002g0070a0001c0002t0002g0075 | 2 | HG00609.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.4363-2307A>G | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 23/31 | chr3 | 127025633 | ||||||
| chr3:127025709
|
C | T | 2 | a0001c0012t0015g0024a0001c0021t0015g0107 | 4 | HG02055.hp2 HG02257.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.4363-2231C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 23/31 | chr3 | 127025709 | ||||||
| chr3:127025797
|
A | T | 1 | a0001c0024t0036g0086 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.4363-2143A>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 23/31 | chr3 | 127025797 | ||||||
| chr3:127025977
|
A | G | 1 | a0001c0004t0004g0174 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.4363-1963A>G | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 23/31 | chr3 | 127025977 | ||||||
| chr3:127026030
|
C | G | 2 | a0001c0008t0013g0030a0001c0008t0013g0053 | 3 | HG01167.hp2 HG01169.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.4363-1910C>G | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 23/31 | chr3 | 127026030 | ||||||
| chr3:127026135
|
G | T | 1 | a0001c0003t0001g0154 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.4363-1805G>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 23/31 | chr3 | 127026135 | ||||||
| chr3:127026136
|
C | T | 1 | a0001c0004t0004g0177 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.4363-1804C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 23/31 | chr3 | 127026136 | ||||||
| chr3:127026153
|
G | T | 5 | a0001c0008t0007g0029a0001c0008t0007g0061a0001c0008t0018g0014others(2): Show | 8 | HG00140.hp2 HG01069.hp1 HG01070.hp1 others(5): Show |
intron_variant | MODIFIER | c.4363-1787G>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 23/31 | chr3 | 127026153 | ||||||
| chr3:127026291
|
C | T | 1 | a0001c0016t0005g0180 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.4363-1649C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 23/31 | chr3 | 127026291 | ||||||
| chr3:127026400
|
A | G | 12 | a0001c0006t0003g0009a0001c0006t0003g0032a0001c0006t0003g0095others(9): Show | 18 | HG02145.hp2 HG02258.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.4363-1540A>G | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 23/31 | chr3 | 127026400 | ||||||
| chr3:127026574
|
T | C | 1 | a0001c0007t0020g0088 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.4363-1366T>C | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 23/31 | chr3 | 127026574 | ||||||
| chr3:127026757
|
G | A | 2 | a0001c0008t0013g0030a0001c0008t0013g0053 | 3 | HG01167.hp2 HG01169.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.4363-1183G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 23/31 | chr3 | 127026757 | ||||||
| chr3:127026825
|
C | T | 1 | a0001c0001t0001g0161 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.4363-1115C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 23/31 | chr3 | 127026825 | ||||||
| chr3:127026835
|
AC | A | 23 | a0001c0001t0039g0132a0001c0002t0004g0069a0001c0004t0004g0010others(20): Show | 32 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(29): Show |
intron_variant | MODIFIER | c.4363-1101delC | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 23/31 | INFO_REALIGN_3_PRIME | chr3 | 127026835 | |||||
| chr3:127026857
|
G | A | 1 | a0001c0002t0006g0068 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.4363-1083G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 23/31 | chr3 | 127026857 | ||||||
| chr3:127026879
|
TCACCCAG others(7): Show |
T | 1 | a0001c0001t0001g0137 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.4363-1060_4363-104 others(18): Show |
PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 23/31 | chr3 | 127026879 | ||||||
| chr3:127027006
|
A | C | 1 | a0001c0001t0001g0145 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.4363-934A>C | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 23/31 | chr3 | 127027006 | ||||||
| chr3:127027240
|
G | A | 1 | a0001c0014t0002g0092 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.4363-700G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 23/31 | chr3 | 127027240 | ||||||
| chr3:127027254
|
A | G | 2 | a0001c0004t0011g0011a0007c0025t0011g0011 | 5 | HG01496.hp1 HG01981.hp1 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.4363-686A>G | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 23/31 | chr3 | 127027254 | ||||||
| chr3:127027390
|
C | A | 7 | a0001c0001t0010g0124a0001c0001t0010g0125a0001c0001t0010g0126others(4): Show | 7 | NA18979.hp2 NA18984.hp1 NA19063.hp1 others(4): Show |
