| geneid | 10564 |
|---|---|
| ensemblid | ENSG00000124198.10 |
| hgncid | 15853 |
| symbol | ARFGEF2 |
| name | ADP ribosylation factor guanine nucleotide exchange factor 2 |
| refseq_nuc | NM_006420.3 |
| refseq_prot | NP_006411.2 |
| ensembl_nuc | ENST00000371917.5 |
| ensembl_prot | ENSP00000360985.4 |
| mane_status | MANE Select |
| chr | chr20 |
| start | 48921711 |
| end | 49036693 |
| strand | + |
| ver | v1.2 |
| region | chr20:48921711-49036693 |
| region5000 | chr20:48916711-49041693 |
| regionname0 | ARFGEF2_chr20_48921711_49036693 |
| regionname5000 | ARFGEF2_chr20_48916711_49041693 |
| 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 | 1785 | 339 | 82 | 61 | 147 | 8 | 39 | 116 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | copy fasta | chr20 | 48916711 | 49041693 |
| a0002 | 0/0 | 1785 | 6 | 0 | 1 | 5 | 0 | 0 | 5 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | copy fasta | chr20 | 48916711 | 49041693 |
| a0003 | 0/0 | 1785 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | copy fasta | chr20 | 48916711 | 49041693 |
| a0004 | 0/0 | 1785 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | copy fasta | chr20 | 48916711 | 49041693 |
| a0005 | 0/0 | 1785 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | copy fasta | chr20 | 48916711 | 49041693 |
| a0006 | 0/0 | 1785 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | copy fasta | chr20 | 48916711 | 49041693 |
| a0007 | 0/0 | 1785 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | copy fasta | chr20 | 48916711 | 49041693 |
| a0008 | 0/0 | 1785 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | copy fasta | chr20 | 48916711 | 49041693 |
| 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 | 5358 | 128 | 46 | 19 | 49 | 3 | 10 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | copy fasta | chr20 | 48916711 | 49041693 |
| c0002 | 1/0 | 5358 | 126 | 28 | 24 | 52 | 5 | 16 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | copy fasta | chr20 | 48916711 | 49041693 |
| c0003 | 0/0 | 5358 | 76 | 4 | 16 | 44 | 0 | 12 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | copy fasta | chr20 | 48916711 | 49041693 |
| c0004 | 0/0 | 5358 | 6 | 0 | 1 | 5 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | copy fasta | chr20 | 48916711 | 49041693 |
| c0005 | 0/0 | 5358 | 3 | 3 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | copy fasta | chr20 | 48916711 | 49041693 |
| c0006 | 0/0 | 5358 | 2 | 0 | 2 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | copy fasta | chr20 | 48916711 | 49041693 |
| c0007 | 0/0 | 5358 | 2 | 0 | 2 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | copy fasta | chr20 | 48916711 | 49041693 |
| c0008 | 0/0 | 5358 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | copy fasta | chr20 | 48916711 | 49041693 |
| c0009 | 0/0 | 5358 | 1 | 0 | 0 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | copy fasta | chr20 | 48916711 | 49041693 |
| c0010 | 0/0 | 5358 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | copy fasta | chr20 | 48916711 | 49041693 |
| c0011 | 0/0 | 5358 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | copy fasta | chr20 | 48916711 | 49041693 |
| c0012 | 0/0 | 5358 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | copy fasta | chr20 | 48916711 | 49041693 |
| c0013 | 0/0 | 5358 | 1 | 0 | 0 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | copy fasta | chr20 | 48916711 | 49041693 |
| c0014 | 0/0 | 5358 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | copy fasta | chr20 | 48916711 | 49041693 |
| c0015 | 0/0 | 5358 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | copy fasta | chr20 | 48916711 | 49041693 |
| c0016 | 0/0 | 5358 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | copy fasta | chr20 | 48916711 | 49041693 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/0 | 3674 | 190 | 17 | 38 | 101 | 4 | 29 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | copy fasta | chr20 | 48916711 | 49041693 |
| t0002 | 0/1 | 3675 | 59 | 35 | 7 | 13 | 1 | 2 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | copy fasta | chr20 | 48916711 | 49041693 |
| t0003 | 0/0 | 3675 | 29 | 2 | 9 | 12 | 2 | 4 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | copy fasta | chr20 | 48916711 | 49041693 |
| t0004 | 0/0 | 3675 | 25 | 0 | 3 | 19 | 0 | 3 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | copy fasta | chr20 | 48916711 | 49041693 |
| t0005 | 0/0 | 3674 | 16 | 15 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | copy fasta | chr20 | 48916711 | 49041693 |
| t0006 | 0/0 | 3675 | 4 | 4 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | copy fasta | chr20 | 48916711 | 49041693 |
| t0007 | 0/0 | 3674 | 4 | 0 | 1 | 2 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | copy fasta | chr20 | 48916711 | 49041693 |
| t0008 | 0/0 | 3675 | 3 | 3 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | copy fasta | chr20 | 48916711 | 49041693 |
| t0009 | 0/0 | 3675 | 3 | 0 | 1 | 2 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | copy fasta | chr20 | 48916711 | 49041693 |
| t0010 | 0/0 | 3674 | 2 | 0 | 2 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | copy fasta | chr20 | 48916711 | 49041693 |
| t0011 | 0/0 | 3675 | 2 | 0 | 0 | 2 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | copy fasta | chr20 | 48916711 | 49041693 |
| t0012 | 0/0 | 3674 | 2 | 0 | 1 | 0 | 1 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | copy fasta | chr20 | 48916711 | 49041693 |
| t0013 | 0/0 | 3675 | 2 | 0 | 0 | 2 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | copy fasta | chr20 | 48916711 | 49041693 |
| t0014 | 0/0 | 3675 | 2 | 2 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | copy fasta | chr20 | 48916711 | 49041693 |
| t0015 | 0/0 | 3674 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | copy fasta | chr20 | 48916711 | 49041693 |
| t0016 | 0/0 | 3675 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | copy fasta | chr20 | 48916711 | 49041693 |
| t0017 | 0/0 | 3674 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | copy fasta | chr20 | 48916711 | 49041693 |
| t0018 | 0/0 | 3674 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | copy fasta | chr20 | 48916711 | 49041693 |
| t0019 | 0/0 | 3675 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | copy fasta | chr20 | 48916711 | 49041693 |
| t0020 | 0/0 | 3675 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | copy fasta | chr20 | 48916711 | 49041693 |
| t0021 | 0/0 | 3675 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | copy fasta | chr20 | 48916711 | 49041693 |
| t0022 | 0/0 | 3674 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | copy fasta | chr20 | 48916711 | 49041693 |
| t0023 | 0/0 | 3675 | 1 | 0 | 0 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | copy fasta | chr20 | 48916711 | 49041693 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0164 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0227 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0348 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| g0350 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| 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 | 5358 | 128 | 46 | 19 | 49 | 3 | 10 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | copy fasta | chr20 | 48916711 | 49041693 |
| a0001c0002 | 1/0 | 5358 | 126 | 28 | 24 | 52 | 5 | 16 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | copy fasta | chr20 | 48916711 | 49041693 |
| a0001c0003 | 0/0 | 5358 | 76 | 4 | 16 | 44 | 0 | 12 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | copy fasta | chr20 | 48916711 | 49041693 |
| a0001c0005 | 0/0 | 5358 | 3 | 3 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | copy fasta | chr20 | 48916711 | 49041693 |
| a0001c0006 | 0/0 | 5358 | 2 | 0 | 2 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | copy fasta | chr20 | 48916711 | 49041693 |
| a0001c0012 | 0/0 | 5358 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | copy fasta | chr20 | 48916711 | 49041693 |
| a0001c0013 | 0/0 | 5358 | 1 | 0 | 0 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | copy fasta | chr20 | 48916711 | 49041693 |
| a0001c0015 | 0/0 | 5358 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | copy fasta | chr20 | 48916711 | 49041693 |
| a0001c0016 | 0/0 | 5358 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | copy fasta | chr20 | 48916711 | 49041693 |
| a0002c0004 | 0/0 | 5358 | 6 | 0 | 1 | 5 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | copy fasta | chr20 | 48916711 | 49041693 |
| a0003c0007 | 0/0 | 5358 | 2 | 0 | 2 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | copy fasta | chr20 | 48916711 | 49041693 |
| a0004c0008 | 0/0 | 5358 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | copy fasta | chr20 | 48916711 | 49041693 |
| a0005c0014 | 0/0 | 5358 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | copy fasta | chr20 | 48916711 | 49041693 |
| a0006c0011 | 0/0 | 5358 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | copy fasta | chr20 | 48916711 | 49041693 |
| a0007c0010 | 0/0 | 5358 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | copy fasta | chr20 | 48916711 | 49041693 |
| a0008c0009 | 0/0 | 5358 | 1 | 0 | 0 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | copy fasta | chr20 | 48916711 | 49041693 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 9031 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | copy fasta | chr20 | 48916711 | 49041693 |
| a0001c0001t0002 | 0/1 | 9032 | 55 | 35 | 5 | 11 | 1 | 2 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | copy fasta | chr20 | 48916711 | 49041693 |
| a0001c0001t0003 | 0/0 | 9032 | 28 | 2 | 9 | 12 | 2 | 3 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | copy fasta | chr20 | 48916711 | 49041693 |
| a0001c0001t0004 | 0/0 | 9032 | 25 | 0 | 3 | 19 | 0 | 3 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | copy fasta | chr20 | 48916711 | 49041693 |
| a0001c0001t0006 | 0/0 | 9032 | 4 | 4 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | copy fasta | chr20 | 48916711 | 49041693 |
| a0001c0001t0007 | 0/0 | 9031 | 4 | 0 | 1 | 2 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | copy fasta | chr20 | 48916711 | 49041693 |
| a0001c0001t0011 | 0/0 | 9032 | 2 | 0 | 0 | 2 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | copy fasta | chr20 | 48916711 | 49041693 |
| a0001c0001t0013 | 0/0 | 9032 | 2 | 0 | 0 | 2 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | copy fasta | chr20 | 48916711 | 49041693 |
| a0001c0001t0014 | 0/0 | 9032 | 2 | 2 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | copy fasta | chr20 | 48916711 | 49041693 |
| a0001c0001t0016 | 0/0 | 9032 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | copy fasta | chr20 | 48916711 | 49041693 |
| a0001c0001t0019 | 0/0 | 9032 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | copy fasta | chr20 | 48916711 | 49041693 |
| a0001c0001t0020 | 0/0 | 9032 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | copy fasta | chr20 | 48916711 | 49041693 |
| a0001c0001t0021 | 0/0 | 9032 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | copy fasta | chr20 | 48916711 | 49041693 |
| a0001c0001t0023 | 0/0 | 9032 | 1 | 0 | 0 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | copy fasta | chr20 | 48916711 | 49041693 |
| a0001c0002t0001 | 1/0 | 9031 | 102 | 11 | 19 | 51 | 4 | 16 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | copy fasta | chr20 | 48916711 | 49041693 |
| a0001c0002t0005 | 0/0 | 9031 | 16 | 15 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | copy fasta | chr20 | 48916711 | 49041693 |
| a0001c0002t0009 | 0/0 | 9032 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | copy fasta | chr20 | 48916711 | 49041693 |
| a0001c0002t0010 | 0/0 | 9031 | 2 | 0 | 2 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | copy fasta | chr20 | 48916711 | 49041693 |
| a0001c0002t0012 | 0/0 | 9031 | 2 | 0 | 1 | 0 | 1 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | copy fasta | chr20 | 48916711 | 49041693 |
| a0001c0002t0015 | 0/0 | 9031 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | copy fasta | chr20 | 48916711 | 49041693 |
| a0001c0002t0017 | 0/0 | 9031 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | copy fasta | chr20 | 48916711 | 49041693 |
| a0001c0002t0022 | 0/0 | 9031 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | copy fasta | chr20 | 48916711 | 49041693 |
| a0001c0003t0001 | 0/0 | 9031 | 74 | 4 | 15 | 43 | 0 | 12 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | copy fasta | chr20 | 48916711 | 49041693 |
| a0001c0003t0009 | 0/0 | 9032 | 2 | 0 | 1 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | copy fasta | chr20 | 48916711 | 49041693 |
| a0001c0005t0008 | 0/0 | 9032 | 3 | 3 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | copy fasta | chr20 | 48916711 | 49041693 |
| a0001c0006t0002 | 0/0 | 9032 | 2 | 0 | 2 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | copy fasta | chr20 | 48916711 | 49041693 |
| a0001c0012t0001 | 0/0 | 9031 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | copy fasta | chr20 | 48916711 | 49041693 |
| a0001c0013t0003 | 0/0 | 9032 | 1 | 0 | 0 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | copy fasta | chr20 | 48916711 | 49041693 |
| a0001c0015t0001 | 0/0 | 9031 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | copy fasta | chr20 | 48916711 | 49041693 |
| a0001c0016t0001 | 0/0 | 9031 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | copy fasta | chr20 | 48916711 | 49041693 |
| a0002c0004t0001 | 0/0 | 9031 | 6 | 0 | 1 | 5 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | copy fasta | chr20 | 48916711 | 49041693 |
| a0003c0007t0001 | 0/0 | 9031 | 2 | 0 | 2 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | copy fasta | chr20 | 48916711 | 49041693 |
| a0004c0008t0002 | 0/0 | 9032 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | copy fasta | chr20 | 48916711 | 49041693 |
| a0005c0014t0018 | 0/0 | 9031 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | copy fasta | chr20 | 48916711 | 49041693 |
| a0006c0011t0001 | 0/0 | 9031 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | copy fasta | chr20 | 48916711 | 49041693 |
| a0007c0010t0002 | 0/0 | 9032 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | copy fasta | chr20 | 48916711 | 49041693 |
| a0008c0009t0001 | 0/0 | 9031 | 1 | 0 | 0 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | copy fasta | chr20 | 48916711 | 49041693 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0002g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0002g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0002g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0002g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0002g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0002g0227 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0002g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0002g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0002g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0002g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0002g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0002g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0002g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0002g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0002g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0002g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0002g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0002g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0002g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0002g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0002g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0003g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0003g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0003g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0003g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0003g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0003g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0003g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0003g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0003g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0003g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0003g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0003g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0003g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0003g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0003g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0003g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0003g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0004g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0004g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0004g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0004g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0004g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0004g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0004g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0004g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0004g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0004g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0004g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0004g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0004g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0004g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0004g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0004g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0004g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0004g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0004g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0004g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0004g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0004g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0004g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0004g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0004g0348 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0006g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0006g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0006g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0006g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0007g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0007g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0007g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0007g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0011g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0011g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0013g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0013g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0014g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0014g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0016g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0019g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0020g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0021g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0023g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0164 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0350 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0005g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0005g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0005g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0005g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0005g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0005g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0005g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0005g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0005g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0005g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0005g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0005g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0005g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0005g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0005g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0009g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0010g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0010g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0012g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0012g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0015g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0017g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0022g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0003t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0003t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0003t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0003t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0003t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0003t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0003t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0003t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0003t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0003t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0003t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0003t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0003t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0003t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0003t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0003t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0003t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0003t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0003t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0003t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0003t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0003t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0003t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0003t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0003t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0003t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0003t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0003t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0003t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0003t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0003t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0003t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0003t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0003t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0003t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0003t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0003t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0003t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0003t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0003t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0003t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0003t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0003t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0003t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0003t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0003t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0003t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0003t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0003t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0003t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0003t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0003t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0003t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0003t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0003t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0003t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0003t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0003t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0003t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0003t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0003t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0003t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0003t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0003t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0003t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0003t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0003t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0003t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0003t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0003t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0003t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0003t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0003t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0003t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0003t0009g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0003t0009g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0005t0008g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0005t0008g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0005t0008g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0006t0002g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0006t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0012t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0013t0003g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0015t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0016t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0002c0004t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0002c0004t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0002c0004t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0002c0004t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0002c0004t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0002c0004t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0003c0007t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0003c0007t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0004c0008t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0005c0014t0018g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0006c0011t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0007c0010t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0008c0009t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0121 | EUR | FIN | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG00280 | hp2 | a0001 | c0002 | t0001 | g0133 | EUR | FIN | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG00323 | hp1 | a0001 | c0002 | t0001 | g0132 | EUR | FIN | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0204 | EUR | FIN | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG00438 | hp1 | a0001 | c0002 | t0001 | g0134 | EAS | CHS | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG00438 | hp2 | a0001 | c0003 | t0001 | g0088 | EAS | CHS | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG00558 | hp1 | a0001 | c0003 | t0001 | g0085 | EAS | CHS | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0116 | EAS | CHS | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG00609 | hp1 | a0001 | c0003 | t0001 | g0083 | EAS | CHS | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG00609 | hp2 | a0001 | c0002 | t0001 | g0187 | EAS | CHS | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG00621 | hp1 | a0001 | c0003 | t0001 | g0050 | EAS | CHS | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG00621 | hp2 | a0001 | c0002 | t0001 | g0126 | EAS | CHS | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG00639 | hp1 | a0006 | c0011 | t0001 | g0301 | AMR | PUR | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG00639 | hp2 | a0001 | c0001 | t0003 | g0199 | AMR | PUR | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG00642 | hp1 | a0001 | c0003 | t0001 | g0066 | AMR | PUR | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG00642 | hp2 | a0001 | c0002 | t0017 | g0007 | AMR | PUR | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG00673 | hp1 | a0001 | c0001 | t0004 | g0337 | EAS | CHS | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG00673 | hp2 | a0001 | c0002 | t0001 | g0282 | EAS | CHS | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG00733 | hp1 | a0005 | c0014 | t0018 | g0136 | AMR | PUR | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG00733 | hp2 | a0001 | c0001 | t0003 | g0234 | AMR | PUR | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG00738 | hp1 | a0001 | c0001 | t0004 | g0332 | AMR | PUR | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG00738 | hp2 | a0001 | c0001 | t0003 | g0203 | AMR | PUR | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG00741 | hp1 | a0001 | c0002 | t0001 | g0294 | AMR | PUR | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG00741 | hp2 | a0001 | c0002 | t0001 | g0314 | AMR | PUR | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG01071 | hp1 | a0001 | c0002 | t0001 | g0295 | AMR | PUR | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG01071 | hp2 | a0001 | c0002 | t0001 | g0163 | AMR | PUR | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG01074 | hp1 | a0001 | c0002 | t0001 | g0156 | AMR | PUR | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG01074 | hp2 | a0001 | c0003 | t0001 | g0100 | AMR | PUR | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG01081 | hp1 | a0001 | c0001 | t0003 | g0205 | AMR | PUR | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG01081 | hp2 | a0003 | c0007 | t0001 | g0302 | AMR | PUR | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG01099 | hp1 | a0001 | c0002 | t0001 | g0180 | AMR | PUR | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG01099 | hp2 | a0001 | c0002 | t0001 | g0293 | AMR | PUR | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG01106 | hp1 | a0001 | c0003 | t0001 | g0317 | AMR | PUR | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0117 | AMR | PUR | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG01109 | hp1 | a0001 | c0002 | t0005 | g0023 | AMR | PUR | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG01109 | hp2 | a0001 | c0002 | t0010 | g0155 | AMR | PUR | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG01169 | hp1 | a0001 | c0002 | t0001 | g0137 | AMR | PUR | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0270 | AMR | PUR | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0250 | AMR | PUR | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0202 | AMR | PUR | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG01192 | hp1 | a0003 | c0007 | t0001 | g0303 | AMR | PUR | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG01192 | hp2 | a0001 | c0003 | t0001 | g0092 | AMR | PUR | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG01243 | hp1 | a0001 | c0003 | t0001 | g0102 | AMR | PUR | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0220 | AMR | PUR | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG01255 | hp1 | a0001 | c0003 | t0001 | g0065 | AMR | CLM | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG01255 | hp2 | a0001 | c0001 | t0003 | g0207 | AMR | CLM | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG01256 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | CLM | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG01256 | hp2 | a0001 | c0003 | t0001 | g0097 | AMR | CLM | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG01257 | hp1 | a0001 | c0001 | t0003 | g0214 | AMR | CLM | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG01257 | hp2 | a0001 | c0006 | t0002 | g0038 | AMR | CLM | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG01258 | hp1 | a0001 | c0006 | t0002 | g0037 | AMR | CLM | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG01258 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | CLM | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG01261 | hp1 | a0001 | c0002 | t0001 | g0173 | AMR | CLM | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG01261 | hp2 | a0001 | c0003 | t0001 | g0057 | AMR | CLM | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG01346 | hp1 | a0001 | c0002 | t0001 | g0142 | AMR | CLM | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0217 | AMR | CLM | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0221 | AMR | CLM | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG01361 | hp2 | a0001 | c0002 | t0012 | g0149 | AMR | CLM | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG01433 | hp1 | a0001 | c0001 | t0007 | g0241 | AMR | CLM | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG01433 | hp2 | a0001 | c0002 | t0001 | g0194 | AMR | CLM | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG01516 | hp1 | a0001 | c0001 | t0003 | g0216 | EUR | IBS | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG01516 | hp2 | a0001 | c0002 | t0001 | g0177 | EUR | IBS | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0281 | AFR | ACB | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG01884 | hp2 | a0001 | c0002 | t0005 | g0001 | AFR | ACB | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG01891 | hp1 | a0001 | c0002 | t0005 | g0025 | AFR | ACB | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | ACB | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG01934 | hp1 | a0001 | c0001 | t0019 | g0345 | AMR | PEL | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG01934 | hp2 | a0001 | c0002 | t0001 | g0165 | AMR | PEL | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG01943 | hp1 | a0001 | c0002 | t0010 | g0153 | AMR | PEL | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG01943 | hp2 | a0001 | c0003 | t0001 | g0076 | AMR | PEL | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG01952 | hp1 | a0001 | c0002 | t0001 | g0159 | AMR | PEL | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG01952 | hp2 | a0001 | c0003 | t0001 | g0068 | AMR | PEL | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG01975 | hp1 | a0001 | c0003 | t0001 | g0081 | AMR | PEL | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG01975 | hp2 | a0001 | c0001 | t0004 | g0343 | AMR | PEL | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG01978 | hp1 | a0001 | c0003 | t0001 | g0054 | AMR | PEL | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0166 | AMR | PEL | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0188 | AMR | PEL | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG01981 | hp2 | a0001 | c0003 | t0009 | g0096 | AMR | PEL | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG02015 | hp1 | a0001 | c0002 | t0001 | g0290 | EAS | KHV | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG02015 | hp2 | a0001 | c0001 | t0013 | g0322 | EAS | KHV | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG02027 | hp1 | a0001 | c0001 | t0003 | g0242 | EAS | KHV | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG02027 | hp2 | a0001 | c0003 | t0001 | g0049 | EAS | KHV | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0275 | AFR | ACB | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG02055 | hp2 | a0001 | c0001 | t0006 | g0274 | AFR | ACB | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG02071 | hp1 | a0001 | c0001 | t0003 | g0246 | EAS | KHV | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG02071 | hp2 | a0001 | c0002 | t0001 | g0300 | EAS | KHV | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG02074 | hp1 | a0001 | c0002 | t0001 | g0161 | EAS | KHV | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG02074 | hp2 | a0001 | c0001 | t0004 | g0325 | EAS | KHV | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG02080 | hp1 | a0001 | c0002 | t0001 | g0192 | EAS | KHV | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG02080 | hp2 | a0001 | c0002 | t0001 | g0124 | EAS | KHV | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG02129 | hp1 | a0001 | c0003 | t0001 | g0095 | EAS | KHV | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0271 | EAS | KHV | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG02132 | hp1 | a0001 | c0002 | t0001 | g0182 | EAS | KHV | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG02132 | hp2 | a0001 | c0003 | t0001 | g0070 | EAS | KHV | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG02135 | hp1 | a0001 | c0003 | t0001 | g0093 | EAS | KHV | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG02135 | hp2 | a0001 | c0002 | t0001 | g0304 | EAS | KHV | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0243 | AFR | ACB | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG02145 | hp2 | a0001 | c0001 | t0006 | g0266 | AFR | ACB | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG02148 | hp1 | a0001 | c0001 | t0004 | g0344 | AMR | PEL | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG02148 | hp2 | a0001 | c0002 | t0001 | g0167 | AMR | PEL | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG02155 | hp1 | a0001 | c0001 | t0013 | g0320 | EAS | CDX | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG02155 | hp2 | a0001 | c0003 | t0001 | g0046 | EAS | CDX | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG02257 | hp1 | a0001 | c0002 | t0001 | g0151 | AFR | ACB | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG02257 | hp2 | a0001 | c0002 | t0001 | g0296 | AFR | ACB | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0201 | AFR | ACB | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0232 | AFR | ACB | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG02273 | hp1 | a0002 | c0004 | t0001 | g0169 | AMR | PEL | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG02273 | hp2 | a0001 | c0003 | t0001 | g0084 | AMR | PEL | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG02293 | hp1 | a0001 | c0001 | t0003 | g0239 | AMR | PEL | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG02293 | hp2 | a0001 | c0003 | t0001 | g0053 | AMR | PEL | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG02451 | hp1 | a0001 | c0016 | t0001 | g0028 | AFR | ACB | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0230 | AFR | ACB | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG02572 | hp1 | a0001 | c0002 | t0001 | g0193 | AFR | GWD | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0119 | AFR | GWD | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0260 | AFR | GWD | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0244 | AFR | GWD | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG02622 | hp1 | a0001 | c0002 | t0005 | g0019 | AFR | GWD | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0229 | AFR | GWD | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0222 | AFR | GWD | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG02647 | hp2 | a0001 | c0003 | t0001 | g0108 | AFR | GWD | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG02683 | hp1 | a0001 | c0003 | t0001 | g0031 | SAS | PJL | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG02683 | hp2 | a0001 | c0002 | t0001 | g0175 | SAS | PJL | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG02717 | hp1 | a0001 | c0003 | t0001 | g0104 | AFR | GWD | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0233 | AFR | GWD | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0279 | AFR | GWD | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0013 | AFR | GWD | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG02735 | hp1 | a0001 | c0002 | t0001 | g0350 | SAS | PJL | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG02735 | hp2 | a0001 | c0001 | t0003 | g0235 | SAS | PJL | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG02738 | hp1 | a0001 | c0001 | t0007 | g0115 | SAS | PJL | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG02738 | hp2 | a0001 | c0002 | t0001 | g0305 | SAS | PJL | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0228 | AFR | GWD | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG02809 | hp2 | a0001 | c0002 | t0005 | g0022 | AFR | GWD | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0261 | AFR | GWD | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG02818 | hp2 | a0001 | c0001 | t0006 | g0273 | AFR | GWD | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0280 | AFR | GWD | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG02895 | hp2 | a0001 | c0001 | t0014 | g0223 | AFR | GWD | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG02896 | hp1 | a0001 | c0003 | t0001 | g0103 | AFR | GWD | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG02896 | hp2 | a0001 | c0002 | t0001 | g0183 | AFR | GWD | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG02897 | hp1 | a0001 | c0001 | t0014 | g0224 | AFR | GWD | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG02897 | hp2 | a0001 | c0002 | t0001 | g0184 | AFR | GWD | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG02965 | hp1 | a0001 | c0001 | t0006 | g0272 | AFR | ESN | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG02965 | hp2 | a0001 | c0002 | t0005 | g0020 | AFR | ESN | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG02970 | hp1 | a0001 | c0002 | t0005 | g0027 | AFR | ESN | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG02970 | hp2 | a0001 | c0005 | t0008 | g0276 | AFR | ESN | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0278 | AFR | ESN | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0249 | AFR | ESN | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0130 | SAS | PJL | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG03017 | hp2 | a0001 | c0003 | t0001 | g0067 | SAS | PJL | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0248 | AFR | GWD | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0277 | AFR | GWD | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0253 | AFR | ESN | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG03139 | hp2 | a0001 | c0002 | t0001 | g0318 | AFR | ESN | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG03209 | hp1 | a0001 | c0001 | t0016 | g0005 | AFR | MSL | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG03209 | hp2 | a0001 | c0003 | t0001 | g0091 | AFR | MSL | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0236 | SAS | PJL | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG03239 | hp2 | a0001 | c0002 | t0001 | g0006 | SAS | PJL | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0219 | AFR | MSL | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG03453 | hp2 | a0001 | c0005 | t0008 | g0268 | AFR | MSL | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0218 | AFR | MSL | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG03486 | hp2 | a0001 | c0002 | t0005 | g0021 | AFR | MSL | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG03490 | hp1 | a0001 | c0002 | t0001 | g0312 | SAS | PJL | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG03490 | hp2 | a0001 | c0001 | t0003 | g0200 | SAS | PJL | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG03491 | hp1 | a0001 | c0003 | t0001 | g0061 | SAS | PJL | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG03491 | hp2 | a0001 | c0002 | t0001 | g0143 | SAS | PJL | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG03492 | hp1 | a0001 | c0003 | t0001 | g0059 | SAS | PJL | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0181 | SAS | PJL | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0255 | AFR | GWD | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG03540 | hp2 | a0001 | c0002 | t0005 | g0024 | AFR | GWD | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG03579 | hp1 | a0001 | c0002 | t0005 | g0018 | AFR | MSL | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | MSL | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG03654 | hp1 | a0001 | c0003 | t0001 | g0072 | SAS | PJL | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG03654 | hp2 | a0008 | c0009 | t0001 | g0289 | SAS | PJL | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG03704 | hp1 | a0001 | c0003 | t0001 | g0029 | SAS | PJL | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG03704 | hp2 | a0001 | c0001 | t0023 | g0215 | SAS | PJL | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG03710 | hp1 | a0001 | c0003 | t0001 | g0082 | SAS | PJL | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0118 | SAS | PJL | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG03831 | hp1 | a0001 | c0002 | t0001 | g0131 | SAS | BEB | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG03831 | hp2 | a0001 | c0003 | t0001 | g0063 | SAS | BEB | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG03834 | hp1 | a0001 | c0002 | t0001 | g0154 | SAS | BEB | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG03834 | hp2 | a0001 | c0001 | t0004 | g0348 | SAS | BEB | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG03927 | hp1 | a0001 | c0003 | t0001 | g0071 | SAS | BEB | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG03927 | hp2 | a0001 | c0002 | t0001 | g0171 | SAS | BEB | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG03942 | hp1 | a0001 | c0002 | t0001 | g0190 | SAS | BEB | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0120 | SAS | BEB | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG04115 | hp1 | a0001 | c0002 | t0001 | g0109 | SAS | STU | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG04115 | hp2 | a0001 | c0001 | t0004 | g0324 | SAS | STU | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG04184 | hp1 | a0001 | c0002 | t0001 | g0112 | SAS | BEB | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG04184 | hp2 | a0001 | c0003 | t0001 | g0035 | SAS | BEB | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG04199 | hp1 | a0001 | c0002 | t0001 | g0179 | SAS | STU | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG04199 | hp2 | a0001 | c0003 | t0001 | g0048 | SAS | STU | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG04228 | hp1 | a0001 | c0001 | t0004 | g0323 | SAS | STU | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG04228 | hp2 | a0001 | c0003 | t0001 | g0080 | SAS | STU | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0014 | AFR | YRI | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA18522 | hp2 | a0001 | c0001 | t0021 | g0225 | AFR | YRI | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA18612 | hp1 | a0001 | c0003 | t0001 | g0047 | EAS | CHB | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA18612 | hp2 | a0001 | c0002 | t0001 | g0125 | EAS | CHB | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA18747 | hp1 | a0007 | c0010 | t0002 | g0262 | EAS | CHB | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA18747 | hp2 | a0001 | c0003 | t0001 | g0039 | EAS | CHB | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0011 | AFR | YRI | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA18906 | hp2 | a0001 | c0002 | t0005 | g0001 | AFR | YRI | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA18939 | hp1 | a0001 | c0001 | t0003 | g0247 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA18939 | hp2 | a0001 | c0003 | t0001 | g0089 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA18941 | hp1 | a0001 | c0001 | t0011 | g0269 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA18941 | hp2 | a0001 | c0003 | t0001 | g0034 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA18944 | hp1 | a0001 | c0003 | t0001 | g0079 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA18944 | hp2 | a0001 | c0002 | t0001 | g0189 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA18945 | hp1 | a0001 | c0003 | t0001 | g0069 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA18945 | hp2 | a0001 | c0001 | t0007 | g0041 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA18946 | hp1 | a0004 | c0008 | t0002 | g0264 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA18946 | hp2 | a0001 | c0001 | t0003 | g0211 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA18948 | hp1 | a0001 | c0001 | t0020 | g0329 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA18948 | hp2 | a0001 | c0003 | t0001 | g0055 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA18949 | hp1 | a0001 | c0002 | t0001 | g0284 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA18949 | hp2 | a0001 | c0003 | t0001 | g0086 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA18950 | hp1 | a0001 | c0002 | t0001 | g0141 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA18950 | hp2 | a0001 | c0002 | t0001 | g0308 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA18951 | hp1 | a0001 | c0002 | t0001 | g0288 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA18951 | hp2 | a0001 | c0003 | t0001 | g0105 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA18952 | hp1 | a0001 | c0001 | t0004 | g0342 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA18952 | hp2 | a0001 | c0003 | t0001 | g0032 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA18954 | hp1 | a0001 | c0003 | t0001 | g0078 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA18954 | hp2 | a0001 | c0001 | t0004 | g0333 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA18956 | hp1 | a0001 | c0003 | t0001 | g0075 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA18956 | hp2 | a0001 | c0002 | t0001 | g0127 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA18959 | hp1 | a0001 | c0002 | t0001 | g0158 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA18959 | hp2 | a0001 | c0001 | t0004 | g0330 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA18960 | hp1 | a0001 | c0002 | t0001 | g0310 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA18960 | hp2 | a0001 | c0001 | t0004 | g0331 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA18963 | hp1 | a0001 | c0001 | t0007 | g0042 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA18963 | hp2 | a0001 | c0003 | t0001 | g0060 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA18964 | hp1 | a0001 | c0002 | t0001 | g0140 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA18964 | hp2 | a0001 | c0003 | t0001 | g0058 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA18965 | hp1 | a0001 | c0002 | t0001 | g0160 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA18965 | hp2 | a0001 | c0003 | t0001 | g0044 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA18966 | hp1 | a0001 | c0001 | t0003 | g0210 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA18966 | hp2 | a0001 | c0001 | t0004 | g0327 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA18968 | hp2 | a0001 | c0015 | t0001 | g0178 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA18970 | hp1 | a0001 | c0002 | t0001 | g0298 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0254 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA18971 | hp2 | a0001 | c0002 | t0001 | g0307 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA18975 | hp1 | a0002 | c0004 | t0001 | g0191 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA18975 | hp2 | a0001 | c0001 | t0003 | g0113 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA18977 | hp1 | a0001 | c0002 | t0001 | g0150 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA18977 | hp2 | a0001 | c0002 | t0001 | g0311 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA18979 | hp1 | a0001 | c0002 | t0001 | g0129 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA18979 | hp2 | a0001 | c0002 | t0001 | g0123 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA18980 | hp1 | a0001 | c0003 | t0001 | g0052 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA18981 | hp1 | a0001 | c0003 | t0001 | g0077 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA18981 | hp2 | a0001 | c0002 | t0001 | g0172 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA18982 | hp1 | a0001 | c0002 | t0001 | g0168 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA18982 | hp2 | a0001 | c0002 | t0001 | g0287 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA18983 | hp1 | a0001 | c0003 | t0001 | g0056 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA18983 | hp2 | a0002 | c0004 | t0001 | g0144 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA18984 | hp1 | a0001 | c0003 | t0001 | g0090 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA18984 | hp2 | a0001 | c0002 | t0001 | g0139 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA18985 | hp1 | a0001 | c0002 | t0001 | g0110 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA18985 | hp2 | a0001 | c0003 | t0001 | g0062 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA18986 | hp1 | a0001 | c0002 | t0001 | g0162 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA18986 | hp2 | a0001 | c0001 | t0003 | g0238 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA18987 | hp1 | a0001 | c0003 | t0009 | g0036 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA18987 | hp2 | a0001 | c0002 | t0001 | g0176 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA18988 | hp1 | a0001 | c0001 | t0004 | g0328 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA18988 | hp2 | a0001 | c0001 | t0003 | g0212 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA18993 | hp1 | a0001 | c0001 | t0004 | g0347 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA18993 | hp2 | a0001 | c0003 | t0001 | g0043 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA18998 | hp1 | a0001 | c0002 | t0001 | g0152 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA18998 | hp2 | a0001 | c0001 | t0004 | g0339 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA18999 | hp1 | a0001 | c0002 | t0001 | g0306 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA18999 | hp2 | a0001 | c0003 | t0001 | g0045 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA19000 | hp1 | a0001 | c0001 | t0004 | g0334 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA19000 | hp2 | a0001 | c0001 | t0003 | g0114 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA19001 | hp1 | a0001 | c0002 | t0001 | g0128 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA19001 | hp2 | a0001 | c0002 | t0001 | g0122 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA19002 | hp1 | a0001 | c0003 | t0001 | g0051 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA19002 | hp2 | a0001 | c0001 | t0004 | g0340 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA19011 | hp1 | a0001 | c0003 | t0001 | g0094 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA19011 | hp2 | a0001 | c0002 | t0001 | g0147 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA19012 | hp1 | a0001 | c0002 | t0009 | g0291 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA19012 | hp2 | a0001 | c0003 | t0001 | g0099 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA19030 | hp1 | a0001 | c0002 | t0001 | g0313 | AFR | LWK | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0245 | AFR | LWK | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA19043 | hp1 | a0001 | c0002 | t0005 | g0349 | AFR | LWK | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA19043 | hp2 | a0001 | c0002 | t0001 | g0315 | AFR | LWK | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA19054 | hp2 | a0001 | c0001 | t0004 | g0341 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA19057 | hp1 | a0001 | c0002 | t0001 | g0185 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA19057 | hp2 | a0001 | c0012 | t0001 | g0033 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA19060 | hp1 | a0001 | c0001 | t0004 | g0321 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0256 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA19063 | hp1 | a0001 | c0002 | t0001 | g0299 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA19063 | hp2 | a0001 | c0001 | t0011 | g0258 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA19065 | hp1 | a0001 | c0001 | t0004 | g0336 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA19065 | hp2 | a0001 | c0003 | t0001 | g0064 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA19067 | hp1 | a0001 | c0003 | t0001 | g0073 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA19067 | hp2 | a0001 | c0002 | t0001 | g0195 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0263 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA19068 | hp2 | a0001 | c0001 | t0004 | g0326 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA19070 | hp1 | a0002 | c0004 | t0001 | g0146 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA19070 | hp2 | a0001 | c0002 | t0001 | g0285 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA19074 | hp1 | a0001 | c0001 | t0003 | g0213 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA19074 | hp2 | a0001 | c0002 | t0001 | g0286 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA19078 | hp1 | a0001 | c0002 | t0001 | g0196 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA19078 | hp2 | a0001 | c0003 | t0001 | g0107 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA19079 | hp1 | a0001 | c0001 | t0003 | g0237 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA19079 | hp2 | a0002 | c0004 | t0001 | g0174 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA19080 | hp1 | a0001 | c0002 | t0001 | g0292 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA19080 | hp2 | a0001 | c0002 | t0001 | g0157 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA19081 | hp1 | a0001 | c0002 | t0001 | g0283 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA19081 | hp2 | a0001 | c0003 | t0001 | g0074 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA19082 | hp1 | a0001 | c0003 | t0001 | g0101 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA19082 | hp2 | a0001 | c0001 | t0004 | g0346 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA19083 | hp1 | a0001 | c0002 | t0001 | g0309 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA19083 | hp2 | a0001 | c0001 | t0004 | g0335 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA19085 | hp1 | a0001 | c0002 | t0001 | g0138 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0265 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA19086 | hp1 | a0002 | c0004 | t0001 | g0145 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA19086 | hp2 | a0001 | c0003 | t0001 | g0087 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA19087 | hp2 | a0001 | c0003 | t0001 | g0030 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA19088 | hp1 | a0001 | c0003 | t0001 | g0106 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA19088 | hp2 | a0001 | c0001 | t0003 | g0209 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA19090 | hp1 | a0001 | c0001 | t0004 | g0338 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA19090 | hp2 | a0001 | c0003 | t0001 | g0098 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA19240 | hp1 | a0001 | c0002 | t0005 | g0016 | AFR | YRI | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | YRI | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0231 | AFR | ASW | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA20129 | hp2 | a0001 | c0002 | t0001 | g0135 | AFR | ASW | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA20805 | hp1 | a0001 | c0002 | t0012 | g0148 | EUR | TSI | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA20805 | hp2 | a0001 | c0002 | t0001 | g0297 | EUR | TSI | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA20905 | hp1 | a0001 | c0002 | t0001 | g0111 | SAS | GIH | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA20905 | hp2 | a0001 | c0013 | t0003 | g0206 | SAS | GIH | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG01123 | hp1 | a0001 | c0002 | t0001 | g0186 | AMR | CLM | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG01123 | hp2 | a0001 | c0003 | t0001 | g0040 | AMR | CLM | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0252 | AFR | ACB | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG02109 | hp2 | a0001 | c0002 | t0005 | g0017 | AFR | ACB | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0010 | AFR | ACB | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG02486 | hp2 | a0001 | c0005 | t0008 | g0267 | AFR | ACB | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG02559 | hp1 | a0001 | c0002 | t0005 | g0015 | AFR | ACB | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0226 | AFR | ACB | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG03471 | hp1 | a0001 | c0002 | t0001 | g0004 | AFR | MSL | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | MSL | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG06807 | hp1 | a0001 | c0002 | t0005 | g0026 | AFR | USA | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG06807 | hp2 | a0001 | c0002 | t0001 | g0316 | AFR | USA | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA20300 | hp1 | a0001 | c0002 | t0015 | g0319 | AFR | USA | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0208 | AFR | USA | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0259 | AFR | LWK | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA21309 | hp2 | a0001 | c0002 | t0022 | g0197 | AFR | LWK | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0227 | REF | REF | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| homoSapiens_grch38 | hp1 | a0001 | c0002 | t0001 | g0164 | REF | REF | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr20:48941880
|
C | T | 1 | a0003 | 2 | HG01081.hp2 HG01192.hp1 |
missense_variant | MODERATE | c.169C>T | p.Pro57Ser | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/39 | 348/9031 | 169/5358 | 57/1785 | chr20 | 48941880 | ||
| chr20:48951384
|
G | A | 1 | a0004 | 1 | NA18946.hp1 | missense_variant | MODERATE | c.338G>A | p.Arg113Gln | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 4/39 | 517/9031 | 338/5358 | 113/1785 | chr20 | 48951384 | ||
| chr20:48953577
|
G | A | 1 | a0002 | 6 | HG02273.hp1 NA18975.hp1 NA18983.hp2 others(3): Show |
missense_variant | MODERATE | c.625G>A | p.Glu209Lys | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/39 | 804/9031 | 625/5358 | 209/1785 | chr20 | 48953577 | ||
| chr20:48963841
|
G | A | 1 | a0008 | 1 | HG03654.hp2 | missense_variant | MODERATE | c.850G>A | p.Gly284Arg | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 7/39 | 1029/9031 | 850/5358 | 284/1785 | chr20 | 48963841 | ||
| chr20:48989390
|
C | T | 1 | a0005 | 1 | HG00733.hp1 | missense_variant | MODERATE | c.2639C>T | p.Pro880Leu | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 19/39 | 2818/9031 | 2639/5358 | 880/1785 | chr20 | 48989390 | ||
| chr20:48989664
|
G | A | 1 | a0007 | 1 | NA18747.hp1 | missense_variant | MODERATE | c.2794G>A | p.Ala932Thr | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 20/39 | 2973/9031 | 2794/5358 | 932/1785 | chr20 | 48989664 | ||
| chr20:48998348
|
G | A | 1 | a0006 | 1 | HG00639.hp1 | missense_variant | MODERATE | c.3275G>A | p.Arg1092His | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 25/39 | 3454/9031 | 3275/5358 | 1092/1785 | chr20 | 48998348 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr20:48969272
|
C | T | 1 | a0001c0016 | 1 | HG02451.hp1 | synonymous_variant | LOW | c.1185C>T | p.Asp395Asp | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 9/39 | 1364/9031 | 1185/5358 | 395/1785 | chr20 | 48969272 | ||
| chr20:48971204
|
C | T | 1 | a0001c0015 | 1 | NA18968.hp2 | synonymous_variant | LOW | c.1275C>T | p.His425His | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 10/39 | 1454/9031 | 1275/5358 | 425/1785 | chr20 | 48971204 | ||
| chr20:48972412
|
G | A | 1 | a0001c0005 | 3 | HG02486.hp2 HG02970.hp2 HG03453.hp2 |
synonymous_variant | LOW | c.1512G>A | p.Thr504Thr | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 11/39 | 1691/9031 | 1512/5358 | 504/1785 | chr20 | 48972412 | ||
| chr20:48995838
|
G | A | 1 | a0001c0006 | 2 | HG01257.hp2 HG01258.hp1 |
synonymous_variant | LOW | c.3177G>A | p.Ser1059Ser | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 23/39 | 3356/9031 | 3177/5358 | 1059/1785 | chr20 | 48995838 | ||
| chr20:49005144
|
T | G | 1 | a0001c0012 | 1 | NA19057.hp2 | synonymous_variant | LOW | c.3507T>G | p.Leu1169Leu | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 26/39 | 3686/9031 | 3507/5358 | 1169/1785 | chr20 | 49005144 | ||
| chr20:49010310
|
T | C | 6 | a0001c0001a0001c0005a0001c0006others(3): Show | 136 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(133): Show |
synonymous_variant | LOW | c.3663T>C | p.Gly1221Gly | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 27/39 | 3842/9031 | 3663/5358 | 1221/1785 | chr20 | 49010310 | ||
| chr20:49013912
|
C | T | 2 | a0001c0003a0001c0012 | 77 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(74): Show |
synonymous_variant | LOW | c.4131C>T | p.Ile1377Ile | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 30/39 | 4310/9031 | 4131/5358 | 1377/1785 | chr20 | 49013912 | ||
| chr20:49025372
|
C | T | 1 | a0001c0013 | 1 | NA20905.hp2 | synonymous_variant | LOW | c.4815C>T | p.Tyr1605Tyr | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 36/39 | 4994/9031 | 4815/5358 | 1605/1785 | chr20 | 49025372 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr20:48921796
|
C | T | 4 | a0001c0001t0003a0001c0001t0007a0001c0001t0023others(1): Show | 34 | HG00323.hp2 HG00639.hp2 HG00733.hp2 others(31): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-94C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/39 | chr20 | 48921796 | ||||||
| chr20:48921889
|
C | T | 1 | a0001c0001t0023 | 1 | HG03704.hp2 | 5_prime_UTR_variant | MODIFIER | c.-1C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/39 | 1 | chr20 | 48921889 | |||||
| chr20:49033237
|
T | C | 1 | a0001c0002t0015 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*38T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 39/39 | 38 | chr20 | 49033237 | |||||
| chr20:49033269
|
C | T | 1 | a0001c0002t0022 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*70C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 39/39 | 70 | chr20 | 49033269 | |||||
| chr20:49033339
|
C | T | 2 | a0001c0001t0014a0001c0001t0021 | 3 | HG02895.hp2 HG02897.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*140C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 39/39 | 140 | chr20 | 49033339 | |||||
| chr20:49033436
|
A | G | 4 | a0001c0001t0004a0001c0001t0013a0001c0001t0019others(1): Show | 29 | HG00673.hp1 HG00738.hp1 HG01934.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*237A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 39/39 | 237 | chr20 | 49033436 | |||||
| chr20:49033567
|
A | G | 1 | a0001c0002t0012 | 2 | HG01361.hp2 NA20805.hp1 |
3_prime_UTR_variant | MODIFIER | c.*368A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 39/39 | 368 | chr20 | 49033567 | |||||
| chr20:49033693
|
G | A | 1 | a0001c0002t0005 | 16 | HG01109.hp1 HG01884.hp2 HG01891.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*494G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 39/39 | 494 | chr20 | 49033693 | |||||
| chr20:49034203
|
G | A | 1 | a0001c0005t0008 | 3 | HG02486.hp2 HG02970.hp2 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1004G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 39/39 | 1004 | chr20 | 49034203 | |||||
| chr20:49034214
|
C | T | 1 | a0001c0005t0008 | 3 | HG02486.hp2 HG02970.hp2 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1015C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 39/39 | 1015 | chr20 | 49034214 | |||||
| chr20:49034432
|
T | C | 1 | a0001c0001t0019 | 1 | HG01934.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1233T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 39/39 | 1233 | chr20 | 49034432 | |||||
| chr20:49034621
|
A | G | 1 | a0001c0001t0011 | 2 | NA18941.hp1 NA19063.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1422A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 39/39 | 1422 | chr20 | 49034621 | |||||
| chr20:49034762
|
C | T | 1 | a0005c0014t0018 | 1 | HG00733.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1563C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 39/39 | 1563 | chr20 | 49034762 | |||||
| chr20:49034802
|
A | G | 1 | a0001c0001t0006 | 4 | HG02055.hp2 HG02145.hp2 HG02818.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1603A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 39/39 | 1603 | chr20 | 49034802 | |||||
| chr20:49034882
|
A | G | 1 | a0001c0001t0020 | 1 | NA18948.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1683A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 39/39 | 1683 | chr20 | 49034882 | |||||
| chr20:49034955
|
G | A | 18 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(15): Show | 135 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(132): Show |
3_prime_UTR_variant | MODIFIER | c.*1756G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 39/39 | 1756 | chr20 | 49034955 | |||||
| chr20:49035075
|
G | A | 1 | a0001c0002t0017 | 1 | HG00642.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1876G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 39/39 | 1876 | chr20 | 49035075 | |||||
| chr20:49035168
|
G | A | 1 | a0001c0002t0010 | 2 | HG01109.hp2 HG01943.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1969G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 39/39 | 1969 | chr20 | 49035168 | |||||
| chr20:49035717
|
A | G | 18 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(15): Show | 135 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(132): Show |
3_prime_UTR_variant | MODIFIER | c.*2518A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 39/39 | 2518 | chr20 | 49035717 | |||||
| chr20:49035801
|
A | G | 18 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(15): Show | 135 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(132): Show |
3_prime_UTR_variant | MODIFIER | c.*2602A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 39/39 | 2602 | chr20 | 49035801 | |||||
| chr20:49035987
|
C | T | 1 | a0001c0001t0013 | 2 | HG02015.hp2 HG02155.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2788C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 39/39 | 2788 | chr20 | 49035987 | |||||
| chr20:49035993
|
G | GA | 19 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(16): Show | 134 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(131): Show |
3_prime_UTR_variant | MODIFIER | c.*2806dupA | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 39/39 | 2807 | INFO_REALIGN_3_PRIME | chr20 | 49035993 | ||||
| chr20:49036154
|
C | T | 1 | a0001c0001t0016 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2955C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 39/39 | 2955 | chr20 | 49036154 | |||||
| chr20:49036653
|
T | C | 1 | a0001c0001t0021 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3454T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 39/39 | 3454 | chr20 | 49036653 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr20:48922217
|
C | T | 1 | a0001c0002t0001g0350 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.121+207C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48922217 | ||||||
| chr20:48922327
|
C | T | 1 | a0001c0002t0005g0349 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.121+317C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48922327 | ||||||
| chr20:48922456
|
G | C | 1 | a0001c0001t0002g0003 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.121+446G>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48922456 | ||||||
| chr20:48922468
|
C | T | 29 | a0001c0001t0004g0321a0001c0001t0004g0323a0001c0001t0004g0324others(26): Show | 29 | HG00673.hp1 HG00738.hp1 HG01934.hp1 others(26): Show |
intron_variant | MODIFIER | c.121+458C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48922468 | ||||||
| chr20:48923214
|
G | C | 1 | a0001c0002t0001g0004 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.121+1204G>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48923214 | ||||||
| chr20:48923238
|
G | A | 1 | a0001c0001t0016g0005 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.121+1228G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48923238 | ||||||
| chr20:48923822
|
C | A | 2 | a0001c0002t0001g0006a0001c0002t0017g0007 | 2 | HG00642.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.121+1812C>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48923822 | ||||||
| chr20:48923834
|
G | A | 7 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0010others(4): Show | 7 | HG01891.hp2 HG02486.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.121+1824G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48923834 | ||||||
| chr20:48923908
|
C | T | 1 | a0001c0001t0004g0348 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.121+1898C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48923908 | ||||||
| chr20:48923973
|
T | C | 16 | a0001c0002t0005g0001a0001c0002t0005g0015a0001c0002t0005g0016others(13): Show | 17 | HG01109.hp1 HG01884.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.121+1963T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48923973 | ||||||
| chr20:48924056
|
A | G | 2 | a0001c0002t0001g0318a0001c0002t0015g0319 | 2 | HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.121+2046A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48924056 | ||||||
| chr20:48924313
|
T | C | 1 | a0001c0001t0002g0003 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.121+2303T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48924313 | ||||||
| chr20:48924511
|
C | CA | 76 | a0001c0001t0007g0041a0001c0001t0007g0042a0001c0002t0001g0109others(73): Show | 76 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(73): Show |
intron_variant | MODIFIER | c.121+2522dupA | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr20 | 48924511 | |||||
| chr20:48924511
|
C | CAA | 8 | a0001c0003t0001g0029a0001c0003t0001g0030a0001c0003t0001g0031others(5): Show | 8 | HG02683.hp1 HG03704.hp1 HG04184.hp2 others(5): Show |
intron_variant | MODIFIER | c.121+2521_121+2522d others(4): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr20 | 48924511 | |||||
| chr20:48924511
|
CA | C | 158 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0010others(155): Show | 158 | HG00323.hp2 HG00639.hp1 HG00639.hp2 others(155): Show |
intron_variant | MODIFIER | c.121+2522delA | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr20 | 48924511 | |||||
| chr20:48924631
|
C | T | 1 | a0001c0003t0001g0317 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.121+2621C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48924631 | ||||||
| chr20:48924672
|
A | G | 2 | a0001c0002t0001g0315a0001c0002t0001g0316 | 2 | HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.121+2662A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48924672 | ||||||
| chr20:48924909
|
A | G | 15 | a0001c0002t0005g0001a0001c0002t0005g0015a0001c0002t0005g0016others(12): Show | 16 | HG01109.hp1 HG01884.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.121+2899A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48924909 | ||||||
| chr20:48924980
|
G | A | 133 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0009others(130): Show | 133 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(130): Show |
intron_variant | MODIFIER | c.121+2970G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48924980 | ||||||
| chr20:48925063
|
G | A | 249 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0009others(246): Show | 249 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(246): Show |
intron_variant | MODIFIER | c.121+3053G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48925063 | ||||||
| chr20:48925199
|
C | T | 2 | a0001c0001t0002g0280a0001c0001t0002g0281 | 2 | HG01884.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.121+3189C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48925199 | ||||||
| chr20:48925536
|
A | G | 2 | a0001c0001t0004g0346a0001c0001t0004g0347 | 2 | NA18993.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.121+3526A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48925536 | ||||||
| chr20:48925564
|
T | C | 1 | a0001c0016t0001g0028 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.121+3554T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48925564 | ||||||
| chr20:48925810
|
C | T | 3 | a0001c0001t0002g0277a0001c0001t0002g0278a0001c0001t0002g0279 | 3 | HG02723.hp1 HG02976.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.121+3800C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48925810 | ||||||
| chr20:48926191
|
T | C | 1 | a0001c0003t0001g0039 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.121+4181T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48926191 | ||||||
| chr20:48926505
|
G | A | 1 | a0001c0016t0001g0028 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.121+4495G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48926505 | ||||||
| chr20:48926658
|
G | A | 1 | a0001c0003t0001g0040 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.121+4648G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48926658 | ||||||
| chr20:48926715
|
T | C | 4 | a0001c0001t0002g0198a0001c0002t0001g0282a0001c0002t0001g0283others(1): Show | 4 | HG00673.hp2 NA18949.hp1 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.121+4705T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48926715 | ||||||
| chr20:48926838
|
C | T | 211 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0009others(208): Show | 212 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(209): Show |
intron_variant | MODIFIER | c.121+4828C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48926838 | ||||||
| chr20:48927067
|
G | A | 249 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0009others(246): Show | 249 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(246): Show |
intron_variant | MODIFIER | c.121+5057G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48927067 | ||||||
| chr20:48927097
|
A | C | 57 | a0001c0001t0002g0218a0001c0001t0002g0219a0001c0001t0002g0220others(54): Show | 57 | HG00323.hp2 HG00639.hp2 HG00733.hp2 others(54): Show |
intron_variant | MODIFIER | c.121+5087A>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48927097 | ||||||
| chr20:48927121
|
GTTGT | G | 13 | a0001c0002t0005g0001a0001c0002t0005g0015a0001c0002t0005g0016others(10): Show | 14 | HG01109.hp1 HG01884.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.121+5118_121+5121d others(6): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr20 | 48927121 | |||||
| chr20:48927909
|
T | G | 2 | a0001c0001t0003g0199a0001c0001t0003g0200 | 2 | HG00639.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.121+5899T>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48927909 | ||||||
| chr20:48927988
|
G | A | 3 | a0001c0001t0002g0248a0001c0001t0002g0249a0001c0001t0002g0250 | 3 | HG01175.hp1 HG02976.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.121+5978G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48927988 | ||||||
| chr20:48928047
|
G | A | 1 | a0001c0002t0001g0122 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.121+6037G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48928047 | ||||||
| chr20:48928192
|
C | CT | 61 | a0001c0001t0002g0121a0001c0001t0002g0198a0001c0001t0002g0243others(58): Show | 61 | HG00280.hp1 HG00609.hp2 HG01106.hp1 others(58): Show |
intron_variant | MODIFIER | c.121+6206dupT | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr20 | 48928192 | |||||
| chr20:48928192
|
CT | C | 23 | a0001c0002t0001g0125a0001c0002t0001g0126a0001c0002t0001g0127others(20): Show | 24 | HG00621.hp2 HG01884.hp2 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.121+6206delT | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr20 | 48928192 | |||||
| chr20:48928251
|
T | G | 1 | a0001c0002t0001g0130 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.121+6241T>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48928251 | ||||||
| chr20:48928347
|
C | T | 1 | a0001c0002t0001g0304 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.121+6337C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48928347 | ||||||
| chr20:48928425
|
C | T | 77 | a0001c0003t0001g0029a0001c0003t0001g0030a0001c0003t0001g0031others(74): Show | 77 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(74): Show |
intron_variant | MODIFIER | c.121+6415C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48928425 | ||||||
| chr20:48928457
|
CAAAGTGC others(289): Show |
C | 5 | a0001c0001t0002g0240a0001c0001t0003g0238a0001c0001t0003g0239others(2): Show | 5 | HG02071.hp1 HG02293.hp1 NA18939.hp1 others(2): Show |
intron_variant | MODIFIER | c.121+6477_121+6772d others(2): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr20 | 48928457 | |||||
| chr20:48928493
|
C | T | 4 | a0001c0002t0001g0185a0001c0005t0008g0267a0001c0005t0008g0268others(1): Show | 4 | HG02486.hp2 HG02970.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.121+6483C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48928493 | ||||||
| chr20:48928497
|
C | T | 2 | a0001c0002t0001g0183a0001c0002t0001g0184 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.121+6487C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48928497 | ||||||
| chr20:48928526
|
G | A | 1 | a0001c0002t0001g0350 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.121+6516G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48928526 | ||||||
| chr20:48928563
|
C | T | 1 | a0001c0001t0003g0237 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.121+6553C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48928563 | ||||||
| chr20:48928568
|
C | T | 1 | a0001c0001t0002g0275 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.121+6558C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48928568 | ||||||
| chr20:48928595
|
C | T | 4 | a0001c0001t0006g0266a0001c0001t0006g0272a0001c0001t0006g0273others(1): Show | 4 | HG02055.hp2 HG02145.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.121+6585C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48928595 | ||||||
| chr20:48928783
|
T | C | 133 | a0001c0001t0002g0198a0001c0002t0001g0122a0001c0002t0001g0123others(130): Show | 134 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(131): Show |
intron_variant | MODIFIER | c.121+6773T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48928783 | ||||||
| chr20:48928928
|
T | A | 45 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0009others(42): Show | 45 | HG00280.hp1 HG00558.hp2 HG01106.hp2 others(42): Show |
intron_variant | MODIFIER | c.121+6918T>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48928928 | ||||||
| chr20:48929100
|
C | G | 2 | a0001c0001t0003g0235a0001c0001t0003g0236 | 2 | HG02735.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.121+7090C>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48929100 | ||||||
| chr20:48929223
|
T | G | 1 | a0001c0002t0022g0197 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.121+7213T>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48929223 | ||||||
| chr20:48929249
|
C | G | 19 | a0001c0001t0004g0325a0001c0001t0004g0326a0001c0001t0004g0327others(16): Show | 19 | HG00673.hp1 HG00738.hp1 HG01934.hp1 others(16): Show |
intron_variant | MODIFIER | c.121+7239C>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48929249 | ||||||
| chr20:48929335
|
C | T | 1 | a0001c0003t0001g0100 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.121+7325C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48929335 | ||||||
| chr20:48929539
|
A | G | 1 | a0001c0001t0003g0234 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.121+7529A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48929539 | ||||||
| chr20:48929552
|
CATA | C | 113 | a0001c0001t0002g0198a0001c0002t0001g0122a0001c0002t0001g0123others(110): Show | 113 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(110): Show |
intron_variant | MODIFIER | c.121+7547_121+7549d others(5): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr20 | 48929552 | |||||
| chr20:48929832
|
G | C | 1 | a0001c0001t0004g0325 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.121+7822G>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48929832 | ||||||
| chr20:48929847
|
G | A | 2 | a0001c0001t0003g0201a0001c0001t0007g0241 | 2 | HG01433.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.121+7837G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48929847 | ||||||
| chr20:48929892
|
T | C | 1 | a0001c0001t0002g0251 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.121+7882T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48929892 | ||||||
| chr20:48929940
|
C | T | 3 | a0001c0001t0002g0231a0001c0001t0002g0232a0001c0001t0002g0233 | 3 | HG02258.hp2 HG02717.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.121+7930C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48929940 | ||||||
| chr20:48929941
|
G | A | 1 | a0001c0001t0002g0008 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.121+7931G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48929941 | ||||||
| chr20:48930280
|
G | A | 132 | a0001c0002t0001g0122a0001c0002t0001g0123a0001c0002t0001g0124others(129): Show | 133 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(130): Show |
intron_variant | MODIFIER | c.121+8270G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48930280 | ||||||
| chr20:48930471
|
A | G | 36 | a0001c0001t0002g0198a0001c0002t0001g0122a0001c0002t0001g0123others(33): Show | 36 | HG00639.hp1 HG00673.hp2 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.121+8461A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48930471 | ||||||
| chr20:48930528
|
A | G | 2 | a0001c0006t0002g0037a0001c0006t0002g0038 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.121+8518A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48930528 | ||||||
| chr20:48930575
|
G | C | 35 | a0001c0001t0002g0240a0001c0001t0003g0113a0001c0001t0003g0114others(32): Show | 35 | HG00323.hp2 HG00639.hp2 HG00733.hp2 others(32): Show |
intron_variant | MODIFIER | c.121+8565G>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48930575 | ||||||
| chr20:48930638
|
A | T | 1 | a0001c0002t0001g0124 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.121+8628A>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48930638 | ||||||
| chr20:48930907
|
G | A | 1 | a0001c0002t0022g0197 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.121+8897G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48930907 | ||||||
| chr20:48930972
|
A | G | 1 | a0001c0002t0001g0182 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.121+8962A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48930972 | ||||||
| chr20:48931162
|
C | G | 112 | a0001c0002t0001g0122a0001c0002t0001g0123a0001c0002t0001g0124others(109): Show | 112 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.121+9152C>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48931162 | ||||||
| chr20:48931442
|
A | T | 1 | a0001c0002t0005g0025 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.121+9432A>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48931442 | ||||||
| chr20:48931457
|
A | G | 2 | a0001c0001t0004g0324a0001c0001t0004g0348 | 2 | HG03834.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.121+9447A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48931457 | ||||||
| chr20:48931565
|
A | C | 1 | a0001c0001t0006g0274 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.121+9555A>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48931565 | ||||||
| chr20:48931627
|
G | T | 97 | a0001c0002t0001g0313a0001c0002t0001g0314a0001c0002t0001g0318others(94): Show | 98 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.122-9572G>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48931627 | ||||||
| chr20:48931736
|
C | A | 1 | a0001c0002t0001g0131 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.122-9463C>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48931736 | ||||||
| chr20:48931854
|
C | T | 29 | a0001c0001t0004g0321a0001c0001t0004g0323a0001c0001t0004g0324others(26): Show | 29 | HG00673.hp1 HG00738.hp1 HG01934.hp1 others(26): Show |
intron_variant | MODIFIER | c.122-9345C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48931854 | ||||||
| chr20:48932419
|
G | C | 1 | a0001c0003t0001g0029 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.122-8780G>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48932419 | ||||||
| chr20:48932510
|
C | T | 132 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0009others(129): Show | 132 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(129): Show |
intron_variant | MODIFIER | c.122-8689C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48932510 | ||||||
| chr20:48932977
|
A | C | 1 | a0001c0003t0001g0099 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.122-8222A>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48932977 | ||||||
| chr20:48933007
|
T | C | 2 | a0001c0002t0001g0132a0001c0002t0001g0133 | 2 | HG00280.hp2 HG00323.hp1 |
intron_variant | MODIFIER | c.122-8192T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48933007 | ||||||
| chr20:48933049
|
T | C | 1 | a0001c0002t0001g0285 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.122-8150T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48933049 | ||||||
| chr20:48933222
|
G | A | 1 | a0001c0002t0001g0109 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.122-7977G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48933222 | ||||||
| chr20:48933268
|
G | A | 3 | a0001c0005t0008g0267a0001c0005t0008g0268a0001c0005t0008g0276 | 3 | HG02486.hp2 HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.122-7931G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48933268 | ||||||
| chr20:48933434
|
A | G | 1 | a0001c0001t0002g0121 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.122-7765A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48933434 | ||||||
| chr20:48933442
|
TA | T | 247 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0009others(244): Show | 247 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(244): Show |
intron_variant | MODIFIER | c.122-7755delA | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr20 | 48933442 | |||||
| chr20:48933701
|
A | T | 1 | a0001c0002t0001g0131 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.122-7498A>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48933701 | ||||||
| chr20:48933842
|
G | A | 16 | a0001c0002t0005g0001a0001c0002t0005g0015a0001c0002t0005g0016others(13): Show | 17 | HG01109.hp1 HG01884.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.122-7357G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48933842 | ||||||
| chr20:48933890
|
C | T | 1 | a0001c0003t0001g0035 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.122-7309C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48933890 | ||||||
| chr20:48933951
|
C | T | 132 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0009others(129): Show | 132 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(129): Show |
intron_variant | MODIFIER | c.122-7248C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48933951 | ||||||
| chr20:48934119
|
C | CA | 31 | a0001c0001t0004g0321a0001c0001t0004g0323a0001c0001t0004g0324others(28): Show | 31 | HG00438.hp1 HG00673.hp1 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.122-7055dupA | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr20 | 48934119 | |||||
| chr20:48934119
|
CA | C | 203 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0009others(200): Show | 203 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(200): Show |
intron_variant | MODIFIER | c.122-7055delA | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr20 | 48934119 | |||||
| chr20:48934119
|
CAA | C | 15 | a0001c0001t0002g0230a0001c0001t0002g0249a0001c0001t0002g0265others(12): Show | 15 | HG00733.hp2 HG01074.hp2 HG01081.hp2 others(12): Show |
intron_variant | MODIFIER | c.122-7056_122-7055d others(4): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr20 | 48934119 | |||||
| chr20:48934413
|
G | C | 2 | a0001c0002t0001g0315a0001c0002t0001g0316 | 2 | HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.122-6786G>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48934413 | ||||||
| chr20:48934691
|
T | A | 1 | a0001c0016t0001g0028 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.122-6508T>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48934691 | ||||||
| chr20:48935095
|
C | CTCTTTTT others(1): Show |
268 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0009others(265): Show | 269 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(266): Show |
intron_variant | MODIFIER | c.122-6094_122-6087d others(10): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr20 | 48935095 | |||||
| chr20:48935235
|
C | T | 1 | a0001c0001t0002g0233 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.122-5964C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48935235 | ||||||
| chr20:48935239
|
G | A | 1 | a0001c0003t0001g0051 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.122-5960G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48935239 | ||||||
| chr20:48935635
|
G | A | 4 | a0001c0001t0006g0266a0001c0001t0006g0272a0001c0001t0006g0273others(1): Show | 4 | HG02055.hp2 HG02145.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.122-5564G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48935635 | ||||||
| chr20:48935667
|
C | T | 35 | a0001c0002t0001g0122a0001c0002t0001g0123a0001c0002t0001g0124others(32): Show | 35 | HG00639.hp1 HG00673.hp2 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.122-5532C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48935667 | ||||||
