Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 394 |
| ensemblid | ENSG00000100852.14 |
| hgncid | 675 |
| symbol | ARHGAP5 |
| name | Rho GTPase activating protein 5 |
| refseq_nuc | NM_001030055.2 |
| refseq_prot | NP_001025226.1 |
| ensembl_nuc | ENST00000345122.8 |
| ensembl_prot | ENSP00000371897.1 |
| mane_status | MANE Select |
| chr | chr14 |
| start | 32077304 |
| end | 32159728 |
| strand | + |
| ver | v1.2 |
| region | chr14:32077304-32159728 |
| region5000 | chr14:32072304-32164728 |
| regionname0 | ARHGAP5_chr14_32077304_32159728 |
| regionname5000 | ARHGAP5_chr14_32072304_32164728 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1502 | 169 | 55 | 37 | 38 | 8 | 29 | 19 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | MMAKN others(1497): Show |
chr14 | 32072304 | 32164728 |
| a0002 | 0/0 | 1502 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | MMAKN others(1497): Show |
chr14 | 32072304 | 32164728 |
| a0003 | 0/0 | 1502 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | MMAKN others(1497): Show |
chr14 | 32072304 | 32164728 |
| a0004 | 0/0 | 1502 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | MMAKN others(1497): Show |
chr14 | 32072304 | 32164728 |
| a0005 | 0/0 | 1502 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | MMAKN others(1497): Show |
chr14 | 32072304 | 32164728 |
| a0006 | 0/0 | 1502 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | MMAKN others(1497): Show |
chr14 | 32072304 | 32164728 |
| a0007 | 0/0 | 1502 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | MMAKN others(1497): Show |
chr14 | 32072304 | 32164728 |
| a0008 | 0/0 | 1502 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | MMAKN others(1497): Show |
chr14 | 32072304 | 32164728 |
| a0009 | 0/0 | 1502 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | MMAKN others(1497): Show |
chr14 | 32072304 | 32164728 |
| a0010 | 0/0 | 1502 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | MMAKN others(1497): Show |
chr14 | 32072304 | 32164728 |
| a0011 | 0/0 | 1502 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | MMAKN others(1497): Show |
chr14 | 32072304 | 32164728 |
| a0012 | 0/0 | 1502 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | MMAKN others(1497): Show |
chr14 | 32072304 | 32164728 |
| a0013 | 0/0 | 1502 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | MMAKN others(1497): Show |
chr14 | 32072304 | 32164728 |
| a0014 | 0/0 | 1502 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | MMAKN others(1497): Show |
chr14 | 32072304 | 32164728 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 4506 | 160 | 48 | 35 | 38 | 8 | 29 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | ATGAT others(4501): Show |
chr14 | 32072304 | 32164728 | ||
| a0001c0002 | 0/0 | 4506 | 5 | 4 | 1 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | ATGAT others(4501): Show |
chr14 | 32072304 | 32164728 | ||
| a0001c0010 | 0/0 | 4506 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | ATGAT others(4501): Show |
chr14 | 32072304 | 32164728 | ||
| a0001c0012 | 0/0 | 4506 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | ATGAT others(4501): Show |
chr14 | 32072304 | 32164728 | ||
| a0001c0018 | 0/0 | 4506 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | ATGAT others(4501): Show |
chr14 | 32072304 | 32164728 | ||
| a0001c0019 | 0/0 | 4506 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | ATGAT others(4501): Show |
chr14 | 32072304 | 32164728 | ||
| a0002c0004 | 0/0 | 4506 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | ATGAT others(4501): Show |
chr14 | 32072304 | 32164728 | ||
| a0003c0003 | 0/0 | 4506 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | ATGAT others(4501): Show |
chr14 | 32072304 | 32164728 | ||
| a0004c0014 | 0/0 | 4506 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | ATGAT others(4501): Show |
chr14 | 32072304 | 32164728 | ||
| a0005c0013 | 0/0 | 4506 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | ATGAT others(4501): Show |
chr14 | 32072304 | 32164728 | ||
| a0006c0016 | 0/0 | 4506 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | ATGAT others(4501): Show |
chr14 | 32072304 | 32164728 | ||
| a0007c0011 | 0/0 | 4506 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | ATGAT others(4501): Show |
chr14 | 32072304 | 32164728 | ||
| a0008c0015 | 0/0 | 4506 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | ATGAT others(4501): Show |
chr14 | 32072304 | 32164728 | ||
| a0009c0009 | 0/0 | 4506 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | ATGAT others(4501): Show |
chr14 | 32072304 | 32164728 | ||
| a0010c0017 | 0/0 | 4506 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | ATGAT others(4501): Show |
chr14 | 32072304 | 32164728 | ||
| a0011c0006 | 0/0 | 4506 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | ATGAT others(4501): Show |
chr14 | 32072304 | 32164728 | ||
| a0012c0005 | 0/0 | 4506 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | ATGAT others(4501): Show |
chr14 | 32072304 | 32164728 | ||
| a0013c0007 | 0/0 | 4506 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | ATGAT others(4501): Show |
chr14 | 32072304 | 32164728 | ||
| a0014c0008 | 0/0 | 4506 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | ATGAT others(4501): Show |
chr14 | 32072304 | 32164728 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 9589 | 109 | 33 | 19 | 27 | 6 | 22 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | GAGGA others(9584): Show |
chr14 | 32072304 | 32164728 |
| a0001c0001t0002 | 0/0 | 9589 | 22 | 1 | 9 | 8 | 1 | 3 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | GAGGA others(9584): Show |
chr14 | 32072304 | 32164728 |
| a0001c0001t0003 | 0/0 | 9589 | 6 | 6 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | GAGGA others(9584): Show |
chr14 | 32072304 | 32164728 |
| a0001c0001t0004 | 0/0 | 9590 | 3 | 1 | 1 | 0 | 0 | 1 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | GAGGA others(9585): Show |
chr14 | 32072304 | 32164728 |
| a0001c0001t0006 | 0/0 | 9589 | 4 | 0 | 4 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | GAGGA others(9584): Show |
chr14 | 32072304 | 32164728 |
| a0001c0001t0007 | 0/0 | 9589 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | GAGGA others(9584): Show |
chr14 | 32072304 | 32164728 |
| a0001c0001t0008 | 0/0 | 9589 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | GAGGA others(9584): Show |
chr14 | 32072304 | 32164728 |
| a0001c0001t0009 | 0/0 | 9602 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | GAGGA others(9597): Show |
chr14 | 32072304 | 32164728 |
| a0001c0001t0010 | 0/0 | 9589 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | GAGGA others(9584): Show |
chr14 | 32072304 | 32164728 |
| a0001c0001t0011 | 0/0 | 9589 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | GAGGA others(9584): Show |
chr14 | 32072304 | 32164728 |
| a0001c0001t0012 | 0/0 | 9589 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | GAGGA others(9584): Show |
chr14 | 32072304 | 32164728 |
| a0001c0001t0013 | 0/0 | 9589 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | GAGGA others(9584): Show |
chr14 | 32072304 | 32164728 |
| a0001c0001t0014 | 0/0 | 9589 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | GAGGA others(9584): Show |
chr14 | 32072304 | 32164728 |
| a0001c0001t0017 | 0/0 | 9589 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | GAGGA others(9584): Show |
chr14 | 32072304 | 32164728 |
| a0001c0001t0020 | 0/0 | 9589 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | GAGGA others(9584): Show |
chr14 | 32072304 | 32164728 |
| a0001c0001t0021 | 0/0 | 9589 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | GAGGA others(9584): Show |
chr14 | 32072304 | 32164728 |
| a0001c0001t0022 | 0/0 | 9589 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | GAGGA others(9584): Show |
chr14 | 32072304 | 32164728 |
| a0001c0001t0026 | 0/0 | 9589 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | GAGGA others(9584): Show |
chr14 | 32072304 | 32164728 |
| a0001c0001t0028 | 0/0 | 9589 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | GAGGA others(9584): Show |
chr14 | 32072304 | 32164728 |
| a0001c0002t0005 | 0/0 | 9589 | 5 | 4 | 1 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | GAGGA others(9584): Show |
chr14 | 32072304 | 32164728 |
| a0001c0010t0025 | 0/0 | 9589 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | GAGGA others(9584): Show |
chr14 | 32072304 | 32164728 |
| a0001c0012t0027 | 0/0 | 9589 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | GAGGA others(9584): Show |
chr14 | 32072304 | 32164728 |
| a0001c0018t0023 | 0/0 | 9589 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | GAGGA others(9584): Show |
chr14 | 32072304 | 32164728 |
| a0001c0019t0001 | 0/0 | 9589 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | GAGGA others(9584): Show |
chr14 | 32072304 | 32164728 |
| a0002c0004t0001 | 0/0 | 9589 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | GAGGA others(9584): Show |
chr14 | 32072304 | 32164728 |
| a0003c0003t0001 | 0/0 | 9589 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | GAGGA others(9584): Show |
chr14 | 32072304 | 32164728 |
| a0003c0003t0019 | 0/0 | 9589 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | GAGGA others(9584): Show |
chr14 | 32072304 | 32164728 |
| a0004c0014t0015 | 0/0 | 9577 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | GAGGA others(9572): Show |
chr14 | 32072304 | 32164728 |
| a0005c0013t0018 | 0/0 | 9589 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | GAGGA others(9584): Show |
chr14 | 32072304 | 32164728 |
| a0006c0016t0004 | 0/0 | 9590 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | GAGGA others(9585): Show |
chr14 | 32072304 | 32164728 |
| a0007c0011t0001 | 0/0 | 9589 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | GAGGA others(9584): Show |
chr14 | 32072304 | 32164728 |
| a0008c0015t0024 | 0/0 | 9589 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | GAGGA others(9584): Show |
chr14 | 32072304 | 32164728 |
| a0009c0009t0003 | 0/0 | 9589 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | GAGGA others(9584): Show |
chr14 | 32072304 | 32164728 |
| a0010c0017t0016 | 0/0 | 9589 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | GAGGA others(9584): Show |
chr14 | 32072304 | 32164728 |
| a0011c0006t0001 | 0/0 | 9589 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | GAGGA others(9584): Show |
chr14 | 32072304 | 32164728 |
| a0012c0005t0004 | 0/0 | 9590 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | GAGGA others(9585): Show |
chr14 | 32072304 | 32164728 |
| a0013c0007t0001 | 0/0 | 9589 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | GAGGA others(9584): Show |
chr14 | 32072304 | 32164728 |
| a0014c0008t0001 | 0/0 | 9589 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | GAGGA others(9584): Show |
chr14 | 32072304 | 32164728 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0023 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0047 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0002g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0003g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0003g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0003g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0003g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0003g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0003g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0004g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0004g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0004g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0006g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0006g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0006g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0006g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0007g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0007g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0007g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0008g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0009g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0010g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0011g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0012g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0013g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0014g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0017g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0020g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0021g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0022g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0026g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0001t0028g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0002t0005g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0002t0005g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0002t0005g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0002t0005g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0010t0025g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0012t0027g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0018t0023g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0001c0019t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0002c0004t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0002c0004t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0002c0004t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0003c0003t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0003c0003t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0003c0003t0019g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0004c0014t0015g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0005c0013t0018g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0006c0016t0004g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0007c0011t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0008c0015t0024g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0009c0009t0003g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0010c0017t0016g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0011c0006t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0012c0005t0004g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0013c0007t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0014c0008t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0080 | EUR | GBR | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0134 | EUR | GBR | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0067 | EUR | GBR | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0024 | EUR | GBR | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | CHS | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | CHS | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | CHS | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG00609 | hp2 | a0004 | c0014 | t0015 | g0159 | EAS | CHS | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | CHS | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | CHS | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | CHS | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | CHS | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0138 | AMR | PUR | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0109 | AMR | PUR | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG01099 | hp1 | a0001 | c0001 | t0006 | g0107 | AMR | PUR | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG01106 | hp1 | a0001 | c0001 | t0020 | g0051 | AMR | PUR | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG01106 | hp2 | a0001 | c0001 | t0028 | g0019 | AMR | PUR | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG01169 | hp2 | a0001 | c0001 | t0004 | g0174 | AMR | PUR | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | PUR | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG01192 | hp2 | a0001 | c0019 | t0001 | g0179 | AMR | PUR | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG01243 | hp1 | a0001 | c0002 | t0005 | g0168 | AMR | PUR | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0045 | AMR | PUR | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | CLM | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG01255 | hp2 | a0005 | c0013 | t0018 | g0062 | AMR | CLM | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG01257 | hp2 | a0001 | c0001 | t0006 | g0154 | AMR | CLM | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG01258 | hp1 | a0001 | c0001 | t0006 | g0155 | AMR | CLM | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | CLM | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0124 | AMR | CLM | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | CLM | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0108 | AMR | CLM | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG01515 | hp1 | a0006 | c0016 | t0004 | g0178 | EUR | IBS | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG01515 | hp2 | a0007 | c0011 | t0001 | g0026 | EUR | IBS | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0083 | EUR | IBS | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG01516 | hp2 | a0001 | c0001 | t0008 | g0139 | EUR | IBS | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG01884 | hp2 | a0001 | c0001 | t0014 | g0170 | AFR | ACB | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0103 | AMR | PEL | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PEL | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0100 | AMR | PEL | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | ACB | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | ACB | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | KHV | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | KHV | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | KHV | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG02145 | hp1 | a0002 | c0004 | t0001 | g0136 | AFR | ACB | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | ACB | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | CDX | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | CDX | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0116 | EAS | CDX | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | CDX | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | ACB | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG02257 | hp2 | a0008 | c0015 | t0024 | g0132 | AFR | ACB | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG02258 | hp1 | a0001 | c0001 | t0010 | g0034 | AFR | ACB | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG02258 | hp2 | a0001 | c0002 | t0005 | g0004 | AFR | ACB | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG02280 | hp1 | a0001 | c0001 | t0004 | g0061 | AFR | ACB | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0148 | AFR | ACB | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0104 | AMR | PEL | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG02293 | hp2 | a0001 | c0001 | t0006 | g0182 | AMR | PEL | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG02451 | hp1 | a0002 | c0004 | t0001 | g0137 | AFR | ACB | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0125 | AFR | ACB | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG02572 | hp1 | a0009 | c0009 | t0003 | g0172 | AFR | GWD | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG02572 | hp2 | a0001 | c0002 | t0005 | g0167 | AFR | GWD | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0096 | SAS | PJL | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG02622 | hp1 | a0001 | c0002 | t0005 | g0169 | AFR | GWD | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0044 | SAS | PJL | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0176 | SAS | PJL | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0068 | SAS | PJL | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | GWD | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG02717 | hp2 | a0001 | c0018 | t0023 | g0181 | AFR | GWD | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | GWD | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0085 | SAS | PJL | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0175 | SAS | PJL | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG02809 | hp1 | a0010 | c0017 | t0016 | g0005 | AFR | GWD | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | GWD | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | GWD | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | GWD | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | GWD | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG02965 | hp1 | a0003 | c0003 | t0001 | g0145 | AFR | ESN | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0070 | SAS | PJL | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG03041 | hp1 | a0001 | c0001 | t0003 | g0144 | AFR | GWD | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG03041 | hp2 | a0001 | c0001 | t0007 | g0003 | AFR | GWD | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG03098 | hp1 | a0003 | c0003 | t0001 | g0147 | AFR | MSL | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | MSL | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | ESN | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | ESN | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG03139 | hp1 | a0001 | c0012 | t0027 | g0131 | AFR | ESN | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG03139 | hp2 | a0001 | c0001 | t0017 | g0123 | AFR | ESN | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG03195 | hp2 | a0002 | c0004 | t0001 | g0135 | AFR | ESN | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | MSL | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0071 | SAS | PJL | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG03453 | hp1 | a0001 | c0001 | t0007 | g0164 | AFR | MSL | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG03453 | hp2 | a0001 | c0001 | t0007 | g0165 | AFR | MSL | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0161 | AFR | MSL | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | MSL | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0043 | SAS | PJL | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | ESN | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | ESN | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG03540 | hp1 | a0011 | c0006 | t0001 | g0072 | AFR | GWD | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | GWD | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0128 | SAS | PJL | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG03704 | hp1 | a0001 | c0001 | t0004 | g0177 | SAS | PJL | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0093 | SAS | PJL | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0094 | SAS | BEB | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG03831 | hp2 | a0012 | c0005 | t0004 | g0173 | SAS | BEB | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0052 | SAS | BEB | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | BEB | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG04115 | hp1 | a0001 | c0001 | t0026 | g0079 | SAS | STU | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | STU | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0101 | SAS | STU | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0053 | SAS | STU | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| NA18522 | hp1 | a0001 | c0001 | t0022 | g0003 | AFR | YRI | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| NA18522 | hp2 | a0003 | c0003 | t0019 | g0146 | AFR | YRI | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | CHB | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| NA18612 | hp2 | a0001 | c0001 | t0011 | g0119 | EAS | CHB | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | CHB | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | CHB | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| NA18906 | hp1 | a0001 | c0002 | t0005 | g0004 | AFR | YRI | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | YRI | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| NA18982 | hp1 | a0001 | c0001 | t0012 | g0055 | EAS | JPT | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | LWK | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| NA19043 | hp2 | a0001 | c0010 | t0025 | g0151 | AFR | LWK | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| NA19065 | hp1 | a0013 | c0007 | t0001 | g0064 | EAS | JPT | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| NA19088 | hp1 | a0001 | c0001 | t0009 | g0171 | EAS | JPT | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | YRI | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | YRI | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0028 | EUR | TSI | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0102 | EUR | TSI | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| NA20905 | hp1 | a0001 | c0001 | t0021 | g0010 | SAS | GIH | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| NA20905 | hp2 | a0001 | c0001 | t0013 | g0007 | SAS | GIH | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0163 | AFR | ACB | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | ACB | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | MSL | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0162 | AFR | MSL | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0160 | AFR | USA | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | USA | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| NA21309 | hp1 | a0014 | c0008 | t0001 | g0130 | AFR | LWK | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | LWK | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0023 | REF | REF | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0047 | REF | REF | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:32091474 | G | C | 1 | a0012 | 1 | HG03831.hp2 | missense_variant | MODERATE | c.805G>C | p.Val269Leu | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/7 | 1105/9589 | 805/4509 | 269/1502 | chr14 | 32091474 | |||
