Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| 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 | 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 | MQESQ others(1780): Show |
chr20 | 48916711 | 49041693 |
| a0002 | 0/0 | 1785 | 6 | 0 | 1 | 5 | 0 | 0 | 5 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | MQESQ others(1780): Show |
chr20 | 48916711 | 49041693 |
| a0003 | 0/0 | 1785 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | MQESQ others(1780): Show |
chr20 | 48916711 | 49041693 |
| a0004 | 0/0 | 1785 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | MQESQ others(1780): Show |
chr20 | 48916711 | 49041693 |
| a0005 | 0/0 | 1785 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | MQESQ others(1780): Show |
chr20 | 48916711 | 49041693 |
| a0006 | 0/0 | 1785 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | MQESQ others(1780): Show |
chr20 | 48916711 | 49041693 |
| a0007 | 0/0 | 1785 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | MQESQ others(1780): Show |
chr20 | 48916711 | 49041693 |
| a0008 | 0/0 | 1785 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | MQESQ others(1780): Show |
chr20 | 48916711 | 49041693 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 5355 | 128 | 46 | 19 | 49 | 3 | 10 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | ATGCA others(5350): Show |
chr20 | 48916711 | 49041693 | ||
| a0001c0002 | 1/0 | 5355 | 126 | 28 | 24 | 52 | 5 | 16 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | ATGCA others(5350): Show |
chr20 | 48916711 | 49041693 | ||
| a0001c0003 | 0/0 | 5355 | 76 | 4 | 16 | 44 | 0 | 12 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | ATGCA others(5350): Show |
chr20 | 48916711 | 49041693 | ||
| a0001c0005 | 0/0 | 5355 | 3 | 3 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | ATGCA others(5350): Show |
chr20 | 48916711 | 49041693 | ||
| a0001c0006 | 0/0 | 5355 | 2 | 0 | 2 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | ATGCA others(5350): Show |
chr20 | 48916711 | 49041693 | ||
| a0001c0012 | 0/0 | 5355 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | ATGCA others(5350): Show |
chr20 | 48916711 | 49041693 | ||
| a0001c0013 | 0/0 | 5355 | 1 | 0 | 0 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | ATGCA others(5350): Show |
chr20 | 48916711 | 49041693 | ||
| a0001c0015 | 0/0 | 5355 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | ATGCA others(5350): Show |
chr20 | 48916711 | 49041693 | ||
| a0001c0016 | 0/0 | 5355 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | ATGCA others(5350): Show |
chr20 | 48916711 | 49041693 | ||
| a0002c0004 | 0/0 | 5355 | 6 | 0 | 1 | 5 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | ATGCA others(5350): Show |
chr20 | 48916711 | 49041693 | ||
| a0003c0007 | 0/0 | 5355 | 2 | 0 | 2 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | ATGCA others(5350): Show |
chr20 | 48916711 | 49041693 | ||
| a0004c0011 | 0/0 | 5355 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | ATGCA others(5350): Show |
chr20 | 48916711 | 49041693 | ||
| a0005c0014 | 0/0 | 5355 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | ATGCA others(5350): Show |
chr20 | 48916711 | 49041693 | ||
| a0006c0009 | 0/0 | 5355 | 1 | 0 | 0 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | ATGCA others(5350): Show |
chr20 | 48916711 | 49041693 | ||
| a0007c0010 | 0/0 | 5355 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | ATGCA others(5350): Show |
chr20 | 48916711 | 49041693 | ||
| a0008c0008 | 0/0 | 5355 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | ATGCA others(5350): Show |
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 | ACGTG others(9026): Show |
chr20 | 48916711 | 49041693 |
| a0001c0001t0002 | 0/1 | 9032 | 55 | 35 | 5 | 11 | 1 | 2 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | ACGTG others(9027): Show |
chr20 | 48916711 | 49041693 |
| a0001c0001t0003 | 0/0 | 9032 | 28 | 2 | 9 | 12 | 2 | 3 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | ACGTG others(9027): Show |
chr20 | 48916711 | 49041693 |
| a0001c0001t0004 | 0/0 | 9032 | 25 | 0 | 3 | 19 | 0 | 3 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | ACGTG others(9027): Show |
chr20 | 48916711 | 49041693 |
| a0001c0001t0006 | 0/0 | 9032 | 4 | 4 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | ACGTG others(9027): Show |
chr20 | 48916711 | 49041693 |
| a0001c0001t0007 | 0/0 | 9031 | 4 | 0 | 1 | 2 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | ACGTG others(9026): Show |
chr20 | 48916711 | 49041693 |
| a0001c0001t0011 | 0/0 | 9032 | 2 | 0 | 0 | 2 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | ACGTG others(9027): Show |
chr20 | 48916711 | 49041693 |
| a0001c0001t0013 | 0/0 | 9032 | 2 | 0 | 0 | 2 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | ACGTG others(9027): Show |
chr20 | 48916711 | 49041693 |
| a0001c0001t0014 | 0/0 | 9032 | 2 | 2 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | ACGTG others(9027): Show |
chr20 | 48916711 | 49041693 |
| a0001c0001t0016 | 0/0 | 9032 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | ACGTG others(9027): Show |
chr20 | 48916711 | 49041693 |
| a0001c0001t0019 | 0/0 | 9032 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | ACGTG others(9027): Show |
chr20 | 48916711 | 49041693 |
| a0001c0001t0020 | 0/0 | 9032 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | ACGTG others(9027): Show |
chr20 | 48916711 | 49041693 |
| a0001c0001t0021 | 0/0 | 9032 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | ACGTG others(9027): Show |
chr20 | 48916711 | 49041693 |
| a0001c0001t0023 | 0/0 | 9032 | 1 | 0 | 0 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | ACGTG others(9027): Show |
chr20 | 48916711 | 49041693 |
| a0001c0002t0001 | 1/0 | 9031 | 102 | 11 | 19 | 51 | 4 | 16 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | ACGTG others(9026): Show |
chr20 | 48916711 | 49041693 |
| a0001c0002t0005 | 0/0 | 9031 | 16 | 15 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | ACGTG others(9026): Show |
chr20 | 48916711 | 49041693 |
| a0001c0002t0009 | 0/0 | 9032 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | ACGTG others(9027): Show |
chr20 | 48916711 | 49041693 |
| a0001c0002t0010 | 0/0 | 9031 | 2 | 0 | 2 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | ACGTG others(9026): Show |
chr20 | 48916711 | 49041693 |
| a0001c0002t0012 | 0/0 | 9031 | 2 | 0 | 1 | 0 | 1 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | ACGTG others(9026): Show |
chr20 | 48916711 | 49041693 |
| a0001c0002t0015 | 0/0 | 9031 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | ACGTG others(9026): Show |
chr20 | 48916711 | 49041693 |
| a0001c0002t0017 | 0/0 | 9031 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | ACGTG others(9026): Show |
chr20 | 48916711 | 49041693 |
| a0001c0002t0022 | 0/0 | 9031 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | ACGTG others(9026): Show |
chr20 | 48916711 | 49041693 |
| a0001c0003t0001 | 0/0 | 9031 | 74 | 4 | 15 | 43 | 0 | 12 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | ACGTG others(9026): Show |
chr20 | 48916711 | 49041693 |
| a0001c0003t0009 | 0/0 | 9032 | 2 | 0 | 1 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | ACGTG others(9027): Show |
chr20 | 48916711 | 49041693 |
| a0001c0005t0008 | 0/0 | 9032 | 3 | 3 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | ACGTG others(9027): Show |
chr20 | 48916711 | 49041693 |
| a0001c0006t0002 | 0/0 | 9032 | 2 | 0 | 2 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | ACGTG others(9027): Show |
chr20 | 48916711 | 49041693 |
| a0001c0012t0001 | 0/0 | 9031 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | ACGTG others(9026): Show |
chr20 | 48916711 | 49041693 |
| a0001c0013t0003 | 0/0 | 9032 | 1 | 0 | 0 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | ACGTG others(9027): Show |
chr20 | 48916711 | 49041693 |
| a0001c0015t0001 | 0/0 | 9031 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | ACGTG others(9026): Show |
chr20 | 48916711 | 49041693 |
| a0001c0016t0001 | 0/0 | 9031 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | ACGTG others(9026): Show |
chr20 | 48916711 | 49041693 |
| a0002c0004t0001 | 0/0 | 9031 | 6 | 0 | 1 | 5 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | ACGTG others(9026): Show |
chr20 | 48916711 | 49041693 |
| a0003c0007t0001 | 0/0 | 9031 | 2 | 0 | 2 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | ACGTG others(9026): Show |
chr20 | 48916711 | 49041693 |
| a0004c0011t0001 | 0/0 | 9031 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | ACGTG others(9026): Show |
chr20 | 48916711 | 49041693 |
| a0005c0014t0018 | 0/0 | 9031 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | ACGTG others(9026): Show |
chr20 | 48916711 | 49041693 |
| a0006c0009t0001 | 0/0 | 9031 | 1 | 0 | 0 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | ACGTG others(9026): Show |
chr20 | 48916711 | 49041693 |
| a0007c0010t0002 | 0/0 | 9032 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | ACGTG others(9027): Show |
chr20 | 48916711 | 49041693 |
| a0008c0008t0002 | 0/0 | 9032 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | ACGTG others(9027): Show |
chr20 | 48916711 | 49041693 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0173 | 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 | 0 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | 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 |
| a0001c0001t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0002g0220 | 0/0 | 1 | 1 | 0 | 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 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 1 | 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 |
| a0001c0001t0002g0234 | 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 |
| a0001c0001t0002g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0002g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0002g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0002g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0002g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0002g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0003g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 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 |
| a0001c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 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 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0003g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0003g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0003g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | 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 | 0 | 0 | 1 | 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 |
| a0001c0001t0006g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0006g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0006g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0006g0275 | 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 |
| a0001c0001t0011g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0011g0271 | 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 |
| a0001c0001t0014g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0014g0225 | 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 |
| a0001c0001t0021g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0001t0023g0216 | 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 |
| a0001c0002t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0002t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0156 | 0/0 | 1 | 1 | 0 | 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 | 1 | 0 | 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 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 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 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0002t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0001g0291 | 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 |
| a0001c0002t0009g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0010g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0010g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0012g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0002t0012g0160 | 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 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0003t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0003t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 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 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0003t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0003t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0003t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 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 | 0 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0003t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0003t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0003t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0003t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0003t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0003t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0003t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0003t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0003t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0003t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0003t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0003t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0003t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 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 | 1 | 0 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0003t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0003t0001g0103 | 0/0 | 1 | 0 | 1 | 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 |
| a0001c0013t0003g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0001c0015t0001g0181 | 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 |
| a0002c0004t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0002c0004t0001g0177 | 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 |
| a0004c0011t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0005c0014t0018g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0006c0009t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0007c0010t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| a0008c0008t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | g0203 | EUR | FIN | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG00438 | hp1 | a0001 | c0002 | t0001 | g0136 | 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 | g0084 | 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 | g0082 | EAS | CHS | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG00609 | hp2 | a0001 | c0002 | t0001 | g0186 | 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 | a0004 | 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 | g0065 | 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 | g0134 | AMR | PUR | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG00733 | hp2 | a0001 | c0001 | t0003 | g0235 | 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 | g0204 | AMR | PUR | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG00741 | hp1 | a0001 | c0002 | t0001 | g0295 | 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 | g0294 | AMR | PUR | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG01071 | hp2 | a0001 | c0002 | t0001 | g0164 | AMR | PUR | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG01074 | hp1 | a0001 | c0002 | t0001 | g0152 | 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 | g0183 | 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 | g0118 | 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 | g0151 | 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 | g0273 | 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 | g0103 | AMR | PUR | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0221 | AMR | PUR | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG01255 | hp1 | a0001 | c0003 | t0001 | g0064 | AMR | CLM | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG01255 | hp2 | a0001 | c0001 | t0003 | g0209 | 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 | g0215 | 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 | g0176 | AMR | CLM | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG01261 | hp2 | a0001 | c0003 | t0001 | g0055 | 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 | g0218 | AMR | CLM | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0223 | AMR | CLM | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG01361 | hp2 | a0001 | c0002 | t0012 | g0160 | 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 | g0217 | EUR | IBS | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG01516 | hp2 | a0001 | c0002 | t0001 | g0180 | 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 | g0166 | AMR | PEL | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG01943 | hp1 | a0001 | c0002 | t0010 | g0147 | AMR | PEL | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG01943 | hp2 | a0001 | c0003 | t0001 | g0078 | AMR | PEL | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG01952 | hp1 | a0001 | c0002 | t0001 | g0158 | AMR | PEL | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG01952 | hp2 | a0001 | c0003 | t0001 | g0067 | AMR | PEL | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG01975 | hp1 | a0001 | c0003 | t0001 | g0075 | 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 | g0087 | AMR | PEL | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0169 | AMR | PEL | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0187 | 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 | g0291 | 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 | g0272 | AFR | ACB | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG02055 | hp2 | a0001 | c0001 | t0006 | g0275 | 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 | g0165 | 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 | g0193 | 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 | g0274 | EAS | KHV | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG02132 | hp1 | a0001 | c0002 | t0001 | g0185 | EAS | KHV | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG02132 | hp2 | a0001 | c0003 | t0001 | g0061 | 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 | g0252 | 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 | g0170 | 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 | g0156 | 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 | g0233 | AFR | ACB | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG02273 | hp1 | a0002 | c0004 | t0001 | g0172 | AMR | PEL | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG02273 | hp2 | a0001 | c0003 | t0001 | g0083 | 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 | g0063 | 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 | g0231 | AFR | ACB | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG02572 | hp1 | a0001 | c0002 | t0001 | g0192 | 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 | g0257 | 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 | g0230 | 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 | g0178 | 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 | g0234 | 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 | g0236 | 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 | g0229 | 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 | g0263 | AFR | GWD | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG02818 | hp2 | a0001 | c0001 | t0006 | g0270 | 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 | g0224 | AFR | GWD | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG02896 | hp1 | a0001 | c0003 | t0001 | g0101 | AFR | GWD | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG02896 | hp2 | a0001 | c0002 | t0001 | g0167 | AFR | GWD | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG02897 | hp1 | a0001 | c0001 | t0014 | g0225 | AFR | GWD | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG02897 | hp2 | a0001 | c0002 | t0001 | g0168 | AFR | GWD | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG02965 | hp1 | a0001 | c0001 | t0006 | g0269 | 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 | g0066 | 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 | g0254 | 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 | g0237 | 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 | g0220 | 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 | g0219 | 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 | g0060 | 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 | g0184 | SAS | PJL | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0256 | 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 | g0173 | AFR | MSL | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG03654 | hp1 | a0001 | c0003 | t0001 | g0070 | SAS | PJL | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG03654 | hp2 | a0006 | c0009 | t0001 | g0288 | 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 | g0216 | SAS | PJL | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG03710 | hp1 | a0001 | c0003 | t0001 | g0081 | SAS | PJL | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0117 | 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 | g0058 | SAS | BEB | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG03834 | hp1 | a0001 | c0002 | t0001 | g0149 | 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 | g0069 | SAS | BEB | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG03927 | hp2 | a0001 | c0002 | t0001 | g0174 | 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 | g0182 | 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 | g0079 | 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 | g0226 | 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 | g0258 | 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 | g0271 | 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 | g0074 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA18944 | hp2 | a0001 | c0002 | t0001 | g0188 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA18945 | hp1 | a0001 | c0003 | t0001 | g0068 | 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 | a0008 | c0008 | t0002 | g0265 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA18946 | hp2 | a0001 | c0001 | t0003 | g0214 | 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 | g0053 | 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 | g0287 | 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 | g0071 | 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 | g0077 | 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 | g0154 | 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 | g0072 | 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 | g0056 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA18965 | hp1 | a0001 | c0002 | t0001 | g0161 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA18965 | hp2 | a0001 | c0003 | t0001 | g0043 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA18966 | hp1 | a0001 | c0001 | t0003 | g0211 | 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 | g0260 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA18968 | hp2 | a0001 | c0015 | t0001 | g0181 | 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 | g0255 | 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 | g0162 | 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 | g0080 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA18981 | hp2 | a0001 | c0002 | t0001 | g0175 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA18982 | hp1 | a0001 | c0002 | t0001 | g0171 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA18982 | hp2 | a0001 | c0002 | t0001 | g0289 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA18983 | hp1 | a0001 | c0003 | t0001 | g0054 | 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 | g0057 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA18986 | hp1 | a0001 | c0002 | t0001 | g0155 | 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 | g0179 | 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 | g0044 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA18998 | hp1 | a0001 | c0002 | t0001 | g0157 | 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 | g0150 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA19012 | hp1 | a0001 | c0002 | t0009 | g0290 | 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 | g0148 | 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 | g0259 | 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 | g0261 | 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 | g0062 | 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 | g0196 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0264 | 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 | g0195 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA19078 | hp2 | a0001 | c0003 | t0001 | g0106 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA19079 | hp1 | a0001 | c0001 | t0003 | g0206 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA19079 | hp2 | a0002 | c0004 | t0001 | g0177 | 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 | g0153 | 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 | g0076 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA19082 | hp1 | a0001 | c0003 | t0001 | g0102 | 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 | g0266 | 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 | g0085 | 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 | g0107 | EAS | JPT | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| NA19088 | hp2 | a0001 | c0001 | t0003 | g0210 | 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 | g0232 | 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 | g0159 | 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 | g0207 | SAS | GIH | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| HG01123 | hp1 | a0001 | c0002 | t0001 | g0189 | 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 | g0253 | 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 | g0228 | 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 | g0262 | 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 | a0001 | c0001 | t0002 | g0227 | REF | REF | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0001 | g0163 | REF | REF | ARFGEF2_chr20_48916711_49041693 | ARFGEF2 | chr20 | 48916711 | 49041693 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | a0008 | 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 | a0006 | 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 | a0004 | 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 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | a0001c0001 a0001c0005 a0001c0006 others(3): Show |
135 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(132): 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 | a0001c0003 a0001c0012 |
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 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr20:48921796 | C | T | 4 | a0001c0001t0003 a0001c0001t0007 a0001c0001t0023 others(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 | a0001c0001t0014 a0001c0001t0021 |
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 | a0001c0001t0004 a0001c0001t0013 a0001c0001t0019 others(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 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(15): Show |
134 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(131): 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 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(15): Show |
134 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(131): 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 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(15): Show |
134 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(131): 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 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(16): Show |
133 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(130): 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 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | a0001c0001t0004g0321 a0001c0001t0004g0323 a0001c0001t0004g0324 others(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 | a0001c0002t0001g0006 a0001c0002t0017g0007 |
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 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0010 others(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 | a0001c0002t0005g0001 a0001c0002t0005g0015 a0001c0002t0005g0016 others(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 | a0001c0002t0001g0318 a0001c0002t0015g0319 |
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 | a0001c0001t0007g0041 a0001c0001t0007g0042 a0001c0002t0001g0109 others(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 | a0001c0003t0001g0029 a0001c0003t0001g0030 a0001c0003t0001g0031 others(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 | 157 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0010 others(154): Show |
157 | HG00323.hp2 HG00639.hp1 HG00639.hp2 others(154): 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 | a0001c0002t0001g0315 a0001c0002t0001g0316 |
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 | a0001c0002t0005g0001 a0001c0002t0005g0015 a0001c0002t0005g0016 others(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 | 132 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(129): Show |
132 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(129): Show |
intron_variant | MODIFIER | c.121+2970G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48924980 | |||||||
| chr20:48925063 | G | A | 248 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(245): Show |
248 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(245): 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 | a0001c0001t0002g0280 a0001c0001t0002g0281 |
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 | a0001c0001t0004g0346 a0001c0001t0004g0347 |
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 | a0001c0001t0002g0277 a0001c0001t0002g0278 a0001c0001t0002g0279 |
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 | a0001c0001t0002g0198 a0001c0002t0001g0282 a0001c0002t0001g0283 others(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 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(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 | 248 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(245): Show |
248 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(245): Show |
intron_variant | MODIFIER | c.121+5057G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48927067 | |||||||
| chr20:48927097 | A | C | 56 | a0001c0001t0002g0219 a0001c0001t0002g0220 a0001c0001t0002g0221 others(53): Show |
56 | HG00323.hp2 HG00639.hp2 HG00733.hp2 others(53): 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 | a0001c0002t0005g0001 a0001c0002t0005g0015 a0001c0002t0005g0016 others(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 | a0001c0001t0003g0199 a0001c0001t0003g0200 |
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 | a0001c0001t0002g0248 a0001c0001t0002g0249 a0001c0001t0002g0250 |
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 | a0001c0001t0002g0121 a0001c0001t0002g0198 a0001c0001t0002g0243 others(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 | a0001c0002t0001g0125 a0001c0002t0001g0126 a0001c0002t0001g0127 others(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 | a0001c0003t0001g0029 a0001c0003t0001g0030 a0001c0003t0001g0031 others(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 | a0001c0001t0002g0240 a0001c0001t0003g0238 a0001c0001t0003g0239 others(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 | a0001c0002t0001g0148 a0001c0005t0008g0267 a0001c0005t0008g0268 others(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 | a0001c0002t0001g0167 a0001c0002t0001g0168 |
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 | a0001c0001t0003g0206 | 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 | a0001c0001t0002g0272 | 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 | a0001c0001t0006g0252 a0001c0001t0006g0269 a0001c0001t0006g0270 others(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 | a0001c0001t0002g0198 a0001c0002t0001g0122 a0001c0002t0001g0123 others(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 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(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 | a0001c0001t0003g0236 a0001c0001t0003g0237 |
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 | a0001c0001t0004g0325 a0001c0001t0004g0326 a0001c0001t0004g0327 others(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 | a0001c0001t0003g0235 | 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 | a0001c0001t0002g0198 a0001c0002t0001g0122 a0001c0002t0001g0123 others(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 | a0001c0001t0003g0201 a0001c0001t0007g0241 |
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 | a0001c0001t0002g0232 a0001c0001t0002g0233 a0001c0001t0002g0234 |
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 | a0001c0002t0001g0122 a0001c0002t0001g0123 a0001c0002t0001g0124 others(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 | a0001c0001t0002g0198 a0001c0002t0001g0122 a0001c0002t0001g0123 others(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 | a0001c0006t0002g0037 a0001c0006t0002g0038 |
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 | a0001c0001t0002g0240 a0001c0001t0003g0113 a0001c0001t0003g0114 others(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 | a0001c0002t0001g0185 | 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 | a0001c0002t0001g0122 a0001c0002t0001g0123 a0001c0002t0001g0124 others(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 | a0001c0001t0004g0324 a0001c0001t0004g0348 |
