| geneid | 57584 |
|---|---|
| ensemblid | ENSG00000107863.20 |
| hgncid | 23725 |
| symbol | ARHGAP21 |
| name | Rho GTPase activating protein 21 |
| refseq_nuc | NM_020824.4 |
| refseq_prot | NP_065875.3 |
| ensembl_nuc | ENST00000396432.7 |
| ensembl_prot | ENSP00000379709.2 |
| mane_status | MANE Select |
| chr | chr10 |
| start | 24583614 |
| end | 24723887 |
| strand | - |
| ver | v1.2 |
| region | chr10:24583614-24723887 |
| region5000 | chr10:24578614-24728887 |
| regionname0 | ARHGAP21_chr10_24583614_24723887 |
| regionname5000 | ARHGAP21_chr10_24578614_24728887 |
| 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 | 1/0 | 1958 | 139 | 43 | 24 | 46 | 7 | 18 | 38 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| a0002 | 0/0 | 1958 | 126 | 21 | 30 | 58 | 7 | 10 | 43 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| a0003 | 0/0 | 1958 | 37 | 0 | 5 | 29 | 0 | 3 | 21 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| a0004 | 0/0 | 1958 | 9 | 9 | 0 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| a0005 | 0/0 | 1958 | 8 | 7 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| a0006 | 0/0 | 1958 | 5 | 0 | 0 | 5 | 0 | 0 | 5 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| a0007 | 0/0 | 1976 | 4 | 0 | 0 | 4 | 0 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| a0008 | 0/0 | 1958 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| a0009 | 0/0 | 1958 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| a0010 | 0/0 | 1958 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| a0011 | 0/0 | 1958 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| a0012 | 0/0 | 1958 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| a0013 | 0/0 | 1958 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| a0014 | 0/0 | 1958 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| a0015 | 0/0 | 1958 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| a0016 | 0/0 | 1958 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| a0017 | 0/0 | 1976 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| a0018 | 0/0 | 1958 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| a0019 | 0/0 | 1958 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| a0020 | 0/0 | 1958 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| a0021 | 0/0 | 1958 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| a0022 | 0/0 | 1976 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| a0023 | 0/1 | 1958 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| a0024 | 0/0 | 1958 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| 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 | 1/0 | 5877 | 138 | 42 | 24 | 46 | 7 | 18 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| c0002 | 0/0 | 5877 | 121 | 20 | 29 | 55 | 7 | 10 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| c0003 | 0/0 | 5877 | 37 | 0 | 5 | 29 | 0 | 3 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| c0004 | 0/0 | 5877 | 9 | 9 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| c0005 | 0/0 | 5877 | 8 | 7 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| c0006 | 0/0 | 5877 | 5 | 0 | 0 | 5 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| c0007 | 0/0 | 5931 | 4 | 0 | 0 | 4 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| c0008 | 0/0 | 5877 | 3 | 0 | 0 | 3 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| c0009 | 0/0 | 5877 | 3 | 0 | 0 | 3 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| c0010 | 0/0 | 5877 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| c0011 | 0/0 | 5877 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| c0012 | 0/0 | 5877 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| c0013 | 0/0 | 5877 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| c0014 | 0/0 | 5877 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| c0015 | 0/0 | 5877 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| c0016 | 0/0 | 5877 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| c0017 | 0/0 | 5877 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| c0018 | 0/0 | 5877 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| c0019 | 0/0 | 5877 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| c0020 | 0/0 | 5877 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| c0021 | 0/0 | 5877 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| c0022 | 0/0 | 5877 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| c0023 | 0/0 | 5877 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| c0024 | 0/0 | 5877 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| c0025 | 0/1 | 5877 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| c0026 | 0/0 | 5877 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| c0027 | 0/0 | 5877 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| c0028 | 0/0 | 5931 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| c0029 | 0/0 | 5931 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| c0030 | 0/0 | 5877 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 1503 | 259 | 72 | 49 | 106 | 8 | 24 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| t0002 | 0/0 | 1502 | 48 | 3 | 10 | 29 | 1 | 5 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| t0003 | 1/1 | 1505 | 9 | 2 | 2 | 2 | 1 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| t0004 | 0/0 | 1500 | 9 | 7 | 0 | 2 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| t0005 | 0/0 | 1509 | 6 | 0 | 1 | 4 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| t0006 | 0/0 | 1504 | 5 | 0 | 0 | 5 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| t0007 | 0/0 | 1506 | 3 | 0 | 0 | 0 | 1 | 2 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| t0008 | 0/0 | 1504 | 3 | 0 | 2 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| t0009 | 0/0 | 1507 | 2 | 0 | 0 | 0 | 2 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| t0010 | 0/0 | 1503 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| t0011 | 0/0 | 1505 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| t0012 | 0/0 | 1505 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| t0013 | 0/0 | 1503 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| t0014 | 0/0 | 1503 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| t0015 | 0/0 | 1502 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| t0016 | 0/0 | 1502 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0008 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0029 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0157 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0323 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| 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 | 1/0 | 5877 | 138 | 42 | 24 | 46 | 7 | 18 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| a0001c0014 | 0/0 | 5877 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| a0002c0002 | 0/0 | 5877 | 121 | 20 | 29 | 55 | 7 | 10 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| a0002c0015 | 0/0 | 5877 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| a0002c0017 | 0/0 | 5877 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| a0002c0018 | 0/0 | 5877 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| a0002c0021 | 0/0 | 5877 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| a0002c0030 | 0/0 | 5877 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| a0003c0003 | 0/0 | 5877 | 37 | 0 | 5 | 29 | 0 | 3 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| a0004c0004 | 0/0 | 5877 | 9 | 9 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| a0005c0005 | 0/0 | 5877 | 8 | 7 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| a0006c0006 | 0/0 | 5877 | 5 | 0 | 0 | 5 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| a0007c0007 | 0/0 | 5931 | 4 | 0 | 0 | 4 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| a0008c0009 | 0/0 | 5877 | 3 | 0 | 0 | 3 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| a0009c0008 | 0/0 | 5877 | 3 | 0 | 0 | 3 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| a0010c0012 | 0/0 | 5877 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| a0011c0011 | 0/0 | 5877 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| a0012c0010 | 0/0 | 5877 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| a0013c0027 | 0/0 | 5877 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| a0014c0024 | 0/0 | 5877 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| a0015c0023 | 0/0 | 5877 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| a0016c0022 | 0/0 | 5877 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| a0017c0029 | 0/0 | 5931 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| a0018c0013 | 0/0 | 5877 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| a0019c0020 | 0/0 | 5877 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| a0020c0019 | 0/0 | 5877 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| a0021c0016 | 0/0 | 5877 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| a0022c0028 | 0/0 | 5931 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| a0023c0025 | 0/1 | 5877 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| a0024c0026 | 0/0 | 5877 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 7379 | 78 | 32 | 12 | 19 | 3 | 12 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| a0001c0001t0002 | 0/0 | 7378 | 42 | 3 | 9 | 24 | 1 | 5 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| a0001c0001t0003 | 1/0 | 7381 | 4 | 2 | 0 | 0 | 1 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| a0001c0001t0004 | 0/0 | 7376 | 4 | 4 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| a0001c0001t0005 | 0/0 | 7385 | 3 | 0 | 1 | 1 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| a0001c0001t0008 | 0/0 | 7380 | 3 | 0 | 2 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| a0001c0001t0009 | 0/0 | 7383 | 2 | 0 | 0 | 0 | 2 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| a0001c0001t0013 | 0/0 | 7379 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| a0001c0001t0016 | 0/0 | 7378 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| a0001c0014t0004 | 0/0 | 7376 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| a0002c0002t0001 | 0/0 | 7379 | 115 | 19 | 29 | 54 | 5 | 8 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| a0002c0002t0004 | 0/0 | 7376 | 2 | 1 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| a0002c0002t0007 | 0/0 | 7382 | 3 | 0 | 0 | 0 | 1 | 2 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| a0002c0002t0014 | 0/0 | 7379 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| a0002c0015t0001 | 0/0 | 7379 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| a0002c0017t0001 | 0/0 | 7379 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| a0002c0018t0001 | 0/0 | 7379 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| a0002c0021t0001 | 0/0 | 7379 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| a0002c0030t0001 | 0/0 | 7379 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| a0003c0003t0001 | 0/0 | 7379 | 36 | 0 | 5 | 28 | 0 | 3 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| a0003c0003t0012 | 0/0 | 7381 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| a0004c0004t0001 | 0/0 | 7379 | 9 | 9 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| a0005c0005t0001 | 0/0 | 7379 | 6 | 6 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| a0005c0005t0003 | 0/0 | 7381 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| a0005c0005t0004 | 0/0 | 7376 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| a0006c0006t0002 | 0/0 | 7378 | 4 | 0 | 0 | 4 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| a0006c0006t0003 | 0/0 | 7381 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| a0007c0007t0006 | 0/0 | 7434 | 3 | 0 | 0 | 3 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| a0007c0007t0015 | 0/0 | 7432 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| a0008c0009t0005 | 0/0 | 7385 | 3 | 0 | 0 | 3 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| a0009c0008t0001 | 0/0 | 7379 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| a0009c0008t0004 | 0/0 | 7376 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| a0010c0012t0010 | 0/0 | 7379 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| a0011c0011t0001 | 0/0 | 7379 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| a0012c0010t0001 | 0/0 | 7379 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| a0013c0027t0001 | 0/0 | 7379 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| a0014c0024t0011 | 0/0 | 7381 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| a0015c0023t0001 | 0/0 | 7379 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| a0016c0022t0002 | 0/0 | 7378 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| a0017c0029t0006 | 0/0 | 7434 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| a0018c0013t0002 | 0/0 | 7378 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| a0019c0020t0001 | 0/0 | 7379 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| a0020c0019t0001 | 0/0 | 7379 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| a0021c0016t0003 | 0/0 | 7381 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| a0022c0028t0006 | 0/0 | 7434 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| a0023c0025t0003 | 0/1 | 7381 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| a0024c0026t0003 | 0/0 | 7381 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | copy fasta | chr10 | 24578614 | 24728887 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0002g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0002g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0002g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0002g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0002g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0002g0323 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0002g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0002g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0002g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0002g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0002g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0002g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0002g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0002g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0002g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0002g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0002g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0002g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0002g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0002g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0002g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0002g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0002g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0002g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0003g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0003g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0003g0157 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0003g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0004g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0004g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0004g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0004g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0005g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0005g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0005g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0008g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0008g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0008g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0009g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0009g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0013g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0001t0016g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0001c0014t0004g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0004g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0004g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0007g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0007g0008 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0007g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0002t0014g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0015t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0017t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0018t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0021t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0002c0030t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0003c0003t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0003c0003t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0003c0003t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0003c0003t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0003c0003t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0003c0003t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0003c0003t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0003c0003t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0003c0003t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0003c0003t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0003c0003t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0003c0003t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0003c0003t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0003c0003t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0003c0003t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0003c0003t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0003c0003t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0003c0003t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0003c0003t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0003c0003t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0003c0003t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0003c0003t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0003c0003t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0003c0003t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0003c0003t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0003c0003t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0003c0003t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0003c0003t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0003c0003t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0003c0003t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0003c0003t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0003c0003t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0003c0003t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0003c0003t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0003c0003t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0003c0003t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0003c0003t0012g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0004c0004t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0004c0004t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0004c0004t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0004c0004t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0004c0004t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0004c0004t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0004c0004t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0004c0004t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0004c0004t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0005c0005t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0005c0005t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0005c0005t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0005c0005t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0005c0005t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0005c0005t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0005c0005t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0005c0005t0004g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0006c0006t0002g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0006c0006t0002g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0006c0006t0002g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0006c0006t0002g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0006c0006t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0007c0007t0006g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0007c0007t0006g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0007c0007t0006g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0007c0007t0015g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0008c0009t0005g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0008c0009t0005g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0008c0009t0005g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0009c0008t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0009c0008t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0009c0008t0004g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0010c0012t0010g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0010c0012t0010g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0011c0011t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0011c0011t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0012c0010t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0012c0010t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0013c0027t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0014c0024t0011g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0015c0023t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0016c0022t0002g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0017c0029t0006g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0018c0013t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0019c0020t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0020c0019t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0021c0016t0003g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0022c0028t0006g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0023c0025t0003g0029 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| a0024c0026t0003g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0001 | g0279 | EUR | GBR | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG00099 | hp2 | a0002 | c0002 | t0001 | g0152 | EUR | GBR | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0241 | EUR | GBR | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG00140 | hp2 | a0002 | c0002 | t0001 | g0278 | EUR | GBR | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG00280 | hp1 | a0002 | c0002 | t0007 | g0008 | EUR | FIN | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG00280 | hp2 | a0001 | c0001 | t0003 | g0155 | EUR | FIN | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0245 | EUR | FIN | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG00323 | hp2 | a0002 | c0002 | t0001 | g0131 | EUR | FIN | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG00408 | hp1 | a0002 | c0002 | t0001 | g0056 | EAS | CHS | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG00408 | hp2 | a0003 | c0003 | t0001 | g0268 | EAS | CHS | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG00423 | hp1 | a0003 | c0003 | t0001 | g0218 | EAS | CHS | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | CHS | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG00438 | hp1 | a0002 | c0002 | t0001 | g0094 | EAS | CHS | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG00438 | hp2 | a0002 | c0002 | t0001 | g0120 | EAS | CHS | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | CHS | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG00597 | hp2 | a0003 | c0003 | t0001 | g0230 | EAS | CHS | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG00609 | hp1 | a0003 | c0003 | t0001 | g0179 | EAS | CHS | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG00609 | hp2 | a0005 | c0005 | t0003 | g0147 | EAS | CHS | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | CHS | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG00621 | hp2 | a0002 | c0002 | t0001 | g0024 | EAS | CHS | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG00639 | hp1 | a0002 | c0002 | t0001 | g0057 | AMR | PUR | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | PUR | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG00642 | hp2 | a0020 | c0019 | t0001 | g0066 | AMR | PUR | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG00673 | hp1 | a0002 | c0002 | t0001 | g0119 | EAS | CHS | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0318 | EAS | CHS | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0315 | AMR | PUR | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG00733 | hp2 | a0002 | c0002 | t0001 | g0130 | AMR | PUR | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG00735 | hp1 | a0002 | c0002 | t0001 | g0126 | AMR | PUR | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG00735 | hp2 | a0002 | c0018 | t0001 | g0097 | AMR | PUR | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG00741 | hp1 | a0002 | c0002 | t0001 | g0080 | AMR | PUR | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG01069 | hp1 | a0002 | c0002 | t0001 | g0099 | AMR | PUR | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | PUR | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG01081 | hp1 | a0024 | c0026 | t0003 | g0156 | AMR | PUR | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG01081 | hp2 | a0002 | c0002 | t0001 | g0132 | AMR | PUR | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG01099 | hp1 | a0002 | c0002 | t0001 | g0123 | AMR | PUR | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG01099 | hp2 | a0001 | c0001 | t0008 | g0327 | AMR | PUR | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG01109 | hp1 | a0016 | c0022 | t0002 | g0339 | AMR | PUR | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0242 | AMR | PUR | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0307 | AMR | PUR | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0341 | AMR | PUR | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG01175 | hp1 | a0002 | c0002 | t0001 | g0128 | AMR | PUR | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG01175 | hp2 | a0002 | c0002 | t0001 | g0086 | AMR | PUR | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG01192 | hp2 | a0002 | c0002 | t0001 | g0048 | AMR | PUR | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG01255 | hp1 | a0002 | c0002 | t0001 | g0060 | AMR | CLM | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG01255 | hp2 | a0001 | c0001 | t0008 | g0324 | AMR | CLM | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0335 | AMR | CLM | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG01256 | hp2 | a0002 | c0002 | t0001 | g0129 | AMR | CLM | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0263 | AMR | CLM | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG01257 | hp2 | a0002 | c0002 | t0001 | g0061 | AMR | CLM | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG01258 | hp1 | a0002 | c0002 | t0001 | g0058 | AMR | CLM | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0322 | AMR | CLM | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | CLM | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG01261 | hp2 | a0019 | c0020 | t0001 | g0112 | AMR | CLM | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG01361 | hp1 | a0002 | c0002 | t0001 | g0081 | AMR | CLM | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0243 | AMR | CLM | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG01433 | hp1 | a0021 | c0016 | t0003 | g0028 | AMR | CLM | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG01433 | hp2 | a0002 | c0002 | t0001 | g0125 | AMR | CLM | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG01496 | hp1 | a0002 | c0002 | t0001 | g0019 | AMR | CLM | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG01496 | hp2 | a0002 | c0002 | t0001 | g0098 | AMR | CLM | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG01516 | hp1 | a0001 | c0001 | t0009 | g0158 | EUR | IBS | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG01516 | hp2 | a0002 | c0002 | t0014 | g0105 | EUR | IBS | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG01517 | hp1 | a0001 | c0001 | t0009 | g0159 | EUR | IBS | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG01517 | hp2 | a0002 | c0002 | t0001 | g0124 | EUR | IBS | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG01884 | hp1 | a0002 | c0002 | t0004 | g0295 | AFR | ACB | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | ACB | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG01891 | hp1 | a0002 | c0002 | t0001 | g0122 | AFR | ACB | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | ACB | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG01928 | hp1 | a0002 | c0002 | t0001 | g0101 | AMR | PEL | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0308 | AMR | PEL | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG01934 | hp1 | a0002 | c0002 | t0001 | g0049 | AMR | PEL | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0340 | AMR | PEL | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG01952 | hp1 | a0003 | c0003 | t0001 | g0212 | AMR | PEL | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG01952 | hp2 | a0002 | c0002 | t0001 | g0053 | AMR | PEL | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG01975 | hp1 | a0002 | c0002 | t0001 | g0078 | AMR | PEL | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0303 | AMR | PEL | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0260 | AMR | PEL | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG01978 | hp2 | a0002 | c0002 | t0001 | g0082 | AMR | PEL | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG01981 | hp1 | a0001 | c0001 | t0005 | g0005 | AMR | PEL | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG01981 | hp2 | a0002 | c0002 | t0001 | g0256 | AMR | PEL | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG01993 | hp1 | a0003 | c0003 | t0001 | g0265 | AMR | PEL | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG01993 | hp2 | a0002 | c0002 | t0001 | g0063 | AMR | PEL | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG02004 | hp1 | a0003 | c0003 | t0001 | g0201 | AMR | PEL | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG02004 | hp2 | a0002 | c0002 | t0001 | g0027 | AMR | PEL | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG02027 | hp1 | a0003 | c0003 | t0001 | g0247 | EAS | KHV | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG02027 | hp2 | a0002 | c0002 | t0001 | g0283 | EAS | KHV | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | KHV | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG02040 | hp2 | a0002 | c0002 | t0001 | g0034 | EAS | KHV | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG02055 | hp1 | a0005 | c0005 | t0001 | g0104 | AFR | ACB | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | ACB | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0319 | EAS | KHV | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG02071 | hp2 | a0002 | c0002 | t0001 | g0127 | EAS | KHV | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG02074 | hp1 | a0002 | c0002 | t0001 | g0010 | EAS | KHV | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG02074 | hp2 | a0002 | c0017 | t0001 | g0041 | EAS | KHV | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG02080 | hp1 | a0002 | c0002 | t0001 | g0118 | EAS | KHV | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0312 | EAS | KHV | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG02083 | hp1 | a0002 | c0015 | t0001 | g0161 | EAS | KHV | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG02083 | hp2 | a0003 | c0003 | t0001 | g0198 | EAS | KHV | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG02129 | hp1 | a0003 | c0003 | t0001 | g0236 | EAS | KHV | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG02129 | hp2 | a0007 | c0007 | t0006 | g0291 | EAS | KHV | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG02145 | hp1 | a0004 | c0004 | t0001 | g0089 | AFR | ACB | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0264 | AFR | ACB | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG02148 | hp1 | a0002 | c0002 | t0001 | g0109 | AMR | PEL | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG02148 | hp2 | a0003 | c0003 | t0001 | g0203 | AMR | PEL | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0316 | EAS | CDX | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG02155 | hp2 | a0002 | c0002 | t0001 | g0083 | EAS | CDX | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG02165 | hp1 | a0002 | c0002 | t0001 | g0026 | EAS | CDX | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG02165 | hp2 | a0003 | c0003 | t0001 | g0213 | EAS | CDX | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | ACB | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG02257 | hp2 | a0002 | c0002 | t0001 | g0134 | AFR | ACB | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG02258 | hp1 | a0002 | c0002 | t0001 | g0111 | AFR | ACB | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG02258 | hp2 | a0002 | c0002 | t0001 | g0135 | AFR | ACB | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | ACB | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | ACB | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0325 | AMR | PEL | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG02300 | hp2 | a0002 | c0002 | t0001 | g0042 | AMR | PEL | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG02451 | hp1 | a0005 | c0005 | t0001 | g0103 | AFR | ACB | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | ACB | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG02523 | hp1 | a0018 | c0013 | t0002 | g0314 | EAS | KHV | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG02523 | hp2 | a0007 | c0007 | t0006 | g0293 | EAS | KHV | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG02572 | hp1 | a0002 | c0002 | t0001 | g0088 | AFR | GWD | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG02602 | hp1 | a0002 | c0002 | t0001 | g0059 | SAS | PJL | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0191 | SAS | PJL | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG02615 | hp1 | a0002 | c0002 | t0001 | g0139 | AFR | GWD | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | GWD | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0255 | AFR | GWD | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | GWD | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG02630 | hp1 | a0002 | c0002 | t0001 | g0107 | AFR | GWD | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0253 | AFR | GWD | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG02647 | hp1 | a0004 | c0004 | t0001 | g0031 | AFR | GWD | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG02647 | hp2 | a0013 | c0027 | t0001 | g0065 | AFR | GWD | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0317 | SAS | PJL | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG02698 | hp2 | a0002 | c0002 | t0001 | g0121 | SAS | PJL | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | GWD | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | GWD | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG02723 | hp1 | a0010 | c0012 | t0010 | g0016 | AFR | GWD | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG02723 | hp2 | a0002 | c0002 | t0001 | g0117 | AFR | GWD | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0257 | SAS | PJL | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG02738 | hp2 | a0015 | c0023 | t0001 | g0090 | SAS | PJL | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG02809 | hp1 | a0002 | c0002 | t0001 | g0136 | AFR | GWD | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG02809 | hp2 | a0004 | c0004 | t0001 | g0100 | AFR | GWD | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG02818 | hp2 | a0011 | c0011 | t0001 | g0258 | AFR | GWD | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG02895 | hp1 | a0001 | c0001 | t0004 | g0298 | AFR | GWD | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG02895 | hp2 | a0002 | c0002 | t0001 | g0110 | AFR | GWD | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG02896 | hp1 | a0010 | c0012 | t0010 | g0015 | AFR | GWD | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0344 | AFR | GWD | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0343 | AFR | GWD | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG02897 | hp2 | a0001 | c0001 | t0004 | g0297 | AFR | GWD | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG02922 | hp1 | a0002 | c0002 | t0001 | g0138 | AFR | ESN | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0294 | AFR | ESN | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG02965 | hp2 | a0001 | c0001 | t0004 | g0299 | AFR | ESN | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG02970 | hp1 | a0004 | c0004 | t0001 | g0032 | AFR | ESN | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0251 | AFR | ESN | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG02976 | hp1 | a0002 | c0021 | t0001 | g0084 | AFR | ESN | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG02976 | hp2 | a0004 | c0004 | t0001 | g0091 | AFR | ESN | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG03017 | hp1 | a0002 | c0002 | t0001 | g0021 | SAS | PJL | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG03017 | hp2 | a0002 | c0002 | t0007 | g0009 | SAS | PJL | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG03041 | hp1 | a0002 | c0002 | t0001 | g0020 | AFR | GWD | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG03130 | hp1 | a0001 | c0001 | t0013 | g0254 | AFR | ESN | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG03130 | hp2 | a0005 | c0005 | t0001 | g0167 | AFR | ESN | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG03139 | hp1 | a0002 | c0002 | t0001 | g0108 | AFR | ESN | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG03139 | hp2 | a0004 | c0004 | t0001 | g0070 | AFR | ESN | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG03195 | hp1 | a0012 | c0010 | t0001 | g0266 | AFR | ESN | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | ESN | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG03209 | hp1 | a0005 | c0005 | t0004 | g0287 | AFR | MSL | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG03209 | hp2 | a0005 | c0005 | t0001 | g0102 | AFR | MSL | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0216 | AFR | MSL | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG03239 | hp1 | a0002 | c0002 | t0001 | g0153 | SAS | PJL | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0196 | SAS | PJL | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG03453 | hp1 | a0002 | c0002 | t0001 | g0106 | AFR | MSL | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | MSL | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG03486 | hp1 | a0002 | c0002 | t0001 | g0017 | AFR | MSL | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG03486 | hp2 | a0011 | c0011 | t0001 | g0259 | AFR | MSL | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0346 | SAS | PJL | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0246 | SAS | PJL | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0240 | SAS | PJL | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG03491 | hp2 | a0002 | c0002 | t0001 | g0054 | SAS | PJL | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0342 | SAS | PJL | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0238 | SAS | PJL | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | GWD | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG03540 | hp2 | a0004 | c0004 | t0001 | g0069 | AFR | GWD | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | MSL | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG03579 | hp2 | a0004 | c0004 | t0001 | g0067 | AFR | MSL | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0178 | SAS | PJL | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG03654 | hp2 | a0002 | c0002 | t0001 | g0079 | SAS | PJL | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG03688 | hp1 | a0002 | c0002 | t0007 | g0007 | SAS | STU | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG03688 | hp2 | a0003 | c0003 | t0001 | g0276 | SAS | STU | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0186 | SAS | PJL | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0336 | SAS | PJL | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0310 | SAS | BEB | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0190 | SAS | BEB | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG03927 | hp1 | a0002 | c0002 | t0001 | g0062 | SAS | BEB | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG03927 | hp2 | a0001 | c0001 | t0005 | g0001 | SAS | BEB | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0170 | SAS | BEB | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG03942 | hp2 | a0003 | c0003 | t0001 | g0211 | SAS | BEB | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0228 | SAS | STU | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG04199 | hp2 | a0002 | c0002 | t0001 | g0077 | SAS | STU | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0244 | SAS | STU | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG04228 | hp2 | a0003 | c0003 | t0001 | g0116 | SAS | STU | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA18522 | hp1 | a0005 | c0005 | t0001 | g0284 | AFR | YRI | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA18522 | hp2 | a0002 | c0002 | t0001 | g0140 | AFR | YRI | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA18747 | hp1 | a0007 | c0007 | t0015 | g0288 | EAS | CHB | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA18747 | hp2 | a0002 | c0002 | t0001 | g0038 | EAS | CHB | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA18906 | hp1 | a0001 | c0014 | t0004 | g0286 | AFR | YRI | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | YRI | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0321 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA18939 | hp2 | a0002 | c0002 | t0001 | g0149 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA18941 | hp1 | a0002 | c0002 | t0001 | g0151 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA18941 | hp2 | a0009 | c0008 | t0001 | g0261 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA18943 | hp1 | a0002 | c0002 | t0001 | g0150 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA18945 | hp1 | a0003 | c0003 | t0001 | g0227 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0333 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA18947 | hp1 | a0003 | c0003 | t0001 | g0209 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA18947 | hp2 | a0002 | c0002 | t0001 | g0039 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0334 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA18951 | hp2 | a0003 | c0003 | t0001 | g0180 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA18953 | hp1 | a0002 | c0002 | t0001 | g0035 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA18953 | hp2 | a0002 | c0002 | t0001 | g0280 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0320 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA18957 | hp1 | a0006 | c0006 | t0002 | g0348 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA18957 | hp2 | a0002 | c0002 | t0001 | g0085 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA18959 | hp1 | a0003 | c0003 | t0001 | g0200 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0309 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0331 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA18961 | hp2 | a0003 | c0003 | t0001 | g0205 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA18963 | hp1 | a0003 | c0003 | t0001 | g0277 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA18963 | hp2 | a0002 | c0002 | t0001 | g0146 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0337 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA18970 | hp2 | a0002 | c0002 | t0001 | g0050 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA18972 | hp1 | a0002 | c0002 | t0001 | g0285 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0305 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0304 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA18974 | hp2 | a0009 | c0008 | t0001 | g0262 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA18975 | hp2 | a0002 | c0002 | t0001 | g0046 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA18978 | hp2 | a0002 | c0002 | t0001 | g0095 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA18979 | hp1 | a0002 | c0002 | t0001 | g0025 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0326 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA18980 | hp1 | a0002 | c0002 | t0001 | g0036 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA18980 | hp2 | a0002 | c0002 | t0001 | g0282 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA18982 | hp1 | a0002 | c0002 | t0004 | g0301 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA18982 | hp2 | a0003 | c0003 | t0001 | g0229 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA18986 | hp2 | a0001 | c0001 | t0008 | g0306 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA18987 | hp1 | a0002 | c0002 | t0001 | g0076 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA18987 | hp2 | a0003 | c0003 | t0001 | g0011 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA18988 | hp2 | a0002 | c0002 | t0001 | g0064 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA18989 | hp1 | a0017 | c0029 | t0006 | g0290 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA18989 | hp2 | a0001 | c0001 | t0016 | g0352 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA18992 | hp1 | a0006 | c0006 | t0002 | g0349 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA18992 | hp2 | a0002 | c0002 | t0001 | g0096 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA18994 | hp1 | a0002 | c0002 | t0001 | g0051 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0311 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA18995 | hp1 | a0002 | c0002 | t0001 | g0113 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA18995 | hp2 | a0008 | c0009 | t0005 | g0004 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0332 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA18998 | hp2 | a0003 | c0003 | t0001 | g0175 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA19002 | hp1 | a0002 | c0002 | t0001 | g0148 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA19002 | hp2 | a0003 | c0003 | t0001 | g0223 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA19003 | hp1 | a0002 | c0002 | t0001 | g0030 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA19003 | hp2 | a0003 | c0003 | t0001 | g0208 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA19004 | hp1 | a0008 | c0009 | t0005 | g0003 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA19004 | hp2 | a0003 | c0003 | t0001 | g0173 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA19005 | hp2 | a0006 | c0006 | t0002 | g0351 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA19007 | hp1 | a0002 | c0002 | t0001 | g0023 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA19007 | hp2 | a0003 | c0003 | t0001 | g0210 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA19009 | hp1 | a0001 | c0001 | t0005 | g0006 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA19009 | hp2 | a0002 | c0002 | t0001 | g0072 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA19011 | hp1 | a0008 | c0009 | t0005 | g0002 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA19011 | hp2 | a0022 | c0028 | t0006 | g0289 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA19030 | hp1 | a0005 | c0005 | t0001 | g0137 | AFR | LWK | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA19030 | hp2 | a0014 | c0024 | t0011 | g0033 | AFR | LWK | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA19054 | hp1 | a0002 | c0002 | t0001 | g0092 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA19054 | hp2 | a0003 | c0003 | t0001 | g0204 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA19055 | hp1 | a0002 | c0002 | t0001 | g0075 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA19056 | hp1 | a0003 | c0003 | t0012 | g0172 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA19056 | hp2 | a0007 | c0007 | t0006 | g0292 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA19057 | hp1 | a0002 | c0002 | t0001 | g0047 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA19057 | hp2 | a0003 | c0003 | t0001 | g0231 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA19058 | hp1 | a0002 | c0002 | t0001 | g0073 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0345 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA19060 | hp1 | a0006 | c0006 | t0002 | g0350 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0302 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA19062 | hp2 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA19064 | hp1 | a0003 | c0003 | t0001 | g0207 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA19064 | hp2 | a0002 | c0002 | t0001 | g0040 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA19065 | hp2 | a0002 | c0002 | t0001 | g0114 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA19066 | hp2 | a0009 | c0008 | t0004 | g0347 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA19070 | hp1 | a0002 | c0002 | t0001 | g0281 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA19070 | hp2 | a0002 | c0002 | t0001 | g0052 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA19072 | hp1 | a0003 | c0003 | t0001 | g0248 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA19072 | hp2 | a0002 | c0002 | t0001 | g0043 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA19074 | hp1 | a0002 | c0002 | t0001 | g0037 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0338 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA19077 | hp1 | a0002 | c0002 | t0001 | g0074 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0330 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA19078 | hp1 | a0003 | c0003 | t0001 | g0215 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA19078 | hp2 | a0002 | c0002 | t0001 | g0093 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA19079 | hp1 | a0002 | c0002 | t0001 | g0045 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0313 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0328 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA19081 | hp1 | a0006 | c0006 | t0003 | g0214 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA19081 | hp2 | a0002 | c0002 | t0001 | g0115 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0329 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA19085 | hp2 | a0003 | c0003 | t0001 | g0206 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0300 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA19087 | hp2 | a0002 | c0030 | t0001 | g0022 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA19088 | hp1 | a0002 | c0002 | t0001 | g0044 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA19088 | hp2 | a0003 | c0003 | t0001 | g0221 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA19090 | hp2 | a0002 | c0002 | t0001 | g0145 | EAS | JPT | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | YRI | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA19240 | hp2 | a0001 | c0001 | t0004 | g0296 | AFR | YRI | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | ASW | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0154 | AFR | ASW | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0323 | EUR | TSI | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0188 | EUR | TSI | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG01123 | hp1 | a0003 | c0003 | t0001 | g0202 | AMR | CLM | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG01123 | hp2 | a0002 | c0002 | t0001 | g0071 | AMR | CLM | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG02109 | hp1 | a0012 | c0010 | t0001 | g0267 | AFR | ACB | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG02109 | hp2 | a0002 | c0002 | t0001 | g0087 | AFR | ACB | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | ACB | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | ACB | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | ACB | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG02559 | hp2 | a0004 | c0004 | t0001 | g0068 | AFR | ACB | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | MSL | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG03471 | hp2 | a0002 | c0002 | t0001 | g0133 | AFR | MSL | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | USA | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| HG06807 | hp2 | a0002 | c0002 | t0001 | g0055 | AFR | USA | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| homoSapiens_chm13v2 | hp1 | a0023 | c0025 | t0003 | g0029 | REF | REF | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0003 | g0157 | REF | REF | ARHGAP21_chr10_24578614_24728887 | ARHGAP21 | chr10 | 24578614 | 24728887 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:24584440
|
C | G | 11 | a0002a0003a0004others(8): Show | 182 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(179): Show |
missense_variant | MODERATE | c.5849G>C | p.Ser1950Thr | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 26/26 | 6555/7381 | 5849/5877 | 1950/1958 | chr10 | 24584440 | ||
| chr10:24584440
|
C | T | 1 | a0006 | 5 | NA18957.hp1 NA18992.hp1 NA19005.hp2 others(2): Show |
missense_variant | MODERATE | c.5849G>A | p.Ser1950Asn | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 26/26 | 6555/7381 | 5849/5877 | 1950/1958 | chr10 | 24584440 | ||
| chr10:24584635
|
G | A | 1 | a0018 | 1 | HG02523.hp1 | missense_variant | MODERATE | c.5654C>T | p.Thr1885Met | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 26/26 | 6360/7381 | 5654/5877 | 1885/1958 | chr10 | 24584635 | ||
| chr10:24584959
|
G | A | 1 | a0020 | 1 | HG00642.hp2 | missense_variant | MODERATE | c.5330C>T | p.Ala1777Val | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 26/26 | 6036/7381 | 5330/5877 | 1777/1958 | chr10 | 24584959 | ||
| chr10:24585182
|
G | A | 1 | a0019 | 1 | HG01261.hp2 | missense_variant | MODERATE | c.5107C>T | p.Leu1703Phe | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 26/26 | 5813/7381 | 5107/5877 | 1703/1958 | chr10 | 24585182 | ||
| chr10:24585335
|
T | C | 1 | a0017 | 1 | NA18989.hp1 | missense_variant | MODERATE | c.4954A>G | p.Arg1652Gly | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 26/26 | 5660/7381 | 4954/5877 | 1652/1958 | chr10 | 24585335 | ||
| chr10:24594993
|
G | GAAAGGAA others(47): Show |
3 | a0007a0017a0022 | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
conservative_inframe_insertion | MODERATE | c.3787-8_3832dupTGTT others(50): Show |
p.Leu1277_Ser1278ins others(54): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 21/26 | 4538/7381 | 3832/5877 | 1278/1958 | chr10 | 24594993 | ||
| chr10:24596856
|
C | T | 2 | a0004a0014 | 10 | HG02145.hp1 HG02559.hp2 HG02647.hp1 others(7): Show |
missense_variant | MODERATE | c.3361G>A | p.Gly1121Ser | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 17/26 | 4067/7381 | 3361/5877 | 1121/1958 | chr10 | 24596856 | ||
| chr10:24600731
|
C | G | 1 | a0011 | 2 | HG02818.hp2 HG03486.hp2 |
missense_variant | MODERATE | c.3047G>C | p.Cys1016Ser | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 14/26 | 3753/7381 | 3047/5877 | 1016/1958 | chr10 | 24600731 | ||
| chr10:24619599
|
C | T | 2 | a0021a0023 | 2 | HG01433.hp1 homoSapiens_chm13v2.hp1 |
missense_variant | MODERATE | c.2296G>A | p.Gly766Arg | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/26 | 3002/7381 | 2296/5877 | 766/1958 | chr10 | 24619599 | ||
| chr10:24619757
|
T | C | 11 | a0002a0004a0005others(8): Show | 152 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(149): Show |
missense_variant | MODERATE | c.2138A>G | p.Asn713Ser | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/26 | 2844/7381 | 2138/5877 | 713/1958 | chr10 | 24619757 | ||
| chr10:24619844
|
G | C | 1 | a0010 | 2 | HG02723.hp1 HG02896.hp1 |
missense_variant | MODERATE | c.2051C>G | p.Ser684Cys | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/26 | 2757/7381 | 2051/5877 | 684/1958 | chr10 | 24619844 | ||
| chr10:24620069
|
C | T | 1 | a0009 | 3 | NA18941.hp2 NA18974.hp2 NA19066.hp2 |
missense_variant | MODERATE | c.1826G>A | p.Arg609Gln | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/26 | 2532/7381 | 1826/5877 | 609/1958 | chr10 | 24620069 | ||
| chr10:24620159
|
G | T | 1 | a0022 | 1 | NA19011.hp2 | missense_variant | MODERATE | c.1736C>A | p.Ser579Tyr | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/26 | 2442/7381 | 1736/5877 | 579/1958 | chr10 | 24620159 | ||
| chr10:24620286
|
T | C | 1 | a0016 | 1 | HG01109.hp1 | missense_variant | MODERATE | c.1609A>G | p.Arg537Gly | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/26 | 2315/7381 | 1609/5877 | 537/1958 | chr10 | 24620286 | ||
| chr10:24620421
|
T | C | 1 | a0015 | 1 | HG02738.hp2 | missense_variant | MODERATE | c.1474A>G | p.Arg492Gly | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/26 | 2180/7381 | 1474/5877 | 492/1958 | chr10 | 24620421 | ||
| chr10:24620630
|
G | A | 1 | a0014 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.1265C>T | p.Thr422Met | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/26 | 1971/7381 | 1265/5877 | 422/1958 | chr10 | 24620630 | ||
| chr10:24620679
|
G | A | 1 | a0023 | 1 | homoSapiens_chm13v2.hp1 | missense_variant | MODERATE | c.1216C>T | p.Arg406Trp | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/26 | 1922/7381 | 1216/5877 | 406/1958 | chr10 | 24620679 | ||
| chr10:24620709
|
T | C | 1 | a0024 | 1 | HG01081.hp1 | missense_variant | MODERATE | c.1186A>G | p.Ile396Val | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/26 | 1892/7381 | 1186/5877 | 396/1958 | chr10 | 24620709 | ||
| chr10:24620916
|
T | C | 1 | a0013 | 1 | HG02647.hp2 | missense_variant | MODERATE | c.979A>G | p.Thr327Ala | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/26 | 1685/7381 | 979/5877 | 327/1958 | chr10 | 24620916 | ||
| chr10:24621258
|
C | T | 1 | a0012 | 2 | HG02109.hp1 HG03195.hp1 |
missense_variant | MODERATE | c.637G>A | p.Ala213Thr | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/26 | 1343/7381 | 637/5877 | 213/1958 | chr10 | 24621258 | ||
| chr10:24670388
|
T | C | 1 | a0008 | 3 | NA18995.hp2 NA19004.hp1 NA19011.hp1 |
missense_variant | MODERATE | c.73A>G | p.Asn25Asp | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 3/26 | 779/7381 | 73/5877 | 25/1958 | chr10 | 24670388 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:24584478
|
C | G | 1 | a0002c0018 | 1 | HG00735.hp2 | synonymous_variant | LOW | c.5811G>C | p.Ala1937Ala | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 26/26 | 6517/7381 | 5811/5877 | 1937/1958 | chr10 | 24584478 | ||
| chr10:24585882
|
C | T | 1 | a0002c0017 | 1 | HG02074.hp2 | synonymous_variant | LOW | c.4407G>A | p.Gln1469Gln | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 26/26 | 5113/7381 | 4407/5877 | 1469/1958 | chr10 | 24585882 | ||
| chr10:24595900
|
A | G | 3 | a0007c0007a0017c0029a0022c0028 | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
synonymous_variant | LOW | c.3621T>C | p.Asp1207Asp | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 18/26 | 4327/7381 | 3621/5877 | 1207/1958 | chr10 | 24595900 | ||
| chr10:24619600
|
G | A | 1 | a0001c0014 | 1 | NA18906.hp1 | synonymous_variant | LOW | c.2295C>T | p.Thr765Thr | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/26 | 3001/7381 | 2295/5877 | 765/1958 | chr10 | 24619600 | ||
| chr10:24619651
|
C | T | 1 | a0002c0015 | 1 | HG02083.hp1 | synonymous_variant | LOW | c.2244G>A | p.Pro748Pro | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/26 | 2950/7381 | 2244/5877 | 748/1958 | chr10 | 24619651 | ||
| chr10:24620152
|
C | A | 1 | a0002c0021 | 1 | HG02976.hp1 | synonymous_variant | LOW | c.1743G>T | p.Ser581Ser | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/26 | 2449/7381 | 1743/5877 | 581/1958 | chr10 | 24620152 | ||
| chr10:24620941
|
T | G | 3 | a0007c0007a0017c0029a0022c0028 | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
synonymous_variant | LOW | c.954A>C | p.Thr318Thr | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/26 | 1660/7381 | 954/5877 | 318/1958 | chr10 | 24620941 | ||
| chr10:24621280
|
G | A | 1 | a0002c0030 | 1 | NA19087.hp2 | synonymous_variant | LOW | c.615C>T | p.Pro205Pro | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/26 | 1321/7381 | 615/5877 | 205/1958 | chr10 | 24621280 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:24583825
|
G | A | 1 | a0002c0002t0014 | 1 | HG01516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*587C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 26/26 | 587 | chr10 | 24583825 | |||||
| chr10:24583830
|
G | A | 1 | a0003c0003t0012 | 1 | NA19056.hp1 | 3_prime_UTR_variant | MODIFIER | c.*582C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 26/26 | 582 | chr10 | 24583830 | |||||
| chr10:24584031
|
T | A | 4 | a0007c0007t0006a0007c0007t0015a0017c0029t0006others(1): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*381A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 26/26 | 381 | chr10 | 24584031 | |||||
| chr10:24584053
|
C | T | 1 | a0010c0012t0010 | 2 | HG02723.hp1 HG02896.hp1 |
3_prime_UTR_variant | MODIFIER | c.*359G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 26/26 | 359 | chr10 | 24584053 | |||||
| chr10:24584181
|
T | C | 1 | a0010c0012t0010 | 2 | HG02723.hp1 HG02896.hp1 |
3_prime_UTR_variant | MODIFIER | c.*231A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 26/26 | 231 | chr10 | 24584181 | |||||
| chr10:24584208
|
C | G | 1 | a0001c0001t0013 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*204G>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 26/26 | 204 | chr10 | 24584208 | |||||
| chr10:24584221
|
A | AAT | 5 | a0001c0001t0008a0001c0001t0009a0007c0007t0006others(2): Show | 10 | HG01099.hp2 HG01255.hp2 HG01516.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*189_*190dupAT | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 26/26 | 190 | chr10 | 24584221 | |||||
| chr10:24584221
|
AAT | A | 28 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(25): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
3_prime_UTR_variant | MODIFIER | c.*189_*190delAT | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 26/26 | 189 | chr10 | 24584221 | |||||
| chr10:24584240
|
A | G | 1 | a0014c0024t0011 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*172T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 26/26 | 172 | chr10 | 24584240 | |||||
| chr10:24723673
|
C | CCCG | 1 | a0002c0002t0007 | 3 | HG00280.hp1 HG03017.hp2 HG03688.hp1 |
5_prime_UTR_variant | MODIFIER | c.-495_-493dupCGG | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 1/26 | 1775 | chr10 | 24723673 | |||||
| chr10:24723673
|
C | CCCGCCG | 2 | a0001c0001t0005a0008c0009t0005 | 6 | HG01981.hp1 HG03927.hp2 NA18995.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-498_-493dupCGGCGG | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 1/26 | 1775 | chr10 | 24723673 | |||||
| chr10:24723673
|
CCCG | C | 15 | a0001c0001t0002a0001c0001t0004a0001c0001t0008others(12): Show | 67 | HG00673.hp2 HG00733.hp1 HG01099.hp2 others(64): Show |
5_prime_UTR_variant | MODIFIER | c.-495_-493delCGG | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 1/26 | 1775 | chr10 | 24723673 | |||||
| chr10:24723846
|
G | A | 1 | a0001c0001t0016 | 1 | NA18989.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-665C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 1/26 | chr10 | 24723846 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:24586167
|
A | G | 2 | a0001c0001t0001g0142a0001c0001t0001g0143 | 2 | HG02451.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.4183-61T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 25/25 | chr10 | 24586167 | ||||||
| chr10:24586501
|
G | A | 1 | a0002c0002t0001g0094 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.4183-395C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 25/25 | chr10 | 24586501 | ||||||
| chr10:24586523
|
T | C | 1 | a0001c0001t0001g0196 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.4183-417A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 25/25 | chr10 | 24586523 | ||||||
| chr10:24586917
|
G | A | 1 | a0001c0001t0004g0296 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.4183-811C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 25/25 | chr10 | 24586917 | ||||||
| chr10:24587244
|
A | G | 1 | a0005c0005t0001g0104 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.4183-1138T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 25/25 | chr10 | 24587244 | ||||||
| chr10:24587285
|
A | G | 2 | a0010c0012t0010g0015a0010c0012t0010g0016 | 2 | HG02723.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.4183-1179T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 25/25 | chr10 | 24587285 | ||||||
| chr10:24587466
|
AAATTTAG others(6): Show |
A | 34 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0176others(31): Show | 34 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(31): Show |
intron_variant | MODIFIER | c.4183-1373_4183-136 others(17): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 25/25 | chr10 | 24587466 | ||||||
| chr10:24587620
|
T | G | 1 | a0001c0001t0002g0319 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.4183-1514A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 25/25 | chr10 | 24587620 | ||||||
| chr10:24587690
|
T | C | 43 | a0002c0002t0001g0017a0002c0002t0001g0019a0002c0002t0001g0056others(40): Show | 43 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(40): Show |
intron_variant | MODIFIER | c.4182+1581A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 25/25 | chr10 | 24587690 | ||||||
| chr10:24587734
|
G | A | 169 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(166): Show | 169 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.4182+1537C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 25/25 | chr10 | 24587734 | ||||||
| chr10:24587827
|
TTACTC | T | 6 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(3): Show | 6 | HG02145.hp2 HG02965.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.4182+1439_4182+144 others(9): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 25/25 | chr10 | 24587827 | ||||||
| chr10:24587840
|
C | G | 16 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(13): Show | 16 | HG01891.hp2 HG02280.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.4182+1431G>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 25/25 | chr10 | 24587840 | ||||||
| chr10:24588347
|
C | CTAGGGTA others(31): Show |
40 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(37): Show | 40 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(37): Show |
intron_variant | MODIFIER | c.4182+886_4182+923d others(40): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 25/25 | chr10 | 24588347 | ||||||
| chr10:24588570
|
T | C | 1 | a0001c0001t0001g0192 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.4182+701A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 25/25 | chr10 | 24588570 | ||||||
| chr10:24588915
|
C | T | 2 | a0002c0002t0001g0034a0002c0002t0001g0052 | 2 | HG02040.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.4182+356G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 25/25 | chr10 | 24588915 | ||||||
| chr10:24588925
|
C | T | 1 | a0001c0001t0008g0324 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.4182+346G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 25/25 | chr10 | 24588925 | ||||||
| chr10:24588954
|
T | A | 1 | a0001c0001t0001g0273 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.4182+317A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 25/25 | chr10 | 24588954 | ||||||
| chr10:24588997
|
T | C | 16 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(13): Show | 16 | HG01891.hp2 HG02280.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.4182+274A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 25/25 | chr10 | 24588997 | ||||||
| chr10:24589093
|
C | T | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.4182+178G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 25/25 | chr10 | 24589093 | ||||||
| chr10:24589113
|
C | A | 145 | a0002c0002t0001g0010a0002c0002t0001g0017a0002c0002t0001g0018others(142): Show | 145 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.4182+158G>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 25/25 | chr10 | 24589113 | ||||||
| chr10:24589173
|
A | G | 2 | a0010c0012t0010g0015a0010c0012t0010g0016 | 2 | HG02723.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.4182+98T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 25/25 | chr10 | 24589173 | ||||||
| chr10:24589179
|
C | T | 3 | a0002c0002t0001g0280a0002c0002t0001g0281a0002c0002t0001g0282 | 3 | NA18953.hp2 NA18980.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.4182+92G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 25/25 | chr10 | 24589179 | ||||||
| chr10:24589200
|
G | A | 291 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(288): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.4182+71C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 25/25 | chr10 | 24589200 | ||||||
| chr10:24589673
|
T | A | 1 | a0003c0003t0001g0179 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.4151-371A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 24/25 | chr10 | 24589673 | ||||||
| chr10:24589905
|
G | A | 144 | a0002c0002t0001g0010a0002c0002t0001g0017a0002c0002t0001g0018others(141): Show | 144 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.4151-603C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 24/25 | chr10 | 24589905 | ||||||
| chr10:24589907
|
G | A | 1 | a0002c0002t0001g0059 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.4151-605C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 24/25 | chr10 | 24589907 | ||||||
| chr10:24590352
|
A | G | 351 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(348): Show | 351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.4150+873T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 24/25 | chr10 | 24590352 | ||||||
| chr10:24590855
|
ATAC | A | 24 | a0002c0002t0001g0017a0002c0002t0001g0117a0002c0002t0001g0118others(21): Show | 24 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(21): Show |
intron_variant | MODIFIER | c.4150+367_4150+369d others(5): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 24/25 | chr10 | 24590855 | ||||||
| chr10:24590940
|
T | TA | 6 | a0001c0001t0001g0176a0001c0001t0001g0257a0001c0001t0002g0321others(3): Show | 6 | HG01261.hp1 HG02083.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.4150+284dupT | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 24/25 | chr10 | 24590940 | ||||||
| chr10:24590940
|
TA | T | 25 | a0001c0001t0001g0174a0001c0001t0001g0217a0001c0001t0001g0219others(22): Show | 25 | HG00323.hp1 HG00609.hp1 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.4150+284delT | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 24/25 | chr10 | 24590940 | ||||||
| chr10:24591447
|
T | C | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.4045-117A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 23/25 | chr10 | 24591447 | ||||||
| chr10:24591484
|
C | T | 7 | a0001c0001t0002g0302a0001c0001t0002g0318a0001c0001t0002g0320others(4): Show | 7 | HG00673.hp2 HG01109.hp1 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.4045-154G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 23/25 | chr10 | 24591484 | ||||||
| chr10:24591572
|
T | C | 1 | a0002c0002t0001g0035 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.4044+70A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 23/25 | chr10 | 24591572 | ||||||
| chr10:24591783
|
G | A | 156 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(153): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.4003-100C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 22/25 | chr10 | 24591783 | ||||||
| chr10:24592156
|
A | AT | 17 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0163others(14): Show | 17 | HG01258.hp2 HG01934.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.3877-145dupA | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 21/25 | chr10 | 24592156 | ||||||
| chr10:24592156
|
AT | A | 189 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0160others(186): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.3877-145delA | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 21/25 | chr10 | 24592156 | ||||||
| chr10:24592156
|
ATT | A | 38 | a0001c0001t0001g0013a0002c0002t0001g0017a0002c0002t0001g0019others(35): Show | 38 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(35): Show |
intron_variant | MODIFIER | c.3877-146_3877-145d others(4): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 21/25 | chr10 | 24592156 | ||||||
| chr10:24592156
|
ATTTTTT | A | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.3877-150_3877-145d others(8): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 21/25 | chr10 | 24592156 | ||||||
| chr10:24592636
|
T | C | 170 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(167): Show | 170 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.3877-624A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 21/25 | chr10 | 24592636 | ||||||
| chr10:24592643
|
C | T | 1 | a0002c0002t0001g0135 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3877-631G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 21/25 | chr10 | 24592643 | ||||||
| chr10:24592714
|
C | T | 160 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(157): Show | 160 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(157): Show |
intron_variant | MODIFIER | c.3877-702G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 21/25 | chr10 | 24592714 | ||||||
| chr10:24592720
|
A | AGTAAGAT others(11): Show |
3 | a0002c0002t0001g0107a0002c0002t0001g0108a0002c0002t0001g0111 | 3 | HG02258.hp1 HG02630.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.3877-726_3877-709d others(20): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 21/25 | chr10 | 24592720 | ||||||
| chr10:24592746
|
G | GA | 16 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(13): Show | 16 | HG01891.hp2 HG02280.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.3877-735dupT | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 21/25 | chr10 | 24592746 | ||||||
| chr10:24592922
|
A | C | 3 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0001g0249 | 3 | HG00621.hp1 NA18954.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.3877-910T>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 21/25 | chr10 | 24592922 | ||||||
| chr10:24592952
|
T | C | 1 | a0001c0001t0001g0143 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3877-940A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 21/25 | chr10 | 24592952 | ||||||
| chr10:24593080
|
CA | C | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.3877-1069delT | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 21/25 | chr10 | 24593080 | ||||||
| chr10:24593172
|
T | C | 16 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(13): Show | 16 | HG01891.hp2 HG02280.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.3877-1160A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 21/25 | chr10 | 24593172 | ||||||
| chr10:24593258
|
A | AGAAAGAA others(7): Show |
1 | a0001c0001t0001g0271 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.3877-1260_3877-124 others(18): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 21/25 | chr10 | 24593258 | ||||||
| chr10:24593267
|
CTA | C | 4 | a0002c0002t0001g0020a0002c0002t0001g0138a0002c0002t0001g0139others(1): Show | 4 | HG02615.hp1 HG02922.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.3877-1257_3877-125 others(6): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 21/25 | chr10 | 24593267 | ||||||
| chr10:24593303
|
C | T | 2 | a0011c0011t0001g0258a0011c0011t0001g0259 | 2 | HG02818.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.3877-1291G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 21/25 | chr10 | 24593303 | ||||||
| chr10:24593492
|
G | GTAATATT others(30): Show |
1 | a0002c0002t0001g0136 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3876+1421_3876+145 others(41): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 21/25 | chr10 | 24593492 | ||||||
| chr10:24593590
|
T | TGAAAGAT others(14): Show |
134 | a0001c0001t0008g0324a0001c0014t0004g0286a0002c0002t0001g0010others(131): Show | 134 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.3876+1339_3876+135 others(25): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 21/25 | chr10 | 24593590 | ||||||
| chr10:24593590
|
T | TGAAAGAT others(14): Show |