| chr14:32092572 | C | T | 1 | a0002 | 3 | HG02145.hp1 HG02451.hp1 HG03195.hp2 |
missense_variant | MODERATE | c.1903C>T | p.Arg635Trp | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/7 | 2203/9589 | 1903/4509 | 635/1502 | chr14 | 32092572 | |||
| chr14:32092703 | A | G | 1 | a0006 | 1 | HG01515.hp1 | missense_variant | MODERATE | c.2034A>G | p.Ile678Met | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/7 | 2334/9589 | 2034/4509 | 678/1502 | chr14 | 32092703 | |||
| chr14:32092969 | T | C | 1 | a0010 | 1 | HG02809.hp1 | missense_variant | MODERATE | c.2300T>C | p.Ile767Thr | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/7 | 2600/9589 | 2300/4509 | 767/1502 | chr14 | 32092969 | |||
| chr14:32092989 | T | C | 1 | a0011 | 1 | HG03540.hp1 | missense_variant | MODERATE | c.2320T>C | p.Ser774Pro | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/7 | 2620/9589 | 2320/4509 | 774/1502 | chr14 | 32092989 | |||
| chr14:32093048 | T | A | 1 | a0013 | 1 | NA19065.hp1 | missense_variant | MODERATE | c.2379T>A | p.Asp793Glu | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/7 | 2679/9589 | 2379/4509 | 793/1502 | chr14 | 32093048 | |||
| chr14:32093204 | T | G | 1 | a0014 | 1 | NA21309.hp1 | missense_variant | MODERATE | c.2535T>G | p.Asp845Glu | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/7 | 2835/9589 | 2535/4509 | 845/1502 | chr14 | 32093204 | |||
| chr14:32093524 | A | G | 1 | a0008 | 1 | HG02257.hp2 | missense_variant | MODERATE | c.2855A>G | p.Asp952Gly | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/7 | 3155/9589 | 2855/4509 | 952/1502 | chr14 | 32093524 | |||
| chr14:32093527 | A | G | 1 | a0003 | 3 | HG02965.hp1 HG03098.hp1 NA18522.hp2 |
missense_variant | MODERATE | c.2858A>G | p.Asn953Ser | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/7 | 3158/9589 | 2858/4509 | 953/1502 | chr14 | 32093527 | |||
| chr14:32093959 | C | A | 1 | a0009 | 1 | HG02572.hp1 | missense_variant | MODERATE | c.3290C>A | p.Thr1097Lys | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/7 | 3590/9589 | 3290/4509 | 1097/1502 | chr14 | 32093959 | |||
| chr14:32093961 | A | G | 1 | a0004 | 1 | HG00609.hp2 | missense_variant | MODERATE | c.3292A>G | p.Ile1098Val | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/7 | 3592/9589 | 3292/4509 | 1098/1502 | chr14 | 32093961 | |||
| chr14:32094246 | C | T | 1 | a0005 | 1 | HG01255.hp2 | missense_variant | MODERATE | c.3577C>T | p.Arg1193Cys | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/7 | 3877/9589 | 3577/4509 | 1193/1502 | chr14 | 32094246 | |||
| chr14:32154655 | G | A | 1 | a0007 | 1 | HG01515.hp2 | missense_variant | MODERATE | c.4216G>A | p.Ala1406Thr | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 7/7 | 4516/9589 | 4216/4509 | 1406/1502 | chr14 | 32154655 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:32091149 | A | G | 1 | a0001c0019 | 1 | HG01192.hp2 | synonymous_variant | LOW | c.480A>G | p.Leu160Leu | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/7 | 780/9589 | 480/4509 | 160/1502 | chr14 | 32091149 | |||
| chr14:32091281 | C | T | 1 | a0001c0018 | 1 | HG02717.hp2 | synonymous_variant | LOW | c.612C>T | p.Cys204Cys | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/7 | 912/9589 | 612/4509 | 204/1502 | chr14 | 32091281 | |||
| chr14:32091923 | A | G | 2 | a0001c0002 a0010c0017 |
6 | HG01243.hp1 HG02258.hp2 HG02572.hp2 others(3): Show |
synonymous_variant | LOW | c.1254A>G | p.Val418Val | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/7 | 1554/9589 | 1254/4509 | 418/1502 | chr14 | 32091923 | |||
| chr14:32092847 | A | G | 2 | a0001c0002 a0010c0017 |
6 | HG01243.hp1 HG02258.hp2 HG02572.hp2 others(3): Show |
synonymous_variant | LOW | c.2178A>G | p.Gln726Gln | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/7 | 2478/9589 | 2178/4509 | 726/1502 | chr14 | 32092847 | |||
| chr14:32093582 | C | T | 1 | a0001c0002 | 5 | HG01243.hp1 HG02258.hp2 HG02572.hp2 others(2): Show |
synonymous_variant | LOW | c.2913C>T | p.Asp971Asp | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/7 | 3213/9589 | 2913/4509 | 971/1502 | chr14 | 32093582 | |||
| chr14:32149990 | T | G | 1 | a0001c0010 | 1 | NA19043.hp2 | synonymous_variant | LOW | c.4032T>G | p.Pro1344Pro | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 5/7 | 4332/9589 | 4032/4509 | 1344/1502 | chr14 | 32149990 | |||
| chr14:32154918 | A | G | 1 | a0001c0010 | 1 | NA19043.hp2 | synonymous_variant | LOW | c.4479A>G | p.Gln1493Gln | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 7/7 | 4779/9589 | 4479/4509 | 1493/1502 | chr14 | 32154918 | |||
| chr14:32154945 | A | T | 1 | a0001c0012 | 1 | HG03139.hp1 | synonymous_variant | LOW | c.4506A>T | p.Ile1502Ile | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 7/7 | 4806/9589 | 4506/4509 | 1502/1502 | chr14 | 32154945 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:32077358 | C | T | 1 | a0001c0001t0028 | 1 | HG01106.hp2 | 5_prime_UTR_variant | MODIFIER | c.-246C>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 1/7 | 13312 | chr14 | 32077358 | ||||||
| chr14:32154967 | C | T | 1 | a0001c0012t0027 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*19C>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 7/7 | 19 | chr14 | 32154967 | ||||||
| chr14:32155300 | A | G | 1 | a0001c0001t0026 | 1 | HG04115.hp1 | 3_prime_UTR_variant | MODIFIER | c.*352A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 7/7 | 352 | chr14 | 32155300 | ||||||
| chr14:32155381 | A | G | 1 | a0001c0010t0025 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*433A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 7/7 | 433 | chr14 | 32155381 | ||||||
| chr14:32155401 | T | C | 1 | a0001c0001t0008 | 1 | HG01516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*453T>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 7/7 | 453 | chr14 | 32155401 | ||||||
| chr14:32155568 | A | C | 1 | a0008c0015t0024 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*620A>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 7/7 | 620 | chr14 | 32155568 | ||||||
| chr14:32155636 | A | G | 2 | a0001c0001t0003 a0009c0009t0003 |
7 | HG02280.hp2 HG02559.hp1 HG02572.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*688A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 7/7 | 688 | chr14 | 32155636 | ||||||
| chr14:32156116 | A | G | 4 | a0001c0001t0007 a0001c0001t0022 a0001c0002t0005 others(1): Show |
10 | HG01243.hp1 HG02258.hp2 HG02572.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1168A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 7/7 | 1168 | chr14 | 32156116 | ||||||
| chr14:32156258 | G | T | 1 | a0001c0001t0021 | 1 | NA20905.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1310G>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 7/7 | 1310 | chr14 | 32156258 | ||||||
| chr14:32156288 | T | TATTTGGT others(6): Show |
1 | a0001c0001t0009 | 1 | NA19088.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1351_*1352insAAAT others(9): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 7/7 | 1352 | INFO_REALIGN_3_PRIME | chr14 | 32156288 | |||||
| chr14:32156633 | A | T | 1 | a0001c0001t0020 | 1 | HG01106.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1685A>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 7/7 | 1685 | chr14 | 32156633 | ||||||
| chr14:32156646 | G | C | 2 | a0001c0001t0006 a0001c0001t0021 |
5 | HG01099.hp1 HG01257.hp2 HG01258.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1698G>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 7/7 | 1698 | chr14 | 32156646 | ||||||
| chr14:32156862 | T | C | 1 | a0001c0001t0022 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1914T>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 7/7 | 1914 | chr14 | 32156862 | ||||||
| chr14:32156887 | G | A | 1 | a0001c0001t0010 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1939G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 7/7 | 1939 | chr14 | 32156887 | ||||||
| chr14:32157096 | T | G | 1 | a0001c0001t0011 | 1 | NA18612.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2148T>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 7/7 | 2148 | chr14 | 32157096 | ||||||
| chr14:32157126 | C | T | 1 | a0001c0002t0005 | 5 | HG01243.hp1 HG02258.hp2 HG02572.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2178C>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 7/7 | 2178 | chr14 | 32157126 | ||||||
| chr14:32157162 | G | A | 1 | a0001c0001t0012 | 1 | NA18982.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2214G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 7/7 | 2214 | chr14 | 32157162 | ||||||
| chr14:32157599 | T | A | 1 | a0001c0001t0002 | 22 | HG00735.hp2 HG01071.hp1 HG01192.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*2651T>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 7/7 | 2651 | chr14 | 32157599 | ||||||
| chr14:32157828 | G | GT | 3 | a0001c0001t0004 a0006c0016t0004 a0012c0005t0004 |
5 | HG01169.hp2 HG01515.hp1 HG02280.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2891dupT | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 7/7 | 2892 | INFO_REALIGN_3_PRIME | chr14 | 32157828 | |||||
| chr14:32158099 | A | G | 1 | a0001c0018t0023 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3151A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 7/7 | 3151 | chr14 | 32158099 | ||||||
| chr14:32158232 | A | G | 1 | a0001c0002t0005 | 5 | HG01243.hp1 HG02258.hp2 HG02572.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3284A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 7/7 | 3284 | chr14 | 32158232 | ||||||
| chr14:32158273 | T | G | 1 | a0001c0001t0013 | 1 | NA20905.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3325T>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 7/7 | 3325 | chr14 | 32158273 | ||||||
| chr14:32158274 | C | T | 1 | a0001c0001t0013 | 1 | NA20905.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3326C>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 7/7 | 3326 | chr14 | 32158274 | ||||||
| chr14:32158431 | G | C | 1 | a0001c0001t0014 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3483G>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 7/7 | 3483 | chr14 | 32158431 | ||||||
| chr14:32158910 | A | G | 1 | a0003c0003t0019 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3962A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 7/7 | 3962 | chr14 | 32158910 | ||||||
| chr14:32158984 | A | G | 1 | a0005c0013t0018 | 1 | HG01255.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4036A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 7/7 | 4036 | chr14 | 32158984 | ||||||
| chr14:32159011 | G | A | 1 | a0001c0018t0023 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4063G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 7/7 | 4063 | chr14 | 32159011 | ||||||
| chr14:32159363 | G | T | 1 | a0001c0001t0017 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4415G>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 7/7 | 4415 | chr14 | 32159363 | ||||||
| chr14:32159387 | TATTTTAG others(5): Show |
T | 1 | a0004c0014t0015 | 1 | HG00609.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4444_*4455delTAGT others(8): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 7/7 | 4444 | INFO_REALIGN_3_PRIME | chr14 | 32159387 | |||||
| chr14:32159423 | T | C | 1 | a0001c0002t0005 | 5 | HG01243.hp1 HG02258.hp2 HG02572.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4475T>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 7/7 | 4475 | chr14 | 32159423 | ||||||
| chr14:32159468 | G | A | 1 | a0010c0017t0016 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4520G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 7/7 | 4520 | chr14 | 32159468 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:32077469 | G | A | 1 | a0010c0017t0016g0005 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-169+34G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 1/6 | chr14 | 32077469 | |||||||
| chr14:32077593 | C | G | 1 | a0001c0001t0006g0182 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-169+158C>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 1/6 | chr14 | 32077593 | |||||||
| chr14:32077627 | C | T | 9 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0180 others(6): Show |
9 | HG01169.hp2 HG01192.hp2 HG01515.hp1 others(6): Show |
intron_variant | MODIFIER | c.-169+192C>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 1/6 | chr14 | 32077627 | |||||||
| chr14:32077983 | C | T | 1 | a0009c0009t0003g0172 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-169+548C>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 1/6 | chr14 | 32077983 | |||||||
| chr14:32077985 | C | T | 1 | a0009c0009t0003g0172 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-169+550C>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 1/6 | chr14 | 32077985 | |||||||
| chr14:32078135 | C | T | 1 | a0001c0001t0009g0171 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-169+700C>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 1/6 | chr14 | 32078135 | |||||||
| chr14:32078268 | G | T | 2 | a0001c0001t0014g0170 a0001c0018t0023g0181 |
2 | HG01884.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-169+833G>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 1/6 | chr14 | 32078268 | |||||||
| chr14:32078360 | A | G | 4 | a0001c0002t0005g0004 a0001c0002t0005g0167 a0001c0002t0005g0168 others(1): Show |
5 | HG01243.hp1 HG02258.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-169+925A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 1/6 | chr14 | 32078360 | |||||||
| chr14:32078518 | C | T | 18 | a0001c0001t0001g0166 a0001c0001t0003g0160 a0001c0001t0003g0161 others(15): Show |
19 | HG00609.hp2 HG01243.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.-169+1083C>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 1/6 | chr14 | 32078518 | |||||||
| chr14:32078550 | T | C | 4 | a0001c0002t0005g0004 a0001c0002t0005g0167 a0001c0002t0005g0168 others(1): Show |
5 | HG01243.hp1 HG02258.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-169+1115T>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 1/6 | chr14 | 32078550 | |||||||
| chr14:32078984 | G | C | 1 | a0004c0014t0015g0159 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-169+1549G>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 1/6 | chr14 | 32078984 | |||||||
| chr14:32079162 | A | T | 1 | a0001c0001t0001g0158 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-169+1727A>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 1/6 | chr14 | 32079162 | |||||||
| chr14:32079282 | T | C | 1 | a0001c0001t0001g0006 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-169+1847T>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 1/6 | chr14 | 32079282 | |||||||
| chr14:32079316 | G | A | 1 | a0001c0001t0013g0007 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-169+1881G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 1/6 | chr14 | 32079316 | |||||||
| chr14:32079395 | A | G | 2 | a0001c0001t0001g0156 a0001c0001t0001g0157 |
2 | HG02559.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-169+1960A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 1/6 | chr14 | 32079395 | |||||||
| chr14:32079433 | C | G | 2 | a0001c0001t0006g0154 a0001c0001t0006g0155 |
2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.-169+1998C>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 1/6 | chr14 | 32079433 | |||||||
| chr14:32079741 | A | G | 9 | a0001c0001t0001g0166 a0001c0001t0007g0003 a0001c0001t0007g0164 others(6): Show |
10 | HG01243.hp1 HG02055.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.-169+2306A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 1/6 | chr14 | 32079741 | |||||||
| chr14:32079850 | A | C | 1 | a0001c0001t0001g0153 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-169+2415A>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 1/6 | chr14 | 32079850 | |||||||
| chr14:32079851 | C | T | 1 | a0001c0001t0001g0152 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-169+2416C>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 1/6 | chr14 | 32079851 | |||||||
| chr14:32080593 | A | G | 1 | a0001c0010t0025g0151 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-169+3158A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 1/6 | chr14 | 32080593 | |||||||
| chr14:32080659 | C | T | 6 | a0001c0001t0001g0150 a0001c0001t0003g0160 a0001c0001t0003g0161 others(3): Show |
6 | HG01109.hp2 HG02559.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.-169+3224C>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 1/6 | chr14 | 32080659 | |||||||
| chr14:32080695 | G | T | 1 | a0001c0001t0001g0149 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-169+3260G>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 1/6 | chr14 | 32080695 | |||||||
| chr14:32080775 | A | AT | 14 | a0001c0001t0001g0150 a0001c0001t0003g0144 a0001c0001t0003g0148 others(11): Show |
15 | HG01109.hp2 HG01243.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.-169+3350dupT | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 32080775 | ||||||
| chr14:32080785 | TC | T | 4 | a0001c0001t0007g0003 a0001c0001t0007g0164 a0001c0001t0007g0165 others(1): Show |
4 | HG03041.hp2 HG03453.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-169+3356delC | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 32080785 | ||||||
| chr14:32080934 | T | C | 1 | a0001c0001t0001g0008 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-169+3499T>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 1/6 | chr14 | 32080934 | |||||||
| chr14:32080944 | G | A | 1 | a0001c0001t0001g0009 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-169+3509G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 1/6 | chr14 | 32080944 | |||||||
| chr14:32081020 | G | A | 1 | a0004c0014t0015g0159 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-169+3585G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 1/6 | chr14 | 32081020 | |||||||
| chr14:32081165 | T | A | 8 | a0001c0001t0007g0003 a0001c0001t0007g0164 a0001c0001t0007g0165 others(5): Show |
9 | HG01243.hp1 HG02258.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.-169+3730T>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 1/6 | chr14 | 32081165 | |||||||
| chr14:32081548 | C | CA | 18 | a0001c0001t0002g0011 a0001c0001t0003g0144 a0001c0001t0003g0160 others(15): Show |
19 | HG01192.hp1 HG01243.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.-169+4136dupA | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 32081548 | ||||||
| chr14:32081548 | CA | C | 10 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0140 others(7): Show |
10 | HG00609.hp2 HG01167.hp2 HG01516.hp2 others(7): Show |
intron_variant | MODIFIER | c.-169+4136delA | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 32081548 | ||||||
| chr14:32081589 | T | A | 2 | a0001c0001t0001g0012 a0001c0001t0001g0013 |
2 | NA18987.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.-169+4154T>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 1/6 | chr14 | 32081589 | |||||||
| chr14:32081709 | T | G | 1 | a0001c0001t0001g0014 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-169+4274T>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 1/6 | chr14 | 32081709 | |||||||
| chr14:32081797 | T | C | 1 | a0001c0001t0001g0015 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-169+4362T>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 1/6 | chr14 | 32081797 | |||||||
| chr14:32081859 | T | C | 1 | a0001c0001t0001g0016 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-169+4424T>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 1/6 | chr14 | 32081859 | |||||||
| chr14:32081956 | C | T | 1 | a0001c0001t0002g0138 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-169+4521C>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 1/6 | chr14 | 32081956 | |||||||
| chr14:32081957 | C | T | 3 | a0002c0004t0001g0135 a0002c0004t0001g0136 a0002c0004t0001g0137 |
3 | HG02145.hp1 HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-169+4522C>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 1/6 | chr14 | 32081957 | |||||||
| chr14:32081979 | A | T | 1 | a0001c0001t0002g0138 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-169+4544A>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 1/6 | chr14 | 32081979 | |||||||
| chr14:32082002 | G | A | 1 | a0001c0001t0002g0017 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-169+4567G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 1/6 | chr14 | 32082002 | |||||||
| chr14:32082052 | A | C | 24 | a0001c0001t0001g0150 a0001c0001t0001g0166 a0001c0001t0003g0144 others(21): Show |
25 | HG00609.hp2 HG01109.hp2 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.-169+4617A>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 1/6 | chr14 | 32082052 | |||||||
| chr14:32082450 | T | C | 1 | a0010c0017t0016g0005 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-169+5015T>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 1/6 | chr14 | 32082450 | |||||||
| chr14:32082752 | C | A | 19 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(16): Show |
20 | HG00140.hp2 HG00735.hp1 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.-169+5317C>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 1/6 | chr14 | 32082752 | |||||||
| chr14:32082860 | G | C | 5 | a0001c0001t0001g0166 a0001c0001t0007g0003 a0001c0001t0007g0164 others(2): Show |
5 | HG02055.hp1 HG03041.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.-169+5425G>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 1/6 | chr14 | 32082860 | |||||||
| chr14:32082881 | G | A | 1 | a0001c0001t0014g0170 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-169+5446G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 1/6 | chr14 | 32082881 | |||||||
| chr14:32082898 | A | G | 1 | a0001c0018t0023g0181 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-169+5463A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 1/6 | chr14 | 32082898 | |||||||
| chr14:32082903 | T | C | 1 | a0010c0017t0016g0005 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-169+5468T>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 1/6 | chr14 | 32082903 | |||||||