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 | a0001c0001t0006g0275 | 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 | a0001c0002t0001g0313 a0001c0002t0001g0314 a0001c0002t0001g0318 others(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 | a0001c0001t0004g0321 a0001c0001t0004g0323 a0001c0001t0004g0324 others(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 | 131 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(128): Show |
131 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(128): 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 | a0001c0002t0001g0132 a0001c0002t0001g0133 |
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 | a0001c0005t0008g0267 a0001c0005t0008g0268 a0001c0005t0008g0276 |
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 | 246 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(243): Show |
246 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(243): 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 | a0001c0002t0005g0001 a0001c0002t0005g0015 a0001c0002t0005g0016 others(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 | 131 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(128): Show |
131 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(128): 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 | a0001c0001t0004g0321 a0001c0001t0004g0323 a0001c0001t0004g0324 others(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 | 202 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(199): Show |
202 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(199): 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 | a0001c0001t0002g0231 a0001c0001t0002g0249 a0001c0001t0002g0266 others(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 | a0001c0002t0001g0315 a0001c0002t0001g0316 |
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 |
267 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(264): Show |
268 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(265): 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 | a0001c0001t0002g0234 | 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 | a0001c0001t0006g0252 a0001c0001t0006g0269 a0001c0001t0006g0270 others(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 | a0001c0002t0001g0122 a0001c0002t0001g0123 a0001c0002t0001g0124 others(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 | 267 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(264): Show |
268 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(265): 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 | a0001c0001t0002g0219 a0001c0001t0002g0220 a0001c0001t0002g0243 |
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 | a0001c0002t0005g0021 a0001c0002t0005g0024 a0001c0002t0005g0025 |
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 | a0004c0011t0001g0301 | 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 | a0001c0001t0003g0202 a0001c0001t0003g0215 a0001c0001t0003g0217 others(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 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(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 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(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 | a0001c0001t0003g0113 a0001c0001t0003g0114 a0001c0001t0003g0210 others(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 | a0001c0002t0001g0182 | 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 | 54 | a0001c0001t0002g0219 a0001c0001t0002g0220 a0001c0001t0002g0221 others(51): Show |
54 | HG00323.hp2 HG00639.hp2 HG00733.hp2 others(51): Show |
intron_variant | MODIFIER | c.122-5269G>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48935930 | |||||||
| chr20:48935937 | C | CG | 39 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(36): Show |
39 | HG01175.hp2 HG01192.hp1 HG01261.hp1 others(36): 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 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0013 others(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 | a0001c0001t0002g0120 a0001c0001t0002g0248 a0001c0001t0002g0250 others(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 | a0001c0005t0008g0267 a0001c0005t0008g0268 a0001c0005t0008g0276 |
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 | a0001c0001t0007g0041 a0001c0001t0007g0042 a0001c0003t0001g0029 others(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 | a0001c0002t0001g0318 a0001c0002t0015g0319 |
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 | 132 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(129): Show |
132 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(129): 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 | a0001c0002t0001g0315 a0001c0002t0001g0316 |
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 | a0001c0001t0002g0272 | 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 | a0001c0001t0002g0232 a0001c0001t0002g0233 a0001c0001t0002g0234 |
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 | a0001c0001t0003g0206 | 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 | a0007c0010t0002g0258 | 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 | a0001c0001t0004g0321 a0001c0001t0004g0323 a0001c0001t0004g0324 others(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 | a0001c0001t0003g0212 a0001c0001t0003g0213 |
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 | a0001c0002t0005g0001 a0001c0002t0005g0015 a0001c0002t0005g0016 others(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 | 132 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(129): Show |
132 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(129): 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 | a0001c0002t0001g0174 | 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 | a0001c0001t0002g0219 | 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 | a0001c0005t0008g0267 a0001c0005t0008g0268 a0001c0005t0008g0276 |
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 | a0001c0001t0003g0236 a0001c0001t0003g0237 |
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 | a0001c0002t0001g0318 a0001c0002t0015g0319 |
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 | a0001c0001t0002g0254 | 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 | 247 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(244): Show |
247 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(244): 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 | a0001c0001t0002g0234 | 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 | a0001c0002t0001g0313 a0001c0002t0005g0001 a0001c0002t0005g0015 others(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 | a0001c0001t0002g0240 a0001c0001t0003g0113 a0001c0001t0003g0114 others(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 | a0001c0001t0004g0327 a0001c0001t0004g0333 a0001c0001t0004g0334 others(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 | a0001c0002t0005g0026 a0001c0002t0005g0027 |
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 | a0001c0001t0004g0321 a0001c0001t0004g0324 a0001c0001t0004g0325 others(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 | a0001c0001t0003g0214 a0001c0002t0001g0309 a0001c0002t0022g0197 others(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 | a0001c0002t0001g0122 a0001c0002t0001g0123 a0001c0002t0001g0124 others(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 | a0001c0001t0002g0253 a0001c0001t0002g0281 a0001c0001t0003g0114 others(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 | a0001c0003t0001g0029 a0001c0003t0001g0030 a0001c0003t0001g0031 others(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 | 271 | a0001c0001t0001g0173 a0001c0001t0002g0003 a0001c0001t0002g0008 others(268): Show |
273 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(270): 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 | a0001c0001t0002g0003 a0001c0001t0002g0116 a0001c0001t0002g0117 others(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 | a0001c0002t0001g0122 a0001c0002t0001g0123 a0001c0002t0001g0124 others(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 | a0001c0003t0001g0034 a0001c0003t0001g0089 a0001c0003t0001g0105 others(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 | a0001c0002t0001g0122 a0001c0002t0001g0123 a0001c0002t0001g0124 others(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 | a0001c0002t0005g0001 a0001c0002t0005g0015 a0001c0002t0005g0016 others(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 | a0002c0004t0001g0172 | 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 | 135 | a0001c0001t0001g0173 a0001c0001t0002g0003 a0001c0001t0002g0008 others(132): Show |
135 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(132): Show |
intron_variant | MODIFIER | c.122-723C>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 1/38 | chr20 | 48940476 | |||||||
| chr20:48940477 | G | A | 134 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(131): Show |
134 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(131): 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 | a0001c0002t0001g0138 a0001c0002t0001g0139 a0001c0002t0001g0175 |
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 | a0001c0001t0002g0240 a0001c0001t0003g0113 a0001c0001t0003g0114 others(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 | a0001c0002t0001g0318 a0001c0002t0015g0319 |
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 | a0001c0001t0002g0280 a0001c0001t0002g0281 |
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 | a0001c0001t0002g0198 a0001c0002t0001g0122 a0001c0002t0001g0123 others(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 | a0001c0001t0002g0198 a0001c0002t0001g0122 a0001c0002t0001g0123 others(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 | a0001c0003t0001g0034 a0001c0003t0001g0089 a0001c0003t0001g0105 others(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 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0011 others(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 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0011 others(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 | a0001c0002t0001g0122 a0001c0002t0001g0123 a0001c0002t0001g0124 others(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 | a0001c0003t0001g0030 a0001c0003t0001g0053 a0001c0003t0001g0054 others(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 | a0001c0001t0001g0173 a0001c0001t0002g0219 a0001c0001t0002g0220 others(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 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(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 | a0001c0001t0002g0255 a0001c0001t0002g0264 a0001c0001t0004g0323 others(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 | a0001c0002t0001g0314 a0001c0002t0001g0318 a0001c0002t0005g0001 others(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 | a0001c0003t0001g0055 a0001c0003t0001g0091 |
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 | a0001c0005t0008g0267 a0001c0005t0008g0268 a0001c0005t0008g0276 |
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 | a0001c0005t0008g0267 a0001c0005t0008g0268 a0001c0005t0008g0276 |
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 | a0001c0002t0001g0318 a0001c0002t0015g0319 |
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 | a0001c0002t0001g0318 a0001c0002t0015g0319 |
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 | a0001c0002t0001g0313 a0001c0002t0001g0314 |
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 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(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 | a0001c0002t0005g0026 a0001c0002t0005g0027 |
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 | a0001c0005t0008g0267 a0001c0005t0008g0268 a0001c0005t0008g0276 |
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 | a0001c0001t0002g0229 a0001c0001t0002g0230 |
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 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(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 | a0001c0001t0002g0198 a0001c0001t0007g0041 a0001c0001t0007g0042 others(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 | a0001c0001t0002g0240 a0001c0001t0003g0238 a0001c0001t0003g0239 |
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 | a0001c0001t0002g0198 a0001c0001t0007g0041 a0001c0001t0007g0042 others(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 | a0001c0001t0002g0219 a0001c0001t0002g0220 a0001c0001t0002g0243 |
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 | 131 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(128): Show |
131 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(128): 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 | a0001c0002t0001g0293 a0001c0002t0001g0294 a0001c0002t0001g0295 |
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 | a0004c0011t0001g0301 | 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 | a0001c0001t0002g0198 a0001c0002t0001g0122 a0001c0002t0001g0123 others(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 | a0001c0001t0002g0274 | 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 | a0001c0003t0001g0084 | 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 | a0001c0002t0001g0167 a0001c0002t0001g0168 |
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 | a0001c0002t0001g0166 | 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 | a0001c0001t0004g0321 a0001c0001t0004g0323 a0001c0001t0004g0324 others(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 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0010 others(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 | a0001c0003t0001g0083 | 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 | a0001c0013t0003g0207 | 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 | a0001c0005t0008g0267 a0001c0005t0008g0268 a0001c0005t0008g0276 |
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 | a0001c0001t0006g0252 a0001c0001t0006g0269 a0001c0001t0006g0270 others(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 | a0001c0001t0002g0198 a0001c0001t0007g0041 a0001c0001t0007g0042 others(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 | a0001c0002t0001g0142 a0001c0002t0001g0143 a0001c0002t0001g0176 others(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 | a0001c0001t0007g0041 a0001c0001t0007g0042 a0001c0002t0001g0122 others(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 | 131 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(128): Show |
131 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(128): 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 | a0001c0001t0002g0198 a0001c0002t0001g0282 a0001c0002t0001g0283 others(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 | a0001c0001t0002g0263 | 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 | a0008c0008t0002g0265 | 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 | a0001c0003t0001g0056 | 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 | a0001c0005t0008g0267 a0001c0005t0008g0268 a0001c0005t0008g0276 |
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 | a0001c0001t0004g0327 a0001c0001t0004g0333 a0001c0001t0004g0334 others(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 | a0001c0013t0003g0207 | 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 | a0001c0001t0002g0274 | 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 | a0001c0001t0002g0221 a0001c0001t0002g0244 a0001c0001t0002g0277 others(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 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0014 |
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 | a0001c0002t0001g0142 a0001c0002t0001g0143 a0001c0002t0001g0176 others(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 | a0001c0002t0005g0001 a0001c0002t0005g0015 a0001c0002t0005g0016 others(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 | a0001c0001t0002g0254 | 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 | a0001c0001t0002g0253 | 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 | a0001c0001t0004g0332 a0001c0001t0004g0343 a0001c0001t0004g0344 others(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 | a0001c0001t0002g0221 a0001c0001t0002g0244 a0001c0001t0002g0277 others(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 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(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 | a0001c0002t0005g0001 a0001c0002t0005g0015 a0001c0002t0005g0016 others(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 | a0001c0001t0014g0224 a0001c0001t0014g0225 a0001c0001t0021g0226 |
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 | a0001c0003t0001g0081 | 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 | a0001c0002t0001g0318 a0001c0002t0015g0319 |
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 | a0001c0002t0001g0318 a0001c0002t0015g0319 |
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 | a0001c0002t0001g0318 a0001c0002t0015g0319 |
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 | a0001c0002t0001g0318 a0001c0002t0015g0319 |
