Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 26130 |
|---|---|
| ensemblid | ENSG00000165219.23 |
| hgncid | 23375 |
| symbol | GAPVD1 |
| name | GTPase activating protein and VPS9 domains 1 |
| refseq_nuc | NM_001282680.3 |
| refseq_prot | NP_001269609.1 |
| ensembl_nuc | ENST00000297933.11 |
| ensembl_prot | ENSP00000297933.6 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 125261826 |
| end | 125367207 |
| strand | + |
| ver | v1.2 |
| region | chr9:125261826-125367207 |
| region5000 | chr9:125256826-125372207 |
| regionname0 | GAPVD1_chr9_125261826_125367207 |
| regionname5000 | GAPVD1_chr9_125256826_125372207 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1460 | 332 | 66 | 53 | 166 | 12 | 33 | 128 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| a0002 | 0/0 | 1460 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| a0003 | 0/0 | 1460 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| a0004 | 0/0 | 1460 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| a0005 | 0/0 | 1460 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| a0006 | 0/0 | 1460 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| a0007 | 0/0 | 1460 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 4383 | 271 | 51 | 41 | 140 | 10 | 28 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| c0002 | 0/0 | 4383 | 31 | 0 | 6 | 24 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| c0003 | 0/0 | 4383 | 17 | 14 | 2 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| c0004 | 1/0 | 4383 | 4 | 0 | 2 | 0 | 1 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| c0005 | 0/0 | 4383 | 3 | 0 | 1 | 0 | 1 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| c0006 | 0/0 | 4383 | 2 | 1 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| c0007 | 0/0 | 4383 | 2 | 0 | 0 | 0 | 0 | 2 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| c0008 | 0/0 | 4383 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| c0009 | 0/0 | 4383 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| c0010 | 0/0 | 4383 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| c0011 | 0/0 | 4383 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| c0012 | 0/0 | 4383 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| c0013 | 0/0 | 4383 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| c0014 | 0/0 | 4383 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| c0015 | 0/0 | 4383 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| c0016 | 0/0 | 4383 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| c0017 | 0/0 | 4383 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 4795 | 130 | 34 | 17 | 56 | 4 | 19 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| t0002 | 1/0 | 4794 | 98 | 3 | 13 | 64 | 6 | 11 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| t0003 | 0/0 | 4795 | 20 | 0 | 0 | 19 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| t0004 | 0/0 | 4794 | 13 | 11 | 2 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| t0005 | 0/0 | 4795 | 13 | 0 | 0 | 13 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| t0006 | 0/0 | 4793 | 12 | 9 | 2 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| t0007 | 0/0 | 4794 | 10 | 0 | 5 | 5 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| t0008 | 0/0 | 4794 | 5 | 0 | 5 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| t0009 | 0/0 | 4793 | 3 | 3 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| t0010 | 0/0 | 4795 | 3 | 0 | 1 | 0 | 2 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| t0011 | 0/0 | 4794 | 2 | 1 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| t0012 | 0/0 | 4794 | 2 | 0 | 2 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| t0013 | 0/0 | 4794 | 2 | 1 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| t0014 | 0/1 | 4795 | 2 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| t0015 | 0/0 | 4793 | 2 | 0 | 0 | 1 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| t0016 | 0/0 | 4795 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| t0017 | 0/0 | 4794 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| t0018 | 0/0 | 4794 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| t0019 | 0/0 | 4794 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| t0020 | 0/0 | 4794 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| t0021 | 0/0 | 4795 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| t0022 | 0/0 | 4795 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| t0023 | 0/0 | 4795 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| t0024 | 0/0 | 4795 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| t0025 | 0/0 | 4795 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| t0026 | 0/0 | 4793 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| t0027 | 0/0 | 4793 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| t0028 | 0/0 | 4794 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| t0029 | 0/0 | 4794 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| t0030 | 0/0 | 4795 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| t0031 | 0/0 | 4794 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| t0032 | 0/0 | 4795 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| t0033 | 0/0 | 4794 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| t0034 | 0/0 | 4795 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| t0035 | 0/0 | 4795 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| t0036 | 0/0 | 4794 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| t0037 | 0/0 | 4793 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| t0038 | 0/0 | 4794 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0019 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0259 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 4383 | 271 | 51 | 41 | 140 | 10 | 28 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| a0001c0002 | 0/0 | 4383 | 31 | 0 | 6 | 24 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| a0001c0003 | 0/0 | 4383 | 17 | 14 | 2 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| a0001c0004 | 1/0 | 4383 | 4 | 0 | 2 | 0 | 1 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| a0001c0005 | 0/0 | 4383 | 3 | 0 | 1 | 0 | 1 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| a0001c0009 | 0/0 | 4383 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| a0001c0010 | 0/0 | 4383 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| a0001c0012 | 0/0 | 4383 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| a0001c0013 | 0/0 | 4383 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| a0001c0014 | 0/0 | 4383 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| a0001c0016 | 0/0 | 4383 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| a0002c0006 | 0/0 | 4383 | 2 | 1 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| a0003c0007 | 0/0 | 4383 | 2 | 0 | 0 | 0 | 0 | 2 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| a0004c0008 | 0/0 | 4383 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| a0005c0015 | 0/0 | 4383 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| a0006c0011 | 0/0 | 4383 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| a0007c0017 | 0/0 | 4383 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 9177 | 120 | 33 | 15 | 55 | 2 | 15 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| a0001c0001t0002 | 0/0 | 9176 | 92 | 3 | 11 | 62 | 6 | 10 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| a0001c0001t0004 | 0/0 | 9176 | 9 | 7 | 2 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| a0001c0001t0005 | 0/0 | 9177 | 12 | 0 | 0 | 12 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| a0001c0001t0008 | 0/0 | 9176 | 5 | 0 | 5 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| a0001c0001t0009 | 0/0 | 9175 | 3 | 3 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| a0001c0001t0010 | 0/0 | 9177 | 3 | 0 | 1 | 0 | 2 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| a0001c0001t0012 | 0/0 | 9176 | 2 | 0 | 2 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| a0001c0001t0013 | 0/0 | 9176 | 2 | 1 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| a0001c0001t0014 | 0/1 | 9177 | 2 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| a0001c0001t0015 | 0/0 | 9175 | 2 | 0 | 0 | 1 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| a0001c0001t0016 | 0/0 | 9177 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| a0001c0001t0017 | 0/0 | 9176 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| a0001c0001t0019 | 0/0 | 9176 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| a0001c0001t0020 | 0/0 | 9176 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| a0001c0001t0021 | 0/0 | 9177 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| a0001c0001t0022 | 0/0 | 9177 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| a0001c0001t0023 | 0/0 | 9177 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| a0001c0001t0024 | 0/0 | 9177 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| a0001c0001t0025 | 0/0 | 9177 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| a0001c0001t0027 | 0/0 | 9175 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| a0001c0001t0028 | 0/0 | 9176 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| a0001c0001t0029 | 0/0 | 9176 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| a0001c0001t0030 | 0/0 | 9177 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| a0001c0001t0031 | 0/0 | 9176 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| a0001c0001t0032 | 0/0 | 9177 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| a0001c0001t0033 | 0/0 | 9176 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| a0001c0001t0034 | 0/0 | 9177 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| a0001c0001t0035 | 0/0 | 9177 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| a0001c0001t0036 | 0/0 | 9176 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| a0001c0002t0003 | 0/0 | 9177 | 20 | 0 | 0 | 19 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| a0001c0002t0007 | 0/0 | 9176 | 10 | 0 | 5 | 5 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| a0001c0002t0038 | 0/0 | 9176 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| a0001c0003t0004 | 0/0 | 9176 | 4 | 4 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| a0001c0003t0006 | 0/0 | 9175 | 11 | 8 | 2 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| a0001c0003t0018 | 0/0 | 9176 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| a0001c0003t0026 | 0/0 | 9175 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| a0001c0004t0001 | 0/0 | 9177 | 1 | 0 | 0 | 0 | 1 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| a0001c0004t0002 | 1/0 | 9176 | 3 | 0 | 2 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| a0001c0005t0001 | 0/0 | 9177 | 3 | 0 | 1 | 0 | 1 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| a0001c0009t0001 | 0/0 | 9177 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| a0001c0010t0006 | 0/0 | 9175 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| a0001c0012t0001 | 0/0 | 9177 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| a0001c0013t0002 | 0/0 | 9176 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| a0001c0014t0001 | 0/0 | 9177 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| a0001c0016t0037 | 0/0 | 9175 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| a0002c0006t0011 | 0/0 | 9176 | 2 | 1 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| a0003c0007t0001 | 0/0 | 9177 | 2 | 0 | 0 | 0 | 0 | 2 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| a0004c0008t0002 | 0/0 | 9176 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| a0005c0015t0002 | 0/0 | 9176 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| a0006c0011t0005 | 0/0 | 9177 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| a0007c0017t0001 | 0/0 | 9177 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | copy fasta | chr9 | 125256826 | 125372207 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0004g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0004g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0004g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0004g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0004g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0004g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0004g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0004g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0004g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0005g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0005g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0005g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0005g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0005g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0005g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0005g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0005g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0005g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0005g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0005g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0005g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0008g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0008g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0008g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0008g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0008g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0009g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0009g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0009g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0010g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0010g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0010g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0012g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0012g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0013g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0013g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0014g0259 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0014g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0015g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0015g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0016g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0017g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0019g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0020g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0021g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0022g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0023g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0024g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0025g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0027g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0028g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0029g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0030g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0031g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0032g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0033g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0034g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0035g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0001t0036g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0002t0003g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0002t0003g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0002t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0002t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0002t0003g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0002t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0002t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0002t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0002t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0002t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0002t0003g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0002t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0002t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0002t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0002t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0002t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0002t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0002t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0002t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0002t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0002t0007g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0002t0007g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0002t0007g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0002t0007g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0002t0007g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0002t0007g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0002t0007g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0002t0007g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0002t0007g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0002t0007g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0002t0038g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0003t0004g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0003t0004g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0003t0004g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0003t0004g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0003t0006g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0003t0006g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0003t0006g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0003t0006g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0003t0006g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0003t0006g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0003t0006g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0003t0006g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0003t0006g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0003t0006g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0003t0006g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0003t0018g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0003t0026g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0004t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0004t0002g0019 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0004t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0004t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0005t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0005t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0005t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0009t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0010t0006g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0012t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0013t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0014t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0001c0016t0037g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0002c0006t0011g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0002c0006t0011g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0003c0007t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0003c0007t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0004c0008t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0005c0015t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0006c0011t0005g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| a0007c0017t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0225 | EUR | GBR | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0066 | EUR | GBR | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0032 | EUR | GBR | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0223 | EUR | GBR | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG00280 | hp1 | a0001 | c0005 | t0001 | g0231 | EUR | FIN | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0048 | EUR | FIN | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | CHS | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0105 | EAS | CHS | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | CHS | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | CHS | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | CHS | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0086 | EAS | CHS | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | CHS | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG00544 | hp2 | a0001 | c0002 | t0007 | g0142 | EAS | CHS | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | CHS | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG00558 | hp2 | a0001 | c0001 | t0027 | g0222 | EAS | CHS | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0095 | EAS | CHS | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | CHS | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG00621 | hp1 | a0001 | c0002 | t0003 | g0144 | EAS | CHS | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0324 | EAS | CHS | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0269 | AMR | PUR | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0260 | AMR | PUR | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG00642 | hp1 | a0001 | c0001 | t0012 | g0099 | AMR | PUR | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0254 | AMR | PUR | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG00673 | hp1 | a0001 | c0001 | t0029 | g0073 | EAS | CHS | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | CHS | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG00733 | hp1 | a0001 | c0001 | t0025 | g0207 | AMR | PUR | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0063 | AMR | PUR | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0079 | AMR | PUR | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0242 | AMR | PUR | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG00738 | hp1 | a0001 | c0001 | t0021 | g0189 | AMR | PUR | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG00738 | hp2 | a0001 | c0001 | t0012 | g0101 | AMR | PUR | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0044 | AMR | PUR | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG00741 | hp2 | a0001 | c0001 | t0014 | g0263 | AMR | PUR | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG01069 | hp1 | a0001 | c0001 | t0004 | g0011 | AMR | PUR | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0061 | AMR | PUR | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG01074 | hp2 | a0001 | c0004 | t0002 | g0041 | AMR | PUR | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0226 | AMR | PUR | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG01081 | hp2 | a0001 | c0002 | t0007 | g0133 | AMR | PUR | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG01099 | hp1 | a0001 | c0001 | t0004 | g0174 | AMR | PUR | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG01109 | hp1 | a0001 | c0003 | t0006 | g0161 | AMR | PUR | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG01109 | hp2 | a0002 | c0006 | t0011 | g0122 | AMR | PUR | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG01167 | hp1 | a0001 | c0003 | t0006 | g0166 | AMR | PUR | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0264 | AMR | PUR | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0155 | AMR | PUR | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG01175 | hp2 | a0001 | c0001 | t0010 | g0255 | AMR | PUR | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0036 | AMR | PUR | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0090 | AMR | PUR | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0261 | AMR | PUR | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG01243 | hp2 | a0001 | c0009 | t0001 | g0190 | AMR | PUR | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0278 | AMR | CLM | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG01255 | hp2 | a0001 | c0002 | t0007 | g0135 | AMR | CLM | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG01257 | hp1 | a0001 | c0002 | t0038 | g0141 | AMR | CLM | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0234 | AMR | CLM | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | CLM | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0235 | AMR | CLM | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0257 | AMR | CLM | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0033 | AMR | CLM | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0072 | AMR | CLM | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG01346 | hp2 | a0001 | c0001 | t0008 | g0112 | AMR | CLM | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | CLM | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG01358 | hp2 | a0001 | c0001 | t0016 | g0046 | AMR | CLM | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG01361 | hp1 | a0001 | c0001 | t0008 | g0047 | AMR | CLM | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG01361 | hp2 | a0001 | c0002 | t0007 | g0124 | AMR | CLM | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG01496 | hp1 | a0001 | c0001 | t0008 | g0110 | AMR | CLM | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG01496 | hp2 | a0001 | c0004 | t0002 | g0042 | AMR | CLM | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG01515 | hp1 | a0001 | c0001 | t0010 | g0266 | EUR | IBS | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0175 | EUR | IBS | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG01517 | hp1 | a0001 | c0001 | t0010 | g0216 | EUR | IBS | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG01517 | hp2 | a0001 | c0004 | t0001 | g0035 | EUR | IBS | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG01884 | hp1 | a0001 | c0003 | t0006 | g0158 | AFR | ACB | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG01884 | hp2 | a0001 | c0001 | t0009 | g0002 | AFR | ACB | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | PEL | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG01993 | hp2 | a0001 | c0002 | t0007 | g0137 | AMR | PEL | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02004 | hp1 | a0001 | c0001 | t0023 | g0301 | AMR | PEL | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02004 | hp2 | a0001 | c0005 | t0001 | g0219 | AMR | PEL | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02027 | hp1 | a0001 | c0002 | t0003 | g0123 | EAS | KHV | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | KHV | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | ACB | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02055 | hp2 | a0001 | c0003 | t0026 | g0118 | AFR | ACB | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | KHV | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | KHV | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | KHV | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | KHV | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02074 | hp1 | a0001 | c0002 | t0003 | g0130 | EAS | KHV | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0103 | EAS | KHV | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0100 | EAS | KHV | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | KHV | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02129 | hp1 | a0001 | c0001 | t0005 | g0340 | EAS | KHV | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02129 | hp2 | a0001 | c0002 | t0003 | g0134 | EAS | KHV | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | KHV | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02132 | hp2 | a0001 | c0001 | t0031 | g0102 | EAS | KHV | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02135 | hp1 | a0001 | c0001 | t0030 | g0120 | EAS | KHV | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0108 | EAS | KHV | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | CDX | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0111 | EAS | CDX | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02257 | hp1 | a0001 | c0001 | t0004 | g0173 | AFR | ACB | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0049 | AFR | ACB | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02258 | hp1 | a0001 | c0003 | t0018 | g0165 | AFR | ACB | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0297 | AFR | ACB | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0247 | AFR | ACB | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02280 | hp2 | a0001 | c0003 | t0006 | g0160 | AFR | ACB | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02300 | hp1 | a0001 | c0001 | t0008 | g0031 | AMR | PEL | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0311 | AMR | PEL | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0319 | AFR | ACB | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02451 | hp2 | a0001 | c0003 | t0004 | g0157 | AFR | ACB | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0253 | AFR | GWD | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02572 | hp2 | a0001 | c0003 | t0006 | g0162 | AFR | GWD | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02602 | hp1 | a0004 | c0008 | t0002 | g0083 | SAS | PJL | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0227 | SAS | PJL | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | GWD | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02615 | hp2 | a0001 | c0001 | t0004 | g0009 | AFR | GWD | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02622 | hp1 | a0001 | c0003 | t0004 | g0170 | AFR | GWD | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0322 | AFR | GWD | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02630 | hp1 | a0001 | c0001 | t0017 | g0013 | AFR | GWD | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | GWD | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02683 | hp1 | a0001 | c0016 | t0037 | g0152 | SAS | PJL | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0221 | SAS | PJL | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0215 | SAS | PJL | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0290 | SAS | PJL | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0318 | AFR | GWD | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02717 | hp2 | a0001 | c0001 | t0013 | g0198 | AFR | GWD | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02723 | hp1 | a0001 | c0001 | t0004 | g0008 | AFR | GWD | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02723 | hp2 | a0007 | c0017 | t0001 | g0250 | AFR | GWD | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02735 | hp1 | a0001 | c0001 | t0034 | g0217 | SAS | PJL | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0034 | SAS | PJL | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0262 | AFR | GWD | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02818 | hp2 | a0001 | c0001 | t0004 | g0007 | AFR | GWD | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0265 | AFR | GWD | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02895 | hp2 | a0001 | c0003 | t0006 | g0169 | AFR | GWD | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02897 | hp1 | a0001 | c0003 | t0006 | g0172 | AFR | GWD | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02897 | hp2 | a0001 | c0001 | t0019 | g0208 | AFR | GWD | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | ESN | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02922 | hp2 | a0001 | c0003 | t0006 | g0159 | AFR | ESN | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02970 | hp1 | a0001 | c0001 | t0004 | g0010 | AFR | ESN | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0298 | AFR | ESN | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0084 | SAS | PJL | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG03017 | hp2 | a0003 | c0007 | t0001 | g0308 | SAS | PJL | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | GWD | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG03041 | hp2 | a0001 | c0001 | t0024 | g0194 | AFR | GWD | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG03098 | hp1 | a0002 | c0006 | t0011 | g0121 | AFR | MSL | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0251 | AFR | MSL | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0320 | AFR | ESN | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0069 | AFR | ESN | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0317 | AFR | ESN | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG03195 | hp2 | a0001 | c0003 | t0006 | g0168 | AFR | ESN | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG03209 | hp1 | a0001 | c0003 | t0004 | g0156 | AFR | MSL | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | MSL | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG03225 | hp1 | a0001 | c0001 | t0009 | g0001 | AFR | MSL | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0249 | AFR | MSL | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | MSL | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG03453 | hp2 | a0001 | c0001 | t0004 | g0006 | AFR | MSL | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG03486 | hp1 | a0001 | c0001 | t0032 | g0295 | AFR | MSL | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG03486 | hp2 | a0001 | c0003 | t0004 | g0164 | AFR | MSL | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0117 | SAS | PJL | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0267 | SAS | PJL | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0240 | SAS | PJL | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0078 | SAS | PJL | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG03540 | hp1 | a0001 | c0003 | t0006 | g0171 | AFR | GWD | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0299 | AFR | GWD | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG03579 | hp1 | a0001 | c0001 | t0004 | g0012 | AFR | MSL | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | MSL | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG03654 | hp1 | a0001 | c0001 | t0022 | g0279 | SAS | PJL | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0213 | SAS | PJL | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0300 | SAS | STU | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0059 | SAS | STU | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG03704 | hp1 | a0003 | c0007 | t0001 | g0302 | SAS | PJL | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0097 | SAS | PJL | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0291 | SAS | PJL | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG03710 | hp2 | a0001 | c0003 | t0006 | g0163 | SAS | PJL | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0065 | SAS | BEB | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0214 | SAS | BEB | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0288 | SAS | BEB | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0098 | SAS | BEB | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0232 | SAS | STU | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0312 | SAS | STU | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG04184 | hp1 | a0001 | c0005 | t0001 | g0199 | SAS | BEB | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG04184 | hp2 | a0001 | c0012 | t0001 | g0282 | SAS | BEB | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0092 | SAS | STU | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0230 | SAS | STU | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0091 | SAS | STU | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG04228 | hp2 | a0001 | c0002 | t0003 | g0126 | SAS | STU | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | CHB | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | CHB | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | CHB | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18747 | hp2 | a0001 | c0001 | t0005 | g0331 | EAS | CHB | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18939 | hp1 | a0001 | c0002 | t0003 | g0132 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0314 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18940 | hp1 | a0001 | c0002 | t0003 | g0138 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18949 | hp2 | a0001 | c0002 | t0003 | g0140 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18950 | hp1 | a0001 | c0001 | t0005 | g0332 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18954 | hp2 | a0001 | c0001 | t0035 | g0303 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18957 | hp2 | a0001 | c0014 | t0001 | g0233 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18959 | hp2 | a0001 | c0013 | t0002 | g0043 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18961 | hp1 | a0001 | c0001 | t0005 | g0339 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18962 | hp1 | a0001 | c0001 | t0036 | g0088 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18962 | hp2 | a0001 | c0001 | t0020 | g0335 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18964 | hp1 | a0001 | c0002 | t0007 | g0143 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18965 | hp1 | a0001 | c0002 | t0003 | g0139 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18966 | hp1 | a0001 | c0002 | t0003 | g0145 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18967 | hp2 | a0001 | c0001 | t0028 | g0154 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18968 | hp1 | a0001 | c0002 | t0007 | g0129 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18970 | hp2 | a0001 | c0002 | t0003 | g0127 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18972 | hp2 | a0001 | c0001 | t0005 | g0338 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18974 | hp1 | a0006 | c0011 | t0005 | g0337 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0309 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18979 | hp2 | a0001 | c0002 | t0003 | g0004 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18980 | hp1 | a0001 | c0001 | t0005 | g0307 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18982 | hp2 | a0001 | c0001 | t0005 | g0328 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18986 | hp1 | a0005 | c0015 | t0002 | g0057 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18986 | hp2 | a0001 | c0002 | t0003 | g0151 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18988 | hp1 | a0001 | c0002 | t0003 | g0146 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18989 | hp1 | a0001 | c0002 | t0003 | g0147 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18990 | hp2 | a0001 | c0001 | t0005 | g0333 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18991 | hp1 | a0001 | c0002 | t0003 | g0005 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0258 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA19002 | hp1 | a0001 | c0002 | t0003 | g0148 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA19002 | hp2 | a0001 | c0001 | t0005 | g0329 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA19005 | hp2 | a0001 | c0002 | t0003 | g0131 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA19007 | hp2 | a0001 | c0002 | t0003 | g0128 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA19010 | hp1 | a0001 | c0001 | t0005 | g0330 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA19012 | hp2 | a0001 | c0002 | t0003 | g0125 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0245 | AFR | LWK | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA19043 | hp2 | a0001 | c0010 | t0006 | g0167 | AFR | LWK | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA19054 | hp1 | a0001 | c0002 | t0007 | g0136 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA19055 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA19060 | hp2 | a0001 | c0001 | t0015 | g0060 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA19082 | hp2 | a0001 | c0001 | t0005 | g0336 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA19087 | hp2 | a0001 | c0002 | t0007 | g0149 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA19088 | hp1 | a0001 | c0001 | t0033 | g0056 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA19089 | hp1 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA19089 | hp2 | a0001 | c0001 | t0013 | g0191 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA19091 | hp1 | a0001 | c0001 | t0005 | g0334 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0296 | AFR | ASW | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | ASW | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0080 | EUR | TSI | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0085 | EUR | TSI | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA20905 | hp1 | a0001 | c0001 | t0015 | g0064 | SAS | GIH | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0202 | SAS | GIH | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG01123 | hp1 | a0001 | c0002 | t0007 | g0150 | AMR | CLM | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG01123 | hp2 | a0001 | c0001 | t0008 | g0050 | AMR | CLM | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | ACB | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | ACB | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02486 | hp1 | a0001 | c0001 | t0009 | g0003 | AFR | ACB | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0323 | AFR | ACB | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0321 | AFR | ACB | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0326 | AFR | ACB | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0067 | AFR | MSL | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | MSL | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0246 | AFR | LWK | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0325 | AFR | LWK | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0014 | g0259 | REF | REF | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| homoSapiens_grch38 | hp1 | a0001 | c0004 | t0002 | g0019 | REF | REF | GAPVD1_chr9_125256826_125372207 | GAPVD1 | chr9 | 125256826 | 125372207 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:125302143
|
G | T | 1 | a0003 | 2 | HG03017.hp2 HG03704.hp1 |
missense_variant | MODERATE | c.346G>T | p.Ala116Ser | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 5/28 | 678/9176 | 346/4383 | 116/1460 | chr9 | 125302143 | ||
| chr9:125302647
|
G | A | 1 | a0004 | 1 | HG02602.hp1 | missense_variant | MODERATE | c.850G>A | p.Val284Met | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 5/28 | 1182/9176 | 850/4383 | 284/1460 | chr9 | 125302647 | ||
| chr9:125307821
|
A | G | 1 | a0007 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.1382A>G | p.Asn461Ser | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 8/28 | 1714/9176 | 1382/4383 | 461/1460 | chr9 | 125307821 | ||
| chr9:125321493
|
C | A | 1 | a0006 | 1 | NA18974.hp1 | missense_variant | MODERATE | c.1663C>A | p.Leu555Ile | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 10/28 | 1995/9176 | 1663/4383 | 555/1460 | chr9 | 125321493 | ||
| chr9:125321494
|
T | C | 1 | a0006 | 1 | NA18974.hp1 | missense_variant | MODERATE | c.1664T>C | p.Leu555Pro | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 10/28 | 1996/9176 | 1664/4383 | 555/1460 | chr9 | 125321494 | ||
| chr9:125326463
|
C | T | 1 | a0005 | 1 | NA18986.hp1 | missense_variant | MODERATE | c.1906C>T | p.Arg636Cys | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 12/28 | 2238/9176 | 1906/4383 | 636/1460 | chr9 | 125326463 | ||
| chr9:125337505
|
C | T | 1 | a0002 | 2 | HG01109.hp2 HG03098.hp1 |