| chr20:48935695
|
T | C | 1 | a0001c0001t0002g0198 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.122-5504T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48935695 | ||||||
| chr20:48935709
|
A | G | 268 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0009others(265): Show | 269 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(266): Show |
intron_variant | MODIFIER | c.122-5490A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48935709 | ||||||
| chr20:48935718
|
G | A | 3 | a0001c0001t0002g0218a0001c0001t0002g0219a0001c0001t0002g0243 | 3 | HG02145.hp1 HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.122-5481G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48935718 | ||||||
| chr20:48935744
|
C | T | 3 | a0001c0002t0005g0021a0001c0002t0005g0024a0001c0002t0005g0025 | 3 | HG01891.hp1 HG03486.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.122-5455C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48935744 | ||||||
| chr20:48935765
|
C | G | 1 | a0006c0011t0001g0301 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.122-5434C>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48935765 | ||||||
| chr20:48935776
|
C | A | 1 | a0001c0002t0001g0137 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.122-5423C>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48935776 | ||||||
| chr20:48935776
|
C | T | 1 | a0001c0003t0001g0097 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.122-5423C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48935776 | ||||||
| chr20:48935782
|
C | CACCTCCC others(42): Show |
1 | a0001c0001t0016g0005 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.122-5384_122-5336d others(51): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr20 | 48935782 | |||||
| chr20:48935810
|
C | T | 7 | a0001c0001t0003g0202a0001c0001t0003g0214a0001c0001t0003g0216others(4): Show | 7 | HG00733.hp2 HG01175.hp2 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.122-5389C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48935810 | ||||||
| chr20:48935869
|
A | G | 46 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0009others(43): Show | 46 | HG00280.hp1 HG00558.hp2 HG01106.hp2 others(43): Show |
intron_variant | MODIFIER | c.122-5330A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48935869 | ||||||
| chr20:48935876
|
T | C | 46 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0009others(43): Show | 46 | HG00280.hp1 HG00558.hp2 HG01106.hp2 others(43): Show |
intron_variant | MODIFIER | c.122-5323T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48935876 | ||||||
| chr20:48935892
|
C | T | 7 | a0001c0001t0003g0113a0001c0001t0003g0114a0001c0001t0003g0209others(4): Show | 7 | NA18946.hp2 NA18966.hp1 NA18975.hp2 others(4): Show |
intron_variant | MODIFIER | c.122-5307C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48935892 | ||||||
| chr20:48935915
|
C | G | 1 | a0001c0002t0001g0179 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.122-5284C>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48935915 | ||||||
| chr20:48935930
|
G | C | 55 | a0001c0001t0002g0218a0001c0001t0002g0219a0001c0001t0002g0220others(52): Show | 55 | HG00323.hp2 HG00639.hp2 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.122-5269G>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48935930 | ||||||
| chr20:48935937
|
C | CG | 40 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0012others(37): Show | 40 | HG01175.hp2 HG01192.hp1 HG01261.hp1 others(37): Show |
intron_variant | MODIFIER | c.122-5251dupG | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr20 | 48935937 | |||||
| chr20:48935937
|
C | CGG | 45 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0013others(42): Show | 45 | HG00280.hp1 HG00558.hp2 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.122-5252_122-5251d others(4): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr20 | 48935937 | |||||
| chr20:48935937
|
C | CGGG | 21 | a0001c0001t0002g0120a0001c0001t0002g0248a0001c0001t0002g0250others(18): Show | 21 | HG00673.hp1 HG01169.hp2 HG01175.hp1 others(18): Show |
intron_variant | MODIFIER | c.122-5253_122-5251d others(5): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr20 | 48935937 | |||||
| chr20:48935940
|
G | T | 1 | a0001c0002t0005g0020 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.122-5259G>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48935940 | ||||||
| chr20:48935942
|
G | C | 1 | a0001c0002t0001g0123 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.122-5257G>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48935942 | ||||||
| chr20:48935942
|
G | GC | 3 | a0001c0005t0008g0267a0001c0005t0008g0268a0001c0005t0008g0276 | 3 | HG02486.hp2 HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.122-5257_122-5256i others(3): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48935942 | ||||||
| chr20:48935943
|
G | C | 78 | a0001c0001t0007g0041a0001c0001t0007g0042a0001c0003t0001g0029others(75): Show | 78 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.122-5256G>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48935943 | ||||||
| chr20:48935979
|
C | A | 1 | a0001c0016t0001g0028 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.122-5220C>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48935979 | ||||||
| chr20:48936052
|
TGGGGCGG others(168): Show |
T | 2 | a0001c0002t0001g0318a0001c0002t0015g0319 | 2 | HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.122-5129_122-4955d others(2): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr20 | 48936052 | |||||
| chr20:48936059
|
G | A | 133 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0009others(130): Show | 133 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(130): Show |
intron_variant | MODIFIER | c.122-5140G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48936059 | ||||||
| chr20:48936080
|
ACCCCCAC others(42): Show |
A | 2 | a0001c0002t0001g0315a0001c0002t0001g0316 | 2 | HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.122-5081_122-5033d others(51): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr20 | 48936080 | |||||
| chr20:48936105
|
C | T | 1 | a0001c0001t0002g0275 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.122-5094C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48936105 | ||||||
| chr20:48936113
|
C | T | 3 | a0001c0001t0002g0231a0001c0001t0002g0232a0001c0001t0002g0233 | 3 | HG02258.hp2 HG02717.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.122-5086C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48936113 | ||||||
| chr20:48936117
|
C | T | 1 | a0001c0002t0001g0122 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.122-5082C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48936117 | ||||||
| chr20:48936119
|
G | A | 1 | a0001c0001t0003g0237 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.122-5080G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48936119 | ||||||
| chr20:48936141
|
C | T | 1 | a0007c0010t0002g0262 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.122-5058C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48936141 | ||||||
| chr20:48936149
|
C | T | 1 | a0001c0002t0022g0197 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.122-5050C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48936149 | ||||||
| chr20:48936195
|
C | T | 29 | a0001c0001t0004g0321a0001c0001t0004g0323a0001c0001t0004g0324others(26): Show | 29 | HG00673.hp1 HG00738.hp1 HG01934.hp1 others(26): Show |
intron_variant | MODIFIER | c.122-5004C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48936195 | ||||||
| chr20:48936209
|
C | T | 2 | a0001c0001t0003g0212a0001c0001t0003g0213 | 2 | NA18988.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.122-4990C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48936209 | ||||||
| chr20:48936217
|
A | ACCTCCCG others(40): Show |
13 | a0001c0002t0005g0001a0001c0002t0005g0015a0001c0002t0005g0016others(10): Show | 14 | HG01109.hp1 HG01884.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.122-4978_122-4932d others(49): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr20 | 48936217 | |||||
| chr20:48936224
|
G | A | 133 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0009others(130): Show | 133 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(130): Show |
intron_variant | MODIFIER | c.122-4975G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48936224 | ||||||
| chr20:48936307
|
C | A | 1 | a0001c0001t0002g0277 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.122-4892C>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48936307 | ||||||
| chr20:48936374
|
G | A | 1 | a0001c0002t0001g0171 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.122-4825G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48936374 | ||||||
| chr20:48936375
|
AGGTGGCT others(33): Show |
A | 1 | a0001c0001t0002g0121 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.122-4814_122-4775d others(42): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr20 | 48936375 | |||||
| chr20:48936454
|
G | A | 1 | a0001c0001t0002g0218 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.122-4745G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48936454 | ||||||
| chr20:48936505
|
C | T | 3 | a0001c0005t0008g0267a0001c0005t0008g0268a0001c0005t0008g0276 | 3 | HG02486.hp2 HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.122-4694C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48936505 | ||||||
| chr20:48936669
|
C | T | 1 | a0001c0001t0004g0340 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.122-4530C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48936669 | ||||||
| chr20:48936845
|
A | G | 1 | a0001c0001t0013g0322 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.122-4354A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48936845 | ||||||
| chr20:48937028
|
A | G | 2 | a0001c0001t0003g0235a0001c0001t0003g0236 | 2 | HG02735.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.122-4171A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48937028 | ||||||
| chr20:48937151
|
G | C | 2 | a0001c0002t0001g0318a0001c0002t0015g0319 | 2 | HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.122-4048G>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48937151 | ||||||
| chr20:48937355
|
T | G | 1 | a0001c0002t0001g0109 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.122-3844T>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48937355 | ||||||
| chr20:48937661
|
G | A | 1 | a0001c0001t0002g0253 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.122-3538G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48937661 | ||||||
| chr20:48937855
|
A | G | 248 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0009others(245): Show | 248 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(245): Show |
intron_variant | MODIFIER | c.122-3344A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48937855 | ||||||
| chr20:48937861
|
T | C | 1 | a0001c0003t0001g0052 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.122-3338T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48937861 | ||||||
| chr20:48937966
|
T | G | 1 | a0001c0001t0002g0233 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.122-3233T>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48937966 | ||||||
| chr20:48938203
|
T | C | 1 | a0001c0002t0001g0006 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.122-2996T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48938203 | ||||||
| chr20:48938302
|
C | T | 18 | a0001c0002t0001g0313a0001c0002t0005g0001a0001c0002t0005g0015others(15): Show | 19 | HG01109.hp1 HG01884.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.122-2897C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48938302 | ||||||
| chr20:48938445
|
T | G | 1 | a0001c0001t0002g0013 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.122-2754T>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48938445 | ||||||
| chr20:48938545
|
A | G | 35 | a0001c0001t0002g0240a0001c0001t0003g0113a0001c0001t0003g0114others(32): Show | 35 | HG00323.hp2 HG00639.hp2 HG00733.hp2 others(32): Show |
intron_variant | MODIFIER | c.122-2654A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48938545 | ||||||
| chr20:48938825
|
C | A | 5 | a0001c0001t0004g0327a0001c0001t0004g0333a0001c0001t0004g0334others(2): Show | 5 | NA18952.hp1 NA18954.hp2 NA18966.hp2 others(2): Show |
intron_variant | MODIFIER | c.122-2374C>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48938825 | ||||||
| chr20:48938891
|
T | G | 2 | a0001c0002t0005g0026a0001c0002t0005g0027 | 2 | HG02970.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.122-2308T>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48938891 | ||||||
| chr20:48938908
|
G | A | 28 | a0001c0001t0004g0321a0001c0001t0004g0324a0001c0001t0004g0325others(25): Show | 28 | HG00673.hp1 HG00738.hp1 HG01934.hp1 others(25): Show |
intron_variant | MODIFIER | c.122-2291G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48938908 | ||||||
| chr20:48938967
|
G | GT | 19 | a0001c0001t0003g0211a0001c0002t0001g0309a0001c0002t0022g0197others(16): Show | 19 | HG00621.hp1 HG01192.hp2 HG01981.hp2 others(16): Show |
intron_variant | MODIFIER | c.122-2224dupT | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr20 | 48938967 | |||||
| chr20:48938976
|
G | T | 129 | a0001c0002t0001g0122a0001c0002t0001g0123a0001c0002t0001g0124others(126): Show | 130 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(127): Show |
intron_variant | MODIFIER | c.122-2223G>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48938976 | ||||||
| chr20:48938980
|
G | GT | 9 | a0001c0001t0002g0252a0001c0001t0002g0281a0001c0001t0003g0114others(6): Show | 9 | HG01884.hp1 HG02109.hp1 HG02738.hp1 others(6): Show |
intron_variant | MODIFIER | c.122-2205dupT | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr20 | 48938980 | |||||
| chr20:48938980
|
G | T | 76 | a0001c0003t0001g0029a0001c0003t0001g0030a0001c0003t0001g0031others(73): Show | 76 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(73): Show |
intron_variant | MODIFIER | c.122-2219G>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48938980 | ||||||
| chr20:48938999
|
A | C | 272 | a0001c0001t0001g0170a0001c0001t0002g0003a0001c0001t0002g0008others(269): Show | 274 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(271): Show |
intron_variant | MODIFIER | c.122-2200A>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48938999 | ||||||
| chr20:48939040
|
T | C | 36 | a0001c0001t0002g0003a0001c0001t0002g0116a0001c0001t0002g0117others(33): Show | 36 | HG00280.hp1 HG00558.hp2 HG01106.hp2 others(33): Show |
intron_variant | MODIFIER | c.122-2159T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48939040 | ||||||
| chr20:48939068
|
G | A | 112 | a0001c0002t0001g0122a0001c0002t0001g0123a0001c0002t0001g0124others(109): Show | 112 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.122-2131G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48939068 | ||||||
| chr20:48939239
|
C | T | 4 | a0001c0003t0001g0034a0001c0003t0001g0089a0001c0003t0001g0105others(1): Show | 4 | NA18939.hp2 NA18941.hp2 NA18951.hp2 others(1): Show |
intron_variant | MODIFIER | c.122-1960C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48939239 | ||||||
| chr20:48939406
|
C | T | 132 | a0001c0002t0001g0122a0001c0002t0001g0123a0001c0002t0001g0124others(129): Show | 133 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(130): Show |
intron_variant | MODIFIER | c.122-1793C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48939406 | ||||||
| chr20:48939612
|
G | A | 16 | a0001c0002t0005g0001a0001c0002t0005g0015a0001c0002t0005g0016others(13): Show | 17 | HG01109.hp1 HG01884.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.122-1587G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48939612 | ||||||
| chr20:48939896
|
T | A | 1 | a0001c0016t0001g0028 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.122-1303T>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48939896 | ||||||
| chr20:48940023
|
A | C | 1 | a0001c0002t0001g0297 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.122-1176A>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48940023 | ||||||
| chr20:48940058
|
G | T | 1 | a0002c0004t0001g0169 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.122-1141G>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48940058 | ||||||
| chr20:48940245
|
C | T | 1 | a0001c0002t0005g0027 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.122-954C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48940245 | ||||||
| chr20:48940329
|
T | C | 1 | a0001c0002t0001g0305 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.122-870T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48940329 | ||||||
| chr20:48940476
|
C | G | 136 | a0001c0001t0001g0170a0001c0001t0002g0003a0001c0001t0002g0008others(133): Show | 136 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(133): Show |
intron_variant | MODIFIER | c.122-723C>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48940476 | ||||||
| chr20:48940477
|
G | A | 135 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0009others(132): Show | 135 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(132): Show |
intron_variant | MODIFIER | c.122-722G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48940477 | ||||||
| chr20:48940515
|
T | C | 3 | a0001c0002t0001g0138a0001c0002t0001g0139a0001c0002t0001g0172 | 3 | NA18981.hp2 NA18984.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.122-684T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48940515 | ||||||
| chr20:48940592
|
C | T | 35 | a0001c0001t0002g0240a0001c0001t0003g0113a0001c0001t0003g0114others(32): Show | 35 | HG00323.hp2 HG00639.hp2 HG00733.hp2 others(32): Show |
intron_variant | MODIFIER | c.122-607C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48940592 | ||||||
| chr20:48940668
|
C | T | 2 | a0001c0002t0001g0318a0001c0002t0015g0319 | 2 | HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.122-531C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48940668 | ||||||
| chr20:48940703
|
A | G | 2 | a0001c0001t0002g0280a0001c0001t0002g0281 | 2 | HG01884.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.122-496A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48940703 | ||||||
| chr20:48940765
|
G | T | 36 | a0001c0001t0002g0198a0001c0002t0001g0122a0001c0002t0001g0123others(33): Show | 36 | HG00639.hp1 HG00673.hp2 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.122-434G>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48940765 | ||||||
| chr20:48940766
|
G | T | 36 | a0001c0001t0002g0198a0001c0002t0001g0122a0001c0002t0001g0123others(33): Show | 36 | HG00639.hp1 HG00673.hp2 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.122-433G>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48940766 | ||||||
| chr20:48941105
|
ATCT | A | 4 | a0001c0003t0001g0034a0001c0003t0001g0089a0001c0003t0001g0105others(1): Show | 4 | NA18939.hp2 NA18941.hp2 NA18951.hp2 others(1): Show |
intron_variant | MODIFIER | c.122-92_122-90delCT others(1): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | INFO_REALIGN_3_PRIME | chr20 | 48941105 | |||||
| chr20:48942086
|
T | A | 5 | a0001c0001t0002g0008a0001c0001t0002g0010a0001c0001t0002g0011others(2): Show | 5 | HG01891.hp2 HG02486.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.276+99T>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | chr20 | 48942086 | ||||||
| chr20:48942093
|
G | A | 5 | a0001c0001t0002g0008a0001c0001t0002g0010a0001c0001t0002g0011others(2): Show | 5 | HG01891.hp2 HG02486.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.276+106G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | chr20 | 48942093 | ||||||
| chr20:48942310
|
CT | C | 35 | a0001c0002t0001g0122a0001c0002t0001g0123a0001c0002t0001g0124others(32): Show | 35 | HG00639.hp1 HG00673.hp2 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.276+329delT | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr20 | 48942310 | |||||
| chr20:48942405
|
T | C | 4 | a0001c0003t0001g0030a0001c0003t0001g0055a0001c0003t0001g0056others(1): Show | 4 | NA18948.hp2 NA18983.hp1 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.276+418T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | chr20 | 48942405 | ||||||
| chr20:48942473
|
G | GT | 34 | a0001c0001t0001g0170a0001c0001t0002g0218a0001c0001t0002g0219others(31): Show | 34 | HG01175.hp2 HG01255.hp2 HG01516.hp2 others(31): Show |
intron_variant | MODIFIER | c.276+513dupT | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr20 | 48942473 | |||||
| chr20:48942473
|
GT | G | 139 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0009others(136): Show | 139 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(136): Show |
intron_variant | MODIFIER | c.276+513delT | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr20 | 48942473 | |||||
| chr20:48942473
|
GTT | G | 32 | a0001c0001t0002g0254a0001c0001t0002g0263a0001c0001t0004g0323others(29): Show | 32 | HG00673.hp1 HG01192.hp2 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.276+512_276+513del others(2): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr20 | 48942473 | |||||
| chr20:48942473
|
GTTT | G | 16 | a0001c0002t0001g0314a0001c0002t0001g0318a0001c0002t0005g0001others(13): Show | 17 | HG00741.hp2 HG01109.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.276+511_276+513del others(3): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr20 | 48942473 | |||||
| chr20:48942473
|
GTTTTTTT others(8): Show |
G | 2 | a0001c0003t0001g0057a0001c0003t0001g0091 | 2 | HG01261.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.276+499_276+513del others(15): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr20 | 48942473 | |||||
| chr20:48942473
|
GTTTTTTT others(9): Show |
G | 3 | a0001c0005t0008g0267a0001c0005t0008g0268a0001c0005t0008g0276 | 3 | HG02486.hp2 HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.276+498_276+513del others(16): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr20 | 48942473 | |||||
| chr20:48942506
|
T | C | 3 | a0001c0005t0008g0267a0001c0005t0008g0268a0001c0005t0008g0276 | 3 | HG02486.hp2 HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.276+519T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | chr20 | 48942506 | ||||||
| chr20:48942541
|
A | G | 2 | a0001c0002t0001g0318a0001c0002t0015g0319 | 2 | HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.276+554A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | chr20 | 48942541 | ||||||
| chr20:48942546
|
G | A | 2 | a0001c0002t0001g0318a0001c0002t0015g0319 | 2 | HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.276+559G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | chr20 | 48942546 | ||||||
| chr20:48942587
|
G | A | 2 | a0001c0002t0001g0313a0001c0002t0001g0314 | 2 | HG00741.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.276+600G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | chr20 | 48942587 | ||||||
| chr20:48942727
|
G | A | 213 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0009others(210): Show | 214 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(211): Show |
intron_variant | MODIFIER | c.276+740G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | chr20 | 48942727 | ||||||
| chr20:48942827
|
T | C | 1 | a0001c0002t0001g0314 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.276+840T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | chr20 | 48942827 | ||||||
| chr20:48942872
|
C | G | 2 | a0001c0002t0005g0026a0001c0002t0005g0027 | 2 | HG02970.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.276+885C>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | chr20 | 48942872 | ||||||
| chr20:48942937
|
T | C | 3 | a0001c0005t0008g0267a0001c0005t0008g0268a0001c0005t0008g0276 | 3 | HG02486.hp2 HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.276+950T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | chr20 | 48942937 | ||||||
| chr20:48943417
|
A | G | 2 | a0001c0001t0002g0228a0001c0001t0002g0229 | 2 | HG02622.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.276+1430A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | chr20 | 48943417 | ||||||
| chr20:48943561
|
A | T | 1 | a0001c0001t0002g0281 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.276+1574A>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | chr20 | 48943561 | ||||||
| chr20:48943637
|
A | C | 213 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0009others(210): Show | 214 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(211): Show |
intron_variant | MODIFIER | c.276+1650A>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | chr20 | 48943637 | ||||||
| chr20:48943663
|
T | C | 136 | a0001c0001t0002g0198a0001c0001t0007g0041a0001c0001t0007g0042others(133): Show | 137 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(134): Show |
intron_variant | MODIFIER | c.276+1676T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | chr20 | 48943663 | ||||||
| chr20:48943664
|
G | A | 1 | a0001c0002t0001g0141 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.276+1677G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | chr20 | 48943664 | ||||||
| chr20:48944013
|
ATATT | A | 3 | a0001c0001t0002g0240a0001c0001t0003g0238a0001c0001t0003g0239 | 3 | HG02293.hp1 NA18986.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.276+2029_276+2032d others(6): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr20 | 48944013 | |||||
| chr20:48944291
|
T | C | 136 | a0001c0001t0002g0198a0001c0001t0007g0041a0001c0001t0007g0042others(133): Show | 137 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(134): Show |
intron_variant | MODIFIER | c.276+2304T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | chr20 | 48944291 | ||||||
| chr20:48944325
|
A | G | 1 | a0001c0002t0001g0299 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.276+2338A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | chr20 | 48944325 | ||||||
| chr20:48944532
|
G | A | 3 | a0001c0001t0002g0218a0001c0001t0002g0219a0001c0001t0002g0243 | 3 | HG02145.hp1 HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.276+2545G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | chr20 | 48944532 | ||||||
| chr20:48944554
|
G | A | 132 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0009others(129): Show | 132 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(129): Show |
intron_variant | MODIFIER | c.276+2567G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | chr20 | 48944554 | ||||||
| chr20:48944749
|
A | G | 3 | a0001c0002t0001g0293a0001c0002t0001g0294a0001c0002t0001g0295 | 3 | HG00741.hp1 HG01071.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.276+2762A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | chr20 | 48944749 | ||||||
| chr20:48944963
|
G | A | 1 | a0001c0001t0013g0322 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.276+2976G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | chr20 | 48944963 | ||||||
| chr20:48945177
|
A | G | 1 | a0001c0001t0004g0321 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.276+3190A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | chr20 | 48945177 | ||||||
| chr20:48945238
|
C | G | 1 | a0001c0002t0001g0310 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.276+3251C>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | chr20 | 48945238 | ||||||
| chr20:48945340
|
C | T | 1 | a0006c0011t0001g0301 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.276+3353C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | chr20 | 48945340 | ||||||
| chr20:48945346
|
G | T | 1 | a0001c0002t0001g0299 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.276+3359G>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | chr20 | 48945346 | ||||||
| chr20:48945404
|
C | G | 36 | a0001c0001t0002g0198a0001c0002t0001g0122a0001c0002t0001g0123others(33): Show | 36 | HG00639.hp1 HG00673.hp2 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.276+3417C>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | chr20 | 48945404 | ||||||
| chr20:48945495
|
C | T | 1 | a0001c0003t0001g0099 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.276+3508C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | chr20 | 48945495 | ||||||
| chr20:48945508
|
T | A | 1 | a0001c0001t0002g0010 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.276+3521T>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | chr20 | 48945508 | ||||||
| chr20:48945536
|
G | C | 1 | a0001c0001t0002g0271 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.276+3549G>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | chr20 | 48945536 | ||||||
| chr20:48945558
|
C | T | 1 | a0001c0003t0001g0085 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.276+3571C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | chr20 | 48945558 | ||||||
| chr20:48945709
|
A | C | 2 | a0001c0002t0001g0183a0001c0002t0001g0184 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.276+3722A>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | chr20 | 48945709 | ||||||
| chr20:48945738
|
C | T | 1 | a0001c0002t0001g0165 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.276+3751C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | chr20 | 48945738 | ||||||
| chr20:48945790
|
G | C | 29 | a0001c0001t0004g0321a0001c0001t0004g0323a0001c0001t0004g0324others(26): Show | 29 | HG00673.hp1 HG00738.hp1 HG01934.hp1 others(26): Show |
intron_variant | MODIFIER | c.276+3803G>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | chr20 | 48945790 | ||||||
| chr20:48945929
|
A | T | 7 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0010others(4): Show | 7 | HG01891.hp2 HG02486.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.276+3942A>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | chr20 | 48945929 | ||||||
| chr20:48945977
|
A | G | 1 | a0001c0003t0001g0084 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.276+3990A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | chr20 | 48945977 | ||||||
| chr20:48946005
|
C | T | 1 | a0001c0013t0003g0206 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.276+4018C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | chr20 | 48946005 | ||||||
| chr20:48946025
|
A | G | 1 | a0001c0001t0002g0240 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.276+4038A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | chr20 | 48946025 | ||||||
| chr20:48946134
|
C | T | 3 | a0001c0005t0008g0267a0001c0005t0008g0268a0001c0005t0008g0276 | 3 | HG02486.hp2 HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.276+4147C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | chr20 | 48946134 | ||||||
| chr20:48946157
|
G | A | 4 | a0001c0001t0006g0266a0001c0001t0006g0272a0001c0001t0006g0273others(1): Show | 4 | HG02055.hp2 HG02145.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.276+4170G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | chr20 | 48946157 | ||||||
| chr20:48946189
|
A | G | 115 | a0001c0001t0002g0198a0001c0001t0007g0041a0001c0001t0007g0042others(112): Show | 115 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.276+4202A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | chr20 | 48946189 | ||||||
| chr20:48946410
|
G | A | 4 | a0001c0002t0001g0142a0001c0002t0001g0143a0001c0002t0001g0173others(1): Show | 4 | HG01261.hp1 HG01346.hp1 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.276+4423G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | chr20 | 48946410 | ||||||
| chr20:48946477
|
T | TTA | 109 | a0001c0001t0007g0041a0001c0001t0007g0042a0001c0002t0001g0122others(106): Show | 109 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(106): Show |
intron_variant | MODIFIER | c.276+4508_276+4509d others(4): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr20 | 48946477 | |||||
| chr20:48946477
|
TTA | T | 132 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0009others(129): Show | 132 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(129): Show |
intron_variant | MODIFIER | c.276+4508_276+4509d others(4): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr20 | 48946477 | |||||
| chr20:48946495
|
A | ATT | 4 | a0001c0001t0002g0198a0001c0002t0001g0282a0001c0002t0001g0283others(1): Show | 4 | HG00673.hp2 NA18949.hp1 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.276+4512_276+4513d others(4): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr20 | 48946495 | |||||
| chr20:48946495
|
A | T | 1 | a0001c0001t0002g0261 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.276+4508A>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | chr20 | 48946495 | ||||||
| chr20:48946579
|
G | A | 1 | a0004c0008t0002g0264 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.276+4592G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | chr20 | 48946579 | ||||||
| chr20:48946727
|
G | A | 1 | a0001c0003t0001g0058 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.277-4596G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | chr20 | 48946727 | ||||||
| chr20:48946753
|
G | A | 3 | a0001c0005t0008g0267a0001c0005t0008g0268a0001c0005t0008g0276 | 3 | HG02486.hp2 HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.277-4570G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | chr20 | 48946753 | ||||||
| chr20:48947081
|
A | T | 1 | a0001c0003t0001g0095 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.277-4242A>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | chr20 | 48947081 | ||||||
| chr20:48947362
|
T | A | 5 | a0001c0001t0004g0327a0001c0001t0004g0333a0001c0001t0004g0334others(2): Show | 5 | NA18952.hp1 NA18954.hp2 NA18966.hp2 others(2): Show |
intron_variant | MODIFIER | c.277-3961T>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | chr20 | 48947362 | ||||||
| chr20:48947397
|
C | T | 1 | a0001c0002t0005g0020 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.277-3926C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | chr20 | 48947397 | ||||||
| chr20:48947599
|
G | A | 1 | a0001c0013t0003g0206 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.277-3724G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | chr20 | 48947599 | ||||||
| chr20:48947742
|
A | C | 1 | a0001c0003t0001g0098 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.277-3581A>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | chr20 | 48947742 | ||||||
| chr20:48948218
|
C | G | 1 | a0001c0001t0002g0271 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.277-3105C>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | chr20 | 48948218 | ||||||
| chr20:48948286
|
G | A | 5 | a0001c0001t0002g0220a0001c0001t0002g0244a0001c0001t0002g0277others(2): Show | 5 | HG01243.hp2 HG02615.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.277-3037G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | chr20 | 48948286 | ||||||
| chr20:48948349
|
C | T | 3 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0014 | 3 | HG01891.hp2 NA18522.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.277-2974C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | chr20 | 48948349 | ||||||
| chr20:48948350
|
G | A | 4 | a0001c0002t0001g0142a0001c0002t0001g0143a0001c0002t0001g0173others(1): Show | 4 | HG01261.hp1 HG01346.hp1 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.277-2973G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | chr20 | 48948350 | ||||||
| chr20:48948525
|
G | A | 1 | a0001c0001t0002g0116 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.277-2798G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | chr20 | 48948525 | ||||||
| chr20:48948525
|
G | T | 15 | a0001c0002t0005g0001a0001c0002t0005g0015a0001c0002t0005g0016others(12): Show | 16 | HG01109.hp1 HG01884.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.277-2798G>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | chr20 | 48948525 | ||||||
| chr20:48948664
|
C | T | 1 | a0001c0001t0002g0253 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.277-2659C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | chr20 | 48948664 | ||||||
| chr20:48948908
|
C | T | 1 | a0001c0003t0001g0104 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.277-2415C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | chr20 | 48948908 | ||||||
| chr20:48948993
|
G | A | 1 | a0001c0001t0002g0252 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.277-2330G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | chr20 | 48948993 | ||||||
| chr20:48949188
|
G | A | 4 | a0001c0001t0004g0332a0001c0001t0004g0343a0001c0001t0004g0344others(1): Show | 4 | HG00738.hp1 HG01934.hp1 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.277-2135G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | chr20 | 48949188 | ||||||
| chr20:48949211
|
C | T | 1 | a0001c0002t0001g0006 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.277-2112C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | chr20 | 48949211 | ||||||
| chr20:48949236
|
G | A | 5 | a0001c0001t0002g0220a0001c0001t0002g0244a0001c0001t0002g0277others(2): Show | 5 | HG01243.hp2 HG02615.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.277-2087G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | chr20 | 48949236 | ||||||
| chr20:48949242
|
C | A | 211 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0009others(208): Show | 212 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(209): Show |
intron_variant | MODIFIER | c.277-2081C>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | chr20 | 48949242 | ||||||
| chr20:48949250
|
A | G | 1 | a0001c0002t0005g0027 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.277-2073A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | chr20 | 48949250 | ||||||
| chr20:48949327
|
C | A | 10 | a0001c0002t0005g0001a0001c0002t0005g0015a0001c0002t0005g0016others(7): Show | 11 | HG01109.hp1 HG01884.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.277-1996C>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | chr20 | 48949327 | ||||||
| chr20:48949693
|
A | G | 3 | a0001c0001t0014g0223a0001c0001t0014g0224a0001c0001t0021g0225 | 3 | HG02895.hp2 HG02897.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.277-1630A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | chr20 | 48949693 | ||||||
| chr20:48950316
|
A | G | 1 | a0001c0003t0001g0082 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.277-1007A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | chr20 | 48950316 | ||||||
| chr20:48950412
|
T | C | 2 | a0001c0002t0001g0318a0001c0002t0015g0319 | 2 | HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.277-911T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | chr20 | 48950412 | ||||||
| chr20:48950626
|
T | C | 2 | a0001c0002t0001g0318a0001c0002t0015g0319 | 2 | HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.277-697T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | chr20 | 48950626 | ||||||
| chr20:48950628
|
T | C | 2 | a0001c0002t0001g0318a0001c0002t0015g0319 | 2 | HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.277-695T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | chr20 | 48950628 | ||||||
| chr20:48950630
|
C | G | 2 | a0001c0002t0001g0318a0001c0002t0015g0319 | 2 | HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.277-693C>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | chr20 | 48950630 | ||||||
| chr20:48950787
|
C | A | 5 | a0002c0004t0001g0144a0002c0004t0001g0145a0002c0004t0001g0146others(2): Show | 5 | NA18975.hp1 NA18983.hp2 NA19070.hp1 others(2): Show |
intron_variant | MODIFIER | c.277-536C>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | chr20 | 48950787 | ||||||
| chr20:48950794
|
TA | T | 6 | a0001c0003t0001g0047a0001c0003t0001g0074a0001c0003t0001g0075others(3): Show | 6 | HG00438.hp2 HG01943.hp2 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.277-511delA | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr20 | 48950794 | |||||
| chr20:48950794
|
TAA | T | 8 | a0001c0003t0001g0032a0001c0003t0001g0057a0001c0003t0001g0077others(5): Show | 8 | HG00639.hp1 HG01243.hp1 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.277-512_277-511del others(2): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr20 | 48950794 | |||||
| chr20:48950805
|
A | AATATATA others(3): Show |
1 | a0001c0002t0009g0291 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.277-517_277-516ins others(10): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr20 | 48950805 | |||||
| chr20:48950805
|
A | AATATATA others(9): Show |
1 | a0001c0002t0001g0290 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.277-517_277-516ins others(16): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr20 | 48950805 | |||||
| chr20:48950805
|
A | ATATATAT others(6): Show |
1 | a0001c0002t0001g0292 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.277-518_277-517ins others(13): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | chr20 | 48950805 | ||||||
| chr20:48950805
|
A | ATATATAT others(18): Show |
1 | a0001c0002t0001g0307 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.277-518_277-517ins others(25): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | chr20 | 48950805 | ||||||
| chr20:48950806
|
AAAAAAAT others(10): Show |
A | 1 | a0001c0016t0001g0028 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.277-515_277-499del others(17): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr20 | 48950806 | |||||
| chr20:48950807
|
A | AATATATA others(5): Show |
1 | a0001c0003t0001g0104 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.277-515_277-514ins others(12): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr20 | 48950807 | |||||
| chr20:48950807
|
A | AATATATA others(7): Show |
2 | a0001c0002t0001g0311a0008c0009t0001g0289 | 2 | HG03654.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.277-515_277-514ins others(14): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr20 | 48950807 | |||||
| chr20:48950807
|
A | AATATATA others(11): Show |
2 | a0001c0002t0001g0283a0001c0002t0001g0309 | 2 | NA19081.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.277-515_277-514ins others(18): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr20 | 48950807 | |||||
| chr20:48950807
|
A | AATATATA others(13): Show |
3 | a0001c0001t0002g0198a0001c0002t0001g0123a0001c0002t0001g0310 | 3 | NA18960.hp1 NA18970.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.277-515_277-514ins others(20): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr20 | 48950807 | |||||
| chr20:48950807
|
A | ATATATAT others(18): Show |
1 | a0001c0002t0001g0284 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.277-516_277-515ins others(25): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | chr20 | 48950807 | ||||||
| chr20:48950807
|
A | T | 7 | a0001c0002t0001g0290a0001c0002t0001g0292a0001c0002t0001g0307others(4): Show | 7 | HG00639.hp1 HG01081.hp2 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.277-516A>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | chr20 | 48950807 | ||||||
| chr20:48950807
|
AAAAAATA others(3): Show |
A | 3 | a0001c0001t0004g0321a0001c0001t0004g0341a0001c0002t0001g0282 | 3 | HG00673.hp2 NA19054.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.277-514_277-505del others(10): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr20 | 48950807 | |||||
| chr20:48950807
|
AAAAAATA others(7): Show |
A | 1 | a0001c0002t0005g0023 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.277-514_277-501del others(14): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr20 | 48950807 | |||||
| chr20:48950807
|
AAAAAATA others(9): Show |
A | 9 | a0001c0002t0001g0314a0001c0002t0005g0001a0001c0002t0005g0015others(6): Show | 10 | HG00741.hp2 HG01884.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.277-514_277-499del others(16): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr20 | 48950807 | |||||
| chr20:48950808
|
AAAAATAT others(4): Show |
A | 1 | a0001c0001t0004g0343 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.277-513_277-503del others(11): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr20 | 48950808 | |||||
| chr20:48950808
|
AAAAATAT others(10): Show |
A | 2 | a0001c0002t0005g0026a0001c0002t0005g0027 | 2 | HG02970.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.277-513_277-497del others(17): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr20 | 48950808 | |||||
| chr20:48950809
|
A | AATATATA others(3): Show |
1 | a0001c0002t0001g0285 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.277-513_277-512ins others(10): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr20 | 48950809 | |||||
| chr20:48950809
|
A | AATATATA others(5): Show |
2 | a0001c0002t0001g0124a0001c0002t0001g0300 | 2 | HG02071.hp2 HG02080.hp2 |
intron_variant | MODIFIER | c.277-513_277-512ins others(12): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr20 | 48950809 | |||||
| chr20:48950809
|
A | AATATATA others(7): Show |
2 | a0001c0002t0001g0286a0001c0002t0001g0295 | 2 | HG01071.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.277-513_277-512ins others(14): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr20 | 48950809 | |||||
| chr20:48950809
|
A | AATATATA others(9): Show |
1 | a0001c0002t0001g0304 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.277-513_277-512ins others(16): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr20 | 48950809 | |||||
| chr20:48950809
|
A | AATATATA others(11): Show |
2 | a0001c0002t0001g0122a0001c0002t0001g0297 | 2 | NA19001.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.277-513_277-512ins others(18): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr20 | 48950809 | |||||
| chr20:48950809
|
A | AATATATA others(13): Show |
1 | a0001c0002t0001g0294 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.277-513_277-512ins others(20): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr20 | 48950809 | |||||
| chr20:48950809
|
A | T | 19 | a0001c0001t0002g0198a0001c0002t0001g0123a0001c0002t0001g0283others(16): Show | 19 | HG00639.hp1 HG01081.hp2 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.277-514A>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | chr20 | 48950809 | ||||||
| chr20:48950809
|
AAAATATA others(3): Show |
A | 21 | a0001c0001t0004g0323a0001c0001t0004g0324a0001c0001t0004g0327others(18): Show | 21 | HG00673.hp1 HG00738.hp1 HG01934.hp1 others(18): Show |
intron_variant | MODIFIER | c.277-512_277-503del others(10): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr20 | 48950809 | |||||
| chr20:48950809
|
AAAATATA others(5): Show |