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 | a0002c0004t0001g0144 a0002c0004t0001g0145 a0002c0004t0001g0146 others(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 | a0001c0003t0001g0047 a0001c0003t0001g0075 a0001c0003t0001g0076 others(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 | a0001c0003t0001g0032 a0001c0003t0001g0055 a0001c0003t0001g0079 others(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 | a0001c0002t0009g0290 | 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 | a0001c0002t0001g0291 | 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 | a0001c0002t0001g0311 a0006c0009t0001g0288 |
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 | a0001c0002t0001g0283 a0001c0002t0001g0309 |
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 | a0001c0001t0002g0198 a0001c0002t0001g0123 a0001c0002t0001g0310 |
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 | a0001c0002t0001g0291 a0001c0002t0001g0292 a0001c0002t0001g0307 others(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 | a0001c0001t0004g0321 a0001c0001t0004g0341 a0001c0002t0001g0282 |
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 | a0001c0002t0001g0314 a0001c0002t0005g0001 a0001c0002t0005g0015 others(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 | a0001c0002t0005g0026 a0001c0002t0005g0027 |
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 | a0001c0002t0001g0124 a0001c0002t0001g0300 |
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 | a0001c0002t0001g0286 a0001c0002t0001g0294 |
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 | a0001c0002t0001g0122 a0001c0002t0001g0297 |
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 | a0001c0002t0001g0295 | 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 | a0001c0001t0002g0198 a0001c0002t0001g0123 a0001c0002t0001g0283 others(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 | a0001c0001t0004g0323 a0001c0001t0004g0324 a0001c0001t0004g0327 others(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 | a0001c0002t0005g0019 a0001c0002t0005g0024 |
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 | a0001c0002t0005g0021 a0001c0002t0005g0025 |
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 | a0001c0001t0002g0257 | 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 | a0001c0001t0014g0224 a0001c0001t0014g0225 a0001c0001t0021g0226 |
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 | a0001c0002t0001g0289 | 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 | a0001c0001t0002g0198 a0001c0002t0001g0122 a0001c0002t0001g0123 others(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 | a0001c0001t0002g0243 a0001c0002t0001g0002 a0001c0002t0001g0004 others(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 | a0001c0001t0002g0221 a0001c0001t0002g0231 a0001c0001t0002g0244 others(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 | 29 | a0001c0001t0002g0009 a0001c0001t0002g0013 a0001c0001t0002g0219 others(26): Show |
29 | HG00323.hp2 HG00639.hp2 HG01081.hp1 others(26): 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 | a0001c0001t0001g0173 a0001c0001t0002g0008 a0001c0001t0002g0010 others(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 | a0001c0002t0001g0137 a0001c0002t0001g0169 a0001c0002t0001g0170 others(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 | a0001c0002t0001g0178 | 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 | a0001c0002t0001g0315 a0001c0002t0001g0316 |
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 | a0001c0003t0001g0030 a0001c0003t0001g0052 a0001c0003t0001g0053 others(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 | a0001c0002t0001g0112 a0001c0002t0001g0127 a0001c0002t0001g0194 |
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 | a0001c0001t0002g0003 a0001c0001t0002g0248 a0001c0001t0007g0241 others(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 | a0001c0001t0002g0119 a0001c0001t0002g0223 a0001c0001t0002g0250 others(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 | a0001c0001t0002g0117 a0001c0001t0002g0118 a0001c0001t0002g0120 others(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 | a0001c0001t0002g0254 a0001c0002t0001g0318 a0001c0002t0015g0319 |
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 | a0001c0003t0001g0106 | 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 | a0001c0002t0001g0109 a0001c0002t0001g0182 a0001c0003t0001g0317 |
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 | a0001c0001t0002g0243 a0001c0002t0001g0002 a0001c0002t0001g0004 others(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 | a0001c0001t0002g0221 a0001c0001t0002g0231 a0001c0001t0002g0243 others(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 | 53 | a0001c0001t0002g0219 a0001c0001t0002g0220 a0001c0001t0002g0221 others(50): Show |
53 | HG00323.hp2 HG00639.hp2 HG00738.hp2 others(50): Show |
intron_variant | MODIFIER | c.277-504T>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3/38 | chr20 | 48950819 | |||||||
| chr20:48950821 | T | A | 44 | a0001c0001t0001g0173 a0001c0001t0002g0118 a0001c0001t0002g0219 others(41): Show |
44 | HG00323.hp2 HG00639.hp2 HG01081.hp1 others(41): 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 | a0001c0001t0002g0222 a0001c0001t0002g0223 a0001c0001t0002g0245 others(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 | a0001c0002t0001g0137 a0001c0002t0001g0169 a0001c0002t0001g0170 others(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 | a0001c0002t0001g0178 | 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 | a0001c0002t0022g0197 a0001c0003t0001g0055 a0001c0003t0001g0091 others(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 | a0001c0003t0001g0035 a0001c0003t0001g0051 a0001c0003t0001g0057 |
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 | a0001c0001t0014g0224 a0001c0001t0014g0225 a0001c0001t0021g0226 others(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 | a0001c0001t0002g0262 a0001c0001t0003g0212 a0001c0002t0001g0196 others(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 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0014 |
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 | a0001c0002t0001g0186 | 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 | a0001c0002t0001g0313 a0001c0002t0001g0314 a0001c0002t0001g0318 others(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 | a0001c0001t0002g0003 a0001c0001t0002g0116 a0001c0001t0002g0117 others(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 | a0001c0003t0001g0078 | 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 | a0001c0002t0001g0313 a0001c0002t0001g0314 a0001c0002t0001g0318 others(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 | a0001c0002t0001g0175 | 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 | a0001c0001t0002g0229 a0001c0001t0002g0230 |
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 | 271 | a0001c0001t0001g0173 a0001c0001t0002g0003 a0001c0001t0002g0008 others(268): Show |
273 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(270): 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 | a0001c0001t0002g0254 a0001c0001t0004g0326 a0001c0001t0004g0334 others(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 | 249 | a0001c0001t0001g0173 a0001c0001t0002g0003 a0001c0001t0002g0008 others(246): Show |
250 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(247): 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 | a0001c0001t0002g0273 a0001c0001t0003g0212 a0001c0001t0003g0238 others(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 | a0001c0002t0001g0195 | 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 | a0001c0001t0002g0223 | 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 | a0001c0002t0001g0122 a0001c0002t0001g0123 a0001c0002t0001g0124 others(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 | a0001c0001t0002g0003 a0001c0001t0002g0116 a0001c0001t0002g0117 others(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 | a0001c0005t0008g0267 a0001c0005t0008g0268 a0001c0005t0008g0276 |
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 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(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 | a0001c0001t0001g0173 | 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 | a0001c0003t0001g0029 a0001c0003t0001g0031 a0001c0003t0001g0059 others(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 | a0001c0001t0002g0255 a0001c0001t0002g0264 a0001c0001t0002g0266 |
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 | a0001c0002t0001g0318 a0001c0002t0015g0319 a0001c0005t0008g0267 others(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 | a0001c0002t0001g0307 a0001c0002t0001g0311 |
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 | a0001c0003t0001g0035 a0001c0003t0001g0051 a0001c0003t0001g0057 others(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 | 268 | a0001c0001t0001g0173 a0001c0001t0002g0003 a0001c0001t0002g0008 others(265): Show |
269 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(266): 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 | a0001c0001t0003g0206 | 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 | a0001c0003t0001g0040 a0001c0003t0001g0092 |
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 | a0001c0002t0001g0122 a0001c0002t0001g0123 a0001c0002t0001g0124 others(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 | a0001c0003t0001g0106 | 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 | a0001c0001t0002g0234 | 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 | 134 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(131): Show |
134 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(131): 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 | a0001c0002t0001g0122 a0001c0002t0001g0123 a0001c0002t0001g0124 others(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 | a0001c0005t0008g0267 a0001c0005t0008g0268 a0001c0005t0008g0276 |
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 | a0001c0001t0002g0254 a0001c0001t0014g0224 a0001c0001t0014g0225 others(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 | a0001c0001t0002g0009 a0001c0001t0002g0013 |
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 | a0001c0003t0001g0032 a0001c0003t0001g0074 a0001c0003t0001g0082 |
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 | a0001c0002t0001g0313 a0001c0002t0001g0314 a0001c0002t0005g0001 others(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 | 50 | a0001c0001t0002g0221 a0001c0001t0002g0222 a0001c0001t0002g0223 others(47): Show |
50 | HG00323.hp2 HG00639.hp2 HG00733.hp2 others(47): 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 | 246 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(243): Show |
246 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(243): 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 | a0001c0002t0001g0136 a0001c0002t0001g0165 a0001c0002t0001g0171 others(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 | a0001c0001t0002g0117 | 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 | a0001c0002t0001g0122 a0001c0002t0001g0123 a0001c0002t0001g0124 others(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 | a0001c0001t0002g0280 a0001c0001t0002g0281 |
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 | a0001c0002t0001g0122 a0001c0002t0001g0123 a0001c0002t0001g0124 others(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 | a0001c0003t0001g0061 a0001c0003t0001g0084 a0001c0003t0001g0093 |
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 | a0001c0003t0001g0072 | 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 | 1 | a0001c0001t0002g0228 | 1 | HG02559.hp2 | 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 | a0001c0001t0002g0120 a0001c0001t0002g0240 a0001c0001t0003g0113 others(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 | a0001c0001t0004g0321 a0001c0001t0004g0323 a0001c0001t0004g0324 others(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 | a0001c0001t0002g0198 a0001c0002t0001g0122 a0001c0002t0001g0123 others(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 | a0001c0003t0001g0032 a0001c0003t0001g0039 a0001c0003t0001g0044 others(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 | a0001c0001t0003g0209 a0001c0001t0011g0271 a0001c0002t0001g0132 others(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 | a0001c0001t0002g0198 a0001c0001t0004g0339 a0001c0001t0011g0271 others(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 | a0001c0003t0001g0076 | 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 | a0001c0002t0001g0138 a0001c0002t0001g0139 a0001c0002t0001g0175 |
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 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(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 | a0004c0011t0001g0301 | 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 | a0001c0003t0001g0076 | 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 | a0001c0003t0001g0076 | 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 | a0001c0002t0001g0314 a0001c0002t0001g0318 a0001c0002t0005g0021 others(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 | a0001c0002t0005g0001 a0001c0002t0005g0015 a0001c0002t0005g0016 others(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 | a0001c0001t0003g0212 a0001c0002t0001g0313 a0001c0002t0001g0314 others(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 | a0001c0001t0003g0212 a0001c0002t0001g0313 a0001c0002t0001g0314 others(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 | a0001c0001t0003g0212 a0001c0002t0001g0313 a0001c0002t0001g0314 others(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 | a0001c0001t0003g0212 a0001c0002t0001g0313 a0001c0002t0001g0314 others(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 | a0001c0003t0001g0062 | 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 | a0001c0003t0001g0076 | 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 | a0001c0001t0003g0212 a0001c0002t0001g0313 a0001c0002t0001g0314 others(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 | a0001c0003t0001g0062 | 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 | a0001c0003t0001g0062 | 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 | a0001c0003t0001g0062 | 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 | a0001c0002t0001g0313 a0001c0002t0001g0314 a0001c0002t0001g0318 others(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 | a0001c0003t0001g0062 | 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 | a0001c0003t0001g0076 | 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 | a0001c0003t0001g0043 a0001c0003t0001g0073 |
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 | a0001c0003t0001g0029 a0001c0003t0001g0030 a0001c0003t0001g0031 others(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 | a0001c0003t0001g0054 | 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 | a0001c0001t0002g0198 a0001c0002t0001g0122 a0001c0002t0001g0123 others(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 | a0001c0001t0002g0223 a0001c0001t0002g0245 |
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 | a0001c0001t0002g0120 a0001c0001t0002g0240 a0001c0001t0003g0113 others(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 | a0001c0002t0001g0006 a0001c0002t0017g0007 |
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 | a0001c0003t0001g0107 | 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 | a0001c0001t0002g0221 a0001c0001t0002g0244 a0001c0001t0002g0277 others(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 |
36 | a0001c0001t0002g0219 a0001c0001t0002g0220 a0001c0001t0002g0228 others(33): Show |
36 | HG00673.hp1 HG00738.hp1 HG01934.hp1 others(33): 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 | a0001c0001t0002g0229 a0001c0001t0002g0230 |
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 | a0001c0002t0001g0196 | 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 | a0001c0003t0001g0106 | 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 | a0001c0001t0002g0262 | 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 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0010 others(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 | a0001c0003t0001g0029 a0001c0003t0001g0030 a0001c0003t0001g0031 others(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 | a0001c0005t0008g0267 a0001c0005t0008g0268 a0001c0005t0008g0276 |
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 | a0001c0001t0002g0263 | 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 | a0001c0003t0001g0076 | 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 | a0001c0003t0001g0076 | 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 | a0001c0001t0002g0198 a0001c0002t0001g0122 a0001c0002t0001g0123 others(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 | a0001c0001t0002g0198 a0001c0001t0011g0271 a0001c0002t0001g0006 others(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 | a0001c0005t0008g0267 a0001c0005t0008g0268 a0001c0005t0008g0276 |