missense_variant | MODERATE | c.2791C>T | p.Pro931Ser | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 17/28 | 3123/9176 | 2791/4383 | 931/1460 | chr9 | 125337505 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:125302394
|
T | G | 1 | a0001c0002 | 31 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(28): Show |
synonymous_variant | LOW | c.597T>G | p.Thr199Thr | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 5/28 | 929/9176 | 597/4383 | 199/1460 | chr9 | 125302394 | ||
| chr9:125302676
|
T | C | 1 | a0001c0009 | 1 | HG01243.hp2 | synonymous_variant | LOW | c.879T>C | p.Cys293Cys | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 5/28 | 1211/9176 | 879/4383 | 293/1460 | chr9 | 125302676 | ||
| chr9:125305140
|
G | A | 2 | a0001c0003a0001c0010 | 18 | HG01109.hp1 HG01167.hp1 HG01884.hp1 others(15): Show |
synonymous_variant | LOW | c.1107G>A | p.Lys369Lys | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 6/28 | 1439/9176 | 1107/4383 | 369/1460 | chr9 | 125305140 | ||
| chr9:125307424
|
C | A | 1 | a0001c0005 | 3 | HG00280.hp1 HG02004.hp2 HG04184.hp1 |
synonymous_variant | LOW | c.1128C>A | p.Ala376Ala | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 7/28 | 1460/9176 | 1128/4383 | 376/1460 | chr9 | 125307424 | ||
| chr9:125312468
|
C | T | 1 | a0001c0016 | 1 | HG02683.hp1 | synonymous_variant | LOW | c.1458C>T | p.Ser486Ser | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/28 | 1790/9176 | 1458/4383 | 486/1460 | chr9 | 125312468 | ||
| chr9:125312528
|
T | C | 16 | a0001c0001a0001c0002a0001c0003others(13): Show | 336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
synonymous_variant | LOW | c.1518T>C | p.Ile506Ile | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/28 | 1850/9176 | 1518/4383 | 506/1460 | chr9 | 125312528 | ||
| chr9:125321495
|
C | T | 1 | a0006c0011 | 1 | NA18974.hp1 | synonymous_variant | LOW | c.1665C>T | p.Leu555Leu | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 10/28 | 1997/9176 | 1665/4383 | 555/1460 | chr9 | 125321495 | ||
| chr9:125330154
|
T | C | 1 | a0001c0012 | 1 | HG04184.hp2 | synonymous_variant | LOW | c.2109T>C | p.Thr703Thr | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 13/28 | 2441/9176 | 2109/4383 | 703/1460 | chr9 | 125330154 | ||
| chr9:125350855
|
G | C | 1 | a0001c0013 | 1 | NA18959.hp2 | synonymous_variant | LOW | c.3552G>C | p.Ser1184Ser | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 23/28 | 3884/9176 | 3552/4383 | 1184/1460 | chr9 | 125350855 | ||
| chr9:125355660
|
C | T | 1 | a0001c0010 | 1 | NA19043.hp2 | synonymous_variant | LOW | c.3774C>T | p.Thr1258Thr | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 25/28 | 4106/9176 | 3774/4383 | 1258/1460 | chr9 | 125355660 | ||
| chr9:125362614
|
A | G | 1 | a0001c0014 | 1 | NA18957.hp2 | synonymous_variant | LOW | c.4251A>G | p.Pro1417Pro | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 28/28 | 4583/9176 | 4251/4383 | 1417/1460 | chr9 | 125362614 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:125261865
|
C | G | 3 | a0001c0002t0003a0001c0002t0007a0001c0002t0038 | 31 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(28): Show |
5_prime_UTR_variant | MODIFIER | c.-293C>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/28 | 37057 | chr9 | 125261865 | |||||
| chr9:125261952
|
C | G | 1 | a0001c0016t0037 | 1 | HG02683.hp1 | 5_prime_UTR_variant | MODIFIER | c.-206C>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/28 | 36970 | chr9 | 125261952 | |||||
| chr9:125295535
|
C | T | 1 | a0001c0001t0036 | 1 | NA18962.hp1 | 5_prime_UTR_variant | MODIFIER | c.-72C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 3/28 | 3387 | chr9 | 125295535 | |||||
| chr9:125362859
|
A | G | 1 | a0001c0001t0035 | 1 | NA18954.hp2 | 3_prime_UTR_variant | MODIFIER | c.*113A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 28/28 | 113 | chr9 | 125362859 | |||||
| chr9:125363149
|
A | G | 1 | a0001c0016t0037 | 1 | HG02683.hp1 | 3_prime_UTR_variant | MODIFIER | c.*403A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 28/28 | 403 | chr9 | 125363149 | |||||
| chr9:125363198
|
C | T | 1 | a0001c0001t0034 | 1 | HG02735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*452C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 28/28 | 452 | chr9 | 125363198 | |||||
| chr9:125363228
|
C | T | 1 | a0001c0001t0008 | 5 | HG01123.hp2 HG01346.hp2 HG01361.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*482C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 28/28 | 482 | chr9 | 125363228 | |||||
| chr9:125363471
|
G | A | 1 | a0001c0001t0008 | 5 | HG01123.hp2 HG01346.hp2 HG01361.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*725G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 28/28 | 725 | chr9 | 125363471 | |||||
| chr9:125363767
|
C | G | 1 | a0001c0001t0033 | 1 | NA19088.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1021C>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 28/28 | 1021 | chr9 | 125363767 | |||||
| chr9:125363919
|
A | G | 1 | a0001c0016t0037 | 1 | HG02683.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1173A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 28/28 | 1173 | chr9 | 125363919 | |||||
| chr9:125364032
|
C | T | 1 | a0001c0001t0032 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1286C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 28/28 | 1286 | chr9 | 125364032 | |||||
| chr9:125364064
|
T | A | 6 | a0001c0001t0016a0001c0002t0003a0001c0002t0007others(3): Show | 35 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*1318T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 28/28 | 1318 | chr9 | 125364064 | |||||
| chr9:125364096
|
G | A | 1 | a0001c0001t0012 | 2 | HG00642.hp1 HG00738.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1350G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 28/28 | 1350 | chr9 | 125364096 | |||||
| chr9:125364103
|
G | A | 4 | a0001c0001t0016a0001c0002t0003a0001c0002t0007others(1): Show | 32 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*1357G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 28/28 | 1357 | chr9 | 125364103 | |||||
| chr9:125364368
|
G | C | 37 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(34): Show | 226 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(223): Show |
3_prime_UTR_variant | MODIFIER | c.*1622G>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 28/28 | 1622 | chr9 | 125364368 | |||||
| chr9:125364382
|
C | G | 1 | a0001c0001t0031 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1636C>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 28/28 | 1636 | chr9 | 125364382 | |||||
| chr9:125364672
|
C | T | 1 | a0002c0006t0011 | 2 | HG01109.hp2 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1926C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 28/28 | 1926 | chr9 | 125364672 | |||||
| chr9:125364758
|
G | A | 1 | a0001c0001t0009 | 3 | HG01884.hp2 HG02486.hp1 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2012G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 28/28 | 2012 | chr9 | 125364758 | |||||
| chr9:125364832
|
C | T | 1 | a0001c0003t0026 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2086C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 28/28 | 2086 | chr9 | 125364832 | |||||
| chr9:125365059
|
G | T | 1 | a0001c0016t0037 | 1 | HG02683.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2313G>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 28/28 | 2313 | chr9 | 125365059 | |||||
| chr9:125365133
|
A | G | 30 | a0001c0001t0001a0001c0001t0005a0001c0001t0010others(27): Show | 196 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(193): Show |
3_prime_UTR_variant | MODIFIER | c.*2387A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 28/28 | 2387 | chr9 | 125365133 | |||||
| chr9:125365318
|
A | AT | 23 | a0001c0001t0001a0001c0001t0005a0001c0001t0010others(20): Show | 178 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(175): Show |
3_prime_UTR_variant | MODIFIER | c.*2589dupT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 28/28 | 2590 | INFO_REALIGN_3_PRIME | chr9 | 125365318 | ||||
| chr9:125365318
|
AT | A | 7 | a0001c0001t0009a0001c0001t0015a0001c0001t0027others(4): Show | 20 | HG00558.hp2 HG01109.hp1 HG01167.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*2589delT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 28/28 | 2589 | INFO_REALIGN_3_PRIME | chr9 | 125365318 | ||||
| chr9:125365724
|
C | T | 3 | a0001c0001t0005a0001c0001t0020a0006c0011t0005 | 14 | HG02129.hp1 NA18747.hp2 NA18950.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*2978C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 28/28 | 2978 | chr9 | 125365724 | |||||
| chr9:125365737
|
C | G | 1 | a0001c0001t0010 | 3 | HG01175.hp2 HG01515.hp1 HG01517.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2991C>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 28/28 | 2991 | chr9 | 125365737 | |||||
| chr9:125365805
|
A | T | 1 | a0001c0001t0027 | 1 | HG00558.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3059A>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 28/28 | 3059 | chr9 | 125365805 | |||||
| chr9:125365928
|
C | T | 1 | a0001c0001t0025 | 1 | HG00733.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3182C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 28/28 | 3182 | chr9 | 125365928 | |||||
| chr9:125366148
|
A | G | 1 | a0001c0001t0014 | 2 | HG00741.hp2 homoSapiens_chm13v2.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3402A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 28/28 | 3402 | chr9 | 125366148 | |||||
| chr9:125366207
|
C | T | 1 | a0001c0001t0029 | 1 | HG00673.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3461C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 28/28 | 3461 | chr9 | 125366207 | |||||
| chr9:125366229
|
G | A | 1 | a0001c0001t0009 | 3 | HG01884.hp2 HG02486.hp1 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3483G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 28/28 | 3483 | chr9 | 125366229 | |||||
| chr9:125366239
|
G | A | 1 | a0001c0002t0038 | 1 | HG01257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3493G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 28/28 | 3493 | chr9 | 125366239 | |||||
| chr9:125366290
|
C | T | 1 | a0001c0001t0019 | 1 | HG02897.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3544C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 28/28 | 3544 | chr9 | 125366290 | |||||
| chr9:125366291
|
G | A | 1 | a0001c0001t0017 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3545G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 28/28 | 3545 | chr9 | 125366291 | |||||
| chr9:125366339
|
G | A | 1 | a0001c0016t0037 | 1 | HG02683.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3593G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 28/28 | 3593 | chr9 | 125366339 | |||||
| chr9:125366503
|
A | G | 30 | a0001c0001t0001a0001c0001t0005a0001c0001t0010others(27): Show | 196 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(193): Show |
3_prime_UTR_variant | MODIFIER | c.*3757A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 28/28 | 3757 | chr9 | 125366503 | |||||
| chr9:125366517
|
T | C | 1 | a0001c0001t0021 | 1 | HG00738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3771T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 28/28 | 3771 | chr9 | 125366517 | |||||
| chr9:125366545
|
C | T | 1 | a0001c0001t0024 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3799C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 28/28 | 3799 | chr9 | 125366545 | |||||
| chr9:125366584
|
C | T | 1 | a0001c0001t0023 | 1 | HG02004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3838C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 28/28 | 3838 | chr9 | 125366584 | |||||
| chr9:125366833
|
A | G | 1 | a0001c0001t0022 | 1 | HG03654.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4087A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 28/28 | 4087 | chr9 | 125366833 | |||||
| chr9:125366848
|
A | G | 1 | a0001c0003t0018 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4102A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 28/28 | 4102 | chr9 | 125366848 | |||||
| chr9:125366955
|
G | A | 1 | a0001c0001t0014 | 2 | HG00741.hp2 homoSapiens_chm13v2.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4209G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 28/28 | 4209 | chr9 | 125366955 | |||||
| chr9:125367107
|
T | C | 1 | a0001c0001t0028 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4361T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 28/28 | 4361 | chr9 | 125367107 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:125262019
|
G | T | 165 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(162): Show | 165 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.-199+60G>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125262019 | ||||||
| chr9:125262038
|
G | T | 1 | a0001c0001t0005g0340 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-199+79G>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125262038 | ||||||
| chr9:125262102
|
T | C | 3 | a0001c0001t0009g0001a0001c0001t0009g0002a0001c0001t0009g0003 | 3 | HG01884.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-199+143T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125262102 | ||||||
| chr9:125262168
|
G | A | 165 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(162): Show | 165 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.-199+209G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125262168 | ||||||
| chr9:125262632
|
CT | C | 13 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(10): Show | 13 | HG00558.hp1 HG02027.hp2 NA18943.hp1 others(10): Show |
intron_variant | MODIFIER | c.-199+674delT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125262632 | ||||||
| chr9:125262714
|
G | A | 5 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(2): Show | 5 | HG02027.hp2 NA18943.hp1 NA18961.hp2 others(2): Show |
intron_variant | MODIFIER | c.-199+755G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125262714 | ||||||
| chr9:125263081
|
T | A | 1 | a0001c0001t0021g0189 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-199+1122T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125263081 | ||||||
| chr9:125263146
|
G | C | 3 | a0001c0001t0009g0001a0001c0001t0009g0002a0001c0001t0009g0003 | 3 | HG01884.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-199+1187G>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125263146 | ||||||
| chr9:125263215
|
C | T | 1 | a0001c0001t0002g0175 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-199+1256C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125263215 | ||||||
| chr9:125263255
|
C | G | 14 | a0001c0001t0001g0327a0001c0001t0005g0328a0001c0001t0005g0329others(11): Show | 14 | HG02129.hp1 NA18747.hp2 NA18950.hp1 others(11): Show |
intron_variant | MODIFIER | c.-199+1296C>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125263255 | ||||||
| chr9:125263321
|
T | C | 2 | a0001c0002t0003g0004a0001c0002t0003g0005 | 2 | NA18979.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.-199+1362T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125263321 | ||||||
| chr9:125263390
|
A | G | 2 | a0001c0001t0001g0325a0001c0001t0001g0326 | 2 | HG02559.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-199+1431A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125263390 | ||||||
| chr9:125263406
|
G | A | 1 | a0001c0001t0001g0176 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-199+1447G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125263406 | ||||||
| chr9:125263478
|
A | C | 2 | a0001c0001t0004g0173a0001c0001t0004g0174 | 2 | HG01099.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.-199+1519A>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125263478 | ||||||
| chr9:125263528
|
G | GT | 7 | a0001c0001t0001g0324a0001c0001t0002g0153a0001c0001t0002g0155others(4): Show | 7 | HG00621.hp2 HG01099.hp1 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.-199+1582dupT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr9 | 125263528 | |||||
| chr9:125263528
|
G | T | 17 | a0001c0003t0004g0156a0001c0003t0004g0157a0001c0003t0004g0164others(14): Show | 17 | HG01109.hp1 HG01167.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.-199+1569G>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125263528 | ||||||
| chr9:125263618
|
G | A | 8 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0008others(5): Show | 8 | HG01069.hp1 HG02615.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.-199+1659G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125263618 | ||||||
| chr9:125263683
|
ACAGCACT others(20): Show |
A | 200 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(197): Show | 200 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.-199+1756_-199+178 others(31): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr9 | 125263683 | |||||
| chr9:125263907
|
A | G | 1 | a0001c0001t0001g0323 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-199+1948A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125263907 | ||||||
| chr9:125263908
|
A | T | 2 | a0001c0001t0001g0179a0001c0001t0001g0180 | 2 | NA19054.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.-199+1949A>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125263908 | ||||||
| chr9:125263984
|
G | A | 2 | a0001c0001t0002g0014a0001c0001t0002g0015 | 2 | NA18977.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.-199+2025G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125263984 | ||||||
| chr9:125263999
|
G | T | 165 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(162): Show | 165 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.-199+2040G>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125263999 | ||||||
| chr9:125264117
|
C | G | 1 | a0001c0001t0001g0322 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-199+2158C>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125264117 | ||||||
| chr9:125264129
|
C | T | 5 | a0001c0001t0001g0317a0001c0001t0001g0318a0001c0001t0001g0319others(2): Show | 5 | HG02451.hp1 HG02559.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.-199+2170C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125264129 | ||||||
| chr9:125264138
|
C | T | 1 | a0001c0016t0037g0152 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-199+2179C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125264138 | ||||||
| chr9:125264208
|
G | A | 2 | a0001c0001t0004g0173a0001c0001t0004g0174 | 2 | HG01099.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.-199+2249G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125264208 | ||||||
| chr9:125264565
|
C | T | 1 | a0001c0001t0002g0119 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.-199+2606C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125264565 | ||||||
| chr9:125264718
|
AT | A | 6 | a0001c0001t0001g0017a0001c0001t0001g0192a0001c0001t0002g0016others(3): Show | 6 | HG01099.hp2 HG01243.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.-199+2775delT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr9 | 125264718 | |||||
| chr9:125264781
|
C | T | 1 | a0001c0001t0002g0155 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-199+2822C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125264781 | ||||||
| chr9:125264924
|
G | A | 2 | a0001c0003t0004g0156a0001c0003t0004g0157 | 2 | HG02451.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-199+2965G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125264924 | ||||||
| chr9:125264987
|
A | G | 31 | a0001c0002t0003g0004a0001c0002t0003g0005a0001c0002t0003g0123others(28): Show | 31 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.-199+3028A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125264987 | ||||||
| chr9:125265039
|
C | G | 2 | a0002c0006t0011g0121a0002c0006t0011g0122 | 2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-199+3080C>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125265039 | ||||||
| chr9:125265227
|
C | A | 1 | a0001c0001t0001g0193 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-199+3268C>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125265227 | ||||||
| chr9:125265428
|
C | T | 230 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(227): Show | 230 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.-199+3469C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125265428 | ||||||
| chr9:125265524
|
C | T | 1 | a0001c0001t0002g0117 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-198-3412C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125265524 | ||||||
| chr9:125265566
|
G | A | 92 | a0001c0001t0001g0193a0001c0001t0001g0195a0001c0001t0001g0196others(89): Show | 92 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(89): Show |
intron_variant | MODIFIER | c.-198-3370G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125265566 | ||||||
| chr9:125265588
|
T | A | 1 | a0001c0001t0001g0269 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-198-3348T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125265588 | ||||||
| chr9:125265628
|
G | A | 1 | a0001c0001t0024g0194 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-198-3308G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125265628 | ||||||
| chr9:125265636
|
C | CTCCTGAC others(827): Show |
1 | a0001c0001t0001g0269 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-198-3279_-198-327 others(838): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr9 | 125265636 | |||||
| chr9:125265636
|
C | CTCCTGAC others(831): Show |
5 | a0001c0003t0006g0158a0001c0003t0006g0159a0001c0003t0006g0160others(2): Show | 5 | HG01109.hp1 HG01884.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.-198-3279_-198-327 others(842): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr9 | 125265636 | |||||
| chr9:125265636
|
C | CTCCTGAC others(831): Show |
31 | a0001c0002t0003g0004a0001c0002t0003g0005a0001c0002t0003g0123others(28): Show | 31 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.-198-3279_-198-327 others(842): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr9 | 125265636 | |||||
| chr9:125265636
|
C | CTCCTGAC others(831): Show |
1 | a0001c0016t0037g0152 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-198-3279_-198-327 others(842): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr9 | 125265636 | |||||
| chr9:125265636
|
C | CTCCTGAC others(831): Show |
2 | a0001c0003t0006g0163a0001c0003t0026g0118 | 2 | HG02055.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.-198-3279_-198-327 others(842): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr9 | 125265636 | |||||
| chr9:125265636
|
C | CTCCTGAC others(831): Show |
7 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0008others(4): Show | 7 | HG01069.hp1 HG02615.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.-198-3279_-198-327 others(842): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr9 | 125265636 | |||||
| chr9:125265636
|
C | CTCCTGAC others(832): Show |
1 | a0001c0001t0001g0195 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.-198-3279_-198-327 others(843): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr9 | 125265636 | |||||
| chr9:125265636
|
C | CTCCTGAC others(831): Show |
3 | a0001c0001t0009g0001a0001c0001t0009g0002a0001c0001t0009g0003 | 3 | HG01884.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-198-3279_-198-327 others(842): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr9 | 125265636 | |||||
| chr9:125265636
|
C | CTCCTGAC others(831): Show |
122 | a0001c0001t0001g0017a0001c0001t0001g0045a0001c0001t0001g0270others(119): Show | 122 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.-198-3279_-198-327 others(842): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr9 | 125265636 | |||||
| chr9:125265636
|
C | CTCCTGAC others(831): Show |
160 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(157): Show | 160 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.-198-3279_-198-327 others(842): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr9 | 125265636 | |||||
| chr9:125265636
|
C | CTCCTGAC others(832): Show |
1 | a0001c0001t0002g0113 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-198-3279_-198-327 others(843): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr9 | 125265636 | |||||
| chr9:125265636
|
C | CTCCTGAC others(832): Show |
1 | a0001c0001t0002g0114 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-198-3279_-198-327 others(843): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr9 | 125265636 | |||||
| chr9:125265636
|
C | CTCCTGAC others(831): Show |
2 | a0001c0001t0002g0115a0001c0001t0002g0116 | 2 | NA18949.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.-198-3279_-198-327 others(842): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr9 | 125265636 | |||||
| chr9:125265636
|
C | CTCCTGAC others(828): Show |
2 | a0001c0001t0001g0315a0001c0001t0001g0316 | 2 | NA19079.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.-198-3279_-198-327 others(839): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr9 | 125265636 | |||||
| chr9:125265836
|
G | A | 1 | a0001c0002t0003g0123 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-198-3100G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125265836 | ||||||
| chr9:125265924
|
T | TA | 9 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0271others(6): Show | 9 | HG01358.hp1 HG01361.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.-198-2995dupA | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr9 | 125265924 | |||||
| chr9:125265924
|
TA | T | 13 | a0001c0001t0001g0192a0001c0001t0001g0268a0001c0001t0001g0313others(10): Show | 13 | HG01515.hp2 HG01884.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.-198-2995delA | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr9 | 125265924 | |||||
| chr9:125265972
|
G | A | 229 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(226): Show | 229 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.-198-2964G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125265972 | ||||||
| chr9:125266074
|
C | T | 1 | a0001c0001t0001g0188 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.-198-2862C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125266074 | ||||||
| chr9:125266127
|
AT | A | 194 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(191): Show | 194 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.-198-2793delT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr9 | 125266127 | |||||
| chr9:125266145
|
A | T | 1 | a0001c0001t0008g0112 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-198-2791A>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125266145 | ||||||
| chr9:125266166
|
G | A | 1 | a0001c0001t0001g0197 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-198-2770G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125266166 | ||||||
| chr9:125266190
|
G | A | 2 | a0001c0001t0004g0173a0001c0001t0004g0174 | 2 | HG01099.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.-198-2746G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125266190 | ||||||
| chr9:125266277
|
C | T | 1 | a0001c0001t0002g0111 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-198-2659C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125266277 | ||||||
| chr9:125266294
|
T | TTTTTA | 5 | a0001c0001t0004g0006a0001c0001t0009g0001a0001c0001t0009g0002others(2): Show | 5 | HG01884.hp2 HG02486.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-198-2617_-198-261 others(9): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr9 | 125266294 | |||||
| chr9:125266319
|
A | T | 1 | a0001c0001t0008g0110 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-198-2617A>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125266319 | ||||||
| chr9:125266324
|
T | A | 235 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(232): Show | 235 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.-198-2612T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125266324 | ||||||
| chr9:125266336
|
C | T | 14 | a0001c0001t0001g0300a0001c0001t0001g0304a0001c0001t0001g0305others(11): Show | 14 | HG02004.hp1 HG02056.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.-198-2600C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125266336 | ||||||
| chr9:125266529
|
G | C | 18 | a0001c0003t0004g0156a0001c0003t0004g0157a0001c0003t0004g0164others(15): Show | 18 | HG01109.hp1 HG01167.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.-198-2407G>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125266529 | ||||||
| chr9:125266532
|
C | G | 1 | a0001c0016t0037g0152 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-198-2404C>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125266532 | ||||||
| chr9:125266579
|
C | T | 1 | a0001c0016t0037g0152 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-198-2357C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125266579 | ||||||
| chr9:125266604
|
C | T | 33 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0021others(30): Show | 33 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.-198-2332C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125266604 | ||||||
| chr9:125266605
|
G | A | 43 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(40): Show | 43 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.-198-2331G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125266605 | ||||||
| chr9:125266662
|
A | G | 1 | a0001c0001t0017g0013 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-198-2274A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125266662 | ||||||
| chr9:125266733
|
C | T | 2 | a0001c0001t0004g0173a0001c0001t0004g0174 | 2 | HG01099.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.-198-2203C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125266733 | ||||||
| chr9:125266748
|
C | G | 1 | a0004c0008t0002g0083 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-198-2188C>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125266748 | ||||||
| chr9:125266908
|
G | A | 31 | a0001c0002t0003g0004a0001c0002t0003g0005a0001c0002t0003g0123others(28): Show | 31 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.-198-2028G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125266908 | ||||||
| chr9:125267238
|
C | T | 6 | a0001c0003t0004g0156a0001c0003t0004g0157a0001c0003t0004g0164others(3): Show | 6 | HG02258.hp1 HG02451.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-198-1698C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125267238 | ||||||
| chr9:125267408
|
G | A | 2 | a0001c0001t0001g0271a0001c0001t0001g0272 | 2 | NA18952.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.-198-1528G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125267408 | ||||||
| chr9:125267720
|
G | T | 1 | a0001c0001t0001g0264 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-198-1216G>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125267720 | ||||||
| chr9:125267794
|
A | G | 1 | a0001c0002t0007g0149 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.-198-1142A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125267794 | ||||||
| chr9:125268194
|
AC | A | 123 | a0001c0001t0001g0193a0001c0001t0001g0195a0001c0001t0001g0196others(120): Show | 123 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.-198-731delC | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr9 | 125268194 | |||||
| chr9:125268205
|
C | A | 4 | a0001c0001t0001g0325a0001c0001t0001g0326a0001c0001t0001g0327others(1): Show | 4 | HG02559.hp2 HG04184.hp1 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.-198-731C>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125268205 | ||||||
| chr9:125268205
|
C | CA | 5 | a0001c0001t0001g0181a0001c0001t0001g0273a0001c0001t0001g0274others(2): Show | 5 | HG00438.hp1 HG02056.hp2 HG03688.hp1 others(2): Show |
intron_variant | MODIFIER | c.-198-722dupA | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr9 | 125268205 | |||||
| chr9:125268206
|
A | C | 1 | a0001c0001t0001g0294 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-198-730A>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125268206 | ||||||
| chr9:125268495
|
G | GT | 28 | a0001c0001t0001g0180a0001c0001t0001g0292a0001c0001t0001g0293others(25): Show | 28 | HG00423.hp1 HG00741.hp2 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.-198-420dupT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr9 | 125268495 | |||||
| chr9:125268495
|
GT | G | 8 | a0001c0001t0001g0200a0001c0001t0002g0201a0001c0001t0005g0328others(5): Show | 8 | HG01167.hp1 HG02109.hp1 HG02683.hp1 others(5): Show |
intron_variant | MODIFIER | c.-198-420delT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr9 | 125268495 | |||||
| chr9:125268558
|
A | G | 204 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(201): Show | 204 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.-198-378A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 1/27 | chr9 | 125268558 | ||||||
| chr9:125269013
|
A | T | 1 | a0001c0001t0002g0080 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-150+29A>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125269013 | ||||||
| chr9:125269019
|
A | T | 2 | a0002c0006t0011g0121a0002c0006t0011g0122 | 2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-150+35A>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125269019 | ||||||
| chr9:125269184
|
C | T | 166 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(163): Show | 166 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.-150+200C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125269184 | ||||||
| chr9:125269259
|
G | A | 1 | a0001c0001t0032g0295 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-150+275G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125269259 | ||||||
| chr9:125269418
|
A | G | 1 | a0001c0001t0001g0291 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-150+434A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125269418 | ||||||
| chr9:125269544
|
C | G | 7 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0008others(4): Show | 7 | HG01069.hp1 HG02615.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.-150+560C>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125269544 | ||||||
| chr9:125269557
|
A | G | 1 | a0001c0001t0017g0013 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-150+573A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125269557 | ||||||
| chr9:125269584
|
C | T | 1 | a0001c0001t0001g0262 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-150+600C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125269584 | ||||||
| chr9:125269710
|
C | CT | 57 | a0001c0001t0001g0017a0001c0001t0001g0178a0001c0001t0001g0246others(54): Show | 57 | HG00423.hp1 HG00544.hp1 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.-150+750dupT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125269710 | |||||
| chr9:125269710
|
CT | C | 24 | a0001c0001t0002g0016a0001c0001t0002g0084a0001c0001t0004g0006others(21): Show | 24 | HG01069.hp1 HG01167.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.-150+750delT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125269710 | |||||
| chr9:125269710
|
CTTTTTTT | C | 31 | a0001c0002t0003g0004a0001c0002t0003g0005a0001c0002t0003g0123others(28): Show | 31 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.-150+744_-150+750d others(9): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125269710 | |||||
| chr9:125269831
|
C | T | 1 | a0001c0001t0001g0245 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-150+847C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125269831 | ||||||
| chr9:125269907
|
C | T | 166 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(163): Show | 166 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.-150+923C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125269907 | ||||||
| chr9:125269947
|
A | G | 231 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(228): Show | 231 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.-150+963A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125269947 | ||||||
| chr9:125270284
|
C | T | 4 | a0001c0001t0001g0192a0001c0001t0001g0269a0001c0001t0001g0298others(1): Show | 4 | HG00639.hp1 HG02622.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-150+1300C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125270284 | ||||||
| chr9:125270298
|
G | A | 2 | a0001c0001t0002g0028a0001c0001t0002g0070 | 2 | HG02071.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.-150+1314G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125270298 | ||||||
| chr9:125270365
|
T | G | 2 | a0001c0003t0006g0163a0001c0003t0026g0118 | 2 | HG02055.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.-150+1381T>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125270365 | ||||||
| chr9:125270544
|
A | G | 6 | a0001c0003t0006g0166a0001c0003t0006g0168a0001c0003t0006g0169others(3): Show | 6 | HG01167.hp1 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-150+1560A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125270544 | ||||||
| chr9:125270665
|
C | T | 3 | a0001c0001t0009g0001a0001c0001t0009g0002a0001c0001t0009g0003 | 3 | HG01884.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-150+1681C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125270665 | ||||||
| chr9:125270791
|
A | C | 5 | a0001c0003t0004g0156a0001c0003t0004g0157a0001c0003t0004g0164others(2): Show | 5 | HG02258.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.-150+1807A>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125270791 | ||||||
| chr9:125270808
|
T | A | 6 | a0001c0003t0006g0166a0001c0003t0006g0168a0001c0003t0006g0169others(3): Show | 6 | HG01167.hp1 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-150+1824T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125270808 | ||||||
| chr9:125270873
|
T | C | 1 | a0001c0001t0002g0071 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.-150+1889T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125270873 | ||||||
| chr9:125270903
|
C | G | 1 | a0001c0001t0002g0109 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-150+1919C>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125270903 | ||||||
| chr9:125271138
|
A | G | 13 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(10): Show | 13 | HG00558.hp1 HG02027.hp2 NA18943.hp1 others(10): Show |
intron_variant | MODIFIER | c.-150+2154A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125271138 | ||||||
| chr9:125271414
|
A | G | 1 | a0001c0001t0001g0261 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-150+2430A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125271414 | ||||||
| chr9:125271531
|
G | A | 2 | a0002c0006t0011g0121a0002c0006t0011g0122 | 2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-150+2547G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125271531 | ||||||
| chr9:125271676
|
G | A | 5 | a0001c0003t0006g0158a0001c0003t0006g0159a0001c0003t0006g0160others(2): Show | 5 | HG01109.hp1 HG01884.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.-150+2692G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125271676 | ||||||
| chr9:125271801
|
T | G | 61 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(58): Show | 61 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.-150+2817T>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125271801 | ||||||
| chr9:125271806
|
T | G | 6 | a0001c0003t0006g0166a0001c0003t0006g0168a0001c0003t0006g0169others(3): Show | 6 | HG01167.hp1 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-150+2822T>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125271806 | ||||||
| chr9:125272188
|
T | C | 1 | a0001c0016t0037g0152 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-150+3204T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125272188 | ||||||
| chr9:125272249
|
C | A | 1 | a0001c0001t0001g0325 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-150+3265C>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125272249 | ||||||
| chr9:125272257
|
C | T | 1 | a0001c0016t0037g0152 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-150+3273C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125272257 | ||||||
| chr9:125272311
|
C | T | 1 | a0001c0001t0002g0069 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-150+3327C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125272311 | ||||||
| chr9:125272383
|
A | G | 1 | a0001c0016t0037g0152 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-150+3399A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125272383 | ||||||
| chr9:125272436
|
G | T | 3 | a0001c0001t0001g0243a0001c0001t0001g0244a0001c0001t0001g0268 | 3 | NA18942.hp2 NA18971.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.-150+3452G>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125272436 | ||||||
| chr9:125272448
|
A | G | 1 | a0001c0016t0037g0152 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-150+3464A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125272448 | ||||||
| chr9:125272876
|
T | G | 33 | a0001c0002t0003g0004a0001c0002t0003g0005a0001c0002t0003g0123others(30): Show | 33 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(30): Show |
intron_variant | MODIFIER | c.-150+3892T>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125272876 | ||||||
| chr9:125272882
|
G | T | 1 | a0001c0002t0003g0145 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-150+3898G>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125272882 | ||||||
| chr9:125273062
|
C | T | 230 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(227): Show | 230 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.-150+4078C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125273062 | ||||||
| chr9:125273170
|
C | A | 163 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(160): Show | 163 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.-150+4186C>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125273170 | ||||||
| chr9:125273278
|
G | T | 3 | a0001c0001t0009g0001a0001c0001t0009g0002a0001c0001t0009g0003 | 3 | HG01884.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-150+4294G>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125273278 | ||||||
| chr9:125273367
|
C | A | 4 | a0001c0002t0003g0004a0001c0002t0003g0005a0001c0002t0003g0125others(1): Show | 4 | NA18979.hp2 NA18988.hp1 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.-150+4383C>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125273367 | ||||||
| chr9:125273471
|
G | T | 4 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0242others(1): Show | 4 | HG00639.hp2 HG00735.hp2 HG01074.hp1 others(1): Show |
intron_variant | MODIFIER | c.-150+4487G>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125273471 | ||||||
| chr9:125273501
|
T | C | 1 | a0001c0001t0002g0085 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-150+4517T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125273501 | ||||||
| chr9:125273511
|
T | A | 1 | a0001c0001t0002g0086 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-150+4527T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125273511 | ||||||
| chr9:125273646
|
C | T | 31 | a0001c0002t0003g0004a0001c0002t0003g0005a0001c0002t0003g0123others(28): Show | 31 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.-150+4662C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125273646 | ||||||
| chr9:125273848