| chr14:32082957 | C | G | 1 | a0001c0001t0001g0134 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-169+5522C>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 1/6 | chr14 | 32082957 | |||||||
| chr14:32083310 | A | C | 3 | a0003c0003t0001g0145 a0003c0003t0001g0147 a0003c0003t0019g0146 |
3 | HG02965.hp1 HG03098.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-169+5875A>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 1/6 | chr14 | 32083310 | |||||||
| chr14:32083608 | G | C | 3 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0153 |
3 | HG01255.hp1 HG02698.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.-169+6173G>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 1/6 | chr14 | 32083608 | |||||||
| chr14:32083762 | T | C | 1 | a0001c0001t0007g0164 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-169+6327T>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 1/6 | chr14 | 32083762 | |||||||
| chr14:32083812 | A | G | 4 | a0001c0001t0001g0133 a0001c0012t0027g0131 a0008c0015t0024g0132 others(1): Show |
4 | HG02257.hp2 HG02886.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-169+6377A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 1/6 | chr14 | 32083812 | |||||||
| chr14:32083923 | T | C | 1 | a0010c0017t0016g0005 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-169+6488T>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 1/6 | chr14 | 32083923 | |||||||
| chr14:32083978 | T | C | 1 | a0001c0001t0001g0140 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.-168-6524T>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 1/6 | chr14 | 32083978 | |||||||
| chr14:32084191 | G | A | 2 | a0001c0001t0001g0033 a0001c0001t0010g0034 |
2 | HG02258.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.-168-6311G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 1/6 | chr14 | 32084191 | |||||||
| chr14:32084564 | T | C | 5 | a0001c0002t0005g0004 a0001c0002t0005g0167 a0001c0002t0005g0168 others(2): Show |
6 | HG01243.hp1 HG02258.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.-168-5938T>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 1/6 | chr14 | 32084564 | |||||||
| chr14:32084591 | T | G | 4 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0020 others(1): Show |
4 | HG01106.hp2 HG02735.hp2 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.-168-5911T>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 1/6 | chr14 | 32084591 | |||||||
| chr14:32085015 | GACAGATT others(22): Show |
G | 1 | a0001c0019t0001g0179 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-168-5482_-168-545 others(33): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 32085015 | ||||||
| chr14:32085133 | A | G | 1 | a0002c0004t0001g0137 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-168-5369A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 1/6 | chr14 | 32085133 | |||||||
| chr14:32085213 | A | G | 1 | a0001c0001t0014g0170 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-168-5289A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 1/6 | chr14 | 32085213 | |||||||
| chr14:32085342 | C | T | 2 | a0001c0001t0001g0128 a0001c0001t0001g0129 |
2 | HG03492.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.-168-5160C>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 1/6 | chr14 | 32085342 | |||||||
| chr14:32085373 | G | A | 4 | a0001c0002t0005g0004 a0001c0002t0005g0167 a0001c0002t0005g0168 others(1): Show |
5 | HG01243.hp1 HG02258.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-168-5129G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 1/6 | chr14 | 32085373 | |||||||
| chr14:32085399 | A | G | 1 | a0003c0003t0001g0147 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-168-5103A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 1/6 | chr14 | 32085399 | |||||||
| chr14:32085587 | A | G | 22 | a0001c0001t0001g0127 a0001c0001t0001g0150 a0001c0001t0001g0166 others(19): Show |
23 | HG00609.hp2 HG01109.hp2 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.-168-4915A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 1/6 | chr14 | 32085587 | |||||||
| chr14:32085697 | G | T | 1 | a0001c0001t0001g0133 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-168-4805G>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 1/6 | chr14 | 32085697 | |||||||
| chr14:32085845 | A | C | 1 | a0001c0001t0001g0126 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-168-4657A>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 1/6 | chr14 | 32085845 | |||||||
| chr14:32085924 | C | T | 3 | a0001c0001t0002g0011 a0001c0001t0002g0124 a0001c0001t0002g0125 |
3 | HG01192.hp1 HG01358.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.-168-4578C>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 1/6 | chr14 | 32085924 | |||||||
| chr14:32086046 | G | T | 8 | a0001c0001t0001g0150 a0001c0001t0003g0144 a0001c0001t0003g0148 others(5): Show |
8 | HG01109.hp2 HG02280.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.-168-4456G>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 1/6 | chr14 | 32086046 | |||||||
| chr14:32086567 | G | A | 1 | a0001c0001t0001g0035 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-168-3935G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 1/6 | chr14 | 32086567 | |||||||
| chr14:32086574 | T | TATA | 5 | a0001c0002t0005g0004 a0001c0002t0005g0167 a0001c0002t0005g0168 others(2): Show |
6 | HG01243.hp1 HG02258.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.-168-3925_-168-392 others(7): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 32086574 | ||||||
| chr14:32086576 | T | C | 1 | a0010c0017t0016g0005 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-168-3926T>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 1/6 | chr14 | 32086576 | |||||||
| chr14:32086728 | G | A | 1 | a0010c0017t0016g0005 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-168-3774G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 1/6 | chr14 | 32086728 | |||||||
| chr14:32086905 | T | C | 1 | a0001c0001t0014g0170 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-168-3597T>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 1/6 | chr14 | 32086905 | |||||||
| chr14:32087179 | G | GA | 20 | a0001c0001t0001g0150 a0001c0001t0001g0166 a0001c0001t0003g0144 others(17): Show |
21 | HG01109.hp2 HG01243.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.-168-3315dupA | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 32087179 | ||||||
| chr14:32087182 | A | G | 1 | a0001c0010t0025g0151 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-168-3320A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 1/6 | chr14 | 32087182 | |||||||
| chr14:32087194 | A | T | 2 | a0001c0001t0006g0154 a0001c0001t0006g0155 |
2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.-168-3308A>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 1/6 | chr14 | 32087194 | |||||||
| chr14:32087261 | G | T | 1 | a0006c0016t0004g0178 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-168-3241G>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 1/6 | chr14 | 32087261 | |||||||
| chr14:32087383 | A | G | 2 | a0001c0001t0001g0166 a0001c0001t0007g0164 |
2 | HG02055.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-168-3119A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 1/6 | chr14 | 32087383 | |||||||
| chr14:32087474 | C | T | 1 | a0001c0001t0001g0030 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-168-3028C>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 1/6 | chr14 | 32087474 | |||||||
| chr14:32087475 | G | A | 1 | a0001c0001t0004g0174 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-168-3027G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 1/6 | chr14 | 32087475 | |||||||
| chr14:32087490 | C | CT | 6 | a0001c0001t0001g0166 a0001c0001t0007g0003 a0001c0001t0007g0164 others(3): Show |
6 | HG02055.hp1 HG03041.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.-168-3000dupT | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 32087490 | ||||||
| chr14:32087512 | G | A | 1 | a0001c0001t0001g0036 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-168-2990G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 1/6 | chr14 | 32087512 | |||||||
| chr14:32087707 | A | G | 5 | a0001c0001t0001g0166 a0001c0001t0007g0003 a0001c0001t0007g0164 others(2): Show |
5 | HG02055.hp1 HG03041.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.-168-2795A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 1/6 | chr14 | 32087707 | |||||||
| chr14:32087834 | T | A | 6 | a0001c0001t0001g0166 a0001c0001t0007g0003 a0001c0001t0007g0164 others(3): Show |
6 | HG01884.hp2 HG02055.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.-168-2668T>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 1/6 | chr14 | 32087834 | |||||||
| chr14:32087844 | C | T | 2 | a0001c0001t0002g0121 a0001c0001t0002g0122 |
2 | NA19060.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.-168-2658C>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 1/6 | chr14 | 32087844 | |||||||
| chr14:32088094 | T | C | 6 | a0001c0001t0001g0166 a0001c0001t0007g0003 a0001c0001t0007g0164 others(3): Show |
6 | HG01884.hp2 HG02055.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.-168-2408T>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 1/6 | chr14 | 32088094 | |||||||
| chr14:32088297 | C | T | 1 | a0001c0001t0001g0002 | 2 | HG02965.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-168-2205C>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 1/6 | chr14 | 32088297 | |||||||
| chr14:32088604 | G | A | 5 | a0001c0001t0001g0166 a0001c0001t0007g0003 a0001c0001t0007g0164 others(2): Show |
5 | HG02055.hp1 HG03041.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.-168-1898G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 1/6 | chr14 | 32088604 | |||||||
| chr14:32088871 | T | C | 5 | a0001c0001t0001g0166 a0001c0001t0007g0003 a0001c0001t0007g0164 others(2): Show |
5 | HG02055.hp1 HG03041.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.-168-1631T>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 1/6 | chr14 | 32088871 | |||||||
| chr14:32088961 | A | G | 1 | a0001c0001t0001g0120 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-168-1541A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 1/6 | chr14 | 32088961 | |||||||
| chr14:32088980 | G | T | 1 | a0001c0018t0023g0181 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-168-1522G>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 1/6 | chr14 | 32088980 | |||||||
| chr14:32089005 | A | C | 5 | a0001c0002t0005g0004 a0001c0002t0005g0167 a0001c0002t0005g0168 others(2): Show |
6 | HG01243.hp1 HG02258.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.-168-1497A>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 1/6 | chr14 | 32089005 | |||||||
| chr14:32089128 | GAATA | G | 2 | a0001c0001t0001g0012 a0001c0001t0001g0013 |
2 | NA18987.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.-168-1370_-168-136 others(8): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | 32089128 | ||||||
| chr14:32089230 | A | G | 5 | a0001c0002t0005g0004 a0001c0002t0005g0167 a0001c0002t0005g0168 others(2): Show |
6 | HG01243.hp1 HG02258.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.-168-1272A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 1/6 | chr14 | 32089230 | |||||||
| chr14:32089448 | C | T | 12 | a0001c0001t0001g0166 a0001c0001t0007g0003 a0001c0001t0007g0164 others(9): Show |
13 | HG01243.hp1 HG01884.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.-168-1054C>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 1/6 | chr14 | 32089448 | |||||||
| chr14:32089545 | T | C | 13 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0040 others(10): Show |
13 | HG00597.hp1 HG00609.hp1 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.-168-957T>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 1/6 | chr14 | 32089545 | |||||||
| chr14:32089696 | G | A | 19 | a0001c0001t0001g0166 a0001c0001t0003g0144 a0001c0001t0003g0148 others(16): Show |
20 | HG01243.hp1 HG01884.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.-168-806G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 1/6 | chr14 | 32089696 | |||||||
| chr14:32089717 | G | A | 5 | a0001c0001t0001g0166 a0001c0001t0007g0003 a0001c0001t0007g0164 others(2): Show |
5 | HG02055.hp1 HG03041.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.-168-785G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 1/6 | chr14 | 32089717 | |||||||
| chr14:32090014 | T | C | 1 | a0001c0001t0001g0042 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-168-488T>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 1/6 | chr14 | 32090014 | |||||||
| chr14:32090116 | G | A | 1 | a0001c0001t0014g0170 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-168-386G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 1/6 | chr14 | 32090116 | |||||||
| chr14:32090152 | C | T | 5 | a0001c0001t0001g0166 a0001c0001t0007g0003 a0001c0001t0007g0164 others(2): Show |
5 | HG02055.hp1 HG03041.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.-168-350C>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 1/6 | chr14 | 32090152 | |||||||
| chr14:32094395 | A | C | 1 | a0001c0001t0001g0134 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.3717+9A>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32094395 | |||||||
| chr14:32094434 | A | G | 174 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(171): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.3717+48A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32094434 | |||||||
| chr14:32094442 | A | C | 1 | a0001c0001t0011g0119 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.3717+56A>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32094442 | |||||||
| chr14:32094724 | G | A | 1 | a0001c0018t0023g0181 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3717+338G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32094724 | |||||||
| chr14:32095366 | G | A | 5 | a0001c0001t0001g0166 a0001c0001t0007g0003 a0001c0001t0007g0164 others(2): Show |
5 | HG02055.hp1 HG03041.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.3717+980G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32095366 | |||||||
| chr14:32095401 | GT | G | 5 | a0001c0001t0001g0166 a0001c0001t0007g0003 a0001c0001t0007g0164 others(2): Show |
5 | HG02055.hp1 HG03041.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.3717+1029delT | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr14 | 32095401 | ||||||
| chr14:32095412 | T | TG | 4 | a0001c0002t0005g0004 a0001c0002t0005g0167 a0001c0002t0005g0168 others(1): Show |
5 | HG01243.hp1 HG02258.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.3717+1026_3717+102 others(5): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32095412 | |||||||
| chr14:32095414 | T | G | 1 | a0001c0001t0001g0175 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.3717+1028T>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32095414 | |||||||
| chr14:32095416 | G | GTT | 4 | a0001c0002t0005g0004 a0001c0002t0005g0167 a0001c0002t0005g0168 others(1): Show |
5 | HG01243.hp1 HG02258.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.3717+1042_3717+104 others(6): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr14 | 32095416 | ||||||
| chr14:32095416 | G | T | 1 | a0001c0018t0023g0181 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3717+1030G>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32095416 | |||||||
| chr14:32095423 | T | G | 1 | a0001c0001t0020g0051 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.3717+1037T>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32095423 | |||||||
| chr14:32095467 | T | C | 13 | a0001c0001t0001g0166 a0001c0001t0007g0003 a0001c0001t0007g0164 others(10): Show |
14 | HG00609.hp2 HG01243.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.3717+1081T>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32095467 | |||||||
| chr14:32095578 | T | C | 1 | a0014c0008t0001g0130 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3717+1192T>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32095578 | |||||||
| chr14:32095593 | A | G | 1 | a0001c0001t0001g0042 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.3717+1207A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32095593 | |||||||
| chr14:32096083 | T | C | 1 | a0001c0001t0002g0011 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.3717+1697T>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32096083 | |||||||
| chr14:32096107 | G | A | 1 | a0001c0001t0017g0123 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.3717+1721G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32096107 | |||||||
| chr14:32096110 | C | T | 1 | a0010c0017t0016g0005 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3717+1724C>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32096110 | |||||||
| chr14:32096141 | GT | G | 4 | a0001c0002t0005g0004 a0001c0002t0005g0167 a0001c0002t0005g0168 others(1): Show |
5 | HG01243.hp1 HG02258.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.3717+1766delT | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr14 | 32096141 | ||||||
| chr14:32096554 | G | A | 5 | a0001c0001t0007g0003 a0001c0001t0007g0164 a0001c0001t0007g0165 others(2): Show |
5 | HG02717.hp2 HG03041.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.3717+2168G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32096554 | |||||||
| chr14:32096562 | A | G | 2 | a0001c0001t0001g0117 a0001c0001t0001g0118 |
2 | HG03540.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.3717+2176A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32096562 | |||||||
| chr14:32096614 | T | C | 1 | a0001c0018t0023g0181 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3717+2228T>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32096614 | |||||||
| chr14:32097044 | A | G | 3 | a0001c0001t0002g0116 a0001c0001t0002g0121 a0001c0001t0002g0122 |
3 | HG02165.hp1 NA19060.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.3717+2658A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32097044 | |||||||
| chr14:32097127 | T | A | 1 | a0001c0001t0003g0163 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.3717+2741T>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32097127 | |||||||
| chr14:32097167 | A | G | 34 | a0001c0001t0001g0099 a0001c0001t0001g0105 a0001c0001t0001g0106 others(31): Show |
34 | HG00735.hp2 HG01071.hp1 HG01099.hp1 others(31): Show |
intron_variant | MODIFIER | c.3717+2781A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32097167 | |||||||
| chr14:32097244 | T | G | 6 | a0001c0001t0003g0144 a0001c0001t0003g0148 a0001c0001t0003g0160 others(3): Show |
6 | HG02280.hp2 HG02572.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.3717+2858T>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32097244 | |||||||
| chr14:32097376 | G | A | 3 | a0001c0001t0007g0003 a0001c0001t0007g0165 a0001c0001t0022g0003 |
3 | HG03041.hp2 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.3717+2990G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32097376 | |||||||
| chr14:32097650 | C | T | 6 | a0001c0002t0005g0004 a0001c0002t0005g0167 a0001c0002t0005g0168 others(3): Show |
7 | HG01243.hp1 HG02258.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.3717+3264C>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32097650 | |||||||
| chr14:32097969 | A | G | 1 | a0001c0018t0023g0181 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3717+3583A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32097969 | |||||||
| chr14:32098310 | G | C | 1 | a0001c0018t0023g0181 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3717+3924G>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32098310 | |||||||
| chr14:32098528 | A | G | 1 | a0001c0001t0001g0098 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3717+4142A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32098528 | |||||||
| chr14:32098580 | A | G | 1 | a0001c0018t0023g0181 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3717+4194A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32098580 | |||||||
| chr14:32098588 | T | C | 6 | a0001c0002t0005g0004 a0001c0002t0005g0167 a0001c0002t0005g0168 others(3): Show |
7 | HG00609.hp2 HG01243.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.3717+4202T>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32098588 | |||||||
| chr14:32098612 | G | C | 6 | a0001c0001t0001g0150 a0001c0001t0003g0160 a0001c0001t0003g0161 others(3): Show |
6 | HG01109.hp2 HG02559.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.3717+4226G>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32098612 | |||||||
| chr14:32098686 | A | C | 3 | a0001c0001t0003g0160 a0001c0001t0003g0161 a0001c0001t0003g0162 |
3 | HG03471.hp2 HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.3717+4300A>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32098686 | |||||||
| chr14:32098801 | A | G | 35 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0032 others(32): Show |
35 | HG00099.hp1 HG00099.hp2 HG00597.hp2 others(32): Show |
intron_variant | MODIFIER | c.3717+4415A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32098801 | |||||||
| chr14:32098810 | G | A | 1 | a0001c0001t0001g0006 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3717+4424G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32098810 | |||||||
| chr14:32098978 | G | A | 1 | a0001c0001t0003g0161 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3717+4592G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32098978 | |||||||
| chr14:32099029 | C | T | 31 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0075 others(28): Show |
32 | HG01243.hp1 HG01884.hp2 HG02055.hp1 others(29): Show |
intron_variant | MODIFIER | c.3717+4643C>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32099029 | |||||||
| chr14:32099054 | C | T | 2 | a0001c0001t0001g0117 a0001c0001t0001g0118 |
2 | HG03540.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.3717+4668C>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32099054 | |||||||
| chr14:32099105 | T | C | 1 | a0001c0001t0021g0010 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.3717+4719T>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32099105 | |||||||
| chr14:32099269 | T | C | 1 | a0001c0001t0001g0127 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3717+4883T>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32099269 | |||||||
| chr14:32099649 | A | T | 16 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0075 others(13): Show |
16 | HG02055.hp1 HG02145.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.3717+5263A>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32099649 | |||||||
| chr14:32099756 | G | A | 1 | a0001c0001t0001g0008 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3717+5370G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32099756 | |||||||
| chr14:32099806 | C | G | 1 | a0001c0001t0001g0158 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.3717+5420C>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32099806 | |||||||
| chr14:32099950 | T | C | 1 | a0001c0001t0001g0052 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.3717+5564T>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32099950 | |||||||
| chr14:32100025 | A | C | 2 | a0001c0001t0001g0001 a0001c0001t0001g0016 |
3 | HG01099.hp2 HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.3717+5639A>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32100025 | |||||||
| chr14:32100116 | G | A | 1 | a0001c0001t0001g0133 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3717+5730G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32100116 | |||||||
| chr14:32100523 | G | A | 1 | a0001c0001t0001g0152 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.3717+6137G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32100523 | |||||||
| chr14:32100539 | C | T | 1 | a0001c0001t0003g0163 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.3717+6153C>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32100539 | |||||||