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 | a0001c0002t0001g0313 a0001c0002t0001g0314 a0001c0002t0001g0318 others(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 | a0001c0001t0002g0255 | 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 | a0001c0001t0002g0219 a0001c0001t0002g0220 a0001c0001t0002g0243 |
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 | a0001c0001t0014g0224 a0001c0001t0014g0225 |
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 | a0001c0003t0001g0029 a0001c0003t0001g0030 a0001c0003t0001g0031 others(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 | a0001c0001t0002g0010 a0001c0001t0002g0248 a0001c0001t0002g0254 others(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 | a0001c0002t0001g0132 a0001c0002t0001g0133 a0001c0002t0001g0318 others(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 | a0001c0002t0001g0304 a0001c0003t0001g0044 a0001c0003t0001g0071 others(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 | a0001c0003t0001g0030 a0001c0003t0001g0040 a0001c0003t0001g0053 others(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 | a0001c0002t0001g0293 a0001c0002t0001g0294 a0001c0002t0001g0295 others(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 | a0001c0002t0001g0123 a0001c0002t0001g0124 a0001c0002t0001g0283 others(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 | a0001c0002t0001g0122 a0001c0002t0001g0282 a0001c0002t0001g0286 others(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 | a0001c0002t0001g0289 a0001c0002t0001g0291 a0001c0002t0001g0292 others(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 | a0001c0003t0001g0032 a0001c0003t0001g0074 a0001c0003t0001g0082 |
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 | a0001c0001t0002g0003 a0001c0001t0002g0116 a0001c0001t0002g0117 others(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 | a0001c0002t0001g0315 a0001c0002t0001g0316 |
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 | a0001c0001t0004g0328 a0001c0001t0004g0342 |
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 | a0001c0001t0004g0327 a0001c0001t0004g0333 |
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 | a0001c0001t0002g0198 a0001c0002t0001g0122 a0001c0002t0001g0123 others(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 | a0001c0005t0008g0267 a0001c0005t0008g0268 a0001c0005t0008g0276 |
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 | a0006c0009t0001g0288 | 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 | a0001c0001t0002g0117 a0001c0001t0002g0198 a0001c0001t0002g0222 others(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 | a0001c0002t0001g0318 a0001c0002t0015g0319 |
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 | a0001c0002t0001g0318 a0001c0002t0015g0319 |
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 | a0001c0002t0001g0318 a0001c0002t0015g0319 |
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 | a0001c0002t0001g0318 a0001c0002t0015g0319 |
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 | 248 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(245): Show |
248 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(245): 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 | a0001c0001t0003g0206 | 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 | a0006c0009t0001g0288 | 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 | a0001c0003t0001g0072 | 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 | a0001c0002t0001g0293 a0001c0002t0001g0294 a0001c0002t0001g0295 |
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 | a0001c0005t0008g0267 a0001c0005t0008g0268 a0001c0005t0008g0276 |
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 | a0001c0001t0002g0255 a0001c0001t0002g0264 |
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 | a0001c0002t0001g0137 a0001c0002t0001g0169 a0001c0003t0001g0064 others(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 | 48 | a0001c0001t0001g0173 a0001c0001t0002g0219 a0001c0001t0002g0220 others(45): Show |
48 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(45): 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 | a0001c0001t0002g0222 a0001c0001t0003g0199 a0001c0001t0003g0200 others(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 | a0001c0001t0002g0009 a0001c0001t0002g0228 a0001c0001t0002g0248 others(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 | a0001c0001t0002g0198 a0001c0001t0002g0250 a0001c0001t0002g0255 others(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 | a0001c0001t0002g0116 a0001c0001t0002g0121 a0001c0001t0002g0254 others(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 | a0001c0001t0002g0117 a0001c0001t0002g0118 a0001c0001t0002g0119 others(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 | a0001c0001t0006g0252 | 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 | a0001c0001t0002g0008 a0001c0001t0006g0275 |
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 | a0001c0001t0002g0011 a0001c0001t0002g0014 |
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 | a0001c0005t0008g0268 a0001c0005t0008g0276 |
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 | a0001c0001t0002g0232 a0001c0001t0002g0233 a0001c0001t0002g0234 |
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 | 135 | a0001c0001t0001g0173 a0001c0001t0002g0003 a0001c0001t0002g0008 others(132): Show |
135 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(132): 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 | a0001c0003t0001g0058 | 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 | a0001c0002t0001g0189 | 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 | a0003c0007t0001g0302 a0003c0007t0001g0303 |
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 | 135 | a0001c0001t0001g0173 a0001c0001t0002g0003 a0001c0001t0002g0008 others(132): Show |
135 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(132): 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 | 244 | a0001c0001t0001g0173 a0001c0001t0002g0003 a0001c0001t0002g0008 others(241): Show |
244 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(241): 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 | a0001c0001t0004g0321 a0001c0001t0004g0323 a0001c0001t0004g0324 others(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 | a0001c0002t0001g0122 a0001c0002t0001g0123 a0001c0002t0001g0124 others(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 | a0001c0001t0003g0200 a0001c0002t0001g0122 a0001c0002t0001g0123 others(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 | a0001c0002t0001g0169 | 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 | a0001c0003t0001g0075 | 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 | a0001c0001t0002g0219 | 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 | a0001c0002t0001g0122 a0001c0002t0001g0123 a0001c0002t0001g0124 others(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 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(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 | a0001c0002t0001g0122 a0001c0002t0001g0123 a0001c0002t0001g0124 others(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 | a0001c0002t0001g0122 a0001c0002t0001g0123 a0001c0002t0001g0124 others(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 | a0001c0002t0010g0147 | 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 | a0001c0002t0001g0122 a0001c0002t0001g0123 a0001c0002t0001g0124 others(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 | a0001c0001t0002g0231 | 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 | a0003c0007t0001g0302 a0003c0007t0001g0303 |
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 | 56 | a0001c0001t0002g0219 a0001c0001t0002g0220 a0001c0001t0002g0221 others(53): Show |
56 | HG00323.hp2 HG00639.hp2 HG00733.hp2 others(53): Show |
intron_variant | MODIFIER | c.1059+225T>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 8/38 | chr20 | 48966248 | |||||||
| chr20:48966347 | G | A | 134 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(131): Show |
134 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(131): Show |
intron_variant | MODIFIER | c.1059+324G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 8/38 | chr20 | 48966347 | |||||||
| chr20:48966421 | A | T | 246 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(243): Show |
246 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(243): 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 | 134 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(131): Show |
134 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(131): 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 | a0001c0002t0001g0122 a0001c0002t0001g0123 a0001c0002t0001g0124 others(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 | 134 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(131): Show |
134 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(131): 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 | a0001c0002t0005g0001 a0001c0002t0005g0015 a0001c0002t0005g0016 others(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 | a0001c0001t0002g0221 | 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 | a0001c0002t0001g0149 a0001c0002t0001g0180 |
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 | a0001c0002t0001g0161 | 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 | a0001c0002t0001g0122 a0001c0002t0001g0123 a0001c0002t0001g0124 others(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 | a0001c0001t0002g0257 | 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 | a0001c0002t0001g0313 a0001c0002t0001g0314 |
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 | a0001c0002t0001g0122 a0001c0002t0001g0123 a0001c0002t0001g0124 others(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 | a0001c0002t0001g0122 a0001c0002t0001g0123 a0001c0002t0001g0124 others(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 | a0001c0002t0001g0122 a0001c0002t0001g0123 a0001c0002t0001g0124 others(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 | a0001c0002t0001g0122 a0001c0002t0001g0123 a0001c0002t0001g0124 others(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 | a0001c0002t0012g0159 a0001c0002t0012g0160 |
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 | a0001c0002t0001g0122 a0001c0002t0001g0123 a0001c0002t0001g0124 others(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 | a0001c0002t0001g0122 a0001c0002t0001g0123 a0001c0002t0001g0124 others(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 | a0001c0001t0004g0321 a0001c0001t0004g0323 a0001c0001t0004g0324 others(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 | a0001c0001t0002g0229 a0001c0001t0002g0230 |
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 | a0001c0002t0001g0122 a0001c0002t0001g0123 a0001c0002t0001g0124 others(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 | a0001c0002t0001g0122 a0001c0002t0001g0123 a0001c0002t0001g0124 others(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 | a0001c0005t0008g0267 a0001c0005t0008g0268 a0001c0005t0008g0276 |
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 | a0001c0002t0001g0122 a0001c0002t0001g0123 a0001c0002t0001g0124 others(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 | a0001c0001t0004g0335 a0003c0007t0001g0302 a0003c0007t0001g0303 others(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 | a0001c0003t0001g0029 a0001c0003t0001g0030 a0001c0003t0001g0031 others(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 | a0001c0002t0001g0175 | 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 | a0001c0002t0001g0318 a0001c0002t0015g0319 |
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 | a0001c0001t0007g0041 a0001c0001t0007g0042 |
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 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(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 | a0001c0003t0001g0061 a0001c0003t0001g0084 a0001c0003t0001g0093 |
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 | a0001c0002t0001g0122 a0001c0002t0001g0123 a0001c0002t0001g0124 others(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 | a0001c0002t0001g0122 a0001c0002t0001g0123 a0001c0002t0001g0124 others(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 | a0001c0002t0001g0318 a0001c0002t0015g0319 |
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 | a0001c0003t0001g0054 | 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 | a0001c0002t0005g0001 a0001c0002t0005g0015 a0001c0002t0005g0016 others(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 | a0001c0002t0005g0021 a0001c0002t0005g0024 a0001c0002t0005g0025 |
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 | a0001c0005t0008g0267 a0001c0005t0008g0268 a0001c0005t0008g0276 |
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 | a0001c0003t0001g0103 | 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 | a0001c0003t0001g0062 | 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 | a0001c0001t0002g0240 a0001c0001t0003g0113 a0001c0001t0003g0114 others(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 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0010 others(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 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(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 | a0001c0001t0002g0116 a0001c0001t0002g0221 a0001c0001t0002g0244 others(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 | a0001c0001t0001g0173 a0001c0001t0002g0220 a0001c0001t0002g0222 others(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 | 7 | a0001c0001t0002g0219 a0001c0001t0002g0223 a0001c0001t0002g0228 others(4): Show |
7 | HG01361.hp1 HG02258.hp2 HG02559.hp2 others(4): 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 | a0001c0002t0001g0122 a0001c0002t0001g0123 a0001c0002t0001g0282 others(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 | a0001c0002t0001g0311 a0001c0002t0001g0313 a0001c0002t0005g0001 others(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 | a0001c0003t0001g0029 a0001c0003t0001g0030 a0001c0003t0001g0031 others(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 | a0001c0002t0005g0026 a0001c0002t0005g0027 |
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 | a0001c0003t0001g0029 a0001c0003t0001g0030 a0001c0003t0001g0031 others(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 | a0001c0003t0001g0062 | 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 | a0001c0003t0001g0055 a0001c0003t0001g0091 |
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 | a0001c0002t0001g0183 | 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 | a0001c0002t0001g0313 a0001c0002t0001g0314 a0001c0002t0005g0001 others(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 | a0001c0003t0001g0086 a0001c0003t0009g0036 |
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 | a0001c0002t0001g0138 a0001c0002t0001g0139 a0001c0002t0001g0175 |
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 | a0001c0002t0001g0122 a0001c0002t0001g0123 a0001c0002t0001g0124 others(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 | a0001c0001t0004g0332 a0001c0001t0004g0343 a0001c0001t0004g0346 others(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 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0010 others(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 | a0001c0001t0002g0003 a0001c0001t0002g0116 a0001c0001t0002g0117 others(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 | a0001c0001t0002g0259 a0001c0003t0001g0035 a0001c0003t0001g0053 others(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 | a0001c0003t0001g0064 | 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 | a0001c0002t0001g0122 a0001c0002t0001g0123 a0001c0002t0001g0124 others(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 | a0001c0002t0001g0318 a0001c0002t0015g0319 |
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 | a0001c0001t0006g0269 | 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 | a0001c0001t0014g0224 a0001c0001t0014g0225 a0001c0001t0021g0226 |
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 | a0001c0001t0006g0269 a0001c0001t0006g0270 |
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 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0010 others(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 | 43 | a0001c0001t0002g0222 a0001c0001t0002g0223 a0001c0001t0002g0229 others(40): Show |
45 | HG01109.hp1 HG01256.hp1 HG01258.hp2 others(42): 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 | a0001c0001t0002g0003 a0001c0001t0002g0117 a0001c0001t0002g0118 others(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 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0010 others(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 | a0001c0001t0002g0014 a0001c0003t0001g0075 |
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 | a0001c0002t0001g0318 a0001c0002t0015g0319 |