4 | a0002c0002t0001g0078a0002c0002t0001g0079a0002c0002t0001g0080others(1): Show | 4 | HG00741.hp1 HG01975.hp1 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.3876+1359_3876+136 others(25): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 21/25 | chr10 | 24593590 | ||||||
| chr10:24593629
|
A | G | 9 | a0002c0002t0001g0057a0002c0002t0001g0058a0002c0002t0001g0059others(6): Show | 9 | HG00639.hp1 HG01069.hp1 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.3876+1321T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 21/25 | chr10 | 24593629 | ||||||
| chr10:24593832
|
G | A | 138 | a0001c0001t0008g0324a0001c0014t0004g0286a0002c0002t0001g0010others(135): Show | 138 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.3876+1118C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 21/25 | chr10 | 24593832 | ||||||
| chr10:24593969
|
A | G | 7 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0164others(4): Show | 7 | HG02559.hp1 HG02572.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.3876+981T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 21/25 | chr10 | 24593969 | ||||||
| chr10:24594171
|
A | G | 1 | a0001c0001t0001g0162 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3876+779T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 21/25 | chr10 | 24594171 | ||||||
| chr10:24594203
|
T | TTAAAATC others(10): Show |
1 | a0002c0002t0001g0071 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.3876+730_3876+746d others(19): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 21/25 | chr10 | 24594203 | ||||||
| chr10:24594329
|
C | T | 1 | a0001c0001t0002g0336 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.3876+621G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 21/25 | chr10 | 24594329 | ||||||
| chr10:24594617
|
G | GTATTCT | 153 | a0001c0001t0008g0324a0001c0014t0004g0286a0002c0002t0001g0010others(150): Show | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.3876+327_3876+332d others(8): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 21/25 | chr10 | 24594617 | ||||||
| chr10:24594844
|
T | G | 168 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.3876+106A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 21/25 | chr10 | 24594844 | ||||||
| chr10:24595102
|
T | C | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.3786+15A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 20/25 | chr10 | 24595102 | ||||||
| chr10:24595227
|
T | C | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.3713-37A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 19/25 | chr10 | 24595227 | ||||||
| chr10:24595294
|
T | C | 1 | a0005c0005t0001g0104 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3713-104A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 19/25 | chr10 | 24595294 | ||||||
| chr10:24595375
|
C | T | 1 | a0002c0002t0001g0092 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.3713-185G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 19/25 | chr10 | 24595375 | ||||||
| chr10:24595390
|
A | C | 168 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.3713-200T>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 19/25 | chr10 | 24595390 | ||||||
| chr10:24595581
|
A | G | 21 | a0001c0001t0002g0302a0001c0001t0002g0310a0001c0001t0002g0311others(18): Show | 21 | HG00673.hp2 HG00733.hp1 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.3712+136T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 19/25 | chr10 | 24595581 | ||||||
| chr10:24595585
|
G | A | 16 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(13): Show | 16 | HG01891.hp2 HG02280.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.3712+132C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 19/25 | chr10 | 24595585 | ||||||
| chr10:24595850
|
GA | G | 109 | a0002c0002t0001g0010a0002c0002t0001g0017a0002c0002t0001g0018others(106): Show | 109 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.3633+37delT | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 18/25 | chr10 | 24595850 | ||||||
| chr10:24596101
|
T | C | 3 | a0001c0001t0002g0337a0001c0001t0002g0338a0016c0022t0002g0339 | 3 | HG01109.hp1 NA18964.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.3478-58A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 17/25 | chr10 | 24596101 | ||||||
| chr10:24596134
|
G | A | 1 | a0015c0023t0001g0090 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.3478-91C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 17/25 | chr10 | 24596134 | ||||||
| chr10:24596242
|
TGAAA | T | 85 | a0002c0002t0001g0010a0002c0002t0001g0018a0002c0002t0001g0020others(82): Show | 85 | HG00140.hp2 HG00438.hp1 HG00609.hp2 others(82): Show |
intron_variant | MODIFIER | c.3478-203_3478-200d others(6): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 17/25 | chr10 | 24596242 | ||||||
| chr10:24596490
|
C | T | 6 | a0002c0002t0001g0078a0002c0002t0001g0079a0002c0002t0001g0080others(3): Show | 6 | HG00741.hp1 HG01361.hp1 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.3477+250G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 17/25 | chr10 | 24596490 | ||||||
| chr10:24596563
|
T | C | 1 | a0019c0020t0001g0112 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.3477+177A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 17/25 | chr10 | 24596563 | ||||||
| chr10:24596570
|
A | G | 16 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(13): Show | 16 | HG01891.hp2 HG02280.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.3477+170T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 17/25 | chr10 | 24596570 | ||||||
| chr10:24596628
|
A | G | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.3477+112T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 17/25 | chr10 | 24596628 | ||||||
| chr10:24596673
|
T | A | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.3477+67A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 17/25 | chr10 | 24596673 | ||||||
| chr10:24596681
|
C | T | 1 | a0001c0001t0001g0257 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.3477+59G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 17/25 | chr10 | 24596681 | ||||||
| chr10:24596716
|
A | G | 2 | a0010c0012t0010g0015a0010c0012t0010g0016 | 2 | HG02723.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.3477+24T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 17/25 | chr10 | 24596716 | ||||||
| chr10:24596718
|
C | T | 2 | a0003c0003t0001g0200a0003c0003t0001g0248 | 2 | NA18959.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.3477+22G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 17/25 | chr10 | 24596718 | ||||||
| chr10:24597066
|
G | A | 1 | a0002c0002t0014g0105 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.3335-184C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 16/25 | chr10 | 24597066 | ||||||
| chr10:24597075
|
TTTTC | T | 148 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(145): Show | 148 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.3335-197_3335-194d others(6): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 16/25 | chr10 | 24597075 | ||||||
| chr10:24597090
|
C | CA | 165 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(162): Show | 165 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.3335-209dupT | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 16/25 | chr10 | 24597090 | ||||||
| chr10:24597372
|
A | C | 1 | a0001c0001t0001g0272 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.3334+75T>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 16/25 | chr10 | 24597372 | ||||||
| chr10:24597395
|
G | A | 16 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(13): Show | 16 | HG01891.hp2 HG02280.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.3334+52C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 16/25 | chr10 | 24597395 | ||||||
| chr10:24597605
|
G | A | 1 | a0001c0001t0001g0264 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3198-22C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 15/25 | chr10 | 24597605 | ||||||
| chr10:24597846
|
A | G | 1 | a0002c0002t0001g0117 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.3197+99T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 15/25 | chr10 | 24597846 | ||||||
| chr10:24598199
|
T | C | 1 | a0002c0030t0001g0022 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.3133-190A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 14/25 | chr10 | 24598199 | ||||||
| chr10:24598264
|
T | C | 175 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(172): Show | 175 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.3133-255A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 14/25 | chr10 | 24598264 | ||||||
| chr10:24598528
|
TAAGAG | T | 6 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0183others(3): Show | 6 | HG00642.hp1 HG01884.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.3133-524_3133-520d others(7): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 14/25 | chr10 | 24598528 | ||||||
| chr10:24598741
|
A | AGTCT | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.3133-736_3133-733d others(6): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 14/25 | chr10 | 24598741 | ||||||
| chr10:24598779
|
T | C | 1 | a0001c0001t0001g0242 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.3133-770A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 14/25 | chr10 | 24598779 | ||||||
| chr10:24598987
|
T | A | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.3133-978A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 14/25 | chr10 | 24598987 | ||||||
| chr10:24598990
|
G | A | 1 | a0001c0001t0002g0336 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.3133-981C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 14/25 | chr10 | 24598990 | ||||||
| chr10:24599003
|
T | C | 46 | a0002c0002t0001g0017a0002c0002t0001g0019a0002c0002t0001g0056others(43): Show | 46 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(43): Show |
intron_variant | MODIFIER | c.3133-994A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 14/25 | chr10 | 24599003 | ||||||
| chr10:24599012
|
T | C | 1 | a0002c0002t0001g0017 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3133-1003A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 14/25 | chr10 | 24599012 | ||||||
| chr10:24599033
|
T | C | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.3133-1024A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 14/25 | chr10 | 24599033 | ||||||
| chr10:24599102
|
A | C | 1 | a0003c0003t0001g0180 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.3133-1093T>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 14/25 | chr10 | 24599102 | ||||||
| chr10:24599113
|
T | C | 42 | a0002c0002t0001g0017a0002c0002t0001g0019a0002c0002t0001g0056others(39): Show | 42 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.3133-1104A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 14/25 | chr10 | 24599113 | ||||||
| chr10:24599161
|
C | T | 77 | a0001c0001t0001g0160a0001c0001t0001g0174a0001c0001t0001g0181others(74): Show | 77 | HG00408.hp2 HG00423.hp1 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.3133-1152G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 14/25 | chr10 | 24599161 | ||||||
| chr10:24599319
|
A | C | 1 | a0002c0002t0001g0045 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.3133-1310T>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 14/25 | chr10 | 24599319 | ||||||
| chr10:24599337
|
T | C | 4 | a0005c0005t0001g0103a0005c0005t0001g0104a0005c0005t0001g0137others(1): Show | 4 | HG02055.hp1 HG02451.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.3132+1309A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 14/25 | chr10 | 24599337 | ||||||
| chr10:24599470
|
G | A | 16 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(13): Show | 16 | HG01891.hp2 HG02280.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.3132+1176C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 14/25 | chr10 | 24599470 | ||||||
| chr10:24599579
|
A | G | 1 | a0001c0001t0001g0183 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3132+1067T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 14/25 | chr10 | 24599579 | ||||||
| chr10:24599616
|
T | C | 1 | a0001c0001t0002g0307 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.3132+1030A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 14/25 | chr10 | 24599616 | ||||||
| chr10:24599696
|
TTCA | T | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.3132+947_3132+949d others(5): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 14/25 | chr10 | 24599696 | ||||||
| chr10:24599718
|
G | A | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.3132+928C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 14/25 | chr10 | 24599718 | ||||||
| chr10:24599791
|
T | C | 5 | a0002c0002t0001g0020a0002c0002t0001g0138a0002c0002t0001g0139others(2): Show | 5 | HG02615.hp1 HG02922.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.3132+855A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 14/25 | chr10 | 24599791 | ||||||
| chr10:24599900
|
G | A | 1 | a0001c0001t0004g0299 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.3132+746C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 14/25 | chr10 | 24599900 | ||||||
| chr10:24599916
|
A | G | 3 | a0001c0001t0001g0171a0001c0001t0004g0297a0001c0001t0004g0298 | 3 | HG01891.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.3132+730T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 14/25 | chr10 | 24599916 | ||||||
| chr10:24600014
|
T | C | 1 | a0002c0002t0001g0060 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.3132+632A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 14/25 | chr10 | 24600014 | ||||||
| chr10:24600128
|
G | A | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.3132+518C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 14/25 | chr10 | 24600128 | ||||||
| chr10:24600132
|
C | CAAAA | 13 | a0001c0001t0001g0142a0001c0001t0001g0144a0001c0001t0001g0162others(10): Show | 13 | HG01891.hp2 HG02451.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.3132+510_3132+513d others(6): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 14/25 | chr10 | 24600132 | ||||||
| chr10:24600132
|
C | CAAAAA | 7 | a0001c0001t0001g0143a0007c0007t0006g0291a0007c0007t0006g0292others(4): Show | 7 | HG02129.hp2 HG02523.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.3132+509_3132+513d others(7): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 14/25 | chr10 | 24600132 | ||||||
| chr10:24600132
|
C | CAAAAAA | 17 | a0001c0014t0004g0286a0002c0002t0001g0061a0002c0002t0001g0076others(14): Show | 17 | HG00099.hp1 HG01069.hp1 HG01257.hp2 others(14): Show |
intron_variant | MODIFIER | c.3132+508_3132+513d others(8): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 14/25 | chr10 | 24600132 | ||||||
| chr10:24600132
|
C | CAAAAAAA | 114 | a0001c0001t0008g0324a0002c0002t0001g0010a0002c0002t0001g0017others(111): Show | 114 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.3132+507_3132+513d others(9): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 14/25 | chr10 | 24600132 | ||||||
| chr10:24600132
|
C | CAAAAAAA others(1): Show |
23 | a0002c0002t0001g0018a0002c0002t0001g0020a0002c0002t0001g0054others(20): Show | 23 | HG00099.hp2 HG00438.hp1 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.3132+506_3132+513d others(10): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 14/25 | chr10 | 24600132 | ||||||
| chr10:24600132
|
CA | C | 7 | a0001c0001t0001g0194a0001c0001t0002g0319a0001c0001t0003g0154others(4): Show | 7 | HG01081.hp1 HG01099.hp2 HG02071.hp1 others(4): Show |
intron_variant | MODIFIER | c.3132+513delT | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 14/25 | chr10 | 24600132 | ||||||
| chr10:24600454
|
G | C | 77 | a0001c0001t0008g0324a0002c0002t0001g0010a0002c0002t0001g0018others(74): Show | 77 | HG00140.hp2 HG00438.hp1 HG00609.hp2 others(74): Show |
intron_variant | MODIFIER | c.3132+192C>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 14/25 | chr10 | 24600454 | ||||||
| chr10:24600543
|
C | T | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.3132+103G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 14/25 | chr10 | 24600543 | ||||||
| chr10:24600972
|
T | G | 154 | a0001c0001t0001g0252a0001c0001t0008g0324a0001c0014t0004g0286others(151): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.2848-42A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 13/25 | chr10 | 24600972 | ||||||
| chr10:24601232
|
C | T | 1 | a0002c0002t0001g0110 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2848-302G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 13/25 | chr10 | 24601232 | ||||||
| chr10:24601401
|
T | C | 1 | a0005c0005t0001g0137 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2848-471A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 13/25 | chr10 | 24601401 | ||||||
| chr10:24601573
|
GAAAC | G | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.2847+401_2847+404d others(6): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 13/25 | chr10 | 24601573 | ||||||
| chr10:24601603
|
A | C | 2 | a0011c0011t0001g0258a0011c0011t0001g0259 | 2 | HG02818.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2847+375T>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 13/25 | chr10 | 24601603 | ||||||
| chr10:24601637
|
T | A | 172 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(169): Show | 172 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.2847+341A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 13/25 | chr10 | 24601637 | ||||||
| chr10:24601742
|
C | T | 1 | a0003c0003t0001g0203 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.2847+236G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 13/25 | chr10 | 24601742 | ||||||
| chr10:24601823
|
G | A | 7 | a0002c0002t0001g0019a0002c0002t0001g0113a0002c0002t0001g0114others(4): Show | 7 | HG01496.hp1 HG01516.hp2 HG02027.hp2 others(4): Show |
intron_variant | MODIFIER | c.2847+155C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 13/25 | chr10 | 24601823 | ||||||
| chr10:24601863
|
T | C | 2 | a0002c0002t0001g0107a0002c0002t0001g0111 | 2 | HG02258.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.2847+115A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 13/25 | chr10 | 24601863 | ||||||
| chr10:24601899
|
T | C | 103 | a0001c0001t0008g0324a0002c0002t0001g0010a0002c0002t0001g0018others(100): Show | 103 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.2847+79A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 13/25 | chr10 | 24601899 | ||||||
| chr10:24602164
|
A | G | 1 | a0002c0002t0001g0042 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.2722-61T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 12/25 | chr10 | 24602164 | ||||||
| chr10:24602235
|
T | C | 1 | a0001c0001t0001g0219 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2722-132A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 12/25 | chr10 | 24602235 | ||||||
| chr10:24602332
|
G | T | 6 | a0001c0001t0005g0001a0001c0001t0005g0005a0001c0001t0005g0006others(3): Show | 6 | HG01981.hp1 HG03927.hp2 NA18995.hp2 others(3): Show |
intron_variant | MODIFIER | c.2722-229C>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 12/25 | chr10 | 24602332 | ||||||
| chr10:24602398
|
C | T | 3 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0255 | 3 | HG02622.hp1 HG02970.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2722-295G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 12/25 | chr10 | 24602398 | ||||||
| chr10:24602423
|
G | A | 1 | a0001c0001t0001g0275 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.2722-320C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 12/25 | chr10 | 24602423 | ||||||
| chr10:24602438
|
C | A | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.2722-335G>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 12/25 | chr10 | 24602438 | ||||||
| chr10:24602708
|
C | T | 1 | a0005c0005t0001g0103 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2722-605G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 12/25 | chr10 | 24602708 | ||||||
| chr10:24602931
|
G | A | 1 | a0002c0002t0001g0118 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.2722-828C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 12/25 | chr10 | 24602931 | ||||||
| chr10:24602977
|
A | G | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.2722-874T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 12/25 | chr10 | 24602977 | ||||||
| chr10:24603470
|
A | C | 1 | a0002c0002t0001g0152 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2721+842T>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 12/25 | chr10 | 24603470 | ||||||
| chr10:24603560
|
A | C | 1 | a0002c0002t0001g0093 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.2721+752T>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 12/25 | chr10 | 24603560 | ||||||
| chr10:24603822
|
A | C | 1 | a0002c0002t0001g0093 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.2721+490T>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 12/25 | chr10 | 24603822 | ||||||
| chr10:24603921
|
G | A | 6 | a0001c0001t0005g0001a0001c0001t0005g0005a0001c0001t0005g0006others(3): Show | 6 | HG01981.hp1 HG03927.hp2 NA18995.hp2 others(3): Show |
intron_variant | MODIFIER | c.2721+391C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 12/25 | chr10 | 24603921 | ||||||
| chr10:24604064
|
G | C | 3 | a0002c0002t0001g0107a0002c0002t0001g0108a0002c0002t0001g0111 | 3 | HG02258.hp1 HG02630.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2721+248C>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 12/25 | chr10 | 24604064 | ||||||
| chr10:24604131
|
C | T | 1 | a0002c0002t0001g0081 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2721+181G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 12/25 | chr10 | 24604131 | ||||||
| chr10:24604453
|
C | T | 1 | a0002c0002t0001g0021 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2685-105G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 11/25 | chr10 | 24604453 | ||||||
| chr10:24604590
|
G | A | 2 | a0001c0014t0004g0286a0005c0005t0004g0287 | 2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2685-242C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 11/25 | chr10 | 24604590 | ||||||
| chr10:24604747
|
C | T | 1 | a0011c0011t0001g0259 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2685-399G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 11/25 | chr10 | 24604747 | ||||||
| chr10:24605008
|
T | TA | 4 | a0005c0005t0001g0103a0005c0005t0001g0104a0005c0005t0001g0137others(1): Show | 4 | HG02055.hp1 HG02451.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.2685-661dupT | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 11/25 | chr10 | 24605008 | ||||||
| chr10:24605132
|
C | T | 2 | a0001c0001t0001g0163a0001c0001t0001g0164 | 2 | HG02572.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.2685-784G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 11/25 | chr10 | 24605132 | ||||||
| chr10:24605191
|
G | A | 5 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0015g0288others(2): Show | 5 | HG02129.hp2 NA18747.hp1 NA18989.hp1 others(2): Show |
intron_variant | MODIFIER | c.2685-843C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 11/25 | chr10 | 24605191 | ||||||
| chr10:24605365
|
T | C | 1 | a0001c0001t0001g0244 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2685-1017A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 11/25 | chr10 | 24605365 | ||||||
| chr10:24605371
|
C | T | 2 | a0001c0001t0002g0322a0001c0001t0002g0335 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.2685-1023G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 11/25 | chr10 | 24605371 | ||||||
| chr10:24605417
|
T | C | 2 | a0001c0001t0002g0320a0001c0001t0002g0345 | 2 | NA18954.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.2685-1069A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 11/25 | chr10 | 24605417 | ||||||
| chr10:24605481
|
C | T | 10 | a0002c0002t0001g0019a0002c0002t0001g0113a0002c0002t0001g0114others(7): Show | 10 | HG01496.hp1 HG01516.hp2 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.2685-1133G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 11/25 | chr10 | 24605481 | ||||||
| chr10:24605502
|
C | T | 60 | a0001c0001t0001g0160a0001c0001t0001g0174a0001c0001t0001g0197others(57): Show | 60 | HG00408.hp2 HG00423.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.2685-1154G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 11/25 | chr10 | 24605502 | ||||||
| chr10:24605514
|
TCCTGCTA others(14): Show |
T | 2 | a0012c0010t0001g0266a0012c0010t0001g0267 | 2 | HG02109.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2685-1187_2685-116 others(25): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 11/25 | chr10 | 24605514 | ||||||
| chr10:24605519
|
C | T | 3 | a0001c0001t0002g0337a0001c0001t0002g0338a0016c0022t0002g0339 | 3 | HG01109.hp1 NA18964.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.2685-1171G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 11/25 | chr10 | 24605519 | ||||||
| chr10:24605731
|
T | C | 1 | a0002c0002t0001g0153 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2685-1383A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 11/25 | chr10 | 24605731 | ||||||
| chr10:24605807
|
T | C | 2 | a0011c0011t0001g0258a0011c0011t0001g0259 | 2 | HG02818.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2685-1459A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 11/25 | chr10 | 24605807 | ||||||
| chr10:24605811
|
CAGG | C | 44 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(41): Show | 44 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(41): Show |
intron_variant | MODIFIER | c.2685-1466_2685-146 others(7): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 11/25 | chr10 | 24605811 | ||||||
| chr10:24605894
|
G | A | 1 | a0001c0001t0002g0307 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.2685-1546C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 11/25 | chr10 | 24605894 | ||||||
| chr10:24605992
|
C | T | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.2684+1507G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 11/25 | chr10 | 24605992 | ||||||
| chr10:24606108
|
C | A | 1 | a0002c0002t0001g0093 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.2684+1391G>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 11/25 | chr10 | 24606108 | ||||||
| chr10:24606115
|
AT | A | 4 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0183others(1): Show | 4 | HG01884.hp2 HG02615.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.2684+1383delA | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 11/25 | chr10 | 24606115 | ||||||
| chr10:24606229
|
A | C | 1 | a0002c0002t0001g0098 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2684+1270T>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 11/25 | chr10 | 24606229 | ||||||
| chr10:24606479
|
A | T | 1 | a0002c0002t0001g0030 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.2684+1020T>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 11/25 | chr10 | 24606479 | ||||||
| chr10:24606487
|
G | A | 1 | a0001c0001t0008g0306 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.2684+1012C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 11/25 | chr10 | 24606487 | ||||||
| chr10:24606510
|
G | A | 5 | a0001c0001t0001g0171a0001c0001t0004g0296a0001c0001t0004g0297others(2): Show | 5 | HG01891.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.2684+989C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 11/25 | chr10 | 24606510 | ||||||
| chr10:24606540
|
T | G | 1 | a0002c0002t0001g0030 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.2684+959A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 11/25 | chr10 | 24606540 | ||||||
| chr10:24606568
|
T | G | 1 | a0002c0002t0001g0030 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.2684+931A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 11/25 | chr10 | 24606568 | ||||||
| chr10:24606831
|
A | G | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.2684+668T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 11/25 | chr10 | 24606831 | ||||||
| chr10:24606937
|
C | A | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.2684+562G>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 11/25 | chr10 | 24606937 | ||||||
| chr10:24607138
|
G | T | 1 | a0002c0002t0001g0030 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.2684+361C>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 11/25 | chr10 | 24607138 | ||||||
| chr10:24607139
|
T | G | 1 | a0002c0002t0001g0030 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.2684+360A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 11/25 | chr10 | 24607139 | ||||||
| chr10:24607140
|
A | T | 1 | a0002c0002t0001g0030 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.2684+359T>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 11/25 | chr10 | 24607140 | ||||||
| chr10:24607219
|
T | C | 2 | a0002c0002t0001g0038a0002c0002t0001g0092 | 2 | NA18747.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.2684+280A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 11/25 | chr10 | 24607219 | ||||||
| chr10:24607231
|
AAAG | A | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.2684+265_2684+267d others(5): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 11/25 | chr10 | 24607231 | ||||||
| chr10:24607259
|
A | T | 1 | a0002c0002t0001g0030 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.2684+240T>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 11/25 | chr10 | 24607259 | ||||||
| chr10:24608065
|
C | CAGTT | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.2423-166_2423-163d others(6): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24608065 | ||||||
| chr10:24608108
|
G | A | 146 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(143): Show | 146 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.2423-205C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24608108 | ||||||
| chr10:24608117
|
T | TAAA | 16 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(13): Show | 16 | HG01891.hp2 HG02280.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.2423-217_2423-215d others(5): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24608117 | ||||||
| chr10:24608435
|
C | T | 1 | a0002c0002t0001g0118 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.2423-532G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24608435 | ||||||
| chr10:24608571
|
T | C | 1 | a0002c0002t0001g0027 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.2423-668A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24608571 | ||||||
| chr10:24608648
|
C | G | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.2423-745G>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24608648 | ||||||
| chr10:24608778
|
TA | T | 124 | a0002c0002t0001g0010a0002c0002t0001g0017a0002c0002t0001g0018others(121): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(121): Show |
intron_variant | MODIFIER | c.2423-876delT | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24608778 | ||||||
| chr10:24608854
|
C | T | 1 | a0001c0001t0008g0327 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2423-951G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24608854 | ||||||
| chr10:24608861
|
T | TTACTATT others(18): Show |
6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.2423-983_2423-959d others(27): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24608861 | ||||||
| chr10:24609108
|
A | C | 1 | a0002c0002t0001g0139 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2423-1205T>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24609108 | ||||||
| chr10:24609161
|
A | G | 1 | a0002c0002t0007g0008 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2423-1258T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24609161 | ||||||
| chr10:24609180
|
T | A | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.2423-1277A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24609180 | ||||||
| chr10:24609419
|
T | C | 1 | a0002c0002t0001g0279 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2423-1516A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24609419 | ||||||
| chr10:24609651
|
G | A | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.2423-1748C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24609651 | ||||||
| chr10:24609662
|
C | T | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.2423-1759G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24609662 | ||||||
| chr10:24609663
|
G | A | 1 | a0001c0001t0001g0192 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2423-1760C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24609663 | ||||||
| chr10:24609679
|
G | GT | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.2423-1777dupA | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24609679 | ||||||
| chr10:24609806
|
A | G | 1 | a0001c0001t0001g0199 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.2423-1903T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24609806 | ||||||
| chr10:24610104
|
G | A | 1 | a0001c0001t0001g0171 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2423-2201C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24610104 | ||||||
| chr10:24610152
|
G | C | 1 | a0002c0002t0001g0038 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2423-2249C>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24610152 | ||||||
| chr10:24610180
|
C | G | 2 | a0002c0002t0001g0109a0002c0002t0001g0110 | 2 | HG02148.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.2423-2277G>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24610180 | ||||||
| chr10:24610185
|
T | C | 1 | a0002c0002t0001g0109 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.2423-2282A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24610185 | ||||||
| chr10:24610249
|
C | T | 3 | a0002c0002t0001g0107a0002c0002t0001g0108a0002c0002t0001g0111 | 3 | HG02258.hp1 HG02630.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2423-2346G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24610249 | ||||||
| chr10:24610372
|
C | CA | 9 | a0001c0001t0001g0171a0001c0001t0001g0189a0001c0001t0002g0318others(6): Show | 9 | HG00673.hp2 HG00741.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.2423-2470dupT | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24610372 | ||||||
| chr10:24610372
|
C | CAA | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.2423-2471_2423-247 others(6): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24610372 | ||||||
| chr10:24610372
|
CA | C | 112 | a0001c0001t0002g0315a0002c0002t0001g0010a0002c0002t0001g0017others(109): Show | 112 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.2423-2470delT | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24610372 | ||||||
| chr10:24610374
|
A | C | 1 | a0001c0001t0001g0190 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2423-2471T>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24610374 | ||||||
| chr10:24610375
|
A | C | 3 | a0005c0005t0001g0102a0005c0005t0001g0103a0005c0005t0001g0284 | 3 | HG02451.hp1 HG03209.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2423-2472T>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24610375 | ||||||
| chr10:24610377
|
A | C | 2 | a0005c0005t0001g0102a0005c0005t0001g0103 | 2 | HG02451.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2423-2474T>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24610377 | ||||||
| chr10:24610877
|
C | T | 1 | a0001c0001t0001g0187 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2423-2974G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24610877 | ||||||
| chr10:24611067
|
T | C | 3 | a0001c0001t0001g0217a0001c0001t0001g0220a0001c0001t0003g0216 | 3 | HG01069.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2423-3164A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24611067 | ||||||
| chr10:24611177
|
C | T | 2 | a0002c0002t0001g0078a0002c0002t0001g0079 | 2 | HG01975.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.2423-3274G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24611177 | ||||||
| chr10:24611211
|
G | A | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.2423-3308C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24611211 | ||||||
| chr10:24611246
|
T | A | 1 | a0019c0020t0001g0112 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2423-3343A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24611246 | ||||||
| chr10:24611341
|
T | C | 2 | a0011c0011t0001g0258a0011c0011t0001g0259 | 2 | HG02818.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2423-3438A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24611341 | ||||||
| chr10:24611450
|
T | C | 1 | a0001c0001t0002g0310 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2423-3547A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24611450 | ||||||
| chr10:24611556
|
T | C | 1 | a0018c0013t0002g0314 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2423-3653A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24611556 | ||||||
| chr10:24611660
|
C | T | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.2423-3757G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24611660 | ||||||
| chr10:24611671
|
G | A | 64 | a0001c0001t0001g0160a0001c0001t0001g0174a0001c0001t0001g0197others(61): Show | 64 | HG00408.hp2 HG00423.hp1 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.2423-3768C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24611671 | ||||||
| chr10:24611833
|
A | T | 1 | a0005c0005t0001g0284 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2423-3930T>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24611833 | ||||||
| chr10:24612022
|
G | C | 1 | a0001c0001t0002g0307 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.2423-4119C>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24612022 | ||||||
| chr10:24612057
|
C | G | 4 | a0003c0003t0001g0198a0003c0003t0001g0213a0003c0003t0001g0218others(1): Show | 4 | HG00423.hp1 HG00597.hp2 HG02083.hp2 others(1): Show |
intron_variant | MODIFIER | c.2423-4154G>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24612057 | ||||||
| chr10:24612218
|
C | T | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.2423-4315G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24612218 | ||||||
| chr10:24612311
|
T | C | 5 | a0001c0001t0001g0171a0001c0001t0004g0296a0001c0001t0004g0297others(2): Show | 5 | HG01891.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.2423-4408A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24612311 | ||||||