| chr14:32101031 | T | C | 3 | a0003c0003t0001g0145 a0003c0003t0001g0147 a0003c0003t0019g0146 |
3 | HG02965.hp1 HG03098.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.3717+6645T>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32101031 | |||||||
| chr14:32101208 | C | T | 3 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 |
3 | HG00597.hp2 HG00621.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.3717+6822C>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32101208 | |||||||
| chr14:32101605 | CA | C | 4 | a0001c0001t0004g0174 a0001c0001t0004g0177 a0001c0019t0001g0179 others(1): Show |
4 | HG01169.hp2 HG01192.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.3717+7220delA | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32101605 | |||||||
| chr14:32101606 | A | G | 7 | a0001c0001t0001g0150 a0001c0001t0003g0144 a0001c0001t0003g0148 others(4): Show |
7 | HG01109.hp2 HG02280.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.3717+7220A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32101606 | |||||||
| chr14:32101652 | C | CA | 11 | a0001c0001t0001g0150 a0001c0001t0003g0144 a0001c0001t0003g0148 others(8): Show |
11 | HG00609.hp2 HG01109.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.3717+7281dupA | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr14 | 32101652 | ||||||
| chr14:32101811 | C | A | 4 | a0001c0001t0001g0133 a0001c0012t0027g0131 a0008c0015t0024g0132 others(1): Show |
4 | HG02257.hp2 HG02886.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.3717+7425C>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32101811 | |||||||
| chr14:32101944 | C | T | 5 | a0001c0002t0005g0004 a0001c0002t0005g0167 a0001c0002t0005g0168 others(2): Show |
6 | HG01243.hp1 HG02258.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.3717+7558C>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32101944 | |||||||
| chr14:32102097 | G | A | 1 | a0001c0001t0001g0042 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.3717+7711G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32102097 | |||||||
| chr14:32102131 | A | G | 4 | a0001c0002t0005g0004 a0001c0002t0005g0167 a0001c0002t0005g0168 others(1): Show |
5 | HG01243.hp1 HG02258.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.3717+7745A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32102131 | |||||||
| chr14:32102202 | T | G | 1 | a0001c0001t0001g0099 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3717+7816T>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32102202 | |||||||
| chr14:32102347 | A | G | 1 | a0001c0001t0001g0120 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.3717+7961A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32102347 | |||||||
| chr14:32102895 | T | C | 6 | a0001c0002t0005g0004 a0001c0002t0005g0167 a0001c0002t0005g0168 others(3): Show |
7 | HG00609.hp2 HG01243.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.3717+8509T>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32102895 | |||||||
| chr14:32102956 | G | A | 3 | a0001c0001t0003g0160 a0001c0001t0003g0161 a0001c0001t0003g0162 |
3 | HG03471.hp2 HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.3717+8570G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32102956 | |||||||
| chr14:32103192 | T | C | 1 | a0001c0018t0023g0181 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3717+8806T>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32103192 | |||||||
| chr14:32103314 | T | G | 1 | a0001c0001t0001g0012 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.3717+8928T>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32103314 | |||||||
| chr14:32103416 | A | G | 1 | a0001c0001t0014g0170 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3717+9030A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32103416 | |||||||
| chr14:32103505 | G | A | 5 | a0001c0001t0001g0166 a0001c0001t0007g0003 a0001c0001t0007g0164 others(2): Show |
5 | HG02055.hp1 HG03041.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.3717+9119G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32103505 | |||||||
| chr14:32103699 | G | GT | 8 | a0001c0001t0001g0150 a0001c0001t0003g0144 a0001c0001t0003g0148 others(5): Show |
8 | HG01109.hp2 HG02280.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.3717+9319dupT | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr14 | 32103699 | ||||||
| chr14:32104699 | G | T | 5 | a0001c0001t0001g0166 a0001c0001t0007g0003 a0001c0001t0007g0164 others(2): Show |
5 | HG02055.hp1 HG03041.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.3717+10313G>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32104699 | |||||||
| chr14:32105060 | T | C | 2 | a0001c0001t0001g0073 a0011c0006t0001g0072 |
2 | HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.3717+10674T>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32105060 | |||||||
| chr14:32105113 | G | A | 1 | a0001c0001t0001g0152 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.3717+10727G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32105113 | |||||||
| chr14:32105362 | G | A | 4 | a0001c0002t0005g0004 a0001c0002t0005g0167 a0001c0002t0005g0168 others(1): Show |
5 | HG01243.hp1 HG02258.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.3717+10976G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32105362 | |||||||
| chr14:32105487 | T | A | 7 | a0001c0001t0003g0144 a0001c0001t0003g0148 a0001c0001t0003g0160 others(4): Show |
7 | HG01169.hp2 HG02280.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.3717+11101T>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32105487 | |||||||
| chr14:32105487 | T | TA | 4 | a0001c0002t0005g0004 a0001c0002t0005g0167 a0001c0002t0005g0168 others(1): Show |
5 | HG01243.hp1 HG02258.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.3717+11101_3717+11 others(7): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32105487 | |||||||
| chr14:32105488 | T | A | 160 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(157): Show |
163 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.3717+11102T>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32105488 | |||||||
| chr14:32105489 | A | T | 4 | a0001c0001t0001g0071 a0003c0003t0001g0145 a0003c0003t0001g0147 others(1): Show |
4 | HG02965.hp1 HG03098.hp1 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.3717+11103A>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32105489 | |||||||
| chr14:32106070 | T | G | 3 | a0003c0003t0001g0145 a0003c0003t0001g0147 a0003c0003t0019g0146 |
3 | HG02965.hp1 HG03098.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.3718-11070T>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32106070 | |||||||
| chr14:32106169 | T | C | 1 | a0001c0018t0023g0181 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3718-10971T>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32106169 | |||||||
| chr14:32106182 | C | T | 3 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0149 |
3 | HG02132.hp1 HG03704.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.3718-10958C>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32106182 | |||||||
| chr14:32106211 | T | C | 1 | a0001c0001t0001g0080 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.3718-10929T>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32106211 | |||||||
| chr14:32106264 | A | G | 12 | a0001c0001t0001g0166 a0001c0001t0007g0003 a0001c0001t0007g0164 others(9): Show |
13 | HG01243.hp1 HG01884.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.3718-10876A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32106264 | |||||||
| chr14:32106410 | C | T | 5 | a0001c0002t0005g0004 a0001c0002t0005g0167 a0001c0002t0005g0168 others(2): Show |
6 | HG01243.hp1 HG02258.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.3718-10730C>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32106410 | |||||||
| chr14:32106649 | C | T | 5 | a0001c0001t0003g0160 a0001c0001t0003g0161 a0001c0001t0003g0162 others(2): Show |
5 | HG02559.hp1 HG02572.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.3718-10491C>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32106649 | |||||||
| chr14:32106685 | C | T | 1 | a0001c0001t0001g0153 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.3718-10455C>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32106685 | |||||||
| chr14:32106794 | T | G | 3 | a0003c0003t0001g0145 a0003c0003t0001g0147 a0003c0003t0019g0146 |
3 | HG02965.hp1 HG03098.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.3718-10346T>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32106794 | |||||||
| chr14:32107030 | A | G | 3 | a0003c0003t0001g0145 a0003c0003t0001g0147 a0003c0003t0019g0146 |
3 | HG02965.hp1 HG03098.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.3718-10110A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32107030 | |||||||
| chr14:32107436 | T | TA | 16 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0075 others(13): Show |
16 | HG02055.hp1 HG02145.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.3718-9703dupA | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr14 | 32107436 | ||||||
| chr14:32107460 | G | C | 16 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0075 others(13): Show |
16 | HG02055.hp1 HG02145.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.3718-9680G>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32107460 | |||||||
| chr14:32108099 | C | A | 4 | a0001c0001t0007g0003 a0001c0001t0007g0164 a0001c0001t0007g0165 others(1): Show |
4 | HG03041.hp2 HG03453.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.3718-9041C>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32108099 | |||||||
| chr14:32108117 | C | T | 1 | a0001c0001t0001g0092 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.3718-9023C>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32108117 | |||||||
| chr14:32108277 | G | C | 1 | a0010c0017t0016g0005 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3718-8863G>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32108277 | |||||||
| chr14:32108408 | AAG | A | 6 | a0001c0001t0001g0099 a0001c0001t0001g0113 a0001c0001t0001g0114 others(3): Show |
6 | HG02055.hp2 HG02257.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.3718-8727_3718-872 others(6): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr14 | 32108408 | ||||||
| chr14:32108586 | C | T | 1 | a0001c0001t0001g0008 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3718-8554C>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32108586 | |||||||
| chr14:32108873 | G | A | 1 | a0001c0001t0014g0170 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3718-8267G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32108873 | |||||||
| chr14:32108891 | A | G | 4 | a0001c0001t0007g0003 a0001c0001t0007g0164 a0001c0001t0007g0165 others(1): Show |
4 | HG03041.hp2 HG03453.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.3718-8249A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32108891 | |||||||
| chr14:32109037 | T | C | 1 | a0001c0001t0001g0052 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.3718-8103T>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32109037 | |||||||
| chr14:32109040 | C | T | 5 | a0001c0001t0001g0150 a0001c0001t0003g0160 a0001c0001t0003g0161 others(2): Show |
5 | HG01109.hp2 HG02572.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.3718-8100C>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32109040 | |||||||
| chr14:32109111 | A | G | 6 | a0001c0001t0001g0150 a0001c0001t0003g0160 a0001c0001t0003g0161 others(3): Show |
6 | HG01109.hp2 HG02559.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.3718-8029A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32109111 | |||||||
| chr14:32109117 | A | G | 4 | a0001c0002t0005g0004 a0001c0002t0005g0167 a0001c0002t0005g0168 others(1): Show |
5 | HG01243.hp1 HG02258.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.3718-8023A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32109117 | |||||||
| chr14:32109333 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3718-7807C>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32109333 | |||||||
| chr14:32109396 | C | T | 1 | a0001c0001t0001g0153 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.3718-7744C>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32109396 | |||||||
| chr14:32109752 | A | T | 1 | a0001c0001t0001g0070 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.3718-7388A>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32109752 | |||||||
| chr14:32109853 | G | C | 1 | a0001c0001t0001g0053 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.3718-7287G>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32109853 | |||||||
| chr14:32109975 | A | G | 7 | a0001c0001t0001g0150 a0001c0001t0003g0160 a0001c0001t0003g0161 others(4): Show |
7 | HG01109.hp2 HG01884.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.3718-7165A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32109975 | |||||||
| chr14:32110062 | A | T | 2 | a0001c0001t0001g0117 a0001c0001t0001g0118 |
2 | HG03540.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.3718-7078A>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32110062 | |||||||
| chr14:32110158 | G | A | 1 | a0001c0001t0001g0021 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.3718-6982G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32110158 | |||||||
| chr14:32110209 | T | TA | 19 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0076 others(16): Show |
19 | HG01192.hp1 HG01192.hp2 HG01358.hp2 others(16): Show |
intron_variant | MODIFIER | c.3718-6917dupA | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr14 | 32110209 | ||||||
| chr14:32110209 | T | TAA | 5 | a0001c0002t0005g0004 a0001c0002t0005g0167 a0001c0002t0005g0168 others(2): Show |
6 | HG01243.hp1 HG02258.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.3718-6918_3718-691 others(6): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr14 | 32110209 | ||||||
| chr14:32110583 | AAATTAGG others(9): Show |
A | 1 | a0010c0017t0016g0005 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3718-6554_3718-653 others(20): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr14 | 32110583 | ||||||
| chr14:32110625 | G | A | 1 | a0010c0017t0016g0005 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3718-6515G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32110625 | |||||||
| chr14:32110625 | G | C | 1 | a0001c0001t0001g0081 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.3718-6515G>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32110625 | |||||||
| chr14:32110637 | C | T | 5 | a0001c0001t0001g0166 a0001c0001t0007g0003 a0001c0001t0007g0164 others(2): Show |
5 | HG02055.hp1 HG03041.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.3718-6503C>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32110637 | |||||||
| chr14:32110728 | A | C | 1 | a0001c0018t0023g0181 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3718-6412A>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32110728 | |||||||
| chr14:32111827 | G | A | 1 | a0001c0012t0027g0131 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3718-5313G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32111827 | |||||||
| chr14:32111839 | A | AT | 24 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0063 others(21): Show |
25 | HG00609.hp2 HG01109.hp2 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.3718-5278dupT | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr14 | 32111839 | ||||||
| chr14:32111839 | AT | A | 53 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(50): Show |
54 | HG00140.hp2 HG00609.hp1 HG00673.hp1 others(51): Show |
intron_variant | MODIFIER | c.3718-5278delT | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr14 | 32111839 | ||||||
| chr14:32111878 | T | G | 4 | a0001c0002t0005g0004 a0001c0002t0005g0167 a0001c0002t0005g0168 others(1): Show |
5 | HG01243.hp1 HG02258.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.3718-5262T>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32111878 | |||||||
| chr14:32111959 | C | T | 1 | a0001c0001t0014g0170 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3718-5181C>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32111959 | |||||||
| chr14:32112398 | C | T | 1 | a0001c0001t0001g0042 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.3718-4742C>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32112398 | |||||||
| chr14:32112423 | T | C | 1 | a0001c0001t0001g0015 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.3718-4717T>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32112423 | |||||||
| chr14:32112449 | G | A | 5 | a0001c0001t0003g0160 a0001c0001t0003g0161 a0001c0001t0003g0162 others(2): Show |
5 | HG02559.hp1 HG02572.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.3718-4691G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32112449 | |||||||
| chr14:32112524 | G | A | 1 | a0001c0018t0023g0181 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3718-4616G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32112524 | |||||||
| chr14:32112670 | A | C | 1 | a0001c0001t0001g0149 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.3718-4470A>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32112670 | |||||||
| chr14:32112815 | G | A | 1 | a0001c0018t0023g0181 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3718-4325G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32112815 | |||||||
| chr14:32113354 | A | C | 1 | a0001c0001t0014g0170 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3718-3786A>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32113354 | |||||||
| chr14:32113535 | G | T | 1 | a0001c0001t0006g0107 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.3718-3605G>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32113535 | |||||||
| chr14:32113674 | A | T | 1 | a0001c0018t0023g0181 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3718-3466A>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32113674 | |||||||
| chr14:32113994 | C | T | 1 | a0001c0001t0002g0138 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.3718-3146C>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32113994 | |||||||
| chr14:32114153 | A | G | 1 | a0001c0001t0001g0030 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.3718-2987A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32114153 | |||||||
| chr14:32114192 | C | T | 22 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0075 others(19): Show |
23 | HG01243.hp1 HG01884.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.3718-2948C>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32114192 | |||||||
| chr14:32114227 | C | CA | 5 | a0001c0001t0001g0021 a0001c0001t0003g0162 a0001c0001t0006g0155 others(2): Show |
5 | HG01258.hp1 HG01884.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.3718-2899dupA | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr14 | 32114227 | ||||||
| chr14:32114227 | C | CAA | 21 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0075 others(18): Show |
22 | HG01243.hp1 HG02055.hp1 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.3718-2900_3718-289 others(6): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr14 | 32114227 | ||||||
| chr14:32114258 | CTCTTT | C | 3 | a0003c0003t0001g0145 a0003c0003t0001g0147 a0003c0003t0019g0146 |
3 | HG02965.hp1 HG03098.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.3718-2880_3718-287 others(9): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr14 | 32114258 | ||||||
| chr14:32114272 | C | T | 1 | a0001c0018t0023g0181 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3718-2868C>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32114272 | |||||||
| chr14:32114545 | C | T | 3 | a0003c0003t0001g0145 a0003c0003t0001g0147 a0003c0003t0019g0146 |
3 | HG02965.hp1 HG03098.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.3718-2595C>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32114545 | |||||||
| chr14:32114624 | A | G | 1 | a0001c0001t0001g0059 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.3718-2516A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32114624 | |||||||
| chr14:32114940 | A | G | 1 | a0010c0017t0016g0005 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3718-2200A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32114940 | |||||||
| chr14:32115131 | T | C | 7 | a0001c0001t0001g0052 a0001c0001t0001g0060 a0001c0001t0001g0065 others(4): Show |
7 | HG00621.hp1 HG02132.hp2 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.3718-2009T>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32115131 | |||||||
| chr14:32115139 | T | C | 1 | a0001c0001t0014g0170 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3718-2001T>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32115139 | |||||||
| chr14:32115465 | T | C | 21 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(18): Show |
22 | HG00099.hp2 HG00140.hp2 HG00735.hp1 others(19): Show |
intron_variant | MODIFIER | c.3718-1675T>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32115465 | |||||||
| chr14:32115634 | C | T | 1 | a0001c0001t0006g0107 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.3718-1506C>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32115634 | |||||||
| chr14:32115663 | C | CA | 17 | a0001c0001t0001g0018 a0001c0001t0001g0063 a0001c0001t0001g0067 others(14): Show |
17 | HG00140.hp1 HG00609.hp2 HG01192.hp2 others(14): Show |
intron_variant | MODIFIER | c.3718-1456dupA | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr14 | 32115663 | ||||||
| chr14:32115663 | C | CAA | 8 | a0001c0001t0001g0038 a0001c0001t0001g0095 a0001c0001t0001g0096 others(5): Show |
8 | HG00597.hp1 HG00597.hp2 HG00621.hp2 others(5): Show |
intron_variant | MODIFIER | c.3718-1457_3718-145 others(6): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr14 | 32115663 | ||||||
| chr14:32115815 | C | CA | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(162): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.3718-1312dupA | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr14 | 32115815 | ||||||
| chr14:32115815 | C | CAA | 13 | a0001c0001t0001g0035 a0001c0001t0001g0150 a0001c0001t0001g0158 others(10): Show |
13 | HG00609.hp2 HG01109.hp2 HG01167.hp2 others(10): Show |
intron_variant | MODIFIER | c.3718-1313_3718-131 others(6): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr14 | 32115815 | ||||||
| chr14:32115852 | T | C | 24 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0075 others(21): Show |
25 | HG00609.hp2 HG01243.hp1 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.3718-1288T>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32115852 | |||||||
| chr14:32115977 | A | G | 1 | a0001c0001t0001g0035 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.3718-1163A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32115977 | |||||||
| chr14:32116112 | C | A | 1 | a0008c0015t0024g0132 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3718-1028C>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32116112 | |||||||
| chr14:32116244 | G | A | 1 | a0001c0001t0001g0092 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.3718-896G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32116244 | |||||||
| chr14:32116266 | G | C | 1 | a0010c0017t0016g0005 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3718-874G>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32116266 | |||||||
| chr14:32116340 | C | G | 2 | a0001c0001t0006g0154 a0001c0001t0006g0155 |
2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.3718-800C>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32116340 | |||||||
| chr14:32116510 | G | T | 1 | a0001c0018t0023g0181 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3718-630G>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32116510 | |||||||
| chr14:32116548 | G | A | 4 | a0001c0001t0007g0003 a0001c0001t0007g0164 a0001c0001t0007g0165 others(1): Show |
