Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| 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 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1502 | 169 | 55 | 37 | 38 | 8 | 29 | 19 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| a0002 | 0/0 | 1502 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| a0003 | 0/0 | 1502 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| a0004 | 0/0 | 1502 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| a0005 | 0/0 | 1502 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| a0006 | 0/0 | 1502 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| a0007 | 0/0 | 1502 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| a0008 | 0/0 | 1502 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| a0009 | 0/0 | 1502 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| a0010 | 0/0 | 1502 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| a0011 | 0/0 | 1502 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| a0012 | 0/0 | 1502 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| a0013 | 0/0 | 1502 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| a0014 | 0/0 | 1502 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 4509 | 160 | 48 | 35 | 38 | 8 | 29 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| c0002 | 0/0 | 4509 | 5 | 4 | 1 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| c0003 | 0/0 | 4509 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| c0004 | 0/0 | 4509 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| c0005 | 0/0 | 4509 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| c0006 | 0/0 | 4509 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| c0007 | 0/0 | 4509 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| c0008 | 0/0 | 4509 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| c0009 | 0/0 | 4509 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| c0010 | 0/0 | 4509 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| c0011 | 0/0 | 4509 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| c0012 | 0/0 | 4509 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| c0013 | 0/0 | 4509 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| c0014 | 0/0 | 4509 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| c0015 | 0/0 | 4509 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| c0016 | 0/0 | 4509 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| c0017 | 0/0 | 4509 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| c0018 | 0/0 | 4509 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| c0019 | 0/0 | 4509 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 5081 | 119 | 40 | 20 | 28 | 7 | 22 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| t0002 | 0/0 | 5081 | 22 | 1 | 9 | 8 | 1 | 3 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| t0003 | 0/0 | 5081 | 7 | 7 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| t0004 | 0/0 | 5082 | 5 | 1 | 1 | 0 | 1 | 2 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| t0005 | 0/0 | 5081 | 5 | 4 | 1 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| t0006 | 0/0 | 5081 | 4 | 0 | 4 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| t0007 | 0/0 | 5081 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| t0008 | 0/0 | 5081 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| t0009 | 0/0 | 5094 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| t0010 | 0/0 | 5081 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| t0011 | 0/0 | 5081 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| t0012 | 0/0 | 5081 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| t0013 | 0/0 | 5081 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| t0014 | 0/0 | 5081 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| t0015 | 0/0 | 5069 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| t0016 | 0/0 | 5081 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| t0017 | 0/0 | 5081 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| t0018 | 0/0 | 5081 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| t0019 | 0/0 | 5081 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| t0020 | 0/0 | 5081 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| t0021 | 0/0 | 5081 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| t0022 | 0/0 | 5081 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| t0023 | 0/0 | 5081 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| t0024 | 0/0 | 5081 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| t0025 | 0/0 | 5081 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| t0026 | 0/0 | 5081 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| t0027 | 0/0 | 5081 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| t0028 | 0/0 | 5081 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0023 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0024 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0047 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 4509 | 160 | 48 | 35 | 38 | 8 | 29 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| a0001c0002 | 0/0 | 4509 | 5 | 4 | 1 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| a0001c0010 | 0/0 | 4509 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| a0001c0012 | 0/0 | 4509 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| a0001c0018 | 0/0 | 4509 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| a0001c0019 | 0/0 | 4509 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| a0002c0003 | 0/0 | 4509 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| a0003c0004 | 0/0 | 4509 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| a0004c0005 | 0/0 | 4509 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| a0005c0006 | 0/0 | 4509 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| a0006c0009 | 0/0 | 4509 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| a0007c0013 | 0/0 | 4509 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| a0008c0011 | 0/0 | 4509 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| a0009c0014 | 0/0 | 4509 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| a0010c0015 | 0/0 | 4509 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| a0011c0008 | 0/0 | 4509 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| a0012c0007 | 0/0 | 4509 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| a0013c0017 | 0/0 | 4509 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| a0014c0016 | 0/0 | 4509 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | 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 | copy fasta | chr14 | 32072304 | 32164728 |
| a0001c0001t0002 | 0/0 | 9589 | 22 | 1 | 9 | 8 | 1 | 3 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| a0001c0001t0003 | 0/0 | 9589 | 6 | 6 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| a0001c0001t0004 | 0/0 | 9590 | 3 | 1 | 1 | 0 | 0 | 1 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| a0001c0001t0006 | 0/0 | 9589 | 4 | 0 | 4 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| a0001c0001t0007 | 0/0 | 9589 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| a0001c0001t0008 | 0/0 | 9589 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| a0001c0001t0009 | 0/0 | 9602 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| a0001c0001t0010 | 0/0 | 9589 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| a0001c0001t0011 | 0/0 | 9589 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| a0001c0001t0012 | 0/0 | 9589 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| a0001c0001t0013 | 0/0 | 9589 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| a0001c0001t0014 | 0/0 | 9589 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| a0001c0001t0017 | 0/0 | 9589 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| a0001c0001t0020 | 0/0 | 9589 