| chr10:24612408
|
T | G | 3 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195 | 3 | HG02280.hp2 HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2423-4505A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24612408 | ||||||
| chr10:24612453
|
A | T | 1 | a0018c0013t0002g0314 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2423-4550T>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24612453 | ||||||
| chr10:24612625
|
C | T | 34 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0176others(31): Show | 34 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(31): Show |
intron_variant | MODIFIER | c.2423-4722G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24612625 | ||||||
| chr10:24612856
|
A | AAAAT | 141 | a0001c0001t0001g0160a0001c0001t0001g0169a0001c0001t0001g0170others(138): Show | 141 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.2423-4957_2423-495 others(8): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24612856 | ||||||
| chr10:24612856
|
A | AAAATAAA others(1): Show |
9 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(6): Show | 9 | HG02818.hp2 HG02965.hp1 HG03225.hp2 others(6): Show |
intron_variant | MODIFIER | c.2423-4961_2423-495 others(12): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24612856 | ||||||
| chr10:24612959
|
C | T | 1 | a0001c0001t0001g0186 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2423-5056G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24612959 | ||||||
| chr10:24613021
|
T | C | 3 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195 | 3 | HG02280.hp2 HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2423-5118A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24613021 | ||||||
| chr10:24613579
|
T | C | 1 | a0001c0001t0002g0318 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.2423-5676A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24613579 | ||||||
| chr10:24613609
|
G | T | 2 | a0001c0001t0001g0232a0001c0001t0001g0235 | 2 | NA18975.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.2423-5706C>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24613609 | ||||||
| chr10:24613682
|
T | C | 1 | a0002c0002t0001g0098 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2423-5779A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24613682 | ||||||
| chr10:24613709
|
T | G | 5 | a0001c0001t0002g0322a0001c0001t0002g0323a0001c0001t0002g0335others(2): Show | 5 | HG01099.hp2 HG01255.hp2 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.2422+5764A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24613709 | ||||||
| chr10:24613817
|
G | C | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.2422+5656C>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24613817 | ||||||
| chr10:24613826
|
C | G | 1 | a0001c0001t0016g0352 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.2422+5647G>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24613826 | ||||||
| chr10:24613873
|
G | A | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.2422+5600C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24613873 | ||||||
| chr10:24613880
|
A | AGGTTACA others(3): Show |
15 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(12): Show | 15 | HG01891.hp2 HG02280.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.2422+5583_2422+559 others(14): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24613880 | ||||||
| chr10:24613992
|
G | A | 23 | a0002c0002t0001g0017a0002c0002t0001g0117a0002c0002t0001g0118others(20): Show | 23 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(20): Show |
intron_variant | MODIFIER | c.2422+5481C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24613992 | ||||||
| chr10:24614398
|
T | G | 1 | a0003c0003t0001g0208 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.2422+5075A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24614398 | ||||||
| chr10:24614399
|
G | T | 1 | a0003c0003t0001g0208 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.2422+5074C>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24614399 | ||||||
| chr10:24614411
|
T | G | 2 | a0001c0001t0001g0169a0001c0001t0001g0187 | 2 | NA18988.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.2422+5062A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24614411 | ||||||
| chr10:24614462
|
A | G | 1 | a0007c0007t0006g0293 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2422+5011T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24614462 | ||||||
| chr10:24614641
|
G | T | 1 | a0003c0003t0001g0208 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.2422+4832C>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24614641 | ||||||
| chr10:24614691
|
G | A | 1 | a0003c0003t0001g0208 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.2422+4782C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24614691 | ||||||
| chr10:24614692
|
A | G | 1 | a0003c0003t0001g0208 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.2422+4781T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24614692 | ||||||
| chr10:24614693
|
G | A | 1 | a0003c0003t0001g0208 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.2422+4780C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24614693 | ||||||
| chr10:24614740
|
G | T | 1 | a0003c0003t0001g0208 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.2422+4733C>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24614740 | ||||||
| chr10:24614782
|
C | CA | 25 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(22): Show | 25 | HG00642.hp1 HG01109.hp1 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.2422+4690dupT | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24614782 | ||||||
| chr10:24614782
|
C | CAA | 137 | a0002c0002t0001g0010a0002c0002t0001g0017a0002c0002t0001g0018others(134): Show | 137 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.2422+4689_2422+469 others(6): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24614782 | ||||||
| chr10:24614782
|
C | CAAA | 14 | a0002c0002t0001g0039a0002c0002t0001g0086a0002c0002t0001g0094others(11): Show | 14 | HG00438.hp1 HG01175.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.2422+4688_2422+469 others(7): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24614782 | ||||||
| chr10:24614845
|
T | C | 1 | a0001c0001t0001g0143 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2422+4628A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24614845 | ||||||
| chr10:24614915
|
G | A | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.2422+4558C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24614915 | ||||||
| chr10:24615017
|
C | T | 1 | a0001c0001t0001g0194 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2422+4456G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24615017 | ||||||
| chr10:24615047
|
G | C | 3 | a0003c0003t0001g0221a0003c0003t0001g0227a0003c0003t0001g0268 | 3 | HG00408.hp2 NA18945.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.2422+4426C>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24615047 | ||||||
| chr10:24615058
|
T | C | 341 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(338): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.2422+4415A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24615058 | ||||||
| chr10:24615105
|
A | T | 2 | a0010c0012t0010g0015a0010c0012t0010g0016 | 2 | HG02723.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.2422+4368T>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24615105 | ||||||
| chr10:24615122
|
G | A | 1 | a0005c0005t0001g0104 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2422+4351C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24615122 | ||||||
| chr10:24615186
|
G | A | 15 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(12): Show | 15 | HG01891.hp2 HG02280.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.2422+4287C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24615186 | ||||||
| chr10:24615388
|
T | G | 2 | a0012c0010t0001g0266a0012c0010t0001g0267 | 2 | HG02109.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2422+4085A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24615388 | ||||||
| chr10:24615421
|
T | C | 1 | a0002c0002t0001g0021 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2422+4052A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24615421 | ||||||
| chr10:24615457
|
C | T | 1 | a0001c0001t0004g0296 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2422+4016G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24615457 | ||||||
| chr10:24615484
|
G | A | 1 | a0001c0001t0001g0244 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2422+3989C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24615484 | ||||||
| chr10:24615491
|
A | C | 23 | a0002c0002t0001g0017a0002c0002t0001g0117a0002c0002t0001g0118others(20): Show | 23 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(20): Show |
intron_variant | MODIFIER | c.2422+3982T>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24615491 | ||||||
| chr10:24615534
|
C | A | 1 | a0003c0003t0001g0208 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.2422+3939G>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24615534 | ||||||
| chr10:24615569
|
T | C | 15 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(12): Show | 15 | HG01891.hp2 HG02280.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.2422+3904A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24615569 | ||||||
| chr10:24615771
|
ATTATT | A | 135 | a0002c0002t0001g0010a0002c0002t0001g0017a0002c0002t0001g0018others(132): Show | 135 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.2422+3697_2422+370 others(9): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24615771 | ||||||
| chr10:24616073
|
C | T | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.2422+3400G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24616073 | ||||||
| chr10:24616221
|
C | A | 1 | a0001c0001t0001g0014 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2422+3252G>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24616221 | ||||||
| chr10:24616345
|
T | A | 1 | a0001c0001t0003g0155 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2422+3128A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24616345 | ||||||
| chr10:24616441
|
C | T | 16 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(13): Show | 16 | HG01891.hp2 HG02280.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.2422+3032G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24616441 | ||||||
| chr10:24616507
|
T | G | 1 | a0002c0002t0004g0295 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2422+2966A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24616507 | ||||||
| chr10:24616631
|
T | C | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.2422+2842A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24616631 | ||||||
| chr10:24616668
|
G | T | 1 | a0003c0003t0001g0208 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.2422+2805C>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24616668 | ||||||
| chr10:24616678
|
G | A | 6 | a0002c0002t0001g0078a0002c0002t0001g0079a0002c0002t0001g0080others(3): Show | 6 | HG00741.hp1 HG01361.hp1 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.2422+2795C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24616678 | ||||||
| chr10:24616904
|
A | G | 1 | a0001c0001t0001g0237 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2422+2569T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24616904 | ||||||
| chr10:24617034
|
G | A | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.2422+2439C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24617034 | ||||||
| chr10:24617214
|
C | T | 112 | a0002c0002t0001g0010a0002c0002t0001g0018a0002c0002t0001g0019others(109): Show | 112 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.2422+2259G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24617214 | ||||||
| chr10:24617244
|
T | G | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.2422+2229A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24617244 | ||||||
| chr10:24617439
|
T | G | 1 | a0001c0001t0001g0189 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2422+2034A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24617439 | ||||||
| chr10:24617535
|
G | C | 1 | a0004c0004t0001g0031 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2422+1938C>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24617535 | ||||||
| chr10:24617595
|
G | A | 1 | a0002c0002t0001g0125 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2422+1878C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24617595 | ||||||
| chr10:24617611
|
T | TA | 7 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0164others(4): Show | 7 | HG02559.hp1 HG02572.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.2422+1861dupT | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24617611 | ||||||
| chr10:24617643
|
A | T | 1 | a0001c0001t0001g0194 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2422+1830T>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24617643 | ||||||
| chr10:24617724
|
T | TAGCTTTA others(37): Show |
23 | a0002c0002t0001g0017a0002c0002t0001g0117a0002c0002t0001g0118others(20): Show | 23 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(20): Show |
intron_variant | MODIFIER | c.2422+1705_2422+174 others(48): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24617724 | ||||||
| chr10:24617740
|
T | TCCGTAGA others(37): Show |
1 | a0002c0002t0001g0279 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2422+1732_2422+173 others(48): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24617740 | ||||||
| chr10:24618012
|
G | A | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.2422+1461C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24618012 | ||||||
| chr10:24618046
|
CT | C | 156 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(153): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.2422+1426delA | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24618046 | ||||||
| chr10:24618136
|
A | G | 2 | a0001c0014t0004g0286a0005c0005t0004g0287 | 2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2422+1337T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24618136 | ||||||
| chr10:24618195
|
T | TA | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.2422+1277dupT | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24618195 | ||||||
| chr10:24618328
|
A | C | 1 | a0005c0005t0001g0284 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2422+1145T>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24618328 | ||||||
| chr10:24618348
|
T | C | 1 | a0002c0002t0001g0106 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2422+1125A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24618348 | ||||||
| chr10:24618649
|
G | C | 1 | a0011c0011t0001g0258 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2422+824C>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24618649 | ||||||
| chr10:24618864
|
A | T | 1 | a0003c0003t0001g0231 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.2422+609T>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24618864 | ||||||
| chr10:24618922
|
G | T | 3 | a0002c0002t0001g0107a0002c0002t0001g0108a0002c0002t0001g0111 | 3 | HG02258.hp1 HG02630.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2422+551C>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24618922 | ||||||
| chr10:24619054
|
GTTAAATT others(3): Show |
G | 1 | a0001c0001t0002g0304 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.2422+409_2422+418d others(12): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24619054 | ||||||
| chr10:24619251
|
T | C | 1 | a0002c0002t0001g0019 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2422+222A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24619251 | ||||||
| chr10:24619261
|
G | GT | 136 | a0001c0001t0001g0260a0002c0002t0001g0010a0002c0002t0001g0017others(133): Show | 136 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(133): Show |
intron_variant | MODIFIER | c.2422+211dupA | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24619261 | ||||||
| chr10:24619261
|
G | T | 1 | a0001c0001t0001g0187 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2422+212C>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24619261 | ||||||
| chr10:24619271
|
T | A | 4 | a0003c0003t0001g0198a0003c0003t0001g0213a0003c0003t0001g0218others(1): Show | 4 | HG00423.hp1 HG00597.hp2 HG02083.hp2 others(1): Show |
intron_variant | MODIFIER | c.2422+202A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24619271 | ||||||
| chr10:24619271
|
T | TA | 14 | a0002c0002t0001g0071a0002c0002t0001g0088a0002c0002t0001g0150others(11): Show | 14 | HG01123.hp2 HG02145.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.2422+201dupT | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24619271 | ||||||
| chr10:24619272
|
A | T | 3 | a0003c0003t0001g0231a0003c0003t0001g0277a0008c0009t0005g0004 | 3 | NA18963.hp1 NA18995.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.2422+201T>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24619272 | ||||||
| chr10:24619290
|
A | G | 1 | a0001c0001t0001g0186 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2422+183T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24619290 | ||||||
| chr10:24619356
|
G | C | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.2422+117C>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 9/25 | chr10 | 24619356 | ||||||
| chr10:24621826
|
G | A | 158 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(155): Show | 158 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.526-457C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 8/25 | chr10 | 24621826 | ||||||
| chr10:24621830
|
A | AATTT | 80 | a0001c0001t0001g0160a0001c0001t0001g0174a0001c0001t0001g0181others(77): Show | 80 | HG00408.hp2 HG00423.hp1 HG00597.hp2 others(77): Show |
intron_variant | MODIFIER | c.526-465_526-462dup others(4): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 8/25 | chr10 | 24621830 | ||||||
| chr10:24621986
|
G | C | 293 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(290): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.526-617C>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 8/25 | chr10 | 24621986 | ||||||
| chr10:24622013
|
G | A | 2 | a0002c0002t0001g0087a0013c0027t0001g0065 | 2 | HG02109.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.526-644C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 8/25 | chr10 | 24622013 | ||||||
| chr10:24622083
|
C | T | 158 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(155): Show | 158 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.525+650G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 8/25 | chr10 | 24622083 | ||||||
| chr10:24622119
|
A | G | 1 | a0001c0001t0001g0195 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.525+614T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 8/25 | chr10 | 24622119 | ||||||
| chr10:24622433
|
C | CAT | 7 | a0001c0001t0001g0170a0001c0001t0001g0238a0001c0001t0001g0240others(4): Show | 7 | HG01256.hp1 HG01258.hp2 HG03491.hp1 others(4): Show |
intron_variant | MODIFIER | c.525+298_525+299dup others(2): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 8/25 | chr10 | 24622433 | ||||||
| chr10:24622433
|
C | CATAT | 5 | a0001c0001t0001g0169a0001c0001t0001g0190a0001c0001t0001g0274others(2): Show | 5 | HG00423.hp2 HG00673.hp2 HG02300.hp1 others(2): Show |
intron_variant | MODIFIER | c.525+296_525+299dup others(4): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 8/25 | chr10 | 24622433 | ||||||
| chr10:24622433
|
C | CATATAT | 4 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0241others(1): Show | 4 | HG00140.hp1 HG03710.hp1 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.525+294_525+299dup others(6): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 8/25 | chr10 | 24622433 | ||||||
| chr10:24622433
|
C | CATATATA others(1): Show |
3 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0275 | 3 | HG02965.hp1 HG03225.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.525+292_525+299dup others(8): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 8/25 | chr10 | 24622433 | ||||||
| chr10:24622433
|
C | CATATATA others(5): Show |
1 | a0001c0001t0001g0188 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.525+288_525+299dup others(12): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 8/25 | chr10 | 24622433 | ||||||
| chr10:24622433
|
CAT | C | 14 | a0001c0001t0001g0142a0001c0001t0001g0178a0001c0001t0002g0302others(11): Show | 14 | HG01099.hp2 HG01168.hp2 HG01256.hp2 others(11): Show |
intron_variant | MODIFIER | c.525+298_525+299del others(2): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 8/25 | chr10 | 24622433 | ||||||
| chr10:24622433
|
CATAT | C | 22 | a0001c0001t0001g0143a0001c0001t0001g0176a0001c0001t0001g0189others(19): Show | 22 | HG00408.hp2 HG00733.hp1 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.525+296_525+299del others(4): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 8/25 | chr10 | 24622433 | ||||||
| chr10:24622433
|
CATATAT | C | 21 | a0001c0001t0001g0239a0001c0001t0002g0300a0001c0001t0002g0303others(18): Show | 21 | HG00639.hp2 HG01109.hp1 HG01175.hp1 others(18): Show |
intron_variant | MODIFIER | c.525+294_525+299del others(6): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 8/25 | chr10 | 24622433 | ||||||
| chr10:24622433
|
CATATATA others(1): Show |
C | 15 | a0001c0001t0001g0160a0001c0001t0001g0195a0001c0001t0001g0197others(12): Show | 15 | HG01517.hp2 HG01928.hp2 HG01952.hp1 others(12): Show |
intron_variant | MODIFIER | c.525+292_525+299del others(8): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 8/25 | chr10 | 24622433 | ||||||
| chr10:24622433
|
CATATATA others(3): Show |
C | 10 | a0001c0001t0001g0182a0001c0001t0001g0193a0001c0001t0002g0326others(7): Show | 10 | HG00597.hp2 HG01891.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.525+290_525+299del others(10): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 8/25 | chr10 | 24622433 | ||||||
| chr10:24622433
|
CATATATA others(5): Show |
C | 12 | a0001c0001t0001g0192a0001c0001t0001g0253a0001c0001t0002g0294others(9): Show | 12 | HG02257.hp1 HG02630.hp2 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.525+288_525+299del others(12): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 8/25 | chr10 | 24622433 | ||||||
| chr10:24622433
|
CATATATA others(7): Show |
C | 21 | a0001c0001t0001g0191a0001c0001t0001g0196a0001c0001t0001g0199others(18): Show | 21 | HG00099.hp2 HG01192.hp1 HG01433.hp2 others(18): Show |
intron_variant | MODIFIER | c.525+286_525+299del others(14): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 8/25 | chr10 | 24622433 | ||||||
| chr10:24622433
|
CATATATA others(9): Show |
C | 43 | a0001c0001t0001g0174a0001c0001t0001g0181a0001c0001t0001g0183others(40): Show | 43 | HG00423.hp1 HG00438.hp2 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.525+284_525+299del others(16): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 8/25 | chr10 | 24622433 | ||||||
| chr10:24622433
|
CATATATA others(11): Show |
C | 13 | a0001c0001t0001g0217a0001c0001t0001g0252a0001c0001t0005g0005others(10): Show | 13 | HG00642.hp1 HG01069.hp2 HG01516.hp2 others(10): Show |
intron_variant | MODIFIER | c.525+282_525+299del others(18): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 8/25 | chr10 | 24622433 | ||||||
| chr10:24622433
|
CATATATA others(13): Show |
C | 30 | a0001c0001t0005g0001a0001c0001t0005g0006a0001c0014t0004g0286others(27): Show | 30 | HG00280.hp1 HG00323.hp2 HG00673.hp1 others(27): Show |
intron_variant | MODIFIER | c.525+280_525+299del others(20): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 8/25 | chr10 | 24622433 | ||||||
| chr10:24622433
|
CATATATA others(15): Show |
C | 13 | a0002c0002t0001g0075a0002c0002t0001g0076a0002c0002t0001g0106others(10): Show | 13 | HG01261.hp2 HG02027.hp2 HG02074.hp2 others(10): Show |
intron_variant | MODIFIER | c.525+278_525+299del others(22): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 8/25 | chr10 | 24622433 | ||||||
| chr10:24622433
|
CATATATA others(17): Show |
C | 87 | a0001c0001t0001g0269a0002c0002t0001g0010a0002c0002t0001g0018others(84): Show | 87 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.525+276_525+299del others(24): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 8/25 | chr10 | 24622433 | ||||||
| chr10:24622433
|
CATATATA others(19): Show |
C | 6 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0164others(3): Show | 6 | HG02559.hp1 HG02572.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.525+274_525+299del others(26): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 8/25 | chr10 | 24622433 | ||||||
| chr10:24622433
|
CATATATA others(21): Show |
C | 3 | a0001c0001t0001g0141a0001c0001t0001g0144a0007c0007t0006g0292 | 3 | HG02280.hp1 HG02486.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.525+272_525+299del others(28): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 8/25 | chr10 | 24622433 | ||||||
| chr10:24622433
|
CATATATA others(23): Show |
C | 7 | a0001c0001t0001g0273a0003c0003t0001g0265a0007c0007t0006g0291others(4): Show | 7 | HG01993.hp1 HG02129.hp2 HG02523.hp2 others(4): Show |
intron_variant | MODIFIER | c.525+270_525+299del others(30): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 8/25 | chr10 | 24622433 | ||||||
| chr10:24622433
|
CATATATA others(31): Show |
C | 1 | a0001c0001t0001g0012 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.525+262_525+299del others(38): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 8/25 | chr10 | 24622433 | ||||||
| chr10:24622441
|
T | A | 1 | a0001c0001t0001g0142 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.525+292A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 8/25 | chr10 | 24622441 | ||||||
| chr10:24622443
|
T | A | 1 | a0001c0001t0001g0143 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.525+290A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 8/25 | chr10 | 24622443 | ||||||
| chr10:24622455
|
T | A | 3 | a0001c0001t0004g0296a0001c0001t0004g0297a0001c0001t0004g0298 | 3 | HG02895.hp1 HG02897.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.525+278A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 8/25 | chr10 | 24622455 | ||||||
| chr10:24622485
|
T | C | 90 | a0002c0002t0001g0010a0002c0002t0001g0018a0002c0002t0001g0020others(87): Show | 90 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.525+248A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 8/25 | chr10 | 24622485 | ||||||
| chr10:24622506
|
C | T | 4 | a0002c0002t0001g0106a0002c0002t0001g0107a0002c0002t0001g0108others(1): Show | 4 | HG02258.hp1 HG02630.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.525+227G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 8/25 | chr10 | 24622506 | ||||||
| chr10:24622607
|
G | T | 2 | a0001c0001t0002g0337a0001c0001t0002g0338 | 2 | NA18964.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.525+126C>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 8/25 | chr10 | 24622607 | ||||||
| chr10:24622611
|
G | C | 1 | a0005c0005t0004g0287 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.525+122C>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 8/25 | chr10 | 24622611 | ||||||
| chr10:24622894
|
G | A | 1 | a0001c0001t0001g0270 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.496-132C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24622894 | ||||||
| chr10:24623118
|
C | G | 17 | a0002c0002t0001g0019a0002c0002t0001g0106a0002c0002t0001g0107others(14): Show | 17 | HG01261.hp2 HG01496.hp1 HG01516.hp2 others(14): Show |
intron_variant | MODIFIER | c.496-356G>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24623118 | ||||||
| chr10:24623430
|
G | T | 1 | a0002c0002t0001g0110 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.496-668C>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24623430 | ||||||
| chr10:24623507
|
C | T | 1 | a0002c0002t0001g0094 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.496-745G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24623507 | ||||||
| chr10:24623681
|
T | C | 1 | a0009c0008t0001g0262 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.496-919A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24623681 | ||||||
| chr10:24623704
|
G | A | 139 | a0002c0002t0001g0010a0002c0002t0001g0017a0002c0002t0001g0018others(136): Show | 139 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.496-942C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24623704 | ||||||
| chr10:24624337
|
C | CT | 32 | a0001c0001t0001g0174a0001c0001t0001g0177a0001c0001t0001g0181others(29): Show | 32 | HG00408.hp2 HG00423.hp1 HG00597.hp2 others(29): Show |
intron_variant | MODIFIER | c.496-1576dupA | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24624337 | ||||||
| chr10:24624337
|
C | CTTTTTTT | 88 | a0002c0002t0001g0010a0002c0002t0001g0017a0002c0002t0001g0018others(85): Show | 88 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(85): Show |
intron_variant | MODIFIER | c.496-1582_496-1576d others(9): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24624337 | ||||||
| chr10:24624337
|
C | CTTTTTTT others(1): Show |
58 | a0002c0002t0001g0025a0002c0002t0001g0035a0002c0002t0001g0036others(55): Show | 58 | HG00438.hp2 HG00642.hp2 HG00735.hp1 others(55): Show |
intron_variant | MODIFIER | c.496-1583_496-1576d others(10): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24624337 | ||||||
| chr10:24624337
|
C | CTTTTTTT others(2): Show |
16 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(13): Show | 16 | HG01433.hp1 HG02280.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.496-1584_496-1576d others(11): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24624337 | ||||||
| chr10:24624337
|
C | CTTTTTTT others(3): Show |
8 | a0001c0001t0001g0144a0001c0001t0001g0162a0001c0001t0001g0163others(5): Show | 8 | HG02486.hp1 HG02717.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.496-1585_496-1576d others(12): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24624337 | ||||||
| chr10:24624337
|
C | CTTTTTTT others(4): Show |
2 | a0001c0001t0001g0166a0001c0001t0001g0171 | 2 | HG01891.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.496-1586_496-1576d others(13): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24624337 | ||||||
| chr10:24624457
|
A | G | 1 | a0001c0001t0001g0228 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.496-1695T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24624457 | ||||||
| chr10:24624557
|
C | T | 1 | a0002c0002t0001g0081 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.496-1795G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24624557 | ||||||
| chr10:24624581
|
C | A | 1 | a0001c0001t0002g0319 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.496-1819G>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24624581 | ||||||
| chr10:24624756
|
C | T | 160 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(157): Show | 160 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(157): Show |
intron_variant | MODIFIER | c.496-1994G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24624756 | ||||||
| chr10:24624901
|
T | C | 1 | a0019c0020t0001g0112 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.496-2139A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24624901 | ||||||
| chr10:24624993
|
C | T | 9 | a0001c0001t0001g0141a0001c0001t0001g0144a0001c0001t0001g0162others(6): Show | 9 | HG02280.hp1 HG02486.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.496-2231G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24624993 | ||||||
| chr10:24625050
|
T | A | 1 | a0007c0007t0006g0293 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.496-2288A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24625050 | ||||||
| chr10:24625050
|
T | TG | 54 | a0001c0001t0002g0294a0001c0001t0002g0310a0001c0001t0002g0317others(51): Show | 54 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.496-2289dupC | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24625050 | ||||||
| chr10:24625050
|
T | TGG | 45 | a0001c0001t0001g0191a0001c0001t0002g0303a0001c0001t0002g0304others(42): Show | 45 | HG00733.hp1 HG01168.hp2 HG01928.hp2 others(42): Show |
intron_variant | MODIFIER | c.496-2290_496-2289d others(4): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24625050 | ||||||
| chr10:24625050
|
T | TGGG | 21 | a0001c0001t0002g0300a0001c0001t0002g0302a0001c0001t0002g0318others(18): Show | 21 | HG00140.hp2 HG00609.hp2 HG00673.hp2 others(18): Show |
intron_variant | MODIFIER | c.496-2291_496-2289d others(5): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24625050 | ||||||
| chr10:24625050
|
T | TGGGGG | 19 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0187others(16): Show | 19 | HG00140.hp1 HG00639.hp2 HG00642.hp2 others(16): Show |
intron_variant | MODIFIER | c.496-2293_496-2289d others(7): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24625050 | ||||||
| chr10:24625050
|
T | TGGGGGGG others(3): Show |
4 | a0001c0001t0001g0181a0001c0001t0001g0183a0001c0001t0001g0195others(1): Show | 4 | HG01884.hp2 HG02622.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.496-2298_496-2289d others(12): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24625050 | ||||||
| chr10:24625050
|
T | TGGGGGGG others(4): Show |
1 | a0001c0001t0001g0193 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.496-2299_496-2289d others(13): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24625050 | ||||||
| chr10:24625051
|
G | A | 2 | a0017c0029t0006g0290a0022c0028t0006g0289 | 2 | NA18989.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.496-2289C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24625051 | ||||||
| chr10:24625052
|
G | A | 3 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0015g0288 | 3 | HG02129.hp2 NA18747.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.496-2290C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24625052 | ||||||
| chr10:24625062
|
G | A | 1 | a0001c0001t0001g0228 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.496-2300C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24625062 | ||||||
| chr10:24625062
|
G | C | 2 | a0011c0011t0001g0258a0011c0011t0001g0259 | 2 | HG02818.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.496-2300C>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24625062 | ||||||
| chr10:24625062
|
G | GGGGGGGG others(4): Show |
3 | a0003c0003t0001g0200a0003c0003t0001g0223a0008c0009t0005g0003 | 3 | NA18959.hp1 NA19002.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.496-2301_496-2300i others(13): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24625062 | ||||||
| chr10:24625062
|
G | GGGGGGGG others(5): Show |
10 | a0001c0001t0001g0197a0003c0003t0001g0173a0003c0003t0001g0180others(7): Show | 10 | HG01952.hp1 HG02040.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.496-2301_496-2300i others(14): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24625062 | ||||||
| chr10:24625062
|
G | GGGGGGGG others(7): Show |
1 | a0003c0003t0001g0231 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.496-2301_496-2300i others(16): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24625062 | ||||||
| chr10:24625062
|
G | GGGGGGGG others(6): Show |
11 | a0001c0001t0001g0217a0001c0001t0001g0225a0001c0001t0001g0249others(8): Show | 11 | HG00621.hp1 HG01069.hp2 HG02970.hp2 others(8): Show |
intron_variant | MODIFIER | c.496-2301_496-2300i others(15): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24625062 | ||||||
| chr10:24625062
|
G | GGGGGGGG others(7): Show |
13 | a0001c0001t0001g0199a0001c0001t0001g0222a0001c0001t0001g0224others(10): Show | 13 | HG00423.hp1 HG00597.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.496-2301_496-2300i others(16): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24625062 | ||||||
| chr10:24625062
|
G | GGGGGGGG others(8): Show |
10 | a0001c0001t0001g0219a0001c0001t0001g0233a0001c0001t0001g0234others(7): Show | 10 | HG00408.hp2 HG01192.hp1 HG01993.hp1 others(7): Show |
intron_variant | MODIFIER | c.496-2301_496-2300i others(17): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24625062 | ||||||
| chr10:24625062
|
G | GGGGGGGG others(9): Show |
6 | a0001c0001t0001g0174a0001c0001t0001g0235a0003c0003t0001g0011others(3): Show | 6 | HG01123.hp1 HG02004.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.496-2301_496-2300i others(18): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24625062 | ||||||
| chr10:24625062
|
G | GGGGGGGG others(10): Show |
3 | a0001c0001t0001g0220a0001c0001t0001g0232a0001c0001t0001g0255 | 3 | HG02622.hp1 HG03453.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.496-2301_496-2300i others(19): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24625062 | ||||||
| chr10:24625062
|
G | GGGGGGGG others(11): Show |
1 | a0003c0003t0001g0179 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.496-2301_496-2300i others(20): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24625062 | ||||||
| chr10:24625062
|
G | GGGGGGGG others(12): Show |
2 | a0001c0001t0001g0226a0003c0003t0001g0203 | 2 | HG02148.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.496-2301_496-2300i others(21): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24625062 | ||||||
| chr10:24625062
|
G | GGGGGGGG others(10): Show |
1 | a0003c0003t0001g0215 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.496-2301_496-2300i others(19): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24625062 | ||||||
| chr10:24625063
|
GGA | G | 18 | a0002c0002t0001g0017a0002c0002t0001g0021a0002c0002t0001g0023others(15): Show | 18 | HG00438.hp2 HG00673.hp1 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.496-2303_496-2302d others(4): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24625063 | ||||||
| chr10:24625064
|
GA | G | 12 | a0002c0002t0001g0038a0002c0002t0001g0109a0002c0002t0001g0113others(9): Show | 12 | HG01256.hp2 HG02027.hp2 HG02074.hp2 others(9): Show |
intron_variant | MODIFIER | c.496-2303delT | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24625064 | ||||||
| chr10:24625065
|
A | G | 98 | a0002c0002t0001g0010a0002c0002t0001g0018a0002c0002t0001g0019others(95): Show | 98 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.496-2303T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24625065 | ||||||
| chr10:24625068
|