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 | a0004c0011t0001g0301 | 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 | a0001c0002t0001g0136 a0001c0002t0001g0165 a0001c0002t0001g0171 others(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 | a0001c0001t0003g0202 a0001c0001t0003g0215 a0001c0001t0003g0217 others(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 | a0001c0003t0001g0101 | 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 | a0001c0002t0001g0004 a0001c0002t0001g0135 a0001c0002t0001g0156 others(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 | a0001c0003t0001g0030 a0001c0003t0001g0053 a0001c0003t0001g0090 |
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 | a0001c0003t0001g0065 | 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 | a0001c0005t0008g0267 a0001c0005t0008g0268 a0001c0005t0008g0276 |
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 | 133 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(130): Show |
133 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(130): 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 | a0001c0001t0006g0270 | 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 | a0001c0002t0001g0122 a0001c0002t0001g0123 a0001c0002t0001g0124 others(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 | a0001c0001t0002g0198 a0001c0002t0001g0122 a0001c0002t0001g0123 others(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 | a0001c0003t0001g0044 | 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 | a0001c0001t0002g0232 a0001c0001t0002g0233 a0001c0001t0002g0234 |
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 | a0001c0002t0001g0318 a0001c0002t0015g0319 |
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 | a0001c0001t0002g0229 a0001c0001t0002g0230 |
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 | a0001c0003t0001g0032 a0001c0003t0001g0039 a0001c0003t0001g0044 others(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 | a0001c0003t0001g0065 | 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 | a0001c0002t0001g0122 a0001c0002t0001g0123 a0001c0002t0001g0124 others(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 | a0001c0002t0001g0293 a0001c0002t0001g0295 |
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 | a0001c0002t0001g0148 | 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 | a0001c0001t0003g0212 a0001c0001t0003g0213 |
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 | 134 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(131): Show |
134 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(131): 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 | a0001c0003t0001g0066 | 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 | 246 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(243): Show |
246 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(243): 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 | 53 | a0001c0001t0002g0219 a0001c0001t0002g0220 a0001c0001t0002g0221 others(50): Show |
53 | HG00323.hp2 HG00639.hp2 HG00733.hp2 others(50): 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 | a0001c0001t0003g0212 a0001c0001t0003g0213 |
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 | a0001c0003t0001g0078 | 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 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0010 others(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 | a0001c0001t0003g0202 a0001c0001t0003g0215 a0001c0001t0003g0217 others(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 | 246 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(243): Show |
246 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(243): 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 | a0001c0005t0008g0267 a0001c0005t0008g0268 a0001c0005t0008g0276 |
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 | a0001c0001t0014g0224 a0001c0001t0014g0225 |
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 | a0001c0003t0001g0029 a0001c0003t0001g0030 a0001c0003t0001g0031 others(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 | a0001c0001t0004g0328 a0001c0001t0004g0331 a0001c0001t0004g0337 |
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 | 248 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(245): Show |
248 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(245): 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 | a0001c0002t0001g0313 a0001c0002t0001g0314 |
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 | a0001c0001t0002g0003 a0001c0001t0002g0116 a0001c0001t0002g0117 others(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 | a0001c0002t0001g0318 a0001c0002t0015g0319 |
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 | a0001c0002t0001g0315 a0001c0002t0001g0316 |
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 | a0001c0001t0002g0254 | 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 | a0001c0002t0001g0122 a0001c0002t0001g0123 a0001c0002t0001g0124 others(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 | a0001c0002t0005g0001 a0001c0002t0005g0015 a0001c0002t0005g0016 others(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 | 134 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(131): Show |
134 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(131): 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 | a0001c0002t0001g0164 | 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 | a0001c0001t0002g0229 a0001c0001t0002g0230 |
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 | a0001c0002t0001g0122 a0001c0002t0001g0123 a0001c0002t0001g0124 others(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 | a0001c0002t0001g0122 a0001c0002t0001g0123 a0001c0002t0001g0124 others(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 | a0008c0008t0002g0265 | 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 | a0001c0001t0002g0280 a0001c0003t0001g0069 |
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 | 134 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(131): Show |
134 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(131): 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 | a0001c0001t0002g0274 | 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 | 124 | a0001c0001t0002g0003 a0001c0001t0002g0116 a0001c0001t0002g0117 others(121): Show |
124 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(121): 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 | a0001c0002t0001g0161 | 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 | 95 | a0001c0001t0002g0003 a0001c0001t0002g0116 a0001c0001t0002g0117 others(92): Show |
95 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(92): 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 | a0001c0013t0003g0207 | 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 | a0001c0001t0023g0216 | 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 | a0001c0003t0001g0053 | 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 | a0001c0003t0001g0043 a0001c0003t0001g0073 |
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 | a0001c0001t0004g0346 a0001c0001t0004g0347 |
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 | a0001c0001t0003g0199 a0001c0001t0003g0200 |
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 | a0001c0002t0001g0122 a0001c0002t0001g0123 a0001c0002t0001g0124 others(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 | a0001c0001t0002g0255 | 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 | a0001c0002t0001g0122 a0001c0002t0001g0123 a0001c0002t0001g0124 others(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 | a0001c0002t0005g0021 a0001c0002t0005g0025 |
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 | a0001c0002t0001g0137 a0001c0002t0001g0169 a0001c0002t0001g0170 |
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 | a0001c0002t0001g0122 a0001c0002t0001g0123 a0001c0002t0001g0124 others(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 | a0001c0003t0001g0055 a0001c0003t0001g0091 |
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 | a0001c0002t0001g0313 a0001c0002t0001g0314 a0001c0002t0005g0001 others(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 | a0001c0001t0004g0321 a0001c0001t0004g0323 a0001c0001t0004g0324 others(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 | a0001c0002t0005g0026 a0001c0002t0005g0027 |
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 | a0001c0001t0002g0229 a0001c0001t0002g0230 |
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 | a0001c0002t0001g0138 a0001c0002t0001g0139 a0001c0002t0001g0140 others(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 | a0001c0002t0005g0001 a0001c0002t0005g0015 a0001c0002t0005g0016 others(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 | a0001c0003t0001g0035 a0001c0003t0001g0051 a0001c0003t0001g0057 others(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 | a0001c0002t0001g0122 a0001c0002t0001g0123 a0001c0002t0001g0124 others(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 | a0001c0002t0001g0004 a0001c0002t0001g0156 |
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 | a0001c0001t0003g0209 | 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 | a0001c0001t0006g0252 a0001c0001t0006g0269 a0001c0001t0006g0270 others(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 | a0001c0001t0004g0325 a0001c0001t0004g0326 a0001c0001t0004g0327 others(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 | a0001c0001t0004g0328 a0001c0002t0001g0110 a0001c0002t0001g0165 others(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 | a0001c0003t0001g0030 a0001c0003t0001g0045 a0001c0003t0001g0046 others(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 | a0001c0005t0008g0267 a0001c0005t0008g0268 a0001c0005t0008g0276 |
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 | a0001c0003t0001g0045 a0001c0003t0001g0046 a0001c0003t0001g0049 others(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 | a0001c0002t0001g0315 a0001c0002t0001g0316 |
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 | a0001c0002t0001g0313 a0001c0002t0001g0314 a0001c0002t0005g0001 others(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 | a0001c0001t0004g0346 a0001c0001t0004g0347 |
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 | a0001c0001t0014g0224 a0001c0001t0014g0225 a0001c0001t0021g0226 |
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 | 134 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(131): Show |
134 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(131): 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 | a0001c0001t0003g0217 | 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 | a0001c0002t0001g0318 a0001c0002t0015g0319 |
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 | a0001c0003t0001g0055 a0001c0003t0001g0091 a0001c0003t0001g0103 |
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 | 134 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(131): Show |
134 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(131): 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 | a0001c0002t0001g0318 a0001c0002t0015g0319 |
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 | a0001c0002t0005g0001 a0001c0002t0005g0015 a0001c0002t0005g0016 others(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 | a0001c0002t0001g0122 a0001c0002t0001g0123 a0001c0002t0001g0124 others(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 | a0001c0002t0001g0307 a0001c0002t0001g0311 |
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 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0010 others(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 | a0001c0001t0002g0277 a0001c0001t0002g0278 a0001c0001t0002g0279 |
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 | a0001c0001t0002g0232 a0001c0001t0002g0233 a0001c0001t0002g0234 |
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 | a0001c0002t0001g0185 | 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 | a0001c0001t0002g0219 a0001c0001t0002g0245 a0001c0001t0002g0255 others(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 | a0001c0001t0003g0114 a0001c0002t0001g0123 a0001c0002t0001g0289 others(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 | a0001c0002t0005g0001 a0001c0002t0005g0015 a0001c0002t0005g0016 others(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 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(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 | a0001c0001t0002g0219 a0001c0001t0003g0214 a0001c0001t0004g0324 others(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 | a0001c0001t0002g0260 a0001c0001t0003g0203 a0001c0001t0003g0247 others(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 | a0001c0002t0001g0122 a0001c0002t0001g0123 a0001c0002t0001g0124 others(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 | a0001c0002t0001g0006 a0001c0002t0017g0007 |
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 | a0001c0001t0003g0211 | 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 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0011 others(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 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0116 others(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 | a0001c0002t0001g0313 a0001c0002t0001g0314 a0001c0002t0005g0001 others(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 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0010 others(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 | a0001c0002t0001g0122 a0001c0002t0001g0123 a0001c0002t0001g0124 others(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 | a0001c0001t0002g0231 | 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 | a0001c0001t0002g0244 a0001c0002t0001g0313 a0001c0002t0001g0314 others(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 | a0001c0002t0001g0122 a0001c0002t0001g0123 a0001c0002t0001g0124 others(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 | a0001c0001t0002g0260 a0001c0001t0003g0237 a0001c0001t0006g0269 others(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 | a0001c0002t0001g0178 | 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 | a0001c0001t0002g0259 | 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 | a0001c0003t0001g0029 a0001c0003t0001g0030 a0001c0003t0001g0031 others(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 | a0001c0001t0006g0252 a0001c0001t0006g0269 a0001c0001t0006g0270 |
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 | a0001c0001t0003g0203 a0001c0001t0003g0204 a0001c0001t0003g0205 others(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 | a0001c0001t0002g0003 a0001c0001t0002g0116 a0001c0001t0002g0117 others(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 | 127 | a0001c0001t0002g0003 a0001c0001t0002g0116 a0001c0001t0002g0117 others(124): Show |
127 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(124): 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 | a0001c0001t0002g0260 a0001c0001t0004g0321 a0001c0001t0004g0335 others(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 | a0001c0002t0001g0313 a0001c0002t0001g0314 a0001c0003t0001g0045 others(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 | a0001c0002t0005g0001 a0001c0002t0005g0015 a0001c0002t0005g0016 others(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 | a0001c0001t0002g0233 a0001c0001t0002g0244 a0001c0003t0001g0055 |
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 | 54 | a0001c0001t0001g0173 a0001c0001t0002g0219 a0001c0001t0002g0220 others(51): Show |
54 | HG00323.hp2 HG00639.hp2 HG00733.hp2 others(51): 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 | a0001c0005t0008g0267 a0001c0005t0008g0268 a0001c0005t0008g0276 |
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 | a0001c0001t0002g0221 a0001c0001t0002g0277 a0001c0001t0002g0278 others(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 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0010 others(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 | 2 | a0001c0001t0002g0228 a0001c0001t0002g0231 |
2 | HG02451.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.3432+1889A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 25/38 | chr20 | 49000394 | |||||||
| chr20:49000402 | G | T | 1 | a0002c0004t0001g0172 | 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 | a0001c0002t0001g0318 a0001c0002t0015g0319 |
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 | a0001c0002t0001g0293 a0001c0002t0001g0294 a0001c0002t0001g0295 |
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 | a0001c0002t0001g0122 a0001c0002t0001g0123 a0001c0002t0001g0124 others(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 | 6 | a0001c0001t0004g0339 a0001c0002t0001g0110 a0001c0003t0001g0083 others(3): Show |
6 | HG02273.hp2 HG02486.hp2 HG02970.hp2 others(3): 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 | a0001c0001t0001g0173 a0001c0001t0002g0008 a0001c0001t0002g0009 others(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 | a0001c0001t0002g0013 a0001c0001t0002g0248 a0001c0001t0002g0249 others(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 | a0001c0002t0001g0289 | 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 | a0001c0003t0001g0078 | 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 | a0001c0002t0001g0142 a0001c0016t0001g0028 |