A | 1 | a0001c0002t0001g0313 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.277-512_277-501del others(12): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr20 | 48950809 | |||||
| chr20:48950809
|
AAAATATA others(7): Show |
A | 2 | a0001c0002t0005g0019a0001c0002t0005g0024 | 2 | HG02622.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.277-512_277-499del others(14): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr20 | 48950809 | |||||
| chr20:48950809
|
AAAATATA others(9): Show |
A | 2 | a0001c0002t0005g0021a0001c0002t0005g0025 | 2 | HG01891.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.277-512_277-497del others(16): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr20 | 48950809 | |||||
| chr20:48950809
|
AAAATATA others(11): Show |
A | 1 | a0001c0001t0013g0322 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.277-512_277-495del others(18): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr20 | 48950809 | |||||
| chr20:48950810
|
AAATATAT others(12): Show |
A | 1 | a0001c0001t0002g0260 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.277-511_277-493del others(19): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr20 | 48950810 | |||||
| chr20:48950810
|
AAATATAT others(14): Show |
A | 3 | a0001c0001t0014g0223a0001c0001t0014g0224a0001c0001t0021g0225 | 3 | HG02895.hp2 HG02897.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.277-511_277-491del others(21): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr20 | 48950810 | |||||
| chr20:48950811
|
A | AATATATA others(3): Show |
1 | a0001c0002t0001g0308 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.277-485_277-476dup others(10): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr20 | 48950811 | |||||
| chr20:48950811
|
A | AATATATA others(5): Show |
1 | a0001c0002t0001g0298 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.277-487_277-476dup others(12): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr20 | 48950811 | |||||
| chr20:48950811
|
A | ATATATAT others(6): Show |
1 | a0001c0002t0001g0287 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.277-512_277-511ins others(13): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | chr20 | 48950811 | ||||||
| chr20:48950811
|
A | ATATATAT others(12): Show |
1 | a0001c0002t0001g0293 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.277-512_277-511ins others(19): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | chr20 | 48950811 | ||||||
| chr20:48950811
|
A | ATATATAT others(14): Show |
1 | a0001c0002t0001g0306 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.277-512_277-511ins others(21): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | chr20 | 48950811 | ||||||
| chr20:48950811
|
A | T | 37 | a0001c0001t0002g0198a0001c0002t0001g0122a0001c0002t0001g0123others(34): Show | 37 | HG00639.hp1 HG00741.hp1 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.277-512A>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | chr20 | 48950811 | ||||||
| chr20:48950811
|
AAT | A | 33 | a0001c0001t0002g0243a0001c0002t0001g0002a0001c0002t0001g0004others(30): Show | 34 | HG00438.hp1 HG01099.hp1 HG01123.hp1 others(31): Show |
intron_variant | MODIFIER | c.277-477_277-476del others(2): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr20 | 48950811 | |||||
| chr20:48950811
|
AATAT | A | 46 | a0001c0001t0002g0220a0001c0001t0002g0230a0001c0001t0002g0244others(43): Show | 46 | HG00280.hp2 HG00323.hp1 HG00609.hp2 others(43): Show |
intron_variant | MODIFIER | c.277-479_277-476del others(4): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr20 | 48950811 | |||||
| chr20:48950811
|
AATATAT | A | 30 | a0001c0001t0002g0009a0001c0001t0002g0013a0001c0001t0002g0218others(27): Show | 30 | HG00323.hp2 HG00639.hp2 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.277-481_277-476del others(6): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr20 | 48950811 | |||||
| chr20:48950811
|
AATATATA others(1): Show |
A | 10 | a0001c0001t0001g0170a0001c0001t0002g0008a0001c0001t0002g0010others(7): Show | 10 | HG01891.hp2 HG02486.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.277-483_277-476del others(8): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr20 | 48950811 | |||||
| chr20:48950811
|
AATATATA others(5): Show |
A | 4 | a0001c0002t0001g0137a0001c0002t0001g0166a0001c0002t0001g0167others(1): Show | 4 | HG01169.hp1 HG01978.hp2 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.277-487_277-476del others(12): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr20 | 48950811 | |||||
| chr20:48950811
|
AATATATA others(7): Show |
A | 1 | a0001c0002t0001g0175 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.277-489_277-476del others(14): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr20 | 48950811 | |||||
| chr20:48950811
|
AATATATA others(9): Show |
A | 2 | a0001c0002t0001g0315a0001c0002t0001g0316 | 2 | HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.277-491_277-476del others(16): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr20 | 48950811 | |||||
| chr20:48950811
|
AATATATA others(13): Show |
A | 7 | a0001c0003t0001g0030a0001c0003t0001g0052a0001c0003t0001g0055others(4): Show | 7 | NA18948.hp2 NA18980.hp1 NA18983.hp1 others(4): Show |
intron_variant | MODIFIER | c.277-495_277-476del others(20): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr20 | 48950811 | |||||
| chr20:48950812
|
AT | A | 3 | a0001c0002t0001g0112a0001c0002t0001g0127a0001c0002t0001g0194 | 3 | HG01433.hp2 HG04184.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.277-510delT | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | chr20 | 48950812 | ||||||
| chr20:48950812
|
ATAT | A | 5 | a0001c0001t0002g0003a0001c0001t0002g0248a0001c0001t0007g0241others(2): Show | 5 | HG01433.hp1 HG03041.hp1 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.277-510_277-508del others(3): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | chr20 | 48950812 | ||||||
| chr20:48950812
|
ATATAT | A | 24 | a0001c0001t0002g0119a0001c0001t0002g0221a0001c0001t0002g0250others(21): Show | 24 | HG00733.hp1 HG01175.hp1 HG01175.hp2 others(21): Show |
intron_variant | MODIFIER | c.277-510_277-506del others(5): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | chr20 | 48950812 | ||||||
| chr20:48950812
|
ATATATAT | A | 26 | a0001c0001t0002g0117a0001c0001t0002g0118a0001c0001t0002g0120others(23): Show | 26 | HG00280.hp1 HG00733.hp2 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.277-510_277-504del others(7): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | chr20 | 48950812 | ||||||
| chr20:48950812
|
ATATATAT others(2): Show |
A | 3 | a0001c0001t0002g0253a0001c0002t0001g0318a0001c0002t0015g0319 | 3 | HG03139.hp1 HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.277-510_277-502del others(9): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | chr20 | 48950812 | ||||||
| chr20:48950812
|
ATATATAT others(12): Show |
A | 1 | a0001c0003t0001g0107 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.277-510_277-492del others(19): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | chr20 | 48950812 | ||||||
| chr20:48950813
|
T | A | 3 | a0001c0002t0001g0109a0001c0002t0001g0179a0001c0003t0001g0317 | 3 | HG01106.hp1 HG04115.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.277-510T>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | chr20 | 48950813 | ||||||
| chr20:48950815
|
T | A | 28 | a0001c0001t0002g0243a0001c0002t0001g0002a0001c0002t0001g0004others(25): Show | 29 | HG00438.hp1 HG01099.hp1 HG01123.hp1 others(26): Show |
intron_variant | MODIFIER | c.277-508T>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | chr20 | 48950815 | ||||||
| chr20:48950817
|
T | A | 48 | a0001c0001t0002g0220a0001c0001t0002g0230a0001c0001t0002g0243others(45): Show | 48 | HG00280.hp2 HG00323.hp1 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.277-506T>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | chr20 | 48950817 | ||||||
| chr20:48950819
|
T | A | 54 | a0001c0001t0002g0218a0001c0001t0002g0219a0001c0001t0002g0220others(51): Show | 54 | HG00323.hp2 HG00639.hp2 HG00738.hp2 others(51): Show |
intron_variant | MODIFIER | c.277-504T>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | chr20 | 48950819 | ||||||
| chr20:48950821
|
T | A | 45 | a0001c0001t0001g0170a0001c0001t0002g0117a0001c0001t0002g0218others(42): Show | 45 | HG00323.hp2 HG00639.hp2 HG01081.hp1 others(42): Show |
intron_variant | MODIFIER | c.277-502T>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | chr20 | 48950821 | ||||||
| chr20:48950823
|
T | A | 13 | a0001c0001t0002g0221a0001c0001t0002g0222a0001c0001t0002g0245others(10): Show | 13 | HG01255.hp2 HG01361.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.277-500T>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | chr20 | 48950823 | ||||||
| chr20:48950825
|
T | A | 4 | a0001c0002t0001g0137a0001c0002t0001g0166a0001c0002t0001g0167others(1): Show | 4 | HG01169.hp1 HG01978.hp2 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.277-498T>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | chr20 | 48950825 | ||||||
| chr20:48950827
|
T | A | 1 | a0001c0002t0001g0175 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.277-496T>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | chr20 | 48950827 | ||||||
| chr20:48950844
|
A | G | 4 | a0001c0002t0022g0197a0001c0003t0001g0057a0001c0003t0001g0091others(1): Show | 4 | HG01243.hp1 HG01261.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.277-479A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | chr20 | 48950844 | ||||||
| chr20:48950846
|
ATG | A | 3 | a0001c0003t0001g0035a0001c0003t0001g0051a0001c0003t0001g0062 | 3 | HG04184.hp2 NA18985.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.277-475_277-474del others(2): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr20 | 48950846 | |||||
| chr20:48950848
|
G | A | 4 | a0001c0001t0014g0223a0001c0001t0014g0224a0001c0001t0021g0225others(1): Show | 4 | HG02895.hp2 HG02897.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.277-475G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | chr20 | 48950848 | ||||||
| chr20:48950862
|
G | GCA | 6 | a0001c0001t0002g0259a0001c0001t0003g0212a0001c0002t0001g0195others(3): Show | 6 | HG00609.hp1 NA18944.hp1 NA18952.hp2 others(3): Show |
intron_variant | MODIFIER | c.277-442_277-441dup others(2): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr20 | 48950862 | |||||
| chr20:48950862
|
GCACA | G | 3 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0014 | 3 | HG01891.hp2 NA18522.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.277-444_277-441del others(4): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr20 | 48950862 | |||||
| chr20:48951183
|
G | A | 1 | a0001c0002t0001g0187 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.277-140G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | chr20 | 48951183 | ||||||
| chr20:48951202
|
C | A | 21 | a0001c0002t0001g0313a0001c0002t0001g0314a0001c0002t0001g0318others(18): Show | 22 | HG00741.hp2 HG01109.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.277-121C>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | chr20 | 48951202 | ||||||
| chr20:48951253
|
G | C | 1 | a0001c0001t0003g0202 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.277-70G>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | chr20 | 48951253 | ||||||
| chr20:48951264
|
C | T | 20 | a0001c0001t0002g0003a0001c0001t0002g0116a0001c0001t0002g0117others(17): Show | 20 | HG00280.hp1 HG00558.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.277-59C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | chr20 | 48951264 | ||||||
| chr20:48951472
|
A | G | 1 | a0001c0003t0001g0076 | 1 | HG01943.hp2 | splice_region_variant&intron_variant | LOW | c.423+3A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 4/38 | chr20 | 48951472 | ||||||
| chr20:48951745
|
A | ACCCTGGA others(71): Show |
1 | a0001c0001t0003g0200 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.423+277_423+354dup others(78): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 4/38 | INFO_REALIGN_3_PRIME | chr20 | 48951745 | |||||
| chr20:48951829
|
G | A | 1 | a0001c0002t0022g0197 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.423+360G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 4/38 | chr20 | 48951829 | ||||||
| chr20:48951867
|
C | T | 21 | a0001c0002t0001g0313a0001c0002t0001g0314a0001c0002t0001g0318others(18): Show | 22 | HG00741.hp2 HG01109.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.423+398C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 4/38 | chr20 | 48951867 | ||||||
| chr20:48951877
|
T | C | 1 | a0001c0002t0001g0172 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.423+408T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 4/38 | chr20 | 48951877 | ||||||
| chr20:48951884
|
A | G | 1 | a0001c0002t0001g0297 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.423+415A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 4/38 | chr20 | 48951884 | ||||||
| chr20:48952034
|
A | G | 2 | a0001c0001t0002g0228a0001c0001t0002g0229 | 2 | HG02622.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.423+565A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 4/38 | chr20 | 48952034 | ||||||
| chr20:48952121
|
G | A | 272 | a0001c0001t0001g0170a0001c0001t0002g0003a0001c0001t0002g0008others(269): Show | 274 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(271): Show |
intron_variant | MODIFIER | c.424-584G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 4/38 | chr20 | 48952121 | ||||||
| chr20:48952148
|
C | CT | 11 | a0001c0001t0002g0253a0001c0001t0004g0326a0001c0001t0004g0334others(8): Show | 11 | HG00621.hp1 HG00673.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.424-532dupT | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 4/38 | INFO_REALIGN_3_PRIME | chr20 | 48952148 | |||||
| chr20:48952148
|
CT | C | 250 | a0001c0001t0001g0170a0001c0001t0002g0003a0001c0001t0002g0008others(247): Show | 251 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(248): Show |
intron_variant | MODIFIER | c.424-532delT | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 4/38 | INFO_REALIGN_3_PRIME | chr20 | 48952148 | |||||
| chr20:48952148
|
CTT | C | 23 | a0001c0001t0002g0270a0001c0001t0003g0212a0001c0001t0003g0238others(20): Show | 24 | HG01109.hp1 HG01169.hp2 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.424-533_424-532del others(2): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 4/38 | INFO_REALIGN_3_PRIME | chr20 | 48952148 | |||||
| chr20:48952387
|
C | T | 1 | a0001c0002t0001g0196 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.424-318C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 4/38 | chr20 | 48952387 | ||||||
| chr20:48952475
|
C | T | 1 | a0001c0001t0002g0221 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.424-230C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 4/38 | chr20 | 48952475 | ||||||
| chr20:48952575
|
C | A | 112 | a0001c0002t0001g0122a0001c0002t0001g0123a0001c0002t0001g0124others(109): Show | 112 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.424-130C>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 4/38 | chr20 | 48952575 | ||||||
| chr20:48952689
|
C | T | 20 | a0001c0001t0002g0003a0001c0001t0002g0116a0001c0001t0002g0117others(17): Show | 20 | HG00280.hp1 HG00558.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.424-16C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 4/38 | chr20 | 48952689 | ||||||
| chr20:48953142
|
TTTTC | T | 3 | a0001c0005t0008g0267a0001c0005t0008g0268a0001c0005t0008g0276 | 3 | HG02486.hp2 HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.603+278_603+281del others(4): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 5/38 | INFO_REALIGN_3_PRIME | chr20 | 48953142 | |||||
| chr20:48953166
|
T | C | 44 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0009others(41): Show | 44 | HG00280.hp1 HG00558.hp2 HG01106.hp2 others(41): Show |
intron_variant | MODIFIER | c.603+282T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 5/38 | chr20 | 48953166 | ||||||
| chr20:48953468
|
G | T | 1 | a0001c0001t0002g0009 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.604-88G>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 5/38 | chr20 | 48953468 | ||||||
| chr20:48953521
|
C | G | 1 | a0001c0001t0001g0170 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.604-35C>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 5/38 | chr20 | 48953521 | ||||||
| chr20:48953972
|
C | A | 1 | a0001c0016t0001g0028 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.838+182C>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48953972 | ||||||
| chr20:48954021
|
G | A | 1 | a0001c0002t0001g0313 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.838+231G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48954021 | ||||||
| chr20:48954036
|
T | C | 5 | a0001c0003t0001g0029a0001c0003t0001g0031a0001c0003t0001g0059others(2): Show | 5 | HG02683.hp1 HG03491.hp1 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.838+246T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48954036 | ||||||
| chr20:48954661
|
A | G | 3 | a0001c0001t0002g0254a0001c0001t0002g0263a0001c0001t0002g0265 | 3 | NA18971.hp1 NA19068.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.838+871A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48954661 | ||||||
| chr20:48954791
|
G | A | 5 | a0001c0002t0001g0318a0001c0002t0015g0319a0001c0005t0008g0267others(2): Show | 5 | HG02486.hp2 HG02970.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.838+1001G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48954791 | ||||||
| chr20:48954817
|
G | A | 2 | a0001c0002t0001g0307a0001c0002t0001g0311 | 2 | NA18971.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.838+1027G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48954817 | ||||||
| chr20:48954861
|
G | A | 4 | a0001c0003t0001g0035a0001c0003t0001g0051a0001c0003t0001g0062others(1): Show | 4 | HG04184.hp2 NA18981.hp1 NA18985.hp2 others(1): Show |
intron_variant | MODIFIER | c.838+1071G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48954861 | ||||||
| chr20:48955014
|
C | G | 269 | a0001c0001t0001g0170a0001c0001t0002g0003a0001c0001t0002g0008others(266): Show | 270 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(267): Show |
intron_variant | MODIFIER | c.838+1224C>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48955014 | ||||||
| chr20:48955124
|
C | G | 1 | a0001c0001t0003g0237 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.838+1334C>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48955124 | ||||||
| chr20:48955197
|
C | T | 2 | a0001c0003t0001g0040a0001c0003t0001g0092 | 2 | HG01123.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.838+1407C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48955197 | ||||||
| chr20:48955330
|
G | A | 112 | a0001c0002t0001g0122a0001c0002t0001g0123a0001c0002t0001g0124others(109): Show | 112 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.838+1540G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48955330 | ||||||
| chr20:48955409
|
C | A | 1 | a0001c0003t0001g0107 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.838+1619C>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48955409 | ||||||
| chr20:48955556
|
A | G | 1 | a0001c0001t0002g0233 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.838+1766A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48955556 | ||||||
| chr20:48955727
|
A | T | 1 | a0001c0003t0001g0092 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.838+1937A>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48955727 | ||||||
| chr20:48955745
|
G | A | 135 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0009others(132): Show | 135 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(132): Show |
intron_variant | MODIFIER | c.838+1955G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48955745 | ||||||
| chr20:48955863
|
A | G | 1 | a0001c0016t0001g0028 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.838+2073A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48955863 | ||||||
| chr20:48956089
|
G | A | 35 | a0001c0002t0001g0122a0001c0002t0001g0123a0001c0002t0001g0124others(32): Show | 35 | HG00639.hp1 HG00673.hp2 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.838+2299G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48956089 | ||||||
| chr20:48956162
|
T | C | 3 | a0001c0005t0008g0267a0001c0005t0008g0268a0001c0005t0008g0276 | 3 | HG02486.hp2 HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.838+2372T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48956162 | ||||||
| chr20:48956309
|
C | G | 4 | a0001c0001t0002g0253a0001c0001t0014g0223a0001c0001t0014g0224others(1): Show | 4 | HG02895.hp2 HG02897.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.838+2519C>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48956309 | ||||||
| chr20:48956780
|
A | G | 2 | a0001c0001t0002g0009a0001c0001t0002g0013 | 2 | HG02723.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.838+2990A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48956780 | ||||||
| chr20:48956795
|
A | G | 3 | a0001c0003t0001g0032a0001c0003t0001g0079a0001c0003t0001g0083 | 3 | HG00609.hp1 NA18944.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.838+3005A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48956795 | ||||||
| chr20:48956871
|
C | T | 19 | a0001c0002t0001g0313a0001c0002t0001g0314a0001c0002t0005g0001others(16): Show | 20 | HG00741.hp2 HG01109.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.838+3081C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48956871 | ||||||
| chr20:48956879
|
C | G | 51 | a0001c0001t0002g0220a0001c0001t0002g0221a0001c0001t0002g0222others(48): Show | 51 | HG00323.hp2 HG00639.hp2 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.838+3089C>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48956879 | ||||||
| chr20:48956972
|
G | A | 1 | a0001c0003t0001g0091 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.838+3182G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48956972 | ||||||
| chr20:48957061
|
G | A | 247 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0009others(244): Show | 247 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(244): Show |
intron_variant | MODIFIER | c.838+3271G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48957061 | ||||||
| chr20:48957163
|
A | T | 4 | a0001c0002t0001g0134a0001c0002t0001g0161a0001c0002t0001g0168others(1): Show | 4 | HG00438.hp1 HG02074.hp1 HG02080.hp1 others(1): Show |
intron_variant | MODIFIER | c.838+3373A>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48957163 | ||||||
| chr20:48957274
|
C | A | 1 | a0001c0001t0002g0118 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.838+3484C>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48957274 | ||||||
| chr20:48957466
|
C | T | 112 | a0001c0002t0001g0122a0001c0002t0001g0123a0001c0002t0001g0124others(109): Show | 112 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.838+3676C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48957466 | ||||||
| chr20:48957513
|
G | A | 2 | a0001c0001t0002g0280a0001c0001t0002g0281 | 2 | HG01884.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.838+3723G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48957513 | ||||||
| chr20:48957515
|
G | T | 35 | a0001c0002t0001g0122a0001c0002t0001g0123a0001c0002t0001g0124others(32): Show | 35 | HG00639.hp1 HG00673.hp2 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.838+3725G>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48957515 | ||||||
| chr20:48957561
|
C | A | 1 | a0001c0001t0003g0246 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.838+3771C>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48957561 | ||||||
| chr20:48957631
|
A | G | 1 | a0001c0001t0003g0208 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.838+3841A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48957631 | ||||||
| chr20:48957643
|
G | A | 3 | a0001c0003t0001g0070a0001c0003t0001g0085a0001c0003t0001g0093 | 3 | HG00558.hp1 HG02132.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.838+3853G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48957643 | ||||||
| chr20:48957658
|
A | G | 1 | a0001c0003t0001g0060 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.838+3868A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48957658 | ||||||
| chr20:48957794
|
A | G | 1 | a0001c0003t0001g0317 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.838+4004A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48957794 | ||||||
| chr20:48957882
|
C | G | 1 | a0001c0002t0001g0304 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.838+4092C>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48957882 | ||||||
| chr20:48957915
|
A | C | 2 | a0001c0001t0002g0226a0001c0001t0002g0227 | 2 | HG02559.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.838+4125A>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48957915 | ||||||
| chr20:48958181
|
A | AACACACA others(20): Show |
1 | a0001c0001t0003g0212 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.838+4392_838+4418d others(29): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr20 | 48958181 | |||||
| chr20:48958210
|
T | A | 36 | a0001c0001t0002g0120a0001c0001t0002g0240a0001c0001t0003g0113others(33): Show | 36 | HG00323.hp2 HG00639.hp2 HG00733.hp2 others(33): Show |
intron_variant | MODIFIER | c.838+4420T>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48958210 | ||||||
| chr20:48958383
|
G | A | 29 | a0001c0001t0004g0321a0001c0001t0004g0323a0001c0001t0004g0324others(26): Show | 29 | HG00673.hp1 HG00738.hp1 HG01934.hp1 others(26): Show |
intron_variant | MODIFIER | c.838+4593G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48958383 | ||||||
| chr20:48958440
|
C | CT | 102 | a0001c0001t0002g0198a0001c0002t0001g0122a0001c0002t0001g0123others(99): Show | 102 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(99): Show |
intron_variant | MODIFIER | c.838+4664dupT | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr20 | 48958440 | |||||
| chr20:48958440
|
C | CTT | 11 | a0001c0003t0001g0032a0001c0003t0001g0039a0001c0003t0001g0043others(8): Show | 11 | HG00438.hp2 HG00609.hp1 HG01981.hp2 others(8): Show |
intron_variant | MODIFIER | c.838+4663_838+4664d others(4): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr20 | 48958440 | |||||
| chr20:48958440
|
CT | C | 7 | a0001c0001t0003g0207a0001c0001t0011g0269a0001c0002t0001g0132others(4): Show | 7 | HG00323.hp1 HG01255.hp2 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.838+4664delT | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr20 | 48958440 | |||||
| chr20:48958449
|
T | C | 1 | a0001c0002t0001g0313 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.838+4659T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48958449 | ||||||
| chr20:48958603
|
AT | A | 134 | a0001c0001t0002g0198a0001c0001t0004g0339a0001c0001t0011g0269others(131): Show | 135 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(132): Show |
intron_variant | MODIFIER | c.838+4825delT | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr20 | 48958603 | |||||
| chr20:48958606
|
T | G | 1 | a0001c0003t0001g0074 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.838+4816T>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48958606 | ||||||
| chr20:48958663
|
C | T | 3 | a0001c0002t0001g0138a0001c0002t0001g0139a0001c0002t0001g0172 | 3 | NA18981.hp2 NA18984.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.838+4873C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48958663 | ||||||
| chr20:48958664
|
G | C | 45 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0009others(42): Show | 45 | HG00280.hp1 HG00558.hp2 HG01106.hp2 others(42): Show |
intron_variant | MODIFIER | c.838+4874G>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48958664 | ||||||
| chr20:48958908
|
T | TGAGGCAA others(4): Show |
1 | a0001c0001t0003g0113 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.839-4920_839-4910d others(13): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr20 | 48958908 | |||||
| chr20:48959065
|
G | A | 1 | a0001c0002t0001g0112 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.839-4765G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48959065 | ||||||
| chr20:48959190
|
A | G | 1 | a0001c0002t0005g0019 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.839-4640A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48959190 | ||||||
| chr20:48959229
|
G | A | 1 | a0006c0011t0001g0301 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.839-4601G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48959229 | ||||||
| chr20:48959271
|
T | C | 1 | a0001c0002t0001g0190 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.839-4559T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48959271 | ||||||
| chr20:48959290
|
A | T | 1 | a0001c0003t0001g0074 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.839-4540A>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48959290 | ||||||
| chr20:48959291
|
T | A | 1 | a0001c0003t0001g0074 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.839-4539T>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48959291 | ||||||
| chr20:48959355
|
C | A | 1 | a0001c0001t0003g0212 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.839-4475C>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48959355 | ||||||
| chr20:48959359
|
T | G | 1 | a0001c0001t0003g0212 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.839-4471T>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48959359 | ||||||
| chr20:48959361
|
A | G | 1 | a0001c0001t0003g0212 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.839-4469A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48959361 | ||||||
| chr20:48959362
|
C | A | 1 | a0001c0001t0003g0212 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.839-4468C>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48959362 | ||||||
| chr20:48959363
|
A | T | 1 | a0001c0001t0003g0212 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.839-4467A>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48959363 | ||||||
| chr20:48959365
|
G | C | 1 | a0001c0001t0003g0212 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.839-4465G>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48959365 | ||||||
| chr20:48959366
|
A | T | 1 | a0001c0001t0003g0212 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.839-4464A>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48959366 | ||||||
| chr20:48959367
|
G | A | 1 | a0001c0001t0003g0212 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.839-4463G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48959367 | ||||||
| chr20:48959372
|
G | C | 1 | a0001c0001t0003g0212 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.839-4458G>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48959372 | ||||||
| chr20:48959389
|
A | C | 1 | a0001c0001t0003g0212 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.839-4441A>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48959389 | ||||||
| chr20:48959390
|
C | CCCTTCCT others(129): Show |
1 | a0001c0002t0001g0313 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.839-4426_839-4425i others(138): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr20 | 48959390 | |||||
| chr20:48959390
|
CCCTTCCT others(5): Show |
C | 1 | a0001c0002t0005g0019 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.839-4425_839-4414d others(14): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr20 | 48959390 | |||||
| chr20:48959394
|
T | C | 1 | a0001c0001t0003g0212 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.839-4436T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48959394 | ||||||
| chr20:48959397
|
T | TTCCCTCC others(133): Show |
10 | a0001c0002t0001g0314a0001c0002t0001g0318a0001c0002t0005g0021others(7): Show | 10 | HG00741.hp2 HG01891.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.839-4426_839-4425i others(142): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr20 | 48959397 | |||||
| chr20:48959397
|
T | TTCCCTCC others(125): Show |
9 | a0001c0002t0005g0001a0001c0002t0005g0015a0001c0002t0005g0016others(6): Show | 10 | HG01109.hp1 HG01884.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.839-4426_839-4425i others(134): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr20 | 48959397 | |||||
| chr20:48959397
|
T | TTCCTTAC others(109): Show |
1 | a0001c0001t0003g0212 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.839-4430_839-4429i others(118): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr20 | 48959397 | |||||
| chr20:48959405
|
T | C | 21 | a0001c0001t0003g0212a0001c0002t0001g0313a0001c0002t0001g0314others(18): Show | 22 | HG00741.hp2 HG01109.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.839-4425T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48959405 | ||||||
| chr20:48959409
|
T | C | 98 | a0001c0001t0003g0212a0001c0002t0001g0313a0001c0002t0001g0314others(95): Show | 99 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(96): Show |
intron_variant | MODIFIER | c.839-4421T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48959409 | ||||||
| chr20:48959417
|
C | A | 21 | a0001c0001t0003g0212a0001c0002t0001g0313a0001c0002t0001g0314others(18): Show | 22 | HG00741.hp2 HG01109.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.839-4413C>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48959417 | ||||||
| chr20:48959427
|
T | G | 21 | a0001c0001t0003g0212a0001c0002t0001g0313a0001c0002t0001g0314others(18): Show | 22 | HG00741.hp2 HG01109.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.839-4403T>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48959427 | ||||||
| chr20:48959449
|
T | C | 1 | a0001c0003t0001g0064 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.839-4381T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48959449 | ||||||
| chr20:48959450
|
T | C | 1 | a0001c0003t0001g0074 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.839-4380T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48959450 | ||||||
| chr20:48959465
|
C | T | 21 | a0001c0001t0003g0212a0001c0002t0001g0313a0001c0002t0001g0314others(18): Show | 22 | HG00741.hp2 HG01109.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.839-4365C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48959465 | ||||||
| chr20:48959467
|
T | C | 1 | a0001c0003t0001g0064 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.839-4363T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48959467 | ||||||
| chr20:48959469
|
T | C | 1 | a0001c0003t0001g0064 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.839-4361T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48959469 | ||||||
| chr20:48959472
|
T | C | 1 | a0001c0003t0001g0064 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.839-4358T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48959472 | ||||||
| chr20:48959479
|
C | CCCTCCCT others(178): Show |
20 | a0001c0002t0001g0313a0001c0002t0001g0314a0001c0002t0001g0318others(17): Show | 21 | HG00741.hp2 HG01109.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.839-4351_839-4350i others(187): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48959479 | ||||||
| chr20:48959479
|
C | CCCTCCCT others(178): Show |
1 | a0001c0001t0003g0212 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.839-4351_839-4350i others(187): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48959479 | ||||||
| chr20:48959479
|
C | CCTCTCCC others(331): Show |
1 | a0001c0001t0013g0320 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.839-4351_839-4350i others(340): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48959479 | ||||||
| chr20:48959479
|
C | CCTTCCCT others(286): Show |
1 | a0001c0003t0001g0064 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.839-4351_839-4350i others(295): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48959479 | ||||||
| chr20:48959479
|
C | CTCTCCCT others(314): Show |
1 | a0001c0003t0001g0074 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.839-4348_839-4347i others(323): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr20 | 48959479 | |||||
| chr20:48959479
|
C | CTCTCCCT others(331): Show |
1 | a0001c0001t0004g0338 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.839-4348_839-4347i others(340): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr20 | 48959479 | |||||
| chr20:48959479
|
C | CTCTCCCT others(330): Show |
2 | a0001c0003t0001g0044a0001c0003t0001g0073 | 2 | NA18965.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.839-4348_839-4347i others(339): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr20 | 48959479 | |||||
| chr20:48959479
|
C | CTCTCCCT others(330): Show |
1 | a0001c0003t0001g0099 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.839-4348_839-4347i others(339): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr20 | 48959479 | |||||
| chr20:48959479
|
C | CTCTCCCT others(334): Show |
1 | a0001c0003t0001g0086 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.839-4348_839-4347i others(343): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr20 | 48959479 | |||||
| chr20:48959479
|
C | CTCTCCCT others(330): Show |
67 | a0001c0003t0001g0029a0001c0003t0001g0030a0001c0003t0001g0031others(64): Show | 67 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.839-4348_839-4347i others(339): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr20 | 48959479 | |||||
| chr20:48959479
|
C | CTCTCCCT others(326): Show |
1 | a0001c0003t0001g0056 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.839-4348_839-4347i others(335): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr20 | 48959479 | |||||
| chr20:48959479
|
C | CTCTCCCT others(326): Show |
1 | a0001c0003t0009g0036 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.839-4348_839-4347i others(335): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr20 | 48959479 | |||||
| chr20:48959479
|
C | CTCTCCCT others(334): Show |
34 | a0001c0001t0002g0198a0001c0002t0001g0122a0001c0002t0001g0123others(31): Show | 34 | HG00639.hp1 HG00673.hp2 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.839-4348_839-4347i others(343): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr20 | 48959479 | |||||
| chr20:48959479
|
C | CTCTCCCT others(333): Show |
1 | a0001c0002t0001g0299 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.839-4348_839-4347i others(342): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr20 | 48959479 | |||||
| chr20:48959479
|
C | CTCTCCCT others(314): Show |
2 | a0001c0001t0002g0221a0001c0001t0002g0245 | 2 | HG01361.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.839-4348_839-4347i others(323): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr20 | 48959479 | |||||
| chr20:48959479
|
C | CTCTCCCT others(346): Show |
1 | a0001c0001t0003g0247 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.839-4348_839-4347i others(355): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr20 | 48959479 | |||||
| chr20:48959479
|
C | CTCTCCCT others(326): Show |
34 | a0001c0001t0002g0120a0001c0001t0002g0240a0001c0001t0003g0113others(31): Show | 34 | HG00323.hp2 HG00639.hp2 HG00733.hp2 others(31): Show |
intron_variant | MODIFIER | c.839-4348_839-4347i others(335): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr20 | 48959479 | |||||
| chr20:48959479
|
C | CTCTCCCT others(306): Show |
2 | a0001c0002t0001g0006a0001c0002t0017g0007 | 2 | HG00642.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.839-4348_839-4347i others(315): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr20 | 48959479 | |||||
| chr20:48959479
|
C | CTCTCCCT others(314): Show |
1 | a0001c0001t0002g0222 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.839-4348_839-4347i others(323): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr20 | 48959479 | |||||
| chr20:48959479
|
C | CTCTCCCT others(326): Show |
1 | a0001c0003t0001g0106 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.839-4348_839-4347i others(335): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr20 | 48959479 | |||||
| chr20:48959479
|
C | CTCTCCCT others(410): Show |
5 | a0001c0001t0002g0220a0001c0001t0002g0244a0001c0001t0002g0277others(2): Show | 5 | HG01243.hp2 HG02615.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.839-4348_839-4347i others(419): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr20 | 48959479 | |||||
| chr20:48959479
|
C | CTCTCCCT others(330): Show |
78 | a0001c0001t0001g0170a0001c0002t0001g0002a0001c0002t0001g0004others(75): Show | 79 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.839-4348_839-4347i others(339): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr20 | 48959479 | |||||
| chr20:48959479
|
C | CTCTCCCT others(330): Show |
37 | a0001c0001t0002g0218a0001c0001t0002g0219a0001c0001t0002g0226others(34): Show | 37 | HG00673.hp1 HG00738.hp1 HG01934.hp1 others(34): Show |
intron_variant | MODIFIER | c.839-4348_839-4347i others(339): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr20 | 48959479 | |||||
| chr20:48959479
|
C | CTCTCCCT others(330): Show |
1 | a0001c0001t0004g0346 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.839-4348_839-4347i others(339): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr20 | 48959479 | |||||
| chr20:48959479
|
C | CTCTCCCT others(326): Show |
2 | a0001c0001t0002g0228a0001c0001t0002g0229 | 2 | HG02622.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.839-4348_839-4347i others(335): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr20 | 48959479 | |||||
| chr20:48959479
|
C | CTCTCCCT others(350): Show |
1 | a0001c0002t0001g0195 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.839-4348_839-4347i others(359): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr20 | 48959479 | |||||
| chr20:48959479
|
C | CTCTCCCT others(329): Show |
1 | a0001c0001t0004g0321 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.839-4348_839-4347i others(338): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr20 | 48959479 | |||||
| chr20:48959479
|
C | CTCTCCCT others(330): Show |
1 | a0001c0003t0001g0107 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.839-4348_839-4347i others(339): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr20 | 48959479 | |||||
| chr20:48959479
|
C | CTCTCCCT others(322): Show |
1 | a0001c0001t0002g0259 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.839-4348_839-4347i others(331): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr20 | 48959479 | |||||
| chr20:48959479
|
C | CTCTCCCT others(326): Show |
45 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0010others(42): Show | 45 | HG00280.hp1 HG00558.hp2 HG01106.hp2 others(42): Show |
intron_variant | MODIFIER | c.839-4348_839-4347i others(335): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr20 | 48959479 | |||||
| chr20:48959479
|
C | CTCTCCCT others(346): Show |
1 | a0001c0001t0002g0003 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.839-4348_839-4347i others(355): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr20 | 48959479 | |||||
| chr20:48959479
|
C | CTCTCCCT others(322): Show |
1 | a0001c0002t0005g0019 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.839-4348_839-4347i others(331): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr20 | 48959479 | |||||
| chr20:48959479
|
C | CTCTCCCT others(334): Show |
1 | a0001c0002t0001g0305 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.839-4348_839-4347i others(343): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr20 | 48959479 | |||||
| chr20:48959519
|
C | G | 76 | a0001c0003t0001g0029a0001c0003t0001g0030a0001c0003t0001g0031others(73): Show | 76 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(73): Show |
intron_variant | MODIFIER | c.839-4311C>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48959519 | ||||||
| chr20:48959550
|
C | T | 1 | a0001c0001t0004g0346 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.839-4280C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48959550 | ||||||
| chr20:48959551
|
T | G | 1 | a0001c0001t0004g0346 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.839-4279T>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48959551 | ||||||
| chr20:48959563
|
C | G | 1 | a0001c0003t0001g0091 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.839-4267C>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48959563 | ||||||
| chr20:48959571
|
C | CTCCT | 3 | a0001c0005t0008g0267a0001c0005t0008g0268a0001c0005t0008g0276 | 3 | HG02486.hp2 HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.839-4251_839-4248d others(6): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr20 | 48959571 | |||||
| chr20:48959671
|
G | A | 1 | a0001c0001t0002g0261 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.839-4159G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48959671 | ||||||
| chr20:48959705
|
G | C | 1 | a0001c0003t0001g0074 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.839-4125G>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48959705 | ||||||
| chr20:48959706
|
C | G | 1 | a0001c0003t0001g0074 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.839-4124C>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48959706 | ||||||
| chr20:48959716
|
C | T | 1 | a0001c0016t0001g0028 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.839-4114C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48959716 | ||||||
| chr20:48959949
|
A | T | 1 | a0001c0016t0001g0028 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.839-3881A>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48959949 | ||||||
| chr20:48960086
|
C | G | 1 | a0001c0002t0001g0112 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.839-3744C>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48960086 | ||||||
| chr20:48960093
|
T | C | 113 | a0001c0001t0002g0198a0001c0002t0001g0122a0001c0002t0001g0123others(110): Show | 113 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(110): Show |
intron_variant | MODIFIER | c.839-3737T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48960093 | ||||||
| chr20:48960447
|
A | ACTGTACA others(3): Show |
1 | a0001c0002t0001g0284 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.839-3382_839-3373d others(12): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr20 | 48960447 | |||||
| chr20:48960488
|
CT | C | 137 | a0001c0001t0002g0198a0001c0001t0011g0269a0001c0002t0001g0006others(134): Show | 138 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(135): Show |