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| a0001c0001t0021 | 0/0 | 9589 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| a0001c0001t0022 | 0/0 | 9589 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| a0001c0001t0026 | 0/0 | 9589 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| a0001c0001t0028 | 0/0 | 9589 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| a0001c0002t0005 | 0/0 | 9589 | 5 | 4 | 1 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| a0001c0010t0025 | 0/0 | 9589 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| a0001c0012t0027 | 0/0 | 9589 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| a0001c0018t0023 | 0/0 | 9589 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| a0001c0019t0001 | 0/0 | 9589 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| a0002c0003t0001 | 0/0 | 9589 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| a0002c0003t0019 | 0/0 | 9589 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| a0003c0004t0001 | 0/0 | 9589 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| a0004c0005t0004 | 0/0 | 9590 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| a0005c0006t0001 | 0/0 | 9589 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| a0006c0009t0003 | 0/0 | 9589 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| a0007c0013t0018 | 0/0 | 9589 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| a0008c0011t0001 | 0/0 | 9589 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| a0009c0014t0015 | 0/0 | 9577 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| a0010c0015t0024 | 0/0 | 9589 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| a0011c0008t0001 | 0/0 | 9589 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| a0012c0007t0001 | 0/0 | 9589 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| a0013c0017t0016 | 0/0 | 9589 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| a0014c0016t0004 | 0/0 | 9590 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | copy fasta | chr14 | 32072304 | 32164728 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 |
| a0002c0003t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0002c0003t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0002c0003t0019g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0003c0004t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0003c0004t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0003c0004t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0004c0005t0004g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0005c0006t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0006c0009t0003g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0007c0013t0018g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0008c0011t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0009c0014t0015g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0010c0015t0024g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0011c0008t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0012c0007t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0013c0017t0016g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| a0014c0016t0004g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 | a0009 | 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 | a0007 | 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 | a0014 | c0016 | t0004 | g0178 | EUR | IBS | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| HG01515 | hp2 | a0008 | 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 | a0003 | 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 | a0010 | 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 | a0003 | 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 | a0006 | 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 | a0013 | 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 | a0002 | 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 | a0002 | 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 | a0003 | 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 | a0005 | 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 | a0004 | 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 | a0002 | 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 | a0012 | 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 | a0011 | 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 | hp1 | a0001 | c0001 | t0001 | g0023 | REF | REF | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0047 | REF | REF | ARHGAP5_chr14_32072304_32164728 | ARHGAP5 | chr14 | 32072304 | 32164728 |
| 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 | a0004 | 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 | a0003 | 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 | a0014 | 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 | a0013 | 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 | a0005 | 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 | a0012 | 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 | a0011 | 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 | a0010 | 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 | a0002 | 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 | a0006 | 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 | a0009 | 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 | a0007 | 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 | a0008 | 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 |
| 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 | a0001c0002a0013c0017 | 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 | a0001c0002a0013c0017 | 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 |
| 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 | a0010c0015t0024 | 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 | a0001c0001t0003a0006c0009t0003 | 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 | a0001c0001t0007a0001c0001t0022a0001c0002t0005others(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 | a0001c0001t0006a0001c0001t0021 | 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 | a0001c0001t0004a0004c0005t0004a0014c0016t0004 | 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 | a0002c0003t0019 | 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 | a0007c0013t0018 | 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 | a0009c0014t0015 | 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 | a0013c0017t0016 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4520G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 7/7 | 4520 | chr14 | 32159468 |
| 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 | a0013c0017t0016g0005 | 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 | a0001c0001t0001g0175a0001c0001t0001g0176a0001c0001t0001g0180others(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 | a0006c0009t0003g0172 | 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 | a0006c0009t0003g0172 | 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 | a0001c0001t0014g0170a0001c0018t0023g0181 | 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 | a0001c0002t0005g0004a0001c0002t0005g0167a0001c0002t0005g0168others(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 | a0001c0001t0001g0166a0001c0001t0003g0160a0001c0001t0003g0161others(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 | a0001c0002t0005g0004a0001c0002t0005g0167a0001c0002t0005g0168others(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 | a0009c0014t0015g0159 | 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 | a0001c0001t0001g0156a0001c0001t0001g0157 | 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 | a0001c0001t0006g0154a0001c0001t0006g0155 | 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 | a0001c0001t0001g0166a0001c0001t0007g0003a0001c0001t0007g0164others(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 | a0001c0001t0001g0150a0001c0001t0003g0160a0001c0001t0003g0161others(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 | a0001c0001t0001g0150a0001c0001t0003g0144a0001c0001t0003g0148others(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 | a0001c0001t0007g0003a0001c0001t0007g0164a0001c0001t0007g0165others(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 | a0009c0014t0015g0159 | 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 | a0001c0001t0007g0003a0001c0001t0007g0164a0001c0001t0007g0165others(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 | a0001c0001t0002g0011a0001c0001t0003g0144a0001c0001t0003g0160others(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 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0140others(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 | a0001c0001t0001g0012a0001c0001t0001g0013 | 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 | a0003c0004t0001g0135a0003c0004t0001g0136a0003c0004t0001g0137 | 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 | a0001c0001t0001g0150a0001c0001t0001g0166a0001c0001t0003g0144others(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 | a0013c0017t0016g0005 | 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 | 20 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0009others(17): Show | 21 | HG00140.hp2 HG00735.hp1 HG01070.hp1 others(18): 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 | a0001c0001t0001g0166a0001c0001t0007g0003a0001c0001t0007g0164others(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 | a0013c0017t0016g0005 | 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 | a0002c0003t0001g0145a0002c0003t0001g0147a0002c0003t0019g0146 | 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 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0153 | 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 | a0001c0001t0001g0133a0001c0012t0027g0131a0010c0015t0024g0132others(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 | a0013c0017t0016g0005 | 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 | a0001c0001t0001g0033a0001c0001t0010g0034 | 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 | a0001c0002t0005g0004a0001c0002t0005g0167a0001c0002t0005g0168others(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 | a0001c0001t0001g0015a0001c0001t0001g0018a0001c0001t0001g0020others(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 | a0003c0004t0001g0137 | 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 | a0001c0001t0001g0128a0001c0001t0001g0129 | 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 | a0001c0002t0005g0004a0001c0002t0005g0167a0001c0002t0005g0168others(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 | a0002c0003t0001g0147 | 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 | a0001c0001t0001g0127a0001c0001t0001g0150a0001c0001t0001g0166others(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 | a0001c0001t0002g0011a0001c0001t0002g0124a0001c0001t0002g0125 | 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 | a0001c0001t0001g0150a0001c0001t0003g0144a0001c0001t0003g0148others(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 | a0001c0002t0005g0004a0001c0002t0005g0167a0001c0002t0005g0168others(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 | a0013c0017t0016g0005 | 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 | a0013c0017t0016g0005 | 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 | a0001c0001t0001g0150a0001c0001t0001g0166a0001c0001t0003g0144others(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 | a0001c0001t0006g0154a0001c0001t0006g0155 | 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 | a0014c0016t0004g0178 | 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 | a0001c0001t0001g0166a0001c0001t0007g0164 | 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 | a0001c0001t0001g0166a0001c0001t0007g0003a0001c0001t0007g0164others(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 | a0001c0001t0001g0166a0001c0001t0007g0003a0001c0001t0007g0164others(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 | a0001c0001t0001g0166a0001c0001t0007g0003a0001c0001t0007g0164others(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 | a0001c0001t0002g0121a0001c0001t0002g0122 | 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 | a0001c0001t0001g0166a0001c0001t0007g0003a0001c0001t0007g0164others(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 | a0001c0001t0001g0166a0001c0001t0007g0003a0001c0001t0007g0164others(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 | a0001c0001t0001g0166a0001c0001t0007g0003a0001c0001t0007g0164others(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 | a0001c0002t0005g0004a0001c0002t0005g0167a0001c0002t0005g0168others(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 | a0001c0001t0001g0012a0001c0001t0001g0013 | 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 | a0001c0002t0005g0004a0001c0002t0005g0167a0001c0002t0005g0168others(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 | a0001c0001t0001g0166a0001c0001t0007g0003a0001c0001t0007g0164others(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 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0040others(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 | a0001c0001t0001g0166a0001c0001t0003g0144a0001c0001t0003g0148others(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 | a0001c0001t0001g0166a0001c0001t0007g0003a0001c0001t0007g0164others(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 | a0001c0001t0001g0166a0001c0001t0007g0003a0001c0001t0007g0164others(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 | 175 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(172): Show | 178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): 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 | a0001c0001t0001g0166a0001c0001t0007g0003a0001c0001t0007g0164others(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 | a0001c0001t0001g0166a0001c0001t0007g0003a0001c0001t0007g0164others(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 | a0001c0002t0005g0004a0001c0002t0005g0167a0001c0002t0005g0168others(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 | a0001c0002t0005g0004a0001c0002t0005g0167a0001c0002t0005g0168others(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 | a0001c0001t0001g0166a0001c0001t0007g0003a0001c0001t0007g0164others(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 | a0011c0008t0001g0130 | 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 | a0013c0017t0016g0005 | 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 | a0001c0002t0005g0004a0001c0002t0005g0167a0001c0002t0005g0168others(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 | a0001c0001t0007g0003a0001c0001t0007g0164a0001c0001t0007g0165others(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 | a0001c0001t0001g0117a0001c0001t0001g0118 | 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 | a0001c0001t0002g0116a0001c0001t0002g0121a0001c0001t0002g0122 | 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 | a0001c0001t0001g0099a0001c0001t0001g0105a0001c0001t0001g0106others(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 | a0001c0001t0003g0144a0001c0001t0003g0148a0001c0001t0003g0160others(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 | a0001c0001t0007g0003a0001c0001t0007g0165a0001c0001t0022g0003 | 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 | a0001c0002t0005g0004a0001c0002t0005g0167a0001c0002t0005g0168others(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 | a0001c0002t0005g0004a0001c0002t0005g0167a0001c0002t0005g0168others(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 | a0001c0001t0001g0150a0001c0001t0003g0160a0001c0001t0003g0161others(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 | a0001c0001t0003g0160a0001c0001t0003g0161a0001c0001t0003g0162 | 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 | a0001c0001t0001g0014a0001c0001t0001g0031a0001c0001t0001g0032others(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 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0075others(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 | a0001c0001t0001g0117a0001c0001t0001g0118 | 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 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0075others(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 | a0001c0001t0001g0001a0001c0001t0001g0016 | 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 | a0002c0003t0001g0145a0002c0003t0001g0147a0002c0003t0019g0146 | 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 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097 | 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 | a0001c0001t0004g0174a0001c0001t0004g0177a0001c0019t0001g0179others(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 | a0001c0001t0001g0150a0001c0001t0003g0144a0001c0001t0003g0148others(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 | a0001c0001t0001g0150a0001c0001t0003g0144a0001c0001t0003g0148others(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 | a0001c0001t0001g0133a0001c0012t0027g0131a0010c0015t0024g0132others(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 | a0001c0002t0005g0004a0001c0002t0005g0167a0001c0002t0005g0168others(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 | a0001c0002t0005g0004a0001c0002t0005g0167a0001c0002t0005g0168others(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 | a0001c0002t0005g0004a0001c0002t0005g0167a0001c0002t0005g0168others(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 | a0001c0001t0003g0160a0001c0001t0003g0161a0001c0001t0003g0162 | 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 | a0001c0001t0001g0166a0001c0001t0007g0003a0001c0001t0007g0164others(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 | a0001c0001t0001g0150a0001c0001t0003g0144a0001c0001t0003g0148others(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 | a0001c0001t0001g0166a0001c0001t0007g0003a0001c0001t0007g0164others(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 | a0001c0001t0001g0073a0005c0006t0001g0072 | 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 | a0001c0002t0005g0004a0001c0002t0005g0167a0001c0002t0005g0168others(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 | a0001c0001t0003g0144a0001c0001t0003g0148a0001c0001t0003g0160others(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 | a0001c0002t0005g0004a0001c0002t0005g0167a0001c0002t0005g0168others(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 | 161 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(158): Show | 164 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(161): 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 | a0001c0001t0001g0071a0002c0003t0001g0145a0002c0003t0001g0147others(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 | a0002c0003t0001g0145a0002c0003t0001g0147a0002c0003t0019g0146 | 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 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0149 | 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 | a0001c0001t0001g0166a0001c0001t0007g0003a0001c0001t0007g0164others(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 | a0001c0002t0005g0004a0001c0002t0005g0167a0001c0002t0005g0168others(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 | a0001c0001t0003g0160a0001c0001t0003g0161a0001c0001t0003g0162others(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 | a0002c0003t0001g0145a0002c0003t0001g0147a0002c0003t0019g0146 | 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 | a0002c0003t0001g0145a0002c0003t0001g0147a0002c0003t0019g0146 | 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 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0075others(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 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0075others(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 | a0001c0001t0007g0003a0001c0001t0007g0164a0001c0001t0007g0165others(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 | a0013c0017t0016g0005 | 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 | a0001c0001t0001g0099a0001c0001t0001g0113a0001c0001t0001g0114others(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 | a0001c0001t0007g0003a0001c0001t0007g0164a0001c0001t0007g0165others(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 | a0001c0001t0001g0150a0001c0001t0003g0160a0001c0001t0003g0161others(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 | a0001c0001t0001g0150a0001c0001t0003g0160a0001c0001t0003g0161others(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 | a0001c0002t0005g0004a0001c0002t0005g0167a0001c0002t0005g0168others(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 | a0001c0001t0001g0150a0001c0001t0003g0160a0001c0001t0003g0161others(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 | a0001c0001t0001g0117a0001c0001t0001g0118 | 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 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076others(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 | a0001c0002t0005g0004a0001c0002t0005g0167a0001c0002t0005g0168others(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 | a0013c0017t0016g0005 | 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 | a0013c0017t0016g0005 | 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 | a0001c0001t0001g0166a0001c0001t0007g0003a0001c0001t0007g0164others(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 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0063others(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 | 54 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(51): Show | 55 | HG00140.hp2 HG00609.hp1 HG00673.hp1 others(52): 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 | a0001c0002t0005g0004a0001c0002t0005g0167a0001c0002t0005g0168others(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 | a0001c0001t0003g0160a0001c0001t0003g0161a0001c0001t0003g0162others(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 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0075others(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 | a0001c0001t0001g0021a0001c0001t0003g0162a0001c0001t0006g0155others(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 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0075others(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 | a0002c0003t0001g0145a0002c0003t0001g0147a0002c0003t0019g0146 | 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 | a0002c0003t0001g0145a0002c0003t0001g0147a0002c0003t0019g0146 | 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 | a0013c0017t0016g0005 | 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 | a0001c0001t0001g0052a0001c0001t0001g0060a0001c0001t0001g0065others(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 | 22 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0009others(19): Show | 23 | HG00099.hp2 HG00140.hp2 HG00735.hp1 others(20): 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 | a0001c0001t0001g0018a0001c0001t0001g0063a0001c0001t0001g0067others(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 | a0001c0001t0001g0038a0001c0001t0001g0095a0001c0001t0001g0096others(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 | 166 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(163): Show | 169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): 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 | a0001c0001t0001g0035a0001c0001t0001g0150a0001c0001t0001g0158others(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 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0075others(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 | a0010c0015t0024g0132 | 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 | a0013c0017t0016g0005 | 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 | a0001c0001t0006g0154a0001c0001t0006g0155 | 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 | a0001c0001t0007g0003a0001c0001t0007g0164a0001c0001t0007g0165others(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 | a0001c0001t0007g0003a0001c0001t0007g0164a0001c0001t0007g0165others(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 | a0001c0001t0001g0150a0001c0001t0003g0144a0001c0001t0003g0148others(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 | a0001c0002t0005g0004a0001c0002t0005g0167a0001c0002t0005g0168others(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 | a0001c0001t0007g0003a0001c0001t0007g0164a0001c0001t0007g0165others(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 | a0001c0001t0007g0003a0001c0001t0007g0164a0001c0001t0007g0165others(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 | a0001c0001t0007g0003a0001c0001t0007g0164a0001c0001t0007g0165others(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 | a0001c0001t0007g0003a0001c0001t0007g0164a0001c0001t0007g0165others(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 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076others(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 | a0002c0003t0001g0145a0002c0003t0001g0147a0002c0003t0019g0146 | 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 | a0001c0002t0005g0004a0001c0002t0005g0167a0001c0002t0005g0168others(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 | a0001c0001t0001g0117a0001c0001t0001g0118 | 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 | a0001c0001t0001g0052a0001c0001t0001g0060a0001c0001t0001g0065others(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 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0075others(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 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0075others(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 | a0013c0017t0016g0005 | 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 | 178 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(175): Show | 181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): 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 | a0001c0002t0005g0004a0001c0002t0005g0167a0001c0002t0005g0168others(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 | a0001c0001t0001g0150a0001c0001t0003g0160a0001c0001t0003g0161others(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 | a0001c0001t0001g0022a0001c0001t0001g0073a0001c0001t0001g0074others(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 | ||||||
| chr14:32120911
|
G | A | 1 | a0001c0001t0001g0023 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.3865+3624G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32120911 | ||||||
| chr14:32120993
|
A | G | 9 | a0001c0001t0001g0150a0001c0001t0003g0144a0001c0001t0003g0148others(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 | 144 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(141): Show | 146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): 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 | a0001c0001t0001g0012a0001c0001t0001g0020a0001c0001t0001g0028others(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 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0075others(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 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0075others(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 | a0001c0001t0002g0116a0001c0001t0002g0121a0001c0001t0002g0122others(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 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0075others(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 | a0013c0017t0016g0005 | 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 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0075others(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 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0075others(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 | a0011c0008t0001g0130 | 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 | a0009c0014t0015g0159 | 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 | a0001c0001t0001g0067a0006c0009t0003g0172 | 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 | a0001c0001t0003g0144a0001c0001t0003g0148a0001c0001t0003g0160others(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 | a0001c0001t0002g0011a0001c0001t0002g0017a0001c0001t0002g0039others(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 | a0009c0014t0015g0159a0013c0017t0016g0005 | 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 | a0013c0017t0016g0005 | 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 | a0001c0001t0002g0011a0001c0001t0002g0124a0001c0001t0002g0125 | 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 | a0001c0001t0007g0003a0001c0001t0007g0164a0001c0001t0007g0165others(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 | a0001c0001t0007g0003a0001c0001t0007g0164a0001c0001t0007g0165others(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 | a0009c0014t0015g0159a0013c0017t0016g0005 | 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 | a0007c0013t0018g0062 | 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 | a0001c0002t0005g0004a0001c0002t0005g0167a0001c0002t0005g0168others(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 | a0001c0002t0005g0004a0001c0002t0005g0167a0001c0002t0005g0168others(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 | a0001c0001t0002g0043a0001c0001t0002g0044a0001c0001t0002g0045 | 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 | a0001c0001t0001g0014a0001c0001t0001g0092 | 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 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0031others(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 | a0001c0001t0007g0003a0001c0001t0007g0164a0001c0001t0007g0165others(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 | a0001c0001t0002g0011a0001c0001t0002g0100a0001c0001t0002g0101others(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 | a0001c0001t0007g0003a0001c0001t0007g0164a0001c0001t0007g0165others(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 | a0001c0002t0005g0004a0001c0002t0005g0167a0001c0002t0005g0168others(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 | a0001c0001t0007g0003a0001c0001t0007g0165a0001c0001t0022g0003 | 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 | a0001c0001t0003g0160a0001c0001t0003g0161a0001c0001t0003g0162others(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 | a0001c0001t0003g0160a0001c0001t0003g0161a0001c0001t0003g0162 | 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 | a0001c0001t0002g0104a0001c0001t0006g0107a0001c0001t0006g0154others(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 | a0013c0017t0016g0005 | 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 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0031others(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 | a0001c0001t0001g0012a0001c0001t0001g0036a0001c0001t0001g0054others(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 | a0001c0001t0001g0080a0001c0001t0001g0083a0001c0001t0001g0084 | 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 | a0001c0001t0007g0003a0001c0001t0007g0164a0001c0001t0007g0165others(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 | a0009c0014t0015g0159a0013c0017t0016g0005 | 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 | 36 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0009others(33): Show | 37 | HG00140.hp1 HG00140.hp2 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.3865+10605G>A | ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | chr14 | 32127892 | ||||||