intron_variant | MODIFIER | c.4363-550C>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 23/31 | chr3 | 127027390 | ||||||
| chr3:127027492
|
G | A | 5 | a0001c0008t0007g0029a0001c0008t0007g0061a0001c0008t0018g0014others(2): Show | 8 | HG00140.hp2 HG01069.hp1 HG01070.hp1 others(5): Show |
intron_variant | MODIFIER | c.4363-448G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 23/31 | chr3 | 127027492 | ||||||
| chr3:127027508
|
T | C | 24 | a0001c0001t0039g0132a0001c0002t0004g0069a0001c0004t0004g0010others(21): Show | 33 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(30): Show |
intron_variant | MODIFIER | c.4363-432T>C | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 23/31 | chr3 | 127027508 | ||||||
| chr3:127027563
|
C | A | 38 | a0000c0028t0034g0052a0001c0002t0002g0002a0001c0002t0002g0013others(35): Show | 60 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.4363-377C>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 23/31 | chr3 | 127027563 | ||||||
| chr3:127027564
|
C | A | 1 | a0001c0001t0001g0137 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.4363-376C>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 23/31 | chr3 | 127027564 | ||||||
| chr3:127027582
|
G | A | 1 | a0001c0038t0038g0158 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.4363-358G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 23/31 | chr3 | 127027582 | ||||||
| chr3:127027587
|
G | T | 1 | a0001c0021t0015g0107 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.4363-353G>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 23/31 | chr3 | 127027587 | ||||||
| chr3:127027671
|
C | T | 2 | a0001c0001t0001g0121a0001c0001t0041g0122 | 2 | HG01074.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.4363-269C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 23/31 | chr3 | 127027671 | ||||||
| chr3:127027847
|
A | G | 94 | a0000c0028t0034g0052a0001c0001t0039g0132a0001c0002t0002g0002others(91): Show | 144 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.4363-93A>G | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 23/31 | chr3 | 127027847 | ||||||
| chr3:127027866
|
C | T | 2 | a0001c0006t0003g0096a0001c0006t0003g0097 | 2 | HG02622.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.4363-74C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 23/31 | chr3 | 127027866 | ||||||
| chr3:127027888
|
T | G | 92 | a0000c0028t0034g0052a0001c0001t0039g0132a0001c0002t0002g0002others(89): Show | 139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.4363-52T>G | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 23/31 | chr3 | 127027888 | ||||||
| chr3:127028093
|
G | A | 3 | a0001c0005t0005g0026a0001c0005t0005g0046a0001c0016t0005g0180 | 4 | HG02132.hp1 NA18947.hp2 NA18999.hp2 others(1): Show |
splice_region_variant&intron_variant | LOW | c.4509+7G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 24/31 | chr3 | 127028093 | ||||||
| chr3:127028158
|
C | G | 23 | a0001c0001t0039g0132a0001c0002t0004g0069a0001c0004t0004g0010others(20): Show | 32 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(29): Show |
intron_variant | MODIFIER | c.4510-23C>G | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 24/31 | chr3 | 127028158 | ||||||
| chr3:127028172
|
C | T | 2 | a0001c0004t0011g0011a0007c0025t0011g0011 | 5 | HG01496.hp1 HG01981.hp1 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.4510-9C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 24/31 | chr3 | 127028172 | ||||||
| chr3:127028177
|
G | A | 3 | a0001c0008t0017g0049a0001c0008t0017g0064a0001c0008t0023g0085 | 3 | HG02258.hp2 HG02886.hp1 NA20300.hp2 |
splice_region_variant&intron_variant | LOW | c.4510-4G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 24/31 | chr3 | 127028177 | ||||||
| chr3:127028367
|
G | T | 1 | a0001c0001t0001g0149 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.4669+27G>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 25/31 | chr3 | 127028367 | ||||||
| chr3:127028491
|
T | G | 1 | a0001c0005t0032g0172 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.4669+151T>G | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 25/31 | chr3 | 127028491 | ||||||
| chr3:127028524
|
T | C | 94 | a0000c0028t0034g0052a0001c0001t0039g0132a0001c0002t0002g0002others(91): Show | 144 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.4669+184T>C | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 25/31 | chr3 | 127028524 | ||||||
| chr3:127028725
|
C | T | 6 | a0001c0008t0013g0030a0001c0008t0013g0053a0001c0008t0013g0063others(3): Show | 7 | HG01167.hp2 HG01169.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.4670-268C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 25/31 | chr3 | 127028725 | ||||||