A | G | 2 | a0002c0002t0001g0128a0002c0002t0001g0129 | 2 | HG01175.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.496-2306T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24625068 | ||||||
| chr10:24625071
|
A | G | 2 | a0002c0002t0001g0128a0002c0002t0001g0129 | 2 | HG01175.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.496-2309T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24625071 | ||||||
| chr10:24625075
|
G | A | 2 | a0012c0010t0001g0266a0012c0010t0001g0267 | 2 | HG02109.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.496-2313C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24625075 | ||||||
| chr10:24625114
|
T | C | 1 | a0007c0007t0006g0293 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.496-2352A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24625114 | ||||||
| chr10:24625282
|
A | G | 1 | a0002c0002t0001g0083 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.496-2520T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24625282 | ||||||
| chr10:24625299
|
G | GC | 77 | a0001c0001t0001g0143a0001c0001t0001g0171a0001c0001t0001g0174others(74): Show | 77 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.496-2538_496-2537i others(3): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24625299 | ||||||
| chr10:24625299
|
G | GCA | 84 | a0001c0001t0001g0183a0001c0001t0004g0297a0001c0001t0016g0352others(81): Show | 84 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.496-2538_496-2537i others(4): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24625299 | ||||||
| chr10:24625299
|
G | GCAA | 16 | a0002c0002t0001g0034a0002c0002t0001g0052a0002c0002t0001g0082others(13): Show | 16 | HG00140.hp2 HG00438.hp1 HG00673.hp1 others(13): Show |
intron_variant | MODIFIER | c.496-2538_496-2537i others(5): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24625299 | ||||||
| chr10:24625299
|
G | GCAAA | 3 | a0002c0002t0001g0045a0002c0002t0001g0050a0002c0002t0001g0134 | 3 | HG02257.hp2 NA18970.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.496-2538_496-2537i others(6): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24625299 | ||||||
| chr10:24625299
|
GA | G | 7 | a0001c0001t0001g0013a0001c0001t0001g0193a0001c0001t0001g0234others(4): Show | 7 | HG01169.hp1 HG01516.hp1 HG01517.hp1 others(4): Show |
intron_variant | MODIFIER | c.496-2538delT | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24625299 | ||||||
| chr10:24625299
|
GAAAAAAA others(5): Show |
G | 1 | a0001c0001t0001g0160 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.496-2549_496-2538d others(14): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24625299 | ||||||
| chr10:24625299
|
GAAAAAAA others(6): Show |
G | 1 | a0001c0001t0001g0192 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.496-2550_496-2538d others(15): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24625299 | ||||||
| chr10:24625300
|
A | C | 161 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0141others(158): Show | 161 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(158): Show |
intron_variant | MODIFIER | c.496-2538T>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24625300 | ||||||
| chr10:24625301
|
A | C | 5 | a0001c0001t0001g0013a0001c0001t0001g0193a0001c0001t0001g0234others(2): Show | 5 | HG01169.hp1 HG02965.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.496-2539T>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24625301 | ||||||
| chr10:24625312
|
A | C | 1 | a0001c0001t0001g0160 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.496-2550T>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24625312 | ||||||
| chr10:24625313
|
A | C | 1 | a0001c0001t0001g0192 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.496-2551T>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24625313 | ||||||
| chr10:24625412
|
T | A | 1 | a0003c0003t0001g0198 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.496-2650A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24625412 | ||||||
| chr10:24625435
|
T | C | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.496-2673A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24625435 | ||||||
| chr10:24625457
|
C | A | 23 | a0002c0002t0001g0017a0002c0002t0001g0117a0002c0002t0001g0118others(20): Show | 23 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(20): Show |
intron_variant | MODIFIER | c.496-2695G>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24625457 | ||||||
| chr10:24625486
|
T | A | 1 | a0003c0003t0001g0215 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.496-2724A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24625486 | ||||||
| chr10:24625530
|
AT | A | 127 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(124): Show | 127 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.496-2769delA | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24625530 | ||||||
| chr10:24625563
|
T | G | 2 | a0001c0001t0001g0142a0001c0001t0001g0143 | 2 | HG02451.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.496-2801A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24625563 | ||||||
| chr10:24625932
|
T | C | 1 | a0011c0011t0001g0259 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.496-3170A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24625932 | ||||||
| chr10:24626073
|
T | C | 1 | a0002c0002t0001g0078 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.496-3311A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24626073 | ||||||
| chr10:24626267
|
G | A | 11 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(8): Show | 11 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.496-3505C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24626267 | ||||||
| chr10:24626292
|
C | T | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.496-3530G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24626292 | ||||||
| chr10:24626392
|
G | A | 3 | a0001c0001t0001g0174a0001c0001t0001g0219a0001c0001t0001g0222 | 3 | HG01192.hp1 HG02055.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.495+3604C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24626392 | ||||||
| chr10:24626513
|
C | T | 6 | a0001c0001t0001g0270a0001c0001t0001g0271a0001c0001t0001g0272others(3): Show | 6 | HG00423.hp2 NA18943.hp2 NA18964.hp1 others(3): Show |
intron_variant | MODIFIER | c.495+3483G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24626513 | ||||||
| chr10:24626637
|
T | G | 2 | a0002c0002t0001g0019a0002c0002t0014g0105 | 2 | HG01496.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.495+3359A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24626637 | ||||||
| chr10:24626701
|
T | C | 1 | a0003c0003t0001g0179 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.495+3295A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24626701 | ||||||
| chr10:24626774
|
A | T | 1 | a0001c0001t0002g0310 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.495+3222T>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24626774 | ||||||
| chr10:24626882
|
T | C | 11 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(8): Show | 11 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.495+3114A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24626882 | ||||||
| chr10:24627125
|
T | C | 5 | a0002c0002t0001g0024a0002c0002t0001g0025a0002c0002t0001g0026others(2): Show | 5 | HG00621.hp2 HG02155.hp2 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.495+2871A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24627125 | ||||||
| chr10:24627176
|
T | G | 1 | a0003c0003t0001g0215 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.495+2820A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24627176 | ||||||
| chr10:24627177
|
G | C | 1 | a0003c0003t0001g0215 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.495+2819C>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24627177 | ||||||
| chr10:24627230
|
C | A | 1 | a0002c0002t0001g0043 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.495+2766G>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24627230 | ||||||
| chr10:24627282
|
T | G | 1 | a0001c0001t0001g0252 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.495+2714A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24627282 | ||||||
| chr10:24627365
|
A | C | 1 | a0002c0002t0001g0126 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.495+2631T>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24627365 | ||||||
| chr10:24627411
|
A | T | 1 | a0003c0003t0001g0211 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.495+2585T>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24627411 | ||||||
| chr10:24627417
|
T | C | 34 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0176others(31): Show | 34 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(31): Show |
intron_variant | MODIFIER | c.495+2579A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24627417 | ||||||
| chr10:24627464
|
A | AAGGAT | 216 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(213): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.495+2531_495+2532i others(7): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24627464 | ||||||
| chr10:24627589
|
C | T | 1 | a0002c0002t0004g0295 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.495+2407G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24627589 | ||||||
| chr10:24627596
|
G | C | 2 | a0011c0011t0001g0258a0011c0011t0001g0259 | 2 | HG02818.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.495+2400C>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24627596 | ||||||
| chr10:24627607
|
C | G | 1 | a0001c0001t0001g0192 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.495+2389G>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24627607 | ||||||
| chr10:24627655
|
T | TACTTTAT others(24): Show |
1 | a0003c0003t0001g0215 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.495+2340_495+2341i others(33): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24627655 | ||||||
| chr10:24627764
|
C | T | 1 | a0002c0002t0001g0095 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.495+2232G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24627764 | ||||||
| chr10:24627767
|
C | G | 350 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(347): Show | 350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.495+2229G>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24627767 | ||||||
| chr10:24627767
|
C | T | 1 | a0002c0002t0001g0043 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.495+2229G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24627767 | ||||||
| chr10:24627805
|
C | T | 11 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(8): Show | 11 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.495+2191G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24627805 | ||||||
| chr10:24628072
|
A | G | 1 | a0011c0011t0001g0258 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.495+1924T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628072 | ||||||
| chr10:24628135
|
G | A | 1 | a0002c0002t0004g0295 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.495+1861C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628135 | ||||||
| chr10:24628219
|
A | C | 1 | a0002c0002t0014g0105 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.495+1777T>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628219 | ||||||
| chr10:24628333
|
T | A | 3 | a0002c0002t0001g0064a0002c0002t0001g0096a0002c0002t0001g0145 | 3 | NA18988.hp2 NA18992.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.495+1663A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628333 | ||||||
| chr10:24628349
|
G | A | 1 | a0003c0003t0001g0204 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.495+1647C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628349 | ||||||
| chr10:24628361
|
T | C | 3 | a0003c0003t0001g0198a0003c0003t0001g0213a0003c0003t0001g0218 | 3 | HG00423.hp1 HG02083.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.495+1635A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628361 | ||||||
| chr10:24628412
|
G | A | 163 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(160): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.495+1584C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628412 | ||||||
| chr10:24628422
|
AT | A | 169 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(166): Show | 169 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.495+1573delA | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628422 | ||||||
| chr10:24628603
|
T | C | 24 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(21): Show | 24 | HG01891.hp2 HG02129.hp2 HG02280.hp1 others(21): Show |
intron_variant | MODIFIER | c.495+1393A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628603 | ||||||
| chr10:24628753
|
A | ATG | 127 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(124): Show | 127 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.495+1241_495+1242d others(4): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628753 | ||||||
| chr10:24628753
|
ATG | A | 3 | a0001c0001t0001g0193a0012c0010t0001g0266a0012c0010t0001g0267 | 3 | HG02109.hp1 HG03195.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.495+1241_495+1242d others(4): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628753 | ||||||
| chr10:24628753
|
ATGTGTG | A | 11 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(8): Show | 11 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.495+1237_495+1242d others(8): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628753 | ||||||
| chr10:24628766
|
T | C | 5 | a0001c0001t0001g0171a0001c0001t0004g0296a0001c0001t0004g0297others(2): Show | 5 | HG01891.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.495+1230A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628766 | ||||||
| chr10:24628767
|
G | A | 5 | a0001c0001t0001g0171a0001c0001t0004g0296a0001c0001t0004g0297others(2): Show | 5 | HG01891.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.495+1229C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628767 | ||||||
| chr10:24628768
|
TGTGC | T | 5 | a0001c0001t0001g0171a0001c0001t0004g0296a0001c0001t0004g0297others(2): Show | 5 | HG01891.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.495+1224_495+1227d others(6): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628768 | ||||||
| chr10:24628770
|
T | C | 3 | a0002c0002t0001g0107a0002c0002t0001g0111a0002c0002t0001g0146 | 3 | HG02258.hp1 HG02630.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.495+1226A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628770 | ||||||
| chr10:24628771
|
G | A | 3 | a0002c0002t0001g0107a0002c0002t0001g0111a0002c0002t0001g0146 | 3 | HG02258.hp1 HG02630.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.495+1225C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628771 | ||||||
| chr10:24628771
|
G | GTGCA | 4 | a0002c0002t0001g0035a0002c0002t0001g0106a0010c0012t0010g0015others(1): Show | 4 | HG02723.hp1 HG02896.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.495+1224_495+1225i others(6): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628771 | ||||||
| chr10:24628772
|
C | CAT | 132 | a0001c0014t0004g0286a0002c0002t0001g0010a0002c0002t0001g0017others(129): Show | 132 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.495+1222_495+1223d others(4): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628772 | ||||||
| chr10:24628772
|
C | T | 7 | a0002c0002t0001g0035a0002c0002t0001g0106a0002c0002t0001g0107others(4): Show | 7 | HG02258.hp1 HG02630.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.495+1224G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628772 | ||||||
| chr10:24628782
|
T | C | 1 | a0001c0001t0001g0171 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.495+1214A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628782 | ||||||
| chr10:24628798
|
C | CAT | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.495+1196_495+1197d others(4): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628798 | ||||||
| chr10:24628808
|
T | C | 1 | a0001c0001t0001g0192 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.495+1188A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628808 | ||||||
| chr10:24628808
|
T | TATATATA others(27): Show |
2 | a0005c0005t0001g0137a0005c0005t0001g0284 | 2 | NA18522.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.495+1187_495+1188i others(36): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628808 | ||||||
| chr10:24628810
|
T | TATATATA others(23): Show |
10 | a0002c0002t0001g0019a0002c0002t0001g0113a0002c0002t0001g0114others(7): Show | 10 | HG01496.hp1 HG01516.hp2 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.495+1185_495+1186i others(32): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628810 | ||||||
| chr10:24628810
|
T | TATATATA others(25): Show |
1 | a0005c0005t0001g0102 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.495+1185_495+1186i others(34): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628810 | ||||||
| chr10:24628810
|
TATATAC | T | 3 | a0002c0002t0001g0108a0002c0002t0001g0109a0002c0002t0001g0110 | 3 | HG02148.hp1 HG02895.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.495+1180_495+1185d others(8): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628810 | ||||||
| chr10:24628812
|
TATAC | T | 26 | a0002c0002t0001g0017a0002c0002t0001g0106a0002c0002t0001g0107others(23): Show | 26 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(23): Show |
intron_variant | MODIFIER | c.495+1180_495+1183d others(6): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628812 | ||||||
| chr10:24628814
|
T | C | 3 | a0002c0002t0001g0058a0002c0002t0001g0061a0002c0002t0001g0078 | 3 | HG01257.hp2 HG01258.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.495+1182A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628814 | ||||||
| chr10:24628816
|
C | CAT | 114 | a0001c0001t0001g0141a0001c0001t0001g0144a0001c0001t0001g0162others(111): Show | 114 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.495+1178_495+1179d others(4): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628816 | ||||||
| chr10:24628816
|
C | CATATATA others(25): Show |
2 | a0001c0001t0001g0142a0001c0001t0001g0143 | 2 | HG02451.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.495+1179_495+1180i others(34): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628816 | ||||||
| chr10:24628816
|
C | T | 16 | a0002c0002t0001g0019a0002c0002t0001g0058a0002c0002t0001g0061others(13): Show | 16 | HG01257.hp2 HG01258.hp1 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.495+1180G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628816 | ||||||
| chr10:24628820
|
T | C | 65 | a0001c0001t0001g0160a0001c0001t0001g0174a0001c0001t0001g0197others(62): Show | 65 | HG00408.hp2 HG00423.hp1 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.495+1176A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628820 | ||||||
| chr10:24628833
|
GTACATAT others(7): Show |
G | 2 | a0001c0001t0009g0158a0001c0001t0009g0159 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.495+1149_495+1162d others(16): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628833 | ||||||
| chr10:24628850
|
CAT | C | 12 | a0001c0001t0001g0014a0001c0001t0001g0171a0001c0001t0001g0226others(9): Show | 12 | HG01891.hp2 HG02895.hp1 HG02897.hp2 others(9): Show |
intron_variant | MODIFIER | c.495+1144_495+1145d others(4): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628850 | ||||||
| chr10:24628872
|
T | TACATATA others(27): Show |
1 | a0001c0001t0001g0252 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.495+1090_495+1123d others(36): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628872 | ||||||
| chr10:24628874
|
C | CAT | 48 | a0002c0002t0001g0017a0002c0002t0001g0019a0002c0002t0001g0106others(45): Show | 48 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(45): Show |
intron_variant | MODIFIER | c.495+1120_495+1121d others(4): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628874 | ||||||
| chr10:24628882
|
C | T | 12 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(9): Show | 12 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.495+1114G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628882 | ||||||
| chr10:24628884
|
CAT | C | 11 | a0001c0001t0001g0171a0001c0001t0002g0302a0001c0001t0004g0296others(8): Show | 11 | HG01891.hp2 HG02895.hp1 HG02897.hp2 others(8): Show |
intron_variant | MODIFIER | c.495+1110_495+1111d others(4): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628884 | ||||||
| chr10:24628886
|
T | C | 12 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(9): Show | 12 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.495+1110A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628886 | ||||||
| chr10:24628896
|
TACATATA others(3): Show |
T | 1 | a0003c0003t0001g0223 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.495+1090_495+1099d others(12): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628896 | ||||||
| chr10:24628898
|
C | CAT | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.495+1096_495+1097d others(4): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628898 | ||||||
| chr10:24628916
|
C | CATATATA others(7): Show |
5 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0015g0288others(2): Show | 5 | HG02129.hp2 NA18747.hp1 NA18989.hp1 others(2): Show |
intron_variant | MODIFIER | c.495+1079_495+1080i others(16): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628916 | ||||||
| chr10:24628916
|
C | CATATATA others(1): Show |
150 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(147): Show | 150 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.495+1079_495+1080i others(10): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628916 | ||||||
| chr10:24628918
|
C | T | 3 | a0007c0007t0006g0293a0010c0012t0010g0015a0010c0012t0010g0016 | 3 | HG02523.hp2 HG02723.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.495+1078G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628918 | ||||||
| chr10:24628924
|
T | C | 1 | a0007c0007t0006g0293 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.495+1072A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628924 | ||||||
| chr10:24628928
|
C | T | 3 | a0002c0002t0001g0130a0002c0002t0001g0131a0007c0007t0006g0293 | 3 | HG00323.hp2 HG00733.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.495+1068G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628928 | ||||||
| chr10:24628940
|
T | C | 1 | a0002c0002t0001g0280 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.495+1056A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628940 | ||||||
| chr10:24628942
|
C | T | 2 | a0002c0002t0001g0150a0002c0002t0001g0151 | 2 | NA18941.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.495+1054G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628942 | ||||||
| chr10:24628944
|
C | T | 1 | a0007c0007t0006g0293 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.495+1052G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628944 | ||||||
| chr10:24628952
|
C | CACTATAT others(3): Show |
1 | a0010c0012t0010g0015 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.495+1043_495+1044i others(12): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628952 | ||||||
| chr10:24628952
|
C | CTA | 18 | a0001c0001t0002g0303a0001c0001t0002g0304a0001c0001t0002g0307others(15): Show | 18 | HG01168.hp2 HG01175.hp2 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.495+1042_495+1043d others(4): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628952 | ||||||
| chr10:24628952
|
C | CTATA | 8 | a0002c0002t0001g0024a0002c0002t0001g0035a0002c0002t0001g0062others(5): Show | 8 | HG00621.hp2 HG02738.hp2 HG03927.hp1 others(5): Show |
intron_variant | MODIFIER | c.495+1040_495+1043d others(6): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628952 | ||||||
| chr10:24628952
|
C | CTATATA | 5 | a0001c0001t0008g0306a0002c0002t0001g0057a0002c0002t0001g0072others(2): Show | 5 | HG00639.hp1 NA18943.hp1 NA18978.hp2 others(2): Show |
intron_variant | MODIFIER | c.495+1038_495+1043d others(8): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628952 | ||||||
| chr10:24628952
|
C | CTATATAT others(1): Show |
5 | a0001c0001t0001g0249a0002c0002t0001g0010a0002c0002t0001g0127others(2): Show | 5 | HG02071.hp2 HG02074.hp1 NA18954.hp2 others(2): Show |
intron_variant | MODIFIER | c.495+1036_495+1043d others(10): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628952 | ||||||
| chr10:24628952
|
C | CTATATAT others(3): Show |
6 | a0001c0001t0001g0269a0001c0001t0005g0005a0001c0001t0005g0006others(3): Show | 6 | HG00597.hp1 HG00673.hp1 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.495+1034_495+1043d others(12): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628952 | ||||||
| chr10:24628952
|
C | CTATATAT others(5): Show |
4 | a0002c0002t0001g0038a0002c0002t0001g0092a0002c0002t0001g0285others(1): Show | 4 | NA18747.hp2 NA18972.hp1 NA19054.hp1 others(1): Show |
intron_variant | MODIFIER | c.495+1032_495+1043d others(14): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628952 | ||||||
| chr10:24628952
|
C | CTATATAT others(7): Show |
3 | a0001c0001t0001g0193a0002c0002t0001g0046a0012c0010t0001g0266 | 3 | HG03195.hp1 HG03195.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.495+1030_495+1043d others(16): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628952 | ||||||
| chr10:24628952
|
C | CTATATAT others(9): Show |
1 | a0012c0010t0001g0267 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.495+1028_495+1043d others(18): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628952 | ||||||
| chr10:24628952
|
C | CTATATAT others(11): Show |
1 | a0002c0002t0001g0256 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.495+1026_495+1043d others(20): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628952 | ||||||
| chr10:24628952
|
CTA | C | 6 | a0001c0001t0003g0154a0003c0003t0001g0204a0003c0003t0001g0205others(3): Show | 6 | HG01081.hp1 HG02818.hp2 NA18961.hp2 others(3): Show |
intron_variant | MODIFIER | c.495+1042_495+1043d others(4): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628952 | ||||||
| chr10:24628952
|
CTATATA | C | 3 | a0001c0001t0001g0272a0001c0001t0002g0316a0001c0001t0002g0326 | 3 | HG02155.hp1 NA18964.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.495+1038_495+1043d others(8): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628952 | ||||||
| chr10:24628952
|
CTATATAT others(1): Show |
C | 3 | a0001c0001t0001g0185a0001c0001t0001g0188a0019c0020t0001g0112 | 3 | HG01169.hp2 HG01261.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.495+1036_495+1043d others(10): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628952 | ||||||
| chr10:24628952
|
CTATATAT others(3): Show |
C | 1 | a0001c0001t0001g0190 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.495+1034_495+1043d others(12): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628952 | ||||||
| chr10:24628952
|
CTATATAT others(5): Show |
C | 1 | a0005c0005t0001g0104 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.495+1032_495+1043d others(14): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628952 | ||||||
| chr10:24628952
|
CTATATAT others(7): Show |
C | 2 | a0002c0002t0014g0105a0005c0005t0001g0284 | 2 | HG01516.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.495+1030_495+1043d others(16): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628952 | ||||||
| chr10:24628952
|
CTATATAT others(9): Show |
C | 1 | a0001c0001t0001g0192 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.495+1028_495+1043d others(18): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628952 | ||||||
| chr10:24628953
|
T | A | 1 | a0010c0012t0010g0016 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.495+1043A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628953 | ||||||
| chr10:24628954
|
A | C | 1 | a0010c0012t0010g0016 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.495+1042T>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628954 | ||||||
| chr10:24628961
|
T | C | 1 | a0007c0007t0006g0293 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.495+1035A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628961 | ||||||
| chr10:24628963
|
T | C | 1 | a0007c0007t0006g0293 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.495+1033A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628963 | ||||||
| chr10:24628965
|
T | C | 1 | a0007c0007t0006g0293 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.495+1031A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628965 | ||||||
| chr10:24628967
|
T | C | 1 | a0007c0007t0006g0293 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.495+1029A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628967 | ||||||
| chr10:24628968
|
ATATATAT others(10): Show |
A | 1 | a0002c0002t0004g0301 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.495+1011_495+1027d others(19): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628968 | ||||||
| chr10:24628969
|
T | C | 1 | a0007c0007t0006g0293 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.495+1027A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628969 | ||||||
| chr10:24628972
|
ATATATAT others(12): Show |
A | 4 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0015g0288others(1): Show | 4 | HG02129.hp2 NA18747.hp1 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.495+1005_495+1023d others(21): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628972 | ||||||
| chr10:24628974
|
ATATATAT others(12): Show |
A | 1 | a0017c0029t0006g0290 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.495+1003_495+1021d others(21): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628974 | ||||||
| chr10:24628976
|
A | T | 2 | a0003c0003t0001g0207a0003c0003t0001g0209 | 2 | NA18947.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.495+1020T>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628976 | ||||||
| chr10:24628978
|
A | T | 6 | a0001c0001t0001g0170a0001c0001t0001g0185a0001c0001t0001g0188others(3): Show | 6 | HG01169.hp2 HG03942.hp1 NA18947.hp1 others(3): Show |
intron_variant | MODIFIER | c.495+1018T>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628978 | ||||||
| chr10:24628980
|
A | T | 16 | a0001c0001t0001g0170a0001c0001t0001g0184a0001c0001t0001g0185others(13): Show | 16 | HG01109.hp1 HG01168.hp1 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.495+1016T>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628980 | ||||||
| chr10:24628982
|
A | ATATATAT others(4): Show |
2 | a0001c0001t0001g0013a0001c0001t0001g0257 | 2 | HG02738.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.495+1013_495+1014i others(13): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | ||||||
| chr10:24628982
|
A | ATATATAT others(6): Show |
1 | a0003c0003t0001g0223 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.495+1013_495+1014i others(15): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | ||||||
| chr10:24628982
|
A | ATATATAT others(8): Show |
1 | a0001c0001t0001g0012 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.495+1013_495+1014i others(17): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | ||||||
| chr10:24628982
|
A | ATATATAT others(25): Show |
1 | a0001c0001t0001g0263 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.495+1013_495+1014i others(34): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | ||||||
| chr10:24628982
|
A | ATATATAT others(23): Show |
1 | a0002c0002t0001g0133 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.495+1013_495+1014i others(32): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | ||||||
| chr10:24628982
|
A | ATATATAT others(20): Show |
1 | a0001c0001t0001g0163 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.495+1013_495+1014i others(29): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | ||||||
| chr10:24628982
|
A | ATATATAT others(24): Show |
1 | a0004c0004t0001g0100 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.495+1013_495+1014i others(33): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | ||||||
| chr10:24628982
|
A | ATATATAT others(25): Show |
1 | a0002c0002t0001g0120 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.495+1013_495+1014i others(34): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | ||||||
| chr10:24628982
|
A | ATATATAT others(18): Show |
1 | a0002c0002t0001g0017 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.495+1013_495+1014i others(27): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | ||||||
| chr10:24628982
|
A | ATATATAT others(16): Show |
2 | a0001c0001t0001g0162a0004c0004t0001g0070 | 2 | HG03139.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.495+1013_495+1014i others(25): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | ||||||
| chr10:24628982
|
A | ATATATAT others(17): Show |
1 | a0001c0001t0001g0165 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.495+1013_495+1014i others(26): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | ||||||
| chr10:24628982
|
A | ATATATAT others(18): Show |
3 | a0001c0001t0001g0164a0004c0004t0001g0069a0005c0005t0001g0167 | 3 | HG02572.hp2 HG03130.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.495+1013_495+1014i others(27): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | ||||||
| chr10:24628982
|
A | ATATATAT others(13): Show |
1 | a0001c0001t0001g0195 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.495+1013_495+1014i others(22): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | ||||||
| chr10:24628982
|
A | ATATATAT others(14): Show |
1 | a0002c0002t0001g0124 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.495+1013_495+1014i others(23): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | ||||||
| chr10:24628982
|
A | ATATATAT others(15): Show |
2 | a0002c0002t0001g0110a0002c0002t0001g0131 | 2 | HG00323.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.495+1013_495+1014i others(24): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | ||||||
| chr10:24628982
|
A | ATATATAT others(16): Show |
2 | a0001c0001t0001g0166a0001c0001t0001g0239 | 2 | HG00639.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.495+1013_495+1014i others(25): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | ||||||
| chr10:24628982
|
A | ATATATAT others(17): Show |
3 | a0001c0001t0001g0014a0004c0004t0001g0068a0004c0004t0001g0091 | 3 | HG02559.hp2 HG02976.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.495+1013_495+1014i others(26): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | ||||||
| chr10:24628982
|
A | ATATATAT others(18): Show |
1 | a0002c0002t0001g0019 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.495+1013_495+1014i others(27): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | ||||||
| chr10:24628982
|
A | ATATATAT others(11): Show |
7 | a0001c0001t0001g0143a0001c0001t0001g0181a0001c0001t0001g0182others(4): Show | 7 | HG01256.hp2 HG02280.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.495+1013_495+1014i others(20): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | ||||||
| chr10:24628982
|
A | ATATATAT others(12): Show |
4 | a0001c0001t0001g0168a0001c0001t0001g0275a0002c0002t0001g0071others(1): Show | 4 | HG00642.hp2 HG01123.hp2 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.495+1013_495+1014i others(21): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | ||||||
| chr10:24628982
|
A | ATATATAT others(13): Show |
1 | a0001c0001t0001g0191 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.495+1013_495+1014i others(22): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | ||||||
| chr10:24628982
|
A | ATATATAT others(14): Show |
4 | a0001c0001t0001g0183a0001c0001t0001g0238a0001c0001t0001g0240others(1): Show | 4 | HG01884.hp2 HG02698.hp2 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.495+1013_495+1014i others(23): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | ||||||
| chr10:24628982
|
A | ATATATAT others(15): Show |
1 | a0004c0004t0001g0089 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.495+1013_495+1014i others(24): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | ||||||
| chr10:24628982
|
A | ATATATAT others(9): Show |
1 | a0002c0002t0001g0128 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.495+1013_495+1014i others(18): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | ||||||
| chr10:24628982
|
A | ATATATAT others(10): Show |
2 | a0002c0002t0007g0009a0003c0003t0001g0203 | 2 | HG02148.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.495+1013_495+1014i others(19): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | ||||||
| chr10:24628982
|
A | ATATATAT others(11): Show |
2 | a0002c0002t0001g0115a0002c0002t0001g0123 | 2 | HG01099.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.495+1013_495+1014i others(20): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | ||||||
| chr10:24628982
|
A | ATATATAT others(16): Show |
1 | a0002c0002t0001g0152 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.495+1013_495+1014i others(25): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | ||||||
| chr10:24628982
|
A | ATATATAT others(7): Show |
2 | a0001c0001t0001g0273a0001c0001t0001g0274 | 2 | HG00423.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.495+1013_495+1014i others(16): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | ||||||
| chr10:24628982
|
A | ATATATAT others(8): Show |
3 | a0001c0001t0001g0224a0002c0002t0001g0125a0002c0002t0004g0295 | 3 | HG01433.hp2 HG01884.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.495+1013_495+1014i others(17): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | ||||||
| chr10:24628982
|
A | ATATATAT others(9): Show |
3 | a0001c0001t0001g0237a0002c0002t0001g0117a0009c0008t0001g0262 | 3 | HG02723.hp2 HG03471.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.495+1013_495+1014i others(18): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | ||||||
| chr10:24628982
|
A | ATATATAT others(10): Show |
4 | a0002c0002t0001g0281a0002c0002t0001g0283a0002c0002t0007g0007others(1): Show | 4 | HG02027.hp2 HG02970.hp1 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.495+1013_495+1014i others(19): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | ||||||
| chr10:24628982
|
A | ATATATAT others(11): Show |
3 | a0002c0002t0001g0280a0002c0002t0001g0282a0004c0004t0001g0031 | 3 | HG02647.hp1 NA18953.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.495+1013_495+1014i others(20): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | ||||||
| chr10:24628982