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 | a0001c0002t0001g0318 a0001c0002t0015g0319 |
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 | a0001c0003t0001g0101 a0001c0003t0001g0104 a0001c0003t0001g0108 |
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 | a0001c0001t0002g0198 a0008c0008t0002g0265 |
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 | a0001c0001t0003g0236 a0001c0001t0003g0237 |
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 | a0001c0002t0001g0313 a0001c0002t0001g0314 a0001c0002t0005g0001 others(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 | a0001c0002t0001g0122 a0001c0002t0001g0123 a0001c0002t0001g0124 others(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 | a0001c0001t0003g0204 | 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 | a0001c0002t0001g0318 a0001c0002t0015g0319 |
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 | a0001c0001t0002g0219 | 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 | a0001c0002t0001g0313 a0001c0002t0001g0314 |
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 | a0001c0001t0002g0240 a0001c0001t0003g0113 a0001c0001t0003g0114 others(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 | a0001c0001t0002g0219 a0001c0001t0002g0220 a0001c0001t0002g0243 |
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 | a0001c0003t0001g0074 | 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 | a0001c0002t0001g0122 a0001c0002t0001g0123 a0001c0002t0001g0124 others(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 | |||||||
| chr20:49002964 | CT | C | 8 | a0001c0001t0002g0273 a0001c0001t0020g0329 a0001c0001t0023g0216 others(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 | a0001c0002t0001g0122 a0001c0002t0001g0123 a0001c0002t0001g0124 others(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 | a0001c0002t0001g0313 a0001c0002t0001g0314 a0001c0002t0005g0001 others(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 | a0001c0002t0001g0318 a0001c0002t0015g0319 |
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 | a0002c0004t0001g0144 a0002c0004t0001g0145 a0002c0004t0001g0191 |
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 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0010 others(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 | a0001c0001t0002g0003 a0001c0001t0002g0116 a0001c0001t0002g0117 others(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 | a0001c0001t0004g0321 a0001c0001t0004g0323 a0001c0001t0004g0324 others(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 | a0001c0002t0001g0318 a0001c0002t0015g0319 |
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 | a0001c0001t0004g0321 a0001c0001t0004g0323 a0001c0001t0004g0324 others(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 | a0001c0003t0001g0079 | 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 | a0001c0001t0023g0216 | 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 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(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 | 266 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(263): Show |
267 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(264): 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 | a0001c0001t0002g0266 | 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 | a0001c0002t0001g0122 a0001c0002t0001g0123 a0001c0002t0001g0124 others(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 | a0001c0002t0001g0313 a0001c0002t0001g0314 |
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 | a0001c0002t0001g0152 | 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 | 2 | a0001c0001t0002g0228 a0001c0001t0002g0231 |
2 | HG02451.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.3584+233A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 26/38 | chr20 | 49005454 | |||||||
| chr20:49005520 | C | T | 2 | a0001c0002t0001g0002 a0001c0002t0001g0174 |
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 | a0001c0001t0002g0273 | 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 | a0001c0001t0003g0239 a0001c0001t0007g0115 a0001c0002t0001g0111 others(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 | a0001c0002t0001g0122 a0001c0002t0001g0123 a0001c0002t0001g0285 others(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 | a0001c0001t0002g0260 a0001c0001t0004g0330 a0001c0002t0001g0002 others(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 | a0001c0003t0001g0048 a0001c0003t0001g0081 a0003c0007t0001g0302 others(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 | a0001c0001t0006g0269 | 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 | a0001c0001t0002g0229 a0001c0001t0002g0230 |
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 | a0001c0002t0001g0313 a0001c0002t0001g0314 a0001c0002t0005g0001 others(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 | a0001c0002t0010g0147 | 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 | a0001c0003t0001g0062 | 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 | a0001c0001t0004g0321 a0001c0001t0004g0323 a0001c0001t0004g0324 others(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 | a0001c0002t0001g0122 a0001c0002t0001g0123 a0001c0002t0001g0124 others(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 | a0001c0003t0001g0056 a0001c0003t0001g0065 a0001c0003t0001g0067 others(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 | 53 | a0001c0001t0002g0219 a0001c0001t0002g0220 a0001c0001t0002g0221 others(50): Show |
53 | HG00323.hp2 HG00639.hp2 HG00733.hp2 others(50): 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 | a0001c0001t0003g0113 a0001c0001t0003g0114 a0001c0001t0003g0210 others(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 | a0001c0002t0001g0122 a0001c0002t0001g0123 a0001c0002t0001g0124 others(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 | a0001c0002t0001g0006 a0001c0002t0017g0007 |
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 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0011 others(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 | a0001c0003t0001g0077 | 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 | a0001c0001t0002g0012 a0001c0001t0002g0233 a0001c0001t0002g0248 others(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 | 247 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(244): Show |
247 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(244): 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 | a0001c0002t0005g0001 a0001c0002t0005g0015 a0001c0002t0005g0016 others(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 | a0001c0001t0002g0003 a0001c0001t0002g0116 a0001c0001t0002g0117 others(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 | 56 | a0001c0001t0002g0219 a0001c0001t0002g0220 a0001c0001t0002g0221 others(53): Show |
56 | HG00323.hp2 HG00639.hp2 HG00733.hp2 others(53): 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 | a0001c0001t0002g0119 a0001c0001t0002g0256 a0001c0001t0002g0272 |
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 | |||||||
| chr20:49007252 | 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 | 258 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(255): Show |
259 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(256): 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 | 347 | a0001c0001t0001g0173 a0001c0001t0002g0003 a0001c0001t0002g0008 others(344): Show |
349 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(346): 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 | a0001c0002t0001g0122 a0001c0002t0001g0123 a0001c0002t0001g0124 others(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 | a0001c0002t0001g0318 a0001c0002t0015g0319 |
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 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0116 others(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 | a0001c0001t0002g0250 a0001c0001t0004g0330 a0001c0001t0006g0252 others(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 | a0001c0001t0004g0321 a0001c0001t0004g0323 a0001c0001t0004g0324 others(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 | a0001c0001t0002g0277 a0001c0001t0003g0200 a0001c0001t0003g0247 others(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 | a0001c0005t0008g0267 a0001c0005t0008g0268 a0001c0005t0008g0276 |
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 | 134 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(131): Show |
134 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(131): 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 | 56 | a0001c0001t0002g0219 a0001c0001t0002g0220 a0001c0001t0002g0221 others(53): Show |
56 | HG00323.hp2 HG00639.hp2 HG00733.hp2 others(53): 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 | a0001c0005t0008g0267 a0001c0005t0008g0268 a0001c0005t0008g0276 |
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 | a0001c0001t0002g0253 | 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 | a0001c0001t0003g0204 | 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 | 347 | a0001c0001t0001g0173 a0001c0001t0002g0003 a0001c0001t0002g0008 others(344): Show |
349 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(346): Show |
intron_variant | MODIFIER | c.3585-1931A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 26/38 | chr20 | 49008301 | |||||||
| chr20:49008561 | C | CA | 132 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(129): Show |
132 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(129): 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 | a0001c0001t0002g0119 a0001c0001t0002g0222 a0001c0001t0002g0243 others(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 | a0001c0002t0001g0313 a0001c0002t0001g0314 |
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 | 347 | a0001c0001t0001g0173 a0001c0001t0002g0003 a0001c0001t0002g0008 others(344): Show |
349 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(346): Show |
intron_variant | MODIFIER | c.3585-1230A>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 26/38 | chr20 | 49009002 | |||||||
| chr20:49009007 | T | C | 268 | a0001c0001t0001g0173 a0001c0001t0002g0003 a0001c0001t0002g0008 others(265): Show |
269 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(266): 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 | a0001c0001t0004g0321 a0001c0001t0004g0323 a0001c0001t0004g0324 others(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 | 135 | a0001c0001t0001g0173 a0001c0001t0002g0003 a0001c0001t0002g0008 others(132): Show |
135 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(132): 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 | a0001c0002t0001g0122 a0001c0002t0001g0123 a0001c0002t0001g0124 others(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 | a0001c0001t0003g0215 a0001c0001t0003g0247 a0001c0001t0004g0330 others(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 | a0001c0002t0001g0122 a0001c0002t0001g0123 a0001c0002t0001g0124 others(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 | 135 | a0001c0001t0001g0173 a0001c0001t0002g0003 a0001c0001t0002g0008 others(132): Show |
135 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(132): 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 | 132 | a0001c0001t0001g0173 a0001c0001t0002g0003 a0001c0001t0002g0008 others(129): Show |
132 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(129): 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 | 135 | a0001c0001t0001g0173 a0001c0001t0002g0003 a0001c0001t0002g0008 others(132): Show |
135 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(132): Show |
intron_variant | MODIFIER | c.3585-33A>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 26/38 | chr20 | 49010199 | |||||||
| chr20:49010558 | A | G | 103 | a0001c0001t0001g0173 a0001c0001t0002g0003 a0001c0001t0002g0008 others(100): Show |
103 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.3757+154A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 27/38 | chr20 | 49010558 | |||||||
| chr20:49010633 | G | T | 247 | a0001c0001t0001g0173 a0001c0001t0002g0003 a0001c0001t0002g0008 others(244): Show |
247 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(244): 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 | a0001c0002t0001g0152 a0001c0002t0012g0159 a0001c0002t0012g0160 |
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 | 132 | a0001c0001t0001g0173 a0001c0001t0002g0003 a0001c0001t0002g0008 others(129): Show |
132 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(129): Show |
intron_variant | MODIFIER | c.3757+631C>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 27/38 | chr20 | 49011035 | |||||||
| chr20:49011068 | C | T | 135 | a0001c0001t0001g0173 a0001c0001t0002g0003 a0001c0001t0002g0008 others(132): Show |
135 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(132): 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 | a0001c0002t0001g0318 a0001c0002t0015g0319 |
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 | 135 | a0001c0001t0001g0173 a0001c0001t0002g0003 a0001c0001t0002g0008 others(132): Show |
135 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(132): 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 | a0001c0001t0002g0117 | 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 | 135 | a0001c0001t0001g0173 a0001c0001t0002g0003 a0001c0001t0002g0008 others(132): Show |
135 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(132): 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 | a0001c0001t0002g0003 a0001c0001t0002g0116 a0001c0001t0002g0117 others(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 | a0001c0003t0001g0029 a0001c0003t0001g0030 a0001c0003t0001g0031 others(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 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(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 | 135 | a0001c0001t0001g0173 a0001c0001t0002g0003 a0001c0001t0002g0008 others(132): Show |
135 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(132): 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 | 246 | a0001c0001t0001g0173 a0001c0001t0002g0003 a0001c0001t0002g0008 others(243): Show |
246 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(243): 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 | 96 | a0001c0001t0001g0173 a0001c0001t0002g0003 a0001c0001t0002g0116 others(93): Show |
96 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(93): 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 | a0001c0001t0002g0003 a0001c0001t0002g0116 a0001c0001t0002g0117 others(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 | a0001c0003t0001g0055 a0001c0003t0001g0091 a0001c0003t0001g0103 |
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 | a0001c0002t0012g0159 | 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 | a0001c0002t0001g0318 a0001c0002t0015g0319 |
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 | a0001c0002t0001g0122 a0001c0002t0001g0123 a0001c0002t0001g0124 others(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 | a0001c0003t0001g0044 a0001c0003t0001g0071 a0001c0003t0001g0085 |
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 | a0001c0002t0001g0186 | 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 | a0001c0002t0001g0122 a0001c0002t0001g0123 a0001c0002t0001g0124 others(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 | a0001c0002t0001g0122 a0001c0002t0001g0123 a0001c0002t0001g0124 others(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 | a0001c0002t0001g0122 a0001c0002t0001g0123 a0001c0002t0001g0124 others(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 | a0001c0002t0001g0122 a0001c0002t0001g0123 a0001c0002t0001g0124 others(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 | a0001c0002t0005g0001 a0001c0002t0005g0015 a0001c0002t0005g0016 others(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 | a0001c0002t0001g0122 a0001c0002t0001g0123 a0001c0002t0001g0124 others(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 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0010 others(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 | a0001c0002t0001g0124 a0001c0002t0001g0285 a0001c0002t0001g0286 others(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 | a0001c0002t0001g0182 | 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 | a0001c0002t0001g0315 a0001c0002t0001g0316 |
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 | a0001c0002t0001g0188 | 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 | a0001c0002t0001g0122 a0001c0002t0001g0123 a0001c0002t0001g0124 others(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 | a0001c0001t0002g0198 a0008c0008t0002g0265 |
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 | a0001c0001t0002g0232 a0001c0001t0002g0233 |
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 | a0001c0002t0001g0136 a0001c0002t0001g0193 |
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 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(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 | a0001c0002t0001g0122 a0001c0002t0001g0123 a0001c0002t0001g0124 others(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 | a0001c0002t0001g0313 a0001c0002t0001g0314 |