| chr3:127028904
|
G | A | 2 | a0001c0008t0013g0030a0001c0008t0013g0053 | 3 | HG01167.hp2 HG01169.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.4670-89G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 25/31 | chr3 | 127028904 | ||||||
| chr3:127028937
|
T | C | 2 | a0001c0012t0015g0024a0001c0021t0015g0107 | 4 | HG02055.hp2 HG02257.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.4670-56T>C | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 25/31 | chr3 | 127028937 | ||||||
| chr3:127028983
|
C | A | 2 | a0001c0001t0001g0113a0001c0001t0001g0144 | 2 | HG02074.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.4670-10C>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 25/31 | chr3 | 127028983 | ||||||
| chr3:127029302
|
T | C | 1 | a0001c0038t0038g0158 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.4774-138T>C | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 26/31 | chr3 | 127029302 | ||||||
| chr3:127029308
|
T | C | 217 | a0000c0028t0034g0052a0001c0001t0001g0001a0001c0001t0001g0003others(214): Show | 345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.4774-132T>C | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 26/31 | chr3 | 127029308 | ||||||
| chr3:127029314
|
C | A | 1 | a0001c0004t0019g0170 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.4774-126C>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 26/31 | chr3 | 127029314 | ||||||
| chr3:127029370
|
C | T | 1 | a0001c0038t0038g0158 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.4774-70C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 26/31 | chr3 | 127029370 | ||||||
| chr3:127029387
|
G | T | 6 | a0001c0008t0013g0030a0001c0008t0013g0053a0001c0008t0013g0063others(3): Show | 7 | HG01167.hp2 HG01169.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.4774-53G>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 26/31 | chr3 | 127029387 | ||||||
| chr3:127029597
|
C | T | 1 | a0001c0006t0003g0095 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.4870+61C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 27/31 | chr3 | 127029597 | ||||||
| chr3:127029685
|
A | G | 1 | a0001c0038t0038g0158 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.4870+149A>G | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 27/31 | chr3 | 127029685 | ||||||
| chr3:127029822
|
C | T | 2 | a0001c0012t0015g0024a0001c0021t0015g0107 | 4 | HG02055.hp2 HG02257.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.4871-52C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 27/31 | chr3 | 127029822 | ||||||
| chr3:127029845
|
A | G | 11 | a0001c0008t0007g0029a0001c0008t0007g0061a0001c0008t0013g0030others(8): Show | 15 | HG00140.hp2 HG01069.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.4871-29A>G | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 27/31 | chr3 | 127029845 | ||||||
| chr3:127029846
|
C | T | 20 | a0001c0005t0005g0004a0001c0005t0005g0025a0001c0005t0005g0026others(17): Show | 31 | HG00323.hp2 HG01168.hp2 HG01169.hp2 others(28): Show |
intron_variant | MODIFIER | c.4871-28C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 27/31 | chr3 | 127029846 | ||||||
| chr3:127029849
|
G | A | 7 | a0001c0001t0001g0012a0001c0001t0001g0023a0001c0003t0001g0016others(4): Show | 17 | HG00735.hp2 HG01074.hp1 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.4871-25G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 27/31 | chr3 | 127029849 | ||||||
| chr3:127030100
|
G | A | 1 | a0001c0005t0005g0046 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.5061+36G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 28/31 | chr3 | 127030100 | ||||||
| chr3:127030129
|
G | A | 1 | a0001c0001t0001g0135 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.5061+65G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 28/31 | chr3 | 127030129 | ||||||
| chr3:127030174
|
T | C | 45 | a0001c0001t0039g0132a0001c0002t0004g0069a0001c0004t0004g0010others(42): Show | 65 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(62): Show |
intron_variant | MODIFIER | c.5062-69T>C | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 28/31 | chr3 | 127030174 | ||||||
| chr3:127030236
|
C | T | 20 | a0001c0001t0039g0132a0001c0002t0004g0069a0001c0004t0004g0010others(17): Show | 26 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(23): Show |
splice_region_variant&intron_variant | LOW | c.5062-7C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 28/31 | chr3 | 127030236 | ||||||
| chr3:127030693
|
G | A | 15 | a0001c0001t0001g0104a0001c0002t0004g0069a0001c0004t0004g0010others(12): Show | 20 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(17): Show |