|
G | C | 2 | a0001c0001t0004g0173a0001c0001t0004g0174 | 2 | HG01099.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.-150+4864G>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125273848 | ||||||
| chr9:125273934
|
T | A | 8 | a0001c0001t0001g0202a0001c0001t0001g0264a0001c0001t0001g0323others(5): Show | 8 | HG00738.hp1 HG01099.hp1 HG01167.hp2 others(5): Show |
intron_variant | MODIFIER | c.-150+4950T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125273934 | ||||||
| chr9:125274029
|
C | T | 7 | a0001c0003t0006g0158a0001c0003t0006g0159a0001c0003t0006g0160others(4): Show | 7 | HG01109.hp1 HG01884.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.-150+5045C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125274029 | ||||||
| chr9:125274066
|
G | A | 7 | a0001c0003t0006g0158a0001c0003t0006g0159a0001c0003t0006g0160others(4): Show | 7 | HG01109.hp1 HG01884.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.-150+5082G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125274066 | ||||||
| chr9:125274130
|
G | T | 31 | a0001c0002t0003g0004a0001c0002t0003g0005a0001c0002t0003g0123others(28): Show | 31 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.-150+5146G>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125274130 | ||||||
| chr9:125274215
|
A | G | 1 | a0001c0001t0030g0120 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-150+5231A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125274215 | ||||||
| chr9:125274267
|
C | T | 2 | a0001c0001t0014g0259a0001c0001t0014g0263 | 2 | HG00741.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-150+5283C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125274267 | ||||||
| chr9:125274312
|
T | C | 200 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(197): Show | 200 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.-150+5328T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125274312 | ||||||
| chr9:125274355
|
A | G | 2 | a0002c0006t0011g0121a0002c0006t0011g0122 | 2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-150+5371A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125274355 | ||||||
| chr9:125274404
|
G | A | 2 | a0001c0003t0006g0163a0001c0003t0026g0118 | 2 | HG02055.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.-150+5420G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125274404 | ||||||
| chr9:125274430
|
A | G | 2 | a0002c0006t0011g0121a0002c0006t0011g0122 | 2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-150+5446A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125274430 | ||||||
| chr9:125274455
|
G | A | 7 | a0001c0001t0001g0200a0001c0001t0013g0198a0001c0003t0004g0156others(4): Show | 7 | HG02109.hp1 HG02258.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.-150+5471G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125274455 | ||||||
| chr9:125274463
|
CT | C | 6 | a0001c0001t0001g0264a0001c0001t0002g0087a0001c0001t0002g0115others(3): Show | 6 | HG01167.hp2 HG02630.hp1 NA18949.hp1 others(3): Show |
intron_variant | MODIFIER | c.-150+5496delT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125274463 | |||||
| chr9:125274497
|
C | G | 31 | a0001c0002t0003g0004a0001c0002t0003g0005a0001c0002t0003g0123others(28): Show | 31 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.-150+5513C>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125274497 | ||||||
| chr9:125274523
|
G | A | 1 | a0001c0001t0002g0084 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-150+5539G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125274523 | ||||||
| chr9:125274614
|
C | A | 1 | a0001c0001t0002g0117 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-150+5630C>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125274614 | ||||||
| chr9:125274722
|
A | G | 1 | a0001c0001t0002g0068 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-150+5738A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125274722 | ||||||
| chr9:125274832
|
A | G | 23 | a0001c0001t0001g0325a0001c0001t0001g0326a0001c0001t0009g0001others(20): Show | 23 | HG01109.hp1 HG01167.hp1 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.-150+5848A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125274832 | ||||||
| chr9:125274966
|
C | T | 197 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(194): Show | 197 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.-150+5982C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125274966 | ||||||
| chr9:125274974
|
T | C | 1 | a0001c0001t0002g0029 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-150+5990T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125274974 | ||||||
| chr9:125275062
|
T | C | 2 | a0001c0003t0006g0163a0001c0003t0026g0118 | 2 | HG02055.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.-150+6078T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125275062 | ||||||
| chr9:125275073
|
A | C | 33 | a0001c0002t0003g0004a0001c0002t0003g0005a0001c0002t0003g0123others(30): Show | 33 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(30): Show |
intron_variant | MODIFIER | c.-150+6089A>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125275073 | ||||||
| chr9:125275096
|
T | G | 2 | a0001c0001t0002g0089a0001c0001t0002g0108 | 2 | HG02135.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.-150+6112T>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125275096 | ||||||
| chr9:125275240
|
T | A | 1 | a0001c0001t0008g0112 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-150+6256T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125275240 | ||||||
| chr9:125275264
|
C | T | 1 | a0001c0001t0002g0028 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.-150+6280C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125275264 | ||||||
| chr9:125275266
|
G | A | 4 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205others(1): Show | 4 | HG02615.hp1 HG02922.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-150+6282G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125275266 | ||||||
| chr9:125275550
|
G | A | 1 | a0001c0001t0017g0013 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-150+6566G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125275550 | ||||||
| chr9:125275597
|
G | A | 1 | a0001c0001t0025g0207 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-150+6613G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125275597 | ||||||
| chr9:125275729
|
C | T | 2 | a0001c0002t0003g0144a0001c0002t0003g0148 | 2 | HG00621.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.-150+6745C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125275729 | ||||||
| chr9:125275747
|
C | T | 31 | a0001c0002t0003g0004a0001c0002t0003g0005a0001c0002t0003g0123others(28): Show | 31 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.-150+6763C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125275747 | ||||||
| chr9:125275927
|
G | T | 2 | a0001c0001t0001g0290a0001c0001t0001g0312 | 2 | HG02698.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.-150+6943G>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125275927 | ||||||
| chr9:125276094
|
C | T | 3 | a0001c0001t0009g0001a0001c0001t0009g0002a0001c0001t0009g0003 | 3 | HG01884.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-150+7110C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125276094 | ||||||
| chr9:125276143
|
A | G | 1 | a0001c0001t0017g0013 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-150+7159A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125276143 | ||||||
| chr9:125276174
|
C | T | 1 | a0001c0001t0001g0241 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-150+7190C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125276174 | ||||||
| chr9:125276181
|
A | G | 31 | a0001c0002t0003g0004a0001c0002t0003g0005a0001c0002t0003g0123others(28): Show | 31 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.-150+7197A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125276181 | ||||||
| chr9:125276216
|
A | G | 20 | a0001c0001t0001g0325a0001c0001t0001g0326a0001c0003t0004g0156others(17): Show | 20 | HG01109.hp1 HG01167.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.-150+7232A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125276216 | ||||||
| chr9:125276273
|
T | C | 1 | a0001c0001t0002g0090 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-150+7289T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125276273 | ||||||
| chr9:125276380
|
A | G | 2 | a0001c0001t0001g0240a0001c0001t0001g0267 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-150+7396A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125276380 | ||||||
| chr9:125276573
|
C | A | 1 | a0001c0001t0004g0007 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-150+7589C>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125276573 | ||||||
| chr9:125276574
|
A | G | 1 | a0001c0001t0004g0007 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-150+7590A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125276574 | ||||||
| chr9:125276623
|
A | T | 1 | a0001c0001t0002g0067 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-150+7639A>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125276623 | ||||||
| chr9:125276638
|
G | A | 33 | a0001c0002t0003g0004a0001c0002t0003g0005a0001c0002t0003g0123others(30): Show | 33 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(30): Show |
intron_variant | MODIFIER | c.-150+7654G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125276638 | ||||||
| chr9:125276683
|
T | C | 1 | a0001c0001t0002g0030 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-150+7699T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125276683 | ||||||
| chr9:125276704
|
A | G | 1 | a0001c0001t0002g0081 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-150+7720A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125276704 | ||||||
| chr9:125276998
|
T | C | 2 | a0002c0006t0011g0121a0002c0006t0011g0122 | 2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-150+8014T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125276998 | ||||||
| chr9:125277243
|
C | T | 3 | a0001c0001t0009g0001a0001c0001t0009g0002a0001c0001t0009g0003 | 3 | HG01884.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-150+8259C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125277243 | ||||||
| chr9:125277372
|
A | G | 1 | a0001c0001t0001g0193 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-150+8388A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125277372 | ||||||
| chr9:125277685
|
G | GT | 19 | a0001c0001t0001g0206a0001c0001t0001g0237a0001c0001t0001g0238others(16): Show | 19 | HG00099.hp2 HG00423.hp2 HG00733.hp2 others(16): Show |
intron_variant | MODIFIER | c.-150+8717dupT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125277685 | |||||
| chr9:125277928
|
G | A | 3 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0299 | 3 | HG02258.hp2 HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-150+8944G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125277928 | ||||||
| chr9:125277971
|
T | C | 4 | a0001c0001t0002g0090a0001c0001t0002g0091a0001c0001t0002g0092others(1): Show | 4 | HG01175.hp1 HG01192.hp2 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.-150+8987T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125277971 | ||||||
| chr9:125278049
|
A | G | 2 | a0002c0006t0011g0121a0002c0006t0011g0122 | 2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-150+9065A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125278049 | ||||||
| chr9:125278254
|
C | T | 1 | a0001c0001t0001g0176 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-150+9270C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125278254 | ||||||
| chr9:125278385
|
G | T | 1 | a0001c0001t0002g0077 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-150+9401G>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125278385 | ||||||
| chr9:125278501
|
A | T | 33 | a0001c0002t0003g0004a0001c0002t0003g0005a0001c0002t0003g0123others(30): Show | 33 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(30): Show |
intron_variant | MODIFIER | c.-150+9517A>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125278501 | ||||||
| chr9:125278574
|
C | G | 1 | a0001c0001t0002g0109 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-150+9590C>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125278574 | ||||||
| chr9:125278750
|
G | T | 163 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(160): Show | 163 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.-150+9766G>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125278750 | ||||||
| chr9:125278835
|
GA | G | 7 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0008others(4): Show | 7 | HG01069.hp1 HG02615.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.-150+9862delA | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125278835 | |||||
| chr9:125278835
|
GAA | G | 31 | a0001c0002t0003g0004a0001c0002t0003g0005a0001c0002t0003g0123others(28): Show | 31 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.-150+9861_-150+986 others(6): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125278835 | |||||
| chr9:125278982
|
A | G | 1 | a0001c0001t0002g0109 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-150+9998A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125278982 | ||||||
| chr9:125278983
|
G | A | 1 | a0001c0001t0002g0109 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-150+9999G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125278983 | ||||||
| chr9:125279209
|
TA | T | 6 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0236others(3): Show | 6 | HG01257.hp2 HG01258.hp2 HG03834.hp1 others(3): Show |
intron_variant | MODIFIER | c.-150+10241delA | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125279209 | |||||
| chr9:125279549
|
C | T | 73 | a0001c0001t0001g0193a0001c0001t0001g0195a0001c0001t0001g0196others(70): Show | 73 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.-150+10565C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125279549 | ||||||
| chr9:125279570
|
CA | C | 61 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(58): Show | 61 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.-150+10603delA | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125279570 | |||||
| chr9:125279637
|
T | TA | 33 | a0001c0002t0003g0004a0001c0002t0003g0005a0001c0002t0003g0123others(30): Show | 33 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(30): Show |
intron_variant | MODIFIER | c.-150+10662dupA | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125279637 | |||||
| chr9:125279656
|
C | A | 1 | a0001c0001t0002g0109 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-150+10672C>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125279656 | ||||||
| chr9:125279670
|
C | T | 1 | a0001c0001t0002g0066 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-150+10686C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125279670 | ||||||
| chr9:125279974
|
CT | C | 7 | a0001c0003t0006g0158a0001c0003t0006g0159a0001c0003t0006g0160others(4): Show | 7 | HG01109.hp1 HG01884.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.-150+10991delT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125279974 | ||||||
| chr9:125280014
|
C | T | 7 | a0001c0001t0002g0089a0001c0001t0002g0103a0001c0001t0002g0104others(4): Show | 7 | HG00408.hp2 HG02074.hp2 HG02135.hp2 others(4): Show |
intron_variant | MODIFIER | c.-150+11030C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125280014 | ||||||
| chr9:125280050
|
G | A | 3 | a0001c0001t0009g0001a0001c0001t0009g0002a0001c0001t0009g0003 | 3 | HG01884.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-150+11066G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125280050 | ||||||
| chr9:125280264
|
T | C | 2 | a0002c0006t0011g0121a0002c0006t0011g0122 | 2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-150+11280T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125280264 | ||||||
| chr9:125280396
|
C | CA | 11 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0002g0025others(8): Show | 11 | HG00733.hp2 HG01175.hp1 HG02300.hp1 others(8): Show |
intron_variant | MODIFIER | c.-150+11436dupA | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125280396 | |||||
| chr9:125280396
|
CA | C | 186 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0179others(183): Show | 186 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.-150+11436delA | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125280396 | |||||
| chr9:125280396
|
CAA | C | 34 | a0001c0001t0001g0192a0001c0001t0001g0236a0001c0001t0001g0239others(31): Show | 34 | HG00423.hp2 HG01099.hp1 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.-150+11435_-150+11 others(8): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125280396 | |||||
| chr9:125280575
|
C | CT | 12 | a0001c0001t0001g0241a0001c0001t0001g0253a0001c0001t0001g0293others(9): Show | 12 | HG00408.hp1 HG00544.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.-150+11609dupT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125280575 | |||||
| chr9:125280575
|
CT | C | 10 | a0001c0001t0001g0213a0001c0001t0001g0236a0001c0001t0002g0109others(7): Show | 10 | HG01069.hp1 HG02615.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.-150+11609delT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125280575 | |||||
| chr9:125280661
|
C | T | 163 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(160): Show | 163 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.-150+11677C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125280661 | ||||||
| chr9:125280779
|
GT | G | 31 | a0001c0002t0003g0004a0001c0002t0003g0005a0001c0002t0003g0123others(28): Show | 31 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.-150+11797delT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125280779 | |||||
| chr9:125280797
|
A | G | 230 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(227): Show | 230 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.-150+11813A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125280797 | ||||||
| chr9:125280952
|
A | G | 1 | a0001c0001t0001g0232 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-150+11968A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125280952 | ||||||
| chr9:125280987
|
G | A | 2 | a0001c0001t0004g0173a0001c0001t0004g0174 | 2 | HG01099.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.-150+12003G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125280987 | ||||||
| chr9:125281525
|
T | G | 231 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(228): Show | 231 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.-150+12541T>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125281525 | ||||||
| chr9:125281581
|
G | C | 33 | a0001c0002t0003g0004a0001c0002t0003g0005a0001c0002t0003g0123others(30): Show | 33 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(30): Show |
intron_variant | MODIFIER | c.-150+12597G>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125281581 | ||||||
| chr9:125281908
|
C | T | 1 | a0001c0001t0002g0059 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-150+12924C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125281908 | ||||||
| chr9:125281986
|
A | G | 2 | a0001c0001t0004g0173a0001c0001t0004g0174 | 2 | HG01099.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.-150+13002A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125281986 | ||||||
| chr9:125282163
|
C | G | 1 | a0001c0002t0007g0142 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-150+13179C>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125282163 | ||||||
| chr9:125282435
|
C | T | 2 | a0001c0001t0004g0173a0001c0001t0004g0174 | 2 | HG01099.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.-149-13023C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125282435 | ||||||
| chr9:125282589
|
T | G | 6 | a0001c0003t0006g0166a0001c0003t0006g0168a0001c0003t0006g0169others(3): Show | 6 | HG01167.hp1 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-149-12869T>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125282589 | ||||||
| chr9:125282595
|
A | G | 1 | a0001c0001t0001g0261 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-149-12863A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125282595 | ||||||
| chr9:125283020
|
A | G | 4 | a0001c0001t0001g0327a0001c0001t0005g0331a0001c0001t0005g0332others(1): Show | 4 | HG02129.hp1 NA18747.hp2 NA18950.hp1 others(1): Show |
intron_variant | MODIFIER | c.-149-12438A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125283020 | ||||||
| chr9:125283028
|
T | TTTTA | 85 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0182others(82): Show | 85 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.-149-12388_-149-12 others(10): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125283028 | |||||
| chr9:125283028
|
T | TTTTATTT others(1): Show |
40 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(37): Show | 40 | HG00609.hp2 HG00621.hp1 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.-149-12392_-149-12 others(14): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125283028 | |||||
| chr9:125283028
|
T | TTTTATTT others(5): Show |
8 | a0001c0001t0001g0212a0001c0001t0001g0286a0001c0001t0001g0315others(5): Show | 8 | HG01257.hp1 HG01884.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.-149-12396_-149-12 others(18): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125283028 | |||||
| chr9:125283028
|
T | TTTTTTTT others(5): Show |
1 | a0001c0001t0001g0287 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-149-12427_-149-12 others(18): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125283028 | |||||
| chr9:125283028
|
TTTTA | T | 7 | a0001c0001t0001g0253a0001c0001t0002g0027a0001c0002t0003g0004others(4): Show | 7 | HG02056.hp2 HG02572.hp1 NA18970.hp2 others(4): Show |
intron_variant | MODIFIER | c.-149-12388_-149-12 others(10): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125283028 | |||||
| chr9:125283028
|
TTTTATTT others(1): Show |
T | 5 | a0001c0001t0001g0327a0001c0001t0005g0331a0001c0001t0005g0332others(2): Show | 5 | HG02129.hp1 HG02630.hp1 NA18747.hp2 others(2): Show |
intron_variant | MODIFIER | c.-149-12392_-149-12 others(14): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125283028 | |||||
| chr9:125283028
|
TTTTATTT others(5): Show |
T | 5 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0214others(2): Show | 5 | HG00639.hp2 HG00735.hp2 HG01074.hp1 others(2): Show |
intron_variant | MODIFIER | c.-149-12396_-149-12 others(18): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125283028 | |||||
| chr9:125283070
|
T | TTATTTAT others(5): Show |
1 | a0001c0001t0009g0001 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-149-12385_-149-12 others(18): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125283070 | |||||
| chr9:125283141
|
C | T | 31 | a0001c0002t0003g0004a0001c0002t0003g0005a0001c0002t0003g0123others(28): Show | 31 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.-149-12317C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125283141 | ||||||
| chr9:125283310
|
C | T | 1 | a0001c0001t0001g0262 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-149-12148C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125283310 | ||||||
| chr9:125283386
|
G | A | 1 | a0001c0016t0037g0152 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-149-12072G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125283386 | ||||||
| chr9:125283449
|
C | T | 2 | a0002c0006t0011g0121a0002c0006t0011g0122 | 2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-149-12009C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125283449 | ||||||
| chr9:125283452
|
C | T | 1 | a0001c0001t0017g0013 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-149-12006C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125283452 | ||||||
| chr9:125283455
|
C | T | 1 | a0001c0001t0002g0021 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-149-12003C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125283455 | ||||||
| chr9:125283787
|
C | G | 2 | a0002c0006t0011g0121a0002c0006t0011g0122 | 2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-149-11671C>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125283787 | ||||||
| chr9:125283872
|
C | CT | 7 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0008others(4): Show | 7 | HG01069.hp1 HG02615.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.-149-11576dupT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125283872 | |||||
| chr9:125283882
|
T | C | 15 | a0001c0001t0001g0270a0001c0001t0001g0271a0001c0001t0001g0272others(12): Show | 15 | HG00609.hp2 HG00673.hp2 HG01255.hp1 others(12): Show |
intron_variant | MODIFIER | c.-149-11576T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125283882 | ||||||
| chr9:125283954
|
C | G | 5 | a0001c0001t0002g0051a0001c0001t0002g0052a0001c0001t0002g0053others(2): Show | 5 | HG00544.hp1 HG02132.hp1 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.-149-11504C>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125283954 | ||||||
| chr9:125283989
|
C | T | 5 | a0001c0003t0004g0156a0001c0003t0004g0157a0001c0003t0004g0164others(2): Show | 5 | HG02258.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.-149-11469C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125283989 | ||||||
| chr9:125283990
|
A | T | 1 | a0001c0001t0002g0021 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-149-11468A>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125283990 | ||||||
| chr9:125284112
|
G | C | 6 | a0001c0003t0006g0166a0001c0003t0006g0168a0001c0003t0006g0169others(3): Show | 6 | HG01167.hp1 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-149-11346G>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125284112 | ||||||
| chr9:125284164
|
C | G | 1 | a0001c0001t0001g0196 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-149-11294C>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125284164 | ||||||
| chr9:125284168
|
G | A | 1 | a0001c0002t0003g0151 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-149-11290G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125284168 | ||||||
| chr9:125284180
|
C | CT | 168 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(165): Show | 168 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.-149-11257dupT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125284180 | |||||
| chr9:125284180
|
C | CTT | 10 | a0001c0001t0001g0229a0001c0001t0001g0269a0001c0001t0001g0289others(7): Show | 10 | HG00639.hp1 HG01109.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.-149-11258_-149-11 others(8): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125284180 | |||||
| chr9:125284180
|
CT | C | 34 | a0001c0001t0002g0069a0001c0001t0002g0084a0001c0002t0003g0004others(31): Show | 34 | HG00544.hp2 HG01081.hp2 HG01123.hp1 others(31): Show |
intron_variant | MODIFIER | c.-149-11257delT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125284180 | |||||
| chr9:125284247
|
C | T | 7 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0008others(4): Show | 7 | HG01069.hp1 HG02615.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.-149-11211C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125284247 | ||||||
| chr9:125284317
|
T | A | 2 | a0001c0001t0001g0215a0001c0001t0001g0254 | 2 | HG00642.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.-149-11141T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125284317 | ||||||
| chr9:125284337
|
C | T | 5 | a0001c0003t0006g0158a0001c0003t0006g0159a0001c0003t0006g0160others(2): Show | 5 | HG01109.hp1 HG01884.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.-149-11121C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125284337 | ||||||
| chr9:125284380
|
A | G | 2 | a0001c0001t0002g0087a0001c0001t0002g0111 | 2 | HG02165.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.-149-11078A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125284380 | ||||||
| chr9:125284437
|
C | G | 3 | a0001c0001t0009g0001a0001c0001t0009g0002a0001c0001t0009g0003 | 3 | HG01884.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-149-11021C>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125284437 | ||||||
| chr9:125284479
|
CT | C | 7 | a0001c0001t0002g0109a0001c0003t0006g0166a0001c0003t0006g0168others(4): Show | 7 | HG01167.hp1 HG02895.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.-149-10966delT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125284479 | |||||
| chr9:125284509
|
G | A | 4 | a0001c0001t0001g0270a0001c0001t0010g0216a0001c0001t0010g0255others(1): Show | 4 | HG00673.hp2 HG01175.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.-149-10949G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125284509 | ||||||
| chr9:125284512
|
A | G | 11 | a0001c0001t0001g0017a0001c0001t0001g0045a0001c0001t0002g0048others(8): Show | 11 | HG00280.hp2 HG01099.hp2 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.-149-10946A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125284512 | ||||||
| chr9:125284567
|
C | T | 1 | a0001c0001t0001g0228 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.-149-10891C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125284567 | ||||||
| chr9:125284707
|
T | C | 1 | a0003c0007t0001g0302 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-149-10751T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125284707 | ||||||
| chr9:125285005
|
G | A | 1 | a0001c0016t0037g0152 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-149-10453G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125285005 | ||||||
| chr9:125285007
|
A | G | 230 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(227): Show | 230 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.-149-10451A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125285007 | ||||||
| chr9:125285015
|
T | G | 1 | a0001c0001t0002g0175 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-149-10443T>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125285015 | ||||||
| chr9:125285056
|
C | T | 1 | a0001c0016t0037g0152 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-149-10402C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125285056 | ||||||
| chr9:125285224
|
T | G | 1 | a0001c0001t0002g0119 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.-149-10234T>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125285224 | ||||||
| chr9:125285306
|
A | G | 2 | a0001c0001t0004g0173a0001c0001t0004g0174 | 2 | HG01099.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.-149-10152A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125285306 | ||||||
| chr9:125285372
|
G | C | 1 | a0001c0001t0002g0066 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-149-10086G>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125285372 | ||||||
| chr9:125285453
|
G | GT | 162 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(159): Show | 162 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.-149-9983dupT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125285453 | |||||
| chr9:125285453
|
G | GTT | 30 | a0001c0001t0001g0188a0001c0001t0001g0195a0001c0001t0001g0226others(27): Show | 30 | HG00438.hp1 HG00609.hp2 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.-149-9984_-149-998 others(6): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125285453 | |||||
| chr9:125285453
|
G | GTTT | 29 | a0001c0001t0004g0011a0001c0001t0030g0120a0001c0002t0003g0004others(26): Show | 29 | HG00544.hp2 HG01069.hp1 HG01081.hp2 others(26): Show |
intron_variant | MODIFIER | c.-149-9985_-149-998 others(7): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125285453 | |||||
| chr9:125285532
|
C | A | 1 | a0001c0001t0002g0089 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.-149-9926C>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125285532 | ||||||
| chr9:125285807
|
T | C | 33 | a0001c0002t0003g0004a0001c0002t0003g0005a0001c0002t0003g0123others(30): Show | 33 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(30): Show |
intron_variant | MODIFIER | c.-149-9651T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125285807 | ||||||
| chr9:125285840
|
A | G | 1 | a0001c0001t0001g0300 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-149-9618A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125285840 | ||||||
| chr9:125286180
|
T | G | 1 | a0001c0003t0006g0166 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-149-9278T>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125286180 | ||||||
| chr9:125286196
|
G | C | 1 | a0001c0016t0037g0152 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-149-9262G>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125286196 | ||||||
| chr9:125286262
|
C | T | 1 | a0001c0001t0004g0012 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-149-9196C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125286262 | ||||||
| chr9:125286294
|
GTTGTTTT others(2): Show |
G | 3 | a0001c0001t0009g0001a0001c0001t0009g0002a0001c0001t0009g0003 | 3 | HG01884.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-149-9156_-149-914 others(13): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125286294 | |||||
| chr9:125286298
|
TTTTC | T | 12 | a0001c0003t0004g0156a0001c0003t0004g0157a0001c0003t0004g0164others(9): Show | 12 | HG01109.hp1 HG01884.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.-149-9156_-149-915 others(8): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125286298 | |||||
| chr9:125286311
|
T | G | 3 | a0001c0001t0009g0001a0001c0001t0009g0002a0001c0001t0009g0003 | 3 | HG01884.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-149-9147T>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125286311 | ||||||
| chr9:125286475
|
G | GT | 13 | a0001c0001t0002g0065a0001c0001t0002g0080a0001c0001t0002g0082others(10): Show | 13 | HG00423.hp1 HG01069.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.-149-8971dupT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125286475 | |||||
| chr9:125286791
|
A | ATTTTCTT others(10): Show |
1 | a0006c0011t0005g0337 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-149-8666_-149-866 others(21): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125286791 | |||||
| chr9:125286809
|
C | T | 1 | a0001c0001t0002g0016 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.-149-8649C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125286809 | ||||||
| chr9:125286874
|
A | C | 1 | a0001c0001t0001g0186 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-149-8584A>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125286874 | ||||||
| chr9:125286900
|
G | A | 2 | a0002c0006t0011g0121a0002c0006t0011g0122 | 2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-149-8558G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125286900 | ||||||
| chr9:125286987
|
G | A | 1 | a0001c0001t0005g0331 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-149-8471G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125286987 | ||||||
| chr9:125287224
|
A | G | 2 | a0001c0002t0003g0131a0001c0002t0003g0151 | 2 | NA18986.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.-149-8234A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125287224 | ||||||
| chr9:125287225
|
G | A | 2 | a0001c0002t0003g0131a0001c0002t0003g0151 | 2 | NA18986.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.-149-8233G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125287225 | ||||||
| chr9:125287324
|
G | A | 31 | a0001c0002t0003g0004a0001c0002t0003g0005a0001c0002t0003g0123others(28): Show | 31 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.-149-8134G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125287324 | ||||||
| chr9:125287765
|
G | A | 1 | a0001c0001t0017g0013 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-149-7693G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125287765 | ||||||
| chr9:125287841
|
A | G | 1 | a0001c0001t0004g0007 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-149-7617A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125287841 | ||||||
| chr9:125287970
|
C | T | 2 | a0001c0001t0001g0262a0007c0017t0001g0250 | 2 | HG02723.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.-149-7488C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125287970 | ||||||
| chr9:125288112
|
A | AT | 10 | a0001c0001t0001g0283a0001c0001t0001g0296a0001c0001t0001g0297others(7): Show | 10 | HG01123.hp2 HG02258.hp2 HG03540.hp2 others(7): Show |
intron_variant | MODIFIER | c.-149-7329dupT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125288112 | |||||
| chr9:125288326
|
G | A | 1 | a0001c0001t0001g0262 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-149-7132G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125288326 | ||||||
| chr9:125288327
|
G | A | 165 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(162): Show | 165 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.-149-7131G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125288327 | ||||||
| chr9:125288503
|
G | A | 2 | a0001c0003t0006g0163a0001c0003t0026g0118 | 2 | HG02055.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.-149-6955G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125288503 | ||||||
| chr9:125288690
|
A | G | 1 | a0001c0001t0002g0100 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-149-6768A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125288690 | ||||||
| chr9:125288887
|
G | A | 2 | a0001c0001t0004g0173a0001c0001t0004g0174 | 2 | HG01099.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.-149-6571G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125288887 | ||||||
| chr9:125288930
|
A | G | 8 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0008others(5): Show | 8 | HG01069.hp1 HG02135.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.-149-6528A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125288930 | ||||||
| chr9:125289158
|
A | G | 1 | a0001c0010t0006g0167 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-149-6300A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125289158 | ||||||
| chr9:125289362
|
GT | G | 31 | a0001c0002t0003g0004a0001c0002t0003g0005a0001c0002t0003g0123others(28): Show | 31 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.-149-6094delT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125289362 | |||||
| chr9:125289408
|
G | A | 7 | a0001c0003t0006g0158a0001c0003t0006g0159a0001c0003t0006g0160others(4): Show | 7 | HG01109.hp1 HG01884.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.-149-6050G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125289408 | ||||||
| chr9:125289795
|
A | C | 3 | a0001c0001t0009g0001a0001c0001t0009g0002a0001c0001t0009g0003 | 3 | HG01884.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-149-5663A>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125289795 | ||||||
| chr9:125289861
|
A | G | 1 | a0001c0001t0017g0013 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-149-5597A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125289861 | ||||||
| chr9:125289925
|
G | A | 1 | a0001c0001t0034g0217 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-149-5533G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125289925 | ||||||
| chr9:125290008
|
A | T | 1 | a0001c0001t0002g0024 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-149-5450A>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125290008 | ||||||
| chr9:125290165
|
C | T | 1 | a0001c0001t0001g0225 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-149-5293C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125290165 | ||||||
| chr9:125290273
|
G | A | 1 | a0001c0001t0017g0013 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-149-5185G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125290273 | ||||||
| chr9:125290353
|
A | G | 21 | a0001c0001t0009g0001a0001c0001t0009g0002a0001c0001t0009g0003others(18): Show | 21 | HG01109.hp1 HG01167.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.-149-5105A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125290353 | ||||||
| chr9:125290409
|
T | G | 1 | a0001c0001t0002g0051 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-149-5049T>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125290409 | ||||||
| chr9:125290419
|
A | G | 1 | a0001c0001t0001g0236 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-149-5039A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125290419 | ||||||
| chr9:125290423
|
G | A | 1 | a0001c0001t0001g0178 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-149-5035G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125290423 | ||||||
| chr9:125290449
|
A | G | 21 | a0001c0001t0009g0001a0001c0001t0009g0002a0001c0001t0009g0003others(18): Show | 21 | HG01109.hp1 HG01167.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.-149-5009A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125290449 | ||||||
| chr9:125290502
|
G | A | 17 | a0001c0001t0002g0021a0001c0001t0002g0086a0001c0001t0002g0087others(14): Show | 17 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(14): Show |
intron_variant | MODIFIER | c.-149-4956G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125290502 | ||||||
| chr9:125290557
|
C | T | 2 | a0001c0001t0001g0290a0001c0001t0001g0312 | 2 | HG02698.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.-149-4901C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125290557 | ||||||
| chr9:125290661
|
G | A | 2 | a0001c0001t0001g0275a0001c0001t0001g0293 | 2 | NA18974.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.-149-4797G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125290661 | ||||||
| chr9:125290686
|
G | A | 1 | a0001c0001t0017g0013 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-149-4772G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125290686 | ||||||
| chr9:125290723
|
A | G | 2 | a0001c0001t0002g0058a0001c0001t0002g0076 | 2 | NA18989.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.-149-4735A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125290723 | ||||||
| chr9:125290977
|
A | G | 231 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(228): Show | 231 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.-149-4481A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125290977 | ||||||
| chr9:125290994
|
T | TA | 154 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(151): Show | 154 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.-149-4446dupA | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125290994 | |||||
| chr9:125290994
|
T | TAA | 8 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0273others(5): Show | 8 | HG00733.hp1 HG02698.hp2 HG03654.hp1 others(5): Show |
intron_variant | MODIFIER | c.-149-4447_-149-444 others(6): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125290994 | |||||
| chr9:125291225
|
G | A | 3 | a0001c0001t0002g0090a0001c0001t0002g0091a0001c0001t0002g0092 | 3 | HG01192.hp2 HG04204.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.-149-4233G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125291225 | ||||||
| chr9:125291450
|
G | A | 3 | a0001c0001t0001g0240a0001c0001t0001g0267a0001c0003t0006g0158 | 3 | HG01884.hp1 HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-149-4008G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125291450 | ||||||
| chr9:125291709
|