4 | HG03041.hp2 HG03453.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.3718-592G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32116548 | |||||||
| chr14:32116561 | C | G | 1 | a0001c0001t0014g0170 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3718-579C>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32116561 | |||||||
| chr14:32116578 | G | A | 1 | a0001c0001t0001g0099 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3718-562G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32116578 | |||||||
| chr14:32116637 | C | T | 12 | a0001c0001t0007g0003 a0001c0001t0007g0164 a0001c0001t0007g0165 others(9): Show |
13 | HG00609.hp2 HG01243.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.3718-503C>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32116637 | |||||||
| chr14:32116788 | A | C | 1 | a0001c0001t0021g0010 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.3718-352A>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32116788 | |||||||
| chr14:32116921 | T | C | 20 | a0001c0001t0001g0150 a0001c0001t0003g0144 a0001c0001t0003g0148 others(17): Show |
21 | HG00609.hp2 HG01109.hp2 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.3718-219T>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32116921 | |||||||
| chr14:32117024 | A | C | 4 | a0001c0002t0005g0004 a0001c0002t0005g0167 a0001c0002t0005g0168 others(1): Show |
5 | HG01243.hp1 HG02258.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.3718-116A>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32117024 | |||||||
| chr14:32117054 | T | C | 1 | a0001c0001t0014g0170 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3718-86T>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32117054 | |||||||
| chr14:32117065 | G | A | 1 | a0001c0012t0027g0131 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3718-75G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32117065 | |||||||
| chr14:32117097 | A | G | 4 | a0001c0001t0007g0003 a0001c0001t0007g0164 a0001c0001t0007g0165 others(1): Show |
4 | HG03041.hp2 HG03453.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.3718-43A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32117097 | |||||||
| chr14:32117136 | A | G | 1 | a0001c0001t0001g0166 | 1 | HG02055.hp1 | splice_region_variant&intron_variant | LOW | c.3718-4A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 2/6 | chr14 | 32117136 | |||||||
| chr14:32117382 | T | C | 1 | a0001c0001t0014g0170 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3865+95T>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32117382 | |||||||
| chr14:32117385 | C | G | 1 | a0001c0001t0021g0010 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.3865+98C>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32117385 | |||||||
| chr14:32117664 | C | T | 4 | a0001c0001t0007g0003 a0001c0001t0007g0164 a0001c0001t0007g0165 others(1): Show |
4 | HG03041.hp2 HG03453.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.3865+377C>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32117664 | |||||||
| chr14:32117708 | C | T | 1 | a0001c0001t0001g0166 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3865+421C>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32117708 | |||||||
| chr14:32117947 | C | CTTAACCA others(10): Show |
8 | a0001c0001t0007g0003 a0001c0001t0007g0164 a0001c0001t0007g0165 others(5): Show |
9 | HG01243.hp1 HG02258.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.3865+660_3865+661i others(19): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32117947 | |||||||
| chr14:32117948 | G | A | 8 | a0001c0001t0007g0003 a0001c0001t0007g0164 a0001c0001t0007g0165 others(5): Show |
9 | HG01243.hp1 HG02258.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.3865+661G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32117948 | |||||||
| chr14:32118094 | G | A | 8 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0076 others(5): Show |
8 | HG02145.hp1 HG02451.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.3865+807G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32118094 | |||||||
| chr14:32118234 | C | T | 3 | a0003c0003t0001g0145 a0003c0003t0001g0147 a0003c0003t0019g0146 |
3 | HG02965.hp1 HG03098.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.3865+947C>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32118234 | |||||||
| chr14:32118345 | A | G | 1 | a0001c0001t0002g0141 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.3865+1058A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32118345 | |||||||
| chr14:32118355 | G | T | 4 | a0001c0002t0005g0004 a0001c0002t0005g0167 a0001c0002t0005g0168 others(1): Show |
5 | HG01243.hp1 HG02258.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.3865+1068G>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32118355 | |||||||
| chr14:32118427 | G | C | 2 | a0001c0001t0001g0117 a0001c0001t0001g0118 |
2 | HG03540.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.3865+1140G>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32118427 | |||||||
| chr14:32118508 | G | A | 13 | a0001c0001t0001g0052 a0001c0001t0001g0060 a0001c0001t0001g0065 others(10): Show |
13 | HG00140.hp1 HG00621.hp1 HG00639.hp1 others(10): Show |
intron_variant | MODIFIER | c.3865+1221G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32118508 | |||||||
| chr14:32119578 | AT | A | 22 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0075 others(19): Show |
23 | HG01243.hp1 HG01884.hp2 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.3865+2293delT | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 32119578 | ||||||
| chr14:32119887 | A | G | 1 | a0001c0019t0001g0179 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.3865+2600A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32119887 | |||||||
| chr14:32119945 | G | A | 20 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0075 others(17): Show |
21 | HG01243.hp1 HG02145.hp1 HG02258.hp2 others(18): Show |
intron_variant | MODIFIER | c.3865+2658G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32119945 | |||||||
| chr14:32120048 | T | G | 1 | a0010c0017t0016g0005 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3865+2761T>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32120048 | |||||||
| chr14:32120133 | T | G | 177 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(174): Show |
180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.3865+2846T>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32120133 | |||||||
| chr14:32120457 | A | G | 4 | a0001c0002t0005g0004 a0001c0002t0005g0167 a0001c0002t0005g0168 others(1): Show |
5 | HG01243.hp1 HG02258.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.3865+3170A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32120457 | |||||||
| chr14:32120479 | T | C | 7 | a0001c0001t0001g0150 a0001c0001t0003g0160 a0001c0001t0003g0161 others(4): Show |
7 | HG01109.hp2 HG01884.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.3865+3192T>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32120479 | |||||||
| chr14:32120547 | G | T | 1 | a0001c0001t0007g0164 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3865+3260G>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32120547 | |||||||
| chr14:32120607 | CT | C | 23 | a0001c0001t0001g0022 a0001c0001t0001g0073 a0001c0001t0001g0074 others(20): Show |
24 | HG01070.hp1 HG01243.hp1 HG02145.hp1 others(21): Show |
intron_variant | MODIFIER | c.3865+3334delT | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 32120607 | ||||||
| chr14:32120681 | T | G | 1 | a0001c0001t0001g0134 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.3865+3394T>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32120681 | |||||||
| chr14:32120993 | A | G | 9 | a0001c0001t0001g0150 a0001c0001t0003g0144 a0001c0001t0003g0148 others(6): Show |
9 | HG01109.hp2 HG01884.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.3865+3706A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32120993 | |||||||
| chr14:32121013 | C | CT | 143 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(140): Show |
145 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(142): Show |
intron_variant | MODIFIER | c.3865+3746dupT | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 32121013 | ||||||
| chr14:32121013 | C | CTT | 20 | a0001c0001t0001g0012 a0001c0001t0001g0020 a0001c0001t0001g0028 others(17): Show |
21 | HG00735.hp1 HG01192.hp2 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.3865+3745_3865+374 others(6): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 32121013 | ||||||
| chr14:32121025 | T | TTA | 12 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0075 others(9): Show |
12 | HG02145.hp1 HG02451.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.3865+3739_3865+374 others(6): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 32121025 | ||||||
| chr14:32121084 | T | C | 31 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0075 others(28): Show |
32 | HG00609.hp2 HG01109.hp2 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.3865+3797T>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32121084 | |||||||
| chr14:32121096 | C | T | 1 | a0001c0001t0001g0058 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.3865+3809C>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32121096 | |||||||
| chr14:32121098 | A | G | 4 | a0001c0001t0002g0116 a0001c0001t0002g0121 a0001c0001t0002g0122 others(1): Show |
4 | HG02165.hp1 NA18971.hp1 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.3865+3811A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32121098 | |||||||
| chr14:32121222 | C | G | 30 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0075 others(27): Show |
31 | HG00609.hp2 HG01243.hp1 HG01884.hp2 others(28): Show |
intron_variant | MODIFIER | c.3865+3935C>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32121222 | |||||||
| chr14:32121223 | G | A | 1 | a0001c0001t0001g0095 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.3865+3936G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32121223 | |||||||
| chr14:32121380 | G | A | 1 | a0001c0001t0014g0170 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3865+4093G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32121380 | |||||||
| chr14:32121948 | G | A | 1 | a0010c0017t0016g0005 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3865+4661G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32121948 | |||||||
| chr14:32122009 | T | G | 23 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0075 others(20): Show |
24 | HG00609.hp2 HG01243.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.3865+4722T>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32122009 | |||||||
| chr14:32122170 | A | C | 15 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0075 others(12): Show |
15 | HG02145.hp1 HG02451.hp1 HG02717.hp1 others(12): Show |
intron_variant | MODIFIER | c.3865+4883A>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32122170 | |||||||
| chr14:32122413 | A | G | 1 | a0001c0010t0025g0151 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3865+5126A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32122413 | |||||||
| chr14:32122416 | T | G | 1 | a0014c0008t0001g0130 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3865+5129T>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32122416 | |||||||
| chr14:32122469 | C | T | 1 | a0001c0001t0001g0042 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.3865+5182C>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32122469 | |||||||
| chr14:32122521 | A | G | 1 | a0004c0014t0015g0159 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.3865+5234A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32122521 | |||||||
| chr14:32122635 | C | T | 2 | a0001c0001t0001g0067 a0009c0009t0003g0172 |
2 | HG00140.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.3865+5348C>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32122635 | |||||||
| chr14:32122822 | A | G | 1 | a0001c0001t0001g0106 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.3865+5535A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32122822 | |||||||
| chr14:32122994 | T | G | 7 | a0001c0001t0003g0144 a0001c0001t0003g0148 a0001c0001t0003g0160 others(4): Show |
7 | HG02280.hp2 HG02559.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.3865+5707T>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32122994 | |||||||
| chr14:32123258 | G | A | 23 | a0001c0001t0002g0011 a0001c0001t0002g0017 a0001c0001t0002g0039 others(20): Show |
23 | HG00735.hp2 HG01071.hp1 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.3865+5971G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32123258 | |||||||
| chr14:32123266 | A | G | 1 | a0001c0001t0001g0142 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3865+5979A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32123266 | |||||||
| chr14:32123349 | A | G | 1 | a0001c0018t0023g0181 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3865+6062A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32123349 | |||||||
| chr14:32123582 | GCTT | G | 2 | a0004c0014t0015g0159 a0010c0017t0016g0005 |
2 | HG00609.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.3865+6299_3865+630 others(7): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 32123582 | ||||||
| chr14:32123695 | C | T | 1 | a0010c0017t0016g0005 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3865+6408C>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32123695 | |||||||
| chr14:32123884 | C | G | 1 | a0001c0001t0002g0111 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.3865+6597C>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32123884 | |||||||
| chr14:32124031 | G | C | 3 | a0001c0001t0002g0011 a0001c0001t0002g0124 a0001c0001t0002g0125 |
3 | HG01192.hp1 HG01358.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.3865+6744G>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32124031 | |||||||
| chr14:32124041 | C | T | 11 | a0001c0001t0007g0003 a0001c0001t0007g0164 a0001c0001t0007g0165 others(8): Show |
12 | HG00609.hp2 HG01243.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.3865+6754C>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32124041 | |||||||
| chr14:32124062 | C | T | 4 | a0001c0001t0007g0003 a0001c0001t0007g0164 a0001c0001t0007g0165 others(1): Show |
4 | HG03041.hp2 HG03453.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.3865+6775C>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32124062 | |||||||
| chr14:32124218 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3865+6931C>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32124218 | |||||||
| chr14:32124252 | G | A | 2 | a0004c0014t0015g0159 a0010c0017t0016g0005 |
2 | HG00609.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.3865+6965G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32124252 | |||||||
| chr14:32124581 | G | A | 1 | a0001c0001t0001g0071 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.3865+7294G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32124581 | |||||||
| chr14:32124708 | C | T | 1 | a0005c0013t0018g0062 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.3865+7421C>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32124708 | |||||||
| chr14:32124710 | G | A | 4 | a0001c0002t0005g0004 a0001c0002t0005g0167 a0001c0002t0005g0168 others(1): Show |
5 | HG01243.hp1 HG02258.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.3865+7423G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32124710 | |||||||
| chr14:32124869 | T | C | 4 | a0001c0002t0005g0004 a0001c0002t0005g0167 a0001c0002t0005g0168 others(1): Show |
5 | HG01243.hp1 HG02258.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.3865+7582T>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32124869 | |||||||
| chr14:32124902 | T | A | 3 | a0001c0001t0002g0043 a0001c0001t0002g0044 a0001c0001t0002g0045 |
3 | HG01243.hp2 HG02683.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.3865+7615T>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32124902 | |||||||
| chr14:32125037 | C | T | 1 | a0001c0001t0002g0111 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.3865+7750C>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32125037 | |||||||
| chr14:32125384 | T | C | 1 | a0001c0001t0001g0068 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.3865+8097T>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32125384 | |||||||
| chr14:32125480 | A | G | 1 | a0001c0001t0001g0025 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.3865+8193A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32125480 | |||||||
| chr14:32125507 | A | G | 1 | a0001c0001t0004g0174 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.3865+8220A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32125507 | |||||||
| chr14:32126218 | G | A | 2 | a0001c0001t0001g0014 a0001c0001t0001g0092 |
2 | NA18612.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.3865+8931G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32126218 | |||||||
| chr14:32126222 | G | GT | 56 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0031 others(53): Show |
57 | HG00099.hp1 HG00099.hp2 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.3865+8943dupT | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 32126222 | ||||||
| chr14:32126270 | A | G | 1 | a0001c0001t0001g0097 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.3865+8983A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32126270 | |||||||
| chr14:32126467 | A | G | 8 | a0001c0001t0007g0003 a0001c0001t0007g0164 a0001c0001t0007g0165 others(5): Show |
9 | HG01243.hp1 HG02258.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.3865+9180A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32126467 | |||||||
| chr14:32126545 | G | A | 1 | a0001c0001t0001g0105 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.3865+9258G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32126545 | |||||||
| chr14:32126794 | T | A | 11 | a0001c0001t0002g0011 a0001c0001t0002g0100 a0001c0001t0002g0101 others(8): Show |
11 | HG00735.hp2 HG01071.hp1 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.3865+9507T>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32126794 | |||||||
| chr14:32126998 | CTT | C | 9 | a0001c0001t0007g0003 a0001c0001t0007g0164 a0001c0001t0007g0165 others(6): Show |
10 | HG01243.hp1 HG02258.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.3865+9727_3865+972 others(6): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 32126998 | ||||||
| chr14:32127031 | T | C | 4 | a0001c0002t0005g0004 a0001c0002t0005g0167 a0001c0002t0005g0168 others(1): Show |
5 | HG01243.hp1 HG02258.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.3865+9744T>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32127031 | |||||||
| chr14:32127046 | G | A | 1 | a0001c0001t0001g0175 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.3865+9759G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32127046 | |||||||
| chr14:32127063 | T | C | 3 | a0001c0001t0007g0003 a0001c0001t0007g0165 a0001c0001t0022g0003 |
3 | HG03041.hp2 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.3865+9776T>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32127063 | |||||||
| chr14:32127163 | G | A | 20 | a0001c0001t0003g0160 a0001c0001t0003g0161 a0001c0001t0003g0162 others(17): Show |
21 | HG00609.hp2 HG01243.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.3865+9876G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32127163 | |||||||
| chr14:32127164 | A | T | 1 | a0001c0001t0001g0112 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.3865+9877A>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32127164 | |||||||
| chr14:32127277 | A | G | 3 | a0001c0001t0003g0160 a0001c0001t0003g0161 a0001c0001t0003g0162 |
3 | HG03471.hp2 HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.3865+9990A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32127277 | |||||||
| chr14:32127443 | T | C | 5 | a0001c0001t0002g0104 a0001c0001t0006g0107 a0001c0001t0006g0154 others(2): Show |
5 | HG01099.hp1 HG01257.hp2 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.3865+10156T>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32127443 | |||||||
| chr14:32127649 | G | A | 1 | a0010c0017t0016g0005 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3865+10362G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32127649 | |||||||
| chr14:32127655 | G | A | 54 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0031 others(51): Show |
55 | HG00099.hp1 HG00099.hp2 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.3865+10368G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32127655 | |||||||
| chr14:32127675 | A | G | 1 | a0001c0018t0023g0181 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3865+10388A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32127675 | |||||||
| chr14:32127701 | C | CG | 6 | a0001c0001t0001g0012 a0001c0001t0001g0036 a0001c0001t0001g0054 others(3): Show |
6 | HG00673.hp1 HG00673.hp2 HG01109.hp2 others(3): Show |
intron_variant | MODIFIER | c.3865+10418dupG | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 32127701 | ||||||
| chr14:32127741 | C | A | 3 | a0001c0001t0001g0080 a0001c0001t0001g0083 a0001c0001t0001g0084 |
3 | HG00099.hp1 HG01258.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.3865+10454C>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32127741 | |||||||
| chr14:32127774 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.3865+10487C>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32127774 | |||||||
| chr14:32127775 | G | C | 12 | a0001c0001t0007g0003 a0001c0001t0007g0164 a0001c0001t0007g0165 others(9): Show |
13 | HG00609.hp2 HG01243.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.3865+10488G>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32127775 | |||||||
| chr14:32127784 | C | T | 2 | a0004c0014t0015g0159 a0010c0017t0016g0005 |
2 | HG00609.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.3865+10497C>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32127784 | |||||||
| chr14:32127786 | G | A | 1 | a0001c0001t0001g0087 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.3865+10499G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32127786 | |||||||
| chr14:32127892 | G | A | 35 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(32): Show |
36 | HG00140.hp1 HG00140.hp2 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.3865+10605G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32127892 | |||||||
| chr14:32127915 | C | G | 35 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(32): Show |
36 | HG00140.hp1 HG00140.hp2 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.3865+10628C>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32127915 | |||||||
| chr14:32127966 | C | CG | 8 | a0001c0001t0001g0012 a0001c0001t0001g0128 a0001c0001t0001g0150 others(5): Show |
8 | HG01099.hp1 HG01109.hp1 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.3865+10683dupG | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 32127966 | ||||||
| chr14:32127966 | C | T | 1 | a0001c0001t0020g0051 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.3865+10679C>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32127966 | |||||||
| chr14:32127979 | G | A | 4 | a0001c0001t0007g0003 a0001c0001t0007g0164 a0001c0001t0007g0165 others(1): Show |
4 | HG03041.hp2 HG03453.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.3865+10692G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32127979 | |||||||
| chr14:32128006 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3865+10719C>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32128006 | |||||||
| chr14:32128047 | A | G | 12 | a0001c0001t0007g0003 a0001c0001t0007g0164 a0001c0001t0007g0165 others(9): Show |
13 | HG00609.hp2 HG01243.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.3865+10760A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32128047 | |||||||
| chr14:32128051 | C | T | 2 | a0001c0001t0001g0002 a0001c0001t0001g0063 |