intron_variant | MODIFIER | c.5231+281G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 29/31 | chr3 | 127030693 | ||||||
| chr3:127030724
|
A | G | 1 | a0001c0001t0001g0131 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.5231+312A>G | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 29/31 | chr3 | 127030724 | ||||||
| chr3:127030742
|
C | A | 2 | a0001c0004t0011g0011a0007c0025t0011g0011 | 5 | HG01496.hp1 HG01981.hp1 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.5231+330C>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 29/31 | chr3 | 127030742 | ||||||
| chr3:127030774
|
C | G | 1 | a0001c0038t0038g0158 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.5231+362C>G | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 29/31 | chr3 | 127030774 | ||||||
| chr3:127030869
|
G | A | 2 | a0001c0004t0011g0011a0007c0025t0011g0011 | 5 | HG01496.hp1 HG01981.hp1 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.5231+457G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 29/31 | chr3 | 127030869 | ||||||
| chr3:127030954
|
A | G | 2 | a0001c0003t0001g0035a0001c0036t0001g0140 | 3 | HG00609.hp2 NA18971.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.5231+542A>G | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 29/31 | chr3 | 127030954 | ||||||
| chr3:127030959
|
T | C | 2 | a0001c0004t0011g0011a0007c0025t0011g0011 | 5 | HG01496.hp1 HG01981.hp1 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.5231+547T>C | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 29/31 | chr3 | 127030959 | ||||||
| chr3:127031098
|
C | T | 1 | a0001c0004t0004g0164 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.5231+686C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 29/31 | chr3 | 127031098 | ||||||
| chr3:127031228
|
C | T | 1 | a0001c0003t0001g0153 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.5231+816C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 29/31 | chr3 | 127031228 | ||||||
| chr3:127031229
|
G | A | 4 | a0001c0003t0001g0016a0001c0003t0001g0017a0001c0003t0001g0152others(1): Show | 9 | HG01243.hp1 HG02622.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.5231+817G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 29/31 | chr3 | 127031229 | ||||||
| chr3:127031241
|
G | C | 44 | a0001c0001t0039g0132a0001c0002t0004g0069a0001c0004t0004g0010others(41): Show | 64 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(61): Show |
intron_variant | MODIFIER | c.5231+829G>C | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 29/31 | chr3 | 127031241 | ||||||
| chr3:127031281
|
G | A | 1 | a0001c0024t0036g0086 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.5231+869G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 29/31 | chr3 | 127031281 | ||||||
| chr3:127031291
|
C | G | 6 | a0001c0008t0013g0030a0001c0008t0013g0053a0001c0008t0013g0063others(3): Show | 7 | HG01167.hp2 HG01169.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.5231+879C>G | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 29/31 | chr3 | 127031291 | ||||||
| chr3:127031307
|
C | T | 1 | a0001c0006t0003g0099 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.5231+895C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 29/31 | chr3 | 127031307 | ||||||
| chr3:127031316
|
G | T | 12 | a0001c0006t0003g0009a0001c0006t0003g0032a0001c0006t0003g0095others(9): Show | 18 | HG02145.hp2 HG02258.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.5231+904G>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 29/31 | chr3 | 127031316 | ||||||
| chr3:127031398
|
C | A | 20 | a0001c0001t0039g0132a0001c0002t0004g0069a0001c0004t0004g0010others(17): Show | 26 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(23): Show |
intron_variant | MODIFIER | c.5231+986C>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 29/31 | chr3 | 127031398 | ||||||
| chr3:127031403
|
C | T | 6 | a0001c0008t0013g0030a0001c0008t0013g0053a0001c0008t0013g0063others(3): Show | 7 | HG01167.hp2 HG01169.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.5232-984C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 29/31 | chr3 | 127031403 | ||||||
| chr3:127031496
|
C | A | 2 | a0001c0006t0014g0019a0001c0006t0014g0098 | 4 | HG02451.hp1 HG02647.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.5232-891C>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 29/31 | chr3 | 127031496 | ||||||
| chr3:127031583
|
C | T | 1 | a0001c0002t0006g0080 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.5232-804C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 29/31 | chr3 | 127031583 | ||||||
| chr3:127031759
|