G | GACCCATA others(10): Show |
1 | a0001c0001t0001g0229 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-149-3748_-149-373 others(21): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125291709 | |||||
| chr9:125291970
|
G | C | 6 | a0001c0003t0006g0166a0001c0003t0006g0168a0001c0003t0006g0169others(3): Show | 6 | HG01167.hp1 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-149-3488G>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125291970 | ||||||
| chr9:125292033
|
A | G | 1 | a0005c0015t0002g0057 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-149-3425A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125292033 | ||||||
| chr9:125292046
|
T | G | 3 | a0001c0001t0002g0087a0001c0001t0002g0111a0001c0001t0028g0154 | 3 | HG02165.hp2 NA18967.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.-149-3412T>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125292046 | ||||||
| chr9:125292117
|
A | C | 337 | a0001c0001t0001g0017a0001c0001t0001g0045a0001c0001t0001g0176others(334): Show | 337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.-149-3341A>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125292117 | ||||||
| chr9:125292130
|
G | A | 1 | a0001c0016t0037g0152 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-149-3328G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125292130 | ||||||
| chr9:125292136
|
C | T | 2 | a0002c0006t0011g0121a0002c0006t0011g0122 | 2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-149-3322C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125292136 | ||||||
| chr9:125292206
|
C | T | 3 | a0001c0001t0001g0298a0001c0002t0007g0143a0001c0002t0007g0149 | 3 | HG02970.hp2 NA18964.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.-149-3252C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125292206 | ||||||
| chr9:125292270
|
A | C | 1 | a0001c0001t0001g0236 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-149-3188A>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125292270 | ||||||
| chr9:125292400
|
A | AT | 9 | a0001c0001t0002g0114a0001c0003t0006g0158a0001c0003t0006g0159others(6): Show | 9 | HG01109.hp1 HG01884.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.-149-3045dupT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125292400 | |||||
| chr9:125292527
|
G | A | 1 | a0001c0001t0002g0016 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.-149-2931G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125292527 | ||||||
| chr9:125292544
|
C | G | 1 | a0001c0001t0001g0236 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-149-2914C>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125292544 | ||||||
| chr9:125292688
|
C | G | 31 | a0001c0002t0003g0004a0001c0002t0003g0005a0001c0002t0003g0123others(28): Show | 31 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.-149-2770C>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125292688 | ||||||
| chr9:125292813
|
T | A | 1 | a0001c0001t0001g0236 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-149-2645T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125292813 | ||||||
| chr9:125293015
|
G | T | 1 | a0001c0001t0017g0013 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-149-2443G>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125293015 | ||||||
| chr9:125293178
|
A | G | 200 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(197): Show | 200 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.-149-2280A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125293178 | ||||||
| chr9:125293543
|
G | A | 1 | a0001c0001t0015g0064 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-149-1915G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125293543 | ||||||
| chr9:125293611
|
A | G | 1 | a0001c0001t0001g0236 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-149-1847A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125293611 | ||||||
| chr9:125293618
|
T | TTTATATA others(32): Show |
61 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(58): Show | 61 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.-149-1829_-149-179 others(43): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293618 | |||||
| chr9:125293618
|
T | TTTATATA others(61): Show |
1 | a0001c0001t0001g0326 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-149-1800_-149-179 others(72): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293618 | |||||
| chr9:125293618
|
T | TTTATATA others(60): Show |
1 | a0001c0001t0001g0325 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-149-1831_-149-176 others(71): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293618 | |||||
| chr9:125293618
|
T | TTTATATA others(62): Show |
89 | a0001c0001t0001g0193a0001c0001t0001g0195a0001c0001t0001g0196others(86): Show | 89 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.-149-1790_-149-178 others(73): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293618 | |||||
| chr9:125293618
|
T | TTTATATA others(92): Show |
3 | a0001c0001t0001g0192a0001c0001t0001g0214a0001c0001t0001g0228 | 3 | HG03041.hp1 HG03831.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.-149-1790_-149-178 others(103): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293618 | |||||
| chr9:125293618
|
T | TTTATATA others(71): Show |
1 | a0001c0001t0001g0277 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-149-1791_-149-179 others(82): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293618 | |||||
| chr9:125293618
|
T | TTTATATA others(59): Show |
1 | a0001c0001t0001g0229 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-149-1810_-149-180 others(70): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293618 | |||||
| chr9:125293618
|
T | TTTATATA others(63): Show |
1 | a0001c0001t0001g0236 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-149-1829_-149-182 others(74): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293618 | |||||
| chr9:125293629
|
T | TATATATA others(21): Show |
1 | a0001c0001t0017g0013 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-149-1828_-149-180 others(32): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293629 | |||||
| chr9:125293630
|
A | ATATATAT others(21): Show |
1 | a0001c0001t0016g0046 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-149-1792_-149-176 others(32): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293630 | |||||
| chr9:125293630
|
A | ATATATAT others(30): Show |
2 | a0001c0001t0002g0309a0001c0001t0002g0314 | 2 | NA18939.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.-149-1827_-149-179 others(41): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293630 | |||||
| chr9:125293630
|
A | ATATATAT others(88): Show |
2 | a0002c0006t0011g0121a0002c0006t0011g0122 | 2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-149-1785_-149-178 others(99): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293630 | |||||
| chr9:125293630
|
A | ATATATAT others(60): Show |
3 | a0001c0001t0001g0246a0001c0001t0001g0247a0001c0001t0001g0298 | 3 | HG02280.hp1 HG02970.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-149-1790_-149-178 others(71): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293630 | |||||
| chr9:125293630
|
ATATATAT others(21): Show |
A | 2 | a0001c0003t0006g0160a0001c0016t0037g0152 | 2 | HG02280.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.-149-1792_-149-176 others(32): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293630 | |||||
| chr9:125293650
|
T | A | 2 | a0001c0001t0001g0017a0001c0001t0001g0045 | 2 | HG01099.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.-149-1808T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125293650 | ||||||
| chr9:125293658
|
T | A | 1 | a0001c0001t0017g0013 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-149-1800T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125293658 | ||||||
| chr9:125293658
|
T | TTA | 3 | a0001c0001t0009g0001a0001c0001t0009g0002a0001c0001t0009g0003 | 3 | HG01884.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-149-1791_-149-179 others(6): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293658 | |||||
| chr9:125293658
|
T | TTATATAT others(34): Show |
2 | a0001c0001t0001g0224a0001c0001t0002g0257 | 2 | HG01261.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.-149-1790_-149-178 others(45): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293658 | |||||
| chr9:125293660
|
A | ATATATAT others(30): Show |
1 | a0001c0001t0002g0311 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-149-1791_-149-179 others(41): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293660 | |||||
| chr9:125293663
|
TATATA | T | 7 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0008others(4): Show | 7 | HG01069.hp1 HG02615.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.-149-1788_-149-178 others(9): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293663 | |||||
| chr9:125293676
|
A | T | 1 | a0001c0001t0002g0044 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-149-1782A>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125293676 | ||||||
| chr9:125293709
|
AT | A | 32 | a0001c0001t0001g0229a0001c0001t0002g0014a0001c0001t0002g0015others(29): Show | 32 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.-149-1744delT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293709 | |||||
| chr9:125293723
|
T | G | 104 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0001g0195others(101): Show | 104 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.-149-1735T>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125293723 | ||||||
| chr9:125293770
|
T | A | 1 | a0001c0001t0001g0229 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-149-1688T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125293770 | ||||||
| chr9:125293771
|
A | T | 1 | a0001c0001t0001g0229 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-149-1687A>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125293771 | ||||||
| chr9:125293784
|
A | T | 3 | a0001c0001t0001g0192a0001c0001t0001g0269a0001c0001t0001g0322 | 3 | HG00639.hp1 HG02622.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-149-1674A>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125293784 | ||||||
| chr9:125293798
|
A | C | 90 | a0001c0001t0001g0193a0001c0001t0001g0195a0001c0001t0001g0196others(87): Show | 90 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.-149-1660A>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125293798 | ||||||
| chr9:125293818
|
G | A | 1 | a0001c0016t0037g0152 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-149-1640G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125293818 | ||||||
| chr9:125293824
|
TA | T | 4 | a0001c0001t0002g0044a0001c0001t0002g0054a0001c0001t0002g0063others(1): Show | 4 | HG00733.hp2 HG00741.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.-149-1627delA | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293824 | |||||
| chr9:125293830
|
A | T | 3 | a0001c0001t0001g0185a0001c0001t0004g0173a0001c0001t0004g0174 | 3 | HG01099.hp1 HG02257.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.-149-1628A>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125293830 | ||||||
| chr9:125293832
|
T | A | 1 | a0001c0001t0015g0064 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-149-1626T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125293832 | ||||||
| chr9:125293840
|
T | A | 2 | a0001c0001t0002g0023a0001c0001t0002g0065 | 2 | HG03831.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.-149-1618T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125293840 | ||||||
| chr9:125293840
|
TA | T | 6 | a0001c0001t0001g0291a0001c0003t0006g0162a0001c0003t0006g0169others(3): Show | 6 | HG02572.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-149-1613delA | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293840 | |||||
| chr9:125293842
|
A | AAAATATA others(14): Show |
5 | a0001c0001t0001g0286a0001c0001t0001g0310a0001c0001t0005g0307others(2): Show | 5 | HG02056.hp1 HG04184.hp2 NA18980.hp1 others(2): Show |
intron_variant | MODIFIER | c.-149-1614_-149-159 others(25): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293842 | |||||
| chr9:125293842
|
A | AAAATATA others(35): Show |
2 | a0001c0001t0001g0283a0001c0001t0001g0316 | 2 | NA18953.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.-149-1594_-149-159 others(46): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293842 | |||||
| chr9:125293842
|
A | AAATATAT others(11): Show |
2 | a0001c0003t0006g0166a0001c0003t0006g0168 | 2 | HG01167.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-149-1614_-149-161 others(22): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293842 | |||||
| chr9:125293842
|
A | T | 10 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0008others(7): Show | 10 | HG01069.hp1 HG01099.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.-149-1616A>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125293842 | ||||||
| chr9:125293844
|
A | ATATATTA others(55): Show |
2 | a0001c0002t0003g0004a0001c0002t0003g0005 | 2 | NA18979.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.-149-1614_-149-161 others(66): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125293844 | ||||||
| chr9:125293844
|
A | T | 2 | a0001c0001t0002g0023a0001c0001t0002g0065 | 2 | HG03831.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.-149-1614A>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125293844 | ||||||
| chr9:125293849
|
A | T | 2 | a0001c0001t0002g0023a0001c0001t0002g0065 | 2 | HG03831.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.-149-1609A>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125293849 | ||||||
| chr9:125293850
|
TTTTATAT others(25): Show |
T | 1 | a0001c0001t0002g0032 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-149-1606_-149-157 others(36): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293850 | |||||
| chr9:125293851
|
T | A | 2 | a0001c0002t0003g0004a0001c0002t0003g0005 | 2 | NA18979.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.-149-1607T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125293851 | ||||||
| chr9:125293851
|
TTTATATA others(6): Show |
T | 1 | a0001c0001t0002g0033 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-149-1605_-149-159 others(17): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293851 | |||||
| chr9:125293852
|
T | A | 35 | a0001c0001t0001g0241a0001c0001t0002g0023a0001c0001t0002g0065others(32): Show | 35 | HG00408.hp1 HG00544.hp2 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.-149-1606T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125293852 | ||||||
| chr9:125293852
|
T | TTA | 10 | a0001c0001t0001g0017a0001c0001t0001g0045a0001c0001t0002g0021others(7): Show | 10 | HG00544.hp1 HG01099.hp2 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.-149-1555_-149-155 others(6): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293852 | |||||
| chr9:125293852
|
T | TTATA | 7 | a0001c0001t0002g0022a0001c0001t0002g0094a0001c0001t0002g0100others(4): Show | 7 | HG00408.hp2 HG01167.hp1 HG02083.hp1 others(4): Show |
intron_variant | MODIFIER | c.-149-1557_-149-155 others(8): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293852 | |||||
| chr9:125293852
|
T | TTATATA | 6 | a0001c0001t0002g0074a0001c0001t0002g0078a0001c0001t0002g0079others(3): Show | 6 | HG00609.hp1 HG00642.hp1 HG00735.hp1 others(3): Show |
intron_variant | MODIFIER | c.-149-1559_-149-155 others(10): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293852 | |||||
| chr9:125293852
|
T | TTATATAT others(1): Show |
4 | a0001c0001t0002g0106a0001c0001t0002g0153a0001c0001t0028g0154others(1): Show | 4 | NA18959.hp2 NA18967.hp2 NA19079.hp1 others(1): Show |
intron_variant | MODIFIER | c.-149-1561_-149-155 others(12): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293852 | |||||
| chr9:125293852
|
T | TTATATAT others(3): Show |
4 | a0001c0001t0002g0111a0001c0001t0002g0114a0001c0001t0002g0119others(1): Show | 4 | HG00738.hp2 HG02165.hp2 NA18943.hp2 others(1): Show |
intron_variant | MODIFIER | c.-149-1563_-149-155 others(14): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293852 | |||||
| chr9:125293852
|
T | TTATATAT others(20): Show |
2 | a0001c0003t0006g0169a0001c0003t0006g0172 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-149-1596_-149-159 others(31): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293852 | |||||
| chr9:125293852
|
T | TTATATAT others(22): Show |
1 | a0001c0003t0006g0171 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-149-1596_-149-159 others(33): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293852 | |||||
| chr9:125293852
|
T | TTATATAT others(41): Show |
1 | a0001c0003t0026g0118 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-149-1596_-149-159 others(52): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293852 | |||||
| chr9:125293852
|
T | TTATATAT others(20): Show |
1 | a0001c0016t0037g0152 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-149-1594_-149-159 others(31): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293852 | |||||
| chr9:125293852
|
T | TTATATAT others(7): Show |
3 | a0001c0001t0002g0025a0001c0001t0002g0059a0001c0001t0002g0068 | 3 | HG03688.hp2 NA18978.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.-149-1567_-149-155 others(18): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293852 | |||||
| chr9:125293852
|
T | TTATATAT others(11): Show |
3 | a0001c0001t0002g0066a0001c0001t0002g0086a0001c0001t0015g0060 | 3 | HG00099.hp2 HG00438.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.-149-1571_-149-155 others(22): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293852 | |||||
| chr9:125293852
|
T | TTATATAT others(13): Show |
1 | a0001c0001t0002g0082 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-149-1573_-149-155 others(24): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293852 | |||||
| chr9:125293852
|
TTA | T | 11 | a0001c0001t0002g0014a0001c0001t0002g0039a0001c0001t0002g0040others(8): Show | 11 | HG02074.hp2 HG02165.hp1 HG02602.hp1 others(8): Show |
intron_variant | MODIFIER | c.-149-1555_-149-155 others(6): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293852 | |||||
| chr9:125293852
|
TTATA | T | 14 | a0001c0001t0002g0020a0001c0001t0002g0026a0001c0001t0002g0027others(11): Show | 14 | HG00280.hp2 HG00673.hp1 HG01069.hp2 others(11): Show |
intron_variant | MODIFIER | c.-149-1557_-149-155 others(8): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293852 | |||||
| chr9:125293852
|
TTATATA | T | 8 | a0001c0001t0002g0018a0001c0001t0002g0024a0001c0001t0002g0028others(5): Show | 8 | HG00733.hp2 HG02071.hp1 NA18957.hp1 others(5): Show |
intron_variant | MODIFIER | c.-149-1559_-149-155 others(10): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293852 | |||||
| chr9:125293852
|
TTATATAT others(1): Show |
T | 7 | a0001c0001t0002g0030a0001c0001t0002g0036a0001c0001t0002g0051others(4): Show | 7 | HG01192.hp1 HG01192.hp2 HG02132.hp1 others(4): Show |
intron_variant | MODIFIER | c.-149-1561_-149-155 others(12): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293852 | |||||
| chr9:125293852
|
TTATATAT others(3): Show |
T | 2 | a0001c0001t0002g0016a0001c0001t0002g0097 | 2 | HG03704.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.-149-1563_-149-155 others(14): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293852 | |||||
| chr9:125293852
|
TTATATAT others(5): Show |
T | 1 | a0001c0001t0002g0091 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-149-1565_-149-155 others(16): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293852 | |||||
| chr9:125293852
|
TTATATAT others(7): Show |
T | 1 | a0001c0004t0001g0035 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-149-1567_-149-155 others(18): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293852 | |||||
| chr9:125293852
|
TTATATAT others(9): Show |
T | 1 | a0001c0001t0002g0034 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-149-1569_-149-155 others(20): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293852 | |||||
| chr9:125293852
|
TTATATAT others(23): Show |
T | 1 | a0001c0001t0002g0072 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-149-1583_-149-155 others(34): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293852 | |||||
| chr9:125293852
|
TTATATAT others(25): Show |
T | 1 | a0001c0001t0030g0120 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-149-1585_-149-155 others(36): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293852 | |||||
| chr9:125293852
|
TTATATAT others(31): Show |
T | 1 | a0001c0001t0002g0029 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-149-1591_-149-155 others(42): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293852 | |||||
| chr9:125293854
|
A | ATATATAT others(8): Show |
1 | a0001c0001t0004g0173 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-149-1596_-149-159 others(19): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293854 | |||||
| chr9:125293854
|
A | ATATATAT others(10): Show |
1 | a0001c0010t0006g0167 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-149-1596_-149-159 others(21): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293854 | |||||
| chr9:125293854
|
A | ATATATAT others(37): Show |
1 | a0001c0003t0006g0163 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-149-1596_-149-159 others(48): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293854 | |||||
| chr9:125293854
|
A | ATATATAT others(12): Show |
6 | a0001c0001t0001g0281a0001c0001t0001g0304a0001c0001t0001g0305others(3): Show | 6 | HG02300.hp2 NA18942.hp1 NA18954.hp2 others(3): Show |
intron_variant | MODIFIER | c.-149-1594_-149-159 others(23): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293854 | |||||
| chr9:125293854
|
A | ATATATAT others(33): Show |
4 | a0001c0001t0001g0270a0001c0001t0001g0272a0001c0001t0001g0293others(1): Show | 4 | HG00673.hp2 NA18952.hp1 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.-149-1594_-149-159 others(44): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293854 | |||||
| chr9:125293854
|
A | T | 1 | a0001c0001t0002g0117 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-149-1604A>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125293854 | ||||||
| chr9:125293856
|
A | ATATATAA others(6): Show |
1 | a0001c0001t0004g0174 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-149-1596_-149-159 others(17): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293856 | |||||
| chr9:125293856
|
A | ATATATAT others(10): Show |
2 | a0001c0001t0001g0184a0001c0001t0001g0188 | 2 | HG00558.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.-149-1594_-149-159 others(21): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293856 | |||||
| chr9:125293858
|
A | ATATATAA others(8): Show |
11 | a0001c0001t0001g0181a0001c0001t0001g0183a0001c0001t0001g0186others(8): Show | 11 | HG00621.hp2 HG02004.hp1 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.-149-1594_-149-159 others(19): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293858 | |||||
| chr9:125293858
|
A | ATATATAA others(29): Show |
4 | a0001c0001t0001g0276a0001c0001t0001g0278a0001c0001t0001g0292others(1): Show | 4 | HG01255.hp1 NA18985.hp2 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.-149-1594_-149-159 others(40): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293858 | |||||
| chr9:125293860
|
A | AAATATAA others(55): Show |
28 | a0001c0002t0003g0123a0001c0002t0003g0125a0001c0002t0003g0127others(25): Show | 28 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(25): Show |
intron_variant | MODIFIER | c.-149-1598_-149-159 others(66): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125293860 | ||||||
| chr9:125293860
|
A | AAATATAA others(53): Show |
1 | a0001c0002t0003g0126 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-149-1598_-149-159 others(64): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125293860 | ||||||
| chr9:125293860
|
A | ATATAAAT others(6): Show |
6 | a0001c0001t0001g0274a0001c0001t0001g0277a0001c0001t0001g0280others(3): Show | 6 | HG00438.hp1 HG01243.hp2 NA18612.hp2 others(3): Show |
intron_variant | MODIFIER | c.-149-1594_-149-159 others(17): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293860 | |||||
| chr9:125293860
|
A | ATATAAAT others(27): Show |
4 | a0001c0001t0001g0271a0001c0001t0001g0275a0001c0001t0001g0284others(1): Show | 4 | HG00609.hp2 NA18974.hp2 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.-149-1594_-149-159 others(38): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293860 | |||||
| chr9:125293862
|
A | ATAAATAT others(4): Show |
7 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0288others(4): Show | 7 | HG03688.hp1 HG03704.hp1 HG03834.hp1 others(4): Show |
intron_variant | MODIFIER | c.-149-1594_-149-159 others(15): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293862 | |||||
| chr9:125293862
|
A | ATATATAA others(6): Show |
1 | a0001c0003t0004g0156 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-149-1590_-149-158 others(17): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293862 | |||||
| chr9:125293863
|
T | A | 8 | a0001c0001t0009g0001a0001c0001t0009g0002a0001c0001t0009g0003others(5): Show | 8 | HG01109.hp1 HG01884.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.-149-1595T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125293863 | ||||||
| chr9:125293864
|
A | AAATATAT | 6 | a0001c0001t0001g0176a0001c0001t0001g0182a0001c0001t0001g0185others(3): Show | 6 | HG03540.hp2 HG03710.hp1 NA18943.hp1 others(3): Show |
intron_variant | MODIFIER | c.-149-1594_-149-159 others(11): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125293864 | ||||||
| chr9:125293864
|
A | AAATATAT others(21): Show |
1 | a0001c0001t0001g0273 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.-149-1594_-149-159 others(32): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125293864 | ||||||
| chr9:125293864
|
A | AAATATAT others(39): Show |
1 | a0001c0001t0001g0178 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-149-1594_-149-159 others(50): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125293864 | ||||||
| chr9:125293864
|
A | AAATATAT others(39): Show |
1 | a0001c0001t0001g0177 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-149-1594_-149-159 others(50): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125293864 | ||||||
| chr9:125293865
|
T | A | 113 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0001g0195others(110): Show | 113 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.-149-1593T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125293865 | ||||||
| chr9:125293866
|
A | AAAATATA others(26): Show |
2 | a0002c0006t0011g0121a0002c0006t0011g0122 | 2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-149-1592_-149-159 others(37): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125293866 | ||||||
| chr9:125293866
|
A | ATATTTTA others(75): Show |
1 | a0001c0003t0006g0160 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-149-1589_-149-158 others(86): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293866 | |||||
| chr9:125293866
|
A | T | 8 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0182others(5): Show | 8 | HG03540.hp2 HG03710.hp1 NA18943.hp1 others(5): Show |
intron_variant | MODIFIER | c.-149-1592A>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125293866 | ||||||
| chr9:125293868
|
A | AT | 29 | a0001c0002t0003g0123a0001c0002t0003g0125a0001c0002t0003g0126others(26): Show | 29 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(26): Show |
intron_variant | MODIFIER | c.-149-1589dupT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293868 | |||||
| chr9:125293868
|
A | ATTTTATA others(75): Show |
1 | a0001c0003t0006g0162 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-149-1589_-149-158 others(86): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293868 | |||||
| chr9:125293868
|
A | ATTTTATA others(127): Show |
1 | a0001c0003t0006g0159 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-149-1589_-149-158 others(138): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293868 | |||||
| chr9:125293868
|
A | ATTTTATA others(77): Show |
1 | a0001c0003t0006g0161 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-149-1589_-149-158 others(88): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293868 | |||||
| chr9:125293870
|
A | AT | 3 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0010 | 3 | HG02615.hp2 HG02723.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-149-1587dupT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293870 | |||||
| chr9:125293870
|
A | ATTT | 3 | a0001c0001t0001g0290a0001c0001t0004g0012a0001c0001t0017g0013 | 3 | HG02630.hp1 HG02698.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-149-1587_-149-158 others(7): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293870 | |||||
| chr9:125293870
|
A | ATTTTATA others(25): Show |
1 | a0001c0001t0004g0011 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-149-1587_-149-158 others(36): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293870 | |||||
| chr9:125293871
|
T | A | 3 | a0001c0003t0004g0157a0001c0003t0004g0170a0001c0003t0018g0165 | 3 | HG02258.hp1 HG02451.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.-149-1587T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125293871 | ||||||
| chr9:125293871
|
TA | T | 3 | a0001c0001t0001g0312a0001c0001t0004g0006a0001c0001t0004g0007 | 3 | HG02818.hp2 HG03453.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.-149-1586delA | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125293871 | ||||||
| chr9:125293871
|
TATATATA others(4): Show |
T | 4 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0001g0212others(1): Show | 4 | HG00408.hp1 HG02630.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-149-1586_-149-157 others(15): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125293871 | ||||||
| chr9:125293871
|
TATATATA others(6): Show |
T | 97 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0001g0195others(94): Show | 97 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.-149-1586_-149-157 others(17): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125293871 | ||||||
| chr9:125293871
|
TATATATA others(8): Show |
T | 1 | a0001c0001t0001g0229 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-149-1586_-149-157 others(19): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125293871 | ||||||
| chr9:125293872
|
A | T | 4 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0010others(1): Show | 4 | HG02615.hp2 HG02630.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.-149-1586A>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125293872 | ||||||
| chr9:125293874
|
A | T | 5 | a0001c0001t0001g0312a0001c0001t0004g0006a0001c0001t0004g0007others(2): Show | 5 | HG02280.hp2 HG02818.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-149-1584A>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125293874 | ||||||
| chr9:125293875
|
T | TA | 3 | a0001c0002t0003g0004a0001c0002t0003g0005a0001c0002t0003g0145 | 3 | NA18966.hp1 NA18979.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.-149-1582dupA | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293875 | |||||
| chr9:125293876
|
A | T | 5 | a0001c0001t0009g0002a0001c0001t0009g0003a0001c0003t0006g0159others(2): Show | 5 | HG01109.hp1 HG01884.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-149-1582A>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125293876 | ||||||
| chr9:125293877
|
T | TA | 28 | a0001c0002t0003g0123a0001c0002t0003g0125a0001c0002t0003g0126others(25): Show | 28 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(25): Show |
intron_variant | MODIFIER | c.-149-1580dupA | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293877 | |||||
| chr9:125293877
|
T | TTATATAT others(9): Show |
2 | a0001c0003t0004g0157a0001c0003t0018g0165 | 2 | HG02258.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.-149-1581_-149-158 others(20): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125293877 | ||||||
| chr9:125293877
|
T | TTATATAT others(13): Show |
1 | a0001c0003t0004g0170 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-149-1581_-149-158 others(24): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125293877 | ||||||
| chr9:125293878
|
A | ATATATAA others(41): Show |
1 | a0001c0003t0006g0158 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-149-1574_-149-157 others(52): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293878 | |||||
| chr9:125293881
|
T | A | 2 | a0002c0006t0011g0121a0002c0006t0011g0122 | 2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-149-1577T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125293881 | ||||||
| chr9:125293884
|
A | T | 4 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0001g0212others(1): Show | 4 | HG00408.hp1 HG02630.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-149-1574A>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125293884 | ||||||
| chr9:125293885
|
TA | T | 3 | a0001c0002t0003g0004a0001c0002t0003g0005a0001c0002t0003g0145 | 3 | NA18966.hp1 NA18979.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.-149-1572delA | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125293885 | ||||||
| chr9:125293886
|
A | AT | 30 | a0001c0002t0003g0123a0001c0002t0003g0125a0001c0002t0003g0126others(27): Show | 30 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.-149-1571dupT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125293886 | |||||
| chr9:125293886
|
A | T | 93 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0001g0195others(90): Show | 93 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.-149-1572A>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125293886 | ||||||
| chr9:125293888
|
A | T | 3 | a0001c0001t0001g0229a0002c0006t0011g0121a0002c0006t0011g0122 | 3 | HG01109.hp2 HG03098.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.-149-1570A>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125293888 | ||||||
| chr9:125293895
|
T | G | 1 | a0001c0001t0002g0311 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-149-1563T>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125293895 | ||||||
| chr9:125293903
|
T | A | 1 | a0001c0010t0006g0167 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-149-1555T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125293903 | ||||||
| chr9:125293940
|
G | A | 1 | a0001c0003t0018g0165 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-149-1518G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125293940 | ||||||
| chr9:125293955
|
C | A | 2 | a0001c0001t0002g0115a0001c0001t0002g0116 | 2 | NA18949.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.-149-1503C>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125293955 | ||||||
| chr9:125294115
|
T | C | 1 | a0001c0010t0006g0167 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-149-1343T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125294115 | ||||||
| chr9:125294149
|
G | A | 8 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0008others(5): Show | 8 | HG01069.hp1 HG02615.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.-149-1309G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125294149 | ||||||
| chr9:125294287
|
C | T | 1 | a0001c0003t0006g0159 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-149-1171C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125294287 | ||||||
| chr9:125294336
|
C | T | 7 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(4): Show | 7 | HG02027.hp2 NA18943.hp1 NA18952.hp2 others(4): Show |
intron_variant | MODIFIER | c.-149-1122C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125294336 | ||||||
| chr9:125294348
|
C | CT | 14 | a0001c0001t0001g0186a0001c0001t0001g0232a0001c0001t0001g0286others(11): Show | 14 | HG02071.hp1 HG02683.hp1 HG02970.hp1 others(11): Show |
intron_variant | MODIFIER | c.-149-1093dupT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125294348 | |||||
| chr9:125294370
|
C | T | 1 | a0001c0001t0008g0031 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-149-1088C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125294370 | ||||||
| chr9:125294386
|
C | T | 1 | a0001c0016t0037g0152 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-149-1072C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125294386 | ||||||
| chr9:125294415
|
C | T | 9 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0008others(6): Show | 9 | HG00738.hp2 HG01069.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.-149-1043C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125294415 | ||||||
| chr9:125294474
|
G | C | 1 | a0001c0001t0001g0286 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.-149-984G>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125294474 | ||||||
| chr9:125294503
|
T | C | 1 | a0001c0001t0004g0006 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-149-955T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125294503 | ||||||
| chr9:125294507
|
C | T | 1 | a0001c0001t0002g0034 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-149-951C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125294507 | ||||||
| chr9:125294522
|
T | G | 1 | a0001c0001t0001g0200 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-149-936T>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125294522 | ||||||
| chr9:125294636
|
G | A | 7 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0008others(4): Show | 7 | HG01069.hp1 HG02615.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.-149-822G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125294636 | ||||||
| chr9:125294652
|
G | GT | 93 | a0001c0001t0001g0184a0001c0001t0001g0193a0001c0001t0001g0195others(90): Show | 93 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.-149-789dupT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125294652 | |||||
| chr9:125294652
|
G | GTT | 12 | a0001c0001t0001g0205a0001c0001t0001g0227a0001c0001t0001g0232others(9): Show | 12 | HG00738.hp1 HG02602.hp2 HG03209.hp2 others(9): Show |
intron_variant | MODIFIER | c.-149-790_-149-789d others(4): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125294652 | |||||
| chr9:125294652
|
G | T | 2 | a0002c0006t0011g0121a0002c0006t0011g0122 | 2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-149-806G>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125294652 | ||||||
| chr9:125294652
|
GT | G | 41 | a0001c0001t0002g0052a0001c0001t0002g0054a0001c0001t0002g0065others(38): Show | 41 | HG00544.hp1 HG00544.hp2 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.-149-789delT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125294652 | |||||
| chr9:125294667
|
T | C | 1 | a0001c0002t0003g0131 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-149-791T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125294667 | ||||||
| chr9:125294670
|
C | T | 1 | a0001c0001t0001g0236 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-149-788C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125294670 | ||||||
| chr9:125294671
|
A | C | 1 | a0001c0001t0001g0236 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-149-787A>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125294671 | ||||||
| chr9:125294746
|
T | G | 1 | a0001c0001t0001g0236 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-149-712T>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125294746 | ||||||
| chr9:125294747
|
G | T | 1 | a0001c0001t0001g0236 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-149-711G>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125294747 | ||||||
| chr9:125294908
|
G | A | 31 | a0001c0002t0003g0004a0001c0002t0003g0005a0001c0002t0003g0123others(28): Show | 31 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.-149-550G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125294908 | ||||||
| chr9:125294930
|
G | T | 1 | a0001c0004t0002g0042 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-149-528G>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125294930 | ||||||
| chr9:125294962
|
T | A | 1 | a0001c0001t0001g0236 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-149-496T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125294962 | ||||||
| chr9:125295254
|
T | C | 1 | a0001c0001t0005g0338 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.-149-204T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125295254 | ||||||
| chr9:125295354
|
T | A | 1 | a0001c0001t0001g0229 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-149-104T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125295354 | ||||||
| chr9:125295358
|
A | C | 1 | a0001c0001t0001g0229 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-149-100A>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125295358 | ||||||
| chr9:125295359
|
T | G | 1 | a0001c0001t0001g0229 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-149-99T>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125295359 | ||||||
| chr9:125295360
|
T | C | 1 | a0001c0001t0001g0229 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-149-98T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125295360 | ||||||
| chr9:125295361
|
A | G | 1 | a0001c0001t0001g0229 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-149-97A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125295361 | ||||||
| chr9:125295363
|
A | G | 1 | a0001c0001t0001g0229 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-149-95A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125295363 | ||||||
| chr9:125295364
|
G | T | 1 | a0001c0001t0001g0229 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-149-94G>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | chr9 | 125295364 | ||||||
| chr9:125295429
|
C | CT | 14 | a0001c0001t0002g0021a0001c0001t0002g0024a0001c0001t0002g0025others(11): Show | 14 | HG00544.hp1 HG00642.hp1 HG00673.hp1 others(11): Show |
splice_region_variant&intron_variant | LOW | c.-149-8dupT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125295429 | |||||
| chr9:125295429
|
CT | C | 183 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(180): Show | 183 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(180): Show |
splice_region_variant&intron_variant | LOW | c.-149-8delT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125295429 | |||||
| chr9:125295429
|
CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0001g0204 | 1 | HG02615.hp1 | splice_region_variant&intron_variant | LOW | c.-149-19_-149-8delT others(11): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr9 | 125295429 | |||||
| chr9:125295643
|
A | G | 166 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(163): Show | 166 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.-33+69A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 3/27 | chr9 | 125295643 | ||||||
| chr9:125296098
|
A | T | 231 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(228): Show | 231 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.-33+524A>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 3/27 | chr9 | 125296098 | ||||||
| chr9:125296108
|
A | T | 33 | a0001c0002t0003g0004a0001c0002t0003g0005a0001c0002t0003g0123others(30): Show | 33 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(30): Show |
intron_variant | MODIFIER | c.-33+534A>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 3/27 | chr9 | 125296108 | ||||||
| chr9:125296140