3 | HG02145.hp2 HG02965.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.3865+10764C>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32128051 | |||||||
| chr14:32128172 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.3865+10885G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32128172 | |||||||
| chr14:32128209 | A | G | 12 | a0001c0001t0007g0003 a0001c0001t0007g0164 a0001c0001t0007g0165 others(9): Show |
13 | HG00609.hp2 HG01243.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.3865+10922A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32128209 | |||||||
| chr14:32128236 | C | T | 1 | a0004c0014t0015g0159 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.3865+10949C>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32128236 | |||||||
| chr14:32128243 | T | C | 22 | a0001c0001t0003g0144 a0001c0001t0003g0148 a0001c0001t0003g0160 others(19): Show |
23 | HG00609.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.3865+10956T>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32128243 | |||||||
| chr14:32128382 | A | G | 22 | a0001c0001t0003g0144 a0001c0001t0003g0148 a0001c0001t0003g0160 others(19): Show |
23 | HG00609.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.3865+11095A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32128382 | |||||||
| chr14:32128459 | G | A | 2 | a0001c0001t0001g0095 a0001c0001t0001g0097 |
2 | HG00597.hp2 HG00621.hp2 |
intron_variant | MODIFIER | c.3865+11172G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32128459 | |||||||
| chr14:32128630 | C | T | 4 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0128 others(1): Show |
5 | HG01099.hp2 HG01167.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.3865+11343C>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32128630 | |||||||
| chr14:32128668 | G | T | 1 | a0001c0018t0023g0181 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3865+11381G>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32128668 | |||||||
| chr14:32128790 | T | C | 1 | a0001c0001t0014g0170 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3865+11503T>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32128790 | |||||||
| chr14:32128797 | A | G | 7 | a0001c0001t0007g0003 a0001c0001t0007g0164 a0001c0001t0007g0165 others(4): Show |
7 | HG02965.hp1 HG03041.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.3865+11510A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32128797 | |||||||
| chr14:32128887 | G | C | 5 | a0001c0001t0003g0160 a0001c0001t0003g0161 a0001c0001t0003g0162 others(2): Show |
5 | HG02559.hp1 HG02572.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.3865+11600G>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32128887 | |||||||
| chr14:32129097 | A | C | 5 | a0001c0001t0001g0060 a0001c0001t0001g0065 a0001c0001t0001g0066 others(2): Show |
5 | HG00621.hp1 HG02132.hp2 HG02165.hp2 others(2): Show |
intron_variant | MODIFIER | c.3865+11810A>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32129097 | |||||||
| chr14:32129158 | G | A | 1 | a0007c0011t0001g0026 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.3865+11871G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32129158 | |||||||
| chr14:32129172 | G | A | 1 | a0004c0014t0015g0159 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.3865+11885G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32129172 | |||||||
| chr14:32129183 | T | C | 177 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(174): Show |
180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.3865+11896T>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32129183 | |||||||
| chr14:32129212 | T | C | 1 | a0001c0018t0023g0181 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3865+11925T>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32129212 | |||||||
| chr14:32129280 | T | C | 2 | a0004c0014t0015g0159 a0010c0017t0016g0005 |
2 | HG00609.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.3865+11993T>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32129280 | |||||||
| chr14:32129435 | C | T | 1 | a0001c0001t0001g0058 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.3865+12148C>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32129435 | |||||||
| chr14:32129878 | A | G | 14 | a0001c0001t0001g0150 a0001c0001t0003g0144 a0001c0001t0003g0148 others(11): Show |
15 | HG01109.hp2 HG01243.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.3865+12591A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32129878 | |||||||
| chr14:32129919 | T | A | 1 | a0001c0001t0002g0043 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.3865+12632T>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32129919 | |||||||
| chr14:32129965 | C | T | 1 | a0001c0001t0010g0034 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3865+12678C>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32129965 | |||||||
| chr14:32129992 | A | G | 4 | a0001c0002t0005g0004 a0001c0002t0005g0167 a0001c0002t0005g0168 others(1): Show |
5 | HG01243.hp1 HG02258.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.3865+12705A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32129992 | |||||||
| chr14:32130004 | A | G | 3 | a0001c0001t0001g0091 a0001c0001t0001g0156 a0001c0001t0001g0157 |
3 | HG02559.hp2 HG02622.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.3865+12717A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32130004 | |||||||
| chr14:32130104 | A | G | 2 | a0004c0014t0015g0159 a0010c0017t0016g0005 |
2 | HG00609.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.3865+12817A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32130104 | |||||||
| chr14:32130123 | A | G | 3 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 |
3 | HG03130.hp2 HG03516.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.3865+12836A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32130123 | |||||||
| chr14:32130209 | A | AT | 7 | a0001c0001t0001g0006 a0001c0001t0001g0041 a0001c0001t0001g0050 others(4): Show |
7 | HG01167.hp2 HG01515.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.3865+12942dupT | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 32130209 | ||||||
| chr14:32130209 | AT | A | 19 | a0001c0001t0001g0028 a0001c0001t0001g0083 a0001c0001t0001g0087 others(16): Show |
20 | HG00609.hp2 HG00639.hp2 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.3865+12942delT | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 32130209 | ||||||
| chr14:32130387 | G | GT | 6 | a0001c0001t0001g0021 a0001c0002t0005g0004 a0001c0002t0005g0167 others(3): Show |
7 | HG01243.hp1 HG02258.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.3865+13115dupT | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 32130387 | ||||||
| chr14:32130389 | T | TC | 5 | a0001c0001t0001g0150 a0001c0001t0003g0161 a0001c0001t0003g0162 others(2): Show |
5 | HG01109.hp2 HG02559.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.3865+13102_3865+13 others(7): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32130389 | |||||||
| chr14:32130525 | C | CATTG | 10 | a0001c0002t0005g0004 a0001c0002t0005g0167 a0001c0002t0005g0168 others(7): Show |
11 | HG00609.hp2 HG01243.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.3865+13266_3865+13 others(10): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 32130525 | ||||||
| chr14:32130525 | CATTGATT others(1): Show |
C | 6 | a0001c0001t0001g0150 a0001c0001t0003g0160 a0001c0001t0003g0161 others(3): Show |
6 | HG01109.hp2 HG02559.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.3865+13262_3865+13 others(14): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 32130525 | ||||||
| chr14:32130547 | T | C | 2 | a0001c0001t0001g0128 a0001c0001t0001g0129 |
2 | HG03492.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.3865+13260T>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32130547 | |||||||
| chr14:32130720 | A | G | 8 | a0001c0001t0007g0003 a0001c0001t0007g0164 a0001c0001t0007g0165 others(5): Show |
9 | HG01243.hp1 HG02258.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.3865+13433A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32130720 | |||||||
| chr14:32130796 | G | T | 19 | a0001c0001t0002g0011 a0001c0001t0002g0017 a0001c0001t0002g0039 others(16): Show |
19 | HG00735.hp2 HG01071.hp1 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.3865+13509G>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32130796 | |||||||
| chr14:32130894 | G | T | 4 | a0001c0001t0007g0003 a0001c0001t0007g0164 a0001c0001t0007g0165 others(1): Show |
4 | HG03041.hp2 HG03453.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.3865+13607G>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32130894 | |||||||
| chr14:32131144 | C | G | 1 | a0001c0010t0025g0151 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3865+13857C>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32131144 | |||||||
| chr14:32131229 | G | A | 4 | a0001c0001t0007g0003 a0001c0001t0007g0164 a0001c0001t0007g0165 others(1): Show |
4 | HG03041.hp2 HG03453.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.3865+13942G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32131229 | |||||||
| chr14:32131252 | CT | C | 23 | a0001c0001t0001g0120 a0001c0001t0001g0150 a0001c0001t0002g0044 others(20): Show |
24 | HG00609.hp2 HG01109.hp2 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.3865+13982delT | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 32131252 | ||||||
| chr14:32131278 | CTTTAT | C | 2 | a0004c0014t0015g0159 a0010c0017t0016g0005 |
2 | HG00609.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.3865+14005_3865+14 others(11): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 32131278 | ||||||
| chr14:32131297 | T | A | 1 | a0001c0001t0001g0088 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.3865+14010T>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32131297 | |||||||
| chr14:32131385 | T | C | 6 | a0001c0001t0001g0150 a0001c0001t0003g0160 a0001c0001t0003g0161 others(3): Show |
6 | HG01109.hp2 HG02559.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.3865+14098T>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32131385 | |||||||
| chr14:32131546 | A | G | 2 | a0001c0001t0001g0012 a0001c0001t0001g0013 |
2 | NA18987.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.3865+14259A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32131546 | |||||||
| chr14:32131553 | TTTTG | T | 8 | a0001c0001t0001g0032 a0001c0001t0001g0099 a0001c0001t0001g0113 others(5): Show |
8 | HG01255.hp1 HG02055.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.3865+14278_3865+14 others(10): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 32131553 | ||||||
| chr14:32131627 | A | G | 1 | a0001c0001t0001g0012 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.3865+14340A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32131627 | |||||||
| chr14:32131679 | A | C | 2 | a0004c0014t0015g0159 a0010c0017t0016g0005 |
2 | HG00609.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.3865+14392A>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32131679 | |||||||
| chr14:32131758 | C | T | 1 | a0001c0001t0011g0119 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.3865+14471C>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32131758 | |||||||
| chr14:32131808 | C | A | 2 | a0001c0001t0006g0154 a0001c0001t0006g0155 |
2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.3866-14455C>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32131808 | |||||||
| chr14:32131817 | G | C | 4 | a0001c0002t0005g0004 a0001c0002t0005g0167 a0001c0002t0005g0168 others(1): Show |
5 | HG01243.hp1 HG02258.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.3866-14446G>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32131817 | |||||||
| chr14:32131979 | T | C | 2 | a0001c0001t0001g0113 a0001c0001t0001g0114 |
2 | HG02055.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.3866-14284T>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32131979 | |||||||
| chr14:32132034 | G | A | 2 | a0004c0014t0015g0159 a0010c0017t0016g0005 |
2 | HG00609.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.3866-14229G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32132034 | |||||||
| chr14:32132036 | A | T | 4 | a0001c0001t0007g0003 a0001c0001t0007g0164 a0001c0001t0007g0165 others(1): Show |
4 | HG03041.hp2 HG03453.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.3866-14227A>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32132036 | |||||||
| chr14:32132053 | A | G | 1 | a0001c0001t0001g0025 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.3866-14210A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32132053 | |||||||
| chr14:32132172 | A | T | 1 | a0001c0001t0001g0073 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3866-14091A>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32132172 | |||||||
| chr14:32132173 | A | C | 1 | a0001c0001t0001g0073 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3866-14090A>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32132173 | |||||||
| chr14:32132176 | G | A | 1 | a0001c0001t0001g0073 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3866-14087G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32132176 | |||||||
| chr14:32132177 | T | A | 1 | a0001c0001t0001g0073 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3866-14086T>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32132177 | |||||||
| chr14:32132178 | T | A | 1 | a0001c0001t0001g0073 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3866-14085T>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32132178 | |||||||
| chr14:32132179 | G | C | 1 | a0001c0001t0001g0073 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3866-14084G>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32132179 | |||||||
| chr14:32132439 | A | T | 8 | a0001c0001t0001g0057 a0001c0001t0001g0059 a0001c0001t0001g0060 others(5): Show |
8 | HG00621.hp1 HG02132.hp2 HG02155.hp2 others(5): Show |
intron_variant | MODIFIER | c.3866-13824A>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32132439 | |||||||
| chr14:32132644 | A | T | 1 | a0001c0001t0020g0051 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.3866-13619A>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32132644 | |||||||
| chr14:32132702 | G | A | 1 | a0001c0001t0001g0025 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.3866-13561G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32132702 | |||||||
| chr14:32132708 | T | TA | 21 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(18): Show |
22 | HG00099.hp2 HG00140.hp2 HG00735.hp1 others(19): Show |
intron_variant | MODIFIER | c.3866-13554dupA | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 32132708 | ||||||
| chr14:32132752 | T | G | 5 | a0001c0001t0001g0060 a0001c0001t0001g0065 a0001c0001t0001g0066 others(2): Show |
5 | HG00621.hp1 HG02132.hp2 HG02165.hp2 others(2): Show |
intron_variant | MODIFIER | c.3866-13511T>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32132752 | |||||||
| chr14:32132762 | G | A | 11 | a0001c0001t0007g0003 a0001c0001t0007g0164 a0001c0001t0007g0165 others(8): Show |
12 | HG00609.hp2 HG01243.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.3866-13501G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32132762 | |||||||
| chr14:32132857 | G | T | 1 | a0004c0014t0015g0159 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.3866-13406G>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32132857 | |||||||
| chr14:32133183 | G | A | 8 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0004g0174 others(5): Show |
8 | HG01169.hp2 HG01192.hp2 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.3866-13080G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32133183 | |||||||
| chr14:32133194 | G | A | 1 | a0001c0001t0001g0166 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3866-13069G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32133194 | |||||||
| chr14:32133199 | T | C | 1 | a0001c0001t0001g0096 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.3866-13064T>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32133199 | |||||||
| chr14:32133221 | T | C | 1 | a0001c0012t0027g0131 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3866-13042T>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32133221 | |||||||
| chr14:32133238 | T | G | 4 | a0001c0002t0005g0004 a0001c0002t0005g0167 a0001c0002t0005g0168 others(1): Show |
5 | HG01243.hp1 HG02258.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.3866-13025T>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32133238 | |||||||
| chr14:32133245 | A | G | 1 | a0001c0012t0027g0131 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3866-13018A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32133245 | |||||||
| chr14:32133256 | T | C | 2 | a0001c0001t0001g0073 a0001c0001t0001g0098 |
2 | HG02717.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.3866-13007T>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32133256 | |||||||
| chr14:32133260 | C | G | 1 | a0001c0012t0027g0131 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3866-13003C>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32133260 | |||||||
| chr14:32133390 | A | G | 4 | a0001c0002t0005g0004 a0001c0002t0005g0167 a0001c0002t0005g0168 others(1): Show |
5 | HG01243.hp1 HG02258.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.3866-12873A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32133390 | |||||||
| chr14:32133402 | G | A | 1 | a0001c0001t0014g0170 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3866-12861G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32133402 | |||||||
| chr14:32133460 | A | G | 5 | a0001c0002t0005g0004 a0001c0002t0005g0167 a0001c0002t0005g0168 others(2): Show |
6 | HG01243.hp1 HG02258.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.3866-12803A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32133460 | |||||||
| chr14:32133662 | G | A | 4 | a0001c0002t0005g0004 a0001c0002t0005g0167 a0001c0002t0005g0168 others(1): Show |
5 | HG01243.hp1 HG02258.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.3866-12601G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32133662 | |||||||
| chr14:32133682 | C | T | 2 | a0001c0001t0001g0068 a0001c0001t0001g0071 |
2 | HG02698.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.3866-12581C>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32133682 | |||||||
| chr14:32133903 | T | G | 1 | a0001c0001t0017g0123 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.3866-12360T>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32133903 | |||||||
| chr14:32133908 | C | A | 3 | a0002c0004t0001g0135 a0002c0004t0001g0136 a0002c0004t0001g0137 |
3 | HG02145.hp1 HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.3866-12355C>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32133908 | |||||||
| chr14:32133910 | G | C | 1 | a0001c0001t0002g0100 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.3866-12353G>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32133910 | |||||||
| chr14:32134003 | G | A | 1 | a0001c0001t0014g0170 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3866-12260G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32134003 | |||||||
| chr14:32134234 | C | T | 1 | a0010c0017t0016g0005 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3866-12029C>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32134234 | |||||||
| chr14:32134329 | C | T | 1 | a0001c0001t0003g0163 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.3866-11934C>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32134329 | |||||||
| chr14:32134453 | G | A | 1 | a0001c0001t0014g0170 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3866-11810G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32134453 | |||||||
| chr14:32134788 | T | C | 1 | a0001c0001t0001g0126 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.3866-11475T>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32134788 | |||||||
| chr14:32134811 | A | G | 9 | a0001c0001t0001g0150 a0001c0001t0003g0144 a0001c0001t0003g0148 others(6): Show |
9 | HG01109.hp2 HG01884.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.3866-11452A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32134811 | |||||||
| chr14:32134885 | G | A | 8 | a0001c0001t0007g0003 a0001c0001t0007g0164 a0001c0001t0007g0165 others(5): Show |
9 | HG01243.hp1 HG02258.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.3866-11378G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32134885 | |||||||
| chr14:32134889 | A | G | 1 | a0001c0001t0002g0011 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.3866-11374A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32134889 | |||||||
| chr14:32134933 | T | C | 2 | a0001c0001t0001g0105 a0001c0001t0004g0061 |
2 | HG02280.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.3866-11330T>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32134933 | |||||||
| chr14:32134993 | ATCTG | A | 8 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0004g0174 others(5): Show |
8 | HG01169.hp2 HG01192.hp2 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.3866-11266_3866-11 others(10): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 32134993 | ||||||
| chr14:32135051 | C | G | 4 | a0001c0002t0005g0004 a0001c0002t0005g0167 a0001c0002t0005g0168 others(1): Show |
5 | HG01243.hp1 HG02258.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.3866-11212C>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32135051 | |||||||
| chr14:32135059 | G | A | 8 | a0001c0001t0007g0003 a0001c0001t0007g0164 a0001c0001t0007g0165 others(5): Show |
9 | HG01243.hp1 HG02258.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.3866-11204G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32135059 | |||||||
| chr14:32135432 | T | C | 8 | a0001c0001t0001g0150 a0001c0001t0003g0144 a0001c0001t0003g0148 others(5): Show |
8 | HG01109.hp2 HG02280.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.3866-10831T>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32135432 | |||||||
| chr14:32135461 | T | A | 3 | a0003c0003t0001g0145 a0003c0003t0001g0147 a0003c0003t0019g0146 |
3 | HG02965.hp1 HG03098.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.3866-10802T>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32135461 | |||||||
| chr14:32135563 | C | G | 54 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0013 others(51): Show |
54 | HG00597.hp1 HG00609.hp1 HG00673.hp1 others(51): Show |
intron_variant | MODIFIER | c.3866-10700C>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32135563 | |||||||
| chr14:32136013 | A | C | 1 | a0001c0001t0001g0031 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.3866-10250A>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32136013 | |||||||
| chr14:32136085 | T | C | 2 | a0004c0014t0015g0159 a0010c0017t0016g0005 |
2 | HG00609.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.3866-10178T>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32136085 | |||||||
| chr14:32136497 | G | T | 12 | a0001c0001t0007g0003 a0001c0001t0007g0164 a0001c0001t0007g0165 others(9): Show |
13 | HG00609.hp2 HG01243.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.3866-9766G>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32136497 | |||||||
| chr14:32136533 | A | G | 8 | a0001c0001t0007g0003 a0001c0001t0007g0164 a0001c0001t0007g0165 others(5): Show |
9 | HG01243.hp1 HG02258.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.3866-9730A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32136533 | |||||||
| chr14:32136690 | T | A | 1 | a0001c0001t0001g0115 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3866-9573T>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32136690 | |||||||
| chr14:32136713 | A | G | 1 | a0010c0017t0016g0005 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3866-9550A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32136713 | |||||||