|
A | ATATATAT others(12): Show |
2 | a0002c0002t0001g0114a0002c0002t0001g0130 | 2 | HG00733.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.495+1013_495+1014i others(21): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | ||||||
| chr10:24628982
|
A | ATATATAT others(20): Show |
1 | a0002c0002t0001g0136 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.495+1013_495+1014i others(29): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | ||||||
| chr10:24628982
|
A | ATATATAT others(6): Show |
1 | a0001c0001t0002g0312 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.495+1013_495+1014i others(15): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | ||||||
| chr10:24628982
|
A | ATATATAT others(7): Show |
3 | a0002c0002t0001g0109a0002c0002t0001g0126a0002c0002t0001g0153 | 3 | HG00735.hp1 HG02148.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.495+1013_495+1014i others(16): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | ||||||
| chr10:24628982
|
A | ATATATAT others(8): Show |
4 | a0001c0001t0001g0142a0001c0001t0001g0260a0003c0003t0001g0202others(1): Show | 4 | HG01123.hp1 HG01978.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.495+1013_495+1014i others(17): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | ||||||
| chr10:24628982
|
A | ATATATAT others(9): Show |
3 | a0001c0001t0001g0241a0002c0017t0001g0041a0009c0008t0001g0261 | 3 | HG00140.hp1 HG02074.hp2 NA18941.hp2 |
intron_variant | MODIFIER | c.495+1013_495+1014i others(18): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | ||||||
| chr10:24628982
|
A | ATATATAT others(11): Show |
3 | a0001c0001t0001g0253a0002c0002t0001g0113a0004c0004t0001g0067 | 3 | HG02630.hp2 HG03579.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.495+1013_495+1014i others(20): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | ||||||
| chr10:24628982
|
A | ATATATAT others(3): Show |
4 | a0003c0003t0001g0212a0003c0003t0001g0215a0003c0003t0001g0265others(1): Show | 4 | HG01952.hp1 HG01993.hp1 NA18963.hp1 others(1): Show |
intron_variant | MODIFIER | c.495+1013_495+1014i others(12): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | ||||||
| chr10:24628982
|
A | ATATATAT others(4): Show |
5 | a0001c0001t0001g0169a0001c0001t0001g0228a0001c0001t0001g0244others(2): Show | 5 | HG04199.hp1 HG04228.hp1 NA18982.hp2 others(2): Show |
intron_variant | MODIFIER | c.495+1013_495+1014i others(13): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | ||||||
| chr10:24628982
|
A | ATATATAT others(5): Show |
4 | a0001c0001t0001g0177a0001c0001t0001g0220a0001c0001t0001g0235others(1): Show | 4 | HG01081.hp2 HG02486.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.495+1013_495+1014i others(14): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | ||||||
| chr10:24628982
|
A | ATATATAT others(6): Show |
3 | a0001c0001t0001g0252a0001c0001t0002g0311a0003c0003t0001g0175 | 3 | HG00642.hp1 NA18994.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.495+1013_495+1014i others(15): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | ||||||
| chr10:24628982
|
A | ATATATAT others(7): Show |
3 | a0003c0003t0001g0173a0003c0003t0012g0172a0014c0024t0011g0033 | 3 | NA19004.hp2 NA19030.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.495+1013_495+1014i others(16): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | ||||||
| chr10:24628982
|
A | ATATATAT others(8): Show |
1 | a0003c0003t0001g0201 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.495+1013_495+1014i others(17): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | ||||||
| chr10:24628982
|
A | ATATATAT others(9): Show |
1 | a0002c0002t0001g0088 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.495+1013_495+1014i others(18): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | ||||||
| chr10:24628982
|
A | ATATATAT others(3): Show |
3 | a0001c0001t0001g0187a0002c0002t0001g0020a0002c0002t0001g0138 | 3 | HG02922.hp1 HG03041.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.495+1013_495+1014i others(12): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | ||||||
| chr10:24628982
|
A | ATATATAT others(4): Show |
4 | a0001c0001t0001g0178a0001c0001t0001g0222a0001c0001t0001g0242others(1): Show | 4 | HG01109.hp2 HG02615.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.495+1013_495+1014i others(13): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | ||||||
| chr10:24628982
|
A | ATATATAT others(5): Show |
2 | a0002c0002t0001g0140a0003c0003t0001g0116 | 2 | HG04228.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.495+1013_495+1014i others(14): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | ||||||
| chr10:24628982
|
A | ATATATAT others(6): Show |
2 | a0001c0001t0001g0217a0001c0001t0001g0271 | 2 | HG01069.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.495+1013_495+1014i others(15): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | ||||||
| chr10:24628982
|
A | ATATATAT others(7): Show |
3 | a0001c0001t0001g0189a0002c0002t0007g0008a0003c0003t0001g0179 | 3 | HG00280.hp1 HG00609.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.495+1013_495+1014i others(16): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | ||||||
| chr10:24628982
|
A | ATATATAT others(8): Show |
1 | a0003c0003t0001g0236 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.495+1013_495+1014i others(17): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | ||||||
| chr10:24628982
|
A | ATATATTT others(3): Show |
2 | a0001c0001t0001g0245a0003c0003t0001g0213 | 2 | HG00323.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.495+1013_495+1014i others(12): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | ||||||
| chr10:24628982
|
A | ATATATTT others(4): Show |
1 | a0001c0001t0001g0232 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.495+1013_495+1014i others(13): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | ||||||
| chr10:24628982
|
A | ATATATTT others(5): Show |
1 | a0001c0001t0001g0186 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.495+1013_495+1014i others(14): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | ||||||
| chr10:24628982
|
A | ATATTTTT others(3): Show |
2 | a0001c0001t0001g0243a0003c0003t0001g0247 | 2 | HG01361.hp2 HG02027.hp1 |
intron_variant | MODIFIER | c.495+1013_495+1014i others(12): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | ||||||
| chr10:24628982
|
A | ATATTTTT others(4): Show |
2 | a0002c0002t0001g0134a0002c0002t0001g0135 | 2 | HG02257.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.495+1013_495+1014i others(13): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | ||||||
| chr10:24628982
|
A | ATT | 8 | a0001c0001t0002g0305a0001c0001t0002g0320a0001c0001t0002g0328others(5): Show | 8 | HG01891.hp1 NA18954.hp1 NA18961.hp1 others(5): Show |
intron_variant | MODIFIER | c.495+1012_495+1013d others(4): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | ||||||
| chr10:24628982
|
A | T | 31 | a0001c0001t0001g0170a0001c0001t0001g0184a0001c0001t0001g0185others(28): Show | 31 | HG00733.hp1 HG01109.hp1 HG01168.hp1 others(28): Show |
intron_variant | MODIFIER | c.495+1014T>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628982 | ||||||
| chr10:24628983
|
T | TA | 5 | a0001c0001t0002g0309a0002c0002t0001g0055a0002c0002t0001g0081others(2): Show | 5 | HG00099.hp1 HG00140.hp2 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.495+1012_495+1013i others(3): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628983 | ||||||
| chr10:24628983
|
T | TATA | 15 | a0001c0001t0009g0158a0001c0001t0009g0159a0002c0002t0001g0034others(12): Show | 15 | HG01516.hp1 HG01517.hp1 HG01952.hp2 others(12): Show |
intron_variant | MODIFIER | c.495+1012_495+1013i others(5): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628983 | ||||||
| chr10:24628983
|
T | TATATA | 14 | a0001c0001t0002g0323a0002c0002t0001g0018a0002c0002t0001g0030others(11): Show | 14 | HG00438.hp1 HG00741.hp1 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.495+1012_495+1013i others(7): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628983 | ||||||
| chr10:24628983
|
T | TATATATA | 5 | a0001c0001t0001g0270a0002c0002t0001g0023a0002c0002t0001g0060others(2): Show | 5 | HG01255.hp1 HG02083.hp1 NA18943.hp2 others(2): Show |
intron_variant | MODIFIER | c.495+1012_495+1013i others(9): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628983 | ||||||
| chr10:24628983
|
T | TATATATA others(2): Show |
7 | a0002c0002t0001g0036a0002c0002t0001g0043a0002c0002t0001g0047others(4): Show | 7 | HG00408.hp1 HG00735.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.495+1012_495+1013i others(11): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628983 | ||||||
| chr10:24628983
|
T | TATATATA others(4): Show |
5 | a0001c0001t0001g0144a0001c0001t0001g0176a0002c0002t0001g0044others(2): Show | 5 | HG01261.hp1 HG02080.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.495+1012_495+1013i others(13): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628983 | ||||||
| chr10:24628983
|
T | TATATATA others(6): Show |
3 | a0001c0001t0001g0141a0001c0001t0005g0001a0002c0002t0001g0051 | 3 | HG02280.hp1 HG03927.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.495+1012_495+1013i others(15): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628983 | ||||||
| chr10:24628983
|
T | TATATATA others(8): Show |
1 | a0002c0021t0001g0084 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.495+1012_495+1013i others(17): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628983 | ||||||
| chr10:24628983
|
T | TATATATA others(12): Show |
1 | a0001c0001t0001g0264 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.495+1012_495+1013i others(21): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628983 | ||||||
| chr10:24628984
|
T | A | 37 | a0001c0001t0001g0269a0001c0001t0002g0341a0001c0001t0005g0005others(34): Show | 37 | HG00597.hp1 HG00639.hp1 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.495+1012A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628984 | ||||||
| chr10:24628985
|
T | A | 27 | a0001c0001t0001g0270a0002c0002t0001g0018a0002c0002t0001g0034others(24): Show | 27 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(24): Show |
intron_variant | MODIFIER | c.495+1011A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628985 | ||||||
| chr10:24628986
|
T | A | 23 | a0001c0001t0001g0269a0001c0001t0013g0254a0001c0014t0004g0286others(20): Show | 23 | HG00597.hp1 HG00639.hp1 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.495+1010A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628986 | ||||||
| chr10:24628987
|
T | A | 5 | a0002c0002t0001g0045a0002c0002t0001g0052a0002c0002t0001g0053others(2): Show | 5 | HG00408.hp1 HG01952.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.495+1009A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628987 | ||||||
| chr10:24628988
|
T | A | 4 | a0001c0001t0001g0269a0001c0001t0013g0254a0002c0002t0001g0096others(1): Show | 4 | HG00597.hp1 HG02523.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.495+1008A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628988 | ||||||
| chr10:24628989
|
T | A | 1 | a0010c0012t0010g0016 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.495+1007A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628989 | ||||||
| chr10:24628990
|
T | A | 4 | a0001c0001t0001g0269a0001c0001t0013g0254a0002c0002t0001g0077others(1): Show | 4 | HG00597.hp1 HG02523.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.495+1006A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628990 | ||||||
| chr10:24628991
|
T | A | 1 | a0010c0012t0010g0016 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.495+1005A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628991 | ||||||
| chr10:24628992
|
T | A | 3 | a0001c0001t0013g0254a0002c0002t0001g0077a0003c0003t0001g0208 | 3 | HG03130.hp1 HG04199.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.495+1004A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628992 | ||||||
| chr10:24628993
|
T | A | 1 | a0010c0012t0010g0016 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.495+1003A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628993 | ||||||
| chr10:24628994
|
T | A | 3 | a0001c0001t0013g0254a0002c0002t0001g0077a0003c0003t0001g0208 | 3 | HG03130.hp1 HG04199.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.495+1002A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628994 | ||||||
| chr10:24628995
|
T | A | 1 | a0010c0012t0010g0016 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.495+1001A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628995 | ||||||
| chr10:24628996
|
T | A | 1 | a0002c0002t0001g0077 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.495+1000A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628996 | ||||||
| chr10:24628997
|
T | A | 1 | a0010c0012t0010g0016 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.495+999A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628997 | ||||||
| chr10:24628998
|
T | A | 1 | a0002c0002t0001g0077 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.495+998A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24628998 | ||||||
| chr10:24629000
|
T | A | 1 | a0002c0002t0001g0077 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.495+996A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24629000 | ||||||
| chr10:24629043
|
TGGAGTGC others(12): Show |
T | 9 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0183others(6): Show | 9 | HG01884.hp2 HG02257.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.495+934_495+952del others(19): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24629043 | ||||||
| chr10:24629057
|
G | A | 6 | a0001c0001t0001g0171a0001c0001t0004g0296a0001c0001t0004g0297others(3): Show | 6 | HG01891.hp2 HG02895.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.495+939C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24629057 | ||||||
| chr10:24629360
|
T | C | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.495+636A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24629360 | ||||||
| chr10:24629392
|
A | C | 1 | a0002c0002t0001g0106 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.495+604T>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24629392 | ||||||
| chr10:24629494
|
C | T | 2 | a0001c0001t0002g0342a0001c0001t0002g0346 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.495+502G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24629494 | ||||||
| chr10:24629607
|
AT | A | 7 | a0001c0001t0001g0271a0007c0007t0006g0291a0007c0007t0006g0292others(4): Show | 7 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(4): Show |
intron_variant | MODIFIER | c.495+388delA | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24629607 | ||||||
| chr10:24629898
|
AT | A | 16 | a0002c0002t0001g0019a0002c0002t0001g0036a0002c0002t0001g0113others(13): Show | 16 | HG01496.hp1 HG01516.hp2 HG02027.hp2 others(13): Show |
intron_variant | MODIFIER | c.495+97delA | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | 24629898 | ||||||
| chr10:24630153
|
G | A | 10 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(7): Show | 10 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.441-103C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 6/25 | chr10 | 24630153 | ||||||
| chr10:24630392
|
T | G | 10 | a0002c0002t0001g0018a0002c0002t0001g0042a0002c0002t0001g0049others(7): Show | 10 | HG00735.hp2 HG01934.hp1 HG01952.hp2 others(7): Show |
intron_variant | MODIFIER | c.441-342A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 6/25 | chr10 | 24630392 | ||||||
| chr10:24630882
|
C | T | 2 | a0003c0003t0001g0200a0003c0003t0001g0248 | 2 | NA18959.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.441-832G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 6/25 | chr10 | 24630882 | ||||||
| chr10:24631063
|
C | T | 2 | a0002c0002t0001g0058a0002c0002t0001g0061 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.441-1013G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 6/25 | chr10 | 24631063 | ||||||
| chr10:24631103
|
G | A | 1 | a0002c0002t0001g0140 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.441-1053C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 6/25 | chr10 | 24631103 | ||||||
| chr10:24631180
|
A | G | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.441-1130T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 6/25 | chr10 | 24631180 | ||||||
| chr10:24631195
|
C | G | 1 | a0001c0001t0001g0191 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.441-1145G>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 6/25 | chr10 | 24631195 | ||||||
| chr10:24631293
|
G | C | 1 | a0009c0008t0001g0262 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.441-1243C>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 6/25 | chr10 | 24631293 | ||||||
| chr10:24631418
|
A | ACTATT | 152 | a0002c0002t0001g0010a0002c0002t0001g0017a0002c0002t0001g0018others(149): Show | 152 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.441-1369_441-1368i others(7): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 6/25 | chr10 | 24631418 | ||||||
| chr10:24631445
|
T | G | 1 | a0001c0001t0001g0220 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.441-1395A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 6/25 | chr10 | 24631445 | ||||||
| chr10:24631465
|
T | G | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.441-1415A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 6/25 | chr10 | 24631465 | ||||||
| chr10:24631699
|
T | C | 152 | a0002c0002t0001g0010a0002c0002t0001g0017a0002c0002t0001g0018others(149): Show | 152 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.441-1649A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 6/25 | chr10 | 24631699 | ||||||
| chr10:24631700
|
G | A | 2 | a0011c0011t0001g0258a0011c0011t0001g0259 | 2 | HG02818.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.441-1650C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 6/25 | chr10 | 24631700 | ||||||
| chr10:24631729
|
T | G | 5 | a0001c0001t0001g0170a0001c0001t0001g0176a0001c0001t0001g0177others(2): Show | 5 | HG01261.hp1 HG02486.hp2 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.440+1673A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 6/25 | chr10 | 24631729 | ||||||
| chr10:24631803
|
C | G | 14 | a0002c0002t0001g0019a0002c0002t0001g0109a0002c0002t0001g0110others(11): Show | 14 | HG01496.hp1 HG01516.hp2 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.440+1599G>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 6/25 | chr10 | 24631803 | ||||||
| chr10:24631828
|
A | G | 13 | a0002c0002t0001g0071a0002c0002t0001g0088a0004c0004t0001g0031others(10): Show | 13 | HG00642.hp2 HG01123.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.440+1574T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 6/25 | chr10 | 24631828 | ||||||
| chr10:24631869
|
C | A | 2 | a0003c0003t0001g0200a0003c0003t0001g0248 | 2 | NA18959.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.440+1533G>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 6/25 | chr10 | 24631869 | ||||||
| chr10:24631984
|
A | G | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.440+1418T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 6/25 | chr10 | 24631984 | ||||||
| chr10:24632062
|
G | C | 2 | a0001c0014t0004g0286a0005c0005t0004g0287 | 2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.440+1340C>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 6/25 | chr10 | 24632062 | ||||||
| chr10:24632139
|
T | G | 11 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(8): Show | 11 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.440+1263A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 6/25 | chr10 | 24632139 | ||||||
| chr10:24632281
|
T | C | 7 | a0001c0001t0001g0171a0001c0001t0004g0296a0001c0001t0004g0297others(4): Show | 7 | HG01891.hp2 HG02895.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.440+1121A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 6/25 | chr10 | 24632281 | ||||||
| chr10:24632359
|
A | T | 2 | a0001c0014t0004g0286a0005c0005t0004g0287 | 2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.440+1043T>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 6/25 | chr10 | 24632359 | ||||||
| chr10:24632468
|
T | C | 1 | a0001c0001t0002g0313 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.440+934A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 6/25 | chr10 | 24632468 | ||||||
| chr10:24633248
|
T | A | 2 | a0001c0001t0001g0250a0001c0001t0001g0251 | 2 | HG02970.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.440+154A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 6/25 | chr10 | 24633248 | ||||||
| chr10:24633290
|
C | T | 2 | a0001c0014t0004g0286a0005c0005t0004g0287 | 2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.440+112G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 6/25 | chr10 | 24633290 | ||||||
| chr10:24633316
|
T | G | 1 | a0001c0001t0002g0315 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.440+86A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 6/25 | chr10 | 24633316 | ||||||
| chr10:24633372
|
C | A | 1 | a0003c0003t0001g0180 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.440+30G>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 6/25 | chr10 | 24633372 | ||||||
| chr10:24633394
|
A | G | 1 | a0005c0005t0001g0137 | 1 | NA19030.hp1 | splice_region_variant&intron_variant | LOW | c.440+8T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 6/25 | chr10 | 24633394 | ||||||
| chr10:24633558
|
T | TA | 11 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(8): Show | 11 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.362-79dupT | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 5/25 | chr10 | 24633558 | ||||||
| chr10:24633819
|
T | C | 1 | a0001c0001t0001g0275 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.362-339A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 5/25 | chr10 | 24633819 | ||||||
| chr10:24633883
|
C | CT | 113 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0174others(110): Show | 113 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.362-404dupA | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 5/25 | chr10 | 24633883 | ||||||
| chr10:24633883
|
C | CTT | 61 | a0001c0001t0001g0253a0002c0002t0001g0010a0002c0002t0001g0017others(58): Show | 61 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(58): Show |
intron_variant | MODIFIER | c.362-405_362-404dup others(2): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 5/25 | chr10 | 24633883 | ||||||
| chr10:24633883
|
C | CTTT | 16 | a0002c0002t0001g0064a0002c0002t0001g0093a0002c0002t0001g0106others(13): Show | 16 | HG00099.hp2 HG00673.hp1 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.362-406_362-404dup others(3): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 5/25 | chr10 | 24633883 | ||||||
| chr10:24633883
|
CT | C | 8 | a0001c0001t0001g0194a0001c0001t0002g0335a0001c0014t0004g0286others(5): Show | 8 | HG01081.hp1 HG01256.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.362-404delA | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 5/25 | chr10 | 24633883 | ||||||
| chr10:24633883
|
CTTTTTTT | C | 12 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(9): Show | 12 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.362-410_362-404del others(7): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 5/25 | chr10 | 24633883 | ||||||
| chr10:24633943
|
G | A | 11 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(8): Show | 11 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.362-463C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 5/25 | chr10 | 24633943 | ||||||
| chr10:24634016
|
G | C | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.362-536C>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 5/25 | chr10 | 24634016 | ||||||
| chr10:24634389
|
A | T | 1 | a0003c0003t0001g0173 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.361+622T>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 5/25 | chr10 | 24634389 | ||||||
| chr10:24634415
|
A | G | 4 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0183others(1): Show | 4 | HG01884.hp2 HG02615.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.361+596T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 5/25 | chr10 | 24634415 | ||||||
| chr10:24634691
|
T | A | 1 | a0002c0002t0001g0133 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.361+320A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 5/25 | chr10 | 24634691 | ||||||
| chr10:24634911
|
T | C | 5 | a0001c0001t0001g0171a0001c0001t0004g0296a0001c0001t0004g0297others(2): Show | 5 | HG01891.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.361+100A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 5/25 | chr10 | 24634911 | ||||||
| chr10:24635138
|
C | T | 1 | a0002c0002t0001g0279 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.269-35G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24635138 | ||||||
| chr10:24635175
|
ATT | A | 3 | a0001c0001t0001g0190a0002c0002t0001g0123a0002c0002t0001g0126 | 3 | HG00735.hp1 HG01099.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.269-74_269-73delAA | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24635175 | ||||||
| chr10:24635255
|
G | A | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.269-152C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24635255 | ||||||
| chr10:24635288
|
C | A | 2 | a0010c0012t0010g0015a0010c0012t0010g0016 | 2 | HG02723.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.269-185G>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24635288 | ||||||
| chr10:24635640
|
G | A | 1 | a0002c0002t0001g0036 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.269-537C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24635640 | ||||||
| chr10:24635790
|
C | T | 2 | a0002c0002t0001g0064a0002c0002t0001g0145 | 2 | NA18988.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.269-687G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24635790 | ||||||
| chr10:24635911
|
T | G | 2 | a0001c0001t0003g0154a0024c0026t0003g0156 | 2 | HG01081.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.269-808A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24635911 | ||||||
| chr10:24636001
|
G | A | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.269-898C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24636001 | ||||||
| chr10:24636033
|
G | A | 1 | a0001c0001t0004g0299 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.269-930C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24636033 | ||||||
| chr10:24636279
|
G | A | 1 | a0002c0002t0001g0124 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.269-1176C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24636279 | ||||||
| chr10:24636316
|
G | A | 1 | a0005c0005t0001g0104 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.269-1213C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24636316 | ||||||
| chr10:24636680
|
C | T | 1 | a0002c0002t0004g0295 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.269-1577G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24636680 | ||||||
| chr10:24636942
|
C | T | 3 | a0001c0001t0001g0174a0001c0001t0001g0219a0001c0001t0001g0222 | 3 | HG01192.hp1 HG02055.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.269-1839G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24636942 | ||||||
| chr10:24636979
|
T | A | 1 | a0002c0002t0001g0076 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.269-1876A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24636979 | ||||||
| chr10:24637172
|
C | T | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.269-2069G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24637172 | ||||||
| chr10:24637254
|
A | G | 78 | a0002c0002t0001g0010a0002c0002t0001g0018a0002c0002t0001g0021others(75): Show | 78 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.269-2151T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24637254 | ||||||
| chr10:24637795
|
T | G | 21 | a0002c0002t0001g0117a0002c0002t0001g0118a0002c0002t0001g0119others(18): Show | 21 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(18): Show |
intron_variant | MODIFIER | c.269-2692A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24637795 | ||||||
| chr10:24637866
|
A | AT | 8 | a0001c0001t0001g0170a0001c0001t0001g0176a0001c0001t0001g0241others(5): Show | 8 | HG00140.hp1 HG01099.hp2 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.269-2764dupA | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24637866 | ||||||
| chr10:24637866
|
AT | A | 27 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(24): Show | 27 | HG00735.hp1 HG01517.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.269-2764delA | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24637866 | ||||||
| chr10:24637972
|
C | T | 1 | a0002c0002t0001g0082 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.269-2869G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24637972 | ||||||
| chr10:24638051
|
G | A | 137 | a0002c0002t0001g0010a0002c0002t0001g0017a0002c0002t0001g0018others(134): Show | 137 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.269-2948C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24638051 | ||||||
| chr10:24638117
|
G | A | 9 | a0002c0002t0001g0057a0002c0002t0001g0058a0002c0002t0001g0059others(6): Show | 9 | HG00639.hp1 HG01069.hp1 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.269-3014C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24638117 | ||||||
| chr10:24638236
|
TAGAG | T | 3 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0255 | 3 | HG02622.hp1 HG02970.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.269-3137_269-3134d others(6): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24638236 | ||||||
| chr10:24638396
|
C | T | 3 | a0001c0001t0002g0300a0001c0001t0002g0340a0001c0001t0002g0341 | 3 | HG01169.hp1 HG01934.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.269-3293G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24638396 | ||||||
| chr10:24638518
|
C | A | 87 | a0002c0002t0001g0010a0002c0002t0001g0018a0002c0002t0001g0020others(84): Show | 87 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.269-3415G>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24638518 | ||||||
| chr10:24638522
|
A | T | 10 | a0002c0002t0001g0018a0002c0002t0001g0042a0002c0002t0001g0049others(7): Show | 10 | HG00735.hp2 HG01934.hp1 HG01952.hp2 others(7): Show |
intron_variant | MODIFIER | c.269-3419T>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24638522 | ||||||
| chr10:24638570
|
T | C | 2 | a0011c0011t0001g0258a0011c0011t0001g0259 | 2 | HG02818.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.269-3467A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24638570 | ||||||
| chr10:24638683
|
A | T | 2 | a0011c0011t0001g0258a0011c0011t0001g0259 | 2 | HG02818.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.269-3580T>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24638683 | ||||||
| chr10:24638708
|
A | C | 1 | a0002c0002t0001g0082 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.269-3605T>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24638708 | ||||||
| chr10:24638756
|
T | C | 2 | a0001c0014t0004g0286a0005c0005t0004g0287 | 2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.269-3653A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24638756 | ||||||
| chr10:24638787
|
A | C | 1 | a0003c0003t0001g0268 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.269-3684T>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24638787 | ||||||
| chr10:24638929
|
C | T | 1 | a0002c0002t0001g0094 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.269-3826G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24638929 | ||||||
| chr10:24639330
|
C | T | 23 | a0002c0002t0001g0017a0002c0002t0001g0117a0002c0002t0001g0118others(20): Show | 23 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(20): Show |
intron_variant | MODIFIER | c.269-4227G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24639330 | ||||||
| chr10:24639636
|
G | A | 2 | a0012c0010t0001g0266a0012c0010t0001g0267 | 2 | HG02109.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.269-4533C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24639636 | ||||||
| chr10:24639747
|
T | C | 11 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(8): Show | 11 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.269-4644A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24639747 | ||||||
| chr10:24639755
|
C | CA | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.269-4653dupT | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24639755 | ||||||
| chr10:24639815
|
T | C | 1 | a0001c0001t0004g0299 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.269-4712A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24639815 | ||||||
| chr10:24639833
|
GAGAAAGC others(3): Show |
G | 2 | a0012c0010t0001g0266a0012c0010t0001g0267 | 2 | HG02109.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.269-4740_269-4731d others(12): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24639833 | ||||||
| chr10:24639919
|
C | CA | 143 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(140): Show | 143 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.269-4817dupT | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24639919 | ||||||
| chr10:24639919
|
C | CAA | 13 | a0001c0001t0001g0189a0003c0003t0001g0116a0003c0003t0001g0180others(10): Show | 13 | HG00423.hp1 HG00597.hp2 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.269-4818_269-4817d others(4): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24639919 | ||||||
| chr10:24640212
|
G | A | 292 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(289): Show | 292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.269-5109C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24640212 | ||||||
| chr10:24640289
|
A | AAT | 7 | a0001c0001t0001g0264a0002c0002t0001g0058a0002c0002t0001g0061others(4): Show | 7 | HG01257.hp2 HG01258.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.269-5188_269-5187d others(4): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24640289 | ||||||
| chr10:24640307
|
T | TATATATA others(1): Show |
6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.269-5205_269-5204i others(10): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24640307 | ||||||
| chr10:24640447
|
T | C | 1 | a0002c0002t0001g0087 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.269-5344A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24640447 | ||||||
| chr10:24640583
|
A | G | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.269-5480T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24640583 | ||||||
| chr10:24640631
|
C | T | 335 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(332): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.269-5528G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24640631 | ||||||
| chr10:24640869
|
A | G | 2 | a0001c0001t0001g0141a0001c0001t0001g0144 | 2 | HG02280.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.269-5766T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24640869 | ||||||
| chr10:24640971
|
G | A | 2 | a0001c0001t0001g0141a0001c0001t0001g0144 | 2 | HG02280.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.269-5868C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24640971 | ||||||
| chr10:24641264
|
G | A | 155 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(152): Show | 155 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.269-6161C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24641264 | ||||||
| chr10:24641354
|
A | G | 1 | a0001c0001t0002g0317 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.269-6251T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24641354 | ||||||
| chr10:24641557
|
T | C | 2 | a0002c0002t0001g0056a0002c0002t0001g0285 | 2 | HG00408.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.269-6454A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24641557 | ||||||
| chr10:24641562
|
T | A | 2 | a0002c0002t0001g0034a0002c0002t0001g0052 | 2 | HG02040.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.269-6459A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24641562 | ||||||
| chr10:24641734
|
G | A | 1 | a0005c0005t0001g0284 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.269-6631C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24641734 | ||||||
| chr10:24641747
|
G | A | 2 | a0002c0002t0001g0134a0002c0002t0001g0135 | 2 | HG02257.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.269-6644C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24641747 | ||||||
| chr10:24641780
|
G | A | 1 | a0002c0002t0007g0009 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.269-6677C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24641780 | ||||||
| chr10:24641872
|
C | T | 2 | a0001c0014t0004g0286a0005c0005t0004g0287 | 2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.269-6769G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24641872 | ||||||
| chr10:24641890
|
G | C | 1 | a0001c0001t0005g0001 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.269-6787C>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24641890 | ||||||
| chr10:24641920
|
C | T | 1 | a0002c0002t0001g0062 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.269-6817G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24641920 | ||||||
| chr10:24641952
|
C | T | 1 | a0003c0003t0001g0223 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.269-6849G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24641952 | ||||||
| chr10:24641953
|
G | A | 78 | a0002c0002t0001g0010a0002c0002t0001g0018a0002c0002t0001g0021others(75): Show | 78 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.269-6850C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24641953 | ||||||
| chr10:24641997
|
G | GA | 82 | a0001c0001t0001g0160a0001c0001t0001g0174a0001c0001t0001g0181others(79): Show | 82 | HG00408.hp2 HG00423.hp1 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.269-6895dupT | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24641997 | ||||||
| chr10:24642080
|
T | A | 2 | a0001c0014t0004g0286a0005c0005t0004g0287 | 2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.269-6977A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24642080 | ||||||
| chr10:24642246
|