|
T | G | 1 | a0001c0001t0001g0265 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-33+566T>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 3/27 | chr9 | 125296140 | ||||||
| chr9:125296271
|
C | T | 1 | a0001c0001t0001g0195 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.-33+697C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 3/27 | chr9 | 125296271 | ||||||
| chr9:125296333
|
A | C | 2 | a0001c0003t0006g0163a0001c0003t0026g0118 | 2 | HG02055.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.-33+759A>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 3/27 | chr9 | 125296333 | ||||||
| chr9:125296357
|
G | GGTTTTTT others(5): Show |
3 | a0001c0002t0003g0132a0002c0006t0011g0121a0002c0006t0011g0122 | 3 | HG01109.hp2 HG03098.hp1 NA18939.hp1 |
intron_variant | MODIFIER | c.-33+784_-33+795dup others(12): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr9 | 125296357 | |||||
| chr9:125296358
|
G | GTTTTTTT others(6): Show |
192 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(189): Show | 192 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.-33+795_-33+796ins others(13): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr9 | 125296358 | |||||
| chr9:125296358
|
G | GTTTTTTT others(7): Show |
27 | a0001c0001t0001g0195a0001c0001t0001g0228a0001c0001t0001g0236others(24): Show | 27 | HG01109.hp1 HG01167.hp1 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.-33+795_-33+796ins others(14): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr9 | 125296358 | |||||
| chr9:125296358
|
G | GTTTTTTT others(7): Show |
1 | a0001c0002t0003g0140 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.-33+796_-33+797ins others(14): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr9 | 125296358 | |||||
| chr9:125296358
|
G | GTTTTTTT others(6): Show |
7 | a0001c0001t0009g0001a0001c0001t0009g0002a0001c0001t0009g0003others(4): Show | 7 | HG01884.hp2 HG02258.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.-33+787_-33+799dup others(13): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr9 | 125296358 | |||||
| chr9:125296358
|
G | GTTTTTTT others(7): Show |
1 | a0001c0003t0004g0170 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-33+786_-33+799dup others(14): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr9 | 125296358 | |||||
| chr9:125296390
|
C | G | 1 | a0001c0001t0001g0320 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-33+816C>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 3/27 | chr9 | 125296390 | ||||||
| chr9:125296487
|
T | G | 31 | a0001c0002t0003g0004a0001c0002t0003g0005a0001c0002t0003g0123others(28): Show | 31 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.-33+913T>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 3/27 | chr9 | 125296487 | ||||||
| chr9:125296653
|
C | CT | 32 | a0001c0001t0002g0038a0001c0001t0004g0006a0001c0001t0004g0007others(29): Show | 32 | HG01069.hp1 HG01099.hp1 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.-33+1093dupT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr9 | 125296653 | |||||
| chr9:125296653
|
C | CTT | 34 | a0001c0001t0001g0273a0001c0002t0003g0004a0001c0002t0003g0005others(31): Show | 34 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(31): Show |
intron_variant | MODIFIER | c.-33+1092_-33+1093d others(4): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr9 | 125296653 | |||||
| chr9:125296653
|
C | CTTT | 163 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(160): Show | 163 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.-33+1091_-33+1093d others(5): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr9 | 125296653 | |||||
| chr9:125296952
|
G | T | 2 | a0001c0001t0001g0277a0001c0001t0001g0287 | 2 | HG02071.hp2 NA18944.hp1 |
intron_variant | MODIFIER | c.-33+1378G>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 3/27 | chr9 | 125296952 | ||||||
| chr9:125297199
|
T | C | 33 | a0001c0002t0003g0004a0001c0002t0003g0005a0001c0002t0003g0123others(30): Show | 33 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(30): Show |
intron_variant | MODIFIER | c.-33+1625T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 3/27 | chr9 | 125297199 | ||||||
| chr9:125297612
|
G | A | 1 | a0001c0016t0037g0152 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-32-1278G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 3/27 | chr9 | 125297612 | ||||||
| chr9:125297714
|
A | G | 1 | a0007c0017t0001g0250 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-32-1176A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 3/27 | chr9 | 125297714 | ||||||
| chr9:125297782
|
A | G | 1 | a0001c0002t0003g0127 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-32-1108A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 3/27 | chr9 | 125297782 | ||||||
| chr9:125297798
|
T | C | 1 | a0001c0016t0037g0152 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-32-1092T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 3/27 | chr9 | 125297798 | ||||||
| chr9:125297894
|
C | T | 3 | a0001c0001t0002g0040a0001c0001t0002g0081a0005c0015t0002g0057 | 3 | NA18941.hp1 NA18964.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.-32-996C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 3/27 | chr9 | 125297894 | ||||||
| chr9:125297966
|
G | A | 5 | a0001c0003t0006g0158a0001c0003t0006g0159a0001c0003t0006g0160others(2): Show | 5 | HG01109.hp1 HG01884.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.-32-924G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 3/27 | chr9 | 125297966 | ||||||
| chr9:125298035
|
C | T | 1 | a0001c0002t0003g0130 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-32-855C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 3/27 | chr9 | 125298035 | ||||||
| chr9:125298041
|
C | T | 8 | a0001c0001t0002g0016a0001c0001t0002g0027a0001c0001t0002g0030others(5): Show | 8 | HG00673.hp1 HG02056.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.-32-849C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 3/27 | chr9 | 125298041 | ||||||
| chr9:125298106
|
G | A | 21 | a0001c0001t0009g0001a0001c0001t0009g0002a0001c0001t0009g0003others(18): Show | 21 | HG01109.hp1 HG01167.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.-32-784G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 3/27 | chr9 | 125298106 | ||||||
| chr9:125298278
|
G | T | 14 | a0001c0001t0001g0300a0001c0001t0001g0304a0001c0001t0001g0305others(11): Show | 14 | HG02004.hp1 HG02056.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.-32-612G>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 3/27 | chr9 | 125298278 | ||||||
| chr9:125298290
|
A | G | 1 | a0001c0001t0001g0288 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-32-600A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 3/27 | chr9 | 125298290 | ||||||
| chr9:125298321
|
C | T | 31 | a0001c0002t0003g0004a0001c0002t0003g0005a0001c0002t0003g0123others(28): Show | 31 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.-32-569C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 3/27 | chr9 | 125298321 | ||||||
| chr9:125298432
|
T | C | 33 | a0001c0002t0003g0004a0001c0002t0003g0005a0001c0002t0003g0123others(30): Show | 33 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(30): Show |
intron_variant | MODIFIER | c.-32-458T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 3/27 | chr9 | 125298432 | ||||||
| chr9:125298481
|
A | AT | 97 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0197others(94): Show | 97 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.-32-383dupT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr9 | 125298481 | |||||
| chr9:125298481
|
A | ATT | 59 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(56): Show | 59 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.-32-384_-32-383dup others(2): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr9 | 125298481 | |||||
| chr9:125298481
|
A | ATTT | 13 | a0001c0001t0001g0230a0001c0001t0001g0253a0001c0001t0001g0283others(10): Show | 13 | HG02071.hp2 HG02559.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.-32-385_-32-383dup others(3): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr9 | 125298481 | |||||
| chr9:125298481
|
AT | A | 45 | a0001c0001t0002g0054a0001c0001t0002g0084a0001c0001t0002g0117others(42): Show | 45 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(42): Show |
intron_variant | MODIFIER | c.-32-383delT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr9 | 125298481 | |||||
| chr9:125298481
|
ATT | A | 9 | a0001c0001t0009g0001a0001c0001t0009g0002a0001c0001t0009g0003others(6): Show | 9 | HG01167.hp1 HG01884.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.-32-384_-32-383del others(2): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr9 | 125298481 | |||||
| chr9:125298481
|
ATTTTTT | A | 7 | a0001c0001t0002g0061a0001c0001t0002g0063a0001c0001t0002g0065others(4): Show | 7 | HG00099.hp2 HG00733.hp2 HG00735.hp1 others(4): Show |
intron_variant | MODIFIER | c.-32-388_-32-383del others(6): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr9 | 125298481 | |||||
| chr9:125298581
|
C | T | 1 | a0001c0001t0001g0221 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-32-309C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 3/27 | chr9 | 125298581 | ||||||
| chr9:125299114
|
G | C | 1 | a0001c0001t0002g0082 | 1 | HG00423.hp1 | splice_region_variant&intron_variant | LOW | c.185+8G>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125299114 | ||||||
| chr9:125299225
|
A | G | 1 | a0001c0016t0037g0152 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.185+119A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125299225 | ||||||
| chr9:125299330
|
C | T | 3 | a0001c0001t0009g0001a0001c0001t0009g0002a0001c0001t0009g0003 | 3 | HG01884.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.185+224C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125299330 | ||||||
| chr9:125299370
|
A | G | 1 | a0001c0001t0004g0010 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.185+264A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125299370 | ||||||
| chr9:125299423
|
C | T | 2 | a0001c0002t0003g0138a0001c0002t0003g0139 | 2 | NA18940.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.185+317C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125299423 | ||||||
| chr9:125299428
|
C | T | 1 | a0001c0016t0037g0152 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.185+322C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125299428 | ||||||
| chr9:125299429
|
G | A | 1 | a0001c0001t0024g0194 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.185+323G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125299429 | ||||||
| chr9:125299666
|
A | C | 1 | a0001c0001t0001g0225 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.185+560A>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125299666 | ||||||
| chr9:125299668
|
A | G | 6 | a0001c0003t0006g0166a0001c0003t0006g0168a0001c0003t0006g0169others(3): Show | 6 | HG01167.hp1 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.185+562A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125299668 | ||||||
| chr9:125299753
|
G | T | 165 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(162): Show | 165 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.185+647G>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125299753 | ||||||
| chr9:125299775
|
C | G | 2 | a0002c0006t0011g0121a0002c0006t0011g0122 | 2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.185+669C>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125299775 | ||||||
| chr9:125299821
|
C | G | 5 | a0001c0003t0004g0156a0001c0003t0004g0157a0001c0003t0004g0164others(2): Show | 5 | HG02258.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.185+715C>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125299821 | ||||||
| chr9:125299846
|
C | G | 1 | a0001c0005t0001g0231 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.185+740C>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125299846 | ||||||
| chr9:125300023
|
G | GAAAA | 6 | a0001c0001t0001g0203a0001c0001t0001g0238a0001c0001t0001g0273others(3): Show | 6 | HG02723.hp1 HG02922.hp1 HG03688.hp1 others(3): Show |
intron_variant | MODIFIER | c.185+930_185+933dup others(4): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr9 | 125300023 | |||||
| chr9:125300023
|
G | GAAAAA | 8 | a0001c0001t0001g0182a0001c0001t0001g0218a0001c0001t0001g0237others(5): Show | 8 | HG02970.hp1 HG03486.hp1 HG03540.hp2 others(5): Show |
intron_variant | MODIFIER | c.185+929_185+933dup others(5): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr9 | 125300023 | |||||
| chr9:125300023
|
G | GAAAAAA | 13 | a0001c0001t0001g0197a0001c0001t0001g0204a0001c0001t0001g0210others(10): Show | 13 | HG00639.hp2 HG01074.hp1 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.185+928_185+933dup others(6): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr9 | 125300023 | |||||
| chr9:125300023
|
G | GAAAAAAA | 10 | a0001c0001t0001g0185a0001c0001t0001g0209a0001c0001t0001g0223others(7): Show | 10 | HG00140.hp2 HG00280.hp1 HG00673.hp2 others(7): Show |
intron_variant | MODIFIER | c.185+927_185+933dup others(7): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr9 | 125300023 | |||||
| chr9:125300023
|
G | GAAAAAAA others(1): Show |
11 | a0001c0001t0001g0192a0001c0001t0001g0246a0001c0001t0001g0256others(8): Show | 11 | HG02622.hp2 HG02717.hp2 HG02735.hp1 others(8): Show |
intron_variant | MODIFIER | c.185+926_185+933dup others(8): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr9 | 125300023 | |||||
| chr9:125300023
|
G | GAAAAAAA others(2): Show |
13 | a0001c0001t0001g0179a0001c0001t0001g0183a0001c0001t0001g0184others(10): Show | 13 | HG00558.hp1 HG01261.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.185+925_185+933dup others(9): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr9 | 125300023 | |||||
| chr9:125300023
|
G | GAAAAAAA others(3): Show |
2 | a0001c0001t0001g0196a0001c0001t0010g0255 | 2 | HG01175.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.185+924_185+933dup others(10): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr9 | 125300023 | |||||
| chr9:125300023
|
G | GAAAAAAA others(4): Show |
8 | a0001c0001t0001g0178a0001c0001t0001g0180a0001c0001t0001g0187others(5): Show | 8 | HG00621.hp2 HG01069.hp1 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.185+923_185+933dup others(11): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr9 | 125300023 | |||||
| chr9:125300023
|
G | GAAAAAAA others(5): Show |
10 | a0001c0001t0001g0181a0001c0001t0001g0225a0001c0001t0001g0234others(7): Show | 10 | HG00099.hp1 HG00408.hp1 HG00733.hp1 others(7): Show |
intron_variant | MODIFIER | c.185+922_185+933dup others(12): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr9 | 125300023 | |||||
| chr9:125300023
|
G | GAAAAAAA others(6): Show |
5 | a0001c0001t0001g0206a0001c0001t0001g0230a0001c0001t0001g0247others(2): Show | 5 | HG02280.hp1 HG04204.hp2 NA18982.hp2 others(2): Show |
intron_variant | MODIFIER | c.185+921_185+933dup others(13): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr9 | 125300023 | |||||
| chr9:125300023
|
G | GAAAAAAA others(7): Show |
3 | a0001c0001t0001g0176a0001c0001t0001g0253a0001c0001t0010g0216 | 3 | HG01517.hp1 HG02572.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.185+920_185+933dup others(14): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr9 | 125300023 | |||||
| chr9:125300023
|
G | GAAAAAAA others(8): Show |
6 | a0001c0001t0001g0224a0001c0001t0001g0268a0001c0001t0001g0327others(3): Show | 6 | HG01993.hp1 NA18747.hp2 NA18942.hp2 others(3): Show |
intron_variant | MODIFIER | c.185+919_185+933dup others(15): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr9 | 125300023 | |||||
| chr9:125300023
|
G | GAAAAAAA others(9): Show |
3 | a0001c0001t0005g0330a0001c0001t0005g0332a0001c0005t0001g0219 | 3 | HG02004.hp2 NA18950.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.185+918_185+933dup others(16): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr9 | 125300023 | |||||
| chr9:125300023
|
G | GAAAAAAA others(10): Show |
3 | a0001c0001t0001g0177a0001c0001t0001g0274a0001c0001t0001g0280 | 3 | HG00438.hp1 NA18612.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.185+933_185+934ins others(17): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr9 | 125300023 | |||||
| chr9:125300023
|
G | GAAAAAAA others(12): Show |
1 | a0001c0001t0001g0214 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.185+933_185+934ins others(19): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr9 | 125300023 | |||||
| chr9:125300023
|
G | GAAAAAAA others(14): Show |
1 | a0001c0001t0005g0340 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.185+933_185+934ins others(21): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr9 | 125300023 | |||||
| chr9:125300023
|
G | T | 5 | a0001c0003t0004g0156a0001c0003t0004g0157a0001c0003t0004g0164others(2): Show | 5 | HG02258.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.185+917G>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125300023 | ||||||
| chr9:125300028
|
A | T | 1 | a0001c0003t0004g0164 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.185+922A>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125300028 | ||||||
| chr9:125300036
|
AAAATATA others(23): Show |
A | 1 | a0001c0016t0037g0152 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.185+932_185+961del others(30): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr9 | 125300036 | |||||
| chr9:125300037
|
AAATATAT others(4): Show |
A | 4 | a0001c0003t0006g0166a0001c0003t0006g0168a0001c0003t0006g0171others(1): Show | 4 | HG01167.hp1 HG03195.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.185+933_185+943del others(11): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr9 | 125300037 | |||||
| chr9:125300037
|
AAATATAT others(6): Show |
A | 1 | a0001c0003t0006g0159 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.185+933_185+945del others(13): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr9 | 125300037 | |||||
| chr9:125300038
|
A | AAAAAAAA others(14): Show |
1 | a0001c0001t0001g0243 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.185+933_185+934ins others(21): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr9 | 125300038 | |||||
| chr9:125300038
|
A | AAAAAAAA others(9): Show |
2 | a0001c0001t0001g0244a0001c0001t0010g0266 | 2 | HG01515.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.185+933_185+934ins others(16): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr9 | 125300038 | |||||
| chr9:125300038
|
AATATAT | A | 8 | a0001c0001t0001g0239a0001c0001t0001g0269a0001c0001t0001g0298others(5): Show | 8 | HG00423.hp2 HG00639.hp1 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.185+983_185+988del others(6): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr9 | 125300038 | |||||
| chr9:125300038
|
AATATATA others(1): Show |
A | 13 | a0001c0001t0001g0249a0001c0001t0001g0251a0001c0001t0001g0304others(10): Show | 13 | HG00735.hp1 HG01346.hp1 HG01515.hp2 others(10): Show |
intron_variant | MODIFIER | c.185+981_185+988del others(8): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr9 | 125300038 | |||||
| chr9:125300038
|
AATATATA others(3): Show |
A | 7 | a0001c0001t0001g0305a0001c0001t0001g0306a0001c0001t0001g0319others(4): Show | 7 | HG02451.hp1 HG02559.hp1 NA18940.hp2 others(4): Show |
intron_variant | MODIFIER | c.185+979_185+988del others(10): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr9 | 125300038 | |||||
| chr9:125300038
|
AATATATA others(5): Show |
A | 10 | a0001c0001t0001g0325a0001c0001t0002g0033a0001c0001t0002g0036others(7): Show | 10 | HG00558.hp2 HG01192.hp1 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.185+977_185+988del others(12): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr9 | 125300038 | |||||
| chr9:125300038
|
AATATATA others(7): Show |
A | 16 | a0001c0001t0001g0323a0001c0001t0002g0153a0001c0001t0002g0309others(13): Show | 16 | HG00738.hp1 HG01993.hp2 HG02074.hp1 others(13): Show |
intron_variant | MODIFIER | c.185+975_185+988del others(14): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr9 | 125300038 | |||||
| chr9:125300038
|
AATATATA others(9): Show |
A | 25 | a0001c0001t0001g0017a0001c0001t0002g0021a0001c0001t0002g0059others(22): Show | 25 | HG00408.hp2 HG00609.hp1 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.185+973_185+988del others(16): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr9 | 125300038 | |||||
| chr9:125300038
|
AATATATA others(11): Show |
A | 4 | a0001c0001t0002g0091a0001c0001t0002g0109a0001c0001t0002g0111others(1): Show | 4 | HG02165.hp2 HG04228.hp1 HG04228.hp2 others(1): Show |
intron_variant | MODIFIER | c.185+971_185+988del others(18): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr9 | 125300038 | |||||
| chr9:125300038
|
AATATATA others(15): Show |
A | 1 | a0001c0001t0001g0205 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.185+967_185+988del others(22): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr9 | 125300038 | |||||
| chr9:125300038
|
AATATATA others(17): Show |
A | 1 | a0001c0001t0014g0259 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.185+965_185+988del others(24): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr9 | 125300038 | |||||
| chr9:125300038
|
AATATATA others(31): Show |
A | 1 | a0001c0003t0006g0162 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.185+951_185+988del others(38): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr9 | 125300038 | |||||
| chr9:125300039
|
ATAT | A | 3 | a0001c0001t0001g0229a0001c0001t0001g0236a0001c0001t0002g0117 | 3 | HG03491.hp1 NA18967.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.185+934_185+936del others(3): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125300039 | ||||||
| chr9:125300039
|
ATATAT | A | 3 | a0001c0001t0001g0193a0001c0001t0001g0211a0001c0001t0001g0221 | 3 | HG02083.hp2 HG02683.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.185+934_185+938del others(5): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125300039 | ||||||
| chr9:125300039
|
ATATATAT | A | 8 | a0001c0001t0001g0248a0001c0001t0001g0310a0001c0001t0001g0320others(5): Show | 8 | HG01517.hp2 HG02056.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.185+934_185+940del others(7): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125300039 | ||||||
| chr9:125300039
|
ATATATAT others(2): Show |
A | 13 | a0001c0001t0001g0317a0001c0001t0002g0022a0001c0001t0002g0024others(10): Show | 13 | HG00423.hp1 HG00673.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.185+934_185+942del others(9): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125300039 | ||||||
| chr9:125300039
|
ATATATAT others(4): Show |
A | 27 | a0001c0001t0001g0326a0001c0001t0002g0016a0001c0001t0002g0026others(24): Show | 27 | HG00140.hp1 HG00621.hp1 HG01074.hp2 others(24): Show |
intron_variant | MODIFIER | c.185+934_185+944del others(11): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125300039 | ||||||
| chr9:125300039
|
ATATATAT others(6): Show |
A | 6 | a0001c0001t0002g0027a0001c0001t0002g0048a0001c0001t0002g0080others(3): Show | 6 | HG00280.hp2 HG02055.hp2 HG02056.hp2 others(3): Show |
intron_variant | MODIFIER | c.185+934_185+946del others(13): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125300039 | ||||||
| chr9:125300039
|
ATATATAT others(8): Show |
A | 22 | a0001c0001t0001g0045a0001c0001t0001g0202a0001c0001t0001g0264others(19): Show | 22 | HG00544.hp2 HG01123.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.185+934_185+948del others(15): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125300039 | ||||||
| chr9:125300039
|
ATATATAT others(10): Show |
A | 22 | a0001c0001t0002g0015a0001c0001t0002g0044a0001c0001t0002g0066others(19): Show | 22 | HG00099.hp2 HG00438.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.185+934_185+950del others(17): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125300039 | ||||||
| chr9:125300039
|
ATATATAT others(12): Show |
A | 4 | a0001c0001t0002g0023a0001c0001t0002g0025a0001c0001t0002g0052others(1): Show | 4 | HG01069.hp2 HG02165.hp1 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.185+934_185+952del others(19): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125300039 | ||||||
| chr9:125300039
|
ATATATAT others(14): Show |
A | 1 | a0001c0001t0001g0227 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.185+934_185+954del others(21): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125300039 | ||||||
| chr9:125300039
|
ATATATAT others(16): Show |
A | 5 | a0001c0001t0005g0329a0001c0001t0005g0333a0001c0001t0005g0336others(2): Show | 5 | HG00741.hp2 NA18961.hp1 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.185+934_185+956del others(23): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125300039 | ||||||
| chr9:125300039
|
ATATATAT others(20): Show |
A | 1 | a0001c0001t0009g0002 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.185+934_185+960del others(27): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125300039 | ||||||
| chr9:125300039
|
ATATATAT others(22): Show |
A | 2 | a0001c0001t0009g0001a0001c0001t0009g0003 | 2 | HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.185+934_185+962del others(29): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125300039 | ||||||
| chr9:125300040
|
T | A | 111 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(108): Show | 111 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.185+934T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125300040 | ||||||
| chr9:125300042
|
T | A | 105 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(102): Show | 105 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.185+936T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125300042 | ||||||
| chr9:125300044
|
T | A | 103 | a0001c0001t0001g0176a0001c0001t0001g0178a0001c0001t0001g0179others(100): Show | 103 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.185+938T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125300044 | ||||||
| chr9:125300046
|
T | A | 101 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0180others(98): Show | 101 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.185+940T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125300046 | ||||||
| chr9:125300048
|
T | A | 97 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0180others(94): Show | 97 | HG00280.hp1 HG00423.hp2 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.185+942T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125300048 | ||||||
| chr9:125300050
|
T | A | 92 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0193others(89): Show | 92 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.185+944T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125300050 | ||||||
| chr9:125300051
|
AT | A | 3 | a0001c0003t0006g0166a0001c0003t0006g0168a0001c0003t0006g0171 | 3 | HG01167.hp1 HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.185+946delT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125300051 | ||||||
| chr9:125300052
|
T | A | 117 | a0001c0001t0001g0193a0001c0001t0001g0200a0001c0001t0001g0211others(114): Show | 117 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.185+946T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125300052 | ||||||
| chr9:125300054
|
T | A | 123 | a0001c0001t0001g0193a0001c0001t0001g0200a0001c0001t0001g0211others(120): Show | 123 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.185+948T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125300054 | ||||||
| chr9:125300056
|
T | A | 159 | a0001c0001t0001g0017a0001c0001t0001g0045a0001c0001t0001g0193others(156): Show | 159 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.185+950T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125300056 | ||||||
| chr9:125300058
|
T | A | 171 | a0001c0001t0001g0017a0001c0001t0001g0045a0001c0001t0001g0193others(168): Show | 171 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.185+952T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125300058 | ||||||
| chr9:125300060
|
T | A | 149 | a0001c0001t0001g0017a0001c0001t0001g0045a0001c0001t0001g0193others(146): Show | 149 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.185+954T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125300060 | ||||||
| chr9:125300062
|
T | A | 137 | a0001c0001t0001g0017a0001c0001t0001g0045a0001c0001t0001g0193others(134): Show | 137 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.185+956T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125300062 | ||||||
| chr9:125300064
|
T | A | 112 | a0001c0001t0001g0017a0001c0001t0001g0045a0001c0001t0001g0193others(109): Show | 112 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.185+958T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125300064 | ||||||
| chr9:125300066
|
T | A | 97 | a0001c0001t0001g0017a0001c0001t0001g0045a0001c0001t0001g0202others(94): Show | 97 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.185+960T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125300066 | ||||||
| chr9:125300068
|
T | A | 60 | a0001c0001t0001g0017a0001c0001t0001g0202a0001c0001t0001g0205others(57): Show | 60 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(57): Show |
intron_variant | MODIFIER | c.185+962T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125300068 | ||||||
| chr9:125300070
|
T | A | 31 | a0001c0001t0001g0202a0001c0001t0001g0205a0001c0001t0001g0227others(28): Show | 31 | HG00408.hp2 HG00642.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.185+964T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125300070 | ||||||
| chr9:125300072
|
T | A | 10 | a0001c0001t0001g0205a0001c0001t0001g0227a0001c0001t0002g0067others(7): Show | 10 | HG00741.hp2 HG02074.hp2 HG02602.hp2 others(7): Show |
intron_variant | MODIFIER | c.185+966T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125300072 | ||||||
| chr9:125300074
|
T | A | 8 | a0001c0001t0001g0205a0001c0001t0001g0227a0001c0001t0005g0329others(5): Show | 8 | HG00741.hp2 HG02602.hp2 HG03209.hp2 others(5): Show |
intron_variant | MODIFIER | c.185+968T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125300074 | ||||||
| chr9:125300076
|
T | A | 7 | a0001c0001t0001g0205a0001c0001t0001g0227a0001c0001t0005g0329others(4): Show | 7 | HG00741.hp2 HG02602.hp2 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.185+970T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125300076 | ||||||
| chr9:125300078
|
T | A | 5 | a0001c0001t0001g0205a0001c0001t0001g0227a0001c0001t0014g0259others(2): Show | 5 | HG00741.hp2 HG02572.hp2 HG02602.hp2 others(2): Show |
intron_variant | MODIFIER | c.185+972T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125300078 | ||||||
| chr9:125300080
|
T | A | 2 | a0001c0001t0014g0259a0001c0001t0014g0263 | 2 | HG00741.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.185+974T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125300080 | ||||||
| chr9:125300095
|
G | A | 1 | a0001c0016t0037g0152 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.185+989G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125300095 | ||||||
| chr9:125300156
|
C | T | 1 | a0001c0001t0002g0029 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.185+1050C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125300156 | ||||||
| chr9:125300189
|
T | A | 240 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(237): Show | 240 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.185+1083T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125300189 | ||||||
| chr9:125300203
|
T | C | 1 | a0001c0001t0002g0175 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.185+1097T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125300203 | ||||||
| chr9:125300212
|
C | T | 33 | a0001c0002t0003g0004a0001c0002t0003g0005a0001c0002t0003g0123others(30): Show | 33 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(30): Show |
intron_variant | MODIFIER | c.185+1106C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125300212 | ||||||
| chr9:125300583
|
A | G | 230 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(227): Show | 230 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.186-1400A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125300583 | ||||||
| chr9:125300933
|
T | C | 1 | a0001c0001t0001g0200 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.186-1050T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125300933 | ||||||
| chr9:125300946
|
G | T | 1 | a0001c0016t0037g0152 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.186-1037G>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125300946 | ||||||
| chr9:125301074
|
A | AT | 34 | a0001c0001t0002g0109a0001c0001t0028g0154a0001c0002t0003g0004others(31): Show | 34 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(31): Show |
intron_variant | MODIFIER | c.186-896dupT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr9 | 125301074 | |||||
| chr9:125301206
|
C | T | 2 | a0001c0001t0001g0318a0001c0001t0001g0320 | 2 | HG02717.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.186-777C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125301206 | ||||||
| chr9:125301623
|
A | G | 1 | a0001c0001t0017g0013 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.186-360A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125301623 | ||||||
| chr9:125301715
|
G | A | 1 | a0001c0001t0002g0018 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.186-268G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125301715 | ||||||
| chr9:125301739
|
C | T | 2 | a0001c0001t0001g0215a0001c0001t0001g0254 | 2 | HG00642.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.186-244C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125301739 | ||||||
| chr9:125301860
|
T | C | 1 | a0001c0005t0001g0231 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.186-123T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | chr9 | 125301860 | ||||||
| chr9:125301963
|
C | CTT | 30 | a0001c0002t0003g0004a0001c0002t0003g0005a0001c0002t0003g0123others(27): Show | 30 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(27): Show |
splice_acceptor_variant&intron_variant | HIGH | c.186-4_186-3dupTT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr9 | 125301963 | |||||
| chr9:125301963
|
CT | C | 19 | a0001c0001t0001g0234a0001c0001t0002g0061a0001c0001t0002g0309others(16): Show | 19 | HG01069.hp2 HG01167.hp1 HG01257.hp2 others(16): Show |
splice_region_variant&intron_variant | LOW | c.186-3delT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr9 | 125301963 | |||||
| chr9:125303005
|
A | G | 1 | a0001c0001t0002g0117 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1029+179A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 5/27 | chr9 | 125303005 | ||||||
| chr9:125303009
|
C | A | 9 | a0001c0001t0001g0274a0001c0001t0001g0277a0001c0001t0001g0280others(6): Show | 9 | HG00438.hp1 HG00621.hp2 HG02071.hp2 others(6): Show |
intron_variant | MODIFIER | c.1029+183C>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 5/27 | chr9 | 125303009 | ||||||
| chr9:125303129
|
A | G | 4 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0276others(1): Show | 4 | HG01255.hp1 NA18952.hp1 NA18985.hp2 others(1): Show |
intron_variant | MODIFIER | c.1029+303A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 5/27 | chr9 | 125303129 | ||||||
| chr9:125303478
|
TA | T | 6 | a0001c0001t0001g0264a0001c0001t0002g0014a0001c0001t0002g0015others(3): Show | 6 | HG01167.hp2 NA18939.hp1 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.1029+666delA | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 5/27 | INFO_REALIGN_3_PRIME | chr9 | 125303478 | |||||
| chr9:125303552
|
G | A | 1 | a0001c0001t0001g0232 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1029+726G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 5/27 | chr9 | 125303552 | ||||||
| chr9:125303656
|
A | G | 1 | a0001c0001t0002g0081 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1029+830A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 5/27 | chr9 | 125303656 | ||||||
| chr9:125303776
|
C | CA | 216 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(213): Show | 216 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1029+966dupA | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 5/27 | INFO_REALIGN_3_PRIME | chr9 | 125303776 | |||||
| chr9:125303776
|
C | CAA | 10 | a0001c0001t0001g0256a0001c0001t0004g0173a0001c0001t0004g0174others(7): Show | 10 | HG01099.hp1 HG01167.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1029+965_1029+966d others(4): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 5/27 | INFO_REALIGN_3_PRIME | chr9 | 125303776 | |||||
| chr9:125303885
|
T | G | 2 | a0001c0001t0001g0275a0001c0001t0001g0293 | 2 | NA18974.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.1029+1059T>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 5/27 | chr9 | 125303885 | ||||||
| chr9:125303892
|
T | C | 1 | a0001c0016t0037g0152 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1029+1066T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 5/27 | chr9 | 125303892 | ||||||
| chr9:125303996
|
A | G | 1 | a0001c0003t0006g0162 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1030-1067A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 5/27 | chr9 | 125303996 | ||||||
| chr9:125303999
|
T | G | 1 | a0001c0001t0002g0038 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1030-1064T>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 5/27 | chr9 | 125303999 | ||||||
| chr9:125304122
|
A | G | 1 | a0001c0001t0001g0213 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1030-941A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 5/27 | chr9 | 125304122 | ||||||
| chr9:125304334
|
C | T | 2 | a0001c0001t0001g0246a0001c0001t0001g0247 | 2 | HG02280.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1030-729C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 5/27 | chr9 | 125304334 | ||||||
| chr9:125304671
|
C | T | 1 | a0001c0001t0002g0078 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1030-392C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 5/27 | chr9 | 125304671 | ||||||
| chr9:125304857
|
T | C | 1 | a0001c0001t0001g0291 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1030-206T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 5/27 | chr9 | 125304857 | ||||||
| chr9:125304942
|
G | A | 8 | a0001c0002t0003g0004a0001c0002t0003g0005a0001c0002t0003g0125others(5): Show | 8 | NA18939.hp1 NA18968.hp1 NA18970.hp2 others(5): Show |
intron_variant | MODIFIER | c.1030-121G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 5/27 | chr9 | 125304942 | ||||||
| chr9:125305002
|
A | G | 1 | a0001c0001t0017g0013 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1030-61A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 5/27 | chr9 | 125305002 | ||||||
| chr9:125305017
|
T | C | 7 | a0001c0003t0006g0158a0001c0003t0006g0159a0001c0003t0006g0160others(4): Show | 7 | HG01109.hp1 HG01884.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.1030-46T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 5/27 | chr9 | 125305017 | ||||||
| chr9:125305223
|
C | T | 1 | a0001c0001t0002g0153 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1116+74C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 6/27 | chr9 | 125305223 | ||||||
| chr9:125305329
|
T | C | 5 | a0001c0003t0006g0158a0001c0003t0006g0159a0001c0003t0006g0160others(2): Show | 5 | HG01109.hp1 HG01884.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.1116+180T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 6/27 | chr9 | 125305329 | ||||||
| chr9:125305371
|
G | GT | 11 | a0001c0001t0002g0022a0001c0001t0002g0068a0001c0001t0002g0071others(8): Show | 11 | HG00621.hp1 NA18949.hp1 NA18950.hp2 others(8): Show |
intron_variant | MODIFIER | c.1116+242dupT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr9 | 125305371 | |||||
| chr9:125305371
|
GT | G | 170 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(167): Show | 170 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.1116+242delT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr9 | 125305371 | |||||
| chr9:125305371
|
GTT | G | 15 | a0001c0001t0001g0312a0001c0001t0009g0001a0001c0001t0009g0002others(12): Show | 15 | HG01109.hp1 HG01167.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.1116+241_1116+242d others(4): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr9 | 125305371 | |||||
| chr9:125305402
|
C | T | 1 | a0001c0003t0006g0171 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1116+253C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 6/27 | chr9 | 125305402 | ||||||
| chr9:125305620
|
C | T | 2 | a0001c0001t0001g0229a0001c0001t0001g0236 | 2 | NA18967.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.1116+471C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 6/27 | chr9 | 125305620 | ||||||
| chr9:125305667
|
C | G | 1 | a0001c0001t0001g0265 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1116+518C>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 6/27 | chr9 | 125305667 | ||||||
| chr9:125305798
|
G | A | 1 | a0001c0016t0037g0152 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1116+649G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 6/27 | chr9 | 125305798 | ||||||
| chr9:125306035
|
C | G | 7 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0008others(4): Show | 7 | HG01069.hp1 HG02615.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1116+886C>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 6/27 | chr9 | 125306035 | ||||||
| chr9:125306109
|
G | A | 104 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0001g0195others(101): Show | 104 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.1116+960G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 6/27 | chr9 | 125306109 | ||||||
| chr9:125306268
|
A | G | 2 | a0001c0001t0025g0207a0001c0001t0034g0217 | 2 | HG00733.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.1116+1119A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 6/27 | chr9 | 125306268 | ||||||
| chr9:125306388
|
G | T | 1 | a0001c0016t0037g0152 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1117-1025G>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 6/27 | chr9 | 125306388 | ||||||
| chr9:125306458
|
T | C | 1 | a0001c0001t0002g0024 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1117-955T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 6/27 | chr9 | 125306458 | ||||||
| chr9:125306715
|
A | G | 1 | a0001c0003t0004g0164 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1117-698A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 6/27 | chr9 | 125306715 | ||||||
| chr9:125306720
|
C | T | 2 | a0001c0001t0001g0318a0001c0001t0001g0320 | 2 | HG02717.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1117-693C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 6/27 | chr9 | 125306720 | ||||||
| chr9:125306758
|
G | T | 1 | a0003c0007t0001g0308 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1117-655G>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 6/27 | chr9 | 125306758 | ||||||
| chr9:125306834
|
T | C | 2 | a0001c0001t0001g0305a0001c0001t0001g0306 | 2 | NA18963.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.1117-579T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 6/27 | chr9 | 125306834 | ||||||