| chr14:32136789 | T | C | 1 | a0001c0001t0001g0070 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.3866-9474T>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32136789 | |||||||
| chr14:32136905 | T | G | 1 | a0004c0014t0015g0159 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.3866-9358T>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32136905 | |||||||
| chr14:32137182 | T | A | 4 | a0001c0002t0005g0004 a0001c0002t0005g0167 a0001c0002t0005g0168 others(1): Show |
5 | HG01243.hp1 HG02258.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.3866-9081T>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32137182 | |||||||
| chr14:32137273 | G | A | 3 | a0003c0003t0001g0145 a0003c0003t0001g0147 a0003c0003t0019g0146 |
3 | HG02965.hp1 HG03098.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.3866-8990G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32137273 | |||||||
| chr14:32137308 | C | G | 1 | a0010c0017t0016g0005 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3866-8955C>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32137308 | |||||||
| chr14:32137308 | C | T | 1 | a0001c0001t0026g0079 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.3866-8955C>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32137308 | |||||||
| chr14:32137533 | A | T | 11 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0075 others(8): Show |
11 | HG02145.hp1 HG02451.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.3866-8730A>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32137533 | |||||||
| chr14:32137678 | A | G | 3 | a0001c0001t0007g0003 a0001c0001t0007g0165 a0001c0001t0022g0003 |
3 | HG03041.hp2 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.3866-8585A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32137678 | |||||||
| chr14:32137791 | A | G | 1 | a0001c0018t0023g0181 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3866-8472A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32137791 | |||||||
| chr14:32137908 | G | A | 1 | a0001c0018t0023g0181 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3866-8355G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32137908 | |||||||
| chr14:32137971 | C | CA | 18 | a0001c0001t0001g0036 a0001c0001t0001g0052 a0001c0001t0001g0060 others(15): Show |
18 | HG00621.hp1 HG00639.hp1 HG01361.hp1 others(15): Show |
intron_variant | MODIFIER | c.3866-8272dupA | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 32137971 | ||||||
| chr14:32137996 | A | G | 20 | a0001c0001t0001g0150 a0001c0001t0003g0144 a0001c0001t0003g0148 others(17): Show |
21 | HG00609.hp2 HG01109.hp2 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.3866-8267A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32137996 | |||||||
| chr14:32138006 | C | T | 1 | a0001c0001t0002g0043 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.3866-8257C>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32138006 | |||||||
| chr14:32138155 | TTTTTCTT others(114): Show |
T | 1 | a0001c0001t0001g0057 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.3866-8104_3866-798 others(4): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 32138155 | ||||||
| chr14:32138442 | C | T | 1 | a0004c0014t0015g0159 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.3866-7821C>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32138442 | |||||||
| chr14:32138452 | T | A | 1 | a0001c0001t0012g0055 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.3866-7811T>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32138452 | |||||||
| chr14:32138531 | G | A | 1 | a0001c0001t0001g0024 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.3866-7732G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32138531 | |||||||
| chr14:32138759 | C | T | 1 | a0001c0001t0004g0174 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.3866-7504C>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32138759 | |||||||
| chr14:32138928 | G | C | 1 | a0010c0017t0016g0005 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3866-7335G>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32138928 | |||||||
| chr14:32139211 | A | G | 15 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0075 others(12): Show |
15 | HG02145.hp1 HG02257.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.3866-7052A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32139211 | |||||||
| chr14:32139587 | C | G | 1 | a0001c0001t0001g0115 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3866-6676C>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32139587 | |||||||
| chr14:32139712 | A | C | 18 | a0001c0001t0001g0150 a0001c0001t0003g0144 a0001c0001t0003g0148 others(15): Show |
19 | HG01109.hp2 HG01243.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.3866-6551A>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32139712 | |||||||
| chr14:32139726 | C | A | 4 | a0001c0001t0007g0003 a0001c0001t0007g0164 a0001c0001t0007g0165 others(1): Show |
4 | HG03041.hp2 HG03453.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.3866-6537C>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32139726 | |||||||
| chr14:32139736 | G | C | 1 | a0001c0001t0002g0111 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.3866-6527G>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32139736 | |||||||
| chr14:32140062 | C | T | 1 | a0001c0001t0001g0029 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.3866-6201C>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32140062 | |||||||
| chr14:32140066 | C | CT | 32 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0037 others(29): Show |
33 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.3866-6179dupT | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 32140066 | ||||||
| chr14:32140066 | CT | C | 5 | a0001c0001t0003g0144 a0001c0001t0007g0003 a0001c0001t0007g0164 others(2): Show |
5 | HG03041.hp1 HG03041.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.3866-6179delT | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 32140066 | ||||||
| chr14:32140068 | T | C | 2 | a0001c0001t0001g0153 a0001c0001t0001g0158 |
2 | HG01167.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.3866-6195T>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32140068 | |||||||
| chr14:32140069 | T | C | 4 | a0001c0001t0007g0003 a0001c0001t0007g0164 a0001c0001t0007g0165 others(1): Show |
4 | HG03041.hp2 HG03453.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.3866-6194T>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32140069 | |||||||
| chr14:32140097 | CT | C | 8 | a0001c0001t0001g0057 a0001c0001t0001g0059 a0001c0001t0001g0087 others(5): Show |
8 | HG00099.hp2 HG00639.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.3866-6150delT | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 32140097 | ||||||
| chr14:32140112 | TTC | T | 5 | a0001c0001t0007g0003 a0001c0001t0007g0164 a0001c0001t0007g0165 others(2): Show |
5 | HG02809.hp1 HG03041.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.3866-6150_3866-614 others(6): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32140112 | |||||||
| chr14:32140114 | C | T | 5 | a0001c0002t0005g0004 a0001c0002t0005g0167 a0001c0002t0005g0168 others(2): Show |
6 | HG01243.hp1 HG02258.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.3866-6149C>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32140114 | |||||||
| chr14:32140115 | C | CT | 9 | a0001c0001t0001g0093 a0001c0001t0001g0150 a0001c0001t0003g0144 others(6): Show |
9 | HG01109.hp2 HG02280.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.3866-6133dupT | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 32140115 | ||||||
| chr14:32140115 | CT | C | 17 | a0001c0001t0001g0025 a0001c0001t0002g0011 a0001c0001t0002g0100 others(14): Show |
17 | HG00609.hp2 HG00735.hp2 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.3866-6133delT | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 32140115 | ||||||
| chr14:32140116 | T | C | 10 | a0001c0001t0007g0003 a0001c0001t0007g0164 a0001c0001t0007g0165 others(7): Show |
11 | HG01243.hp1 HG02258.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.3866-6147T>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32140116 | |||||||
| chr14:32140238 | G | A | 20 | a0001c0001t0001g0150 a0001c0001t0003g0144 a0001c0001t0003g0148 others(17): Show |
21 | HG00609.hp2 HG01109.hp2 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.3866-6025G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32140238 | |||||||
| chr14:32140251 | A | G | 3 | a0003c0003t0001g0145 a0003c0003t0001g0147 a0003c0003t0019g0146 |
3 | HG02965.hp1 HG03098.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.3866-6012A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32140251 | |||||||
| chr14:32140425 | C | CA | 8 | a0001c0001t0001g0021 a0001c0001t0001g0150 a0001c0001t0003g0144 others(5): Show |
8 | HG01109.hp2 HG02559.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.3866-5826dupA | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 32140425 | ||||||
| chr14:32140425 | CA | C | 48 | a0001c0001t0001g0014 a0001c0001t0001g0033 a0001c0001t0001g0036 others(45): Show |
48 | HG00099.hp1 HG00597.hp2 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.3866-5826delA | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 32140425 | ||||||
| chr14:32140460 | G | A | 2 | a0001c0012t0027g0131 a0008c0015t0024g0132 |
2 | HG02257.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.3866-5803G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32140460 | |||||||
| chr14:32140522 | G | A | 1 | a0001c0001t0007g0164 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3866-5741G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32140522 | |||||||
| chr14:32141099 | A | G | 1 | a0001c0018t0023g0181 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3866-5164A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32141099 | |||||||
| chr14:32141183 | C | G | 1 | a0001c0001t0001g0069 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.3866-5080C>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32141183 | |||||||
| chr14:32141615 | A | G | 8 | a0001c0001t0001g0150 a0001c0001t0003g0144 a0001c0001t0003g0148 others(5): Show |
8 | HG01109.hp2 HG02280.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.3866-4648A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32141615 | |||||||
| chr14:32141727 | A | G | 8 | a0001c0001t0007g0003 a0001c0001t0007g0164 a0001c0001t0007g0165 others(5): Show |
9 | HG01243.hp1 HG02258.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.3866-4536A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32141727 | |||||||
| chr14:32141760 | CAT | C | 2 | a0001c0001t0001g0031 a0001c0001t0001g0088 |
2 | HG02698.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.3866-4501_3866-450 others(6): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 32141760 | ||||||
| chr14:32141868 | G | A | 4 | a0001c0001t0007g0003 a0001c0001t0007g0164 a0001c0001t0007g0165 others(1): Show |
4 | HG03041.hp2 HG03453.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.3866-4395G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32141868 | |||||||
| chr14:32142359 | T | C | 20 | a0001c0001t0001g0150 a0001c0001t0003g0144 a0001c0001t0003g0148 others(17): Show |
21 | HG00609.hp2 HG01109.hp2 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.3866-3904T>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32142359 | |||||||
| chr14:32142527 | C | T | 1 | a0004c0014t0015g0159 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.3866-3736C>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32142527 | |||||||
| chr14:32142558 | C | T | 1 | a0001c0001t0001g0015 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.3866-3705C>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32142558 | |||||||
| chr14:32142617 | C | G | 1 | a0001c0001t0014g0170 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3866-3646C>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32142617 | |||||||
| chr14:32142873 | G | A | 3 | a0003c0003t0001g0145 a0003c0003t0001g0147 a0003c0003t0019g0146 |
3 | HG02965.hp1 HG03098.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.3866-3390G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32142873 | |||||||
| chr14:32142913 | T | C | 4 | a0001c0002t0005g0004 a0001c0002t0005g0167 a0001c0002t0005g0168 others(1): Show |
5 | HG01243.hp1 HG02258.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.3866-3350T>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32142913 | |||||||
| chr14:32143043 | A | G | 1 | a0001c0018t0023g0181 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3866-3220A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32143043 | |||||||
| chr14:32143085 | A | G | 1 | a0001c0001t0001g0133 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3866-3178A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32143085 | |||||||
| chr14:32143181 | A | G | 1 | a0004c0014t0015g0159 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.3866-3082A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32143181 | |||||||
| chr14:32143202 | A | AGTT | 79 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(76): Show |
80 | HG00140.hp2 HG00609.hp1 HG00621.hp2 others(77): Show |
intron_variant | MODIFIER | c.3866-3024_3866-302 others(7): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 32143202 | ||||||
| chr14:32143202 | A | AGTTGTT | 31 | a0001c0001t0001g0008 a0001c0001t0001g0032 a0001c0001t0001g0053 others(28): Show |
31 | HG00099.hp1 HG00099.hp2 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.3866-3027_3866-302 others(10): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 32143202 | ||||||
| chr14:32143202 | A | AGTTGTTG others(2): Show |
2 | a0001c0001t0001g0038 a0001c0001t0001g0140 |
2 | HG00597.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.3866-3030_3866-302 others(13): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 32143202 | ||||||
| chr14:32143202 | AGTT | A | 5 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(2): Show |
5 | HG02132.hp1 HG03130.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.3866-3024_3866-302 others(7): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 32143202 | ||||||
| chr14:32143202 | AGTTGTT | A | 3 | a0001c0001t0001g0093 a0001c0001t0001g0157 a0004c0014t0015g0159 |
3 | HG00609.hp2 HG03130.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.3866-3027_3866-302 others(10): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 32143202 | ||||||
| chr14:32143202 | AGTTGTTG others(2): Show |
A | 5 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0003c0003t0001g0145 others(2): Show |
5 | HG02965.hp1 HG03098.hp1 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.3866-3030_3866-302 others(13): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 32143202 | ||||||
| chr14:32143224 | G | A | 1 | a0010c0017t0016g0005 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3866-3039G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32143224 | |||||||
| chr14:32143227 | G | A | 2 | a0001c0018t0023g0181 a0010c0017t0016g0005 |
2 | HG02717.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.3866-3036G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32143227 | |||||||
| chr14:32143227 | G | GTTATTA | 2 | a0001c0001t0003g0161 a0001c0001t0014g0170 |
2 | HG01884.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.3866-3034_3866-303 others(10): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 32143227 | ||||||
| chr14:32143227 | G | GTTATTAT others(14): Show |
1 | a0001c0001t0003g0160 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.3866-3034_3866-303 others(25): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 32143227 | ||||||
| chr14:32143230 | G | A | 5 | a0001c0001t0003g0160 a0001c0001t0003g0161 a0001c0001t0014g0170 others(2): Show |
5 | HG01884.hp2 HG02717.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.3866-3033G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32143230 | |||||||
| chr14:32143230 | G | GTTATTAT others(2): Show |
4 | a0001c0001t0003g0144 a0001c0001t0003g0148 a0001c0001t0003g0162 others(1): Show |
4 | HG02280.hp2 HG02572.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.3866-3031_3866-303 others(13): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 32143230 | ||||||
| chr14:32143233 | G | A | 10 | a0001c0001t0003g0144 a0001c0001t0003g0148 a0001c0001t0003g0160 others(7): Show |
10 | HG00609.hp2 HG01884.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.3866-3030G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32143233 | |||||||
| chr14:32143233 | GTTGTTGT others(2): Show |
G | 2 | a0001c0001t0001g0091 a0001c0001t0001g0156 |
2 | HG02559.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.3866-3027_3866-301 others(13): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 32143233 | ||||||
| chr14:32143236 | G | A | 10 | a0001c0001t0003g0144 a0001c0001t0003g0148 a0001c0001t0003g0160 others(7): Show |
10 | HG00609.hp2 HG01884.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.3866-3027G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32143236 | |||||||
| chr14:32143236 | G | GTTATTAT others(14): Show |
1 | a0001c0001t0003g0163 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.3866-3025_3866-302 others(25): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 32143236 | ||||||
| chr14:32143239 | G | A | 14 | a0001c0001t0003g0144 a0001c0001t0003g0148 a0001c0001t0003g0160 others(11): Show |
15 | HG00609.hp2 HG01243.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.3866-3024G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32143239 | |||||||
| chr14:32143239 | G | GTTATTA | 3 | a0001c0001t0007g0003 a0001c0001t0007g0165 a0001c0001t0022g0003 |
3 | HG03041.hp2 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.3866-3009_3866-300 others(10): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 32143239 | ||||||
| chr14:32143239 | GTTA | G | 5 | a0001c0001t0001g0002 a0001c0001t0001g0028 a0001c0001t0001g0068 others(2): Show |
6 | HG01255.hp2 HG02698.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.3866-3006_3866-300 others(7): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 32143239 | ||||||
| chr14:32143242 | A | G | 54 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(51): Show |
55 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(52): Show |
intron_variant | MODIFIER | c.3866-3021A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32143242 | |||||||
| chr14:32143245 | A | G | 3 | a0001c0001t0001g0009 a0001c0001t0001g0074 a0001c0001t0001g0083 |
3 | HG01516.hp1 HG01975.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.3866-3018A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32143245 | |||||||
| chr14:32143268 | A | G | 1 | a0001c0010t0025g0151 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3866-2995A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32143268 | |||||||
| chr14:32143327 | C | G | 1 | a0001c0001t0014g0170 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3866-2936C>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32143327 | |||||||
| chr14:32143347 | A | G | 1 | a0001c0001t0001g0050 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3866-2916A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32143347 | |||||||
| chr14:32143854 | G | T | 1 | a0001c0001t0014g0170 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3866-2409G>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32143854 | |||||||
| chr14:32143856 | G | A | 1 | a0001c0001t0001g0036 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.3866-2407G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32143856 | |||||||
| chr14:32143984 | A | G | 1 | a0001c0001t0001g0080 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.3866-2279A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32143984 | |||||||
| chr14:32144058 | T | G | 20 | a0001c0001t0001g0150 a0001c0001t0003g0144 a0001c0001t0003g0148 others(17): Show |
21 | HG00609.hp2 HG01109.hp2 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.3866-2205T>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32144058 | |||||||
| chr14:32144060 | C | G | 23 | a0001c0001t0001g0150 a0001c0001t0003g0144 a0001c0001t0003g0148 others(20): Show |
24 | HG00609.hp2 HG01109.hp2 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.3866-2203C>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32144060 | |||||||
| chr14:32144063 | G | C | 1 | a0001c0001t0002g0111 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.3866-2200G>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32144063 | |||||||
| chr14:32144135 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3866-2128C>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32144135 | |||||||
| chr14:32144257 | G | C | 1 | a0001c0001t0002g0116 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.3866-2006G>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32144257 | |||||||
| chr14:32144578 | G | A | 1 | a0001c0001t0014g0170 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3866-1685G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32144578 | |||||||
| chr14:32144591 | C | T | 2 | a0001c0001t0002g0044 a0001c0001t0002g0045 |
2 | HG01243.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.3866-1672C>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32144591 | |||||||
| chr14:32144629 | G | A | 1 | a0001c0001t0003g0163 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.3866-1634G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32144629 | |||||||
| chr14:32144701 | C | T | 1 | a0001c0001t0001g0021 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.3866-1562C>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32144701 | |||||||
| chr14:32144847 | A | T | 12 | a0001c0001t0007g0003 a0001c0001t0007g0164 a0001c0001t0007g0165 others(9): Show |
13 | HG00609.hp2 HG01243.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.3866-1416A>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32144847 | |||||||
| chr14:32144853 | A | C | 4 | a0001c0001t0007g0003 a0001c0001t0007g0164 a0001c0001t0007g0165 others(1): Show |
4 | HG03041.hp2 HG03453.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.3866-1410A>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32144853 | |||||||
| chr14:32145106 | G | A | 1 | a0001c0001t0014g0170 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3866-1157G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32145106 | |||||||
| chr14:32145188 | G | T | 1 | a0001c0001t0001g0150 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.3866-1075G>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32145188 | |||||||
| chr14:32145268 | G | T | 7 | a0001c0001t0001g0099 a0001c0001t0001g0113 a0001c0001t0001g0114 others(4): Show |
7 | HG02055.hp2 HG02257.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.3866-995G>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32145268 | |||||||
| chr14:32145456 | C | CTGT | 22 | a0001c0001t0001g0150 a0001c0001t0003g0144 a0001c0001t0003g0148 others(19): Show |
23 | HG00609.hp2 HG01109.hp2 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.3866-801_3866-799d others(5): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | 32145456 | ||||||
| chr14:32145617 | G | A | 1 | a0001c0001t0009g0171 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.3866-646G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32145617 | |||||||
| chr14:32145644 | G | A | 9 | a0001c0001t0007g0003 a0001c0001t0007g0164 a0001c0001t0007g0165 others(6): Show |
10 | HG01243.hp1 HG02258.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.3866-619G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32145644 | |||||||
| chr14:32145644 | G | T | 1 | a0001c0001t0001g0115 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3866-619G>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32145644 | |||||||
| chr14:32145703 | A | T | 1 | a0010c0017t0016g0005 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3866-560A>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32145703 | |||||||