G | T | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.269-7143C>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24642246 | ||||||
| chr10:24642342
|
C | T | 38 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(35): Show | 38 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(35): Show |
intron_variant | MODIFIER | c.269-7239G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24642342 | ||||||
| chr10:24642376
|
G | A | 1 | a0003c0003t0001g0116 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.269-7273C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24642376 | ||||||
| chr10:24642514
|
C | CA | 37 | a0001c0001t0001g0199a0001c0001t0001g0264a0001c0001t0002g0305others(34): Show | 37 | HG00323.hp2 HG00642.hp2 HG01123.hp1 others(34): Show |
intron_variant | MODIFIER | c.269-7412dupT | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24642514 | ||||||
| chr10:24642514
|
CA | C | 10 | a0001c0001t0001g0144a0001c0001t0001g0178a0001c0001t0001g0273others(7): Show | 10 | HG01069.hp1 HG01975.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.269-7412delT | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24642514 | ||||||
| chr10:24642830
|
C | T | 1 | a0002c0002t0001g0024 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.269-7727G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24642830 | ||||||
| chr10:24642933
|
T | C | 7 | a0001c0001t0001g0171a0001c0001t0004g0296a0001c0001t0004g0297others(4): Show | 7 | HG01891.hp2 HG02895.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.269-7830A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24642933 | ||||||
| chr10:24643119
|
C | T | 5 | a0001c0001t0001g0171a0001c0001t0004g0296a0001c0001t0004g0297others(2): Show | 5 | HG01891.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.269-8016G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24643119 | ||||||
| chr10:24643243
|
A | G | 1 | a0005c0005t0003g0147 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.269-8140T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24643243 | ||||||
| chr10:24643294
|
G | A | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.269-8191C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24643294 | ||||||
| chr10:24643303
|
T | C | 11 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(8): Show | 11 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.269-8200A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24643303 | ||||||
| chr10:24643480
|
T | C | 11 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(8): Show | 11 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.269-8377A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24643480 | ||||||
| chr10:24643754
|
G | T | 292 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(289): Show | 292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.269-8651C>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24643754 | ||||||
| chr10:24644032
|
T | C | 1 | a0001c0001t0002g0326 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.269-8929A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24644032 | ||||||
| chr10:24644200
|
C | T | 1 | a0002c0002t0001g0117 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.269-9097G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24644200 | ||||||
| chr10:24644465
|
G | A | 4 | a0002c0002t0001g0133a0002c0002t0001g0134a0002c0002t0001g0135others(1): Show | 4 | HG02257.hp2 HG02258.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.269-9362C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24644465 | ||||||
| chr10:24644543
|
G | C | 1 | a0002c0002t0001g0078 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.269-9440C>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24644543 | ||||||
| chr10:24644559
|
C | T | 1 | a0002c0002t0001g0094 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.269-9456G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24644559 | ||||||
| chr10:24644608
|
A | C | 1 | a0003c0003t0001g0223 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.269-9505T>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24644608 | ||||||
| chr10:24644771
|
G | T | 203 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(200): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.269-9668C>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24644771 | ||||||
| chr10:24644871
|
A | G | 1 | a0002c0002t0001g0149 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.269-9768T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24644871 | ||||||
| chr10:24644883
|
C | A | 7 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0164others(4): Show | 7 | HG02559.hp1 HG02572.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.269-9780G>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24644883 | ||||||
| chr10:24644973
|
T | C | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.269-9870A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24644973 | ||||||
| chr10:24644980
|
C | A | 3 | a0001c0001t0002g0311a0001c0001t0002g0312a0001c0001t0002g0321 | 3 | HG02080.hp2 NA18939.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.269-9877G>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24644980 | ||||||
| chr10:24645003
|
T | G | 11 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(8): Show | 11 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.269-9900A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24645003 | ||||||
| chr10:24645027
|
G | A | 154 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(151): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.269-9924C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24645027 | ||||||
| chr10:24645142
|
A | G | 1 | a0002c0002t0001g0059 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.269-10039T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24645142 | ||||||
| chr10:24645317
|
A | G | 5 | a0001c0001t0001g0171a0001c0001t0004g0296a0001c0001t0004g0297others(2): Show | 5 | HG01891.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.269-10214T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24645317 | ||||||
| chr10:24645379
|
G | C | 4 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0183others(1): Show | 4 | HG01884.hp2 HG02615.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.269-10276C>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24645379 | ||||||
| chr10:24645517
|
T | C | 3 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0001g0249 | 3 | HG00621.hp1 NA18954.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.269-10414A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24645517 | ||||||
| chr10:24645585
|
GA | G | 141 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(138): Show | 141 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.269-10483delT | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24645585 | ||||||
| chr10:24645666
|
C | T | 292 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(289): Show | 292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.269-10563G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24645666 | ||||||
| chr10:24645674
|
T | C | 150 | a0002c0002t0001g0010a0002c0002t0001g0017a0002c0002t0001g0018others(147): Show | 150 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.269-10571A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24645674 | ||||||
| chr10:24645749
|
T | C | 2 | a0002c0002t0001g0109a0002c0002t0001g0110 | 2 | HG02148.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.269-10646A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24645749 | ||||||
| chr10:24646100
|
C | T | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.269-10997G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24646100 | ||||||
| chr10:24646270
|
A | G | 167 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(164): Show | 167 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.269-11167T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24646270 | ||||||
| chr10:24646339
|
A | T | 11 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(8): Show | 11 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.269-11236T>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24646339 | ||||||
| chr10:24646497
|
G | A | 2 | a0005c0005t0001g0102a0005c0005t0001g0103 | 2 | HG02451.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.269-11394C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24646497 | ||||||
| chr10:24646516
|
T | G | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.269-11413A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24646516 | ||||||
| chr10:24646637
|
T | C | 2 | a0004c0004t0001g0068a0004c0004t0001g0069 | 2 | HG02559.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.269-11534A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24646637 | ||||||
| chr10:24646767
|
G | A | 2 | a0001c0001t0002g0320a0001c0001t0002g0345 | 2 | NA18954.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.269-11664C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24646767 | ||||||
| chr10:24646796
|
T | C | 1 | a0003c0003t0001g0180 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.269-11693A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24646796 | ||||||
| chr10:24647003
|
T | C | 11 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(8): Show | 11 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.269-11900A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24647003 | ||||||
| chr10:24647021
|
G | A | 1 | a0001c0001t0001g0014 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.269-11918C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24647021 | ||||||
| chr10:24647030
|
A | G | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.269-11927T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24647030 | ||||||
| chr10:24647085
|
G | A | 1 | a0001c0001t0002g0319 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.269-11982C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24647085 | ||||||
| chr10:24647216
|
G | T | 1 | a0002c0002t0001g0136 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.269-12113C>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24647216 | ||||||
| chr10:24647612
|
C | T | 7 | a0001c0001t0001g0171a0001c0001t0004g0296a0001c0001t0004g0297others(4): Show | 7 | HG01891.hp2 HG02895.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.269-12509G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24647612 | ||||||
| chr10:24647760
|
G | C | 1 | a0007c0007t0015g0288 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.269-12657C>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24647760 | ||||||
| chr10:24647900
|
C | T | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.269-12797G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24647900 | ||||||
| chr10:24648169
|
C | T | 1 | a0002c0002t0001g0083 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.269-13066G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24648169 | ||||||
| chr10:24648170
|
G | A | 2 | a0002c0002t0001g0036a0006c0006t0003g0214 | 2 | NA18980.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.269-13067C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24648170 | ||||||
| chr10:24648501
|
C | T | 152 | a0002c0002t0001g0010a0002c0002t0001g0017a0002c0002t0001g0018others(149): Show | 152 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.269-13398G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24648501 | ||||||
| chr10:24648546
|
G | A | 5 | a0001c0001t0001g0171a0001c0001t0004g0296a0001c0001t0004g0297others(2): Show | 5 | HG01891.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.269-13443C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24648546 | ||||||
| chr10:24648641
|
G | A | 3 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0255 | 3 | HG02622.hp1 HG02970.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.269-13538C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24648641 | ||||||
| chr10:24648702
|
C | T | 7 | a0001c0001t0001g0171a0001c0001t0004g0296a0001c0001t0004g0297others(4): Show | 7 | HG01891.hp2 HG02895.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.269-13599G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24648702 | ||||||
| chr10:24648709
|
G | A | 1 | a0003c0003t0001g0180 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.269-13606C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24648709 | ||||||
| chr10:24648728
|
G | A | 1 | a0002c0002t0001g0079 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.269-13625C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24648728 | ||||||
| chr10:24648732
|
T | C | 1 | a0002c0002t0001g0010 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.269-13629A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24648732 | ||||||
| chr10:24648779
|
C | CA | 86 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(83): Show | 86 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.269-13677dupT | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24648779 | ||||||
| chr10:24648779
|
C | CAA | 78 | a0002c0002t0001g0010a0002c0002t0001g0018a0002c0002t0001g0023others(75): Show | 78 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.269-13678_269-1367 others(6): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24648779 | ||||||
| chr10:24648814
|
T | C | 2 | a0002c0002t0001g0134a0002c0002t0001g0135 | 2 | HG02257.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.269-13711A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24648814 | ||||||
| chr10:24648961
|
T | C | 152 | a0002c0002t0001g0010a0002c0002t0001g0017a0002c0002t0001g0018others(149): Show | 152 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.269-13858A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24648961 | ||||||
| chr10:24649314
|
T | C | 14 | a0002c0002t0001g0019a0002c0002t0001g0106a0002c0002t0001g0107others(11): Show | 14 | HG01496.hp1 HG01516.hp2 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.269-14211A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24649314 | ||||||
| chr10:24649629
|
G | A | 1 | a0002c0002t0004g0295 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.269-14526C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24649629 | ||||||
| chr10:24649705
|
T | TAA | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.269-14604_269-1460 others(6): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24649705 | ||||||
| chr10:24649751
|
TAGAAAAC others(7): Show |
T | 1 | a0002c0002t0001g0138 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.269-14662_269-1464 others(18): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24649751 | ||||||
| chr10:24649946
|
T | C | 1 | a0001c0001t0002g0310 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.269-14843A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24649946 | ||||||
| chr10:24649962
|
AAACTT | A | 17 | a0002c0002t0001g0019a0002c0002t0001g0106a0002c0002t0001g0107others(14): Show | 17 | HG01261.hp2 HG01496.hp1 HG01516.hp2 others(14): Show |
intron_variant | MODIFIER | c.269-14864_269-1486 others(9): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24649962 | ||||||
| chr10:24650179
|
A | G | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.269-15076T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24650179 | ||||||
| chr10:24650181
|
A | G | 3 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014 | 3 | HG02965.hp1 HG03225.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.269-15078T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24650181 | ||||||
| chr10:24650591
|
A | G | 1 | a0002c0002t0001g0038 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.269-15488T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24650591 | ||||||
| chr10:24650622
|
A | G | 40 | a0002c0002t0001g0017a0002c0002t0001g0019a0002c0002t0001g0106others(37): Show | 40 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.269-15519T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24650622 | ||||||
| chr10:24650736
|
T | C | 169 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(166): Show | 169 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.269-15633A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24650736 | ||||||
| chr10:24650834
|
T | G | 1 | a0003c0003t0001g0175 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.269-15731A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24650834 | ||||||
| chr10:24650965
|
CA | C | 7 | a0001c0001t0002g0300a0007c0007t0006g0291a0007c0007t0006g0292others(4): Show | 7 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(4): Show |
intron_variant | MODIFIER | c.269-15863delT | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24650965 | ||||||
| chr10:24650981
|
C | T | 5 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0001g0249others(2): Show | 5 | HG00621.hp1 HG01496.hp1 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.269-15878G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24650981 | ||||||
| chr10:24651088
|
T | C | 2 | a0002c0002t0001g0109a0002c0002t0001g0110 | 2 | HG02148.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.268+15897A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24651088 | ||||||
| chr10:24651191
|
T | A | 10 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0183others(7): Show | 10 | HG01884.hp2 HG02257.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.268+15794A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24651191 | ||||||
| chr10:24651321
|
G | C | 14 | a0001c0001t0002g0302a0001c0001t0002g0318a0001c0001t0002g0320others(11): Show | 14 | HG00673.hp2 HG01109.hp1 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.268+15664C>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24651321 | ||||||
| chr10:24651446
|
A | G | 1 | a0001c0001t0003g0155 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.268+15539T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24651446 | ||||||
| chr10:24651492
|
T | G | 3 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195 | 3 | HG02280.hp2 HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.268+15493A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24651492 | ||||||
| chr10:24651774
|
G | A | 1 | a0006c0006t0002g0349 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.268+15211C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24651774 | ||||||
| chr10:24651830
|
T | C | 1 | a0002c0002t0004g0295 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.268+15155A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24651830 | ||||||
| chr10:24651885
|
A | G | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.268+15100T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24651885 | ||||||
| chr10:24652024
|
G | A | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.268+14961C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24652024 | ||||||
| chr10:24652076
|
C | T | 3 | a0002c0002t0001g0280a0002c0002t0001g0281a0002c0002t0001g0282 | 3 | NA18953.hp2 NA18980.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.268+14909G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24652076 | ||||||
| chr10:24652118
|
G | A | 1 | a0003c0003t0001g0205 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.268+14867C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24652118 | ||||||
| chr10:24652123
|
A | G | 5 | a0005c0005t0001g0102a0005c0005t0001g0103a0005c0005t0001g0104others(2): Show | 5 | HG02055.hp1 HG02451.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.268+14862T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24652123 | ||||||
| chr10:24652210
|
A | G | 7 | a0003c0003t0001g0212a0003c0003t0001g0215a0003c0003t0001g0221others(4): Show | 7 | HG00408.hp2 HG01952.hp1 HG01993.hp1 others(4): Show |
intron_variant | MODIFIER | c.268+14775T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24652210 | ||||||
| chr10:24652479
|
A | T | 1 | a0003c0003t0001g0277 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.268+14506T>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24652479 | ||||||
| chr10:24652569
|
T | C | 6 | a0001c0001t0001g0174a0001c0001t0001g0217a0001c0001t0001g0219others(3): Show | 6 | HG01069.hp2 HG01192.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.268+14416A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24652569 | ||||||
| chr10:24652728
|
C | A | 1 | a0002c0002t0001g0146 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.268+14257G>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24652728 | ||||||
| chr10:24653087
|
C | G | 3 | a0005c0005t0001g0102a0005c0005t0001g0103a0005c0005t0001g0284 | 3 | HG02451.hp1 HG03209.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.268+13898G>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24653087 | ||||||
| chr10:24653122
|
T | A | 2 | a0002c0002t0001g0058a0002c0002t0001g0061 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.268+13863A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24653122 | ||||||
| chr10:24653222
|
A | C | 1 | a0001c0001t0001g0220 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.268+13763T>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24653222 | ||||||
| chr10:24653346
|
G | A | 1 | a0002c0002t0014g0105 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.268+13639C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24653346 | ||||||
| chr10:24653453
|
A | G | 1 | a0003c0003t0001g0212 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.268+13532T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24653453 | ||||||
| chr10:24653551
|
C | T | 1 | a0001c0001t0001g0164 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.268+13434G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24653551 | ||||||
| chr10:24653552
|
G | A | 1 | a0001c0001t0001g0186 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.268+13433C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24653552 | ||||||
| chr10:24653662
|
T | C | 1 | a0001c0001t0001g0160 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.268+13323A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24653662 | ||||||
| chr10:24653696
|
C | T | 28 | a0003c0003t0001g0011a0003c0003t0001g0173a0003c0003t0001g0175others(25): Show | 28 | HG00408.hp2 HG00609.hp1 HG01123.hp1 others(25): Show |
intron_variant | MODIFIER | c.268+13289G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24653696 | ||||||
| chr10:24653724
|
G | T | 2 | a0002c0002t0001g0078a0002c0002t0001g0079 | 2 | HG01975.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.268+13261C>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24653724 | ||||||
| chr10:24653996
|
C | T | 2 | a0002c0002t0001g0058a0002c0002t0001g0061 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.268+12989G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24653996 | ||||||
| chr10:24654265
|
C | A | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.268+12720G>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24654265 | ||||||
| chr10:24654340
|
CCT | C | 6 | a0001c0001t0005g0001a0001c0001t0005g0005a0001c0001t0005g0006others(3): Show | 6 | HG01981.hp1 HG03927.hp2 NA18995.hp2 others(3): Show |
intron_variant | MODIFIER | c.268+12643_268+1264 others(6): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24654340 | ||||||
| chr10:24654371
|
GA | G | 60 | a0001c0001t0001g0160a0001c0001t0001g0174a0001c0001t0001g0197others(57): Show | 60 | HG00408.hp2 HG00423.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.268+12613delT | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24654371 | ||||||
| chr10:24654459
|
C | G | 1 | a0002c0002t0001g0038 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.268+12526G>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24654459 | ||||||
| chr10:24654464
|
G | A | 1 | a0001c0001t0001g0241 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.268+12521C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24654464 | ||||||
| chr10:24654490
|
G | A | 1 | a0001c0001t0002g0310 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.268+12495C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24654490 | ||||||
| chr10:24654523
|
T | C | 1 | a0001c0001t0001g0166 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.268+12462A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24654523 | ||||||
| chr10:24654609
|
G | A | 1 | a0002c0002t0004g0295 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.268+12376C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24654609 | ||||||
| chr10:24654647
|
A | G | 6 | a0001c0001t0005g0001a0001c0001t0005g0005a0001c0001t0005g0006others(3): Show | 6 | HG01981.hp1 HG03927.hp2 NA18995.hp2 others(3): Show |
intron_variant | MODIFIER | c.268+12338T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24654647 | ||||||
| chr10:24654649
|
G | A | 1 | a0003c0003t0001g0229 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.268+12336C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24654649 | ||||||
| chr10:24654698
|
A | G | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.268+12287T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24654698 | ||||||
| chr10:24654728
|
C | G | 1 | a0002c0002t0001g0023 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.268+12257G>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24654728 | ||||||
| chr10:24654790
|
A | G | 2 | a0003c0003t0001g0200a0003c0003t0001g0248 | 2 | NA18959.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.268+12195T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24654790 | ||||||
| chr10:24654841
|
G | GA | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.268+12143dupT | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24654841 | ||||||
| chr10:24654851
|
A | G | 2 | a0002c0002t0001g0071a0020c0019t0001g0066 | 2 | HG00642.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.268+12134T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24654851 | ||||||
| chr10:24655040
|
A | C | 2 | a0010c0012t0010g0015a0010c0012t0010g0016 | 2 | HG02723.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.268+11945T>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24655040 | ||||||
| chr10:24655097
|
T | C | 1 | a0003c0003t0001g0277 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.268+11888A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24655097 | ||||||
| chr10:24655124
|
A | G | 1 | a0001c0001t0001g0186 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.268+11861T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24655124 | ||||||
| chr10:24655210
|
G | A | 1 | a0003c0003t0001g0247 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.268+11775C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24655210 | ||||||
| chr10:24655272
|
G | T | 2 | a0001c0001t0002g0322a0001c0001t0002g0335 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.268+11713C>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24655272 | ||||||
| chr10:24655330
|
G | C | 3 | a0002c0002t0001g0043a0002c0002t0001g0044a0002c0002t0001g0046 | 3 | NA18975.hp2 NA19072.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.268+11655C>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24655330 | ||||||
| chr10:24655375
|
A | G | 3 | a0002c0002t0001g0043a0002c0002t0001g0044a0002c0002t0001g0046 | 3 | NA18975.hp2 NA19072.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.268+11610T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24655375 | ||||||
| chr10:24655546
|
G | A | 1 | a0001c0001t0002g0336 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.268+11439C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24655546 | ||||||
| chr10:24655557
|
G | A | 1 | a0005c0005t0004g0287 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.268+11428C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24655557 | ||||||
| chr10:24655583
|
G | A | 1 | a0002c0002t0001g0088 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.268+11402C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24655583 | ||||||
| chr10:24655618
|
C | T | 3 | a0002c0002t0001g0027a0021c0016t0003g0028a0023c0025t0003g0029 | 3 | HG01433.hp1 HG02004.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.268+11367G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24655618 | ||||||
| chr10:24655743
|
G | A | 1 | a0002c0002t0001g0281 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.268+11242C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24655743 | ||||||
| chr10:24655787
|
G | A | 1 | a0003c0003t0001g0198 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.268+11198C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24655787 | ||||||
| chr10:24655809
|
G | A | 10 | a0002c0002t0001g0020a0002c0002t0001g0138a0002c0002t0001g0139others(7): Show | 10 | HG02129.hp2 HG02523.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.268+11176C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24655809 | ||||||
| chr10:24655814
|
TCTCTGCC others(69): Show |
T | 1 | a0003c0003t0001g0179 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.268+11095_268+1117 others(80): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24655814 | ||||||
| chr10:24655925
|
G | C | 3 | a0005c0005t0001g0102a0005c0005t0001g0103a0005c0005t0001g0284 | 3 | HG02451.hp1 HG03209.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.268+11060C>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24655925 | ||||||
| chr10:24655929
|
G | T | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.268+11056C>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24655929 | ||||||
| chr10:24655943
|
A | G | 293 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(290): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.268+11042T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24655943 | ||||||
| chr10:24655948
|
G | A | 1 | a0002c0002t0004g0295 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.268+11037C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24655948 | ||||||
| chr10:24655992
|
GAGAAGTG others(73): Show |
G | 4 | a0002c0002t0001g0020a0002c0002t0001g0138a0002c0002t0001g0139others(1): Show | 4 | HG02615.hp1 HG02922.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.268+10913_268+1099 others(84): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24655992 | ||||||
| chr10:24655998
|
T | C | 11 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(8): Show | 11 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.268+10987A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24655998 | ||||||
| chr10:24656065
|
C | A | 7 | a0001c0001t0001g0171a0001c0001t0004g0296a0001c0001t0004g0297others(4): Show | 7 | HG01891.hp2 HG02895.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.268+10920G>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656065 | ||||||
| chr10:24656067
|
C | T | 8 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0183others(5): Show | 8 | HG01884.hp2 HG02257.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.268+10918G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656067 | ||||||
| chr10:24656072
|
A | G | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.268+10913T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656072 | ||||||
| chr10:24656112
|
G | A | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.268+10873C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656112 | ||||||
| chr10:24656162
|
T | TG | 99 | a0001c0001t0001g0269a0002c0002t0001g0010a0002c0002t0001g0018others(96): Show | 99 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.268+10822dupC | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656162 | ||||||
| chr10:24656168
|
G | A | 1 | a0001c0001t0005g0006 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.268+10817C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656168 | ||||||
| chr10:24656198
|
A | G | 11 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(8): Show | 11 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.268+10787T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656198 | ||||||
| chr10:24656201
|
C | T | 11 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(8): Show | 11 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.268+10784G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656201 | ||||||
| chr10:24656213
|
GGGGGGGT others(718): Show |
G | 6 | a0001c0001t0001g0144a0001c0001t0001g0162a0001c0001t0001g0163others(3): Show | 6 | HG02486.hp1 HG02559.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.268+10047_268+1077 others(4): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656213 | ||||||
| chr10:24656214
|
GGGGGGTC others(717): Show |
G | 5 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(2): Show | 5 | HG02280.hp1 HG02451.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.268+10047_268+1077 others(4): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656214 | ||||||
| chr10:24656250
|
CGGGAGGT others(979): Show |
C | 1 | a0002c0002t0001g0023 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.268+9749_268+10734 others(3): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656250 | ||||||
| chr10:24656251
|
G | A | 1 | a0004c0004t0001g0068 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.268+10734C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656251 | ||||||
| chr10:24656301
|
C | T | 5 | a0001c0001t0001g0171a0001c0001t0004g0296a0001c0001t0004g0297others(2): Show | 5 | HG01891.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.268+10684G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656301 | ||||||
| chr10:24656308
|
GCCTGGCC others(43): Show |
G | 1 | a0006c0006t0003g0214 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.268+10627_268+1067 others(54): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656308 | ||||||
| chr10:24656311
|
T | C | 338 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(335): Show | 338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.268+10674A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656311 | ||||||
| chr10:24656312
|
G | A | 1 | a0003c0003t0001g0116 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.268+10673C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656312 | ||||||
| chr10:24656370
|
G | A | 1 | a0006c0006t0003g0214 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.268+10615C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656370 | ||||||
| chr10:24656375
|
G | A | 1 | a0002c0002t0001g0149 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.268+10610C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656375 | ||||||
| chr10:24656389
|
T | TG | 16 | a0001c0001t0001g0219a0001c0001t0001g0252a0001c0001t0002g0345others(13): Show | 16 | HG00642.hp1 HG01192.hp1 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.268+10595dupC | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656389 | ||||||
| chr10:24656391
|
G | A | 2 | a0001c0001t0002g0315a0001c0001t0002g0325 | 2 | HG00733.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.268+10594C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656391 | ||||||
| chr10:24656400
|
G | T | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.268+10585C>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656400 | ||||||
| chr10:24656404
|
T | C | 9 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(6): Show | 9 | HG02129.hp2 HG02523.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.268+10581A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656404 | ||||||
| chr10:24656411
|
G | A | 1 | a0001c0001t0005g0006 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.268+10574C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656411 | ||||||
| chr10:24656427
|
T | C | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.268+10558A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656427 | ||||||
| chr10:24656432
|
G | A | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.268+10553C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656432 | ||||||
| chr10:24656438
|
G | A | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.268+10547C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656438 | ||||||
| chr10:24656442
|
G | A | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.268+10543C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656442 | ||||||
| chr10:24656456
|
A | G | 157 | a0002c0002t0001g0010a0002c0002t0001g0017a0002c0002t0001g0018others(154): Show | 157 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.268+10529T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656456 | ||||||
| chr10:24656464
|
TGTGAAGT others(866): Show |
T | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.268+9648_268+10520 others(3): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656464 | ||||||
| chr10:24656466
|
T | G | 158 | a0001c0001t0001g0171a0001c0001t0004g0296a0001c0001t0004g0297others(155): Show | 158 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.268+10519A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656466 | ||||||
| chr10:24656467
|
GAAGTGAG others(546): Show |
G | 1 | a0001c0001t0002g0321 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.268+9965_268+10517 others(3): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656467 | ||||||
| chr10:24656502
|
G | A | 3 | a0001c0001t0001g0264a0002c0002t0001g0150a0002c0002t0001g0151 | 3 | HG02145.hp2 NA18941.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.268+10483C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656502 | ||||||
| chr10:24656506
|
G | A | 3 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0001g0249 | 3 | HG00621.hp1 NA18954.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.268+10479C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656506 | ||||||
| chr10:24656534
|
G | A | 4 | a0002c0002t0001g0042a0002c0002t0001g0049a0002c0002t0001g0053others(1): Show | 4 | HG01934.hp1 HG01952.hp2 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.268+10451C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656534 | ||||||
| chr10:24656550
|
T | C | 119 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(116): Show | 119 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.268+10435A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656550 | ||||||
| chr10:24656581
|
T | TCCGCCCA others(5): Show |
1 | a0002c0002t0001g0120 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.268+10392_268+1040 others(16): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656581 | ||||||
| chr10:24656595
|
C | T | 1 | a0001c0001t0001g0272 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.268+10390G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656595 | ||||||