| chr9:125306881
|
G | T | 1 | a0001c0016t0037g0152 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1117-532G>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 6/27 | chr9 | 125306881 | ||||||
| chr9:125306945
|
C | T | 1 | a0001c0016t0037g0152 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1117-468C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 6/27 | chr9 | 125306945 | ||||||
| chr9:125307084
|
G | A | 1 | a0001c0001t0001g0315 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1117-329G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 6/27 | chr9 | 125307084 | ||||||
| chr9:125307133
|
G | A | 1 | a0001c0001t0002g0068 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1117-280G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 6/27 | chr9 | 125307133 | ||||||
| chr9:125307157
|
C | T | 1 | a0001c0001t0017g0013 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1117-256C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 6/27 | chr9 | 125307157 | ||||||
| chr9:125307201
|
A | C | 2 | a0001c0001t0004g0173a0001c0001t0004g0174 | 2 | HG01099.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.1117-212A>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 6/27 | chr9 | 125307201 | ||||||
| chr9:125307229
|
A | G | 2 | a0001c0001t0030g0120a0001c0016t0037g0152 | 2 | HG02135.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.1117-184A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 6/27 | chr9 | 125307229 | ||||||
| chr9:125307268
|
C | CA | 19 | a0001c0001t0001g0179a0001c0001t0001g0212a0001c0001t0001g0215others(16): Show | 19 | HG00280.hp1 HG00408.hp1 HG00642.hp2 others(16): Show |
intron_variant | MODIFIER | c.1117-128dupA | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr9 | 125307268 | |||||
| chr9:125307361
|
G | A | 1 | a0001c0001t0025g0207 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1117-52G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 6/27 | chr9 | 125307361 | ||||||
| chr9:125307598
|
G | A | 33 | a0001c0002t0003g0004a0001c0002t0003g0005a0001c0002t0003g0123others(30): Show | 33 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(30): Show |
intron_variant | MODIFIER | c.1251+51G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 7/27 | chr9 | 125307598 | ||||||
| chr9:125307676
|
C | T | 1 | a0001c0001t0002g0072 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1252-15C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 7/27 | chr9 | 125307676 | ||||||
| chr9:125307948
|
G | C | 199 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(196): Show | 199 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.1441+68G>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 8/27 | chr9 | 125307948 | ||||||
| chr9:125308217
|
G | A | 6 | a0001c0003t0006g0166a0001c0003t0006g0168a0001c0003t0006g0169others(3): Show | 6 | HG01167.hp1 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1441+337G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 8/27 | chr9 | 125308217 | ||||||
| chr9:125308231
|
T | A | 231 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(228): Show | 231 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.1441+351T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 8/27 | chr9 | 125308231 | ||||||
| chr9:125308326
|
ACC | A | 336 | a0001c0001t0001g0017a0001c0001t0001g0045a0001c0001t0001g0176others(333): Show | 336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.1441+448_1441+449d others(4): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr9 | 125308326 | |||||
| chr9:125308330
|
T | A | 336 | a0001c0001t0001g0017a0001c0001t0001g0045a0001c0001t0001g0176others(333): Show | 336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.1441+450T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 8/27 | chr9 | 125308330 | ||||||
| chr9:125308347
|
C | CA | 17 | a0001c0003t0004g0156a0001c0003t0004g0157a0001c0003t0004g0164others(14): Show | 17 | HG01109.hp1 HG01167.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.1441+481dupA | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr9 | 125308347 | |||||
| chr9:125308347
|
CA | C | 35 | a0001c0001t0002g0094a0001c0001t0017g0013a0001c0002t0003g0004others(32): Show | 35 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(32): Show |
intron_variant | MODIFIER | c.1441+481delA | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr9 | 125308347 | |||||
| chr9:125308461
|
A | G | 1 | a0001c0016t0037g0152 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1441+581A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 8/27 | chr9 | 125308461 | ||||||
| chr9:125308475
|
C | T | 230 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(227): Show | 230 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.1441+595C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 8/27 | chr9 | 125308475 | ||||||
| chr9:125308513
|
A | G | 336 | a0001c0001t0001g0017a0001c0001t0001g0045a0001c0001t0001g0176others(333): Show | 336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.1441+633A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 8/27 | chr9 | 125308513 | ||||||
| chr9:125308650
|
G | A | 1 | a0001c0001t0002g0054 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1441+770G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 8/27 | chr9 | 125308650 | ||||||
| chr9:125308738
|
G | A | 165 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(162): Show | 165 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.1441+858G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 8/27 | chr9 | 125308738 | ||||||
| chr9:125308768
|
C | G | 1 | a0001c0002t0003g0151 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1441+888C>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 8/27 | chr9 | 125308768 | ||||||
| chr9:125308830
|
A | G | 5 | a0001c0001t0001g0317a0001c0001t0001g0318a0001c0001t0001g0319others(2): Show | 5 | HG02451.hp1 HG02559.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1441+950A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 8/27 | chr9 | 125308830 | ||||||
| chr9:125308898
|
T | C | 1 | a0001c0001t0002g0082 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1441+1018T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 8/27 | chr9 | 125308898 | ||||||
| chr9:125308912
|
A | G | 34 | a0001c0002t0003g0004a0001c0002t0003g0005a0001c0002t0003g0123others(31): Show | 34 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(31): Show |
intron_variant | MODIFIER | c.1441+1032A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 8/27 | chr9 | 125308912 | ||||||
| chr9:125308960
|
T | C | 1 | a0006c0011t0005g0337 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1441+1080T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 8/27 | chr9 | 125308960 | ||||||
| chr9:125309192
|
C | T | 5 | a0001c0003t0006g0158a0001c0003t0006g0159a0001c0003t0006g0160others(2): Show | 5 | HG01109.hp1 HG01884.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.1441+1312C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 8/27 | chr9 | 125309192 | ||||||
| chr9:125309240
|
T | C | 3 | a0001c0001t0009g0001a0001c0001t0009g0002a0001c0001t0009g0003 | 3 | HG01884.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1441+1360T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 8/27 | chr9 | 125309240 | ||||||
| chr9:125309323
|
T | G | 2 | a0001c0001t0001g0325a0001c0001t0001g0326 | 2 | HG02559.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1441+1443T>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 8/27 | chr9 | 125309323 | ||||||
| chr9:125309335
|
G | A | 6 | a0001c0003t0006g0166a0001c0003t0006g0168a0001c0003t0006g0169others(3): Show | 6 | HG01167.hp1 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1441+1455G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 8/27 | chr9 | 125309335 | ||||||
| chr9:125309375
|
C | G | 3 | a0001c0001t0009g0001a0001c0001t0009g0002a0001c0001t0009g0003 | 3 | HG01884.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1441+1495C>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 8/27 | chr9 | 125309375 | ||||||
| chr9:125309499
|
T | C | 2 | a0001c0001t0001g0215a0001c0001t0001g0254 | 2 | HG00642.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.1441+1619T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 8/27 | chr9 | 125309499 | ||||||
| chr9:125309587
|
G | A | 2 | a0001c0001t0002g0097a0001c0001t0002g0098 | 2 | HG03704.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1441+1707G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 8/27 | chr9 | 125309587 | ||||||
| chr9:125309605
|
G | A | 1 | a0001c0001t0002g0059 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1441+1725G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 8/27 | chr9 | 125309605 | ||||||
| chr9:125309754
|
G | A | 1 | a0001c0016t0037g0152 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1441+1874G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 8/27 | chr9 | 125309754 | ||||||
| chr9:125309994
|
G | C | 202 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(199): Show | 202 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.1441+2114G>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 8/27 | chr9 | 125309994 | ||||||
| chr9:125310427
|
T | C | 2 | a0001c0001t0004g0173a0001c0001t0004g0174 | 2 | HG01099.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.1442-2025T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 8/27 | chr9 | 125310427 | ||||||
| chr9:125310537
|
A | AT | 6 | a0001c0001t0002g0016a0001c0001t0002g0030a0001c0001t0002g0077others(3): Show | 6 | HG00544.hp1 HG01175.hp1 NA18940.hp2 others(3): Show |
intron_variant | MODIFIER | c.1442-1896dupT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr9 | 125310537 | |||||
| chr9:125310537
|
AT | A | 45 | a0001c0001t0001g0179a0001c0001t0002g0032a0001c0001t0002g0114others(42): Show | 45 | HG00140.hp1 HG00544.hp2 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.1442-1896delT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr9 | 125310537 | |||||
| chr9:125310537
|
ATT | A | 186 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(183): Show | 186 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.1442-1897_1442-189 others(6): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr9 | 125310537 | |||||
| chr9:125310644
|
A | G | 5 | a0001c0003t0004g0156a0001c0003t0004g0157a0001c0003t0004g0164others(2): Show | 5 | HG02258.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1442-1808A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 8/27 | chr9 | 125310644 | ||||||
| chr9:125310705
|
ATTTTGTA others(296): Show |
A | 1 | a0001c0016t0037g0152 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1442-1726_1442-142 others(4): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr9 | 125310705 | |||||
| chr9:125310801
|
G | A | 2 | a0002c0006t0011g0121a0002c0006t0011g0122 | 2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1442-1651G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 8/27 | chr9 | 125310801 | ||||||
| chr9:125310818
|
G | A | 229 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(226): Show | 229 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.1442-1634G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 8/27 | chr9 | 125310818 | ||||||
| chr9:125310843
|
CT | C | 31 | a0001c0002t0003g0004a0001c0002t0003g0005a0001c0002t0003g0123others(28): Show | 31 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.1442-1595delT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr9 | 125310843 | |||||
| chr9:125310903
|
G | A | 1 | a0001c0001t0001g0202 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1442-1549G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 8/27 | chr9 | 125310903 | ||||||
| chr9:125311029
|
C | T | 31 | a0001c0002t0003g0004a0001c0002t0003g0005a0001c0002t0003g0123others(28): Show | 31 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.1442-1423C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 8/27 | chr9 | 125311029 | ||||||
| chr9:125311061
|
A | G | 1 | a0001c0016t0037g0152 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1442-1391A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 8/27 | chr9 | 125311061 | ||||||
| chr9:125311207
|
C | A | 5 | a0001c0003t0004g0156a0001c0003t0004g0157a0001c0003t0004g0164others(2): Show | 5 | HG02258.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1442-1245C>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 8/27 | chr9 | 125311207 | ||||||
| chr9:125311207
|
C | G | 1 | a0001c0001t0002g0072 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1442-1245C>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 8/27 | chr9 | 125311207 | ||||||
| chr9:125311221
|
T | C | 2 | a0001c0001t0004g0173a0001c0001t0004g0174 | 2 | HG01099.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.1442-1231T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 8/27 | chr9 | 125311221 | ||||||
| chr9:125311265
|
A | T | 5 | a0001c0003t0004g0156a0001c0003t0004g0157a0001c0003t0004g0164others(2): Show | 5 | HG02258.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1442-1187A>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 8/27 | chr9 | 125311265 | ||||||
| chr9:125311451
|
G | C | 31 | a0001c0002t0003g0004a0001c0002t0003g0005a0001c0002t0003g0123others(28): Show | 31 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.1442-1001G>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 8/27 | chr9 | 125311451 | ||||||
| chr9:125311538
|
T | G | 1 | a0001c0013t0002g0043 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1442-914T>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 8/27 | chr9 | 125311538 | ||||||
| chr9:125311559
|
C | T | 7 | a0001c0001t0001g0304a0001c0001t0001g0305a0001c0001t0001g0306others(4): Show | 7 | HG02056.hp1 NA18942.hp1 NA18954.hp2 others(4): Show |
intron_variant | MODIFIER | c.1442-893C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 8/27 | chr9 | 125311559 | ||||||
| chr9:125311580
|
C | T | 1 | a0001c0001t0002g0081 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1442-872C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 8/27 | chr9 | 125311580 | ||||||
| chr9:125311724
|
CT | C | 163 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(160): Show | 163 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.1442-715delT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr9 | 125311724 | |||||
| chr9:125311988
|
A | G | 1 | a0001c0001t0002g0069 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1442-464A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 8/27 | chr9 | 125311988 | ||||||
| chr9:125312082
|
G | A | 31 | a0001c0002t0003g0004a0001c0002t0003g0005a0001c0002t0003g0123others(28): Show | 31 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.1442-370G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 8/27 | chr9 | 125312082 | ||||||
| chr9:125312319
|
C | G | 1 | a0001c0001t0004g0006 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1442-133C>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 8/27 | chr9 | 125312319 | ||||||
| chr9:125313111
|
C | T | 2 | a0002c0006t0011g0121a0002c0006t0011g0122 | 2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1602+499C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125313111 | ||||||
| chr9:125313112
|
G | A | 3 | a0001c0001t0009g0001a0001c0001t0009g0002a0001c0001t0009g0003 | 3 | HG01884.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1602+500G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125313112 | ||||||
| chr9:125313264
|
A | G | 2 | a0002c0006t0011g0121a0002c0006t0011g0122 | 2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1602+652A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125313264 | ||||||
| chr9:125313439
|
G | C | 2 | a0001c0001t0002g0061a0001c0001t0002g0066 | 2 | HG00099.hp2 HG01069.hp2 |
intron_variant | MODIFIER | c.1602+827G>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125313439 | ||||||
| chr9:125313592
|
C | T | 31 | a0001c0002t0003g0004a0001c0002t0003g0005a0001c0002t0003g0123others(28): Show | 31 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.1602+980C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125313592 | ||||||
| chr9:125313790
|
G | A | 165 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(162): Show | 165 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.1602+1178G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125313790 | ||||||
| chr9:125313827
|
C | T | 1 | a0001c0001t0036g0088 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1602+1215C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125313827 | ||||||
| chr9:125313890
|
T | G | 31 | a0001c0002t0003g0004a0001c0002t0003g0005a0001c0002t0003g0123others(28): Show | 31 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.1602+1278T>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125313890 | ||||||
| chr9:125313943
|
A | G | 3 | a0001c0001t0010g0216a0001c0001t0010g0255a0001c0001t0010g0266 | 3 | HG01175.hp2 HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1602+1331A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125313943 | ||||||
| chr9:125314011
|
G | C | 31 | a0001c0002t0003g0004a0001c0002t0003g0005a0001c0002t0003g0123others(28): Show | 31 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.1602+1399G>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125314011 | ||||||
| chr9:125314054
|
C | T | 4 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0242others(1): Show | 4 | HG00639.hp2 HG00735.hp2 HG01074.hp1 others(1): Show |
intron_variant | MODIFIER | c.1602+1442C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125314054 | ||||||
| chr9:125314176
|
T | G | 5 | a0001c0003t0004g0156a0001c0003t0004g0157a0001c0003t0004g0164others(2): Show | 5 | HG02258.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1602+1564T>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125314176 | ||||||
| chr9:125314239
|
G | A | 5 | a0001c0003t0006g0158a0001c0003t0006g0159a0001c0003t0006g0160others(2): Show | 5 | HG01109.hp1 HG01884.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.1602+1627G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125314239 | ||||||
| chr9:125314262
|
A | G | 199 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(196): Show | 199 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.1602+1650A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125314262 | ||||||
| chr9:125314340
|
A | G | 1 | a0001c0003t0026g0118 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1602+1728A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125314340 | ||||||
| chr9:125314480
|
A | C | 1 | a0006c0011t0005g0337 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1602+1868A>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125314480 | ||||||
| chr9:125314520
|
G | A | 1 | a0001c0001t0004g0009 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1602+1908G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125314520 | ||||||
| chr9:125314624
|
A | G | 201 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(198): Show | 201 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.1602+2012A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125314624 | ||||||
| chr9:125314653
|
TCAAAACA others(3): Show |
T | 2 | a0003c0007t0001g0302a0003c0007t0001g0308 | 2 | HG03017.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.1602+2057_1602+206 others(14): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | INFO_REALIGN_3_PRIME | chr9 | 125314653 | |||||
| chr9:125314681
|
CAG | C | 7 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0008others(4): Show | 7 | HG01069.hp1 HG02615.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1602+2071_1602+207 others(6): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | INFO_REALIGN_3_PRIME | chr9 | 125314681 | |||||
| chr9:125314702
|
C | G | 165 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(162): Show | 165 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.1602+2090C>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125314702 | ||||||
| chr9:125314789
|
C | CT | 7 | a0001c0001t0001g0298a0001c0001t0002g0076a0001c0001t0004g0173others(4): Show | 7 | HG01099.hp1 HG01109.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1602+2193dupT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | INFO_REALIGN_3_PRIME | chr9 | 125314789 | |||||
| chr9:125314826
|
C | T | 1 | a0001c0001t0015g0060 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1602+2214C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125314826 | ||||||
| chr9:125314839
|
G | T | 5 | a0001c0003t0004g0156a0001c0003t0004g0157a0001c0003t0004g0164others(2): Show | 5 | HG02258.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1602+2227G>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125314839 | ||||||
| chr9:125314856
|
C | T | 1 | a0001c0001t0001g0278 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1602+2244C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125314856 | ||||||
| chr9:125314949
|
G | A | 1 | a0001c0001t0001g0256 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1602+2337G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125314949 | ||||||
| chr9:125314996
|
C | T | 3 | a0001c0001t0009g0001a0001c0001t0009g0002a0001c0001t0009g0003 | 3 | HG01884.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1602+2384C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125314996 | ||||||
| chr9:125315019
|
C | G | 3 | a0001c0001t0002g0103a0001c0001t0002g0105a0001c0001t0002g0106 | 3 | HG00408.hp2 HG02074.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.1602+2407C>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125315019 | ||||||
| chr9:125315022
|
C | T | 10 | a0001c0001t0001g0192a0001c0001t0001g0269a0001c0001t0001g0298others(7): Show | 10 | HG00639.hp1 HG02451.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.1602+2410C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125315022 | ||||||
| chr9:125315031
|
C | T | 6 | a0001c0003t0006g0166a0001c0003t0006g0168a0001c0003t0006g0169others(3): Show | 6 | HG01167.hp1 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1602+2419C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125315031 | ||||||
| chr9:125315053
|
C | G | 1 | a0001c0001t0002g0069 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1602+2441C>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125315053 | ||||||
| chr9:125315060
|
T | C | 1 | a0001c0010t0006g0167 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1602+2448T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125315060 | ||||||
| chr9:125315255
|
A | G | 1 | a0001c0001t0001g0180 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1602+2643A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125315255 | ||||||
| chr9:125315345
|
C | T | 31 | a0001c0002t0003g0004a0001c0002t0003g0005a0001c0002t0003g0123others(28): Show | 31 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.1602+2733C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125315345 | ||||||
| chr9:125315519
|
A | C | 1 | a0001c0001t0017g0013 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1602+2907A>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125315519 | ||||||
| chr9:125315561
|
G | A | 9 | a0001c0002t0003g0128a0001c0002t0003g0131a0001c0002t0003g0134others(6): Show | 9 | HG01081.hp2 HG02129.hp2 NA18940.hp1 others(6): Show |
intron_variant | MODIFIER | c.1602+2949G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125315561 | ||||||
| chr9:125315824
|
G | A | 1 | a0001c0001t0001g0273 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1602+3212G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125315824 | ||||||
| chr9:125315892
|
G | A | 1 | a0001c0001t0001g0211 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1602+3280G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125315892 | ||||||
| chr9:125315957
|
C | T | 6 | a0001c0003t0006g0166a0001c0003t0006g0168a0001c0003t0006g0169others(3): Show | 6 | HG01167.hp1 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1602+3345C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125315957 | ||||||
| chr9:125316062
|
C | T | 5 | a0001c0003t0004g0156a0001c0003t0004g0157a0001c0003t0004g0164others(2): Show | 5 | HG02258.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1602+3450C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125316062 | ||||||
| chr9:125316308
|
C | G | 9 | a0001c0001t0002g0061a0001c0001t0002g0063a0001c0001t0002g0065others(6): Show | 9 | HG00099.hp2 HG00733.hp2 HG00735.hp1 others(6): Show |
intron_variant | MODIFIER | c.1602+3696C>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125316308 | ||||||
| chr9:125316308
|
C | T | 5 | a0001c0003t0004g0156a0001c0003t0004g0157a0001c0003t0004g0164others(2): Show | 5 | HG02258.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1602+3696C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125316308 | ||||||
| chr9:125316327
|
T | C | 1 | a0006c0011t0005g0337 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1602+3715T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125316327 | ||||||
| chr9:125316328
|
A | T | 1 | a0006c0011t0005g0337 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1602+3716A>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125316328 | ||||||
| chr9:125316330
|
C | A | 1 | a0006c0011t0005g0337 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1602+3718C>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125316330 | ||||||
| chr9:125316580
|
T | C | 1 | a0001c0003t0006g0158 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1602+3968T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125316580 | ||||||
| chr9:125316617
|
G | A | 165 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(162): Show | 165 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.1602+4005G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125316617 | ||||||
| chr9:125316637
|
T | C | 230 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(227): Show | 230 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.1602+4025T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125316637 | ||||||
| chr9:125316697
|
C | T | 3 | a0001c0002t0003g0147a0002c0006t0011g0121a0002c0006t0011g0122 | 3 | HG01109.hp2 HG03098.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.1602+4085C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125316697 | ||||||
| chr9:125316969
|
T | C | 2 | a0001c0001t0001g0262a0007c0017t0001g0250 | 2 | HG02723.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1602+4357T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125316969 | ||||||
| chr9:125317156
|
A | G | 1 | a0001c0016t0037g0152 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1603-4277A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125317156 | ||||||
| chr9:125317179
|
G | A | 5 | a0001c0003t0006g0158a0001c0003t0006g0159a0001c0003t0006g0160others(2): Show | 5 | HG01109.hp1 HG01884.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.1603-4254G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125317179 | ||||||
| chr9:125317304
|
C | T | 2 | a0001c0001t0004g0173a0001c0001t0004g0174 | 2 | HG01099.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.1603-4129C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125317304 | ||||||
| chr9:125317317
|
C | CA | 7 | a0001c0001t0002g0071a0001c0001t0002g0155a0001c0001t0013g0191others(4): Show | 7 | HG01109.hp2 HG01175.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.1603-4103dupA | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | INFO_REALIGN_3_PRIME | chr9 | 125317317 | |||||
| chr9:125317360
|
T | C | 1 | a0001c0001t0022g0279 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1603-4073T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125317360 | ||||||
| chr9:125317372
|
T | C | 2 | a0001c0002t0003g0134a0001c0002t0007g0133 | 2 | HG01081.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.1603-4061T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125317372 | ||||||
| chr9:125317410
|
G | C | 1 | a0001c0003t0006g0161 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1603-4023G>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125317410 | ||||||
| chr9:125317612
|
C | T | 31 | a0001c0002t0003g0004a0001c0002t0003g0005a0001c0002t0003g0123others(28): Show | 31 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.1603-3821C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125317612 | ||||||
| chr9:125317623
|
CT | C | 30 | a0001c0002t0003g0004a0001c0002t0003g0005a0001c0002t0003g0123others(27): Show | 30 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.1603-3809delT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125317623 | ||||||
| chr9:125317624
|
T | A | 1 | a0001c0002t0003g0125 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1603-3809T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125317624 | ||||||
| chr9:125317625
|
C | A | 31 | a0001c0002t0003g0004a0001c0002t0003g0005a0001c0002t0003g0123others(28): Show | 31 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.1603-3808C>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125317625 | ||||||
| chr9:125317625
|
C | CA | 10 | a0001c0001t0001g0176a0001c0001t0001g0178a0001c0001t0001g0180others(7): Show | 10 | HG02027.hp2 HG02055.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1603-3791dupA | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | INFO_REALIGN_3_PRIME | chr9 | 125317625 | |||||
| chr9:125317625
|
C | T | 2 | a0002c0006t0011g0121a0002c0006t0011g0122 | 2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1603-3808C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125317625 | ||||||
| chr9:125317742
|
A | G | 14 | a0001c0001t0001g0300a0001c0001t0001g0304a0001c0001t0001g0305others(11): Show | 14 | HG02004.hp1 HG02056.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.1603-3691A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125317742 | ||||||
| chr9:125317816
|
G | T | 31 | a0001c0002t0003g0004a0001c0002t0003g0005a0001c0002t0003g0123others(28): Show | 31 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.1603-3617G>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125317816 | ||||||
| chr9:125317973
|
G | A | 1 | a0002c0006t0011g0122 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1603-3460G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125317973 | ||||||
| chr9:125317977
|
A | C | 1 | a0001c0003t0006g0158 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1603-3456A>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125317977 | ||||||
| chr9:125318095
|
C | T | 1 | a0001c0016t0037g0152 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1603-3338C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125318095 | ||||||
| chr9:125318109
|
C | G | 2 | a0001c0003t0006g0169a0001c0003t0006g0172 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1603-3324C>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125318109 | ||||||
| chr9:125318359
|
A | G | 1 | a0001c0001t0002g0084 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1603-3074A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125318359 | ||||||
| chr9:125318509
|
A | G | 7 | a0001c0003t0006g0158a0001c0003t0006g0159a0001c0003t0006g0160others(4): Show | 7 | HG01109.hp1 HG01884.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.1603-2924A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125318509 | ||||||
| chr9:125318667
|
A | T | 2 | a0001c0001t0001g0184a0001c0001t0001g0187 | 2 | HG00558.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.1603-2766A>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125318667 | ||||||
| chr9:125318736
|
G | T | 1 | a0001c0001t0002g0065 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1603-2697G>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125318736 | ||||||
| chr9:125318907
|
G | T | 56 | a0001c0001t0001g0176a0001c0001t0001g0178a0001c0001t0001g0179others(53): Show | 56 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.1603-2526G>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125318907 | ||||||
| chr9:125318908
|
G | T | 56 | a0001c0001t0001g0176a0001c0001t0001g0178a0001c0001t0001g0179others(53): Show | 56 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.1603-2525G>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125318908 | ||||||
| chr9:125318990
|
A | G | 2 | a0001c0001t0001g0215a0001c0001t0001g0254 | 2 | HG00642.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.1603-2443A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125318990 | ||||||
| chr9:125319157
|
A | C | 231 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(228): Show | 231 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.1603-2276A>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125319157 | ||||||
| chr9:125319211
|
T | TA | 337 | a0001c0001t0001g0017a0001c0001t0001g0045a0001c0001t0001g0176others(334): Show | 337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.1603-2218dupA | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | INFO_REALIGN_3_PRIME | chr9 | 125319211 | |||||
| chr9:125319380
|
T | A | 2 | a0002c0006t0011g0121a0002c0006t0011g0122 | 2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1603-2053T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125319380 | ||||||
| chr9:125319390
|
T | A | 1 | a0001c0001t0001g0215 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1603-2043T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125319390 | ||||||
| chr9:125319430
|
A | C | 7 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0008others(4): Show | 7 | HG01069.hp1 HG02615.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1603-2003A>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125319430 | ||||||
| chr9:125319563
|
C | G | 3 | a0001c0001t0009g0001a0001c0001t0009g0002a0001c0001t0009g0003 | 3 | HG01884.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1603-1870C>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125319563 | ||||||
| chr9:125319601
|
C | CT | 14 | a0001c0001t0001g0273a0001c0001t0001g0281a0001c0001t0001g0292others(11): Show | 14 | HG01175.hp1 HG02004.hp1 HG02074.hp2 others(11): Show |
intron_variant | MODIFIER | c.1603-1814dupT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | INFO_REALIGN_3_PRIME | chr9 | 125319601 | |||||
| chr9:125319627
|
A | G | 6 | a0001c0003t0006g0166a0001c0003t0006g0168a0001c0003t0006g0169others(3): Show | 6 | HG01167.hp1 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1603-1806A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125319627 | ||||||
| chr9:125319704
|
C | T | 1 | a0001c0001t0001g0223 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1603-1729C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125319704 | ||||||
| chr9:125319903
|
A | C | 2 | a0001c0005t0001g0219a0001c0005t0001g0231 | 2 | HG00280.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.1603-1530A>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125319903 | ||||||
| chr9:125319950
|
A | T | 1 | a0001c0016t0037g0152 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1603-1483A>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125319950 | ||||||
| chr9:125320054
|
A | G | 1 | a0001c0001t0001g0230 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1603-1379A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125320054 | ||||||
| chr9:125320061
|
T | A | 2 | a0001c0001t0001g0182a0001c0001t0001g0185 | 2 | NA18952.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.1603-1372T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125320061 | ||||||
| chr9:125320109
|
C | T | 33 | a0001c0002t0003g0004a0001c0002t0003g0005a0001c0002t0003g0123others(30): Show | 33 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(30): Show |
intron_variant | MODIFIER | c.1603-1324C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125320109 | ||||||
| chr9:125320289
|
A | G | 1 | a0001c0001t0002g0089 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1603-1144A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125320289 | ||||||
| chr9:125320294
|
C | A | 1 | a0006c0011t0005g0337 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1603-1139C>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125320294 | ||||||
| chr9:125320376
|
A | G | 2 | a0001c0001t0001g0224a0001c0001t0002g0257 | 2 | HG01261.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.1603-1057A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125320376 | ||||||
| chr9:125320480
|
G | A | 31 | a0001c0002t0003g0004a0001c0002t0003g0005a0001c0002t0003g0123others(28): Show | 31 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.1603-953G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125320480 | ||||||
| chr9:125320531
|
C | T | 1 | a0001c0001t0002g0092 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1603-902C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125320531 | ||||||
| chr9:125320726
|
C | T | 1 | a0001c0009t0001g0190 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1603-707C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125320726 | ||||||
| chr9:125320767
|
A | G | 1 | a0001c0001t0002g0030 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1603-666A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125320767 | ||||||
| chr9:125320820
|
G | T | 1 | a0006c0011t0005g0337 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1603-613G>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125320820 | ||||||
| chr9:125320823
|
T | A | 1 | a0006c0011t0005g0337 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1603-610T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125320823 | ||||||
| chr9:125320861
|
C | T | 3 | a0001c0001t0001g0181a0002c0006t0011g0121a0002c0006t0011g0122 | 3 | HG01109.hp2 HG03098.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.1603-572C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125320861 | ||||||
| chr9:125320884
|
C | T | 1 | a0001c0001t0002g0051 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1603-549C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125320884 | ||||||
| chr9:125320906
|
G | A | 1 | a0001c0001t0017g0013 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1603-527G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125320906 | ||||||
| chr9:125320913
|
T | A | 1 | a0006c0011t0005g0337 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1603-520T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125320913 | ||||||
| chr9:125320917
|
C | T | 1 | a0001c0001t0002g0114 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1603-516C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125320917 | ||||||
| chr9:125321288
|
T | A | 1 | a0006c0011t0005g0337 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1603-145T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125321288 | ||||||
| chr9:125321306
|
T | C | 2 | a0001c0001t0001g0289a0001c0001t0001g0313 | 2 | NA18959.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.1603-127T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125321306 | ||||||
| chr9:125321310
|
A | C | 2 | a0001c0005t0001g0219a0001c0005t0001g0231 | 2 | HG00280.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.1603-123A>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125321310 | ||||||
| chr9:125321356
|
A | G | 1 | a0001c0002t0003g0123 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1603-77A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 9/27 | chr9 | 125321356 | ||||||
| chr9:125321886
|
G | T | 200 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(197): Show | 200 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.1732+324G>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 10/27 | chr9 | 125321886 | ||||||
| chr9:125321890
|
C | T | 1 | a0001c0009t0001g0190 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1732+328C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 10/27 | chr9 | 125321890 | ||||||
| chr9:125321904
|
C | G | 1 | a0001c0016t0037g0152 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1732+342C>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 10/27 | chr9 | 125321904 | ||||||
| chr9:125321981
|
G | C | 2 | a0001c0001t0004g0173a0001c0001t0004g0174 | 2 | HG01099.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.1732+419G>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 10/27 | chr9 | 125321981 | ||||||
| chr9:125322113
|
G | A | 1 | a0001c0001t0001g0299 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1732+551G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 10/27 | chr9 | 125322113 | ||||||
| chr9:125322125
|
C | T | 1 | a0001c0001t0002g0085 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1732+563C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 10/27 | chr9 | 125322125 | ||||||
| chr9:125322126
|
G | C | 1 | a0001c0001t0002g0085 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1732+564G>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 10/27 | chr9 | 125322126 | ||||||
| chr9:125322157
|
C | T | 1 | a0001c0009t0001g0190 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1732+595C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 10/27 | chr9 | 125322157 | ||||||
| chr9:125322254
|
C | T | 6 | a0001c0001t0001g0181a0001c0001t0001g0183a0001c0001t0001g0184others(3): Show | 6 | HG00558.hp1 NA18973.hp1 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.1732+692C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 10/27 | chr9 | 125322254 | ||||||
| chr9:125322265
|
C | T | 1 | a0001c0016t0037g0152 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1732+703C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 10/27 | chr9 | 125322265 | ||||||
| chr9:125322285
|
C | T | 1 | a0001c0001t0001g0230 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1732+723C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 10/27 | chr9 | 125322285 | ||||||
| chr9:125322353
|
C | T | 7 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0008others(4): Show | 7 | HG01069.hp1 HG02615.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1732+791C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 10/27 | chr9 | 125322353 | ||||||
| chr9:125322359
|
T | C | 1 | a0001c0016t0037g0152 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1732+797T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 10/27 | chr9 | 125322359 | ||||||
| chr9:125322363
|
C | T | 1 | a0001c0001t0001g0298 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1732+801C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 10/27 | chr9 | 125322363 | ||||||
| chr9:125322478
|
T | C | 1 | a0001c0001t0001g0226 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1732+916T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 10/27 | chr9 | 125322478 | ||||||
| chr9:125322517
|
A | G | 6 | a0001c0001t0001g0317a0001c0001t0001g0318a0001c0001t0001g0319others(3): Show | 6 | HG02451.hp1 HG02559.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1732+955A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 10/27 | chr9 | 125322517 | ||||||
| chr9:125322690
|
T | TG | 232 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(229): Show | 232 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.1733-1106dupG | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr9 | 125322690 | |||||
| chr9:125322977
|