| chr14:32145956 | T | G | 1 | a0001c0001t0001g0058 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.3866-307T>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32145956 | |||||||
| chr14:32145964 | T | G | 19 | a0001c0001t0001g0150 a0001c0001t0003g0144 a0001c0001t0003g0148 others(16): Show |
20 | HG00609.hp2 HG01109.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.3866-299T>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32145964 | |||||||
| chr14:32146131 | C | G | 1 | a0005c0013t0018g0062 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.3866-132C>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32146131 | |||||||
| chr14:32146681 | G | A | 23 | a0001c0001t0001g0014 a0001c0001t0001g0033 a0001c0001t0001g0036 others(20): Show |
23 | HG00099.hp1 HG00597.hp2 HG00621.hp2 others(20): Show |
intron_variant | MODIFIER | c.3943+341G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 4/6 | chr14 | 32146681 | |||||||
| chr14:32146846 | T | G | 1 | a0004c0014t0015g0159 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.3943+506T>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 4/6 | chr14 | 32146846 | |||||||
| chr14:32146944 | C | T | 9 | a0001c0001t0007g0003 a0001c0001t0007g0164 a0001c0001t0007g0165 others(6): Show |
10 | HG01243.hp1 HG02258.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.3943+604C>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 4/6 | chr14 | 32146944 | |||||||
| chr14:32146963 | C | T | 24 | a0001c0001t0001g0014 a0001c0001t0001g0033 a0001c0001t0001g0036 others(21): Show |
24 | HG00099.hp1 HG00597.hp2 HG00621.hp2 others(21): Show |
intron_variant | MODIFIER | c.3943+623C>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 4/6 | chr14 | 32146963 | |||||||
| chr14:32147067 | T | G | 1 | a0001c0001t0001g0113 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3943+727T>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 4/6 | chr14 | 32147067 | |||||||
| chr14:32147208 | T | C | 4 | a0001c0002t0005g0004 a0001c0002t0005g0167 a0001c0002t0005g0168 others(1): Show |
5 | HG01243.hp1 HG02258.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.3943+868T>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 4/6 | chr14 | 32147208 | |||||||
| chr14:32147737 | A | G | 8 | a0001c0001t0001g0150 a0001c0001t0003g0144 a0001c0001t0003g0148 others(5): Show |
8 | HG01109.hp2 HG02280.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.3943+1397A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 4/6 | chr14 | 32147737 | |||||||
| chr14:32147782 | C | T | 4 | a0001c0001t0007g0003 a0001c0001t0007g0164 a0001c0001t0007g0165 others(1): Show |
4 | HG03041.hp2 HG03453.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.3943+1442C>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 4/6 | chr14 | 32147782 | |||||||
| chr14:32147814 | C | T | 32 | a0001c0001t0001g0099 a0001c0001t0001g0113 a0001c0001t0001g0114 others(29): Show |
32 | HG00735.hp2 HG01071.hp1 HG01099.hp1 others(29): Show |
intron_variant | MODIFIER | c.3943+1474C>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 4/6 | chr14 | 32147814 | |||||||
| chr14:32147838 | G | C | 1 | a0001c0001t0001g0021 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.3943+1498G>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 4/6 | chr14 | 32147838 | |||||||
| chr14:32148015 | T | C | 4 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0089 others(1): Show |
4 | HG01255.hp1 HG02698.hp2 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.3943+1675T>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 4/6 | chr14 | 32148015 | |||||||
| chr14:32148163 | A | AATCT | 49 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0014 others(46): Show |
50 | HG00609.hp1 HG00639.hp1 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.3944-1692_3944-168 others(8): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr14 | 32148163 | ||||||
| chr14:32148163 | A | AATCTATC others(1): Show |
52 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0013 others(49): Show |
52 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(49): Show |
intron_variant | MODIFIER | c.3944-1696_3944-168 others(12): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr14 | 32148163 | ||||||
| chr14:32148163 | A | AATCTATC others(5): Show |
4 | a0001c0001t0001g0050 a0001c0001t0001g0128 a0001c0001t0001g0175 others(1): Show |
4 | HG02738.hp2 HG03516.hp1 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.3944-1700_3944-168 others(16): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr14 | 32148163 | ||||||
| chr14:32148163 | AATCT | A | 16 | a0001c0001t0002g0011 a0001c0001t0002g0039 a0001c0001t0002g0100 others(13): Show |
16 | HG01071.hp1 HG01192.hp1 HG01358.hp2 others(13): Show |
intron_variant | MODIFIER | c.3944-1692_3944-168 others(8): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr14 | 32148163 | ||||||
| chr14:32148163 | AATCTATC others(1): Show |
A | 3 | a0001c0001t0002g0045 a0001c0001t0002g0102 a0001c0001t0002g0138 |
3 | HG00735.hp2 HG01243.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.3944-1696_3944-168 others(12): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr14 | 32148163 | ||||||
| chr14:32148163 | AATCTATC others(9): Show |
A | 3 | a0003c0003t0001g0145 a0003c0003t0001g0147 a0003c0003t0019g0146 |
3 | HG02965.hp1 HG03098.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.3944-1704_3944-168 others(20): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr14 | 32148163 | ||||||
| chr14:32148167 | T | A | 1 | a0004c0014t0015g0159 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.3944-1735T>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 4/6 | chr14 | 32148167 | |||||||
| chr14:32148206 | CTATCTAT others(1): Show |
C | 3 | a0001c0001t0007g0003 a0001c0001t0022g0003 a0010c0017t0016g0005 |
3 | HG02809.hp1 HG03041.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.3944-1692_3944-168 others(12): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr14 | 32148206 | ||||||
| chr14:32148210 | CTATG | C | 4 | a0001c0001t0007g0165 a0001c0002t0005g0167 a0001c0018t0023g0181 others(1): Show |
4 | HG00609.hp2 HG02572.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.3944-1688_3944-168 others(8): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr14 | 32148210 | ||||||
| chr14:32148214 | G | C | 5 | a0001c0001t0001g0025 a0001c0001t0007g0164 a0001c0002t0005g0004 others(2): Show |
6 | HG01243.hp1 HG01257.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.3944-1688G>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 4/6 | chr14 | 32148214 | |||||||
| chr14:32148226 | A | C | 1 | a0001c0001t0009g0171 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.3944-1676A>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 4/6 | chr14 | 32148226 | |||||||
| chr14:32148255 | G | A | 8 | a0001c0001t0007g0003 a0001c0001t0007g0164 a0001c0001t0007g0165 others(5): Show |
9 | HG01243.hp1 HG02258.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.3944-1647G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 4/6 | chr14 | 32148255 | |||||||
| chr14:32148535 | A | T | 1 | a0001c0001t0017g0123 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.3944-1367A>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 4/6 | chr14 | 32148535 | |||||||
| chr14:32148657 | A | G | 1 | a0001c0001t0007g0164 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3944-1245A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 4/6 | chr14 | 32148657 | |||||||
| chr14:32148670 | A | G | 2 | a0001c0001t0003g0161 a0001c0001t0003g0162 |
2 | HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.3944-1232A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 4/6 | chr14 | 32148670 | |||||||
| chr14:32148855 | A | G | 7 | a0001c0001t0001g0150 a0001c0001t0003g0144 a0001c0001t0003g0148 others(4): Show |
7 | HG01109.hp2 HG02280.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.3944-1047A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 4/6 | chr14 | 32148855 | |||||||
| chr14:32148939 | T | C | 8 | a0001c0001t0007g0003 a0001c0001t0007g0164 a0001c0001t0007g0165 others(5): Show |
9 | HG01243.hp1 HG02258.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.3944-963T>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 4/6 | chr14 | 32148939 | |||||||
| chr14:32149002 | C | T | 11 | a0001c0001t0007g0003 a0001c0001t0007g0164 a0001c0001t0007g0165 others(8): Show |
12 | HG00609.hp2 HG01243.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.3944-900C>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 4/6 | chr14 | 32149002 | |||||||
| chr14:32149102 | G | A | 8 | a0001c0001t0001g0150 a0001c0001t0003g0144 a0001c0001t0003g0148 others(5): Show |
8 | HG01109.hp2 HG02280.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.3944-800G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 4/6 | chr14 | 32149102 | |||||||
| chr14:32149346 | C | CA | 7 | a0001c0001t0001g0150 a0001c0001t0003g0144 a0001c0001t0003g0148 others(4): Show |
7 | HG01109.hp2 HG02280.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.3944-546dupA | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr14 | 32149346 | ||||||
| chr14:32149441 | G | T | 1 | a0001c0001t0001g0086 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.3944-461G>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 4/6 | chr14 | 32149441 | |||||||
| chr14:32149495 | C | T | 1 | a0001c0001t0001g0112 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.3944-407C>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 4/6 | chr14 | 32149495 | |||||||
| chr14:32149760 | T | C | 1 | a0001c0001t0001g0025 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.3944-142T>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 4/6 | chr14 | 32149760 | |||||||
| chr14:32149808 | T | G | 1 | a0001c0018t0023g0181 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3944-94T>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 4/6 | chr14 | 32149808 | |||||||
| chr14:32149838 | A | G | 8 | a0001c0001t0001g0150 a0001c0001t0003g0144 a0001c0001t0003g0148 others(5): Show |
8 | HG01109.hp2 HG02280.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.3944-64A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 4/6 | chr14 | 32149838 | |||||||
| chr14:32149869 | A | G | 1 | a0001c0001t0001g0158 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.3944-33A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 4/6 | chr14 | 32149869 | |||||||
| chr14:32150309 | A | G | 1 | a0001c0010t0025g0151 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.4075+276A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 5/6 | chr14 | 32150309 | |||||||
| chr14:32150512 | T | C | 1 | a0001c0018t0023g0181 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.4075+479T>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 5/6 | chr14 | 32150512 | |||||||
| chr14:32150525 | T | C | 25 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0013 others(22): Show |
25 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(22): Show |
intron_variant | MODIFIER | c.4075+492T>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 5/6 | chr14 | 32150525 | |||||||
| chr14:32150639 | G | T | 1 | a0001c0001t0001g0080 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.4075+606G>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 5/6 | chr14 | 32150639 | |||||||
| chr14:32150844 | G | T | 18 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0013 others(15): Show |
18 | HG00597.hp1 HG00609.hp1 HG00673.hp1 others(15): Show |
intron_variant | MODIFIER | c.4075+811G>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 5/6 | chr14 | 32150844 | |||||||
| chr14:32150883 | A | G | 3 | a0003c0003t0001g0145 a0003c0003t0001g0147 a0003c0003t0019g0146 |
3 | HG02965.hp1 HG03098.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.4075+850A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 5/6 | chr14 | 32150883 | |||||||
| chr14:32150942 | C | T | 3 | a0003c0003t0001g0145 a0003c0003t0001g0147 a0003c0003t0019g0146 |
3 | HG02965.hp1 HG03098.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.4075+909C>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 5/6 | chr14 | 32150942 | |||||||
| chr14:32151377 | T | C | 5 | a0001c0002t0005g0004 a0001c0002t0005g0167 a0001c0002t0005g0168 others(2): Show |
6 | HG01243.hp1 HG02258.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.4076-1046T>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 5/6 | chr14 | 32151377 | |||||||
| chr14:32151463 | A | G | 2 | a0001c0001t0001g0020 a0001c0001t0028g0019 |
2 | HG01106.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.4076-960A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 5/6 | chr14 | 32151463 | |||||||
| chr14:32151662 | C | T | 1 | a0004c0014t0015g0159 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.4076-761C>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 5/6 | chr14 | 32151662 | |||||||
| chr14:32151999 | G | T | 1 | a0001c0001t0002g0017 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.4076-424G>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 5/6 | chr14 | 32151999 | |||||||
| chr14:32152049 | C | T | 1 | a0001c0001t0002g0109 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.4076-374C>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 5/6 | chr14 | 32152049 | |||||||
| chr14:32152127 | A | G | 22 | a0001c0001t0003g0144 a0001c0001t0003g0148 a0001c0001t0003g0160 others(19): Show |
23 | HG00609.hp2 HG01243.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.4076-296A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 5/6 | chr14 | 32152127 | |||||||
| chr14:32152356 | G | C | 4 | a0001c0001t0003g0160 a0001c0001t0003g0161 a0001c0001t0003g0162 others(1): Show |
4 | HG02572.hp1 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.4076-67G>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 5/6 | chr14 | 32152356 | |||||||
| chr14:32152383 | G | A | 4 | a0001c0002t0005g0004 a0001c0002t0005g0167 a0001c0002t0005g0168 others(1): Show |
5 | HG01243.hp1 HG02258.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.4076-40G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 5/6 | chr14 | 32152383 | |||||||
| chr14:32153041 | GGTTTTTT others(2): Show |
G | 57 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0013 others(54): Show |
57 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(54): Show |
intron_variant | MODIFIER | c.4181+523_4181+531d others(11): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr14 | 32153041 | ||||||
| chr14:32153051 | GT | G | 7 | a0001c0001t0001g0014 a0001c0001t0007g0003 a0001c0001t0007g0164 others(4): Show |
7 | HG00609.hp2 HG02809.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.4181+538delT | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr14 | 32153051 | ||||||
| chr14:32153064 | T | A | 1 | a0005c0013t0018g0062 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.4181+536T>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 6/6 | chr14 | 32153064 | |||||||
| chr14:32153313 | G | A | 1 | a0001c0001t0001g0057 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.4181+785G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 6/6 | chr14 | 32153313 | |||||||
| chr14:32153375 | T | C | 11 | a0001c0001t0007g0003 a0001c0001t0007g0164 a0001c0001t0007g0165 others(8): Show |
12 | HG00609.hp2 HG01243.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.4181+847T>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 6/6 | chr14 | 32153375 | |||||||
| chr14:32153399 | T | G | 2 | a0001c0001t0001g0156 a0001c0001t0001g0157 |
2 | HG02559.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.4181+871T>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 6/6 | chr14 | 32153399 | |||||||
| chr14:32153406 | C | CA | 11 | a0001c0001t0001g0030 a0001c0001t0001g0067 a0001c0001t0001g0069 others(8): Show |
11 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(8): Show |
intron_variant | MODIFIER | c.4181+918dupA | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr14 | 32153406 | ||||||
| chr14:32153406 | C | CAAAA | 5 | a0001c0001t0001g0060 a0001c0001t0001g0066 a0001c0001t0003g0144 others(2): Show |
5 | HG01884.hp2 HG02132.hp2 HG02165.hp2 others(2): Show |
intron_variant | MODIFIER | c.4181+915_4181+918d others(6): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr14 | 32153406 | ||||||
| chr14:32153406 | C | CAAAAAAA others(3): Show |
2 | a0001c0001t0001g0166 a0009c0009t0003g0172 |
2 | HG02055.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.4181+909_4181+918d others(12): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr14 | 32153406 | ||||||
| chr14:32153406 | C | CAAAAAAA others(4): Show |
1 | a0001c0001t0003g0160 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.4181+908_4181+918d others(13): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr14 | 32153406 | ||||||
| chr14:32153406 | C | CAAAAAAA others(8): Show |
1 | a0001c0001t0001g0129 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.4181+904_4181+918d others(17): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr14 | 32153406 | ||||||
| chr14:32153406 | C | CAAAAAAA others(16): Show |
1 | a0001c0001t0001g0128 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.4181+896_4181+918d others(25): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr14 | 32153406 | ||||||
| chr14:32153406 | CA | C | 40 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0016 others(37): Show |
41 | HG00140.hp2 HG00621.hp1 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.4181+918delA | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr14 | 32153406 | ||||||
| chr14:32153406 | CAA | C | 26 | a0001c0001t0001g0006 a0001c0001t0001g0028 a0001c0001t0001g0038 others(23): Show |
26 | HG00597.hp1 HG00735.hp2 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.4181+917_4181+918d others(4): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr14 | 32153406 | ||||||
| chr14:32153406 | CAAA | C | 20 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0013 others(17): Show |
20 | HG00609.hp1 HG01169.hp2 HG01192.hp2 others(17): Show |
intron_variant | MODIFIER | c.4181+916_4181+918d others(5): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr14 | 32153406 | ||||||
| chr14:32153406 | CAAAA | C | 15 | a0001c0001t0001g0086 a0001c0001t0001g0099 a0001c0001t0001g0114 others(12): Show |
15 | HG01071.hp1 HG01106.hp1 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.4181+915_4181+918d others(6): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr14 | 32153406 | ||||||
| chr14:32153406 | CAAAAA | C | 6 | a0001c0001t0001g0115 a0001c0001t0002g0039 a0001c0001t0002g0103 others(3): Show |
6 | HG01257.hp2 HG01975.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.4181+914_4181+918d others(7): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr14 | 32153406 | ||||||
| chr14:32153406 | CAAAAAAA others(3): Show |
C | 1 | a0001c0002t0005g0167 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.4181+909_4181+918d others(12): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr14 | 32153406 | ||||||
| chr14:32153406 | CAAAAAAA others(4): Show |
C | 4 | a0001c0002t0005g0004 a0001c0002t0005g0168 a0001c0002t0005g0169 others(1): Show |
5 | HG00609.hp2 HG01243.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.4181+908_4181+918d others(13): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr14 | 32153406 | ||||||
| chr14:32153406 | CAAAAAAA others(5): Show |
C | 1 | a0001c0018t0023g0181 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.4181+907_4181+918d others(14): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr14 | 32153406 | ||||||
| chr14:32153406 | CAAAAAAA others(6): Show |
C | 1 | a0010c0017t0016g0005 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.4181+906_4181+918d others(15): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr14 | 32153406 | ||||||
| chr14:32153406 | CAAAAAAA others(7): Show |
C | 1 | a0001c0001t0001g0089 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.4181+905_4181+918d others(16): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr14 | 32153406 | ||||||
| chr14:32153406 | CAAAAAAA others(8): Show |
C | 3 | a0001c0001t0007g0003 a0001c0001t0007g0165 a0001c0001t0022g0003 |
3 | HG03041.hp2 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.4181+904_4181+918d others(17): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr14 | 32153406 | ||||||
| chr14:32153406 | CAAAAAAA others(9): Show |
C | 1 | a0001c0001t0007g0164 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.4181+903_4181+918d others(18): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr14 | 32153406 | ||||||
| chr14:32153406 | CAAAAAAA others(10): Show |
C | 2 | a0001c0001t0001g0150 a0001c0001t0002g0043 |
2 | HG01109.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.4181+902_4181+918d others(19): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr14 | 32153406 | ||||||
| chr14:32153406 | CAAAAAAA others(11): Show |
C | 1 | a0001c0001t0001g0014 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.4181+901_4181+918d others(20): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr14 | 32153406 | ||||||
| chr14:32153406 | CAAAAAAA others(12): Show |
C | 3 | a0003c0003t0001g0145 a0003c0003t0001g0147 a0003c0003t0019g0146 |
3 | HG02965.hp1 HG03098.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.4181+900_4181+918d others(21): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr14 | 32153406 | ||||||
| chr14:32153406 | CAAAAAAA others(13): Show |
C | 3 | a0001c0001t0001g0002 a0001c0001t0001g0063 a0002c0004t0001g0136 |
4 | HG02145.hp1 HG02145.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.4181+899_4181+918d others(22): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr14 | 32153406 | ||||||
| chr14:32153488 | T | C | 4 | a0001c0001t0001g0133 a0001c0012t0027g0131 a0008c0015t0024g0132 others(1): Show |
4 | HG02257.hp2 HG02886.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.4181+960T>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 6/6 | chr14 | 32153488 | |||||||
| chr14:32153559 | G | A | 1 | a0001c0001t0001g0158 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.4181+1031G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 6/6 | chr14 | 32153559 | |||||||
| chr14:32153755 | T | G | 11 | a0001c0001t0007g0003 a0001c0001t0007g0164 a0001c0001t0007g0165 others(8): Show |
12 | HG00609.hp2 HG01243.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.4182-866T>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 6/6 | chr14 | 32153755 | |||||||
| chr14:32153921 | A | G | 2 | a0001c0001t0007g0003 a0001c0001t0022g0003 |
2 | HG03041.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.4182-700A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 6/6 | chr14 | 32153921 | |||||||
| chr14:32154146 | T | C | 2 | a0001c0001t0001g0156 a0001c0001t0001g0157 |
2 | HG02559.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.4182-475T>C | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 6/6 | chr14 | 32154146 | |||||||
| chr14:32154253 | C | T | 2 | a0001c0001t0001g0001 a0001c0001t0001g0016 |
3 | HG01099.hp2 HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.4182-368C>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 6/6 | chr14 | 32154253 | |||||||
| chr14:32154391 | C | T | 1 | a0001c0001t0002g0045 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.4182-230C>T | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 6/6 | chr14 | 32154391 | |||||||
| chr14:32154466 | A | G | 1 | a0001c0018t0023g0181 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.4182-155A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 6/6 | chr14 | 32154466 | |||||||
| chr14:32154598 | G | GT | 5 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0134 others(2): Show |
5 | HG00099.hp2 HG02132.hp1 HG03704.hp2 others(2): Show |
intron_variant | MODIFIER | c.4182-17dupT | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr14 | 32154598 | ||||||
| chr14:32154611 | A | G | 1 | a0001c0001t0017g0123 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.4182-10A>G | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 6/6 | chr14 | 32154611 |