intron_variant | MODIFIER | c.839-3330delT | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr20 | 48960488 | |||||
| chr20:48960506
|
C | T | 3 | a0001c0005t0008g0267a0001c0005t0008g0268a0001c0005t0008g0276 | 3 | HG02486.hp2 HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.839-3324C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48960506 | ||||||
| chr20:48960670
|
G | A | 21 | a0001c0002t0001g0313a0001c0002t0001g0314a0001c0002t0001g0318others(18): Show | 22 | HG00741.hp2 HG01109.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.839-3160G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48960670 | ||||||
| chr20:48960682
|
G | T | 1 | a0001c0002t0001g0314 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.839-3148G>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48960682 | ||||||
| chr20:48960687
|
T | A | 1 | a0001c0001t0002g0254 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.839-3143T>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48960687 | ||||||
| chr20:48960820
|
G | A | 1 | a0001c0003t0001g0105 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.839-3010G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48960820 | ||||||
| chr20:48960925
|
C | T | 3 | a0001c0001t0002g0218a0001c0001t0002g0219a0001c0001t0002g0243 | 3 | HG02145.hp1 HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.839-2905C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48960925 | ||||||
| chr20:48961004
|
C | A | 1 | a0001c0002t0005g0020 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.839-2826C>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48961004 | ||||||
| chr20:48961016
|
G | T | 2 | a0001c0001t0014g0223a0001c0001t0014g0224 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.839-2814G>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48961016 | ||||||
| chr20:48961047
|
T | A | 1 | a0001c0001t0004g0346 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.839-2783T>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48961047 | ||||||
| chr20:48961048
|
C | T | 77 | a0001c0003t0001g0029a0001c0003t0001g0030a0001c0003t0001g0031others(74): Show | 77 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(74): Show |
intron_variant | MODIFIER | c.839-2782C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48961048 | ||||||
| chr20:48961083
|
T | TATA | 40 | a0001c0001t0002g0010a0001c0001t0002g0248a0001c0001t0002g0253others(37): Show | 40 | HG00673.hp1 HG00738.hp1 HG01256.hp2 others(37): Show |
intron_variant | MODIFIER | c.839-2720_839-2718d others(5): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr20 | 48961083 | |||||
| chr20:48961083
|
T | TATAATA | 5 | a0001c0002t0001g0132a0001c0002t0001g0133a0001c0002t0001g0318others(2): Show | 5 | HG00280.hp2 HG00323.hp1 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.839-2723_839-2718d others(8): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr20 | 48961083 | |||||
| chr20:48961083
|
T | TATAATAA others(2): Show |
5 | a0001c0002t0001g0304a0001c0003t0001g0043a0001c0003t0001g0078others(2): Show | 5 | HG01975.hp1 HG02135.hp2 NA18954.hp1 others(2): Show |
intron_variant | MODIFIER | c.839-2726_839-2718d others(11): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr20 | 48961083 | |||||
| chr20:48961083
|
T | TATAATAA others(5): Show |
6 | a0001c0003t0001g0030a0001c0003t0001g0040a0001c0003t0001g0055others(3): Show | 6 | HG01123.hp2 HG02647.hp2 HG03710.hp1 others(3): Show |
intron_variant | MODIFIER | c.839-2729_839-2718d others(14): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr20 | 48961083 | |||||
| chr20:48961083
|
T | TATAATAA others(8): Show |
59 | a0001c0002t0001g0293a0001c0002t0001g0294a0001c0002t0001g0295others(56): Show | 59 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.839-2732_839-2718d others(17): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr20 | 48961083 | |||||
| chr20:48961083
|
T | TATAATAA others(11): Show |
18 | a0001c0002t0001g0123a0001c0002t0001g0124a0001c0002t0001g0283others(15): Show | 18 | HG01074.hp2 HG01081.hp2 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.839-2735_839-2718d others(20): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr20 | 48961083 | |||||
| chr20:48961083
|
T | TATAATAA others(14): Show |
14 | a0001c0002t0001g0122a0001c0002t0001g0282a0001c0002t0001g0286others(11): Show | 14 | HG00673.hp2 HG02683.hp1 HG02896.hp1 others(11): Show |
intron_variant | MODIFIER | c.839-2738_839-2718d others(23): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr20 | 48961083 | |||||
| chr20:48961083
|
T | TATAATAA others(17): Show |
6 | a0001c0002t0001g0287a0001c0002t0001g0290a0001c0002t0001g0292others(3): Show | 6 | HG02015.hp1 HG02071.hp2 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.839-2741_839-2718d others(26): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr20 | 48961083 | |||||
| chr20:48961111
|
A | ATAATAAT others(15): Show |
1 | a0001c0003t0009g0036 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.839-2718_839-2717i others(24): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr20 | 48961111 | |||||
| chr20:48961112
|
T | TAATAATA others(13): Show |
1 | a0001c0002t0001g0284 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.839-2718_839-2717i others(22): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48961112 | ||||||
| chr20:48961224
|
A | G | 3 | a0001c0003t0001g0032a0001c0003t0001g0079a0001c0003t0001g0083 | 3 | HG00609.hp1 NA18944.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.839-2606A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48961224 | ||||||
| chr20:48961392
|
C | T | 34 | a0001c0001t0002g0003a0001c0001t0002g0116a0001c0001t0002g0117others(31): Show | 34 | HG00280.hp1 HG00558.hp2 HG01106.hp2 others(31): Show |
intron_variant | MODIFIER | c.839-2438C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48961392 | ||||||
| chr20:48961428
|
G | A | 2 | a0001c0002t0001g0315a0001c0002t0001g0316 | 2 | HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.839-2402G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48961428 | ||||||
| chr20:48961527
|
T | TAACTTTT others(3101): Show |
1 | a0001c0001t0004g0325 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.839-2288_839-2287i others(3110): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr20 | 48961527 | |||||
| chr20:48961527
|
T | TAACTTTT others(3097): Show |
1 | a0001c0001t0004g0321 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.839-2288_839-2287i others(3106): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr20 | 48961527 | |||||
| chr20:48961527
|
T | TAACTTTT others(3100): Show |
1 | a0001c0001t0013g0322 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.839-2288_839-2287i others(3109): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr20 | 48961527 | |||||
| chr20:48961527
|
T | TAACTTTT others(3101): Show |
1 | a0001c0001t0004g0341 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.839-2288_839-2287i others(3110): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr20 | 48961527 | |||||
| chr20:48961527
|
T | TAACTTTT others(3106): Show |
1 | a0001c0001t0004g0323 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.839-2288_839-2287i others(3115): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr20 | 48961527 | |||||
| chr20:48961527
|
T | TAACTTTT others(3118): Show |
1 | a0001c0001t0004g0338 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.839-2288_839-2287i others(3127): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr20 | 48961527 | |||||
| chr20:48961527
|
T | TAACTTTT others(3114): Show |
1 | a0001c0001t0004g0332 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.839-2288_839-2287i others(3123): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr20 | 48961527 | |||||
| chr20:48961527
|
T | TAACTTTT others(3126): Show |
1 | a0001c0001t0004g0346 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.839-2288_839-2287i others(3135): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr20 | 48961527 | |||||
| chr20:48961527
|
T | TAACTTTT others(3111): Show |
1 | a0001c0001t0004g0347 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.839-2288_839-2287i others(3120): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr20 | 48961527 | |||||
| chr20:48961527
|
T | TAACTTTT others(3111): Show |
1 | a0001c0001t0004g0339 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.839-2288_839-2287i others(3120): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr20 | 48961527 | |||||
| chr20:48961527
|
T | TAACTTTT others(3121): Show |
1 | a0001c0001t0004g0340 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.839-2288_839-2287i others(3130): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr20 | 48961527 | |||||
| chr20:48961527
|
T | TAACTTTT others(3113): Show |
2 | a0001c0001t0004g0328a0001c0001t0004g0342 | 2 | NA18952.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.839-2288_839-2287i others(3122): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr20 | 48961527 | |||||
| chr20:48961527
|
T | TAACTTTT others(3114): Show |
2 | a0001c0001t0004g0327a0001c0001t0004g0333 | 2 | NA18954.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.839-2288_839-2287i others(3123): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr20 | 48961527 | |||||
| chr20:48961527
|
T | TAACTTTT others(3114): Show |
1 | a0001c0001t0004g0343 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.839-2288_839-2287i others(3123): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr20 | 48961527 | |||||
| chr20:48961527
|
T | TAACTTTT others(3118): Show |
1 | a0001c0001t0004g0337 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.839-2288_839-2287i others(3127): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr20 | 48961527 | |||||
| chr20:48961527
|
T | TAACTTTT others(3122): Show |
1 | a0001c0001t0004g0335 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.839-2288_839-2287i others(3131): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr20 | 48961527 | |||||
| chr20:48961527
|
T | TAACTTTT others(3109): Show |
1 | a0001c0001t0020g0329 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.839-2288_839-2287i others(3118): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr20 | 48961527 | |||||
| chr20:48961527
|
T | TAACTTTT others(3115): Show |
1 | a0001c0001t0004g0334 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.839-2288_839-2287i others(3124): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr20 | 48961527 | |||||
| chr20:48961527
|
T | TAACTTTT others(3115): Show |
1 | a0001c0001t0004g0330 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.839-2288_839-2287i others(3124): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr20 | 48961527 | |||||
| chr20:48961527
|
T | TAACTTTT others(3117): Show |
1 | a0001c0001t0004g0344 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.839-2288_839-2287i others(3126): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr20 | 48961527 | |||||
| chr20:48961527
|
T | TAACTTTT others(3370): Show |
1 | a0001c0001t0004g0331 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.839-2288_839-2287i others(3379): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr20 | 48961527 | |||||
| chr20:48961527
|
T | TAACTTTT others(3117): Show |
1 | a0001c0001t0004g0336 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.839-2288_839-2287i others(3126): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr20 | 48961527 | |||||
| chr20:48961527
|
T | TAACTTTT others(3120): Show |
1 | a0001c0001t0019g0345 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.839-2288_839-2287i others(3129): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr20 | 48961527 | |||||
| chr20:48961527
|
T | TAACTTTT others(3118): Show |
1 | a0001c0001t0004g0324 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.839-2288_839-2287i others(3127): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr20 | 48961527 | |||||
| chr20:48961527
|
T | TAACTTTT others(3118): Show |
1 | a0001c0001t0004g0348 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.839-2288_839-2287i others(3127): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr20 | 48961527 | |||||
| chr20:48961527
|
T | TAACTTTT others(3118): Show |
1 | a0001c0001t0013g0320 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.839-2288_839-2287i others(3127): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr20 | 48961527 | |||||
| chr20:48961527
|
T | TAACTTTT others(3130): Show |
1 | a0001c0001t0004g0326 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.839-2288_839-2287i others(3139): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr20 | 48961527 | |||||
| chr20:48961602
|
A | G | 34 | a0001c0001t0002g0198a0001c0002t0001g0122a0001c0002t0001g0123others(31): Show | 34 | HG00639.hp1 HG00673.hp2 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.839-2228A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48961602 | ||||||
| chr20:48961737
|
G | A | 3 | a0001c0005t0008g0267a0001c0005t0008g0268a0001c0005t0008g0276 | 3 | HG02486.hp2 HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.839-2093G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48961737 | ||||||
| chr20:48961787
|
C | G | 1 | a0001c0002t0001g0111 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.839-2043C>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48961787 | ||||||
| chr20:48961796
|
G | A | 1 | a0008c0009t0001g0289 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.839-2034G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48961796 | ||||||
| chr20:48961861
|
C | CA | 53 | a0001c0001t0002g0118a0001c0001t0002g0198a0001c0001t0002g0222others(50): Show | 53 | HG00639.hp1 HG00673.hp2 HG00741.hp1 others(50): Show |
intron_variant | MODIFIER | c.839-1954dupA | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr20 | 48961861 | |||||
| chr20:48961957
|
T | C | 2 | a0001c0002t0001g0318a0001c0002t0015g0319 | 2 | HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.839-1873T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48961957 | ||||||
| chr20:48961958
|
C | T | 2 | a0001c0002t0001g0318a0001c0002t0015g0319 | 2 | HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.839-1872C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48961958 | ||||||
| chr20:48961959
|
A | G | 2 | a0001c0002t0001g0318a0001c0002t0015g0319 | 2 | HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.839-1871A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48961959 | ||||||
| chr20:48961961
|
C | T | 2 | a0001c0002t0001g0318a0001c0002t0015g0319 | 2 | HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.839-1869C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48961961 | ||||||
| chr20:48962069
|
G | A | 249 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0009others(246): Show | 249 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(246): Show |
intron_variant | MODIFIER | c.839-1761G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48962069 | ||||||
| chr20:48962112
|
G | A | 1 | a0001c0001t0003g0237 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.839-1718G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48962112 | ||||||
| chr20:48962119
|
G | A | 1 | a0008c0009t0001g0289 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.839-1711G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48962119 | ||||||
| chr20:48962190
|
A | G | 1 | a0001c0003t0001g0032 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.839-1640A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48962190 | ||||||
| chr20:48962211
|
A | G | 1 | a0001c0003t0001g0060 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.839-1619A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48962211 | ||||||
| chr20:48962351
|
A | T | 3 | a0001c0002t0001g0293a0001c0002t0001g0294a0001c0002t0001g0295 | 3 | HG00741.hp1 HG01071.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.839-1479A>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48962351 | ||||||
| chr20:48962450
|
CGTT | C | 3 | a0001c0005t0008g0267a0001c0005t0008g0268a0001c0005t0008g0276 | 3 | HG02486.hp2 HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.839-1376_839-1374d others(5): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr20 | 48962450 | |||||
| chr20:48962688
|
G | A | 2 | a0001c0001t0002g0254a0001c0001t0002g0263 | 2 | NA18971.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.839-1142G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48962688 | ||||||
| chr20:48962817
|
G | T | 1 | a0001c0002t0001g0304 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.839-1013G>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48962817 | ||||||
| chr20:48963175
|
C | CA | 6 | a0001c0002t0001g0137a0001c0002t0001g0166a0001c0003t0001g0065others(3): Show | 6 | HG01169.hp1 HG01255.hp1 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.839-641dupA | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr20 | 48963175 | |||||
| chr20:48963175
|
C | CAAAAAA | 49 | a0001c0001t0001g0170a0001c0001t0002g0218a0001c0001t0002g0219others(46): Show | 49 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(46): Show |
intron_variant | MODIFIER | c.839-646_839-641dup others(6): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr20 | 48963175 | |||||
| chr20:48963175
|
C | CAAAAAAA | 8 | a0001c0001t0002g0222a0001c0001t0003g0199a0001c0001t0003g0200others(5): Show | 8 | HG00639.hp2 HG01175.hp2 HG02027.hp1 others(5): Show |
intron_variant | MODIFIER | c.839-647_839-641dup others(7): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr20 | 48963175 | |||||
| chr20:48963175
|
C | CAAAAAAA others(4): Show |
1 | a0001c0001t0002g0003 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.839-651_839-641dup others(11): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr20 | 48963175 | |||||
| chr20:48963175
|
C | CAAAAAAA others(7): Show |
1 | a0001c0001t0016g0005 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.839-654_839-641dup others(14): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr20 | 48963175 | |||||
| chr20:48963175
|
C | CAAAAAAA others(11): Show |
1 | a0001c0001t0002g0013 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.839-641_839-640ins others(18): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr20 | 48963175 | |||||
| chr20:48963175
|
C | CAAAAAAA others(12): Show |
1 | a0001c0001t0002g0249 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.839-641_839-640ins others(19): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr20 | 48963175 | |||||
| chr20:48963175
|
C | CAAAAAAA others(13): Show |
19 | a0001c0001t0002g0009a0001c0001t0002g0226a0001c0001t0002g0248others(16): Show | 19 | HG00738.hp1 HG01975.hp2 HG02148.hp1 others(16): Show |
intron_variant | MODIFIER | c.839-641_839-640ins others(20): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr20 | 48963175 | |||||
| chr20:48963175
|
C | CAAAAAAA others(14): Show |
20 | a0001c0001t0002g0198a0001c0001t0002g0250a0001c0001t0002g0254others(17): Show | 20 | HG00673.hp1 HG01175.hp1 HG01257.hp2 others(17): Show |
intron_variant | MODIFIER | c.839-641_839-640ins others(21): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr20 | 48963175 | |||||
| chr20:48963175
|
C | CAAAAAAA others(15): Show |
14 | a0001c0001t0002g0116a0001c0001t0002g0121a0001c0001t0002g0253others(11): Show | 14 | HG00280.hp1 HG00558.hp2 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.839-641_839-640ins others(22): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr20 | 48963175 | |||||
| chr20:48963175
|
C | CAAAAAAA others(16): Show |
11 | a0001c0001t0002g0117a0001c0001t0002g0118a0001c0001t0002g0119others(8): Show | 11 | HG01106.hp2 HG02055.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.839-641_839-640ins others(23): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr20 | 48963175 | |||||
| chr20:48963175
|
C | CAAAAAAA others(17): Show |
1 | a0001c0001t0006g0266 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.839-641_839-640ins others(24): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr20 | 48963175 | |||||
| chr20:48963175
|
C | CAAAAAAA others(18): Show |
2 | a0001c0001t0002g0008a0001c0001t0006g0274 | 2 | HG02055.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.839-641_839-640ins others(25): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr20 | 48963175 | |||||
| chr20:48963175
|
C | CAAAAAAA others(19): Show |
2 | a0001c0001t0002g0011a0001c0001t0002g0014 | 2 | NA18522.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.839-641_839-640ins others(26): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr20 | 48963175 | |||||
| chr20:48963175
|
C | CAAAAAAA others(21): Show |
1 | a0001c0001t0002g0012 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.839-641_839-640ins others(28): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr20 | 48963175 | |||||
| chr20:48963175
|
C | CAAAAAAA others(25): Show |
1 | a0001c0001t0002g0010 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.839-641_839-640ins others(32): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr20 | 48963175 | |||||
| chr20:48963175
|
C | CAAAAAAA others(28): Show |
2 | a0001c0005t0008g0268a0001c0005t0008g0276 | 2 | HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.839-641_839-640ins others(35): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr20 | 48963175 | |||||
| chr20:48963175
|
C | CAAAAAAA others(29): Show |
1 | a0001c0005t0008g0267 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.839-641_839-640ins others(36): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr20 | 48963175 | |||||
| chr20:48963207
|
A | G | 3 | a0001c0001t0002g0231a0001c0001t0002g0232a0001c0001t0002g0233 | 3 | HG02258.hp2 HG02717.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.839-623A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48963207 | ||||||
| chr20:48963243
|
T | C | 136 | a0001c0001t0001g0170a0001c0001t0002g0003a0001c0001t0002g0008others(133): Show | 136 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(133): Show |
intron_variant | MODIFIER | c.839-587T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48963243 | ||||||
| chr20:48963342
|
G | C | 1 | a0001c0003t0001g0063 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.839-488G>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48963342 | ||||||
| chr20:48963409
|
G | A | 1 | a0001c0002t0022g0197 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.839-421G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48963409 | ||||||
| chr20:48963483
|
C | T | 1 | a0001c0002t0001g0186 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.839-347C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48963483 | ||||||
| chr20:48963574
|
A | C | 2 | a0003c0007t0001g0302a0003c0007t0001g0303 | 2 | HG01081.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.839-256A>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48963574 | ||||||
| chr20:48963810
|
A | G | 136 | a0001c0001t0001g0170a0001c0001t0002g0003a0001c0001t0002g0008others(133): Show | 136 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(133): Show |
intron_variant | MODIFIER | c.839-20A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 6/38 | chr20 | 48963810 | ||||||
| chr20:48964144
|
C | T | 1 | a0001c0002t0001g0002 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.907+246C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 7/38 | chr20 | 48964144 | ||||||
| chr20:48964162
|
T | A | 245 | a0001c0001t0001g0170a0001c0001t0002g0003a0001c0001t0002g0008others(242): Show | 245 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(242): Show |
intron_variant | MODIFIER | c.907+264T>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 7/38 | chr20 | 48964162 | ||||||
| chr20:48964190
|
C | T | 1 | a0001c0002t0001g0296 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.907+292C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 7/38 | chr20 | 48964190 | ||||||
| chr20:48964261
|
C | T | 29 | a0001c0001t0004g0321a0001c0001t0004g0323a0001c0001t0004g0324others(26): Show | 29 | HG00673.hp1 HG00738.hp1 HG01934.hp1 others(26): Show |
intron_variant | MODIFIER | c.907+363C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 7/38 | chr20 | 48964261 | ||||||
| chr20:48964262
|
G | A | 112 | a0001c0002t0001g0122a0001c0002t0001g0123a0001c0002t0001g0124others(109): Show | 112 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.907+364G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 7/38 | chr20 | 48964262 | ||||||
| chr20:48964359
|
C | T | 134 | a0001c0001t0003g0200a0001c0002t0001g0122a0001c0002t0001g0123others(131): Show | 135 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(132): Show |
intron_variant | MODIFIER | c.907+461C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 7/38 | chr20 | 48964359 | ||||||
| chr20:48964370
|
A | G | 1 | a0001c0002t0001g0166 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.907+472A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 7/38 | chr20 | 48964370 | ||||||
| chr20:48964468
|
C | T | 1 | a0001c0003t0001g0081 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.907+570C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 7/38 | chr20 | 48964468 | ||||||
| chr20:48964524
|
A | T | 1 | a0001c0001t0002g0218 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.907+626A>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 7/38 | chr20 | 48964524 | ||||||
| chr20:48965201
|
C | T | 35 | a0001c0002t0001g0122a0001c0002t0001g0123a0001c0002t0001g0124others(32): Show | 35 | HG00639.hp1 HG00673.hp2 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.908-671C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 7/38 | chr20 | 48965201 | ||||||
| chr20:48965588
|
T | C | 211 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0009others(208): Show | 212 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(209): Show |
intron_variant | MODIFIER | c.908-284T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 7/38 | chr20 | 48965588 | ||||||
| chr20:48965592
|
G | A | 112 | a0001c0002t0001g0122a0001c0002t0001g0123a0001c0002t0001g0124others(109): Show | 112 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.908-280G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 7/38 | chr20 | 48965592 | ||||||
| chr20:48965603
|
G | A | 133 | a0001c0002t0001g0122a0001c0002t0001g0123a0001c0002t0001g0124others(130): Show | 134 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(131): Show |
intron_variant | MODIFIER | c.908-269G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 7/38 | chr20 | 48965603 | ||||||
| chr20:48965637
|
A | G | 1 | a0001c0002t0010g0153 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.908-235A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 7/38 | chr20 | 48965637 | ||||||
| chr20:48965711
|
C | G | 35 | a0001c0002t0001g0122a0001c0002t0001g0123a0001c0002t0001g0124others(32): Show | 35 | HG00639.hp1 HG00673.hp2 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.908-161C>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 7/38 | chr20 | 48965711 | ||||||
| chr20:48966095
|
T | A | 1 | a0001c0001t0002g0230 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1059+72T>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 8/38 | chr20 | 48966095 | ||||||
| chr20:48966175
|
G | C | 2 | a0003c0007t0001g0302a0003c0007t0001g0303 | 2 | HG01081.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1059+152G>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 8/38 | chr20 | 48966175 | ||||||
| chr20:48966248
|
T | A | 57 | a0001c0001t0002g0218a0001c0001t0002g0219a0001c0001t0002g0220others(54): Show | 57 | HG00323.hp2 HG00639.hp2 HG00733.hp2 others(54): Show |
intron_variant | MODIFIER | c.1059+225T>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 8/38 | chr20 | 48966248 | ||||||
| chr20:48966347
|
G | A | 135 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0009others(132): Show | 135 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(132): Show |
intron_variant | MODIFIER | c.1059+324G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 8/38 | chr20 | 48966347 | ||||||
| chr20:48966421
|
A | T | 247 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0009others(244): Show | 247 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(244): Show |
intron_variant | MODIFIER | c.1059+398A>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 8/38 | chr20 | 48966421 | ||||||
| chr20:48966810
|
T | G | 1 | a0002c0004t0001g0191 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1059+787T>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 8/38 | chr20 | 48966810 | ||||||
| chr20:48966835
|
T | G | 135 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0009others(132): Show | 135 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(132): Show |
intron_variant | MODIFIER | c.1059+812T>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 8/38 | chr20 | 48966835 | ||||||
| chr20:48966927
|
G | T | 112 | a0001c0002t0001g0122a0001c0002t0001g0123a0001c0002t0001g0124others(109): Show | 112 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.1059+904G>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 8/38 | chr20 | 48966927 | ||||||
| chr20:48966943
|
C | A | 135 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0009others(132): Show | 135 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(132): Show |
intron_variant | MODIFIER | c.1059+920C>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 8/38 | chr20 | 48966943 | ||||||
| chr20:48966947
|
A | G | 16 | a0001c0002t0005g0001a0001c0002t0005g0015a0001c0002t0005g0016others(13): Show | 17 | HG01109.hp1 HG01884.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.1059+924A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 8/38 | chr20 | 48966947 | ||||||
| chr20:48967035
|
G | C | 1 | a0001c0002t0022g0197 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1059+1012G>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 8/38 | chr20 | 48967035 | ||||||
| chr20:48967133
|
A | T | 1 | a0001c0001t0002g0220 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1059+1110A>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 8/38 | chr20 | 48967133 | ||||||
| chr20:48967699
|
T | C | 2 | a0001c0002t0001g0154a0001c0002t0001g0177 | 2 | HG01516.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.1060-1448T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 8/38 | chr20 | 48967699 | ||||||
| chr20:48967821
|
C | G | 1 | a0001c0002t0001g0160 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1060-1326C>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 8/38 | chr20 | 48967821 | ||||||
| chr20:48967847
|
C | A | 133 | a0001c0002t0001g0122a0001c0002t0001g0123a0001c0002t0001g0124others(130): Show | 134 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(131): Show |
intron_variant | MODIFIER | c.1060-1300C>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 8/38 | chr20 | 48967847 | ||||||
| chr20:48968058
|
A | G | 1 | a0001c0001t0002g0260 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1060-1089A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 8/38 | chr20 | 48968058 | ||||||
| chr20:48968088
|
G | C | 2 | a0001c0002t0001g0313a0001c0002t0001g0314 | 2 | HG00741.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1060-1059G>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 8/38 | chr20 | 48968088 | ||||||
| chr20:48968134
|
C | T | 133 | a0001c0002t0001g0122a0001c0002t0001g0123a0001c0002t0001g0124others(130): Show | 134 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(131): Show |
intron_variant | MODIFIER | c.1060-1013C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 8/38 | chr20 | 48968134 | ||||||
| chr20:48968178
|
A | G | 1 | a0001c0001t0002g0116 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1060-969A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 8/38 | chr20 | 48968178 | ||||||
| chr20:48968210
|
A | G | 133 | a0001c0002t0001g0122a0001c0002t0001g0123a0001c0002t0001g0124others(130): Show | 134 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(131): Show |
intron_variant | MODIFIER | c.1060-937A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 8/38 | chr20 | 48968210 | ||||||
| chr20:48968215
|
G | A | 111 | a0001c0002t0001g0122a0001c0002t0001g0123a0001c0002t0001g0124others(108): Show | 111 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(108): Show |
intron_variant | MODIFIER | c.1060-932G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 8/38 | chr20 | 48968215 | ||||||
| chr20:48968285
|
G | T | 133 | a0001c0002t0001g0122a0001c0002t0001g0123a0001c0002t0001g0124others(130): Show | 134 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(131): Show |
intron_variant | MODIFIER | c.1060-862G>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 8/38 | chr20 | 48968285 | ||||||
| chr20:48968375
|
A | G | 2 | a0001c0002t0012g0148a0001c0002t0012g0149 | 2 | HG01361.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1060-772A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 8/38 | chr20 | 48968375 | ||||||
| chr20:48968600
|
G | A | 1 | a0001c0001t0004g0339 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1060-547G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 8/38 | chr20 | 48968600 | ||||||
| chr20:48968615
|
G | A | 1 | a0001c0001t0004g0340 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1060-532G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 8/38 | chr20 | 48968615 | ||||||
| chr20:48968995
|
A | G | 112 | a0001c0002t0001g0122a0001c0002t0001g0123a0001c0002t0001g0124others(109): Show | 112 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.1060-152A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 8/38 | chr20 | 48968995 | ||||||
| chr20:48969105
|
T | C | 133 | a0001c0002t0001g0122a0001c0002t0001g0123a0001c0002t0001g0124others(130): Show | 134 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(131): Show |
intron_variant | MODIFIER | c.1060-42T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 8/38 | chr20 | 48969105 | ||||||
| chr20:48969347
|
C | T | 29 | a0001c0001t0004g0321a0001c0001t0004g0323a0001c0001t0004g0324others(26): Show | 29 | HG00673.hp1 HG00738.hp1 HG01934.hp1 others(26): Show |
intron_variant | MODIFIER | c.1190+70C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 9/38 | chr20 | 48969347 | ||||||
| chr20:48969504
|
T | C | 1 | a0001c0001t0002g0003 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1190+227T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 9/38 | chr20 | 48969504 | ||||||
| chr20:48969527
|
A | T | 2 | a0001c0001t0002g0228a0001c0001t0002g0229 | 2 | HG02622.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1190+250A>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 9/38 | chr20 | 48969527 | ||||||
| chr20:48969633
|
T | G | 1 | a0001c0001t0003g0242 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1190+356T>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 9/38 | chr20 | 48969633 | ||||||
| chr20:48969721
|
T | C | 1 | a0001c0003t0001g0032 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1190+444T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 9/38 | chr20 | 48969721 | ||||||
| chr20:48969761
|
G | C | 1 | a0001c0002t0005g0023 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1190+484G>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 9/38 | chr20 | 48969761 | ||||||
| chr20:48969764
|
T | C | 1 | a0001c0001t0003g0242 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1190+487T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 9/38 | chr20 | 48969764 | ||||||
| chr20:48970043
|
G | A | 1 | a0001c0001t0004g0332 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1190+766G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 9/38 | chr20 | 48970043 | ||||||
| chr20:48970053
|
A | G | 133 | a0001c0002t0001g0122a0001c0002t0001g0123a0001c0002t0001g0124others(130): Show | 134 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(131): Show |
intron_variant | MODIFIER | c.1190+776A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 9/38 | chr20 | 48970053 | ||||||
| chr20:48970081
|
A | G | 133 | a0001c0002t0001g0122a0001c0002t0001g0123a0001c0002t0001g0124others(130): Show | 134 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(131): Show |
intron_variant | MODIFIER | c.1190+804A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 9/38 | chr20 | 48970081 | ||||||
| chr20:48970212
|
A | G | 3 | a0001c0005t0008g0267a0001c0005t0008g0268a0001c0005t0008g0276 | 3 | HG02486.hp2 HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1191-908A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 9/38 | chr20 | 48970212 | ||||||
| chr20:48970230
|
G | A | 33 | a0001c0002t0001g0122a0001c0002t0001g0123a0001c0002t0001g0124others(30): Show | 33 | HG00639.hp1 HG00673.hp2 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.1191-890G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 9/38 | chr20 | 48970230 | ||||||
| chr20:48970477
|
G | A | 1 | a0001c0001t0002g0251 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1191-643G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 9/38 | chr20 | 48970477 | ||||||
| chr20:48970482
|
C | T | 4 | a0001c0001t0004g0335a0003c0007t0001g0302a0003c0007t0001g0303others(1): Show | 4 | HG00639.hp1 HG01081.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.1191-638C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 9/38 | chr20 | 48970482 | ||||||
| chr20:48970561
|
G | C | 77 | a0001c0003t0001g0029a0001c0003t0001g0030a0001c0003t0001g0031others(74): Show | 77 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(74): Show |
intron_variant | MODIFIER | c.1191-559G>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 9/38 | chr20 | 48970561 | ||||||
| chr20:48970848
|
C | T | 1 | a0001c0003t0001g0048 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1191-272C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 9/38 | chr20 | 48970848 | ||||||
| chr20:48970953
|
T | G | 1 | a0001c0002t0001g0172 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1191-167T>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 9/38 | chr20 | 48970953 | ||||||
| chr20:48971365
|
C | T | 2 | a0001c0002t0001g0318a0001c0002t0015g0319 | 2 | HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1425+11C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 10/38 | chr20 | 48971365 | ||||||
| chr20:48971491
|
C | A | 1 | a0001c0016t0001g0028 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1425+137C>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 10/38 | chr20 | 48971491 | ||||||
| chr20:48971613
|
G | A | 2 | a0001c0001t0007g0041a0001c0001t0007g0042 | 2 | NA18945.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.1425+259G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 10/38 | chr20 | 48971613 | ||||||
| chr20:48971620
|
G | C | 46 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0009others(43): Show | 46 | HG00280.hp1 HG00558.hp2 HG01106.hp2 others(43): Show |
intron_variant | MODIFIER | c.1425+266G>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 10/38 | chr20 | 48971620 | ||||||
| chr20:48971774
|
G | A | 1 | a0001c0002t0001g0141 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1425+420G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 10/38 | chr20 | 48971774 | ||||||
| chr20:48971823
|
C | T | 3 | a0001c0003t0001g0070a0001c0003t0001g0085a0001c0003t0001g0093 | 3 | HG00558.hp1 HG02132.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.1425+469C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 10/38 | chr20 | 48971823 | ||||||
| chr20:48972011
|
T | G | 1 | a0001c0001t0002g0121 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1426-315T>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 10/38 | chr20 | 48972011 | ||||||
| chr20:48972031
|
G | A | 132 | a0001c0002t0001g0122a0001c0002t0001g0123a0001c0002t0001g0124others(129): Show | 133 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(130): Show |
intron_variant | MODIFIER | c.1426-295G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 10/38 | chr20 | 48972031 | ||||||
| chr20:48972585
|
T | C | 132 | a0001c0002t0001g0122a0001c0002t0001g0123a0001c0002t0001g0124others(129): Show | 133 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(130): Show |
intron_variant | MODIFIER | c.1525+160T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 11/38 | chr20 | 48972585 | ||||||
| chr20:48972617
|
C | T | 2 | a0001c0002t0001g0318a0001c0002t0015g0319 | 2 | HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1525+192C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 11/38 | chr20 | 48972617 | ||||||
| chr20:48972626
|
G | A | 1 | a0001c0003t0001g0056 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1525+201G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 11/38 | chr20 | 48972626 | ||||||
| chr20:48972777
|
C | T | 15 | a0001c0002t0005g0001a0001c0002t0005g0015a0001c0002t0005g0016others(12): Show | 16 | HG01109.hp1 HG01884.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.1525+352C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 11/38 | chr20 | 48972777 | ||||||
| chr20:48972948
|
A | G | 3 | a0001c0002t0005g0021a0001c0002t0005g0024a0001c0002t0005g0025 | 3 | HG01891.hp1 HG03486.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1526-197A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 11/38 | chr20 | 48972948 | ||||||
| chr20:48972963
|
G | A | 3 | a0001c0005t0008g0267a0001c0005t0008g0268a0001c0005t0008g0276 | 3 | HG02486.hp2 HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1526-182G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 11/38 | chr20 | 48972963 | ||||||
| chr20:48973654
|
T | C | 1 | a0001c0003t0001g0102 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1665+370T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 12/38 | chr20 | 48973654 | ||||||
| chr20:48973880
|
A | G | 1 | a0001c0002t0022g0197 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1665+596A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 12/38 | chr20 | 48973880 | ||||||
| chr20:48973910
|
C | T | 1 | a0001c0003t0001g0064 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1665+626C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 12/38 | chr20 | 48973910 | ||||||
| chr20:48974027
|
T | C | 36 | a0001c0001t0002g0240a0001c0001t0003g0113a0001c0001t0003g0114others(33): Show | 36 | HG00323.hp2 HG00639.hp2 HG00733.hp2 others(33): Show |
intron_variant | MODIFIER | c.1666-739T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 12/38 | chr20 | 48974027 | ||||||
| chr20:48974099
|
A | C | 7 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0010others(4): Show | 7 | HG01891.hp2 HG02486.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1666-667A>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 12/38 | chr20 | 48974099 | ||||||
| chr20:48974118
|
A | AT | 87 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0009others(84): Show | 87 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(84): Show |
intron_variant | MODIFIER | c.1666-623dupT | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 12/38 | INFO_REALIGN_3_PRIME | chr20 | 48974118 | |||||
| chr20:48974118
|
A | ATT | 83 | a0001c0001t0002g0116a0001c0001t0002g0220a0001c0001t0002g0244others(80): Show | 84 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.1666-624_1666-623d others(4): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 12/38 | INFO_REALIGN_3_PRIME | chr20 | 48974118 | |||||
| chr20:48974118
|
A | ATTT | 28 | a0001c0001t0001g0170a0001c0001t0002g0219a0001c0001t0002g0222others(25): Show | 28 | HG00621.hp2 HG01361.hp2 HG01433.hp2 others(25): Show |
intron_variant | MODIFIER | c.1666-625_1666-623d others(5): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 12/38 | INFO_REALIGN_3_PRIME | chr20 | 48974118 | |||||
| chr20:48974118
|
A | ATTTT | 8 | a0001c0001t0002g0218a0001c0001t0002g0221a0001c0001t0002g0226others(5): Show | 8 | HG01361.hp1 HG02258.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1666-626_1666-623d others(6): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 12/38 | INFO_REALIGN_3_PRIME | chr20 | 48974118 | |||||
| chr20:48974118
|
AT | A | 90 | a0001c0002t0001g0122a0001c0002t0001g0123a0001c0002t0001g0282others(87): Show | 90 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(87): Show |
intron_variant | MODIFIER | c.1666-623delT | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 12/38 | INFO_REALIGN_3_PRIME | chr20 | 48974118 | |||||
| chr20:48974118
|
ATT | A | 23 | a0001c0002t0001g0311a0001c0002t0001g0313a0001c0002t0005g0001others(20): Show | 24 | HG01884.hp2 HG01891.hp1 HG01978.hp1 others(21): Show |
intron_variant | MODIFIER | c.1666-624_1666-623d others(4): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 12/38 | INFO_REALIGN_3_PRIME | chr20 | 48974118 | |||||
| chr20:48974295
|
T | G | 75 | a0001c0003t0001g0029a0001c0003t0001g0030a0001c0003t0001g0031others(72): Show | 75 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(72): Show |
intron_variant | MODIFIER | c.1666-471T>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 12/38 | chr20 | 48974295 | ||||||
| chr20:48974303
|
G | C | 1 | a0001c0001t0002g0251 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1666-463G>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 12/38 | chr20 | 48974303 | ||||||
| chr20:48974310
|
C | T | 1 | a0001c0002t0005g0021 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1666-456C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 12/38 | chr20 | 48974310 | ||||||
| chr20:48974348
|
G | A | 2 | a0001c0002t0005g0026a0001c0002t0005g0027 | 2 | HG02970.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1666-418G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 12/38 | chr20 | 48974348 | ||||||
| chr20:48974545
|
C | A | 76 | a0001c0003t0001g0029a0001c0003t0001g0030a0001c0003t0001g0031others(73): Show | 76 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(73): Show |
intron_variant | MODIFIER | c.1666-221C>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 12/38 | chr20 | 48974545 | ||||||
| chr20:48974626
|
T | C | 1 | a0001c0003t0001g0064 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1666-140T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 12/38 | chr20 | 48974626 | ||||||
| chr20:48975129
|
A | G | 2 | a0001c0003t0001g0057a0001c0003t0001g0091 | 2 | HG01261.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1774+255A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 13/38 | chr20 | 48975129 | ||||||
| chr20:48975174
|
C | T | 1 | a0001c0002t0001g0314 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1774+300C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 13/38 | chr20 | 48975174 | ||||||