A | G | 201 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(198): Show | 201 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.1733-821A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 10/27 | chr9 | 125322977 | ||||||
| chr9:125323051
|
T | TA | 13 | a0001c0001t0001g0180a0001c0001t0001g0187a0001c0001t0001g0271others(10): Show | 13 | HG00733.hp2 HG01109.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.1733-729dupA | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr9 | 125323051 | |||||
| chr9:125323051
|
TA | T | 7 | a0001c0001t0001g0203a0001c0001t0001g0236a0001c0001t0002g0028others(4): Show | 7 | HG02922.hp1 HG03491.hp1 HG03704.hp2 others(4): Show |
intron_variant | MODIFIER | c.1733-729delA | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr9 | 125323051 | |||||
| chr9:125323064
|
A | G | 5 | a0001c0003t0004g0156a0001c0003t0004g0157a0001c0003t0004g0164others(2): Show | 5 | HG02258.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1733-734A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 10/27 | chr9 | 125323064 | ||||||
| chr9:125323067
|
A | G | 12 | a0001c0001t0002g0070a0001c0003t0004g0156a0001c0003t0004g0157others(9): Show | 12 | HG01167.hp1 HG02071.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1733-731A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 10/27 | chr9 | 125323067 | ||||||
| chr9:125323148
|
C | T | 34 | a0001c0001t0016g0046a0001c0002t0003g0004a0001c0002t0003g0005others(31): Show | 34 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(31): Show |
intron_variant | MODIFIER | c.1733-650C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 10/27 | chr9 | 125323148 | ||||||
| chr9:125323166
|
A | G | 232 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(229): Show | 232 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.1733-632A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 10/27 | chr9 | 125323166 | ||||||
| chr9:125323169
|
C | T | 2 | a0001c0001t0004g0173a0001c0001t0004g0174 | 2 | HG01099.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.1733-629C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 10/27 | chr9 | 125323169 | ||||||
| chr9:125323198
|
C | T | 1 | a0001c0001t0001g0221 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1733-600C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 10/27 | chr9 | 125323198 | ||||||
| chr9:125323200
|
G | A | 158 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(155): Show | 158 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.1733-598G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 10/27 | chr9 | 125323200 | ||||||
| chr9:125323242
|
G | C | 1 | a0001c0001t0002g0153 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1733-556G>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 10/27 | chr9 | 125323242 | ||||||
| chr9:125323252
|
A | G | 1 | a0001c0001t0002g0015 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1733-546A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 10/27 | chr9 | 125323252 | ||||||
| chr9:125323754
|
T | C | 31 | a0001c0001t0016g0046a0001c0002t0003g0004a0001c0002t0003g0005others(28): Show | 31 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.1733-44T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 10/27 | chr9 | 125323754 | ||||||
| chr9:125323997
|
A | G | 1 | a0001c0001t0002g0085 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1858+74A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 11/27 | chr9 | 125323997 | ||||||
| chr9:125324397
|
C | T | 1 | a0001c0001t0001g0253 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1858+474C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 11/27 | chr9 | 125324397 | ||||||
| chr9:125324405
|
A | G | 1 | a0001c0001t0025g0207 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1858+482A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 11/27 | chr9 | 125324405 | ||||||
| chr9:125324453
|
G | A | 2 | a0002c0006t0011g0121a0002c0006t0011g0122 | 2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1858+530G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 11/27 | chr9 | 125324453 | ||||||
| chr9:125324478
|
A | G | 1 | a0001c0016t0037g0152 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1858+555A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 11/27 | chr9 | 125324478 | ||||||
| chr9:125324543
|
C | T | 1 | a0001c0001t0004g0007 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1858+620C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 11/27 | chr9 | 125324543 | ||||||
| chr9:125324689
|
G | T | 31 | a0001c0002t0003g0004a0001c0002t0003g0005a0001c0002t0003g0123others(28): Show | 31 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.1858+766G>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 11/27 | chr9 | 125324689 | ||||||
| chr9:125324732
|
G | C | 31 | a0001c0002t0003g0004a0001c0002t0003g0005a0001c0002t0003g0123others(28): Show | 31 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.1858+809G>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 11/27 | chr9 | 125324732 | ||||||
| chr9:125324838
|
A | G | 1 | a0001c0016t0037g0152 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1858+915A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 11/27 | chr9 | 125324838 | ||||||
| chr9:125324850
|
G | C | 2 | a0001c0002t0003g0125a0001c0002t0003g0146 | 2 | NA18988.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.1858+927G>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 11/27 | chr9 | 125324850 | ||||||
| chr9:125324916
|
G | A | 1 | a0001c0003t0004g0156 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1858+993G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 11/27 | chr9 | 125324916 | ||||||
| chr9:125324921
|
G | C | 93 | a0001c0001t0001g0193a0001c0001t0001g0195a0001c0001t0001g0196others(90): Show | 93 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.1858+998G>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 11/27 | chr9 | 125324921 | ||||||
| chr9:125324960
|
C | T | 1 | a0001c0001t0004g0006 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1858+1037C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 11/27 | chr9 | 125324960 | ||||||
| chr9:125325260
|
A | G | 231 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(228): Show | 231 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.1859-1156A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 11/27 | chr9 | 125325260 | ||||||
| chr9:125325294
|
A | G | 232 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(229): Show | 232 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.1859-1122A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 11/27 | chr9 | 125325294 | ||||||
| chr9:125325393
|
G | T | 33 | a0001c0002t0003g0004a0001c0002t0003g0005a0001c0002t0003g0123others(30): Show | 33 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(30): Show |
intron_variant | MODIFIER | c.1859-1023G>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 11/27 | chr9 | 125325393 | ||||||
| chr9:125325509
|
G | A | 1 | a0001c0001t0024g0194 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1859-907G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 11/27 | chr9 | 125325509 | ||||||
| chr9:125325519
|
C | CA | 162 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(159): Show | 162 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.1859-877dupA | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 11/27 | INFO_REALIGN_3_PRIME | chr9 | 125325519 | |||||
| chr9:125325519
|
CA | C | 70 | a0001c0001t0002g0018a0001c0001t0002g0026a0001c0001t0002g0055others(67): Show | 70 | HG00544.hp2 HG00621.hp1 HG01069.hp1 others(67): Show |
intron_variant | MODIFIER | c.1859-877delA | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 11/27 | INFO_REALIGN_3_PRIME | chr9 | 125325519 | |||||
| chr9:125325616
|
C | G | 7 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0008others(4): Show | 7 | HG01069.hp1 HG02615.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1859-800C>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 11/27 | chr9 | 125325616 | ||||||
| chr9:125325632
|
C | A | 1 | a0001c0003t0004g0157 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1859-784C>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 11/27 | chr9 | 125325632 | ||||||
| chr9:125325671
|
A | G | 1 | a0001c0001t0001g0177 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1859-745A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 11/27 | chr9 | 125325671 | ||||||
| chr9:125325712
|
T | C | 3 | a0001c0001t0001g0317a0001c0001t0001g0319a0001c0001t0001g0321 | 3 | HG02451.hp1 HG02559.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1859-704T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 11/27 | chr9 | 125325712 | ||||||
| chr9:125325954
|
A | G | 1 | a0001c0001t0001g0310 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1859-462A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 11/27 | chr9 | 125325954 | ||||||
| chr9:125326065
|
G | C | 2 | a0001c0001t0002g0014a0001c0001t0002g0015 | 2 | NA18977.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.1859-351G>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 11/27 | chr9 | 125326065 | ||||||
| chr9:125326069
|
C | T | 1 | a0001c0001t0017g0013 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1859-347C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 11/27 | chr9 | 125326069 | ||||||
| chr9:125326207
|
A | G | 1 | a0001c0001t0001g0253 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1859-209A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 11/27 | chr9 | 125326207 | ||||||
| chr9:125326236
|
G | A | 1 | a0001c0001t0002g0034 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1859-180G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 11/27 | chr9 | 125326236 | ||||||
| chr9:125326240
|
A | G | 1 | a0001c0016t0037g0152 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1859-176A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 11/27 | chr9 | 125326240 | ||||||
| chr9:125326316
|
G | A | 1 | a0001c0001t0017g0013 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1859-100G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 11/27 | chr9 | 125326316 | ||||||
| chr9:125326716
|
T | C | 1 | a0001c0009t0001g0190 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2032+127T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 12/27 | chr9 | 125326716 | ||||||
| chr9:125326826
|
C | CA | 9 | a0001c0001t0002g0024a0001c0001t0004g0006a0001c0001t0004g0007others(6): Show | 9 | HG01069.hp1 HG02615.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.2032+249dupA | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr9 | 125326826 | |||||
| chr9:125327139
|
G | C | 1 | a0001c0016t0037g0152 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2032+550G>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 12/27 | chr9 | 125327139 | ||||||
| chr9:125327397
|
T | A | 1 | a0001c0001t0001g0326 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2032+808T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 12/27 | chr9 | 125327397 | ||||||
| chr9:125327439
|
G | A | 1 | a0001c0001t0001g0316 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.2032+850G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 12/27 | chr9 | 125327439 | ||||||
| chr9:125327479
|
T | C | 166 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(163): Show | 166 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.2032+890T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 12/27 | chr9 | 125327479 | ||||||
| chr9:125327482
|
T | C | 5 | a0001c0003t0004g0156a0001c0003t0004g0157a0001c0003t0004g0164others(2): Show | 5 | HG02258.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.2032+893T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 12/27 | chr9 | 125327482 | ||||||
| chr9:125327529
|
G | A | 5 | a0001c0003t0004g0156a0001c0003t0004g0157a0001c0003t0004g0164others(2): Show | 5 | HG02258.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.2032+940G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 12/27 | chr9 | 125327529 | ||||||
| chr9:125327606
|
T | C | 4 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0242others(1): Show | 4 | HG00639.hp2 HG00735.hp2 HG01074.hp1 others(1): Show |
intron_variant | MODIFIER | c.2032+1017T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 12/27 | chr9 | 125327606 | ||||||
| chr9:125327663
|
C | A | 7 | a0001c0003t0006g0158a0001c0003t0006g0159a0001c0003t0006g0160others(4): Show | 7 | HG01109.hp1 HG01884.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.2032+1074C>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 12/27 | chr9 | 125327663 | ||||||
| chr9:125327665
|
A | G | 1 | a0001c0001t0001g0210 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2032+1076A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 12/27 | chr9 | 125327665 | ||||||
| chr9:125328134
|
T | C | 2 | a0001c0001t0004g0173a0001c0001t0004g0174 | 2 | HG01099.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.2032+1545T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 12/27 | chr9 | 125328134 | ||||||
| chr9:125328188
|
C | CT | 61 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(58): Show | 61 | HG00438.hp1 HG00558.hp1 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.2032+1616dupT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr9 | 125328188 | |||||
| chr9:125328188
|
CT | C | 38 | a0001c0001t0002g0023a0001c0001t0002g0072a0001c0001t0002g0094others(35): Show | 38 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(35): Show |
intron_variant | MODIFIER | c.2032+1616delT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr9 | 125328188 | |||||
| chr9:125328189
|
T | C | 1 | a0001c0001t0008g0112 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2032+1600T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 12/27 | chr9 | 125328189 | ||||||
| chr9:125328205
|
T | A | 1 | a0001c0001t0002g0076 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.2032+1616T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 12/27 | chr9 | 125328205 | ||||||
| chr9:125328205
|
TA | T | 5 | a0001c0001t0001g0197a0001c0001t0001g0234a0001c0001t0001g0238others(2): Show | 5 | HG01074.hp1 HG01167.hp2 HG01257.hp2 others(2): Show |
intron_variant | MODIFIER | c.2032+1619delA | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr9 | 125328205 | |||||
| chr9:125328206
|
A | T | 115 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0001g0195others(112): Show | 115 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.2032+1617A>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 12/27 | chr9 | 125328206 | ||||||
| chr9:125328333
|
C | T | 1 | a0001c0002t0003g0144 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2032+1744C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 12/27 | chr9 | 125328333 | ||||||
| chr9:125328390
|
G | T | 230 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(227): Show | 230 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.2033-1688G>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 12/27 | chr9 | 125328390 | ||||||
| chr9:125328454
|
T | C | 1 | a0001c0016t0037g0152 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2033-1624T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 12/27 | chr9 | 125328454 | ||||||
| chr9:125328615
|
G | C | 1 | a0001c0001t0002g0020 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.2033-1463G>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 12/27 | chr9 | 125328615 | ||||||
| chr9:125328616
|
G | A | 1 | a0001c0001t0002g0020 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.2033-1462G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 12/27 | chr9 | 125328616 | ||||||
| chr9:125328636
|
A | G | 2 | a0001c0001t0002g0153a0001c0001t0031g0102 | 2 | HG02132.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.2033-1442A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 12/27 | chr9 | 125328636 | ||||||
| chr9:125328671
|
A | G | 31 | a0001c0002t0003g0004a0001c0002t0003g0005a0001c0002t0003g0123others(28): Show | 31 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.2033-1407A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 12/27 | chr9 | 125328671 | ||||||
| chr9:125328710
|
G | A | 1 | a0001c0001t0002g0082 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2033-1368G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 12/27 | chr9 | 125328710 | ||||||
| chr9:125328824
|
A | G | 1 | a0001c0016t0037g0152 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2033-1254A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 12/27 | chr9 | 125328824 | ||||||
| chr9:125328831
|
T | C | 1 | a0001c0016t0037g0152 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2033-1247T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 12/27 | chr9 | 125328831 | ||||||
| chr9:125328833
|
ACC | A | 227 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(224): Show | 227 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.2033-1236_2033-123 others(6): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr9 | 125328833 | |||||
| chr9:125328836
|
C | A | 4 | a0001c0001t0002g0201a0001c0001t0002g0220a0001c0001t0002g0258others(1): Show | 4 | HG00558.hp2 NA18941.hp2 NA18965.hp2 others(1): Show |
intron_variant | MODIFIER | c.2033-1242C>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 12/27 | chr9 | 125328836 | ||||||
| chr9:125328839
|
C | T | 1 | a0001c0001t0002g0104 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.2033-1239C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 12/27 | chr9 | 125328839 | ||||||
| chr9:125328899
|
G | A | 1 | a0001c0001t0002g0079 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2033-1179G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 12/27 | chr9 | 125328899 | ||||||
| chr9:125328918
|
C | T | 5 | a0001c0003t0006g0158a0001c0003t0006g0159a0001c0003t0006g0160others(2): Show | 5 | HG01109.hp1 HG01884.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.2033-1160C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 12/27 | chr9 | 125328918 | ||||||
| chr9:125328952
|
T | C | 231 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(228): Show | 231 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.2033-1126T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 12/27 | chr9 | 125328952 | ||||||
| chr9:125329067
|
G | A | 5 | a0001c0003t0004g0156a0001c0003t0004g0157a0001c0003t0004g0164others(2): Show | 5 | HG02258.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.2033-1011G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 12/27 | chr9 | 125329067 | ||||||
| chr9:125329070
|
G | C | 1 | a0001c0016t0037g0152 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2033-1008G>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 12/27 | chr9 | 125329070 | ||||||
| chr9:125329088
|
G | A | 1 | a0001c0001t0002g0096 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.2033-990G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 12/27 | chr9 | 125329088 | ||||||
| chr9:125329094
|
G | A | 31 | a0001c0002t0003g0004a0001c0002t0003g0005a0001c0002t0003g0123others(28): Show | 31 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.2033-984G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 12/27 | chr9 | 125329094 | ||||||
| chr9:125329112
|
GGGGAGA | G | 7 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0008others(4): Show | 7 | HG01069.hp1 HG02615.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.2033-945_2033-940d others(8): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr9 | 125329112 | |||||
| chr9:125329222
|
C | T | 1 | a0001c0003t0004g0170 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2033-856C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 12/27 | chr9 | 125329222 | ||||||
| chr9:125329387
|
A | G | 1 | a0001c0001t0002g0044 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2033-691A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 12/27 | chr9 | 125329387 | ||||||
| chr9:125329400
|
C | T | 1 | a0001c0001t0002g0044 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2033-678C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 12/27 | chr9 | 125329400 | ||||||
| chr9:125329566
|
T | C | 1 | a0001c0001t0002g0096 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.2033-512T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 12/27 | chr9 | 125329566 | ||||||
| chr9:125329634
|
G | GT | 14 | a0001c0001t0002g0024a0001c0001t0002g0025a0001c0001t0002g0044others(11): Show | 14 | HG00423.hp1 HG00609.hp1 HG00733.hp2 others(11): Show |
intron_variant | MODIFIER | c.2033-428dupT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr9 | 125329634 | |||||
| chr9:125329634
|
GT | G | 11 | a0001c0001t0001g0183a0001c0001t0001g0240a0001c0001t0001g0317others(8): Show | 11 | HG02451.hp1 HG02559.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.2033-428delT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr9 | 125329634 | |||||
| chr9:125329634
|
GTT | G | 185 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(182): Show | 185 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.2033-429_2033-428d others(4): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr9 | 125329634 | |||||
| chr9:125329637
|
T | G | 2 | a0002c0006t0011g0121a0002c0006t0011g0122 | 2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2033-441T>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 12/27 | chr9 | 125329637 | ||||||
| chr9:125329823
|
C | T | 17 | a0001c0001t0002g0052a0001c0001t0002g0068a0001c0001t0002g0086others(14): Show | 17 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(14): Show |
intron_variant | MODIFIER | c.2033-255C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 12/27 | chr9 | 125329823 | ||||||
| chr9:125329824
|
G | T | 1 | a0001c0016t0037g0152 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2033-254G>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 12/27 | chr9 | 125329824 | ||||||
| chr9:125330015
|
C | G | 1 | a0001c0016t0037g0152 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2033-63C>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 12/27 | chr9 | 125330015 | ||||||
| chr9:125330381
|
C | T | 1 | a0001c0002t0003g0123 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2173+163C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 13/27 | chr9 | 125330381 | ||||||
| chr9:125330702
|
G | A | 1 | a0001c0016t0037g0152 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2173+484G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 13/27 | chr9 | 125330702 | ||||||
| chr9:125330745
|
C | A | 1 | a0001c0004t0002g0041 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2173+527C>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 13/27 | chr9 | 125330745 | ||||||
| chr9:125330812
|
T | C | 1 | a0001c0002t0007g0150 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2173+594T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 13/27 | chr9 | 125330812 | ||||||
| chr9:125330816
|
A | G | 1 | a0001c0001t0001g0269 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2173+598A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 13/27 | chr9 | 125330816 | ||||||
| chr9:125330851
|
A | G | 1 | a0001c0009t0001g0190 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2173+633A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 13/27 | chr9 | 125330851 | ||||||
| chr9:125330986
|
A | AT | 171 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(168): Show | 171 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.2173+778dupT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 13/27 | INFO_REALIGN_3_PRIME | chr9 | 125330986 | |||||
| chr9:125330989
|
T | C | 1 | a0001c0002t0007g0136 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.2173+771T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 13/27 | chr9 | 125330989 | ||||||
| chr9:125331076
|
G | T | 1 | a0001c0001t0002g0061 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.2174-850G>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 13/27 | chr9 | 125331076 | ||||||
| chr9:125331204
|
AT | A | 231 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(228): Show | 231 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.2174-708delT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 13/27 | INFO_REALIGN_3_PRIME | chr9 | 125331204 | |||||
| chr9:125331272
|
C | T | 31 | a0001c0002t0003g0004a0001c0002t0003g0005a0001c0002t0003g0123others(28): Show | 31 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.2174-654C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 13/27 | chr9 | 125331272 | ||||||
| chr9:125331387
|
G | A | 5 | a0001c0003t0006g0158a0001c0003t0006g0159a0001c0003t0006g0160others(2): Show | 5 | HG01109.hp1 HG01884.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.2174-539G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 13/27 | chr9 | 125331387 | ||||||
| chr9:125331447
|
G | A | 6 | a0001c0003t0006g0166a0001c0003t0006g0168a0001c0003t0006g0169others(3): Show | 6 | HG01167.hp1 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.2174-479G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 13/27 | chr9 | 125331447 | ||||||
| chr9:125331829
|
C | T | 1 | a0001c0001t0001g0178 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2174-97C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 13/27 | chr9 | 125331829 | ||||||
| chr9:125331862
|
A | G | 1 | a0001c0001t0001g0248 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2174-64A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 13/27 | chr9 | 125331862 | ||||||
| chr9:125331920
|
A | G | 1 | a0001c0001t0002g0117 | 1 | HG03491.hp1 | splice_region_variant&intron_variant | LOW | c.2174-6A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 13/27 | chr9 | 125331920 | ||||||
| chr9:125332125
|
A | T | 1 | a0001c0001t0002g0051 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.2308+65A>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 14/27 | chr9 | 125332125 | ||||||
| chr9:125332292
|
G | A | 2 | a0002c0006t0011g0121a0002c0006t0011g0122 | 2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2309-218G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 14/27 | chr9 | 125332292 | ||||||
| chr9:125332412
|
A | G | 2 | a0002c0006t0011g0121a0002c0006t0011g0122 | 2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2309-98A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 14/27 | chr9 | 125332412 | ||||||
| chr9:125333031
|
A | T | 2 | a0001c0003t0006g0166a0001c0003t0006g0168 | 2 | HG01167.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.2428+402A>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 15/27 | chr9 | 125333031 | ||||||
| chr9:125333080
|
G | GT | 6 | a0001c0001t0002g0054a0001c0003t0004g0156a0001c0003t0004g0157others(3): Show | 6 | HG02258.hp1 HG02451.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.2428+461dupT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr9 | 125333080 | |||||
| chr9:125333095
|
C | T | 9 | a0001c0001t0002g0018a0001c0001t0002g0026a0001c0001t0002g0058others(6): Show | 9 | NA18954.hp1 NA18957.hp1 NA18971.hp1 others(6): Show |
intron_variant | MODIFIER | c.2428+466C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 15/27 | chr9 | 125333095 | ||||||
| chr9:125333369
|
C | T | 13 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(10): Show | 13 | HG00558.hp1 HG02027.hp2 NA18943.hp1 others(10): Show |
intron_variant | MODIFIER | c.2428+740C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 15/27 | chr9 | 125333369 | ||||||
| chr9:125333442
|
G | C | 3 | a0001c0001t0009g0001a0001c0001t0009g0002a0001c0001t0009g0003 | 3 | HG01884.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2428+813G>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 15/27 | chr9 | 125333442 | ||||||
| chr9:125333485
|
C | CT | 44 | a0001c0001t0001g0213a0001c0001t0001g0229a0001c0001t0001g0230others(41): Show | 44 | HG00544.hp2 HG01081.hp2 HG01123.hp1 others(41): Show |
intron_variant | MODIFIER | c.2428+876dupT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr9 | 125333485 | |||||
| chr9:125333485
|
CT | C | 8 | a0001c0001t0001g0234a0001c0001t0001g0265a0001c0001t0001g0276others(5): Show | 8 | HG01099.hp1 HG01109.hp2 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.2428+876delT | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr9 | 125333485 | |||||
| chr9:125333550
|
G | A | 6 | a0001c0001t0004g0007a0001c0001t0004g0008a0001c0001t0004g0009others(3): Show | 6 | HG01069.hp1 HG02615.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.2428+921G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 15/27 | chr9 | 125333550 | ||||||
| chr9:125333551
|
C | T | 5 | a0001c0003t0004g0156a0001c0003t0004g0157a0001c0003t0004g0164others(2): Show | 5 | HG02258.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.2428+922C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 15/27 | chr9 | 125333551 | ||||||
| chr9:125333558
|
G | A | 3 | a0001c0003t0004g0156a0001c0003t0004g0157a0001c0003t0004g0170 | 3 | HG02451.hp2 HG02622.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2428+929G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 15/27 | chr9 | 125333558 | ||||||
| chr9:125333882
|
T | C | 32 | a0001c0001t0016g0046a0001c0002t0003g0004a0001c0002t0003g0005others(29): Show | 32 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.2428+1253T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 15/27 | chr9 | 125333882 | ||||||
| chr9:125333927
|
G | T | 2 | a0001c0001t0001g0290a0001c0001t0001g0312 | 2 | HG02698.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.2428+1298G>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 15/27 | chr9 | 125333927 | ||||||
| chr9:125334143
|
A | G | 1 | a0001c0016t0037g0152 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2428+1514A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 15/27 | chr9 | 125334143 | ||||||
| chr9:125334170
|
G | A | 1 | a0001c0016t0037g0152 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2428+1541G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 15/27 | chr9 | 125334170 | ||||||
| chr9:125334232
|
G | A | 1 | a0001c0001t0001g0230 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2428+1603G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 15/27 | chr9 | 125334232 | ||||||
| chr9:125334242
|
G | A | 4 | a0001c0001t0008g0031a0001c0001t0008g0047a0001c0001t0008g0050others(1): Show | 4 | HG01123.hp2 HG01346.hp2 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.2428+1613G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 15/27 | chr9 | 125334242 | ||||||
| chr9:125334270
|
T | TA | 48 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0234others(45): Show | 48 | HG00544.hp2 HG00621.hp1 HG00741.hp2 others(45): Show |
intron_variant | MODIFIER | c.2428+1663dupA | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr9 | 125334270 | |||||
| chr9:125334270
|
TA | T | 16 | a0001c0001t0001g0238a0001c0001t0001g0319a0001c0001t0002g0061others(13): Show | 16 | HG01069.hp1 HG01069.hp2 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.2428+1663delA | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr9 | 125334270 | |||||
| chr9:125334323
|
A | G | 32 | a0001c0001t0016g0046a0001c0002t0003g0004a0001c0002t0003g0005others(29): Show | 32 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.2428+1694A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 15/27 | chr9 | 125334323 | ||||||
| chr9:125334340
|
A | C | 2 | a0001c0002t0003g0138a0001c0002t0003g0139 | 2 | NA18940.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.2428+1711A>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 15/27 | chr9 | 125334340 | ||||||
| chr9:125334390
|
A | G | 1 | a0001c0001t0001g0294 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2428+1761A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 15/27 | chr9 | 125334390 | ||||||
| chr9:125334511
|
G | T | 21 | a0001c0001t0009g0001a0001c0001t0009g0002a0001c0001t0009g0003others(18): Show | 21 | HG01109.hp1 HG01167.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.2428+1882G>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 15/27 | chr9 | 125334511 | ||||||
| chr9:125334658
|
G | C | 4 | a0001c0001t0002g0201a0001c0001t0002g0220a0001c0001t0002g0258others(1): Show | 4 | HG00558.hp2 NA18941.hp2 NA18965.hp2 others(1): Show |
intron_variant | MODIFIER | c.2428+2029G>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 15/27 | chr9 | 125334658 | ||||||
| chr9:125334678
|
G | T | 1 | a0001c0016t0037g0152 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2428+2049G>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 15/27 | chr9 | 125334678 | ||||||
| chr9:125334749
|
A | G | 1 | a0004c0008t0002g0083 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2428+2120A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 15/27 | chr9 | 125334749 | ||||||
| chr9:125334787
|
G | A | 2 | a0001c0001t0002g0052a0001c0001t0002g0087 | 2 | HG02165.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.2428+2158G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 15/27 | chr9 | 125334787 | ||||||
| chr9:125334797
|
T | TA | 163 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(160): Show | 163 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(160): Show |
intron_variant | MODIFIER | c.2428+2181dupA | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr9 | 125334797 | |||||
| chr9:125334805
|
A | G | 5 | a0001c0003t0006g0158a0001c0003t0006g0159a0001c0003t0006g0160others(2): Show | 5 | HG01109.hp1 HG01884.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.2428+2176A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 15/27 | chr9 | 125334805 | ||||||
| chr9:125334827
|
GTTTC | G | 3 | a0001c0001t0002g0103a0001c0001t0002g0105a0001c0001t0002g0106 | 3 | HG00408.hp2 HG02074.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.2429-2188_2429-218 others(8): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr9 | 125334827 | |||||
| chr9:125335388
|
A | T | 165 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(162): Show | 165 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.2429-1630A>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 15/27 | chr9 | 125335388 | ||||||
| chr9:125335403
|
C | T | 3 | a0001c0001t0002g0022a0001c0001t0002g0024a0001c0013t0002g0043 | 3 | NA18959.hp2 NA18995.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.2429-1615C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 15/27 | chr9 | 125335403 | ||||||
| chr9:125335484
|
T | A | 5 | a0001c0003t0006g0158a0001c0003t0006g0159a0001c0003t0006g0160others(2): Show | 5 | HG01109.hp1 HG01884.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.2429-1534T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 15/27 | chr9 | 125335484 | ||||||
| chr9:125335550
|
G | A | 1 | a0001c0001t0001g0316 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.2429-1468G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 15/27 | chr9 | 125335550 | ||||||
| chr9:125335551
|
C | T | 1 | a0001c0001t0001g0316 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.2429-1467C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 15/27 | chr9 | 125335551 | ||||||
| chr9:125335604
|
G | A | 1 | a0001c0002t0007g0136 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.2429-1414G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 15/27 | chr9 | 125335604 | ||||||
| chr9:125335844
|
T | C | 1 | a0001c0001t0002g0153 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.2429-1174T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 15/27 | chr9 | 125335844 | ||||||
| chr9:125336145
|
C | CA | 28 | a0001c0001t0001g0180a0001c0001t0001g0195a0001c0001t0001g0200others(25): Show | 28 | HG01109.hp2 HG01167.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.2429-857dupA | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr9 | 125336145 | |||||
| chr9:125336145
|
C | CAAA | 27 | a0001c0001t0016g0046a0001c0002t0003g0004a0001c0002t0003g0123others(24): Show | 27 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(24): Show |
intron_variant | MODIFIER | c.2429-859_2429-857d others(5): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr9 | 125336145 | |||||
| chr9:125336245
|
G | A | 1 | a0001c0001t0035g0303 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.2429-773G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 15/27 | chr9 | 125336245 | ||||||
| chr9:125336276
|
A | G | 7 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0008others(4): Show | 7 | HG01069.hp1 HG02615.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.2429-742A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 15/27 | chr9 | 125336276 | ||||||
| chr9:125336290
|
C | CA | 18 | a0001c0001t0002g0015a0001c0001t0002g0018a0001c0001t0002g0026others(15): Show | 18 | HG01515.hp2 HG03688.hp2 NA18949.hp1 others(15): Show |
intron_variant | MODIFIER | c.2429-713dupA | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr9 | 125336290 | |||||
| chr9:125336290
|
CA | C | 16 | a0001c0001t0001g0218a0001c0001t0001g0274a0001c0001t0001g0277others(13): Show | 16 | HG00438.hp1 HG01167.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.2429-713delA | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr9 | 125336290 | |||||
| chr9:125336290
|
CAA | C | 167 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(164): Show | 167 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.2429-714_2429-713d others(4): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr9 | 125336290 | |||||
| chr9:125336299
|
A | C | 1 | a0001c0016t0037g0152 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2429-719A>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 15/27 | chr9 | 125336299 | ||||||
| chr9:125336306
|
C | A | 1 | a0001c0002t0003g0146 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.2429-712C>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 15/27 | chr9 | 125336306 | ||||||
| chr9:125336306
|
C | CA | 31 | a0001c0001t0016g0046a0001c0002t0003g0004a0001c0002t0003g0005others(28): Show | 31 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.2429-706dupA | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr9 | 125336306 | |||||
| chr9:125336313
|
C | A | 32 | a0001c0001t0016g0046a0001c0002t0003g0004a0001c0002t0003g0005others(29): Show | 32 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.2429-705C>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 15/27 | chr9 | 125336313 | ||||||
| chr9:125336313
|
CA | C | 7 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(4): Show | 7 | HG02027.hp2 NA18943.hp1 NA18952.hp2 others(4): Show |
intron_variant | MODIFIER | c.2429-699delA | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr9 | 125336313 | |||||
| chr9:125336578
|
G | A | 1 | a0001c0016t0037g0152 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2429-440G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 15/27 | chr9 | 125336578 | ||||||
| chr9:125336771
|
A | G | 1 | a0001c0001t0001g0224 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.2429-247A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 15/27 | chr9 | 125336771 | ||||||
| chr9:125337856
|
T | A | 4 | a0001c0003t0006g0159a0001c0003t0006g0160a0001c0003t0006g0161others(1): Show | 4 | HG01109.hp1 HG02280.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.2877+265T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 17/27 | chr9 | 125337856 | ||||||
| chr9:125337969
|
A | G | 1 | a0001c0005t0001g0199 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2877+378A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 17/27 | chr9 | 125337969 | ||||||
| chr9:125337980
|
A | G | 5 | a0001c0003t0004g0156a0001c0003t0004g0157a0001c0003t0004g0164others(2): Show | 5 | HG02258.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.2877+389A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 17/27 | chr9 | 125337980 | ||||||
| chr9:125338164
|
C | G | 2 | a0001c0001t0004g0173a0001c0001t0004g0174 | 2 | HG01099.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.2877+573C>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 17/27 | chr9 | 125338164 | ||||||
| chr9:125338555
|
C | T | 1 | a0001c0001t0002g0063 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2877+964C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 17/27 | chr9 | 125338555 | ||||||
| chr9:125338927
|
ATTTGTGT others(7): Show |
A | 2 | a0001c0003t0006g0163a0001c0003t0026g0118 | 2 | HG02055.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.2877+1338_2877+135 others(18): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 17/27 | INFO_REALIGN_3_PRIME | chr9 | 125338927 | |||||
| chr9:125338929
|
T | G | 2 | a0001c0001t0001g0206a0001c0001t0001g0213 | 2 | HG03654.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2877+1338T>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 17/27 | chr9 | 125338929 | ||||||
| chr9:125338929
|
T | TTG | 34 | a0001c0001t0001g0017a0001c0001t0001g0045a0001c0001t0001g0182others(31): Show | 34 | HG00280.hp2 HG00639.hp1 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.2877+1366_2877+136 others(6): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 17/27 | INFO_REALIGN_3_PRIME | chr9 | 125338929 | |||||
| chr9:125338929
|
T | TTGTG | 86 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(83): Show | 86 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.2877+1364_2877+136 others(8): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 17/27 | INFO_REALIGN_3_PRIME | chr9 | 125338929 | |||||
| chr9:125338929
|
T | TTGTGTG | 5 | a0001c0002t0007g0135a0001c0012t0001g0282a0002c0006t0011g0121others(2): Show | 5 | HG01109.hp2 HG01255.hp2 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.2877+1362_2877+136 others(10): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 17/27 | INFO_REALIGN_3_PRIME | chr9 | 125338929 | |||||
| chr9:125338929
|
T | TTGTGTGT others(1): Show |
5 | a0001c0001t0001g0297a0001c0001t0001g0299a0001c0001t0010g0216others(2): Show | 5 | HG01515.hp1 HG01517.hp1 HG02135.hp1 others(2): Show |
intron_variant | MODIFIER | c.2877+1360_2877+136 others(12): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 17/27 | INFO_REALIGN_3_PRIME | chr9 | 125338929 | |||||
| chr9:125338929
|
T | TTGTGTGT others(7): Show |
1 | a0001c0001t0001g0214 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2877+1354_2877+136 others(18): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 17/27 | INFO_REALIGN_3_PRIME | chr9 | 125338929 | |||||
| chr9:125338929
|
TTGTG | T | 12 | a0001c0001t0002g0053a0001c0003t0004g0156a0001c0003t0004g0157others(9): Show | 12 | HG01167.hp1 HG02258.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.2877+1364_2877+136 others(8): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 17/27 | INFO_REALIGN_3_PRIME | chr9 | 125338929 | |||||
| chr9:125338955
|
GTGTATA | G | 3 | a0001c0001t0001g0317a0001c0001t0001g0319a0001c0001t0001g0321 | 3 | HG02451.hp1 HG02559.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2877+1366_2877+137 others(10): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 17/27 | INFO_REALIGN_3_PRIME | chr9 | 125338955 | |||||
| chr9:125338959
|
A | G | 197 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(194): Show | 197 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.2877+1368A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 17/27 | chr9 | 125338959 | ||||||
| chr9:125338961
|