C | T | 20 | a0001c0001t0039g0132a0001c0002t0004g0069a0001c0004t0004g0010others(17): Show | 26 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(23): Show |
intron_variant | MODIFIER | c.5232-628C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 29/31 | chr3 | 127031759 | ||||||
| chr3:127031867
|
G | A | 3 | a0001c0004t0004g0044a0001c0004t0004g0167a0001c0004t0019g0044 | 3 | HG02559.hp1 HG03209.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.5232-520G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 29/31 | chr3 | 127031867 | ||||||
| chr3:127032015
|
G | A | 24 | a0001c0001t0039g0132a0001c0002t0004g0069a0001c0004t0004g0010others(21): Show | 33 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(30): Show |
intron_variant | MODIFIER | c.5232-372G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 29/31 | chr3 | 127032015 | ||||||
| chr3:127032086
|
CTG | C | 2 | a0001c0001t0001g0038a0001c0001t0001g0137 | 3 | NA18986.hp2 NA18997.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.5232-296_5232-295d others(4): Show |
PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 29/31 | INFO_REALIGN_3_PRIME | chr3 | 127032086 | |||||
| chr3:127032153
|
C | T | 12 | a0001c0008t0007g0029a0001c0008t0007g0061a0001c0008t0013g0030others(9): Show | 16 | HG00140.hp2 HG01069.hp1 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.5232-234C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 29/31 | chr3 | 127032153 | ||||||
| chr3:127032211
|
T | A | 1 | a0000c0028t0034g0052 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.5232-176T>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 29/31 | chr3 | 127032211 | ||||||
| chr3:127032266
|
C | T | 1 | a0001c0003t0048g0160 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.5232-121C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 29/31 | chr3 | 127032266 | ||||||
| chr3:127032275
|
G | T | 1 | a0001c0001t0001g0109 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.5232-112G>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 29/31 | chr3 | 127032275 | ||||||
| chr3:127032378
|
C | T | 1 | a0001c0003t0048g0160 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.5232-9C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 29/31 | chr3 | 127032378 | ||||||
| chr3:127032635
|
C | T | 50 | a0001c0001t0039g0132a0001c0002t0004g0069a0001c0004t0004g0010others(47): Show | 71 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.5444+36C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 30/31 | chr3 | 127032635 | ||||||
| chr3:127032845
|
C | A | 1 | a0001c0013t0007g0060 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.5595+9C>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 31/31 | chr3 | 127032845 | ||||||
| chr3:127032846
|
G | A | 217 | a0000c0028t0034g0052a0001c0001t0001g0001a0001c0001t0001g0003others(214): Show | 345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.5595+10G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 31/31 | chr3 | 127032846 | ||||||
| chr3:127033031
|
G | A | 1 | a0001c0006t0001g0020 | 3 | HG01255.hp1 HG02809.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.5595+195G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 31/31 | chr3 | 127033031 | ||||||
| chr3:127033108
|
G | C | 20 | a0001c0001t0039g0132a0001c0002t0004g0069a0001c0004t0004g0010others(17): Show | 26 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(23): Show |
intron_variant | MODIFIER | c.5595+272G>C | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 31/31 | chr3 | 127033108 | ||||||
| chr3:127033127
|
A | G | 1 | a0001c0004t0004g0167 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.5595+291A>G | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 31/31 | chr3 | 127033127 | ||||||
| chr3:127033200
|
C | T | 1 | a0001c0024t0036g0086 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.5595+364C>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 31/31 | chr3 | 127033200 | ||||||
| chr3:127033234
|
T | TG | 2 | a0001c0004t0011g0011a0007c0025t0011g0011 | 5 | HG01496.hp1 HG01981.hp1 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.5595+400dupG | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 31/31 | INFO_REALIGN_3_PRIME | chr3 | 127033234 | |||||
| chr3:127033452
|
G | T | 1 | a0001c0001t0010g0128 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.5596-470G>T | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 31/31 | chr3 | 127033452 | ||||||
| chr3:127033779
|
G | A | 1 | a0001c0001t0001g0136 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.5596-143G>A | PLXNA1 | ENSG00000114554.12 | transcript | ENST00000393409.3 | protein_coding | 31/31 | chr3 | 127033779 |