| chr20:48975328
|
G | T | 1 | a0001c0003t0001g0048 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1774+454G>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 13/38 | chr20 | 48975328 | ||||||
| chr20:48975340
|
G | T | 1 | a0001c0001t0004g0332 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1774+466G>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 13/38 | chr20 | 48975340 | ||||||
| chr20:48975484
|
T | A | 1 | a0001c0002t0001g0180 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1775-532T>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 13/38 | chr20 | 48975484 | ||||||
| chr20:48975499
|
A | G | 19 | a0001c0002t0001g0313a0001c0002t0001g0314a0001c0002t0005g0001others(16): Show | 20 | HG00741.hp2 HG01109.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.1775-517A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 13/38 | chr20 | 48975499 | ||||||
| chr20:48975567
|
C | T | 1 | a0001c0001t0002g0250 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1775-449C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 13/38 | chr20 | 48975567 | ||||||
| chr20:48975614
|
A | T | 2 | a0001c0003t0001g0086a0001c0003t0009g0036 | 2 | NA18949.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.1775-402A>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 13/38 | chr20 | 48975614 | ||||||
| chr20:48975656
|
C | T | 3 | a0001c0002t0001g0138a0001c0002t0001g0139a0001c0002t0001g0172 | 3 | NA18981.hp2 NA18984.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1775-360C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 13/38 | chr20 | 48975656 | ||||||
| chr20:48975658
|
G | A | 1 | a0001c0001t0002g0280 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1775-358G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 13/38 | chr20 | 48975658 | ||||||
| chr20:48975759
|
C | T | 1 | a0001c0003t0001g0090 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1775-257C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 13/38 | chr20 | 48975759 | ||||||
| chr20:48975800
|
C | CAAAAAAA others(3): Show |
36 | a0001c0002t0001g0122a0001c0002t0001g0123a0001c0002t0001g0124others(33): Show | 36 | HG00639.hp1 HG00673.hp2 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.1775-213_1775-204d others(12): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 13/38 | INFO_REALIGN_3_PRIME | chr20 | 48975800 | |||||
| chr20:48975800
|
C | CAAAAAAA others(4): Show |
18 | a0001c0001t0004g0332a0001c0001t0004g0343a0001c0001t0004g0346others(15): Show | 19 | HG00738.hp1 HG00741.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.1775-214_1775-204d others(13): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 13/38 | INFO_REALIGN_3_PRIME | chr20 | 48975800 | |||||
| chr20:48975800
|
C | CAAAAAAA others(5): Show |
46 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0010others(43): Show | 46 | HG00609.hp1 HG00673.hp1 HG01106.hp1 others(43): Show |
intron_variant | MODIFIER | c.1775-215_1775-204d others(14): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 13/38 | INFO_REALIGN_3_PRIME | chr20 | 48975800 | |||||
| chr20:48975800
|
C | CAAAAAAA others(6): Show |
101 | a0001c0001t0002g0003a0001c0001t0002g0116a0001c0001t0002g0117others(98): Show | 101 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.1775-204_1775-203i others(15): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 13/38 | INFO_REALIGN_3_PRIME | chr20 | 48975800 | |||||
| chr20:48975800
|
C | CAAAAAAA others(7): Show |
9 | a0001c0001t0002g0256a0001c0003t0001g0035a0001c0003t0001g0055others(6): Show | 9 | HG00642.hp1 HG01243.hp1 HG04184.hp2 others(6): Show |
intron_variant | MODIFIER | c.1775-204_1775-203i others(16): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 13/38 | INFO_REALIGN_3_PRIME | chr20 | 48975800 | |||||
| chr20:48975800
|
C | CAAAAAAA others(19): Show |
1 | a0001c0003t0001g0065 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1775-204_1775-203i others(28): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 13/38 | INFO_REALIGN_3_PRIME | chr20 | 48975800 | |||||
| chr20:48975813
|
G | A | 35 | a0001c0002t0001g0122a0001c0002t0001g0123a0001c0002t0001g0124others(32): Show | 35 | HG00639.hp1 HG00673.hp2 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.1775-203G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 13/38 | chr20 | 48975813 | ||||||
| chr20:48975951
|
C | G | 1 | a0001c0002t0001g0124 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1775-65C>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 13/38 | chr20 | 48975951 | ||||||
| chr20:48975969
|
G | T | 2 | a0001c0002t0001g0318a0001c0002t0015g0319 | 2 | HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1775-47G>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 13/38 | chr20 | 48975969 | ||||||
| chr20:48976340
|
G | A | 1 | a0001c0001t0006g0272 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1958+141G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 14/38 | chr20 | 48976340 | ||||||
| chr20:48976357
|
G | A | 3 | a0001c0001t0014g0223a0001c0001t0014g0224a0001c0001t0021g0225 | 3 | HG02895.hp2 HG02897.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1958+158G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 14/38 | chr20 | 48976357 | ||||||
| chr20:48976364
|
T | C | 2 | a0001c0001t0006g0272a0001c0001t0006g0273 | 2 | HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1958+165T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 14/38 | chr20 | 48976364 | ||||||
| chr20:48976458
|
C | T | 1 | a0001c0001t0002g0243 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1958+259C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 14/38 | chr20 | 48976458 | ||||||
| chr20:48976739
|
C | T | 1 | a0001c0001t0016g0005 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1958+540C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 14/38 | chr20 | 48976739 | ||||||
| chr20:48976866
|
A | G | 39 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0010others(36): Show | 39 | HG00609.hp1 HG00673.hp1 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.1958+667A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 14/38 | chr20 | 48976866 | ||||||
| chr20:48976935
|
C | CATTTT | 44 | a0001c0001t0002g0221a0001c0001t0002g0222a0001c0001t0002g0227others(41): Show | 46 | HG01109.hp1 HG01256.hp1 HG01258.hp2 others(43): Show |
intron_variant | MODIFIER | c.1958+779_1958+783d others(7): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 14/38 | INFO_REALIGN_3_PRIME | chr20 | 48976935 | |||||
| chr20:48976935
|
C | CATTTTAT others(3): Show |
1 | a0001c0002t0005g0020 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1958+774_1958+783d others(12): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 14/38 | INFO_REALIGN_3_PRIME | chr20 | 48976935 | |||||
| chr20:48976935
|
CATTTT | C | 132 | a0001c0001t0002g0003a0001c0001t0002g0117a0001c0001t0002g0118others(129): Show | 132 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(129): Show |
intron_variant | MODIFIER | c.1958+779_1958+783d others(7): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 14/38 | INFO_REALIGN_3_PRIME | chr20 | 48976935 | |||||
| chr20:48976935
|
CATTTTAT others(3): Show |
C | 14 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0010others(11): Show | 14 | HG01169.hp1 HG01891.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.1958+774_1958+783d others(12): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 14/38 | INFO_REALIGN_3_PRIME | chr20 | 48976935 | |||||
| chr20:48976935
|
CATTTTAT others(8): Show |
C | 2 | a0001c0001t0002g0014a0001c0003t0001g0081 | 2 | HG01975.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1958+769_1958+783d others(17): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 14/38 | INFO_REALIGN_3_PRIME | chr20 | 48976935 | |||||
| chr20:48977196
|
T | A | 2 | a0001c0002t0001g0318a0001c0002t0015g0319 | 2 | HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1958+997T>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 14/38 | chr20 | 48977196 | ||||||
| chr20:48977421
|
G | C | 1 | a0001c0002t0001g0109 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1958+1222G>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 14/38 | chr20 | 48977421 | ||||||
| chr20:48977654
|
T | C | 1 | a0006c0011t0001g0301 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1958+1455T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 14/38 | chr20 | 48977654 | ||||||
| chr20:48977748
|
T | A | 4 | a0001c0002t0001g0134a0001c0002t0001g0161a0001c0002t0001g0168others(1): Show | 4 | HG00438.hp1 HG02074.hp1 HG02080.hp1 others(1): Show |
intron_variant | MODIFIER | c.1958+1549T>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 14/38 | chr20 | 48977748 | ||||||
| chr20:48977879
|
C | T | 7 | a0001c0001t0003g0202a0001c0001t0003g0214a0001c0001t0003g0216others(4): Show | 7 | HG00733.hp2 HG01175.hp2 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1958+1680C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 14/38 | chr20 | 48977879 | ||||||
| chr20:48977894
|
T | C | 1 | a0001c0003t0001g0103 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1958+1695T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 14/38 | chr20 | 48977894 | ||||||
| chr20:48977906
|
A | G | 9 | a0001c0002t0001g0004a0001c0002t0001g0135a0001c0002t0001g0151others(6): Show | 9 | HG01099.hp1 HG02257.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1958+1707A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 14/38 | chr20 | 48977906 | ||||||
| chr20:48978071
|
G | A | 1 | a0001c0003t0001g0317 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1958+1872G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 14/38 | chr20 | 48978071 | ||||||
| chr20:48978071
|
G | C | 3 | a0001c0003t0001g0030a0001c0003t0001g0055a0001c0003t0001g0090 | 3 | NA18948.hp2 NA18984.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.1958+1872G>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 14/38 | chr20 | 48978071 | ||||||
| chr20:48978090
|
C | G | 1 | a0001c0003t0001g0066 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1958+1891C>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 14/38 | chr20 | 48978090 | ||||||
| chr20:48978303
|
C | T | 1 | a0001c0001t0007g0241 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1958+2104C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 14/38 | chr20 | 48978303 | ||||||
| chr20:48978326
|
T | C | 1 | a0001c0002t0001g0297 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1958+2127T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 14/38 | chr20 | 48978326 | ||||||
| chr20:48978345
|
G | T | 3 | a0001c0005t0008g0267a0001c0005t0008g0268a0001c0005t0008g0276 | 3 | HG02486.hp2 HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1958+2146G>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 14/38 | chr20 | 48978345 | ||||||
| chr20:48978652
|
G | A | 1 | a0001c0001t0002g0222 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1958+2453G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 14/38 | chr20 | 48978652 | ||||||
| chr20:48979013
|
G | T | 1 | a0001c0002t0005g0016 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1958+2814G>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 14/38 | chr20 | 48979013 | ||||||
| chr20:48979424
|
G | A | 134 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0009others(131): Show | 134 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(131): Show |
intron_variant | MODIFIER | c.1958+3225G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 14/38 | chr20 | 48979424 | ||||||
| chr20:48979731
|
C | A | 1 | a0001c0001t0006g0273 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1958+3532C>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 14/38 | chr20 | 48979731 | ||||||
| chr20:48979920
|
A | T | 112 | a0001c0002t0001g0122a0001c0002t0001g0123a0001c0002t0001g0124others(109): Show | 112 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.1958+3721A>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 14/38 | chr20 | 48979920 | ||||||
| chr20:48979942
|
T | A | 1 | a0001c0002t0001g0300 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1958+3743T>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 14/38 | chr20 | 48979942 | ||||||
| chr20:48979945
|
A | AT | 114 | a0001c0001t0002g0198a0001c0002t0001g0122a0001c0002t0001g0123others(111): Show | 114 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(111): Show |
intron_variant | MODIFIER | c.1958+3755dupT | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 14/38 | INFO_REALIGN_3_PRIME | chr20 | 48979945 | |||||
| chr20:48979975
|
A | G | 1 | a0001c0003t0001g0043 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1958+3776A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 14/38 | chr20 | 48979975 | ||||||
| chr20:48980331
|
A | C | 3 | a0001c0001t0002g0231a0001c0001t0002g0232a0001c0001t0002g0233 | 3 | HG02258.hp2 HG02717.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1958+4132A>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 14/38 | chr20 | 48980331 | ||||||
| chr20:48980347
|
C | T | 1 | a0001c0002t0001g0318 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1958+4148C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 14/38 | chr20 | 48980347 | ||||||
| chr20:48980404
|
A | G | 2 | a0001c0002t0001g0318a0001c0002t0015g0319 | 2 | HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1958+4205A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 14/38 | chr20 | 48980404 | ||||||
| chr20:48980430
|
A | G | 1 | a0001c0002t0001g0111 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1958+4231A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 14/38 | chr20 | 48980430 | ||||||
| chr20:48980524
|
T | C | 1 | a0001c0001t0003g0208 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1959-4205T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 14/38 | chr20 | 48980524 | ||||||
| chr20:48980797
|
A | G | 2 | a0001c0001t0002g0228a0001c0001t0002g0229 | 2 | HG02622.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1959-3932A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 14/38 | chr20 | 48980797 | ||||||
| chr20:48980967
|
T | A | 11 | a0001c0003t0001g0032a0001c0003t0001g0039a0001c0003t0001g0043others(8): Show | 11 | HG00438.hp2 HG00609.hp1 HG01981.hp2 others(8): Show |
intron_variant | MODIFIER | c.1959-3762T>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 14/38 | chr20 | 48980967 | ||||||
| chr20:48981292
|
A | G | 1 | a0001c0002t0001g0313 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1959-3437A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 14/38 | chr20 | 48981292 | ||||||
| chr20:48981307
|
C | T | 1 | a0001c0003t0001g0066 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1959-3422C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 14/38 | chr20 | 48981307 | ||||||
| chr20:48981582
|
A | G | 112 | a0001c0002t0001g0122a0001c0002t0001g0123a0001c0002t0001g0124others(109): Show | 112 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.1959-3147A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 14/38 | chr20 | 48981582 | ||||||
| chr20:48981689
|
C | A | 2 | a0001c0002t0001g0293a0001c0002t0001g0294 | 2 | HG00741.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.1959-3040C>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 14/38 | chr20 | 48981689 | ||||||
| chr20:48981706
|
C | A | 1 | a0001c0002t0001g0185 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1959-3023C>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 14/38 | chr20 | 48981706 | ||||||
| chr20:48981717
|
T | G | 2 | a0001c0001t0003g0212a0001c0001t0003g0213 | 2 | NA18988.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.1959-3012T>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 14/38 | chr20 | 48981717 | ||||||
| chr20:48981761
|
A | C | 135 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0009others(132): Show | 135 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(132): Show |
intron_variant | MODIFIER | c.1959-2968A>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 14/38 | chr20 | 48981761 | ||||||
| chr20:48981793
|
T | C | 1 | a0001c0003t0001g0067 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1959-2936T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 14/38 | chr20 | 48981793 | ||||||
| chr20:48981960
|
G | C | 247 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0009others(244): Show | 247 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(244): Show |
intron_variant | MODIFIER | c.1959-2769G>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 14/38 | chr20 | 48981960 | ||||||
| chr20:48982062
|
G | A | 1 | a0001c0001t0003g0213 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1959-2667G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 14/38 | chr20 | 48982062 | ||||||
| chr20:48982124
|
C | A | 54 | a0001c0001t0002g0218a0001c0001t0002g0219a0001c0001t0002g0220others(51): Show | 54 | HG00323.hp2 HG00639.hp2 HG00733.hp2 others(51): Show |
intron_variant | MODIFIER | c.1959-2605C>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 14/38 | chr20 | 48982124 | ||||||
| chr20:48982218
|
C | T | 1 | a0001c0002t0022g0197 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1959-2511C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 14/38 | chr20 | 48982218 | ||||||
| chr20:48982222
|
C | G | 2 | a0001c0001t0003g0212a0001c0001t0003g0213 | 2 | NA18988.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.1959-2507C>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 14/38 | chr20 | 48982222 | ||||||
| chr20:48982416
|
G | A | 1 | a0001c0003t0001g0076 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1959-2313G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 14/38 | chr20 | 48982416 | ||||||
| chr20:48982494
|
G | A | 7 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0010others(4): Show | 7 | HG01891.hp2 HG02486.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1959-2235G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 14/38 | chr20 | 48982494 | ||||||
| chr20:48982519
|
A | C | 1 | a0001c0001t0004g0332 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1959-2210A>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 14/38 | chr20 | 48982519 | ||||||
| chr20:48982657
|
C | T | 7 | a0001c0001t0003g0202a0001c0001t0003g0214a0001c0001t0003g0216others(4): Show | 7 | HG00733.hp2 HG01175.hp2 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1959-2072C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 14/38 | chr20 | 48982657 | ||||||
| chr20:48982668
|
A | G | 247 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0009others(244): Show | 247 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(244): Show |
intron_variant | MODIFIER | c.1959-2061A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 14/38 | chr20 | 48982668 | ||||||
| chr20:48982769
|
A | G | 3 | a0001c0005t0008g0267a0001c0005t0008g0268a0001c0005t0008g0276 | 3 | HG02486.hp2 HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1959-1960A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 14/38 | chr20 | 48982769 | ||||||
| chr20:48982785
|
C | T | 2 | a0001c0001t0014g0223a0001c0001t0014g0224 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1959-1944C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 14/38 | chr20 | 48982785 | ||||||
| chr20:48982935
|
C | T | 77 | a0001c0003t0001g0029a0001c0003t0001g0030a0001c0003t0001g0031others(74): Show | 77 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(74): Show |
intron_variant | MODIFIER | c.1959-1794C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 14/38 | chr20 | 48982935 | ||||||
| chr20:48982952
|
C | T | 1 | a0001c0003t0001g0093 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1959-1777C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 14/38 | chr20 | 48982952 | ||||||
| chr20:48982990
|
A | G | 3 | a0001c0001t0004g0328a0001c0001t0004g0331a0001c0001t0004g0337 | 3 | HG00673.hp1 NA18960.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.1959-1739A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 14/38 | chr20 | 48982990 | ||||||
| chr20:48983153
|
C | T | 249 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0009others(246): Show | 249 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(246): Show |
intron_variant | MODIFIER | c.1959-1576C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 14/38 | chr20 | 48983153 | ||||||
| chr20:48983197
|
C | A | 2 | a0001c0002t0001g0313a0001c0002t0001g0314 | 2 | HG00741.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1959-1532C>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 14/38 | chr20 | 48983197 | ||||||
| chr20:48983204
|
C | A | 39 | a0001c0001t0002g0003a0001c0001t0002g0116a0001c0001t0002g0117others(36): Show | 39 | HG00280.hp1 HG00558.hp2 HG01106.hp2 others(36): Show |
intron_variant | MODIFIER | c.1959-1525C>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 14/38 | chr20 | 48983204 | ||||||
| chr20:48983323
|
C | T | 1 | a0001c0002t0001g0318 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1959-1406C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 14/38 | chr20 | 48983323 | ||||||
| chr20:48983365
|
T | C | 1 | a0001c0001t0004g0326 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1959-1364T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 14/38 | chr20 | 48983365 | ||||||
| chr20:48983439
|
C | T | 1 | a0001c0003t0001g0095 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1959-1290C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 14/38 | chr20 | 48983439 | ||||||
| chr20:48983624
|
A | G | 2 | a0001c0002t0001g0318a0001c0002t0015g0319 | 2 | HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1959-1105A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 14/38 | chr20 | 48983624 | ||||||
| chr20:48983625
|
A | G | 2 | a0001c0002t0001g0315a0001c0002t0001g0316 | 2 | HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1959-1104A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 14/38 | chr20 | 48983625 | ||||||
| chr20:48983643
|
G | C | 1 | a0001c0002t0001g0111 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1959-1086G>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 14/38 | chr20 | 48983643 | ||||||
| chr20:48983816
|
C | T | 1 | a0001c0016t0001g0028 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1959-913C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 14/38 | chr20 | 48983816 | ||||||
| chr20:48983941
|
T | C | 1 | a0001c0001t0002g0278 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1959-788T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 14/38 | chr20 | 48983941 | ||||||
| chr20:48983946
|
G | A | 1 | a0001c0001t0002g0253 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1959-783G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 14/38 | chr20 | 48983946 | ||||||
| chr20:48984063
|
A | G | 1 | a0001c0003t0001g0049 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1959-666A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 14/38 | chr20 | 48984063 | ||||||
| chr20:48984149
|
C | T | 1 | a0001c0003t0001g0035 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1959-580C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 14/38 | chr20 | 48984149 | ||||||
| chr20:48984281
|
G | A | 112 | a0001c0002t0001g0122a0001c0002t0001g0123a0001c0002t0001g0124others(109): Show | 112 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.1959-448G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 14/38 | chr20 | 48984281 | ||||||
| chr20:48984677
|
A | G | 15 | a0001c0002t0005g0001a0001c0002t0005g0015a0001c0002t0005g0016others(12): Show | 16 | HG01109.hp1 HG01884.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.1959-52A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 14/38 | chr20 | 48984677 | ||||||
| chr20:48984972
|
A | G | 135 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0009others(132): Show | 135 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(132): Show |
intron_variant | MODIFIER | c.2070+132A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 15/38 | chr20 | 48984972 | ||||||
| chr20:48985087
|
G | A | 1 | a0001c0002t0001g0163 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.2070+247G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 15/38 | chr20 | 48985087 | ||||||
| chr20:48985130
|
C | T | 2 | a0001c0001t0002g0228a0001c0001t0002g0229 | 2 | HG02622.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.2071-278C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 15/38 | chr20 | 48985130 | ||||||
| chr20:48985159
|
G | T | 35 | a0001c0002t0001g0122a0001c0002t0001g0123a0001c0002t0001g0124others(32): Show | 35 | HG00639.hp1 HG00673.hp2 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.2071-249G>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 15/38 | chr20 | 48985159 | ||||||
| chr20:48985168
|
G | A | 35 | a0001c0002t0001g0122a0001c0002t0001g0123a0001c0002t0001g0124others(32): Show | 35 | HG00639.hp1 HG00673.hp2 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.2071-240G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 15/38 | chr20 | 48985168 | ||||||
| chr20:48985206
|
C | T | 1 | a0004c0008t0002g0264 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.2071-202C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 15/38 | chr20 | 48985206 | ||||||
| chr20:48985365
|
G | A | 2 | a0001c0001t0002g0280a0001c0003t0001g0071 | 2 | HG02895.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.2071-43G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 15/38 | chr20 | 48985365 | ||||||
| chr20:48985383
|
A | T | 1 | a0001c0003t0001g0099 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.2071-25A>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 15/38 | chr20 | 48985383 | ||||||
| chr20:48985667
|
G | A | 1 | a0001c0002t0022g0197 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2276+54G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 16/38 | chr20 | 48985667 | ||||||
| chr20:48985802
|
A | G | 135 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0009others(132): Show | 135 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(132): Show |
intron_variant | MODIFIER | c.2276+189A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 16/38 | chr20 | 48985802 | ||||||
| chr20:48986076
|
G | A | 1 | a0001c0001t0002g0013 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2276+463G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 16/38 | chr20 | 48986076 | ||||||
| chr20:48986110
|
G | C | 1 | a0001c0001t0002g0271 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2276+497G>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 16/38 | chr20 | 48986110 | ||||||
| chr20:48986295
|
G | T | 125 | a0001c0001t0002g0003a0001c0001t0002g0116a0001c0001t0002g0117others(122): Show | 125 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(122): Show |
intron_variant | MODIFIER | c.2276+682G>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 16/38 | chr20 | 48986295 | ||||||
| chr20:48986332
|
A | T | 1 | a0003c0007t0001g0303 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2276+719A>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 16/38 | chr20 | 48986332 | ||||||
| chr20:48986355
|
G | A | 1 | a0001c0002t0001g0160 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.2276+742G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 16/38 | chr20 | 48986355 | ||||||
| chr20:48986704
|
A | G | 96 | a0001c0001t0002g0003a0001c0001t0002g0116a0001c0001t0002g0117others(93): Show | 96 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.2276+1091A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 16/38 | chr20 | 48986704 | ||||||
| chr20:48987196
|
G | A | 1 | a0001c0003t0001g0035 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2277-1108G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 16/38 | chr20 | 48987196 | ||||||
| chr20:48987603
|
G | C | 1 | a0001c0013t0003g0206 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2277-701G>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 16/38 | chr20 | 48987603 | ||||||
| chr20:48987624
|
G | C | 1 | a0001c0001t0023g0215 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2277-680G>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 16/38 | chr20 | 48987624 | ||||||
| chr20:48987706
|
A | T | 1 | a0001c0003t0001g0055 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.2277-598A>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 16/38 | chr20 | 48987706 | ||||||
| chr20:48987740
|
A | T | 1 | a0001c0002t0001g0313 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2277-564A>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 16/38 | chr20 | 48987740 | ||||||
| chr20:48987815
|
T | G | 2 | a0001c0003t0001g0044a0001c0003t0001g0073 | 2 | NA18965.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.2277-489T>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 16/38 | chr20 | 48987815 | ||||||
| chr20:48987889
|
G | A | 2 | a0001c0001t0004g0346a0001c0001t0004g0347 | 2 | NA18993.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.2277-415G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 16/38 | chr20 | 48987889 | ||||||
| chr20:48987944
|
C | T | 1 | a0001c0002t0001g0311 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.2277-360C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 16/38 | chr20 | 48987944 | ||||||
| chr20:48988039
|
C | T | 2 | a0001c0001t0003g0199a0001c0001t0003g0200 | 2 | HG00639.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.2277-265C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 16/38 | chr20 | 48988039 | ||||||
| chr20:48988063
|
C | T | 35 | a0001c0002t0001g0122a0001c0002t0001g0123a0001c0002t0001g0124others(32): Show | 35 | HG00639.hp1 HG00673.hp2 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.2277-241C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 16/38 | chr20 | 48988063 | ||||||
| chr20:48988214
|
C | T | 1 | a0001c0001t0002g0254 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.2277-90C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 16/38 | chr20 | 48988214 | ||||||
| chr20:48988288
|
G | A | 112 | a0001c0002t0001g0122a0001c0002t0001g0123a0001c0002t0001g0124others(109): Show | 112 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.2277-16G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 16/38 | chr20 | 48988288 | ||||||
| chr20:48988721
|
A | T | 2 | a0001c0002t0005g0021a0001c0002t0005g0025 | 2 | HG01891.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2533+59A>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 18/38 | chr20 | 48988721 | ||||||
| chr20:48988813
|
C | CA | 3 | a0001c0002t0001g0137a0001c0002t0001g0166a0001c0002t0001g0167 | 3 | HG01169.hp1 HG01978.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.2533+151_2533+152i others(3): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 18/38 | chr20 | 48988813 | ||||||
| chr20:48988877
|
A | G | 1 | a0001c0002t0001g0135 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2533+215A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 18/38 | chr20 | 48988877 | ||||||
| chr20:48989075
|
C | A | 133 | a0001c0002t0001g0122a0001c0002t0001g0123a0001c0002t0001g0124others(130): Show | 134 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(131): Show |
intron_variant | MODIFIER | c.2534-210C>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 18/38 | chr20 | 48989075 | ||||||
| chr20:48989237
|
C | T | 2 | a0001c0003t0001g0057a0001c0003t0001g0091 | 2 | HG01261.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2534-48C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 18/38 | chr20 | 48989237 | ||||||
| chr20:48989490
|
G | A | 19 | a0001c0002t0001g0313a0001c0002t0001g0314a0001c0002t0005g0001others(16): Show | 20 | HG00741.hp2 HG01109.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.2685+54G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 19/38 | chr20 | 48989490 | ||||||
| chr20:48989506
|
C | G | 29 | a0001c0001t0004g0321a0001c0001t0004g0323a0001c0001t0004g0324others(26): Show | 29 | HG00673.hp1 HG00738.hp1 HG01934.hp1 others(26): Show |
intron_variant | MODIFIER | c.2686-50C>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 19/38 | chr20 | 48989506 | ||||||
| chr20:48989719
|
G | A | 2 | a0001c0002t0005g0026a0001c0002t0005g0027 | 2 | HG02970.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2814+35G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 20/38 | chr20 | 48989719 | ||||||
| chr20:48989813
|
T | G | 2 | a0001c0001t0002g0228a0001c0001t0002g0229 | 2 | HG02622.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.2814+129T>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 20/38 | chr20 | 48989813 | ||||||
| chr20:48989908
|
A | G | 1 | a0001c0002t0001g0304 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2814+224A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 20/38 | chr20 | 48989908 | ||||||
| chr20:48990009
|
A | G | 23 | a0001c0002t0001g0138a0001c0002t0001g0139a0001c0002t0001g0140others(20): Show | 23 | HG00609.hp2 HG00733.hp1 HG01123.hp1 others(20): Show |
intron_variant | MODIFIER | c.2814+325A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 20/38 | chr20 | 48990009 | ||||||
| chr20:48990035
|
C | T | 1 | a0001c0002t0001g0004 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2814+351C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 20/38 | chr20 | 48990035 | ||||||
| chr20:48990119
|
C | T | 15 | a0001c0002t0005g0001a0001c0002t0005g0015a0001c0002t0005g0016others(12): Show | 16 | HG01109.hp1 HG01884.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.2814+435C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 20/38 | chr20 | 48990119 | ||||||
| chr20:48990305
|
A | G | 1 | a0001c0001t0002g0243 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2814+621A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 20/38 | chr20 | 48990305 | ||||||
| chr20:48990328
|
G | A | 4 | a0001c0003t0001g0035a0001c0003t0001g0051a0001c0003t0001g0062others(1): Show | 4 | HG04184.hp2 NA18981.hp1 NA18985.hp2 others(1): Show |
intron_variant | MODIFIER | c.2814+644G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 20/38 | chr20 | 48990328 | ||||||
| chr20:48990596
|
A | G | 1 | a0001c0001t0002g0222 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2815-444A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 20/38 | chr20 | 48990596 | ||||||
| chr20:48990609
|
G | A | 112 | a0001c0002t0001g0122a0001c0002t0001g0123a0001c0002t0001g0124others(109): Show | 112 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.2815-431G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 20/38 | chr20 | 48990609 | ||||||
| chr20:48990679
|
T | C | 2 | a0001c0002t0001g0004a0001c0002t0001g0151 | 2 | HG02257.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2815-361T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 20/38 | chr20 | 48990679 | ||||||
| chr20:48991219
|
C | G | 1 | a0001c0002t0001g0297 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2973+21C>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 21/38 | chr20 | 48991219 | ||||||
| chr20:48991223
|
T | C | 1 | a0001c0001t0003g0207 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2973+25T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 21/38 | chr20 | 48991223 | ||||||
| chr20:48991229
|
G | C | 4 | a0001c0001t0006g0266a0001c0001t0006g0272a0001c0001t0006g0273others(1): Show | 4 | HG02055.hp2 HG02145.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.2973+31G>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 21/38 | chr20 | 48991229 | ||||||
| chr20:48991410
|
T | C | 19 | a0001c0001t0004g0325a0001c0001t0004g0326a0001c0001t0004g0327others(16): Show | 19 | HG00673.hp1 HG00738.hp1 HG01934.hp1 others(16): Show |
intron_variant | MODIFIER | c.2973+212T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 21/38 | chr20 | 48991410 | ||||||
| chr20:48991464
|
A | AT | 6 | a0001c0001t0004g0328a0001c0002t0001g0110a0001c0002t0001g0161others(3): Show | 6 | HG02074.hp1 HG02970.hp1 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.2973+283dupT | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 21/38 | INFO_REALIGN_3_PRIME | chr20 | 48991464 | |||||
| chr20:48991856
|
T | C | 1 | a0001c0001t0002g0251 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.2973+658T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 21/38 | chr20 | 48991856 | ||||||
| chr20:48991951
|
T | C | 14 | a0001c0003t0001g0030a0001c0003t0001g0045a0001c0003t0001g0046others(11): Show | 14 | HG00621.hp1 HG02027.hp2 HG02155.hp2 others(11): Show |
intron_variant | MODIFIER | c.2973+753T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 21/38 | chr20 | 48991951 | ||||||
| chr20:48991961
|
A | G | 1 | a0001c0002t0022g0197 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2973+763A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 21/38 | chr20 | 48991961 | ||||||
| chr20:48992242
|
T | C | 3 | a0001c0005t0008g0267a0001c0005t0008g0268a0001c0005t0008g0276 | 3 | HG02486.hp2 HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2973+1044T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 21/38 | chr20 | 48992242 | ||||||
| chr20:48992323
|
T | A | 1 | a0001c0002t0001g0112 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2973+1125T>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 21/38 | chr20 | 48992323 | ||||||
| chr20:48992674
|
C | T | 4 | a0001c0003t0001g0045a0001c0003t0001g0046a0001c0003t0001g0049others(1): Show | 4 | HG00621.hp1 HG02027.hp2 HG02155.hp2 others(1): Show |
intron_variant | MODIFIER | c.2973+1476C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 21/38 | chr20 | 48992674 | ||||||
| chr20:48992869
|
C | T | 2 | a0001c0002t0001g0315a0001c0002t0001g0316 | 2 | HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2974-1582C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 21/38 | chr20 | 48992869 | ||||||
| chr20:48993094
|
C | A | 19 | a0001c0002t0001g0313a0001c0002t0001g0314a0001c0002t0005g0001others(16): Show | 20 | HG00741.hp2 HG01109.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.2974-1357C>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 21/38 | chr20 | 48993094 | ||||||
| chr20:48993428
|
C | G | 1 | a0001c0002t0001g0297 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2974-1023C>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 21/38 | chr20 | 48993428 | ||||||
| chr20:48993527
|
T | C | 2 | a0001c0001t0004g0346a0001c0001t0004g0347 | 2 | NA18993.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.2974-924T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 21/38 | chr20 | 48993527 | ||||||
| chr20:48993629
|
C | T | 3 | a0001c0001t0014g0223a0001c0001t0014g0224a0001c0001t0021g0225 | 3 | HG02895.hp2 HG02897.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2974-822C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 21/38 | chr20 | 48993629 | ||||||
| chr20:48993704
|
A | G | 1 | a0001c0002t0022g0197 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2974-747A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 21/38 | chr20 | 48993704 | ||||||
| chr20:48993760
|
G | T | 135 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0009others(132): Show | 135 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(132): Show |
intron_variant | MODIFIER | c.2974-691G>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 21/38 | chr20 | 48993760 | ||||||
| chr20:48993774
|
G | A | 1 | a0001c0001t0003g0216 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.2974-677G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 21/38 | chr20 | 48993774 | ||||||
| chr20:48993886
|
A | G | 2 | a0001c0002t0001g0318a0001c0002t0015g0319 | 2 | HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2974-565A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 21/38 | chr20 | 48993886 | ||||||
| chr20:48993942
|
T | C | 1 | a0001c0002t0001g0112 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2974-509T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 21/38 | chr20 | 48993942 | ||||||
| chr20:48994262
|
G | A | 3 | a0001c0003t0001g0057a0001c0003t0001g0091a0001c0003t0001g0102 | 3 | HG01243.hp1 HG01261.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2974-189G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 21/38 | chr20 | 48994262 | ||||||
| chr20:48994359
|
C | T | 135 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0009others(132): Show | 135 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(132): Show |
intron_variant | MODIFIER | c.2974-92C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 21/38 | chr20 | 48994359 | ||||||
| chr20:48994713
|
G | A | 1 | a0001c0002t0001g0313 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3121+115G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 22/38 | chr20 | 48994713 | ||||||
| chr20:48995082
|
G | A | 2 | a0001c0002t0001g0318a0001c0002t0015g0319 | 2 | HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.3121+484G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 22/38 | chr20 | 48995082 | ||||||
| chr20:48995148
|
A | G | 9 | a0001c0002t0005g0001a0001c0002t0005g0015a0001c0002t0005g0016others(6): Show | 10 | HG01109.hp1 HG01884.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.3121+550A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 22/38 | chr20 | 48995148 | ||||||
| chr20:48995370
|
T | C | 109 | a0001c0002t0001g0122a0001c0002t0001g0123a0001c0002t0001g0124others(106): Show | 109 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(106): Show |
intron_variant | MODIFIER | c.3122-413T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 22/38 | chr20 | 48995370 | ||||||
| chr20:48995645
|
G | A | 2 | a0001c0002t0001g0307a0001c0002t0001g0311 | 2 | NA18971.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.3122-138G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 22/38 | chr20 | 48995645 | ||||||
| chr20:48995721
|
T | G | 7 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0010others(4): Show | 7 | HG01891.hp2 HG02486.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.3122-62T>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 22/38 | chr20 | 48995721 | ||||||
| chr20:48995960
|
T | G | 3 | a0001c0001t0002g0277a0001c0001t0002g0278a0001c0001t0002g0279 | 3 | HG02723.hp1 HG02976.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.3221+78T>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 23/38 | chr20 | 48995960 | ||||||
| chr20:48996025
|
G | C | 3 | a0001c0001t0002g0231a0001c0001t0002g0232a0001c0001t0002g0233 | 3 | HG02258.hp2 HG02717.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.3221+143G>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 23/38 | chr20 | 48996025 | ||||||
| chr20:48996127
|
C | T | 1 | a0001c0002t0001g0141 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.3221+245C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 23/38 | chr20 | 48996127 | ||||||
| chr20:48996170
|
G | A | 1 | a0001c0002t0001g0182 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.3221+288G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 23/38 | chr20 | 48996170 | ||||||
| chr20:48996337
|
C | G | 1 | a0001c0016t0001g0028 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3221+455C>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 23/38 | chr20 | 48996337 | ||||||
| chr20:48996455
|
C | CA | 127 | a0001c0001t0002g0218a0001c0001t0002g0245a0001c0001t0002g0254others(124): Show | 127 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(124): Show |
intron_variant | MODIFIER | c.3221+583dupA | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 23/38 | INFO_REALIGN_3_PRIME | chr20 | 48996455 | |||||
| chr20:48996455
|
C | CAA | 11 | a0001c0001t0003g0114a0001c0002t0001g0123a0001c0002t0001g0287others(8): Show | 11 | HG02135.hp1 HG02135.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.3221+582_3221+583d others(4): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 23/38 | INFO_REALIGN_3_PRIME | chr20 | 48996455 | |||||
| chr20:48996495
|
A | G | 16 | a0001c0002t0005g0001a0001c0002t0005g0015a0001c0002t0005g0016others(13): Show | 17 | HG01109.hp1 HG01884.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.3221+613A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 23/38 | chr20 | 48996495 | ||||||
| chr20:48996559
|
A | C | 1 | a0001c0001t0004g0344 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.3221+677A>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 23/38 | chr20 | 48996559 | ||||||
| chr20:48996620
|
A | T | 208 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0009others(205): Show | 209 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(206): Show |
intron_variant | MODIFIER | c.3221+738A>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 23/38 | chr20 | 48996620 | ||||||
| chr20:48996741
|
T | TA | 7 | a0001c0001t0002g0218a0001c0001t0003g0211a0001c0001t0004g0324others(4): Show | 7 | HG03486.hp1 HG04115.hp2 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.3221+877dupA | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 23/38 | INFO_REALIGN_3_PRIME | chr20 | 48996741 | |||||
| chr20:48996741
|
TA | T | 6 | a0001c0001t0002g0257a0001c0001t0003g0204a0001c0001t0003g0247others(3): Show | 6 | HG00323.hp2 NA18939.hp1 NA18948.hp1 others(3): Show |
intron_variant | MODIFIER | c.3221+877delA | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 23/38 | INFO_REALIGN_3_PRIME | chr20 | 48996741 | |||||
| chr20:48996741
|
TAAA | T | 128 | a0001c0002t0001g0122a0001c0002t0001g0123a0001c0002t0001g0124others(125): Show | 129 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(126): Show |
intron_variant | MODIFIER | c.3221+875_3221+877d others(5): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 23/38 | INFO_REALIGN_3_PRIME | chr20 | 48996741 | |||||
| chr20:48996797
|
T | C | 1 | a0001c0001t0004g0339 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.3221+915T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 23/38 | chr20 | 48996797 | ||||||
| chr20:48996811
|
T | C | 2 | a0001c0002t0001g0006a0001c0002t0017g0007 | 2 | HG00642.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.3221+929T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 23/38 | chr20 | 48996811 | ||||||
| chr20:48997250
|
G | T | 1 | a0001c0001t0003g0210 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3222-943G>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 23/38 | chr20 | 48997250 | ||||||
| chr20:48997265
|
T | TATTG | 125 | a0001c0001t0002g0008a0001c0001t0002g0010a0001c0001t0002g0011others(122): Show | 125 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(122): Show |