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 | a0001c0003t0001g0044 a0001c0003t0001g0071 a0001c0003t0001g0085 |
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 | a0001c0001t0002g0118 | 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 | a0001c0001t0002g0003 a0001c0001t0002g0116 a0001c0001t0002g0117 others(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 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(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 | a0001c0001t0003g0235 | 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 | a0001c0001t0001g0173 a0001c0001t0002g0003 a0001c0001t0002g0008 others(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 | a0001c0002t0001g0174 | 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 | a0001c0001t0002g0116 a0001c0001t0002g0251 a0001c0001t0002g0255 others(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 | a0001c0001t0002g0003 a0001c0001t0002g0116 a0001c0001t0002g0117 others(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 | a0001c0003t0001g0043 | 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 | a0001c0002t0001g0122 a0001c0002t0001g0123 a0001c0002t0001g0124 others(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 | a0001c0003t0001g0072 | 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 | a0001c0002t0001g0122 a0001c0002t0001g0123 a0001c0002t0001g0124 others(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 | a0001c0001t0014g0224 a0001c0001t0014g0225 a0001c0001t0021g0226 |
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 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(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 | a0001c0002t0001g0122 a0001c0002t0001g0123 a0001c0002t0001g0124 others(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 | 177 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(174): Show |
177 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(174): 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 | 2 | a0001c0001t0002g0228 a0001c0001t0002g0231 |
2 | HG02451.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.4625-952G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 34/38 | chr20 | 49022099 | |||||||
| chr20:49022154 | C | CA | 95 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0010 others(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 | a0001c0001t0002g0003 a0001c0001t0002g0116 a0001c0001t0002g0117 others(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 | a0001c0001t0004g0323 a0001c0001t0004g0325 a0001c0001t0004g0326 others(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 | 56 | a0001c0001t0002g0219 a0001c0001t0002g0220 a0001c0001t0002g0221 others(53): Show |
56 | HG00323.hp2 HG00639.hp2 HG00733.hp2 others(53): 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 | a0001c0002t0005g0001 a0001c0002t0005g0015 a0001c0002t0005g0016 others(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 | 271 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(268): Show |
272 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(269): Show |
intron_variant | MODIFIER | c.4625-619A>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 34/38 | chr20 | 49022432 | |||||||
| chr20:49022435 | A | C | 137 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(134): Show |
137 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(134): Show |
intron_variant | MODIFIER | c.4625-616A>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 34/38 | chr20 | 49022435 | |||||||
| chr20:49022438 | A | C | 131 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(128): Show |
131 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(128): Show |
intron_variant | MODIFIER | c.4625-613A>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 34/38 | chr20 | 49022438 | |||||||
| chr20:49022442 | C | A | 248 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(245): Show |
248 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(245): 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 | a0001c0003t0001g0058 | 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 | a0001c0002t0001g0318 a0001c0002t0015g0319 |
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 | a0007c0010t0002g0258 | 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 | 246 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(243): Show |
246 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(243): Show |
intron_variant | MODIFIER | c.4625-124G>C | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 34/38 | chr20 | 49022927 | |||||||
| chr20:49023200 | A | G | 134 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(131): Show |
134 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(131): Show |
intron_variant | MODIFIER | c.4755+19A>G | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 35/38 | chr20 | 49023200 | |||||||
| chr20:49023454 | A | G | 236 | a0001c0001t0001g0173 a0001c0001t0002g0003 a0001c0001t0002g0008 others(233): Show |
238 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(235): 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 | 134 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(131): Show |
134 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(131): 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 | a0001c0002t0001g0122 a0001c0002t0001g0123 a0001c0002t0001g0124 others(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 | 134 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(131): Show |
134 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(131): 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 | a0001c0002t0001g0182 | 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 | 134 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(131): Show |
134 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(131): 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 | a0001c0001t0002g0003 a0001c0001t0002g0116 a0001c0001t0002g0117 others(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 | 135 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(132): Show |
135 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(132): 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 | 246 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(243): Show |
246 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(243): 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 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0010 others(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 | a0001c0002t0005g0021 a0001c0002t0005g0024 a0001c0002t0005g0025 |
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 | a0001c0002t0001g0309 a0001c0002t0001g0310 |
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 | a0001c0001t0006g0275 | 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 | a0008c0008t0002g0265 | 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 | 134 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(131): Show |
134 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(131): 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 | a0001c0001t0004g0321 a0001c0001t0004g0323 a0001c0001t0004g0324 others(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 | 134 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(131): Show |
134 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(131): 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 | a0001c0001t0002g0232 a0001c0001t0002g0233 a0001c0001t0002g0234 |
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 | a0001c0002t0001g0156 a0001c0002t0001g0196 a0001c0002t0001g0315 others(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 | a0001c0002t0001g0123 a0001c0002t0001g0124 a0001c0002t0001g0282 others(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 | a0001c0002t0005g0001 a0001c0002t0005g0015 a0001c0002t0005g0016 others(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 | 134 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(131): Show |
134 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(131): 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 | a0001c0001t0002g0244 a0001c0001t0002g0266 a0001c0001t0003g0246 others(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 | a0001c0001t0006g0270 | 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 | a0001c0002t0005g0021 a0001c0002t0005g0024 a0001c0002t0005g0025 |
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 | 134 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(131): Show |
134 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(131): 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 | a0001c0002t0001g0291 a0001c0002t0001g0292 a0001c0002t0001g0307 others(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 | a0001c0001t0002g0240 a0001c0001t0003g0238 a0001c0001t0003g0239 others(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 | 134 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(131): Show |
134 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(131): 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 | a0001c0003t0001g0076 | 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 | 134 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(131): Show |
134 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(131): 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 | a0001c0001t0002g0240 a0001c0001t0003g0238 a0001c0001t0003g0239 others(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 | a0001c0001t0002g0222 a0001c0001t0002g0223 a0001c0001t0002g0245 |
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 | 134 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(131): Show |
134 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(131): 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 | 266 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(263): Show |
267 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(264): 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 | a0001c0002t0001g0148 | 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 | 134 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(131): Show |
134 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(131): 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 | a0001c0002t0001g0122 a0001c0002t0001g0123 a0001c0002t0001g0124 others(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 | a0001c0002t0001g0122 a0001c0002t0001g0123 a0001c0002t0001g0124 others(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 | 134 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(131): Show |
134 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(131): 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 | a0001c0001t0006g0252 a0001c0001t0006g0269 a0001c0001t0006g0270 others(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 | 266 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(263): Show |
267 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(264): 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 | a0001c0002t0001g0122 a0001c0002t0001g0123 a0001c0002t0001g0124 others(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 | a0001c0001t0001g0173 a0001c0002t0001g0002 a0001c0002t0001g0004 others(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 | a0001c0001t0002g0266 | 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 | 118 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(115): Show |
118 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(115): 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 | a0001c0001t0002g0118 a0001c0001t0002g0119 a0001c0001t0002g0219 others(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 | a0001c0002t0001g0112 a0001c0002t0001g0128 a0001c0002t0001g0136 others(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 | a0001c0002t0001g0123 a0001c0002t0001g0305 a0001c0002t0001g0313 others(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 | a0001c0002t0001g0122 a0001c0002t0001g0124 a0001c0002t0001g0282 others(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 | a0001c0001t0002g0240 a0001c0001t0002g0253 |
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 | a0001c0001t0002g0219 a0001c0001t0002g0220 a0001c0001t0002g0243 |
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 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(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 | 134 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(131): Show |
134 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(131): Show |
intron_variant | MODIFIER | c.5063+1416G>A | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 37/38 | chr20 | 49030084 | |||||||
| chr20:49030395 | C | T | 131 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(128): Show |
131 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(128): 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 | a0001c0001t0002g0120 a0001c0001t0002g0244 a0001c0001t0007g0042 others(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 | 247 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(244): Show |
247 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(244): 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 | a0001c0001t0003g0199 a0001c0001t0003g0200 |
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 | 134 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(131): Show |
134 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(131): 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 | a0001c0001t0002g0240 a0001c0001t0003g0113 a0001c0001t0003g0114 others(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 | 134 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(131): Show |
134 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(131): 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 | a0001c0002t0001g0125 a0001c0002t0001g0128 a0001c0002t0001g0137 others(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 | a0001c0001t0002g0010 a0001c0001t0006g0252 a0001c0002t0001g0167 others(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 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0011 others(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 | a0001c0001t0002g0003 a0001c0001t0002g0116 a0001c0001t0002g0117 others(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 | a0001c0001t0002g0234 a0001c0001t0002g0249 a0001c0001t0002g0255 others(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 | 49 | a0001c0001t0002g0219 a0001c0001t0002g0220 a0001c0001t0002g0222 others(46): Show |
49 | HG00323.hp2 HG00639.hp2 HG00733.hp2 others(46): 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 | a0001c0001t0002g0221 a0001c0001t0002g0231 a0001c0001t0002g0277 others(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 | a0001c0001t0004g0321 a0001c0001t0004g0323 a0001c0001t0004g0324 others(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 | a0001c0002t0001g0291 a0001c0002t0001g0292 a0001c0002t0001g0307 others(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 | 133 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(130): Show |
133 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(130): 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 | 245 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(242): Show |
245 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(242): 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 | a0001c0002t0001g0122 a0001c0002t0001g0123 a0001c0002t0001g0124 others(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 | a0001c0001t0003g0209 | 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 | a0001c0001t0002g0222 a0001c0001t0002g0223 a0001c0001t0002g0245 |
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 | a0001c0002t0001g0195 | 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 | 247 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(244): Show |
247 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(244): Show |
intron_variant | MODIFIER | c.5181+151C>T | ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 38/38 | chr20 | 49032317 | |||||||
| chr20:49032319 | G | A | 136 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(133): Show |
137 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(134): 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 | a0001c0001t0003g0113 a0001c0001t0003g0210 a0001c0001t0003g0211 others(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 | a0001c0001t0003g0202 a0001c0001t0003g0217 a0001c0001t0023g0216 |
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 | a0001c0001t0002g0008 a0001c0001t0002g0009 a0001c0001t0002g0010 others(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 | a0001c0001t0014g0224 a0001c0001t0014g0225 |
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 | a0001c0002t0001g0192 | 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 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(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 |