| chr14:32127915
|
C | G | 36 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0009others(33): Show | 37 | HG00140.hp1 HG00140.hp2 HG00621.hp1 others(34): 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 | a0001c0001t0001g0012a0001c0001t0001g0128a0001c0001t0001g0150others(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 | a0001c0001t0007g0003a0001c0001t0007g0164a0001c0001t0007g0165others(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 | a0001c0001t0007g0003a0001c0001t0007g0164a0001c0001t0007g0165others(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 | a0001c0001t0001g0002a0001c0001t0001g0063 | 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 | a0001c0001t0007g0003a0001c0001t0007g0164a0001c0001t0007g0165others(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 | a0009c0014t0015g0159 | 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 | a0001c0001t0003g0144a0001c0001t0003g0148a0001c0001t0003g0160others(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 | a0001c0001t0003g0144a0001c0001t0003g0148a0001c0001t0003g0160others(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 | a0001c0001t0001g0095a0001c0001t0001g0097 | 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 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0128others(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 | a0001c0001t0007g0003a0001c0001t0007g0164a0001c0001t0007g0165others(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 | a0001c0001t0003g0160a0001c0001t0003g0161a0001c0001t0003g0162others(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 | a0001c0001t0001g0060a0001c0001t0001g0065a0001c0001t0001g0066others(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 | a0008c0011t0001g0026 | 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 | a0009c0014t0015g0159 | 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 | 178 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(175): Show | 181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): 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 | a0009c0014t0015g0159a0013c0017t0016g0005 | 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 | a0001c0001t0001g0150a0001c0001t0003g0144a0001c0001t0003g0148others(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 | a0001c0002t0005g0004a0001c0002t0005g0167a0001c0002t0005g0168others(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 | a0001c0001t0001g0091a0001c0001t0001g0156a0001c0001t0001g0157 | 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 | a0009c0014t0015g0159a0013c0017t0016g0005 | 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 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0050 | 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 | a0001c0001t0001g0006a0001c0001t0001g0041a0001c0001t0001g0050others(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 | a0001c0001t0001g0028a0001c0001t0001g0083a0001c0001t0001g0087others(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 | a0001c0001t0001g0021a0001c0002t0005g0004a0001c0002t0005g0167others(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 | a0001c0001t0001g0150a0001c0001t0003g0161a0001c0001t0003g0162others(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 | a0001c0002t0005g0004a0001c0002t0005g0167a0001c0002t0005g0168others(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 | a0001c0001t0001g0150a0001c0001t0003g0160a0001c0001t0003g0161others(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 | a0001c0001t0001g0128a0001c0001t0001g0129 | 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 | a0001c0001t0007g0003a0001c0001t0007g0164a0001c0001t0007g0165others(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 | a0001c0001t0002g0011a0001c0001t0002g0017a0001c0001t0002g0039others(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 | a0001c0001t0007g0003a0001c0001t0007g0164a0001c0001t0007g0165others(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 | a0001c0001t0007g0003a0001c0001t0007g0164a0001c0001t0007g0165others(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 | a0001c0001t0001g0120a0001c0001t0001g0150a0001c0001t0002g0044others(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 | a0009c0014t0015g0159a0013c0017t0016g0005 | 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 | a0001c0001t0001g0150a0001c0001t0003g0160a0001c0001t0003g0161others(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 | a0001c0001t0001g0012a0001c0001t0001g0013 | 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 | a0001c0001t0001g0032a0001c0001t0001g0099a0001c0001t0001g0113others(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 | a0009c0014t0015g0159a0013c0017t0016g0005 | 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 | a0001c0001t0006g0154a0001c0001t0006g0155 | 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 | a0001c0002t0005g0004a0001c0002t0005g0167a0001c0002t0005g0168others(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 | a0001c0001t0001g0113a0001c0001t0001g0114 | 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 | a0009c0014t0015g0159a0013c0017t0016g0005 | 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 | a0001c0001t0007g0003a0001c0001t0007g0164a0001c0001t0007g0165others(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 | a0001c0001t0001g0057a0001c0001t0001g0059a0001c0001t0001g0060others(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 | 22 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0009others(19): Show | 23 | HG00099.hp2 HG00140.hp2 HG00735.hp1 others(20): 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 | a0001c0001t0001g0060a0001c0001t0001g0065a0001c0001t0001g0066others(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 | a0001c0001t0007g0003a0001c0001t0007g0164a0001c0001t0007g0165others(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 | a0009c0014t0015g0159 | 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 | a0001c0001t0001g0175a0001c0001t0001g0176a0001c0001t0004g0174others(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 | a0001c0002t0005g0004a0001c0002t0005g0167a0001c0002t0005g0168others(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 | a0001c0001t0001g0073a0001c0001t0001g0098 | 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 | a0001c0002t0005g0004a0001c0002t0005g0167a0001c0002t0005g0168others(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 | a0001c0002t0005g0004a0001c0002t0005g0167a0001c0002t0005g0168others(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 | a0001c0002t0005g0004a0001c0002t0005g0167a0001c0002t0005g0168others(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 | a0001c0001t0001g0068a0001c0001t0001g0071 | 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 | a0003c0004t0001g0135a0003c0004t0001g0136a0003c0004t0001g0137 | 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 | a0013c0017t0016g0005 | 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 | a0001c0001t0001g0150a0001c0001t0003g0144a0001c0001t0003g0148others(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 | a0001c0001t0007g0003a0001c0001t0007g0164a0001c0001t0007g0165others(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 | a0001c0001t0001g0105a0001c0001t0004g0061 | 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 | a0001c0001t0001g0175a0001c0001t0001g0176a0001c0001t0004g0174others(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 | a0001c0002t0005g0004a0001c0002t0005g0167a0001c0002t0005g0168others(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 | a0001c0001t0007g0003a0001c0001t0007g0164a0001c0001t0007g0165others(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 | a0001c0001t0001g0150a0001c0001t0003g0144a0001c0001t0003g0148others(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 | a0002c0003t0001g0145a0002c0003t0001g0147a0002c0003t0019g0146 | 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 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(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 | a0009c0014t0015g0159a0013c0017t0016g0005 | 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 | a0001c0001t0007g0003a0001c0001t0007g0164a0001c0001t0007g0165others(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 | a0001c0001t0007g0003a0001c0001t0007g0164a0001c0001t0007g0165others(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 | a0013c0017t0016g0005 | 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 | a0009c0014t0015g0159 | 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 | a0001c0002t0005g0004a0001c0002t0005g0167a0001c0002t0005g0168others(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 | a0002c0003t0001g0145a0002c0003t0001g0147a0002c0003t0019g0146 | 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 | a0013c0017t0016g0005 | 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 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0075others(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 | a0001c0001t0007g0003a0001c0001t0007g0165a0001c0001t0022g0003 | 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 | a0001c0001t0001g0036a0001c0001t0001g0052a0001c0001t0001g0060others(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 | a0001c0001t0001g0150a0001c0001t0003g0144a0001c0001t0003g0148others(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 | a0009c0014t0015g0159 | 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 | a0013c0017t0016g0005 | 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 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0075others(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 | a0001c0001t0001g0150a0001c0001t0003g0144a0001c0001t0003g0148others(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 | a0001c0001t0007g0003a0001c0001t0007g0164a0001c0001t0007g0165others(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 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0037others(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 | a0001c0001t0003g0144a0001c0001t0007g0003a0001c0001t0007g0164others(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 | a0001c0001t0001g0153a0001c0001t0001g0158 | 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 | a0001c0001t0007g0003a0001c0001t0007g0164a0001c0001t0007g0165others(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 | a0001c0001t0001g0057a0001c0001t0001g0059a0001c0001t0001g0087others(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 | a0001c0001t0007g0003a0001c0001t0007g0164a0001c0001t0007g0165others(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 | a0001c0002t0005g0004a0001c0002t0005g0167a0001c0002t0005g0168others(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 | a0001c0001t0001g0093a0001c0001t0001g0150a0001c0001t0003g0144others(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 | a0001c0001t0001g0025a0001c0001t0002g0011a0001c0001t0002g0100others(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 | a0001c0001t0007g0003a0001c0001t0007g0164a0001c0001t0007g0165others(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 | a0001c0001t0001g0150a0001c0001t0003g0144a0001c0001t0003g0148others(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 | a0002c0003t0001g0145a0002c0003t0001g0147a0002c0003t0019g0146 | 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 | a0001c0001t0001g0021a0001c0001t0001g0150a0001c0001t0003g0144others(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 | a0001c0001t0001g0014a0001c0001t0001g0033a0001c0001t0001g0036others(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 | a0001c0012t0027g0131a0010c0015t0024g0132 | 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 | a0001c0001t0001g0150a0001c0001t0003g0144a0001c0001t0003g0148others(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 | a0001c0001t0007g0003a0001c0001t0007g0164a0001c0001t0007g0165others(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 | a0001c0001t0001g0031a0001c0001t0001g0088 | 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 | a0001c0001t0007g0003a0001c0001t0007g0164a0001c0001t0007g0165others(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 | a0001c0001t0001g0150a0001c0001t0003g0144a0001c0001t0003g0148others(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 | a0009c0014t0015g0159 | 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 | a0002c0003t0001g0145a0002c0003t0001g0147a0002c0003t0019g0146 | 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 | a0001c0002t0005g0004a0001c0002t0005g0167a0001c0002t0005g0168others(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 | a0009c0014t0015g0159 | 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 | 80 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0009others(77): Show | 81 | HG00140.hp2 HG00609.hp1 HG00621.hp2 others(78): 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 | a0001c0001t0001g0008a0001c0001t0001g0032a0001c0001t0001g0053others(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 | a0001c0001t0001g0038a0001c0001t0001g0140 | 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 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0050others(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 | a0001c0001t0001g0093a0001c0001t0001g0157a0009c0014t0015g0159 | 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 | a0001c0001t0001g0012a0001c0001t0001g0013a0002c0003t0001g0145others(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 | a0013c0017t0016g0005 | 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 | a0001c0018t0023g0181a0013c0017t0016g0005 | 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 | a0001c0001t0003g0161a0001c0001t0014g0170 | 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 | a0001c0001t0003g0160a0001c0001t0003g0161a0001c0001t0014g0170others(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 | a0001c0001t0003g0144a0001c0001t0003g0148a0001c0001t0003g0162others(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 | a0001c0001t0003g0144a0001c0001t0003g0148a0001c0001t0003g0160others(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 | a0001c0001t0001g0091a0001c0001t0001g0156 | 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 | a0001c0001t0003g0144a0001c0001t0003g0148a0001c0001t0003g0160others(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 | a0001c0001t0003g0144a0001c0001t0003g0148a0001c0001t0003g0160others(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 | a0001c0001t0007g0003a0001c0001t0007g0165a0001c0001t0022g0003 | 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 | a0001c0001t0001g0002a0001c0001t0001g0028a0001c0001t0001g0068others(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 | 55 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0009others(52): Show | 56 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(53): 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 | a0001c0001t0001g0009a0001c0001t0001g0074a0001c0001t0001g0083 | 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 | a0001c0001t0001g0150a0001c0001t0003g0144a0001c0001t0003g0148others(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 | a0001c0001t0001g0150a0001c0001t0003g0144a0001c0001t0003g0148others(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 | a0001c0001t0002g0044a0001c0001t0002g0045 | 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 | a0001c0001t0007g0003a0001c0001t0007g0164a0001c0001t0007g0165others(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 | a0001c0001t0007g0003a0001c0001t0007g0164a0001c0001t0007g0165others(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 | a0001c0001t0001g0099a0001c0001t0001g0113a0001c0001t0001g0114others(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 | a0001c0001t0001g0150a0001c0001t0003g0144a0001c0001t0003g0148others(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 | a0001c0001t0007g0003a0001c0001t0007g0164a0001c0001t0007g0165others(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 | a0013c0017t0016g0005 | 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 | a0001c0001t0001g0150a0001c0001t0003g0144a0001c0001t0003g0148others(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 | a0007c0013t0018g0062 | 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 | a0001c0001t0001g0014a0001c0001t0001g0033a0001c0001t0001g0036others(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 | a0009c0014t0015g0159 | 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 | a0001c0001t0007g0003a0001c0001t0007g0164a0001c0001t0007g0165others(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 | a0001c0001t0001g0014a0001c0001t0001g0033a0001c0001t0001g0036others(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 | a0001c0002t0005g0004a0001c0002t0005g0167a0001c0002t0005g0168others(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 | a0001c0001t0001g0150a0001c0001t0003g0144a0001c0001t0003g0148others(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 | a0001c0001t0007g0003a0001c0001t0007g0164a0001c0001t0007g0165others(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 | a0001c0001t0001g0099a0001c0001t0001g0113a0001c0001t0001g0114others(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 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0089others(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 | 50 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0014others(47): Show | 51 | HG00609.hp1 HG00639.hp1 HG00639.hp2 others(48): 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 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0013others(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 | a0001c0001t0001g0050a0001c0001t0001g0128a0001c0001t0001g0175others(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 | a0001c0001t0002g0011a0001c0001t0002g0039a0001c0001t0002g0100others(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 | a0001c0001t0002g0045a0001c0001t0002g0102a0001c0001t0002g0138 | 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 | a0002c0003t0001g0145a0002c0003t0001g0147a0002c0003t0019g0146 | 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 | a0009c0014t0015g0159 | 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 | a0001c0001t0007g0003a0001c0001t0022g0003a0013c0017t0016g0005 | 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 | a0001c0001t0007g0165a0001c0002t0005g0167a0001c0018t0023g0181others(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 | a0001c0001t0001g0025a0001c0001t0007g0164a0001c0002t0005g0004others(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 | a0001c0001t0007g0003a0001c0001t0007g0164a0001c0001t0007g0165others(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 | a0001c0001t0003g0161a0001c0001t0003g0162 | 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 | a0001c0001t0001g0150a0001c0001t0003g0144a0001c0001t0003g0148others(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 | a0001c0001t0007g0003a0001c0001t0007g0164a0001c0001t0007g0165others(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 | a0001c0001t0007g0003a0001c0001t0007g0164a0001c0001t0007g0165others(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 | a0001c0001t0001g0150a0001c0001t0003g0144a0001c0001t0003g0148others(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 | a0001c0001t0001g0150a0001c0001t0003g0144a0001c0001t0003g0148others(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 | a0001c0001t0001g0150a0001c0001t0003g0144a0001c0001t0003g0148others(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 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(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 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(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 | a0002c0003t0001g0145a0002c0003t0001g0147a0002c0003t0019g0146 | 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 | a0002c0003t0001g0145a0002c0003t0001g0147a0002c0003t0019g0146 | 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 | a0001c0002t0005g0004a0001c0002t0005g0167a0001c0002t0005g0168others(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 | a0001c0001t0001g0020a0001c0001t0028g0019 | 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 | a0009c0014t0015g0159 | 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 | a0001c0001t0003g0144a0001c0001t0003g0148a0001c0001t0003g0160others(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 | a0001c0001t0003g0160a0001c0001t0003g0161a0001c0001t0003g0162others(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 | a0001c0002t0005g0004a0001c0002t0005g0167a0001c0002t0005g0168others(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 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(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 | a0001c0001t0001g0014a0001c0001t0007g0003a0001c0001t0007g0164others(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 | a0007c0013t0018g0062 | 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 | a0001c0001t0007g0003a0001c0001t0007g0164a0001c0001t0007g0165others(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 | a0001c0001t0001g0156a0001c0001t0001g0157 | 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 | 12 | a0001c0001t0001g0023a0001c0001t0001g0030a0001c0001t0001g0067others(9): Show | 12 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(9): 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 | a0001c0001t0001g0060a0001c0001t0001g0066a0001c0001t0003g0144others(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 | a0001c0001t0001g0166a0006c0009t0003g0172 | 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 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(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 | a0001c0001t0001g0006a0001c0001t0001g0028a0001c0001t0001g0038others(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 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(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 | a0001c0001t0001g0086a0001c0001t0001g0099a0001c0001t0001g0114others(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 | a0001c0001t0001g0115a0001c0001t0002g0039a0001c0001t0002g0103others(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 | a0001c0002t0005g0004a0001c0002t0005g0168a0001c0002t0005g0169others(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 | a0013c0017t0016g0005 | 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 | a0001c0001t0007g0003a0001c0001t0007g0165a0001c0001t0022g0003 | 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 | a0001c0001t0001g0150a0001c0001t0002g0043 | 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 | a0002c0003t0001g0145a0002c0003t0001g0147a0002c0003t0019g0146 | 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 | a0001c0001t0001g0002a0001c0001t0001g0063a0003c0004t0001g0136 | 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 | a0001c0001t0001g0133a0001c0012t0027g0131a0010c0015t0024g0132others(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 | a0001c0001t0007g0003a0001c0001t0007g0164a0001c0001t0007g0165others(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 | a0001c0001t0007g0003a0001c0001t0022g0003 | 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 | a0001c0001t0001g0156a0001c0001t0001g0157 | 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 | a0001c0001t0001g0001a0001c0001t0001g0016 | 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 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0134others(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 |