intron_variant | MODIFIER | c.3222-902_3222-899d others(6): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 23/38 | INFO_REALIGN_3_PRIME | chr20 | 48997265 | |||||
| chr20:48997265
|
T | TATTGATT others(1): Show |
64 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0116others(61): Show | 64 | HG00280.hp1 HG00558.hp2 HG00673.hp2 others(61): Show |
intron_variant | MODIFIER | c.3222-906_3222-899d others(10): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 23/38 | INFO_REALIGN_3_PRIME | chr20 | 48997265 | |||||
| chr20:48997265
|
TATTG | T | 19 | a0001c0002t0001g0313a0001c0002t0001g0314a0001c0002t0005g0001others(16): Show | 20 | HG00741.hp2 HG01109.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.3222-902_3222-899d others(6): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 23/38 | INFO_REALIGN_3_PRIME | chr20 | 48997265 | |||||
| chr20:48997299
|
G | A | 1 | a0001c0002t0001g0296 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3222-894G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 23/38 | chr20 | 48997299 | ||||||
| chr20:48997336
|
G | C | 1 | a0001c0002t0005g0027 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.3222-857G>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 23/38 | chr20 | 48997336 | ||||||
| chr20:48997462
|
A | G | 7 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0010others(4): Show | 7 | HG01891.hp2 HG02486.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.3222-731A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 23/38 | chr20 | 48997462 | ||||||
| chr20:48997960
|
C | A | 109 | a0001c0002t0001g0122a0001c0002t0001g0123a0001c0002t0001g0124others(106): Show | 109 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(106): Show |
intron_variant | MODIFIER | c.3222-233C>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 23/38 | chr20 | 48997960 | ||||||
| chr20:48997961
|
G | A | 1 | a0001c0001t0002g0230 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3222-232G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 23/38 | chr20 | 48997961 | ||||||
| chr20:48998015
|
G | A | 20 | a0001c0001t0002g0244a0001c0002t0001g0313a0001c0002t0001g0314others(17): Show | 21 | HG00741.hp2 HG01109.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.3222-178G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 23/38 | chr20 | 48998015 | ||||||
| chr20:48998128
|
G | A | 109 | a0001c0002t0001g0122a0001c0002t0001g0123a0001c0002t0001g0124others(106): Show | 109 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(106): Show |
intron_variant | MODIFIER | c.3222-65G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 23/38 | chr20 | 48998128 | ||||||
| chr20:48998537
|
TA | T | 131 | a0001c0001t0002g0257a0001c0001t0003g0236a0001c0001t0006g0272others(128): Show | 132 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(129): Show |
intron_variant | MODIFIER | c.3432+46delA | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 25/38 | INFO_REALIGN_3_PRIME | chr20 | 48998537 | |||||
| chr20:48998694
|
G | T | 1 | a0001c0002t0001g0175 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.3432+189G>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 25/38 | chr20 | 48998694 | ||||||
| chr20:48999036
|
G | C | 1 | a0001c0001t0002g0256 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.3432+531G>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 25/38 | chr20 | 48999036 | ||||||
| chr20:48999155
|
T | G | 74 | a0001c0003t0001g0029a0001c0003t0001g0030a0001c0003t0001g0031others(71): Show | 74 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.3432+650T>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 25/38 | chr20 | 48999155 | ||||||
| chr20:48999178
|
C | T | 3 | a0001c0001t0006g0266a0001c0001t0006g0272a0001c0001t0006g0273 | 3 | HG02145.hp2 HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.3432+673C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 25/38 | chr20 | 48999178 | ||||||
| chr20:48999605
|
G | A | 6 | a0001c0001t0003g0203a0001c0001t0003g0204a0001c0001t0003g0205others(3): Show | 6 | HG00323.hp2 HG00738.hp2 HG01081.hp1 others(3): Show |
intron_variant | MODIFIER | c.3432+1100G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 25/38 | chr20 | 48999605 | ||||||
| chr20:48999607
|
C | T | 35 | a0001c0001t0002g0003a0001c0001t0002g0116a0001c0001t0002g0117others(32): Show | 35 | HG00280.hp1 HG00558.hp2 HG01106.hp2 others(32): Show |
intron_variant | MODIFIER | c.3432+1102C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 25/38 | chr20 | 48999607 | ||||||
| chr20:48999608
|
G | A | 1 | a0001c0002t0005g0021 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3432+1103G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 25/38 | chr20 | 48999608 | ||||||
| chr20:48999734
|
G | A | 128 | a0001c0001t0002g0003a0001c0001t0002g0116a0001c0001t0002g0117others(125): Show | 128 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(125): Show |
intron_variant | MODIFIER | c.3432+1229G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 25/38 | chr20 | 48999734 | ||||||
| chr20:48999746
|
T | TA | 109 | a0001c0001t0002g0257a0001c0001t0004g0321a0001c0001t0004g0335others(106): Show | 109 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(106): Show |
intron_variant | MODIFIER | c.3432+1263dupA | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 25/38 | INFO_REALIGN_3_PRIME | chr20 | 48999746 | |||||
| chr20:48999746
|
T | TAA | 6 | a0001c0002t0001g0313a0001c0002t0001g0314a0001c0003t0001g0045others(3): Show | 6 | HG00741.hp2 HG02027.hp2 NA18987.hp1 others(3): Show |
intron_variant | MODIFIER | c.3432+1262_3432+126 others(6): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 25/38 | INFO_REALIGN_3_PRIME | chr20 | 48999746 | |||||
| chr20:48999762
|
A | AG | 10 | a0001c0002t0005g0001a0001c0002t0005g0015a0001c0002t0005g0016others(7): Show | 11 | HG01109.hp1 HG01884.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.3432+1257_3432+125 others(5): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 25/38 | chr20 | 48999762 | ||||||
| chr20:48999764
|
A | AC | 3 | a0001c0001t0002g0232a0001c0001t0002g0244a0001c0003t0001g0057 | 3 | HG01261.hp2 HG02258.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.3432+1259_3432+126 others(5): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 25/38 | chr20 | 48999764 | ||||||
| chr20:48999764
|
A | C | 55 | a0001c0001t0001g0170a0001c0001t0002g0218a0001c0001t0002g0219others(52): Show | 55 | HG00323.hp2 HG00639.hp2 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.3432+1259A>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 25/38 | chr20 | 48999764 | ||||||
| chr20:48999988
|
T | C | 3 | a0001c0005t0008g0267a0001c0005t0008g0268a0001c0005t0008g0276 | 3 | HG02486.hp2 HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.3432+1483T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 25/38 | chr20 | 48999988 | ||||||
| chr20:49000092
|
A | G | 4 | a0001c0001t0002g0220a0001c0001t0002g0277a0001c0001t0002g0278others(1): Show | 4 | HG01243.hp2 HG02723.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.3432+1587A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 25/38 | chr20 | 49000092 | ||||||
| chr20:49000182
|
A | T | 1 | a0001c0002t0001g0350 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.3432+1677A>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 25/38 | chr20 | 49000182 | ||||||
| chr20:49000237
|
A | G | 7 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0010others(4): Show | 7 | HG01891.hp2 HG02486.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.3432+1732A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 25/38 | chr20 | 49000237 | ||||||
| chr20:49000394
|
A | G | 3 | a0001c0001t0002g0226a0001c0001t0002g0227a0001c0001t0002g0230 | 3 | HG02451.hp2 HG02559.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.3432+1889A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 25/38 | chr20 | 49000394 | ||||||
| chr20:49000402
|
G | T | 1 | a0002c0004t0001g0169 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.3432+1897G>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 25/38 | chr20 | 49000402 | ||||||
| chr20:49000528
|
C | T | 2 | a0001c0002t0001g0318a0001c0002t0015g0319 | 2 | HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.3432+2023C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 25/38 | chr20 | 49000528 | ||||||
| chr20:49000703
|
C | G | 3 | a0001c0002t0001g0293a0001c0002t0001g0294a0001c0002t0001g0295 | 3 | HG00741.hp1 HG01071.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.3432+2198C>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 25/38 | chr20 | 49000703 | ||||||
| chr20:49001028
|
A | C | 35 | a0001c0002t0001g0122a0001c0002t0001g0123a0001c0002t0001g0124others(32): Show | 35 | HG00639.hp1 HG00673.hp2 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.3432+2523A>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 25/38 | chr20 | 49001028 | ||||||
| chr20:49001033
|
G | A | 1 | a0001c0001t0004g0340 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.3432+2528G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 25/38 | chr20 | 49001033 | ||||||
| chr20:49001054
|
C | CT | 7 | a0001c0001t0002g0227a0001c0001t0004g0339a0001c0002t0001g0110others(4): Show | 7 | HG02273.hp2 HG02486.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.3432+2574dupT | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 25/38 | INFO_REALIGN_3_PRIME | chr20 | 49001054 | |||||
| chr20:49001054
|
CT | C | 210 | a0001c0001t0001g0170a0001c0001t0002g0008a0001c0001t0002g0009others(207): Show | 211 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.3432+2574delT | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 25/38 | INFO_REALIGN_3_PRIME | chr20 | 49001054 | |||||
| chr20:49001054
|
CTT | C | 60 | a0001c0001t0002g0013a0001c0001t0002g0248a0001c0001t0002g0249others(57): Show | 61 | HG00639.hp1 HG00673.hp2 HG00741.hp1 others(58): Show |
intron_variant | MODIFIER | c.3432+2573_3432+257 others(6): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 25/38 | INFO_REALIGN_3_PRIME | chr20 | 49001054 | |||||
| chr20:49001082
|
G | C | 1 | a0001c0002t0001g0287 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.3432+2577G>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 25/38 | chr20 | 49001082 | ||||||
| chr20:49001090
|
T | G | 1 | a0001c0003t0001g0076 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.3432+2585T>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 25/38 | chr20 | 49001090 | ||||||
| chr20:49001112
|
C | T | 2 | a0001c0002t0001g0142a0001c0016t0001g0028 | 2 | HG01346.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.3432+2607C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 25/38 | chr20 | 49001112 | ||||||
| chr20:49001421
|
C | A | 2 | a0001c0002t0001g0318a0001c0002t0015g0319 | 2 | HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.3432+2916C>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 25/38 | chr20 | 49001421 | ||||||
| chr20:49001517
|
A | G | 3 | a0001c0003t0001g0103a0001c0003t0001g0104a0001c0003t0001g0108 | 3 | HG02647.hp2 HG02717.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.3432+3012A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 25/38 | chr20 | 49001517 | ||||||
| chr20:49001555
|
A | G | 2 | a0001c0001t0002g0198a0004c0008t0002g0264 | 2 | NA18946.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.3432+3050A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 25/38 | chr20 | 49001555 | ||||||
| chr20:49001814
|
A | G | 2 | a0001c0001t0003g0235a0001c0001t0003g0236 | 2 | HG02735.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.3433-3256A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 25/38 | chr20 | 49001814 | ||||||
| chr20:49001932
|
C | G | 19 | a0001c0002t0001g0313a0001c0002t0001g0314a0001c0002t0005g0001others(16): Show | 20 | HG00741.hp2 HG01109.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.3433-3138C>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 25/38 | chr20 | 49001932 | ||||||
| chr20:49001956
|
C | T | 130 | a0001c0002t0001g0122a0001c0002t0001g0123a0001c0002t0001g0124others(127): Show | 131 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(128): Show |
intron_variant | MODIFIER | c.3433-3114C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 25/38 | chr20 | 49001956 | ||||||
| chr20:49002032
|
G | A | 1 | a0001c0001t0003g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.3433-3038G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 25/38 | chr20 | 49002032 | ||||||
| chr20:49002043
|
C | T | 2 | a0001c0002t0001g0318a0001c0002t0015g0319 | 2 | HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.3433-3027C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 25/38 | chr20 | 49002043 | ||||||
| chr20:49002098
|
C | T | 1 | a0001c0001t0002g0218 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3433-2972C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 25/38 | chr20 | 49002098 | ||||||
| chr20:49002099
|
G | A | 1 | a0001c0003t0001g0048 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.3433-2971G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 25/38 | chr20 | 49002099 | ||||||
| chr20:49002211
|
C | G | 2 | a0001c0002t0001g0313a0001c0002t0001g0314 | 2 | HG00741.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.3433-2859C>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 25/38 | chr20 | 49002211 | ||||||
| chr20:49002298
|
G | A | 38 | a0001c0001t0002g0240a0001c0001t0003g0113a0001c0001t0003g0114others(35): Show | 38 | HG00323.hp2 HG00639.hp2 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.3433-2772G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 25/38 | chr20 | 49002298 | ||||||
| chr20:49002302
|
G | A | 3 | a0001c0001t0002g0218a0001c0001t0002g0219a0001c0001t0002g0243 | 3 | HG02145.hp1 HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.3433-2768G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 25/38 | chr20 | 49002302 | ||||||
| chr20:49002386
|
C | G | 1 | a0001c0001t0003g0200 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.3433-2684C>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 25/38 | chr20 | 49002386 | ||||||
| chr20:49002414
|
C | T | 1 | a0001c0003t0001g0079 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.3433-2656C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 25/38 | chr20 | 49002414 | ||||||
| chr20:49002608
|
A | ATTAT | 33 | a0001c0002t0001g0122a0001c0002t0001g0123a0001c0002t0001g0124others(30): Show | 33 | HG00639.hp1 HG00673.hp2 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.3433-2447_3433-244 others(8): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 25/38 | INFO_REALIGN_3_PRIME | chr20 | 49002608 | |||||
| chr20:49002760
|
C | A | 1 | a0001c0016t0001g0028 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3433-2310C>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 25/38 | chr20 | 49002760 | ||||||
| chr20:49002762
|
GC | G | 349 | a0001c0001t0001g0170a0001c0001t0002g0003a0001c0001t0002g0008others(346): Show | 351 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(348): Show |
intron_variant | MODIFIER | c.3433-2305delC | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 25/38 | INFO_REALIGN_3_PRIME | chr20 | 49002762 | |||||
| chr20:49002964
|
CT | C | 8 | a0001c0001t0002g0270a0001c0001t0020g0329a0001c0001t0023g0215others(5): Show | 8 | HG01169.hp2 HG01516.hp2 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.3433-2085delT | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 25/38 | INFO_REALIGN_3_PRIME | chr20 | 49002964 | |||||
| chr20:49002964
|
CTT | C | 125 | a0001c0002t0001g0122a0001c0002t0001g0123a0001c0002t0001g0124others(122): Show | 126 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(123): Show |
intron_variant | MODIFIER | c.3433-2086_3433-208 others(6): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 25/38 | INFO_REALIGN_3_PRIME | chr20 | 49002964 | |||||
| chr20:49002964
|
CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0002g0013 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.3433-2096_3433-208 others(16): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 25/38 | INFO_REALIGN_3_PRIME | chr20 | 49002964 | |||||
| chr20:49003156
|
CAG | C | 19 | a0001c0002t0001g0313a0001c0002t0001g0314a0001c0002t0005g0001others(16): Show | 20 | HG00741.hp2 HG01109.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.3433-1913_3433-191 others(6): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 25/38 | chr20 | 49003156 | ||||||
| chr20:49003420
|
C | T | 2 | a0001c0002t0001g0318a0001c0002t0015g0319 | 2 | HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.3433-1650C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 25/38 | chr20 | 49003420 | ||||||
| chr20:49003474
|
G | A | 3 | a0002c0004t0001g0144a0002c0004t0001g0145a0002c0004t0001g0191 | 3 | NA18975.hp1 NA18983.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.3433-1596G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 25/38 | chr20 | 49003474 | ||||||
| chr20:49003606
|
AAAAAT | A | 9 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0010others(6): Show | 9 | HG01891.hp2 HG02486.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.3433-1439_3433-143 others(9): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 25/38 | INFO_REALIGN_3_PRIME | chr20 | 49003606 | |||||
| chr20:49003640
|
A | G | 1 | a0001c0001t0002g0244 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.3433-1430A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 25/38 | chr20 | 49003640 | ||||||
| chr20:49003687
|
G | C | 39 | a0001c0001t0002g0003a0001c0001t0002g0116a0001c0001t0002g0117others(36): Show | 39 | HG00280.hp1 HG00558.hp2 HG01106.hp2 others(36): Show |
intron_variant | MODIFIER | c.3433-1383G>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 25/38 | chr20 | 49003687 | ||||||
| chr20:49003695
|
T | A | 1 | a0001c0002t0001g0109 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.3433-1375T>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 25/38 | chr20 | 49003695 | ||||||
| chr20:49003717
|
G | A | 29 | a0001c0001t0004g0321a0001c0001t0004g0323a0001c0001t0004g0324others(26): Show | 29 | HG00673.hp1 HG00738.hp1 HG01934.hp1 others(26): Show |
intron_variant | MODIFIER | c.3433-1353G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 25/38 | chr20 | 49003717 | ||||||
| chr20:49003996
|
A | G | 2 | a0001c0002t0001g0318a0001c0002t0015g0319 | 2 | HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.3433-1074A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 25/38 | chr20 | 49003996 | ||||||
| chr20:49004091
|
G | T | 1 | a0001c0002t0001g0130 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.3433-979G>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 25/38 | chr20 | 49004091 | ||||||
| chr20:49004132
|
G | A | 29 | a0001c0001t0004g0321a0001c0001t0004g0323a0001c0001t0004g0324others(26): Show | 29 | HG00673.hp1 HG00738.hp1 HG01934.hp1 others(26): Show |
intron_variant | MODIFIER | c.3433-938G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 25/38 | chr20 | 49004132 | ||||||
| chr20:49004159
|
G | A | 1 | a0001c0003t0001g0080 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.3433-911G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 25/38 | chr20 | 49004159 | ||||||
| chr20:49004311
|
G | A | 1 | a0001c0001t0023g0215 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.3433-759G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 25/38 | chr20 | 49004311 | ||||||
| chr20:49004684
|
T | C | 211 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0009others(208): Show | 212 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(209): Show |
intron_variant | MODIFIER | c.3433-386T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 25/38 | chr20 | 49004684 | ||||||
| chr20:49004835
|
G | A | 267 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0009others(264): Show | 268 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(265): Show |
intron_variant | MODIFIER | c.3433-235G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 25/38 | chr20 | 49004835 | ||||||
| chr20:49004839
|
G | A | 1 | a0001c0001t0002g0265 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.3433-231G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 25/38 | chr20 | 49004839 | ||||||
| chr20:49005017
|
G | A | 133 | a0001c0002t0001g0122a0001c0002t0001g0123a0001c0002t0001g0124others(130): Show | 134 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(131): Show |
intron_variant | MODIFIER | c.3433-53G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 25/38 | chr20 | 49005017 | ||||||
| chr20:49005254
|
A | G | 2 | a0001c0002t0001g0313a0001c0002t0001g0314 | 2 | HG00741.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.3584+33A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 26/38 | chr20 | 49005254 | ||||||
| chr20:49005289
|
A | G | 1 | a0001c0002t0001g0156 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.3584+68A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 26/38 | chr20 | 49005289 | ||||||
| chr20:49005296
|
A | G | 1 | a0001c0002t0022g0197 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3584+75A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 26/38 | chr20 | 49005296 | ||||||
| chr20:49005410
|
A | G | 1 | a0001c0001t0004g0340 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.3584+189A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 26/38 | chr20 | 49005410 | ||||||
| chr20:49005454
|
A | G | 3 | a0001c0001t0002g0226a0001c0001t0002g0227a0001c0001t0002g0230 | 3 | HG02451.hp2 HG02559.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.3584+233A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 26/38 | chr20 | 49005454 | ||||||
| chr20:49005520
|
C | T | 2 | a0001c0002t0001g0002a0001c0002t0001g0171 | 3 | HG01256.hp1 HG01258.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.3584+299C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 26/38 | chr20 | 49005520 | ||||||
| chr20:49005633
|
G | A | 1 | a0001c0003t0001g0104 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3584+412G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 26/38 | chr20 | 49005633 | ||||||
| chr20:49005732
|
C | T | 1 | a0001c0001t0002g0270 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.3584+511C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 26/38 | chr20 | 49005732 | ||||||
| chr20:49005737
|
C | CA | 99 | a0001c0001t0003g0239a0001c0001t0007g0115a0001c0002t0001g0111others(96): Show | 99 | HG00438.hp1 HG00558.hp1 HG00609.hp1 others(96): Show |
intron_variant | MODIFIER | c.3584+537dupA | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 26/38 | INFO_REALIGN_3_PRIME | chr20 | 49005737 | |||||
| chr20:49005737
|
C | CAA | 8 | a0001c0002t0001g0122a0001c0002t0001g0123a0001c0002t0001g0285others(5): Show | 8 | HG00438.hp2 HG01123.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.3584+536_3584+537d others(4): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 26/38 | INFO_REALIGN_3_PRIME | chr20 | 49005737 | |||||
| chr20:49005737
|
CA | C | 26 | a0001c0001t0002g0257a0001c0001t0004g0330a0001c0002t0001g0002others(23): Show | 28 | HG00741.hp2 HG01109.hp1 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.3584+537delA | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 26/38 | INFO_REALIGN_3_PRIME | chr20 | 49005737 | |||||
| chr20:49005754
|
A | AG | 4 | a0001c0003t0001g0048a0001c0003t0001g0082a0003c0007t0001g0302others(1): Show | 4 | HG01081.hp2 HG01192.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.3584+533_3584+534i others(3): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 26/38 | chr20 | 49005754 | ||||||
| chr20:49005827
|
G | A | 1 | a0001c0001t0006g0272 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3584+606G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 26/38 | chr20 | 49005827 | ||||||
| chr20:49005870
|
T | C | 1 | a0001c0002t0001g0314 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.3584+649T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 26/38 | chr20 | 49005870 | ||||||
| chr20:49005886
|
C | G | 2 | a0001c0001t0002g0228a0001c0001t0002g0229 | 2 | HG02622.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.3584+665C>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 26/38 | chr20 | 49005886 | ||||||
| chr20:49005945
|
C | G | 19 | a0001c0002t0001g0313a0001c0002t0001g0314a0001c0002t0005g0001others(16): Show | 20 | HG00741.hp2 HG01109.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.3584+724C>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 26/38 | chr20 | 49005945 | ||||||
| chr20:49005958
|
T | C | 1 | a0001c0002t0010g0153 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.3584+737T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 26/38 | chr20 | 49005958 | ||||||
| chr20:49006023
|
C | T | 1 | a0001c0003t0001g0064 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.3584+802C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 26/38 | chr20 | 49006023 | ||||||
| chr20:49006024
|
G | A | 29 | a0001c0001t0004g0321a0001c0001t0004g0323a0001c0001t0004g0324others(26): Show | 29 | HG00673.hp1 HG00738.hp1 HG01934.hp1 others(26): Show |
intron_variant | MODIFIER | c.3584+803G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 26/38 | chr20 | 49006024 | ||||||
| chr20:49006053
|
T | C | 1 | a0001c0002t0001g0123 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.3584+832T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 26/38 | chr20 | 49006053 | ||||||
| chr20:49006154
|
C | T | 133 | a0001c0002t0001g0122a0001c0002t0001g0123a0001c0002t0001g0124others(130): Show | 134 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(131): Show |
intron_variant | MODIFIER | c.3584+933C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 26/38 | chr20 | 49006154 | ||||||
| chr20:49006167
|
G | A | 10 | a0001c0003t0001g0058a0001c0003t0001g0066a0001c0003t0001g0068others(7): Show | 10 | HG00642.hp1 HG01074.hp2 HG01256.hp2 others(7): Show |
intron_variant | MODIFIER | c.3584+946G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 26/38 | chr20 | 49006167 | ||||||
| chr20:49006192
|
A | G | 54 | a0001c0001t0002g0218a0001c0001t0002g0219a0001c0001t0002g0220others(51): Show | 54 | HG00323.hp2 HG00639.hp2 HG00733.hp2 others(51): Show |
intron_variant | MODIFIER | c.3584+971A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 26/38 | chr20 | 49006192 | ||||||
| chr20:49006206
|
A | G | 7 | a0001c0001t0003g0113a0001c0001t0003g0114a0001c0001t0003g0209others(4): Show | 7 | NA18946.hp2 NA18966.hp1 NA18975.hp2 others(4): Show |
intron_variant | MODIFIER | c.3584+985A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 26/38 | chr20 | 49006206 | ||||||
| chr20:49006233
|
A | G | 112 | a0001c0002t0001g0122a0001c0002t0001g0123a0001c0002t0001g0124others(109): Show | 112 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.3584+1012A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 26/38 | chr20 | 49006233 | ||||||
| chr20:49006755
|
C | A | 2 | a0001c0002t0001g0006a0001c0002t0017g0007 | 2 | HG00642.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.3584+1534C>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 26/38 | chr20 | 49006755 | ||||||
| chr20:49006763
|
G | T | 5 | a0001c0001t0002g0008a0001c0001t0002g0010a0001c0001t0002g0011others(2): Show | 5 | HG01891.hp2 HG02486.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.3584+1542G>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 26/38 | chr20 | 49006763 | ||||||
| chr20:49006770
|
A | C | 1 | a0001c0001t0002g0013 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.3584+1549A>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 26/38 | chr20 | 49006770 | ||||||
| chr20:49006841
|
T | C | 1 | a0001c0003t0001g0075 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.3584+1620T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 26/38 | chr20 | 49006841 | ||||||
| chr20:49006877
|
G | GT | 24 | a0001c0001t0002g0012a0001c0001t0002g0232a0001c0001t0002g0248others(21): Show | 24 | HG01106.hp1 HG01175.hp1 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.3584+1661dupT | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 26/38 | INFO_REALIGN_3_PRIME | chr20 | 49006877 | |||||
| chr20:49006883
|
G | T | 248 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0009others(245): Show | 248 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(245): Show |
intron_variant | MODIFIER | c.3584+1662G>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 26/38 | chr20 | 49006883 | ||||||
| chr20:49006884
|
T | G | 15 | a0001c0002t0005g0001a0001c0002t0005g0015a0001c0002t0005g0016others(12): Show | 16 | HG01109.hp1 HG01884.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.3584+1663T>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 26/38 | chr20 | 49006884 | ||||||
| chr20:49006916
|
A | G | 35 | a0001c0001t0002g0003a0001c0001t0002g0116a0001c0001t0002g0117others(32): Show | 35 | HG00280.hp1 HG00558.hp2 HG01106.hp2 others(32): Show |
intron_variant | MODIFIER | c.3584+1695A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 26/38 | chr20 | 49006916 | ||||||
| chr20:49006961
|
C | T | 57 | a0001c0001t0002g0218a0001c0001t0002g0219a0001c0001t0002g0220others(54): Show | 57 | HG00323.hp2 HG00639.hp2 HG00733.hp2 others(54): Show |
intron_variant | MODIFIER | c.3584+1740C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 26/38 | chr20 | 49006961 | ||||||
| chr20:49007022
|
A | G | 3 | a0001c0001t0002g0119a0001c0001t0002g0255a0001c0001t0002g0275 | 3 | HG02055.hp1 HG02572.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.3584+1801A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 26/38 | chr20 | 49007022 | ||||||
| chr20:49007064
|
C | G | 349 | a0001c0001t0001g0170a0001c0001t0002g0003a0001c0001t0002g0008others(346): Show | 351 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(348): Show |
intron_variant | MODIFIER | c.3584+1843C>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 26/38 | chr20 | 49007064 | ||||||
| chr20:49007067
|
T | G | 349 | a0001c0001t0001g0170a0001c0001t0002g0003a0001c0001t0002g0008others(346): Show | 351 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(348): Show |
intron_variant | MODIFIER | c.3584+1846T>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 26/38 | chr20 | 49007067 | ||||||
| chr20:49007252
|
C | T | 1 | a0001c0016t0001g0028 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3584+2031C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 26/38 | chr20 | 49007252 | ||||||
| chr20:49007290
|
C | CT | 259 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0009others(256): Show | 260 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(257): Show |
intron_variant | MODIFIER | c.3584+2085dupT | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 26/38 | INFO_REALIGN_3_PRIME | chr20 | 49007290 | |||||
| chr20:49007311
|
C | T | 1 | a0001c0003t0001g0095 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.3584+2090C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 26/38 | chr20 | 49007311 | ||||||
| chr20:49007320
|
G | C | 1 | a0001c0002t0022g0197 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3584+2099G>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 26/38 | chr20 | 49007320 | ||||||
| chr20:49007344
|
T | C | 348 | a0001c0001t0001g0170a0001c0001t0002g0003a0001c0001t0002g0008others(345): Show | 350 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(347): Show |
intron_variant | MODIFIER | c.3584+2123T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 26/38 | chr20 | 49007344 | ||||||
| chr20:49007440
|
C | T | 112 | a0001c0002t0001g0122a0001c0002t0001g0123a0001c0002t0001g0124others(109): Show | 112 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.3584+2219C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 26/38 | chr20 | 49007440 | ||||||
| chr20:49007537
|
C | T | 2 | a0001c0002t0001g0318a0001c0002t0015g0319 | 2 | HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.3584+2316C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 26/38 | chr20 | 49007537 | ||||||
| chr20:49007592
|
C | CT | 102 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0116others(99): Show | 102 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.3584+2395dupT | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 26/38 | INFO_REALIGN_3_PRIME | chr20 | 49007592 | |||||
| chr20:49007592
|
C | CTT | 13 | a0001c0001t0002g0250a0001c0001t0004g0330a0001c0001t0006g0266others(10): Show | 13 | HG00621.hp1 HG01175.hp1 HG02015.hp2 others(10): Show |
intron_variant | MODIFIER | c.3584+2394_3584+239 others(6): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 26/38 | INFO_REALIGN_3_PRIME | chr20 | 49007592 | |||||
| chr20:49007592
|
C | CTTT | 23 | a0001c0001t0004g0321a0001c0001t0004g0323a0001c0001t0004g0324others(20): Show | 23 | HG00673.hp1 HG00738.hp1 HG01934.hp1 others(20): Show |
intron_variant | MODIFIER | c.3584+2393_3584+239 others(7): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 26/38 | INFO_REALIGN_3_PRIME | chr20 | 49007592 | |||||
| chr20:49007592
|
CT | C | 12 | a0001c0001t0002g0277a0001c0001t0003g0200a0001c0001t0003g0247others(9): Show | 12 | HG01943.hp1 HG02897.hp1 HG02965.hp2 others(9): Show |
intron_variant | MODIFIER | c.3584+2395delT | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 26/38 | INFO_REALIGN_3_PRIME | chr20 | 49007592 | |||||
| chr20:49007592
|
CTTTTTTT others(7): Show |
C | 3 | a0001c0005t0008g0267a0001c0005t0008g0268a0001c0005t0008g0276 | 3 | HG02486.hp2 HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.3584+2382_3584+239 others(18): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 26/38 | INFO_REALIGN_3_PRIME | chr20 | 49007592 | |||||
| chr20:49007949
|
ATTT | A | 135 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0009others(132): Show | 135 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(132): Show |
intron_variant | MODIFIER | c.3585-2282_3585-228 others(7): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 26/38 | chr20 | 49007949 | ||||||
| chr20:49008063
|
T | A | 57 | a0001c0001t0002g0218a0001c0001t0002g0219a0001c0001t0002g0220others(54): Show | 57 | HG00323.hp2 HG00639.hp2 HG00733.hp2 others(54): Show |
intron_variant | MODIFIER | c.3585-2169T>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 26/38 | chr20 | 49008063 | ||||||
| chr20:49008113
|
C | T | 3 | a0001c0005t0008g0267a0001c0005t0008g0268a0001c0005t0008g0276 | 3 | HG02486.hp2 HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.3585-2119C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 26/38 | chr20 | 49008113 | ||||||
| chr20:49008153
|
C | T | 1 | a0001c0016t0001g0028 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3585-2079C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 26/38 | chr20 | 49008153 | ||||||
| chr20:49008177
|
T | C | 1 | a0001c0001t0002g0252 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3585-2055T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 26/38 | chr20 | 49008177 | ||||||
| chr20:49008232
|
C | T | 1 | a0001c0001t0003g0203 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.3585-2000C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 26/38 | chr20 | 49008232 | ||||||
| chr20:49008301
|
A | G | 348 | a0001c0001t0001g0170a0001c0001t0002g0003a0001c0001t0002g0008others(345): Show | 350 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(347): Show |
intron_variant | MODIFIER | c.3585-1931A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 26/38 | chr20 | 49008301 | ||||||
| chr20:49008561
|
C | CA | 133 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0009others(130): Show | 133 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(130): Show |
intron_variant | MODIFIER | c.3585-1659dupA | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 26/38 | INFO_REALIGN_3_PRIME | chr20 | 49008561 | |||||
| chr20:49008707
|
G | GT | 43 | a0001c0001t0002g0119a0001c0001t0002g0222a0001c0001t0002g0243others(40): Show | 43 | HG00438.hp1 HG00438.hp2 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.3585-1504dupT | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 26/38 | INFO_REALIGN_3_PRIME | chr20 | 49008707 | |||||
| chr20:49008707
|
GTTTTTTT others(3): Show |
G | 2 | a0001c0002t0001g0313a0001c0002t0001g0314 | 2 | HG00741.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.3585-1513_3585-150 others(14): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 26/38 | INFO_REALIGN_3_PRIME | chr20 | 49008707 | |||||
| chr20:49009002
|
A | C | 348 | a0001c0001t0001g0170a0001c0001t0002g0003a0001c0001t0002g0008others(345): Show | 350 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(347): Show |
intron_variant | MODIFIER | c.3585-1230A>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 26/38 | chr20 | 49009002 | ||||||
| chr20:49009007
|
T | C | 269 | a0001c0001t0001g0170a0001c0001t0002g0003a0001c0001t0002g0008others(266): Show | 270 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(267): Show |
intron_variant | MODIFIER | c.3585-1225T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 26/38 | chr20 | 49009007 | ||||||
| chr20:49009077
|
A | T | 1 | a0001c0001t0002g0012 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3585-1155A>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 26/38 | chr20 | 49009077 | ||||||
| chr20:49009082
|
G | A | 1 | a0001c0002t0001g0123 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.3585-1150G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 26/38 | chr20 | 49009082 | ||||||
| chr20:49009083
|
G | A | 29 | a0001c0001t0004g0321a0001c0001t0004g0323a0001c0001t0004g0324others(26): Show | 29 | HG00673.hp1 HG00738.hp1 HG01934.hp1 others(26): Show |
intron_variant | MODIFIER | c.3585-1149G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 26/38 | chr20 | 49009083 | ||||||
| chr20:49009368
|
T | C | 136 | a0001c0001t0001g0170a0001c0001t0002g0003a0001c0001t0002g0008others(133): Show | 136 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(133): Show |
intron_variant | MODIFIER | c.3585-864T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 26/38 | chr20 | 49009368 | ||||||
| chr20:49009415
|
A | C | 112 | a0001c0002t0001g0122a0001c0002t0001g0123a0001c0002t0001g0124others(109): Show | 112 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.3585-817A>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 26/38 | chr20 | 49009415 | ||||||
| chr20:49009449
|
CA | C | 7 | a0001c0001t0003g0214a0001c0001t0003g0247a0001c0001t0004g0330others(4): Show | 7 | HG00323.hp1 HG01257.hp1 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.3585-767delA | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 26/38 | INFO_REALIGN_3_PRIME | chr20 | 49009449 | |||||
| chr20:49009879
|
A | G | 112 | a0001c0002t0001g0122a0001c0002t0001g0123a0001c0002t0001g0124others(109): Show | 112 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.3585-353A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 26/38 | chr20 | 49009879 | ||||||
| chr20:49009948
|
G | C | 136 | a0001c0001t0001g0170a0001c0001t0002g0003a0001c0001t0002g0008others(133): Show | 136 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(133): Show |
intron_variant | MODIFIER | c.3585-284G>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 26/38 | chr20 | 49009948 | ||||||
| chr20:49010051
|
G | T | 1 | a0001c0003t0001g0317 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.3585-181G>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 26/38 | chr20 | 49010051 | ||||||
| chr20:49010064
|
G | C | 133 | a0001c0001t0001g0170a0001c0001t0002g0003a0001c0001t0002g0008others(130): Show | 133 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(130): Show |
intron_variant | MODIFIER | c.3585-168G>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 26/38 | chr20 | 49010064 | ||||||
| chr20:49010195
|
A | G | 1 | a0001c0001t0002g0010 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3585-37A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 26/38 | chr20 | 49010195 | ||||||
| chr20:49010199
|
A | T | 136 | a0001c0001t0001g0170a0001c0001t0002g0003a0001c0001t0002g0008others(133): Show | 136 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(133): Show |
intron_variant | MODIFIER | c.3585-33A>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 26/38 | chr20 | 49010199 | ||||||
| chr20:49010558
|
A | G | 104 | a0001c0001t0001g0170a0001c0001t0002g0003a0001c0001t0002g0008others(101): Show | 104 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.3757+154A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 27/38 | chr20 | 49010558 | ||||||
| chr20:49010633
|
G | T | 248 | a0001c0001t0001g0170a0001c0001t0002g0003a0001c0001t0002g0008others(245): Show | 248 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(245): Show |
intron_variant | MODIFIER | c.3757+229G>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 27/38 | chr20 | 49010633 | ||||||
| chr20:49010681
|
G | C | 3 | a0001c0002t0001g0156a0001c0002t0012g0148a0001c0002t0012g0149 | 3 | HG01074.hp1 HG01361.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.3757+277G>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 27/38 | chr20 | 49010681 | ||||||
| chr20:49010999
|
T | C | 1 | a0001c0001t0002g0013 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.3757+595T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 27/38 | chr20 | 49010999 | ||||||
| chr20:49011035
|
C | A | 133 | a0001c0001t0001g0170a0001c0001t0002g0003a0001c0001t0002g0008others(130): Show | 133 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(130): Show |
intron_variant | MODIFIER | c.3757+631C>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 27/38 | chr20 | 49011035 | ||||||
| chr20:49011068
|
C | T | 136 | a0001c0001t0001g0170a0001c0001t0002g0003a0001c0001t0002g0008others(133): Show | 136 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(133): Show |
intron_variant | MODIFIER | c.3757+664C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 27/38 | chr20 | 49011068 | ||||||
| chr20:49011148
|
A | G | 2 | a0001c0002t0001g0318a0001c0002t0015g0319 | 2 | HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.3757+744A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 27/38 | chr20 | 49011148 | ||||||
| chr20:49011308
|
C | T | 136 | a0001c0001t0001g0170a0001c0001t0002g0003a0001c0001t0002g0008others(133): Show | 136 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(133): Show |
intron_variant | MODIFIER | c.3758-616C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 27/38 | chr20 | 49011308 | ||||||
| chr20:49011506
|
C | T | 1 | a0001c0001t0002g0244 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.3758-418C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 27/38 | chr20 | 49011506 | ||||||
| chr20:49011515
|
G | A | 1 | a0001c0001t0002g0118 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.3758-409G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 27/38 | chr20 | 49011515 | ||||||
| chr20:49011633
|
T | C | 136 | a0001c0001t0001g0170a0001c0001t0002g0003a0001c0001t0002g0008others(133): Show | 136 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(133): Show |
intron_variant | MODIFIER | c.3758-291T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 27/38 | chr20 | 49011633 | ||||||
| chr20:49011662
|
A | G | 39 | a0001c0001t0002g0003a0001c0001t0002g0116a0001c0001t0002g0117others(36): Show | 39 | HG00280.hp1 HG00558.hp2 HG01106.hp2 others(36): Show |
intron_variant | MODIFIER | c.3758-262A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 27/38 | chr20 | 49011662 | ||||||
| chr20:49011826
|
G | A | 70 | a0001c0003t0001g0029a0001c0003t0001g0030a0001c0003t0001g0031others(67): Show | 70 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.3758-98G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 27/38 | chr20 | 49011826 | ||||||
| chr20:49011831
|
A | ATG | 45 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0009others(42): Show | 45 | HG00280.hp1 HG00558.hp2 HG01074.hp1 others(42): Show |
intron_variant | MODIFIER | c.3758-74_3758-73dup others(2): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 27/38 | INFO_REALIGN_3_PRIME | chr20 | 49011831 | |||||
| chr20:49011897
|
T | C | 136 | a0001c0001t0001g0170a0001c0001t0002g0003a0001c0001t0002g0008others(133): Show | 136 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(133): Show |
intron_variant | MODIFIER | c.3758-27T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 27/38 | chr20 | 49011897 | ||||||
| chr20:49012209
|
G | T | 1 | a0001c0001t0002g0012 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3918+125G>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 28/38 | chr20 | 49012209 | ||||||
| chr20:49012496
|
T | TTTTG | 247 | a0001c0001t0001g0170a0001c0001t0002g0003a0001c0001t0002g0008others(244): Show | 247 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(244): Show |
intron_variant | MODIFIER | c.3918+428_3918+431d others(6): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 28/38 | INFO_REALIGN_3_PRIME | chr20 | 49012496 | |||||
| chr20:49012516
|
T | G | 97 | a0001c0001t0001g0170a0001c0001t0002g0003a0001c0001t0002g0116others(94): Show | 97 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(94): Show |
intron_variant | MODIFIER | c.3918+432T>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 28/38 | chr20 | 49012516 | ||||||
| chr20:49013285
|
C | T | 39 | a0001c0001t0002g0003a0001c0001t0002g0116a0001c0001t0002g0117others(36): Show | 39 | HG00280.hp1 HG00558.hp2 HG01106.hp2 others(36): Show |
intron_variant | MODIFIER | c.3919-279C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 28/38 | chr20 | 49013285 | ||||||
| chr20:49013455
|
G | T | 1 | a0001c0002t0001g0109 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.3919-109G>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 28/38 | chr20 | 49013455 | ||||||
| chr20:49013537
|
C | T | 3 | a0001c0003t0001g0057a0001c0003t0001g0091a0001c0003t0001g0102 | 3 | HG01243.hp1 HG01261.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.3919-27C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 28/38 | chr20 | 49013537 | ||||||
| chr20:49014448
|
T | C | 1 | a0001c0002t0012g0148 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.4179+488T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 30/38 | chr20 | 49014448 | ||||||
| chr20:49014581
|
A | C | 1 | a0001c0002t0001g0318 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.4179+621A>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 30/38 | chr20 | 49014581 | ||||||
| chr20:49014711
|
A | G | 1 | a0001c0002t0022g0197 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.4179+751A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 30/38 | chr20 | 49014711 | ||||||