A | G | 159 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(156): Show | 159 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.2877+1370A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 17/27 | chr9 | 125338961 | ||||||
| chr9:125338963
|
A | G | 3 | a0001c0001t0001g0246a0001c0001t0001g0247a0001c0001t0001g0265 | 3 | HG02280.hp1 HG02895.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2877+1372A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 17/27 | chr9 | 125338963 | ||||||
| chr9:125338965
|
A | T | 41 | a0001c0001t0002g0016a0001c0001t0002g0021a0001c0001t0002g0027others(38): Show | 41 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.2877+1374A>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 17/27 | chr9 | 125338965 | ||||||
| chr9:125339086
|
A | G | 6 | a0001c0001t0001g0205a0001c0003t0004g0156a0001c0003t0004g0157others(3): Show | 6 | HG02258.hp1 HG02451.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.2877+1495A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 17/27 | chr9 | 125339086 | ||||||
| chr9:125339229
|
G | A | 1 | a0001c0001t0013g0198 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2877+1638G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 17/27 | chr9 | 125339229 | ||||||
| chr9:125339363
|
A | G | 232 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(229): Show | 232 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.2877+1772A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 17/27 | chr9 | 125339363 | ||||||
| chr9:125339567
|
G | A | 1 | a0001c0001t0008g0112 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2878-1610G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 17/27 | chr9 | 125339567 | ||||||
| chr9:125339598
|
A | T | 1 | a0001c0001t0001g0227 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2878-1579A>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 17/27 | chr9 | 125339598 | ||||||
| chr9:125339712
|
A | G | 32 | a0001c0001t0016g0046a0001c0002t0003g0004a0001c0002t0003g0005others(29): Show | 32 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.2878-1465A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 17/27 | chr9 | 125339712 | ||||||
| chr9:125339776
|
A | G | 2 | a0001c0001t0001g0271a0001c0001t0001g0272 | 2 | NA18952.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.2878-1401A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 17/27 | chr9 | 125339776 | ||||||
| chr9:125339971
|
A | G | 2 | a0001c0001t0004g0173a0001c0001t0004g0174 | 2 | HG01099.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.2878-1206A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 17/27 | chr9 | 125339971 | ||||||
| chr9:125340089
|
C | T | 5 | a0001c0003t0004g0156a0001c0003t0004g0157a0001c0003t0004g0164others(2): Show | 5 | HG02258.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.2878-1088C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 17/27 | chr9 | 125340089 | ||||||
| chr9:125340221
|
T | A | 336 | a0001c0001t0001g0017a0001c0001t0001g0045a0001c0001t0001g0176others(333): Show | 336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.2878-956T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 17/27 | chr9 | 125340221 | ||||||
| chr9:125340269
|
C | T | 2 | a0002c0006t0011g0121a0002c0006t0011g0122 | 2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2878-908C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 17/27 | chr9 | 125340269 | ||||||
| chr9:125340327
|
T | G | 231 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(228): Show | 231 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.2878-850T>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 17/27 | chr9 | 125340327 | ||||||
| chr9:125340586
|
T | C | 201 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(198): Show | 201 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.2878-591T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 17/27 | chr9 | 125340586 | ||||||
| chr9:125340787
|
C | T | 1 | a0001c0001t0001g0017 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2878-390C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 17/27 | chr9 | 125340787 | ||||||
| chr9:125340911
|
C | T | 232 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(229): Show | 232 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.2878-266C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 17/27 | chr9 | 125340911 | ||||||
| chr9:125341010
|
G | C | 2 | a0002c0006t0011g0121a0002c0006t0011g0122 | 2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2878-167G>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 17/27 | chr9 | 125341010 | ||||||
| chr9:125341517
|
A | G | 7 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0008others(4): Show | 7 | HG01069.hp1 HG02615.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.2965+253A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 18/27 | chr9 | 125341517 | ||||||
| chr9:125341765
|
G | A | 2 | a0001c0001t0001g0325a0001c0001t0001g0326 | 2 | HG02559.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2966-454G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 18/27 | chr9 | 125341765 | ||||||
| chr9:125341781
|
C | T | 6 | a0001c0003t0006g0166a0001c0003t0006g0168a0001c0003t0006g0169others(3): Show | 6 | HG01167.hp1 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.2966-438C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 18/27 | chr9 | 125341781 | ||||||
| chr9:125341826
|
A | C | 231 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(228): Show | 231 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.2966-393A>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 18/27 | chr9 | 125341826 | ||||||
| chr9:125341988
|
A | G | 1 | a0001c0001t0004g0011 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2966-231A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 18/27 | chr9 | 125341988 | ||||||
| chr9:125342594
|
G | A | 2 | a0002c0006t0011g0121a0002c0006t0011g0122 | 2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.3046+295G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 19/27 | chr9 | 125342594 | ||||||
| chr9:125343062
|
T | C | 2 | a0001c0001t0002g0153a0001c0001t0031g0102 | 2 | HG02132.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.3046+763T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 19/27 | chr9 | 125343062 | ||||||
| chr9:125343195
|
T | C | 1 | a0001c0004t0002g0041 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.3046+896T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 19/27 | chr9 | 125343195 | ||||||
| chr9:125343459
|
A | G | 7 | a0001c0001t0001g0304a0001c0001t0001g0305a0001c0001t0001g0306others(4): Show | 7 | HG02056.hp1 NA18942.hp1 NA18954.hp2 others(4): Show |
intron_variant | MODIFIER | c.3046+1160A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 19/27 | chr9 | 125343459 | ||||||
| chr9:125343464
|
T | C | 2 | a0002c0006t0011g0121a0002c0006t0011g0122 | 2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.3046+1165T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 19/27 | chr9 | 125343464 | ||||||
| chr9:125343548
|
G | A | 2 | a0001c0001t0002g0028a0001c0001t0002g0070 | 2 | HG02071.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.3046+1249G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 19/27 | chr9 | 125343548 | ||||||
| chr9:125343752
|
C | A | 14 | a0001c0001t0005g0307a0001c0001t0005g0328a0001c0001t0005g0329others(11): Show | 14 | HG02129.hp1 NA18747.hp2 NA18950.hp1 others(11): Show |
intron_variant | MODIFIER | c.3046+1453C>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 19/27 | chr9 | 125343752 | ||||||
| chr9:125343820
|
G | A | 2 | a0001c0003t0006g0166a0001c0003t0006g0168 | 2 | HG01167.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.3046+1521G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 19/27 | chr9 | 125343820 | ||||||
| chr9:125343985
|
A | G | 4 | a0001c0001t0002g0068a0001c0001t0002g0086a0001c0001t0002g0094others(1): Show | 4 | HG00438.hp2 NA18978.hp1 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.3046+1686A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 19/27 | chr9 | 125343985 | ||||||
| chr9:125344103
|
G | C | 34 | a0001c0001t0016g0046a0001c0002t0003g0004a0001c0002t0003g0005others(31): Show | 34 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(31): Show |
intron_variant | MODIFIER | c.3046+1804G>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 19/27 | chr9 | 125344103 | ||||||
| chr9:125344201
|
T | A | 2 | a0001c0001t0001g0240a0001c0001t0001g0267 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.3046+1902T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 19/27 | chr9 | 125344201 | ||||||
| chr9:125344206
|
A | G | 32 | a0001c0001t0016g0046a0001c0002t0003g0004a0001c0002t0003g0005others(29): Show | 32 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.3046+1907A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 19/27 | chr9 | 125344206 | ||||||
| chr9:125344354
|
T | C | 1 | a0001c0016t0037g0152 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.3046+2055T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 19/27 | chr9 | 125344354 | ||||||
| chr9:125344408
|
G | A | 1 | a0001c0001t0001g0229 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.3046+2109G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 19/27 | chr9 | 125344408 | ||||||
| chr9:125344807
|
TA | T | 10 | a0001c0001t0001g0230a0001c0001t0002g0016a0001c0001t0002g0048others(7): Show | 10 | HG00280.hp2 HG02258.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.3047-1997delA | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 19/27 | INFO_REALIGN_3_PRIME | chr9 | 125344807 | |||||
| chr9:125344964
|
A | G | 10 | a0001c0001t0001g0192a0001c0001t0001g0269a0001c0001t0001g0298others(7): Show | 10 | HG00639.hp1 HG02451.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.3047-1855A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 19/27 | chr9 | 125344964 | ||||||
| chr9:125345071
|
C | T | 1 | a0001c0001t0001g0291 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.3047-1748C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 19/27 | chr9 | 125345071 | ||||||
| chr9:125345181
|
T | C | 2 | a0001c0002t0007g0133a0001c0002t0007g0150 | 2 | HG01081.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.3047-1638T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 19/27 | chr9 | 125345181 | ||||||
| chr9:125345226
|
G | A | 1 | a0001c0005t0001g0199 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.3047-1593G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 19/27 | chr9 | 125345226 | ||||||
| chr9:125345427
|
C | T | 166 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(163): Show | 166 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.3047-1392C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 19/27 | chr9 | 125345427 | ||||||
| chr9:125345606
|
A | G | 166 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(163): Show | 166 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.3047-1213A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 19/27 | chr9 | 125345606 | ||||||
| chr9:125345677
|
G | A | 32 | a0001c0001t0016g0046a0001c0002t0003g0004a0001c0002t0003g0005others(29): Show | 32 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.3047-1142G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 19/27 | chr9 | 125345677 | ||||||
| chr9:125345789
|
C | A | 1 | a0001c0001t0017g0013 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3047-1030C>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 19/27 | chr9 | 125345789 | ||||||
| chr9:125345821
|
A | G | 1 | a0001c0013t0002g0043 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.3047-998A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 19/27 | chr9 | 125345821 | ||||||
| chr9:125345825
|
A | AAC | 4 | a0001c0001t0005g0307a0001c0001t0005g0331a0001c0001t0005g0332others(1): Show | 4 | HG02129.hp1 NA18747.hp2 NA18950.hp1 others(1): Show |
intron_variant | MODIFIER | c.3047-982_3047-981d others(4): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 19/27 | INFO_REALIGN_3_PRIME | chr9 | 125345825 | |||||
| chr9:125345834
|
A | C | 3 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0001g0236 | 3 | HG04204.hp2 NA18967.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.3047-985A>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 19/27 | chr9 | 125345834 | ||||||
| chr9:125345866
|
A | AGT | 4 | a0001c0001t0002g0049a0001c0001t0002g0116a0001c0001t0004g0173others(1): Show | 4 | HG01099.hp1 HG02257.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.3047-936_3047-935d others(4): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 19/27 | INFO_REALIGN_3_PRIME | chr9 | 125345866 | |||||
| chr9:125345883
|
G | GTA | 3 | a0001c0001t0001g0261a0001c0001t0017g0013a0001c0009t0001g0190 | 3 | HG01243.hp1 HG01243.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.3047-923_3047-922d others(4): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 19/27 | INFO_REALIGN_3_PRIME | chr9 | 125345883 | |||||
| chr9:125345885
|
A | G | 7 | a0001c0001t0001g0192a0001c0001t0001g0269a0001c0001t0001g0322others(4): Show | 7 | HG00639.hp1 HG02622.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.3047-934A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 19/27 | chr9 | 125345885 | ||||||
| chr9:125345913
|
G | A | 2 | a0001c0005t0001g0219a0001c0005t0001g0231 | 2 | HG00280.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.3047-906G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 19/27 | chr9 | 125345913 | ||||||
| chr9:125345963
|
T | C | 2 | a0003c0007t0001g0302a0003c0007t0001g0308 | 2 | HG03017.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.3047-856T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 19/27 | chr9 | 125345963 | ||||||
| chr9:125347115
|
A | G | 2 | a0001c0001t0001g0215a0001c0001t0001g0254 | 2 | HG00642.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.3169+174A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 20/27 | chr9 | 125347115 | ||||||
| chr9:125347120
|
C | A | 2 | a0002c0006t0011g0121a0002c0006t0011g0122 | 2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.3169+179C>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 20/27 | chr9 | 125347120 | ||||||
| chr9:125347148
|
C | T | 1 | a0001c0001t0004g0007 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3169+207C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 20/27 | chr9 | 125347148 | ||||||
| chr9:125347247
|
A | G | 6 | a0001c0003t0006g0166a0001c0003t0006g0168a0001c0003t0006g0169others(3): Show | 6 | HG01167.hp1 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.3169+306A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 20/27 | chr9 | 125347247 | ||||||
| chr9:125347258
|
G | A | 2 | a0001c0001t0001g0325a0001c0001t0001g0326 | 2 | HG02559.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3169+317G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 20/27 | chr9 | 125347258 | ||||||
| chr9:125347454
|
G | A | 1 | a0001c0002t0007g0133 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.3169+513G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 20/27 | chr9 | 125347454 | ||||||
| chr9:125347463
|
C | T | 2 | a0001c0003t0006g0163a0001c0003t0026g0118 | 2 | HG02055.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.3169+522C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 20/27 | chr9 | 125347463 | ||||||
| chr9:125347720
|
CA | C | 220 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(217): Show | 220 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.3169+792delA | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr9 | 125347720 | |||||
| chr9:125347730
|
A | C | 1 | a0001c0001t0002g0048 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.3169+789A>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 20/27 | chr9 | 125347730 | ||||||
| chr9:125347733
|
A | G | 1 | a0001c0001t0002g0054 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.3169+792A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 20/27 | chr9 | 125347733 | ||||||
| chr9:125347884
|
A | G | 1 | a0001c0016t0037g0152 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.3169+943A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 20/27 | chr9 | 125347884 | ||||||
| chr9:125347887
|
T | A | 2 | a0001c0003t0006g0163a0001c0003t0026g0118 | 2 | HG02055.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.3169+946T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 20/27 | chr9 | 125347887 | ||||||
| chr9:125348006
|
C | T | 1 | a0001c0001t0001g0214 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.3169+1065C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 20/27 | chr9 | 125348006 | ||||||
| chr9:125348033
|
G | GTA | 37 | a0001c0001t0016g0046a0001c0002t0003g0004a0001c0002t0003g0005others(34): Show | 37 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(34): Show |
intron_variant | MODIFIER | c.3169+1102_3169+110 others(6): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr9 | 125348033 | |||||
| chr9:125348076
|
C | T | 165 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(162): Show | 165 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.3169+1135C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 20/27 | chr9 | 125348076 | ||||||
| chr9:125348086
|
A | G | 7 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0008others(4): Show | 7 | HG01069.hp1 HG02615.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.3169+1145A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 20/27 | chr9 | 125348086 | ||||||
| chr9:125348274
|
C | T | 165 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(162): Show | 165 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.3170-1116C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 20/27 | chr9 | 125348274 | ||||||
| chr9:125348314
|
C | T | 1 | a0001c0001t0015g0064 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.3170-1076C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 20/27 | chr9 | 125348314 | ||||||
| chr9:125348479
|
G | A | 7 | a0001c0001t0004g0006a0001c0001t0004g0007a0001c0001t0004g0008others(4): Show | 7 | HG01069.hp1 HG02615.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.3170-911G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 20/27 | chr9 | 125348479 | ||||||
| chr9:125348497
|
T | C | 2 | a0001c0001t0002g0153a0001c0001t0031g0102 | 2 | HG02132.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.3170-893T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 20/27 | chr9 | 125348497 | ||||||
| chr9:125348573
|
T | C | 232 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(229): Show | 232 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.3170-817T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 20/27 | chr9 | 125348573 | ||||||
| chr9:125348605
|
C | T | 1 | a0001c0001t0001g0204 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3170-785C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 20/27 | chr9 | 125348605 | ||||||
| chr9:125348655
|
G | A | 2 | a0001c0001t0001g0318a0001c0001t0001g0320 | 2 | HG02717.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.3170-735G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 20/27 | chr9 | 125348655 | ||||||
| chr9:125348698
|
G | A | 2 | a0001c0001t0001g0325a0001c0001t0001g0326 | 2 | HG02559.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3170-692G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 20/27 | chr9 | 125348698 | ||||||
| chr9:125349002
|
T | C | 1 | a0001c0001t0001g0312 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.3170-388T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 20/27 | chr9 | 125349002 | ||||||
| chr9:125349071
|
T | C | 1 | a0001c0001t0001g0252 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3170-319T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 20/27 | chr9 | 125349071 | ||||||
| chr9:125349147
|
G | A | 3 | a0001c0001t0010g0216a0001c0001t0010g0255a0001c0001t0010g0266 | 3 | HG01175.hp2 HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.3170-243G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 20/27 | chr9 | 125349147 | ||||||
| chr9:125349213
|
G | A | 1 | a0001c0001t0002g0037 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.3170-177G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 20/27 | chr9 | 125349213 | ||||||
| chr9:125349556
|
G | A | 1 | a0001c0001t0001g0325 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3299+37G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 21/27 | chr9 | 125349556 | ||||||
| chr9:125349724
|
C | T | 9 | a0001c0002t0007g0124a0001c0002t0007g0135a0001c0002t0007g0136others(6): Show | 9 | HG00544.hp2 HG01123.hp1 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.3299+205C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 21/27 | chr9 | 125349724 | ||||||
| chr9:125349804
|
G | T | 3 | a0001c0001t0001g0237a0001c0001t0001g0238a0001c0001t0001g0239 | 3 | HG00423.hp2 NA18969.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.3299+285G>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 21/27 | chr9 | 125349804 | ||||||
| chr9:125349826
|
C | A | 1 | a0001c0001t0001g0262 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3299+307C>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 21/27 | chr9 | 125349826 | ||||||
| chr9:125349905
|
G | A | 2 | a0001c0001t0001g0017a0001c0001t0001g0045 | 2 | HG01099.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.3299+386G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 21/27 | chr9 | 125349905 | ||||||
| chr9:125349961
|
A | G | 200 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(197): Show | 200 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.3300-334A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 21/27 | chr9 | 125349961 | ||||||
| chr9:125350009
|
C | T | 1 | a0001c0001t0017g0013 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3300-286C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 21/27 | chr9 | 125350009 | ||||||
| chr9:125350490
|
A | G | 1 | a0001c0002t0007g0149 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.3409+86A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 22/27 | chr9 | 125350490 | ||||||
| chr9:125350617
|
G | A | 200 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(197): Show | 200 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.3410-96G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 22/27 | chr9 | 125350617 | ||||||
| chr9:125351021
|
C | T | 1 | a0001c0009t0001g0190 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.3569+149C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 23/27 | chr9 | 125351021 | ||||||
| chr9:125351122
|
G | A | 3 | a0001c0001t0009g0001a0001c0001t0009g0002a0001c0001t0009g0003 | 3 | HG01884.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.3569+250G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 23/27 | chr9 | 125351122 | ||||||
| chr9:125351168
|
A | G | 4 | a0001c0001t0009g0001a0001c0001t0009g0002a0001c0001t0009g0003others(1): Show | 4 | HG01884.hp2 HG02486.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.3569+296A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 23/27 | chr9 | 125351168 | ||||||
| chr9:125351273
|
C | T | 1 | a0001c0002t0003g0126 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.3569+401C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 23/27 | chr9 | 125351273 | ||||||
| chr9:125351300
|
A | C | 1 | a0001c0001t0017g0013 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3569+428A>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 23/27 | chr9 | 125351300 | ||||||
| chr9:125351416
|
G | T | 32 | a0001c0001t0016g0046a0001c0002t0003g0004a0001c0002t0003g0005others(29): Show | 32 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.3569+544G>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 23/27 | chr9 | 125351416 | ||||||
| chr9:125351440
|
C | T | 32 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0036others(29): Show | 32 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.3569+568C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 23/27 | chr9 | 125351440 | ||||||
| chr9:125351627
|
A | G | 1 | a0001c0001t0002g0087 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.3569+755A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 23/27 | chr9 | 125351627 | ||||||
| chr9:125351688
|
G | A | 1 | a0001c0016t0037g0152 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.3569+816G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 23/27 | chr9 | 125351688 | ||||||
| chr9:125351752
|
T | C | 1 | a0001c0003t0004g0156 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3569+880T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 23/27 | chr9 | 125351752 | ||||||
| chr9:125351796
|
A | G | 1 | a0001c0001t0002g0155 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.3569+924A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 23/27 | chr9 | 125351796 | ||||||
| chr9:125351929
|
T | A | 3 | a0001c0001t0009g0001a0001c0001t0009g0002a0001c0001t0009g0003 | 3 | HG01884.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.3569+1057T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 23/27 | chr9 | 125351929 | ||||||
| chr9:125352067
|
C | T | 4 | a0001c0001t0002g0309a0001c0001t0002g0311a0001c0001t0002g0314others(1): Show | 4 | HG02300.hp2 HG02630.hp1 NA18939.hp2 others(1): Show |
intron_variant | MODIFIER | c.3569+1195C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 23/27 | chr9 | 125352067 | ||||||
| chr9:125352319
|
C | T | 6 | a0001c0003t0006g0166a0001c0003t0006g0168a0001c0003t0006g0169others(3): Show | 6 | HG01167.hp1 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.3569+1447C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 23/27 | chr9 | 125352319 | ||||||
| chr9:125352441
|
G | A | 1 | a0001c0001t0002g0053 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.3569+1569G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 23/27 | chr9 | 125352441 | ||||||
| chr9:125352514
|
G | A | 1 | a0001c0001t0002g0079 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.3569+1642G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 23/27 | chr9 | 125352514 | ||||||
| chr9:125352661
|
T | G | 1 | a0001c0001t0002g0048 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.3569+1789T>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 23/27 | chr9 | 125352661 | ||||||
| chr9:125352723
|
C | T | 1 | a0001c0001t0002g0078 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.3569+1851C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 23/27 | chr9 | 125352723 | ||||||
| chr9:125352777
|
C | G | 2 | a0002c0006t0011g0121a0002c0006t0011g0122 | 2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.3570-1877C>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 23/27 | chr9 | 125352777 | ||||||
| chr9:125352871
|
C | T | 2 | a0001c0003t0006g0163a0001c0003t0026g0118 | 2 | HG02055.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.3570-1783C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 23/27 | chr9 | 125352871 | ||||||
| chr9:125352890
|
C | T | 1 | a0001c0001t0002g0029 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.3570-1764C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 23/27 | chr9 | 125352890 | ||||||
| chr9:125352919
|
T | C | 289 | a0001c0001t0001g0017a0001c0001t0001g0045a0001c0001t0001g0176others(286): Show | 289 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(286): Show |
intron_variant | MODIFIER | c.3570-1735T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 23/27 | chr9 | 125352919 | ||||||
| chr9:125353261
|
G | A | 1 | a0001c0001t0017g0013 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3570-1393G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 23/27 | chr9 | 125353261 | ||||||
| chr9:125353391
|
A | T | 1 | a0001c0016t0037g0152 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.3570-1263A>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 23/27 | chr9 | 125353391 | ||||||
| chr9:125353404
|
C | G | 105 | a0001c0001t0001g0176a0001c0001t0001g0192a0001c0001t0001g0193others(102): Show | 105 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.3570-1250C>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 23/27 | chr9 | 125353404 | ||||||
| chr9:125353662
|
A | G | 124 | a0001c0001t0001g0176a0001c0001t0001g0178a0001c0001t0001g0179others(121): Show | 124 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.3570-992A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 23/27 | chr9 | 125353662 | ||||||
| chr9:125353799
|
A | G | 3 | a0001c0001t0009g0001a0001c0001t0009g0002a0001c0001t0009g0003 | 3 | HG01884.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.3570-855A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 23/27 | chr9 | 125353799 | ||||||
| chr9:125353812
|
A | G | 5 | a0001c0003t0006g0158a0001c0003t0006g0159a0001c0003t0006g0160others(2): Show | 5 | HG01109.hp1 HG01884.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.3570-842A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 23/27 | chr9 | 125353812 | ||||||
| chr9:125353860
|
A | G | 1 | a0001c0001t0008g0112 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.3570-794A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 23/27 | chr9 | 125353860 | ||||||
| chr9:125353882
|
T | G | 1 | a0001c0003t0026g0118 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3570-772T>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 23/27 | chr9 | 125353882 | ||||||
| chr9:125353966
|
A | T | 5 | a0001c0003t0004g0156a0001c0003t0004g0157a0001c0003t0004g0164others(2): Show | 5 | HG02258.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.3570-688A>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 23/27 | chr9 | 125353966 | ||||||
| chr9:125353979
|
T | C | 1 | a0001c0001t0001g0178 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.3570-675T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 23/27 | chr9 | 125353979 | ||||||
| chr9:125354303
|
A | T | 1 | a0001c0001t0002g0054 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.3570-351A>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 23/27 | chr9 | 125354303 | ||||||
| chr9:125354306
|
T | G | 1 | a0001c0001t0002g0054 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.3570-348T>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 23/27 | chr9 | 125354306 | ||||||
| chr9:125354538
|
A | G | 162 | a0001c0001t0001g0017a0001c0001t0001g0045a0001c0001t0001g0176others(159): Show | 162 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.3570-116A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 23/27 | chr9 | 125354538 | ||||||
| chr9:125354565
|
T | A | 2 | a0001c0001t0001g0240a0001c0001t0001g0267 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.3570-89T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 23/27 | chr9 | 125354565 | ||||||
| chr9:125355097
|
T | G | 2 | a0001c0003t0006g0163a0001c0003t0026g0118 | 2 | HG02055.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.3757+256T>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 24/27 | chr9 | 125355097 | ||||||
| chr9:125355185
|
C | T | 1 | a0001c0016t0037g0152 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.3757+344C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 24/27 | chr9 | 125355185 | ||||||
| chr9:125355213
|
T | TTCA | 227 | a0001c0001t0001g0017a0001c0001t0001g0045a0001c0001t0001g0176others(224): Show | 227 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.3757+372_3757+373i others(5): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 24/27 | chr9 | 125355213 | ||||||
| chr9:125355215
|
G | GGGATTCT others(1): Show |
227 | a0001c0001t0001g0017a0001c0001t0001g0045a0001c0001t0001g0176others(224): Show | 227 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.3757+374_3757+375i others(10): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 24/27 | chr9 | 125355215 | ||||||
| chr9:125355315
|
A | G | 1 | a0001c0001t0002g0063 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.3758-329A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 24/27 | chr9 | 125355315 | ||||||
| chr9:125355355
|
C | T | 2 | a0001c0002t0003g0125a0001c0002t0003g0146 | 2 | NA18988.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.3758-289C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 24/27 | chr9 | 125355355 | ||||||
| chr9:125355866
|
T | A | 1 | a0001c0001t0001g0195 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.3971+9T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 25/27 | chr9 | 125355866 | ||||||
| chr9:125356067
|
T | C | 1 | a0001c0002t0003g0127 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.3971+210T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 25/27 | chr9 | 125356067 | ||||||
| chr9:125356152
|
C | A | 3 | a0001c0001t0009g0001a0001c0001t0009g0002a0001c0001t0009g0003 | 3 | HG01884.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.3971+295C>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 25/27 | chr9 | 125356152 | ||||||
| chr9:125356281
|
T | A | 2 | a0002c0006t0011g0121a0002c0006t0011g0122 | 2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.3971+424T>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 25/27 | chr9 | 125356281 | ||||||
| chr9:125356351
|
C | T | 1 | a0001c0001t0001g0313 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.3971+494C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 25/27 | chr9 | 125356351 | ||||||
| chr9:125356387
|
T | G | 1 | a0001c0009t0001g0190 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.3971+530T>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 25/27 | chr9 | 125356387 | ||||||
| chr9:125356922
|
G | T | 1 | a0001c0016t0037g0152 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.3971+1065G>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 25/27 | chr9 | 125356922 | ||||||
| chr9:125357184
|
A | G | 32 | a0001c0001t0016g0046a0001c0002t0003g0004a0001c0002t0003g0005others(29): Show | 32 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.3971+1327A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 25/27 | chr9 | 125357184 | ||||||
| chr9:125357187
|
C | A | 54 | a0001c0001t0001g0177a0001c0001t0001g0178a0001c0001t0001g0179others(51): Show | 54 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.3971+1330C>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 25/27 | chr9 | 125357187 | ||||||
| chr9:125357194
|
C | T | 1 | a0001c0009t0001g0190 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.3971+1337C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 25/27 | chr9 | 125357194 | ||||||
| chr9:125357300
|
C | T | 3 | a0001c0001t0001g0290a0001c0001t0001g0312a0001c0001t0022g0279 | 3 | HG02698.hp2 HG03654.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.3971+1443C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 25/27 | chr9 | 125357300 | ||||||
| chr9:125357326
|
C | T | 1 | a0001c0001t0012g0101 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.3971+1469C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 25/27 | chr9 | 125357326 | ||||||
| chr9:125357890
|
G | C | 2 | a0002c0006t0011g0121a0002c0006t0011g0122 | 2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.3972-1530G>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 25/27 | chr9 | 125357890 | ||||||
| chr9:125357904
|
G | T | 14 | a0001c0001t0002g0068a0001c0001t0002g0086a0001c0001t0002g0089others(11): Show | 14 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(11): Show |
intron_variant | MODIFIER | c.3972-1516G>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 25/27 | chr9 | 125357904 | ||||||
| chr9:125357984
|
A | C | 3 | a0001c0001t0009g0001a0001c0001t0009g0002a0001c0001t0009g0003 | 3 | HG01884.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.3972-1436A>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 25/27 | chr9 | 125357984 | ||||||
| chr9:125357986
|
A | AAC | 12 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0001g0211others(9): Show | 12 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.3972-1414_3972-141 others(6): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr9 | 125357986 | |||||
| chr9:125357986
|
A | C | 6 | a0001c0001t0001g0248a0001c0001t0001g0323a0001c0001t0002g0038others(3): Show | 6 | HG01884.hp2 HG02109.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.3972-1434A>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 25/27 | chr9 | 125357986 | ||||||
| chr9:125357988
|
C | A | 10 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0232others(7): Show | 10 | HG00639.hp2 HG00735.hp2 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.3972-1432C>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 25/27 | chr9 | 125357988 | ||||||
| chr9:125358035
|
C | G | 1 | a0001c0001t0004g0012 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3972-1385C>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 25/27 | chr9 | 125358035 | ||||||
| chr9:125358533
|
A | T | 1 | a0001c0001t0002g0086 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.3972-887A>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 25/27 | chr9 | 125358533 | ||||||
| chr9:125358539
|
G | C | 1 | a0001c0001t0001g0211 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3972-881G>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 25/27 | chr9 | 125358539 | ||||||
| chr9:125358834
|
C | G | 3 | a0001c0001t0002g0085a0001c0001t0012g0099a0001c0001t0012g0101 | 3 | HG00642.hp1 HG00738.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.3972-586C>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 25/27 | chr9 | 125358834 | ||||||
| chr9:125359097
|
C | G | 1 | a0001c0001t0001g0221 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.3972-323C>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 25/27 | chr9 | 125359097 | ||||||
| chr9:125359099
|
T | C | 3 | a0001c0001t0009g0001a0001c0001t0009g0002a0001c0001t0009g0003 | 3 | HG01884.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.3972-321T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 25/27 | chr9 | 125359099 | ||||||
| chr9:125359313
|
A | G | 101 | a0001c0001t0001g0017a0001c0001t0001g0045a0001c0001t0001g0192others(98): Show | 101 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.3972-107A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 25/27 | chr9 | 125359313 | ||||||
| chr9:125359527
|
C | T | 1 | a0001c0013t0002g0043 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.4044+35C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 26/27 | chr9 | 125359527 | ||||||
| chr9:125359545
|
T | C | 1 | a0001c0001t0002g0016 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.4044+53T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 26/27 | chr9 | 125359545 | ||||||
| chr9:125359574
|
G | GGAACTGA others(3): Show |
1 | a0001c0002t0007g0149 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.4044+84_4044+93dup others(10): Show |
GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 26/27 | INFO_REALIGN_3_PRIME | chr9 | 125359574 | |||||
| chr9:125359687
|
A | T | 1 | a0001c0001t0015g0064 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.4044+195A>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 26/27 | chr9 | 125359687 | ||||||
| chr9:125359748
|
G | A | 2 | a0002c0006t0011g0121a0002c0006t0011g0122 | 2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.4044+256G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 26/27 | chr9 | 125359748 | ||||||
| chr9:125359835
|
T | C | 1 | a0001c0016t0037g0152 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.4044+343T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 26/27 | chr9 | 125359835 | ||||||
| chr9:125359927
|
A | G | 1 | a0001c0001t0002g0094 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.4044+435A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 26/27 | chr9 | 125359927 | ||||||
| chr9:125360041
|
A | G | 283 | a0001c0001t0001g0017a0001c0001t0001g0045a0001c0001t0001g0176others(280): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(280): Show |
intron_variant | MODIFIER | c.4045-487A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 26/27 | chr9 | 125360041 | ||||||
| chr9:125360316
|
G | T | 1 | a0001c0001t0001g0230 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.4045-212G>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 26/27 | chr9 | 125360316 | ||||||
| chr9:125360760
|
G | A | 1 | a0001c0001t0008g0050 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.4242+35G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 27/27 | chr9 | 125360760 | ||||||
| chr9:125360805
|
A | G | 1 | a0001c0001t0002g0111 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.4242+80A>G | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 27/27 | chr9 | 125360805 | ||||||
| chr9:125361055
|
G | A | 157 | a0001c0001t0001g0017a0001c0001t0001g0045a0001c0001t0001g0176others(154): Show | 157 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.4242+330G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 27/27 | chr9 | 125361055 | ||||||
| chr9:125361277
|
C | T | 1 | a0001c0001t0001g0214 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.4242+552C>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 27/27 | chr9 | 125361277 | ||||||
| chr9:125361278
|
G | A | 1 | a0001c0001t0002g0026 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.4242+553G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 27/27 | chr9 | 125361278 | ||||||
| chr9:125361341
|
T | C | 227 | a0001c0001t0001g0017a0001c0001t0001g0045a0001c0001t0001g0176others(224): Show | 227 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.4242+616T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 27/27 | chr9 | 125361341 | ||||||
| chr9:125361473
|
G | A | 34 | a0001c0001t0016g0046a0001c0002t0003g0004a0001c0002t0003g0005others(31): Show | 34 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(31): Show |
intron_variant | MODIFIER | c.4242+748G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 27/27 | chr9 | 125361473 | ||||||
| chr9:125361513
|
G | A | 157 | a0001c0001t0001g0017a0001c0001t0001g0045a0001c0001t0001g0176others(154): Show | 157 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.4242+788G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 27/27 | chr9 | 125361513 | ||||||
| chr9:125361540
|
G | A | 1 | a0001c0001t0017g0013 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.4242+815G>A | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 27/27 | chr9 | 125361540 | ||||||
| chr9:125361608
|
T | C | 1 | a0001c0001t0002g0027 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.4242+883T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 27/27 | chr9 | 125361608 | ||||||
| chr9:125362030
|
T | C | 35 | a0001c0001t0016g0046a0001c0002t0003g0004a0001c0002t0003g0005others(32): Show | 35 | HG00544.hp2 HG00621.hp1 HG01081.hp2 others(32): Show |
intron_variant | MODIFIER | c.4243-576T>C | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 27/27 | chr9 | 125362030 | ||||||
| chr9:125362373
|
A | T | 2 | a0002c0006t0011g0121a0002c0006t0011g0122 | 2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.4243-233A>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 27/27 | chr9 | 125362373 | ||||||
| chr9:125362519
|
A | T | 91 | a0001c0001t0001g0017a0001c0001t0001g0045a0001c0001t0001g0193others(88): Show | 91 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.4243-87A>T | GAPVD1 | ENSG00000165219.23 | transcript | ENST00000297933.11 | protein_coding | 27/27 | chr9 | 125362519 |