| chr20:49014814
|
C | A | 2 | a0001c0002t0001g0318a0001c0002t0015g0319 | 2 | HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.4179+854C>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 30/38 | chr20 | 49014814 | ||||||
| chr20:49014862
|
A | G | 35 | a0001c0002t0001g0122a0001c0002t0001g0123a0001c0002t0001g0124others(32): Show | 35 | HG00639.hp1 HG00673.hp2 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.4179+902A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 30/38 | chr20 | 49014862 | ||||||
| chr20:49014929
|
C | T | 1 | a0001c0003t0001g0317 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.4179+969C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 30/38 | chr20 | 49014929 | ||||||
| chr20:49014975
|
A | G | 3 | a0001c0003t0001g0043a0001c0003t0001g0078a0001c0003t0001g0087 | 3 | NA18954.hp1 NA18993.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.4179+1015A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 30/38 | chr20 | 49014975 | ||||||
| chr20:49014988
|
C | G | 1 | a0001c0002t0001g0187 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.4179+1028C>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 30/38 | chr20 | 49014988 | ||||||
| chr20:49015255
|
A | G | 112 | a0001c0002t0001g0122a0001c0002t0001g0123a0001c0002t0001g0124others(109): Show | 112 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.4180-1025A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 30/38 | chr20 | 49015255 | ||||||
| chr20:49015331
|
C | A | 1 | a0001c0002t0022g0197 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.4180-949C>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 30/38 | chr20 | 49015331 | ||||||
| chr20:49015780
|
T | C | 35 | a0001c0002t0001g0122a0001c0002t0001g0123a0001c0002t0001g0124others(32): Show | 35 | HG00639.hp1 HG00673.hp2 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.4180-500T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 30/38 | chr20 | 49015780 | ||||||
| chr20:49015944
|
T | C | 1 | a0001c0002t0022g0197 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.4180-336T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 30/38 | chr20 | 49015944 | ||||||
| chr20:49016020
|
C | G | 112 | a0001c0002t0001g0122a0001c0002t0001g0123a0001c0002t0001g0124others(109): Show | 112 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.4180-260C>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 30/38 | chr20 | 49016020 | ||||||
| chr20:49016217
|
A | G | 112 | a0001c0002t0001g0122a0001c0002t0001g0123a0001c0002t0001g0124others(109): Show | 112 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.4180-63A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 30/38 | chr20 | 49016217 | ||||||
| chr20:49016235
|
C | T | 1 | a0001c0001t0004g0341 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.4180-45C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 30/38 | chr20 | 49016235 | ||||||
| chr20:49016545
|
C | T | 15 | a0001c0002t0005g0001a0001c0002t0005g0015a0001c0002t0005g0016others(12): Show | 16 | HG01109.hp1 HG01884.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.4315+130C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 31/38 | chr20 | 49016545 | ||||||
| chr20:49016572
|
G | GC | 33 | a0001c0002t0001g0122a0001c0002t0001g0123a0001c0002t0001g0124others(30): Show | 33 | HG00639.hp1 HG00673.hp2 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.4315+165dupC | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 31/38 | INFO_REALIGN_3_PRIME | chr20 | 49016572 | |||||
| chr20:49016591
|
A | G | 1 | a0001c0002t0001g0109 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.4315+176A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 31/38 | chr20 | 49016591 | ||||||
| chr20:49016679
|
A | G | 7 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0010others(4): Show | 7 | HG01891.hp2 HG02486.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.4315+264A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 31/38 | chr20 | 49016679 | ||||||
| chr20:49016782
|
A | G | 10 | a0001c0002t0001g0124a0001c0002t0001g0285a0001c0002t0001g0286others(7): Show | 10 | HG02071.hp2 HG02080.hp2 NA18950.hp2 others(7): Show |
intron_variant | MODIFIER | c.4315+367A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 31/38 | chr20 | 49016782 | ||||||
| chr20:49016838
|
G | A | 1 | a0001c0002t0001g0179 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.4316-411G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 31/38 | chr20 | 49016838 | ||||||
| chr20:49016854
|
T | G | 2 | a0001c0002t0001g0315a0001c0002t0001g0316 | 2 | HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.4316-395T>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 31/38 | chr20 | 49016854 | ||||||
| chr20:49016961
|
G | A | 1 | a0001c0003t0001g0048 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.4316-288G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 31/38 | chr20 | 49016961 | ||||||
| chr20:49017456
|
T | C | 1 | a0001c0002t0001g0189 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.4455-40T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 32/38 | chr20 | 49017456 | ||||||
| chr20:49017469
|
A | AT | 111 | a0001c0002t0001g0122a0001c0002t0001g0123a0001c0002t0001g0124others(108): Show | 111 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(108): Show |
intron_variant | MODIFIER | c.4455-19dupT | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 32/38 | INFO_REALIGN_3_PRIME | chr20 | 49017469 | |||||
| chr20:49017693
|
T | G | 2 | a0001c0001t0002g0198a0004c0008t0002g0264 | 2 | NA18946.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.4509+143T>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 33/38 | chr20 | 49017693 | ||||||
| chr20:49017870
|
C | T | 1 | a0001c0001t0002g0013 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.4509+320C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 33/38 | chr20 | 49017870 | ||||||
| chr20:49017882
|
A | G | 2 | a0001c0001t0002g0231a0001c0001t0002g0232 | 2 | HG02258.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.4509+332A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 33/38 | chr20 | 49017882 | ||||||
| chr20:49018100
|
C | T | 2 | a0001c0002t0001g0134a0001c0002t0001g0192 | 2 | HG00438.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.4509+550C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 33/38 | chr20 | 49018100 | ||||||
| chr20:49018153
|
A | G | 46 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0009others(43): Show | 46 | HG00280.hp1 HG00558.hp2 HG01106.hp2 others(43): Show |
intron_variant | MODIFIER | c.4509+603A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 33/38 | chr20 | 49018153 | ||||||
| chr20:49018158
|
C | T | 109 | a0001c0002t0001g0122a0001c0002t0001g0123a0001c0002t0001g0124others(106): Show | 109 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(106): Show |
intron_variant | MODIFIER | c.4509+608C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 33/38 | chr20 | 49018158 | ||||||
| chr20:49018219
|
T | G | 2 | a0001c0002t0001g0313a0001c0002t0001g0314 | 2 | HG00741.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.4510-665T>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 33/38 | chr20 | 49018219 | ||||||
| chr20:49018631
|
A | G | 3 | a0001c0003t0001g0043a0001c0003t0001g0078a0001c0003t0001g0087 | 3 | NA18954.hp1 NA18993.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.4510-253A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 33/38 | chr20 | 49018631 | ||||||
| chr20:49018721
|
C | T | 1 | a0001c0001t0002g0117 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.4510-163C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 33/38 | chr20 | 49018721 | ||||||
| chr20:49018802
|
A | G | 35 | a0001c0001t0002g0003a0001c0001t0002g0116a0001c0001t0002g0117others(32): Show | 35 | HG00280.hp1 HG00558.hp2 HG01106.hp2 others(32): Show |
intron_variant | MODIFIER | c.4510-82A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 33/38 | chr20 | 49018802 | ||||||
| chr20:49019178
|
G | A | 244 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0009others(241): Show | 244 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(241): Show |
intron_variant | MODIFIER | c.4624+180G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 34/38 | chr20 | 49019178 | ||||||
| chr20:49019179
|
T | G | 1 | a0001c0001t0003g0234 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.4624+181T>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 34/38 | chr20 | 49019179 | ||||||
| chr20:49019232
|
C | A | 1 | a0001c0003t0001g0048 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.4624+234C>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 34/38 | chr20 | 49019232 | ||||||
| chr20:49019281
|
G | C | 136 | a0001c0001t0001g0170a0001c0001t0002g0003a0001c0001t0002g0008others(133): Show | 136 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(133): Show |
intron_variant | MODIFIER | c.4624+283G>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 34/38 | chr20 | 49019281 | ||||||
| chr20:49019618
|
G | A | 1 | a0001c0002t0001g0171 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.4624+620G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 34/38 | chr20 | 49019618 | ||||||
| chr20:49019936
|
G | A | 9 | a0001c0001t0002g0116a0001c0001t0002g0251a0001c0001t0002g0254others(6): Show | 9 | HG00558.hp2 NA18941.hp1 NA18968.hp1 others(6): Show |
intron_variant | MODIFIER | c.4624+938G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 34/38 | chr20 | 49019936 | ||||||
| chr20:49020136
|
G | C | 35 | a0001c0001t0002g0003a0001c0001t0002g0116a0001c0001t0002g0117others(32): Show | 35 | HG00280.hp1 HG00558.hp2 HG01106.hp2 others(32): Show |
intron_variant | MODIFIER | c.4624+1138G>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 34/38 | chr20 | 49020136 | ||||||
| chr20:49020285
|
T | G | 1 | a0001c0003t0001g0044 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.4624+1287T>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 34/38 | chr20 | 49020285 | ||||||
| chr20:49020363
|
T | A | 1 | a0001c0001t0002g0121 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.4624+1365T>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 34/38 | chr20 | 49020363 | ||||||
| chr20:49020521
|
T | C | 1 | a0001c0002t0022g0197 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.4624+1523T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 34/38 | chr20 | 49020521 | ||||||
| chr20:49020606
|
C | T | 112 | a0001c0002t0001g0122a0001c0002t0001g0123a0001c0002t0001g0124others(109): Show | 112 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.4624+1608C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 34/38 | chr20 | 49020606 | ||||||
| chr20:49020642
|
C | T | 1 | a0001c0002t0005g0025 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.4624+1644C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 34/38 | chr20 | 49020642 | ||||||
| chr20:49020684
|
C | T | 1 | a0001c0003t0001g0060 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.4624+1686C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 34/38 | chr20 | 49020684 | ||||||
| chr20:49020845
|
T | C | 112 | a0001c0002t0001g0122a0001c0002t0001g0123a0001c0002t0001g0124others(109): Show | 112 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.4624+1847T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 34/38 | chr20 | 49020845 | ||||||
| chr20:49021067
|
A | T | 3 | a0001c0001t0014g0223a0001c0001t0014g0224a0001c0001t0021g0225 | 3 | HG02895.hp2 HG02897.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.4625-1984A>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 34/38 | chr20 | 49021067 | ||||||
| chr20:49021122
|
C | T | 1 | a0001c0001t0002g0009 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.4625-1929C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 34/38 | chr20 | 49021122 | ||||||
| chr20:49021719
|
G | A | 132 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0009others(129): Show | 132 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(129): Show |
intron_variant | MODIFIER | c.4625-1332G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 34/38 | chr20 | 49021719 | ||||||
| chr20:49021832
|
G | A | 112 | a0001c0002t0001g0122a0001c0002t0001g0123a0001c0002t0001g0124others(109): Show | 112 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.4625-1219G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 34/38 | chr20 | 49021832 | ||||||
| chr20:49021844
|
C | CA | 178 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0009others(175): Show | 178 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(175): Show |
intron_variant | MODIFIER | c.4625-1191dupA | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 34/38 | INFO_REALIGN_3_PRIME | chr20 | 49021844 | |||||
| chr20:49022099
|
G | A | 3 | a0001c0001t0002g0226a0001c0001t0002g0227a0001c0001t0002g0230 | 3 | HG02451.hp2 HG02559.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.4625-952G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 34/38 | chr20 | 49022099 | ||||||
| chr20:49022154
|
C | CA | 95 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0010others(92): Show | 96 | HG00280.hp2 HG00323.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.4625-875dupA | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 34/38 | INFO_REALIGN_3_PRIME | chr20 | 49022154 | |||||
| chr20:49022154
|
C | CAA | 62 | a0001c0001t0002g0003a0001c0001t0002g0116a0001c0001t0002g0117others(59): Show | 63 | HG00280.hp1 HG00558.hp2 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.4625-876_4625-875d others(4): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 34/38 | INFO_REALIGN_3_PRIME | chr20 | 49022154 | |||||
| chr20:49022154
|
C | CAAA | 22 | a0001c0001t0004g0323a0001c0001t0004g0325a0001c0001t0004g0326others(19): Show | 22 | HG00673.hp1 HG00738.hp1 HG01934.hp1 others(19): Show |
intron_variant | MODIFIER | c.4625-877_4625-875d others(5): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 34/38 | INFO_REALIGN_3_PRIME | chr20 | 49022154 | |||||
| chr20:49022212
|
A | C | 1 | a0001c0001t0002g0010 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.4625-839A>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 34/38 | chr20 | 49022212 | ||||||
| chr20:49022411
|
A | AAAC | 57 | a0001c0001t0002g0218a0001c0001t0002g0219a0001c0001t0002g0220others(54): Show | 57 | HG00323.hp2 HG00639.hp2 HG00733.hp2 others(54): Show |
intron_variant | MODIFIER | c.4625-622_4625-620d others(5): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 34/38 | INFO_REALIGN_3_PRIME | chr20 | 49022411 | |||||
| chr20:49022411
|
A | AAACAAC | 9 | a0001c0002t0005g0001a0001c0002t0005g0015a0001c0002t0005g0016others(6): Show | 10 | HG01109.hp1 HG01884.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.4625-625_4625-620d others(8): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 34/38 | INFO_REALIGN_3_PRIME | chr20 | 49022411 | |||||
| chr20:49022432
|
A | C | 272 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0009others(269): Show | 273 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(270): Show |
intron_variant | MODIFIER | c.4625-619A>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 34/38 | chr20 | 49022432 | ||||||
| chr20:49022435
|
A | C | 138 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0009others(135): Show | 138 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(135): Show |
intron_variant | MODIFIER | c.4625-616A>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 34/38 | chr20 | 49022435 | ||||||
| chr20:49022438
|
A | C | 132 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0009others(129): Show | 132 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(129): Show |
intron_variant | MODIFIER | c.4625-613A>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 34/38 | chr20 | 49022438 | ||||||
| chr20:49022442
|
C | A | 249 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0009others(246): Show | 249 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(246): Show |
intron_variant | MODIFIER | c.4625-609C>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 34/38 | chr20 | 49022442 | ||||||
| chr20:49022474
|
G | A | 1 | a0001c0003t0001g0063 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.4625-577G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 34/38 | chr20 | 49022474 | ||||||
| chr20:49022500
|
C | G | 2 | a0001c0002t0001g0318a0001c0002t0015g0319 | 2 | HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.4625-551C>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 34/38 | chr20 | 49022500 | ||||||
| chr20:49022754
|
T | C | 1 | a0001c0002t0005g0015 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.4625-297T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 34/38 | chr20 | 49022754 | ||||||
| chr20:49022856
|
T | C | 1 | a0007c0010t0002g0262 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.4625-195T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 34/38 | chr20 | 49022856 | ||||||
| chr20:49022927
|
G | C | 247 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0009others(244): Show | 247 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(244): Show |
intron_variant | MODIFIER | c.4625-124G>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 34/38 | chr20 | 49022927 | ||||||
| chr20:49023200
|
A | G | 135 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0009others(132): Show | 135 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(132): Show |
intron_variant | MODIFIER | c.4755+19A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 35/38 | chr20 | 49023200 | ||||||
| chr20:49023454
|
A | G | 237 | a0001c0001t0001g0170a0001c0001t0002g0003a0001c0001t0002g0008others(234): Show | 239 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.4755+273A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 35/38 | chr20 | 49023454 | ||||||
| chr20:49023481
|
A | G | 1 | a0001c0002t0001g0314 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.4755+300A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 35/38 | chr20 | 49023481 | ||||||
| chr20:49023492
|
T | A | 135 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0009others(132): Show | 135 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(132): Show |
intron_variant | MODIFIER | c.4755+311T>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 35/38 | chr20 | 49023492 | ||||||
| chr20:49023523
|
GT | G | 110 | a0001c0002t0001g0122a0001c0002t0001g0123a0001c0002t0001g0124others(107): Show | 110 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(107): Show |
intron_variant | MODIFIER | c.4755+355delT | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 35/38 | INFO_REALIGN_3_PRIME | chr20 | 49023523 | |||||
| chr20:49023524
|
TTTTTTTT others(6): Show |
T | 135 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0009others(132): Show | 135 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(132): Show |
intron_variant | MODIFIER | c.4755+355_4755+367d others(15): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 35/38 | INFO_REALIGN_3_PRIME | chr20 | 49023524 | |||||
| chr20:49023533
|
T | G | 1 | a0001c0002t0001g0179 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.4755+352T>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 35/38 | chr20 | 49023533 | ||||||
| chr20:49023542
|
T | A | 135 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0009others(132): Show | 135 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(132): Show |
intron_variant | MODIFIER | c.4755+361T>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 35/38 | chr20 | 49023542 | ||||||
| chr20:49023562
|
G | A | 35 | a0001c0001t0002g0003a0001c0001t0002g0116a0001c0001t0002g0117others(32): Show | 35 | HG00280.hp1 HG00558.hp2 HG01106.hp2 others(32): Show |
intron_variant | MODIFIER | c.4755+381G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 35/38 | chr20 | 49023562 | ||||||
| chr20:49023599
|
C | T | 1 | a0001c0003t0001g0048 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.4755+418C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 35/38 | chr20 | 49023599 | ||||||
| chr20:49023631
|
T | C | 136 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0009others(133): Show | 136 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(133): Show |
intron_variant | MODIFIER | c.4755+450T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 35/38 | chr20 | 49023631 | ||||||
| chr20:49023632
|
G | C | 1 | a0001c0002t0001g0286 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.4755+451G>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 35/38 | chr20 | 49023632 | ||||||
| chr20:49023696
|
G | A | 1 | a0001c0003t0001g0088 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.4755+515G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 35/38 | chr20 | 49023696 | ||||||
| chr20:49023781
|
G | A | 1 | a0001c0001t0002g0010 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.4755+600G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 35/38 | chr20 | 49023781 | ||||||
| chr20:49023929
|
C | G | 247 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0009others(244): Show | 247 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(244): Show |
intron_variant | MODIFIER | c.4755+748C>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 35/38 | chr20 | 49023929 | ||||||
| chr20:49024047
|
C | G | 7 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0010others(4): Show | 7 | HG01891.hp2 HG02486.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.4755+866C>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 35/38 | chr20 | 49024047 | ||||||
| chr20:49024118
|
C | T | 1 | a0001c0001t0002g0120 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.4755+937C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 35/38 | chr20 | 49024118 | ||||||
| chr20:49024138
|
A | T | 3 | a0001c0002t0005g0021a0001c0002t0005g0024a0001c0002t0005g0025 | 3 | HG01891.hp1 HG03486.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.4755+957A>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 35/38 | chr20 | 49024138 | ||||||
| chr20:49024143
|
T | C | 2 | a0001c0002t0001g0309a0001c0002t0001g0310 | 2 | NA18960.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.4755+962T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 35/38 | chr20 | 49024143 | ||||||
| chr20:49024243
|
G | A | 1 | a0001c0001t0006g0274 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.4755+1062G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 35/38 | chr20 | 49024243 | ||||||
| chr20:49024742
|
G | T | 1 | a0004c0008t0002g0264 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.4756-571G>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 35/38 | chr20 | 49024742 | ||||||
| chr20:49024787
|
C | T | 1 | a0001c0003t0009g0096 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.4756-526C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 35/38 | chr20 | 49024787 | ||||||
| chr20:49024802
|
T | C | 135 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0009others(132): Show | 135 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(132): Show |
intron_variant | MODIFIER | c.4756-511T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 35/38 | chr20 | 49024802 | ||||||
| chr20:49024921
|
G | A | 1 | a0001c0001t0002g0119 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.4756-392G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 35/38 | chr20 | 49024921 | ||||||
| chr20:49025180
|
G | T | 1 | a0001c0003t0001g0317 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.4756-133G>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 35/38 | chr20 | 49025180 | ||||||
| chr20:49025210
|
G | A | 29 | a0001c0001t0004g0321a0001c0001t0004g0323a0001c0001t0004g0324others(26): Show | 29 | HG00673.hp1 HG00738.hp1 HG01934.hp1 others(26): Show |
intron_variant | MODIFIER | c.4756-103G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 35/38 | chr20 | 49025210 | ||||||
| chr20:49025292
|
A | G | 1 | a0001c0002t0022g0197 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.4756-21A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 35/38 | chr20 | 49025292 | ||||||
| chr20:49025506
|
A | G | 1 | a0001c0002t0001g0313 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.4924+25A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 36/38 | chr20 | 49025506 | ||||||
| chr20:49025873
|
T | C | 1 | a0001c0001t0020g0329 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.4924+392T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 36/38 | chr20 | 49025873 | ||||||
| chr20:49025939
|
G | A | 135 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0009others(132): Show | 135 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(132): Show |
intron_variant | MODIFIER | c.4924+458G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 36/38 | chr20 | 49025939 | ||||||
| chr20:49025953
|
G | C | 3 | a0001c0001t0002g0231a0001c0001t0002g0232a0001c0001t0002g0233 | 3 | HG02258.hp2 HG02717.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.4924+472G>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 36/38 | chr20 | 49025953 | ||||||
| chr20:49025982
|
G | GA | 77 | a0001c0002t0001g0151a0001c0002t0001g0195a0001c0002t0001g0315others(74): Show | 77 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(74): Show |
intron_variant | MODIFIER | c.4924+517dupA | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 36/38 | INFO_REALIGN_3_PRIME | chr20 | 49025982 | |||||
| chr20:49025982
|
G | GAA | 34 | a0001c0002t0001g0123a0001c0002t0001g0124a0001c0002t0001g0282others(31): Show | 34 | HG00639.hp1 HG00673.hp2 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.4924+516_4924+517d others(4): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 36/38 | INFO_REALIGN_3_PRIME | chr20 | 49025982 | |||||
| chr20:49025983
|
A | G | 15 | a0001c0002t0005g0001a0001c0002t0005g0015a0001c0002t0005g0016others(12): Show | 16 | HG01109.hp1 HG01884.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.4924+502A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 36/38 | chr20 | 49025983 | ||||||
| chr20:49026042
|
A | G | 135 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0009others(132): Show | 135 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(132): Show |
intron_variant | MODIFIER | c.4924+561A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 36/38 | chr20 | 49026042 | ||||||
| chr20:49026584
|
C | CT | 43 | a0001c0001t0002g0244a0001c0001t0002g0265a0001c0001t0003g0246others(40): Show | 43 | HG00438.hp2 HG00673.hp1 HG00738.hp1 others(40): Show |
intron_variant | MODIFIER | c.4924+1122dupT | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 36/38 | INFO_REALIGN_3_PRIME | chr20 | 49026584 | |||||
| chr20:49026798
|
C | A | 1 | a0001c0001t0002g0248 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.4924+1317C>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 36/38 | chr20 | 49026798 | ||||||
| chr20:49026870
|
G | T | 1 | a0001c0001t0006g0273 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.4924+1389G>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 36/38 | chr20 | 49026870 | ||||||
| chr20:49026891
|
A | G | 3 | a0001c0002t0005g0021a0001c0002t0005g0024a0001c0002t0005g0025 | 3 | HG01891.hp1 HG03486.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.4924+1410A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 36/38 | chr20 | 49026891 | ||||||
| chr20:49027017
|
C | G | 135 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0009others(132): Show | 135 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(132): Show |
intron_variant | MODIFIER | c.4925-1513C>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 36/38 | chr20 | 49027017 | ||||||
| chr20:49027078
|
T | A | 5 | a0001c0002t0001g0290a0001c0002t0001g0292a0001c0002t0001g0307others(2): Show | 5 | HG02015.hp1 NA18971.hp2 NA18977.hp2 others(2): Show |
intron_variant | MODIFIER | c.4925-1452T>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 36/38 | chr20 | 49027078 | ||||||
| chr20:49027250
|
G | A | 4 | a0001c0001t0002g0240a0001c0001t0003g0238a0001c0001t0003g0239others(1): Show | 4 | HG02293.hp1 NA18939.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.4925-1280G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 36/38 | chr20 | 49027250 | ||||||
| chr20:49027489
|
G | A | 1 | a0001c0002t0022g0197 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.4925-1041G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 36/38 | chr20 | 49027489 | ||||||
| chr20:49027495
|
A | G | 135 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0009others(132): Show | 135 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(132): Show |
intron_variant | MODIFIER | c.4925-1035A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 36/38 | chr20 | 49027495 | ||||||
| chr20:49027718
|
G | GAAGAACA others(3): Show |
1 | a0001c0003t0001g0074 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.4925-811_4925-802d others(12): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 36/38 | INFO_REALIGN_3_PRIME | chr20 | 49027718 | |||||
| chr20:49027755
|
TGTA | T | 135 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0009others(132): Show | 135 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(132): Show |
intron_variant | MODIFIER | c.4925-774_4925-772d others(5): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 36/38 | chr20 | 49027755 | ||||||
| chr20:49027914
|
G | A | 4 | a0001c0001t0002g0240a0001c0001t0003g0238a0001c0001t0003g0239others(1): Show | 4 | HG02293.hp1 NA18939.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.4925-616G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 36/38 | chr20 | 49027914 | ||||||
| chr20:49027989
|
C | T | 1 | a0001c0003t0001g0104 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.4925-541C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 36/38 | chr20 | 49027989 | ||||||
| chr20:49028115
|
C | T | 1 | a0001c0002t0001g0350 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.4925-415C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 36/38 | chr20 | 49028115 | ||||||
| chr20:49028187
|
G | A | 1 | a0001c0002t0005g0025 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.4925-343G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 36/38 | chr20 | 49028187 | ||||||
| chr20:49028350
|
T | C | 3 | a0001c0001t0002g0221a0001c0001t0002g0222a0001c0001t0002g0245 | 3 | HG01361.hp1 HG02647.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.4925-180T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 36/38 | chr20 | 49028350 | ||||||
| chr20:49028465
|
G | GT | 135 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0009others(132): Show | 135 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(132): Show |
intron_variant | MODIFIER | c.4925-64dupT | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 36/38 | INFO_REALIGN_3_PRIME | chr20 | 49028465 | |||||
| chr20:49028890
|
G | T | 267 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0009others(264): Show | 268 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(265): Show |
intron_variant | MODIFIER | c.5063+222G>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 37/38 | chr20 | 49028890 | ||||||
| chr20:49029203
|
G | C | 1 | a0001c0001t0002g0009 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.5063+535G>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 37/38 | chr20 | 49029203 | ||||||
| chr20:49029241
|
T | G | 1 | a0001c0002t0001g0185 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.5063+573T>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 37/38 | chr20 | 49029241 | ||||||
| chr20:49029452
|
A | C | 135 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0009others(132): Show | 135 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(132): Show |
intron_variant | MODIFIER | c.5063+784A>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 37/38 | chr20 | 49029452 | ||||||
| chr20:49029455
|
A | C | 35 | a0001c0002t0001g0122a0001c0002t0001g0123a0001c0002t0001g0124others(32): Show | 35 | HG00639.hp1 HG00673.hp2 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.5063+787A>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 37/38 | chr20 | 49029455 | ||||||
| chr20:49029531
|
A | G | 35 | a0001c0002t0001g0122a0001c0002t0001g0123a0001c0002t0001g0124others(32): Show | 35 | HG00639.hp1 HG00673.hp2 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.5063+863A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 37/38 | chr20 | 49029531 | ||||||
| chr20:49029595
|
AT | A | 135 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0009others(132): Show | 135 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(132): Show |
intron_variant | MODIFIER | c.5063+941delT | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 37/38 | INFO_REALIGN_3_PRIME | chr20 | 49029595 | |||||
| chr20:49029614
|
C | T | 4 | a0001c0001t0006g0266a0001c0001t0006g0272a0001c0001t0006g0273others(1): Show | 4 | HG02055.hp2 HG02145.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.5063+946C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 37/38 | chr20 | 49029614 | ||||||
| chr20:49029673
|
G | C | 267 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0009others(264): Show | 268 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(265): Show |
intron_variant | MODIFIER | c.5063+1005G>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 37/38 | chr20 | 49029673 | ||||||
| chr20:49029779
|
G | A | 111 | a0001c0002t0001g0122a0001c0002t0001g0123a0001c0002t0001g0124others(108): Show | 111 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(108): Show |
intron_variant | MODIFIER | c.5063+1111G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 37/38 | chr20 | 49029779 | ||||||
| chr20:49029784
|
G | C | 103 | a0001c0001t0001g0170a0001c0002t0001g0002a0001c0002t0001g0004others(100): Show | 105 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.5063+1116G>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 37/38 | chr20 | 49029784 | ||||||
| chr20:49029882
|
C | T | 1 | a0001c0001t0002g0265 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.5063+1214C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 37/38 | chr20 | 49029882 | ||||||
| chr20:49029900
|
G | GA | 119 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0009others(116): Show | 119 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.5063+1234dupA | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 37/38 | INFO_REALIGN_3_PRIME | chr20 | 49029900 | |||||
| chr20:49029902
|
A | AAT | 13 | a0001c0001t0002g0117a0001c0001t0002g0119a0001c0001t0002g0218others(10): Show | 13 | HG00738.hp1 HG01106.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.5063+1234_5063+123 others(6): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 37/38 | chr20 | 49029902 | ||||||
| chr20:49029902
|
A | AT | 10 | a0001c0002t0001g0112a0001c0002t0001g0128a0001c0002t0001g0134others(7): Show | 10 | HG00438.hp1 HG01361.hp2 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.5063+1257dupT | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 37/38 | INFO_REALIGN_3_PRIME | chr20 | 49029902 | |||||
| chr20:49029902
|
AT | A | 29 | a0001c0002t0001g0123a0001c0002t0001g0305a0001c0002t0001g0313others(26): Show | 30 | HG00639.hp1 HG00741.hp2 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.5063+1257delT | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 37/38 | INFO_REALIGN_3_PRIME | chr20 | 49029902 | |||||
| chr20:49029902
|
ATT | A | 103 | a0001c0002t0001g0122a0001c0002t0001g0124a0001c0002t0001g0282others(100): Show | 103 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(100): Show |
intron_variant | MODIFIER | c.5063+1256_5063+125 others(6): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 37/38 | INFO_REALIGN_3_PRIME | chr20 | 49029902 | |||||
| chr20:49029903
|
T | A | 2 | a0001c0001t0002g0240a0001c0001t0002g0252 | 2 | HG02109.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.5063+1235T>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 37/38 | chr20 | 49029903 | ||||||
| chr20:49029932
|
G | C | 1 | a0001c0002t0001g0141 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.5063+1264G>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 37/38 | chr20 | 49029932 | ||||||
| chr20:49029947
|
A | T | 3 | a0001c0001t0002g0218a0001c0001t0002g0219a0001c0001t0002g0243 | 3 | HG02145.hp1 HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.5063+1279A>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 37/38 | chr20 | 49029947 | ||||||
| chr20:49030001
|
G | A | 1 | a0001c0001t0004g0323 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.5063+1333G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 37/38 | chr20 | 49030001 | ||||||
| chr20:49030083
|
T | C | 46 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0009others(43): Show | 46 | HG00280.hp1 HG00558.hp2 HG01106.hp2 others(43): Show |
intron_variant | MODIFIER | c.5063+1415T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 37/38 | chr20 | 49030083 | ||||||
| chr20:49030084
|
G | A | 135 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0009others(132): Show | 135 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(132): Show |
intron_variant | MODIFIER | c.5063+1416G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 37/38 | chr20 | 49030084 | ||||||
| chr20:49030395
|
C | T | 132 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0009others(129): Show | 132 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(129): Show |
intron_variant | MODIFIER | c.5064-1654C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 37/38 | chr20 | 49030395 | ||||||
| chr20:49030466
|
C | CA | 11 | a0001c0001t0002g0120a0001c0001t0002g0244a0001c0001t0007g0042others(8): Show | 11 | HG00438.hp2 HG02615.hp2 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.5064-1569dupA | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 37/38 | INFO_REALIGN_3_PRIME | chr20 | 49030466 | |||||
| chr20:49030531
|
G | A | 248 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0009others(245): Show | 248 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(245): Show |
intron_variant | MODIFIER | c.5064-1518G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 37/38 | chr20 | 49030531 | ||||||
| chr20:49030723
|
G | A | 2 | a0001c0001t0003g0199a0001c0001t0003g0200 | 2 | HG00639.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.5064-1326G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 37/38 | chr20 | 49030723 | ||||||
| chr20:49030880
|
T | C | 135 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0009others(132): Show | 135 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(132): Show |
intron_variant | MODIFIER | c.5064-1169T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 37/38 | chr20 | 49030880 | ||||||
| chr20:49030900
|
G | C | 35 | a0001c0001t0002g0240a0001c0001t0003g0113a0001c0001t0003g0114others(32): Show | 35 | HG00323.hp2 HG00639.hp2 HG00733.hp2 others(32): Show |
intron_variant | MODIFIER | c.5064-1149G>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 37/38 | chr20 | 49030900 | ||||||
| chr20:49030906
|
C | T | 1 | a0001c0002t0001g0112 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.5064-1143C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 37/38 | chr20 | 49030906 | ||||||
| chr20:49031125
|
T | C | 135 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0009others(132): Show | 135 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(132): Show |
intron_variant | MODIFIER | c.5064-924T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 37/38 | chr20 | 49031125 | ||||||
| chr20:49031220
|
C | CT | 21 | a0001c0002t0001g0125a0001c0002t0001g0128a0001c0002t0001g0137others(18): Show | 21 | HG01074.hp1 HG01123.hp1 HG01169.hp1 others(18): Show |
intron_variant | MODIFIER | c.5064-800dupT | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 37/38 | INFO_REALIGN_3_PRIME | chr20 | 49031220 | |||||
| chr20:49031220
|
CT | C | 26 | a0001c0001t0002g0010a0001c0001t0006g0266a0001c0002t0001g0168others(23): Show | 27 | HG00609.hp2 HG00741.hp2 HG01074.hp2 others(24): Show |
intron_variant | MODIFIER | c.5064-800delT | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 37/38 | INFO_REALIGN_3_PRIME | chr20 | 49031220 | |||||
| chr20:49031220
|
CTT | C | 84 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0011others(81): Show | 84 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.5064-801_5064-800d others(4): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 37/38 | INFO_REALIGN_3_PRIME | chr20 | 49031220 | |||||
| chr20:49031220
|
CTTT | C | 89 | a0001c0001t0002g0003a0001c0001t0002g0116a0001c0001t0002g0117others(86): Show | 89 | HG00280.hp1 HG00558.hp2 HG00639.hp1 others(86): Show |
intron_variant | MODIFIER | c.5064-802_5064-800d others(5): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 37/38 | INFO_REALIGN_3_PRIME | chr20 | 49031220 | |||||
| chr20:49031220
|
CTTTT | C | 8 | a0001c0001t0002g0233a0001c0001t0002g0249a0001c0001t0002g0254others(5): Show | 8 | HG01175.hp2 HG02717.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.5064-803_5064-800d others(6): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 37/38 | INFO_REALIGN_3_PRIME | chr20 | 49031220 | |||||
| chr20:49031220
|
CTTTTT | C | 50 | a0001c0001t0002g0218a0001c0001t0002g0219a0001c0001t0002g0221others(47): Show | 50 | HG00323.hp2 HG00639.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.5064-804_5064-800d others(7): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 37/38 | INFO_REALIGN_3_PRIME | chr20 | 49031220 | |||||
| chr20:49031220
|
CTTTTTT | C | 7 | a0001c0001t0002g0220a0001c0001t0002g0230a0001c0001t0002g0277others(4): Show | 7 | HG01243.hp2 HG02293.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.5064-805_5064-800d others(8): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 37/38 | INFO_REALIGN_3_PRIME | chr20 | 49031220 | |||||
| chr20:49031248
|
T | C | 29 | a0001c0001t0004g0321a0001c0001t0004g0323a0001c0001t0004g0324others(26): Show | 29 | HG00673.hp1 HG00738.hp1 HG01934.hp1 others(26): Show |
intron_variant | MODIFIER | c.5064-801T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 37/38 | chr20 | 49031248 | ||||||
| chr20:49031256
|
G | C | 5 | a0001c0002t0001g0290a0001c0002t0001g0292a0001c0002t0001g0307others(2): Show | 5 | HG02015.hp1 NA18971.hp2 NA18977.hp2 others(2): Show |
intron_variant | MODIFIER | c.5064-793G>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 37/38 | chr20 | 49031256 | ||||||
| chr20:49031339
|
T | C | 134 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0009others(131): Show | 134 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(131): Show |
intron_variant | MODIFIER | c.5064-710T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 37/38 | chr20 | 49031339 | ||||||
| chr20:49031477
|
C | T | 1 | a0001c0002t0001g0305 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.5064-572C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 37/38 | chr20 | 49031477 | ||||||
| chr20:49031816
|
A | G | 246 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0009others(243): Show | 246 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(243): Show |
intron_variant | MODIFIER | c.5064-233A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 37/38 | chr20 | 49031816 | ||||||
| chr20:49031917
|
CA | C | 111 | a0001c0002t0001g0122a0001c0002t0001g0123a0001c0002t0001g0124others(108): Show | 111 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(108): Show |
intron_variant | MODIFIER | c.5064-120delA | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 37/38 | INFO_REALIGN_3_PRIME | chr20 | 49031917 | |||||
| chr20:49031961
|
A | T | 1 | a0001c0001t0003g0207 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.5064-88A>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 37/38 | chr20 | 49031961 | ||||||
| chr20:49032012
|
A | G | 3 | a0001c0001t0002g0221a0001c0001t0002g0222a0001c0001t0002g0245 | 3 | HG01361.hp1 HG02647.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.5064-37A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 37/38 | chr20 | 49032012 | ||||||
| chr20:49032191
|
A | G | 1 | a0001c0002t0001g0196 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.5181+25A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 38/38 | chr20 | 49032191 | ||||||
| chr20:49032317
|
C | T | 248 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0009others(245): Show | 248 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(245): Show |
intron_variant | MODIFIER | c.5181+151C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 38/38 | chr20 | 49032317 | ||||||
| chr20:49032319
|
G | A | 137 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0009others(134): Show | 138 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(135): Show |
intron_variant | MODIFIER | c.5181+153G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 38/38 | chr20 | 49032319 | ||||||
| chr20:49032500
|
TAAAAG | T | 6 | a0001c0001t0003g0113a0001c0001t0003g0209a0001c0001t0003g0210others(3): Show | 6 | NA18946.hp2 NA18966.hp1 NA18975.hp2 others(3): Show |
intron_variant | MODIFIER | c.5181+336_5181+340d others(7): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 38/38 | INFO_REALIGN_3_PRIME | chr20 | 49032500 | |||||
| chr20:49032593
|
A | G | 3 | a0001c0001t0003g0202a0001c0001t0003g0216a0001c0001t0023g0215 | 3 | HG01175.hp2 HG01516.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.5181+427A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 38/38 | chr20 | 49032593 | ||||||
| chr20:49032597
|
C | CT | 15 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0010others(12): Show | 15 | HG01891.hp2 HG02129.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.5182-413dupT | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 38/38 | INFO_REALIGN_3_PRIME | chr20 | 49032597 | |||||
| chr20:49032653
|
C | T | 2 | a0001c0001t0014g0223a0001c0001t0014g0224 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.5182-370C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 38/38 | chr20 | 49032653 | ||||||
| chr20:49032844
|
C | T | 1 | a0001c0002t0001g0193 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.5182-179C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 38/38 | chr20 | 49032844 | ||||||
| chr20:49032988
|
T | C | 46 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0009others(43): Show | 46 | HG00280.hp1 HG00558.hp2 HG01106.hp2 others(43): Show |
intron_variant | MODIFIER | c.5182-35T>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 38/38 | chr20 | 49032988 |