| chr10:24656596
|
G | A | 5 | a0001c0001t0001g0170a0001c0001t0001g0176a0001c0001t0001g0177others(2): Show | 5 | HG01261.hp1 HG02486.hp2 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.268+10389C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656596 | ||||||
| chr10:24656597
|
C | A | 1 | a0001c0001t0001g0170 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.268+10388G>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656597 | ||||||
| chr10:24656619
|
G | A | 4 | a0001c0001t0001g0171a0001c0001t0004g0296a0001c0001t0004g0297others(1): Show | 4 | HG01891.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.268+10366C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656619 | ||||||
| chr10:24656661
|
T | TGCCCGGC others(42): Show |
12 | a0001c0001t0002g0303a0001c0001t0002g0304a0001c0001t0002g0307others(9): Show | 12 | HG01168.hp2 HG01975.hp2 NA18906.hp1 others(9): Show |
intron_variant | MODIFIER | c.268+10275_268+1032 others(53): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656661 | ||||||
| chr10:24656661
|
TGCCCGGC others(42): Show |
T | 2 | a0001c0001t0002g0345a0001c0001t0004g0296 | 2 | NA19058.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.268+10275_268+1032 others(53): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656661 | ||||||
| chr10:24656661
|
TGCCCGGC others(91): Show |
T | 34 | a0001c0001t0003g0155a0002c0002t0001g0017a0002c0002t0001g0019others(31): Show | 34 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.268+10226_268+1032 others(102): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656661 | ||||||
| chr10:24656673
|
C | CGCCCCGT others(42): Show |
1 | a0003c0003t0001g0179 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.268+10311_268+1031 others(53): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656673 | ||||||
| chr10:24656683
|
G | A | 2 | a0001c0001t0001g0174a0001c0001t0001g0222 | 2 | HG02055.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.268+10302C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656683 | ||||||
| chr10:24656694
|
GGGGGGGT others(90): Show |
G | 3 | a0002c0002t0001g0049a0002c0002t0007g0007a0015c0023t0001g0090 | 3 | HG01934.hp1 HG02738.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.268+10194_268+1029 others(101): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656694 | ||||||
| chr10:24656704
|
G | GCCCCCCG others(43): Show |
1 | a0005c0005t0004g0287 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.268+10231_268+1028 others(54): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656704 | ||||||
| chr10:24656705
|
CCCCCCGC others(90): Show |
C | 3 | a0002c0002t0001g0048a0002c0002t0001g0057a0002c0002t0001g0128 | 3 | HG00639.hp1 HG01175.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.268+10183_268+1027 others(101): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656705 | ||||||
| chr10:24656722
|
C | T | 53 | a0001c0001t0001g0160a0001c0001t0001g0174a0001c0001t0001g0181others(50): Show | 53 | HG00423.hp1 HG00597.hp2 HG01069.hp2 others(50): Show |
intron_variant | MODIFIER | c.268+10263G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656722 | ||||||
| chr10:24656742
|
T | TGGGGGGG others(43): Show |
1 | a0001c0001t0002g0305 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.268+10242_268+1024 others(54): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656742 | ||||||
| chr10:24656750
|
T | A | 113 | a0001c0001t0001g0191a0001c0001t0001g0196a0001c0001t0001g0246others(110): Show | 113 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(110): Show |
intron_variant | MODIFIER | c.268+10235A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656750 | ||||||
| chr10:24656753
|
G | GC | 9 | a0001c0001t0001g0176a0001c0001t0001g0228a0001c0001t0001g0257others(6): Show | 9 | HG01261.hp1 HG02071.hp1 HG02080.hp2 others(6): Show |
intron_variant | MODIFIER | c.268+10231dupG | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656753 | ||||||
| chr10:24656753
|
G | GCCCCCCG others(44): Show |
1 | a0001c0001t0001g0252 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.268+10231_268+1023 others(55): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656753 | ||||||
| chr10:24656754
|
CCCCCCGC others(90): Show |
C | 2 | a0005c0005t0001g0102a0019c0020t0001g0112 | 2 | HG01261.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.268+10134_268+1023 others(101): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656754 | ||||||
| chr10:24656766
|
C | T | 1 | a0001c0001t0001g0260 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.268+10219G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656766 | ||||||
| chr10:24656792
|
GGGGGGGT others(90): Show |
G | 2 | a0002c0002t0001g0120a0002c0002t0001g0127 | 2 | HG00438.hp2 HG02071.hp2 |
intron_variant | MODIFIER | c.268+10096_268+1019 others(101): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656792 | ||||||
| chr10:24656793
|
GGGGGGTC others(138): Show |
G | 1 | a0003c0003t0001g0248 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.268+10047_268+1019 others(4): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656793 | ||||||
| chr10:24656794
|
GGGGGTCG others(137): Show |
G | 1 | a0003c0003t0001g0200 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.268+10047_268+1019 others(4): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656794 | ||||||
| chr10:24656799
|
T | A | 5 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0257others(2): Show | 5 | HG00597.hp1 HG01261.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.268+10186A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656799 | ||||||
| chr10:24656801
|
G | A | 1 | a0002c0002t0001g0093 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.268+10184C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656801 | ||||||
| chr10:24656801
|
GGCCCCCC others(449): Show |
G | 1 | a0005c0005t0001g0137 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.268+9728_268+10183 others(3): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656801 | ||||||
| chr10:24656802
|
G | GC | 9 | a0001c0001t0001g0244a0001c0001t0001g0252a0001c0001t0002g0337others(6): Show | 9 | HG00642.hp1 HG01934.hp1 HG02074.hp1 others(6): Show |
intron_variant | MODIFIER | c.268+10182dupG | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656802 | ||||||
| chr10:24656841
|
GGGGGGGT others(90): Show |
G | 15 | a0002c0002t0001g0043a0002c0002t0001g0046a0002c0002t0001g0050others(12): Show | 15 | HG00099.hp2 HG01081.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.268+10047_268+1014 others(101): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656841 | ||||||
| chr10:24656842
|
GGGGGGTC others(89): Show |
G | 41 | a0002c0002t0001g0010a0002c0002t0001g0021a0002c0002t0001g0025others(38): Show | 41 | HG00099.hp1 HG00642.hp2 HG01361.hp1 others(38): Show |
intron_variant | MODIFIER | c.268+10047_268+1014 others(100): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656842 | ||||||
| chr10:24656843
|
GGGGGTCG others(88): Show |
G | 44 | a0001c0001t0001g0191a0001c0001t0001g0196a0001c0001t0001g0246others(41): Show | 44 | HG00408.hp1 HG00609.hp2 HG00621.hp2 others(41): Show |
intron_variant | MODIFIER | c.268+10047_268+1014 others(99): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656843 | ||||||
| chr10:24656844
|
GGGGTCGG others(87): Show |
G | 6 | a0002c0002t0001g0060a0002c0002t0001g0062a0002c0002t0001g0094others(3): Show | 6 | HG00438.hp1 HG01255.hp1 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.268+10047_268+1014 others(98): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656844 | ||||||
| chr10:24656845
|
GGGTCGGC others(86): Show |
G | 2 | a0002c0002t0001g0138a0002c0002t0001g0278 | 2 | HG00140.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.268+10047_268+1013 others(97): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656845 | ||||||
| chr10:24656848
|
T | A | 47 | a0001c0001t0001g0178a0001c0001t0001g0252a0001c0001t0001g0263others(44): Show | 47 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.268+10137A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656848 | ||||||
| chr10:24656848
|
T | TCGGCCCC others(43): Show |
3 | a0001c0001t0001g0242a0001c0001t0001g0270a0003c0003t0001g0116 | 3 | HG01109.hp2 HG04228.hp2 NA18943.hp2 |
intron_variant | MODIFIER | c.268+10136_268+1013 others(54): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656848 | ||||||
| chr10:24656848
|
T | TCGGCCCC others(44): Show |
1 | a0001c0001t0001g0170 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.268+10136_268+1013 others(55): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656848 | ||||||
| chr10:24656848
|
T | TCGGCCCC others(43): Show |
2 | a0001c0001t0001g0219a0003c0003t0001g0205 | 2 | HG01192.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.268+10136_268+1013 others(54): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656848 | ||||||
| chr10:24656848
|
TCGGCCCC others(90): Show |
T | 1 | a0002c0002t0001g0133 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.268+10040_268+1013 others(101): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656848 | ||||||
| chr10:24656851
|
G | GC | 8 | a0001c0001t0001g0176a0001c0001t0002g0302a0001c0001t0002g0341others(5): Show | 8 | HG00639.hp1 HG01169.hp1 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.268+10133dupG | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656851 | ||||||
| chr10:24656851
|
G | GCCCCCCG others(43): Show |
1 | a0001c0001t0001g0174 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.268+10133_268+1013 others(54): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656851 | ||||||
| chr10:24656889
|
TGGGGGGG others(43): Show |
T | 2 | a0001c0001t0002g0342a0001c0001t0002g0346 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.268+10046_268+1009 others(54): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656889 | ||||||
| chr10:24656890
|
GGGGGGGT others(41): Show |
G | 1 | a0001c0001t0002g0320 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.268+10047_268+1009 others(52): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656890 | ||||||
| chr10:24656892
|
GGGGGTCG others(39): Show |
G | 4 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0257others(1): Show | 4 | HG00597.hp1 HG01261.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.268+10047_268+1009 others(50): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656892 | ||||||
| chr10:24656893
|
GGGGTCGG others(38): Show |
G | 1 | a0003c0003t0001g0276 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.268+10047_268+1009 others(49): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656893 | ||||||
| chr10:24656897
|
T | A | 94 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(91): Show | 94 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.268+10088A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656897 | ||||||
| chr10:24656938
|
T | TCGGGGGG others(44): Show |
1 | a0001c0001t0001g0253 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.268+10046_268+1004 others(55): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656938 | ||||||
| chr10:24656938
|
T | TGGGGGGG others(47): Show |
1 | a0001c0001t0001g0228 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.268+10046_268+1004 others(58): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656938 | ||||||
| chr10:24656938
|
T | TGGGGGGG others(46): Show |
1 | a0003c0003t0001g0208 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.268+10046_268+1004 others(57): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656938 | ||||||
| chr10:24656938
|
T | TGGGGGGG others(43): Show |
4 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0001g0240others(1): Show | 4 | HG00741.hp2 HG02257.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.268+10046_268+1004 others(54): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656938 | ||||||
| chr10:24656938
|
T | TGGGGGGG others(44): Show |
24 | a0001c0001t0001g0012a0001c0001t0001g0169a0001c0001t0001g0185others(21): Show | 24 | HG00323.hp1 HG00639.hp2 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.268+10046_268+1004 others(55): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656938 | ||||||
| chr10:24656938
|
T | TGGGGGGG others(45): Show |
49 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0160others(46): Show | 49 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(46): Show |
intron_variant | MODIFIER | c.268+10046_268+1004 others(56): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656938 | ||||||
| chr10:24656938
|
T | TGGGGGGG others(46): Show |
4 | a0001c0001t0001g0220a0001c0001t0003g0216a0003c0003t0001g0221others(1): Show | 4 | HG03225.hp1 HG03453.hp2 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.268+10046_268+1004 others(57): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656938 | ||||||
| chr10:24656940
|
G | GGGGGGGT others(41): Show |
1 | a0001c0001t0005g0001 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.268+10044_268+1004 others(52): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656940 | ||||||
| chr10:24656944
|
GGGGGTCA others(124): Show |
G | 6 | a0001c0001t0005g0005a0001c0001t0005g0006a0003c0003t0001g0202others(3): Show | 6 | HG01123.hp1 HG01981.hp1 NA18995.hp2 others(3): Show |
intron_variant | MODIFIER | c.268+9910_268+10040 others(3): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656944 | ||||||
| chr10:24656951
|
A | G | 108 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(105): Show | 108 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.268+10034T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656951 | ||||||
| chr10:24656954
|
C | T | 2 | a0001c0001t0001g0142a0001c0001t0001g0143 | 2 | HG02451.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.268+10031G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656954 | ||||||
| chr10:24656958
|
CTGCCCGG others(72): Show |
C | 1 | a0001c0001t0001g0275 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.268+9948_268+10026 others(82): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656958 | ||||||
| chr10:24656960
|
G | A | 2 | a0005c0005t0001g0102a0005c0005t0001g0103 | 2 | HG02451.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.268+10025C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656960 | ||||||
| chr10:24656963
|
C | T | 1 | a0001c0001t0001g0162 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.268+10022G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656963 | ||||||
| chr10:24656995
|
G | A | 148 | a0002c0002t0001g0010a0002c0002t0001g0017a0002c0002t0001g0018others(145): Show | 148 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.268+9990C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24656995 | ||||||
| chr10:24657020
|
A | G | 1 | a0001c0001t0005g0001 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.268+9965T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657020 | ||||||
| chr10:24657049
|
C | T | 112 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(109): Show | 112 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.268+9936G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657049 | ||||||
| chr10:24657069
|
TGGGGGTG others(43): Show |
T | 1 | a0002c0002t0001g0121 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.268+9866_268+9915d others(52): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657069 | ||||||
| chr10:24657075
|
T | G | 1 | a0001c0001t0005g0001 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.268+9910A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657075 | ||||||
| chr10:24657079
|
A | G | 6 | a0001c0001t0005g0005a0001c0001t0005g0006a0003c0003t0001g0202others(3): Show | 6 | HG01123.hp1 HG01981.hp1 NA18995.hp2 others(3): Show |
intron_variant | MODIFIER | c.268+9906T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657079 | ||||||
| chr10:24657080
|
G | GCCCCCGG others(603): Show |
1 | a0001c0001t0005g0001 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.268+9904_268+9905i others(612): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657080 | ||||||
| chr10:24657086
|
C | G | 7 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0164others(4): Show | 7 | HG02559.hp1 HG02572.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.268+9899G>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657086 | ||||||
| chr10:24657087
|
G | A | 1 | a0001c0001t0001g0141 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.268+9898C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657087 | ||||||
| chr10:24657090
|
C | T | 1 | a0003c0003t0001g0179 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.268+9895G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657090 | ||||||
| chr10:24657099
|
G | A | 5 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(2): Show | 5 | HG01516.hp1 HG01517.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.268+9886C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657099 | ||||||
| chr10:24657118
|
TG | T | 24 | a0001c0001t0001g0171a0001c0001t0004g0297a0001c0001t0004g0298others(21): Show | 24 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(21): Show |
intron_variant | MODIFIER | c.268+9866delC | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657118 | ||||||
| chr10:24657132
|
C | T | 1 | a0002c0002t0001g0062 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.268+9853G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657132 | ||||||
| chr10:24657137
|
T | C | 1 | a0002c0002t0001g0088 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.268+9848A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657137 | ||||||
| chr10:24657142
|
G | A | 1 | a0003c0003t0001g0268 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.268+9843C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657142 | ||||||
| chr10:24657155
|
G | A | 1 | a0001c0001t0001g0242 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.268+9830C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657155 | ||||||
| chr10:24657173
|
GCCTCTGC others(30): Show |
G | 102 | a0002c0002t0001g0010a0002c0002t0001g0018a0002c0002t0001g0020others(99): Show | 102 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.268+9775_268+9811d others(39): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657173 | ||||||
| chr10:24657182
|
C | T | 3 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0255 | 3 | HG02622.hp1 HG02970.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.268+9803G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657182 | ||||||
| chr10:24657184
|
G | A | 1 | a0003c0003t0001g0223 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.268+9801C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657184 | ||||||
| chr10:24657187
|
A | G | 183 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(180): Show | 183 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.268+9798T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657187 | ||||||
| chr10:24657198
|
G | A | 2 | a0001c0001t0001g0163a0001c0001t0001g0164 | 2 | HG02572.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.268+9787C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657198 | ||||||
| chr10:24657210
|
C | G | 1 | a0011c0011t0001g0259 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.268+9775G>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657210 | ||||||
| chr10:24657236
|
A | C | 286 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(283): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.268+9749T>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657236 | ||||||
| chr10:24657248
|
G | C | 2 | a0011c0011t0001g0258a0011c0011t0001g0259 | 2 | HG02818.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.268+9737C>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657248 | ||||||
| chr10:24657265
|
GCCGGCCA others(124): Show |
G | 1 | a0003c0003t0001g0211 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.268+9589_268+9719d others(2): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657265 | ||||||
| chr10:24657276
|
G | A | 7 | a0001c0001t0001g0171a0001c0001t0004g0296a0001c0001t0004g0297others(4): Show | 7 | HG01891.hp2 HG02895.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.268+9709C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657276 | ||||||
| chr10:24657295
|
TG | T | 265 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(262): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.268+9689delC | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657295 | ||||||
| chr10:24657297
|
G | T | 3 | a0002c0002t0001g0118a0002c0002t0001g0119a0002c0002t0001g0127 | 3 | HG00673.hp1 HG02071.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.268+9688C>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657297 | ||||||
| chr10:24657301
|
G | A | 11 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(8): Show | 11 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.268+9684C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657301 | ||||||
| chr10:24657310
|
CCCCCTCG others(120): Show |
C | 6 | a0001c0001t0001g0162a0001c0001t0001g0165a0001c0001t0001g0166others(3): Show | 6 | HG02559.hp1 HG03130.hp2 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.268+9548_268+9674d others(2): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657310 | ||||||
| chr10:24657315
|
T | C | 280 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(277): Show | 280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.268+9670A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657315 | ||||||
| chr10:24657328
|
C | T | 1 | a0019c0020t0001g0112 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.268+9657G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657328 | ||||||
| chr10:24657329
|
G | A | 1 | a0001c0001t0001g0260 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.268+9656C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657329 | ||||||
| chr10:24657342
|
G | A | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.268+9643C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657342 | ||||||
| chr10:24657351
|
T | C | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.268+9634A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657351 | ||||||
| chr10:24657362
|
G | A | 4 | a0002c0002t0001g0020a0002c0002t0001g0138a0002c0002t0001g0139others(1): Show | 4 | HG02615.hp1 HG02922.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.268+9623C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657362 | ||||||
| chr10:24657397
|
C | T | 1 | a0003c0003t0001g0204 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.268+9588G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657397 | ||||||
| chr10:24657399
|
G | A | 2 | a0001c0001t0001g0238a0001c0001t0001g0240 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.268+9586C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657399 | ||||||
| chr10:24657416
|
G | A | 1 | a0001c0001t0001g0192 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.268+9569C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657416 | ||||||
| chr10:24657427
|
T | G | 2 | a0001c0001t0001g0163a0001c0001t0001g0164 | 2 | HG02572.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.268+9558A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657427 | ||||||
| chr10:24657465
|
G | A | 4 | a0002c0002t0001g0130a0002c0002t0001g0131a0002c0002t0001g0152others(1): Show | 4 | HG00099.hp2 HG00323.hp2 HG00733.hp2 others(1): Show |
intron_variant | MODIFIER | c.268+9520C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657465 | ||||||
| chr10:24657478
|
C | A | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.268+9507G>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657478 | ||||||
| chr10:24657478
|
C | T | 8 | a0001c0001t0001g0162a0001c0001t0001g0165a0001c0001t0001g0166others(5): Show | 8 | HG01099.hp2 HG01255.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.268+9507G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657478 | ||||||
| chr10:24657591
|
T | G | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.268+9394A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657591 | ||||||
| chr10:24657598
|
T | A | 2 | a0002c0002t0001g0038a0002c0002t0001g0092 | 2 | NA18747.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.268+9387A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657598 | ||||||
| chr10:24657611
|
C | T | 2 | a0002c0002t0001g0120a0002c0002t0001g0132 | 2 | HG00438.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.268+9374G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657611 | ||||||
| chr10:24657626
|
A | G | 11 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(8): Show | 11 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.268+9359T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657626 | ||||||
| chr10:24657639
|
C | T | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.268+9346G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657639 | ||||||
| chr10:24657640
|
C | T | 1 | a0001c0001t0001g0143 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.268+9345G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657640 | ||||||
| chr10:24657652
|
G | A | 3 | a0001c0014t0004g0286a0002c0002t0001g0043a0005c0005t0004g0287 | 3 | HG03209.hp1 NA18906.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.268+9333C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657652 | ||||||
| chr10:24657693
|
T | G | 4 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0188others(1): Show | 4 | HG01168.hp1 HG01169.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.268+9292A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657693 | ||||||
| chr10:24657700
|
A | G | 288 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(285): Show | 288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.268+9285T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657700 | ||||||
| chr10:24657859
|
C | T | 1 | a0002c0002t0001g0096 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.268+9126G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657859 | ||||||
| chr10:24657883
|
A | G | 2 | a0011c0011t0001g0258a0011c0011t0001g0259 | 2 | HG02818.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.268+9102T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24657883 | ||||||
| chr10:24658033
|
C | T | 1 | a0005c0005t0001g0137 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.268+8952G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24658033 | ||||||
| chr10:24658060
|
T | TA | 62 | a0001c0001t0002g0294a0001c0001t0002g0300a0001c0001t0002g0302others(59): Show | 62 | HG00280.hp2 HG00673.hp2 HG00733.hp1 others(59): Show |
intron_variant | MODIFIER | c.268+8924dupT | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24658060 | ||||||
| chr10:24658060
|
T | TAA | 14 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0144others(11): Show | 14 | HG01891.hp2 HG02280.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.268+8923_268+8924d others(4): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24658060 | ||||||
| chr10:24658060
|
T | TAAA | 9 | a0001c0001t0001g0143a0001c0001t0001g0162a0001c0001t0001g0163others(6): Show | 9 | HG02559.hp1 HG02572.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.268+8922_268+8924d others(5): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24658060 | ||||||
| chr10:24658060
|
T | TTA | 257 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(254): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.268+8924_268+8925i others(4): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24658060 | ||||||
| chr10:24658060
|
T | TTAA | 4 | a0002c0002t0001g0018a0002c0002t0001g0073a0002c0002t0001g0074others(1): Show | 4 | NA18978.hp2 NA19058.hp1 NA19062.hp2 others(1): Show |
intron_variant | MODIFIER | c.268+8924_268+8925i others(5): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24658060 | ||||||
| chr10:24658116
|
C | T | 2 | a0001c0001t0001g0141a0001c0001t0001g0144 | 2 | HG02280.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.268+8869G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24658116 | ||||||
| chr10:24658261
|
G | A | 1 | a0001c0001t0004g0296 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.268+8724C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24658261 | ||||||
| chr10:24658379
|
CAT | C | 15 | a0001c0001t0001g0186a0002c0002t0001g0019a0002c0002t0001g0106others(12): Show | 15 | HG01261.hp2 HG01496.hp1 HG01516.hp2 others(12): Show |
intron_variant | MODIFIER | c.268+8604_268+8605d others(4): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24658379 | ||||||
| chr10:24658389
|
T | C | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.268+8596A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24658389 | ||||||
| chr10:24658392
|
C | T | 1 | a0002c0002t0001g0152 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.268+8593G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24658392 | ||||||
| chr10:24658571
|
C | T | 1 | a0003c0003t0012g0172 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.268+8414G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24658571 | ||||||
| chr10:24658734
|
G | A | 1 | a0002c0030t0001g0022 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.268+8251C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24658734 | ||||||
| chr10:24658741
|
C | T | 1 | a0001c0001t0001g0264 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.268+8244G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24658741 | ||||||
| chr10:24658797
|
T | C | 2 | a0010c0012t0010g0015a0010c0012t0010g0016 | 2 | HG02723.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.268+8188A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24658797 | ||||||
| chr10:24658809
|
C | CTAGAACT | 289 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(286): Show | 289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.268+8175_268+8176i others(9): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24658809 | ||||||
| chr10:24658902
|
A | G | 1 | a0002c0002t0001g0057 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.268+8083T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24658902 | ||||||
| chr10:24659143
|
T | C | 148 | a0002c0002t0001g0010a0002c0002t0001g0017a0002c0002t0001g0018others(145): Show | 148 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.268+7842A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24659143 | ||||||
| chr10:24659401
|
C | T | 1 | a0002c0015t0001g0161 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.268+7584G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24659401 | ||||||
| chr10:24659408
|
C | T | 1 | a0004c0004t0001g0089 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.268+7577G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24659408 | ||||||
| chr10:24659454
|
T | C | 2 | a0001c0014t0004g0286a0005c0005t0004g0287 | 2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.268+7531A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24659454 | ||||||
| chr10:24659503
|
T | C | 1 | a0002c0002t0001g0094 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.268+7482A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24659503 | ||||||
| chr10:24659539
|
T | C | 2 | a0012c0010t0001g0266a0012c0010t0001g0267 | 2 | HG02109.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.268+7446A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24659539 | ||||||
| chr10:24659680
|
T | G | 1 | a0002c0002t0001g0059 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.268+7305A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24659680 | ||||||
| chr10:24659689
|
G | A | 1 | a0001c0001t0001g0228 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.268+7296C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24659689 | ||||||
| chr10:24659718
|
G | C | 1 | a0001c0001t0002g0336 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.268+7267C>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24659718 | ||||||
| chr10:24659747
|
T | C | 1 | a0001c0001t0001g0274 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.268+7238A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24659747 | ||||||
| chr10:24659794
|
A | G | 7 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0164others(4): Show | 7 | HG02559.hp1 HG02572.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.268+7191T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24659794 | ||||||
| chr10:24659907
|
A | G | 2 | a0001c0001t0003g0154a0024c0026t0003g0156 | 2 | HG01081.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.268+7078T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24659907 | ||||||
| chr10:24659981
|
T | TC | 5 | a0001c0001t0001g0171a0001c0001t0004g0296a0001c0001t0004g0297others(2): Show | 5 | HG01891.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.268+7003dupG | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24659981 | ||||||
| chr10:24660053
|
T | C | 148 | a0002c0002t0001g0010a0002c0002t0001g0017a0002c0002t0001g0018others(145): Show | 148 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.268+6932A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24660053 | ||||||
| chr10:24660262
|
T | C | 1 | a0002c0002t0001g0131 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.268+6723A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24660262 | ||||||
| chr10:24660309
|
AT | A | 105 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(102): Show | 105 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.268+6675delA | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24660309 | ||||||
| chr10:24660386
|
T | TAA | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.268+6597_268+6598d others(4): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24660386 | ||||||
| chr10:24660386
|
T | TAAA | 17 | a0002c0002t0001g0021a0002c0002t0001g0035a0002c0002t0001g0037others(14): Show | 17 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(14): Show |
intron_variant | MODIFIER | c.268+6596_268+6598d others(5): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24660386 | ||||||
| chr10:24660386
|
T | TAAAA | 75 | a0002c0002t0001g0010a0002c0002t0001g0018a0002c0002t0001g0019others(72): Show | 75 | HG00099.hp2 HG00408.hp1 HG00609.hp1 others(72): Show |
intron_variant | MODIFIER | c.268+6595_268+6598d others(6): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24660386 | ||||||
| chr10:24660386
|
T | TAAAAA | 108 | a0001c0001t0001g0160a0001c0001t0001g0185a0001c0001t0001g0186others(105): Show | 108 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.268+6594_268+6598d others(7): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24660386 | ||||||
| chr10:24660386
|
T | TAAAAAA | 47 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(44): Show | 47 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(44): Show |
intron_variant | MODIFIER | c.268+6593_268+6598d others(8): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24660386 | ||||||
| chr10:24660386
|
T | TAAAAAAA | 15 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0182others(12): Show | 15 | HG00642.hp1 HG01175.hp1 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.268+6592_268+6598d others(9): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24660386 | ||||||
| chr10:24660386
|
T | TAAAAAAA others(3): Show |
2 | a0001c0014t0004g0286a0005c0005t0004g0287 | 2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.268+6589_268+6598d others(12): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24660386 | ||||||
| chr10:24660386
|
TA | T | 7 | a0001c0001t0002g0303a0001c0001t0002g0317a0001c0001t0002g0321others(4): Show | 7 | HG00280.hp2 HG01099.hp2 HG01975.hp2 others(4): Show |
intron_variant | MODIFIER | c.268+6598delT | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24660386 | ||||||
| chr10:24660386
|
TAAAAAAA others(2): Show |
T | 11 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(8): Show | 11 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.268+6590_268+6598d others(11): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24660386 | ||||||
| chr10:24660433
|
G | T | 150 | a0002c0002t0001g0010a0002c0002t0001g0017a0002c0002t0001g0018others(147): Show | 150 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.268+6552C>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24660433 | ||||||
| chr10:24660507
|
C | T | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.268+6478G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24660507 | ||||||
| chr10:24660566
|
C | G | 1 | a0016c0022t0002g0339 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.268+6419G>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24660566 | ||||||
| chr10:24660786
|
A | C | 2 | a0002c0002t0001g0064a0002c0002t0001g0145 | 2 | NA18988.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.268+6199T>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24660786 | ||||||
| chr10:24660814
|
G | C | 105 | a0002c0002t0001g0010a0002c0002t0001g0018a0002c0002t0001g0020others(102): Show | 105 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.268+6171C>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24660814 | ||||||
| chr10:24660836
|
T | A | 1 | a0002c0002t0001g0055 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.268+6149A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24660836 | ||||||
| chr10:24661046
|
T | C | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.268+5939A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24661046 | ||||||
| chr10:24661200
|
G | A | 8 | a0001c0001t0001g0191a0001c0001t0001g0196a0001c0001t0001g0238others(5): Show | 8 | HG00639.hp2 HG01257.hp1 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.268+5785C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24661200 | ||||||
| chr10:24661266
|
C | T | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.268+5719G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24661266 | ||||||
| chr10:24661305
|
T | C | 1 | a0002c0002t0004g0295 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.268+5680A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24661305 | ||||||
| chr10:24661423
|
C | T | 7 | a0002c0002t0001g0019a0002c0002t0001g0280a0002c0002t0001g0281others(4): Show | 7 | HG01496.hp1 HG01516.hp2 HG02027.hp2 others(4): Show |
intron_variant | MODIFIER | c.268+5562G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24661423 | ||||||
| chr10:24661738
|
T | C | 1 | a0001c0001t0004g0296 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.268+5247A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24661738 | ||||||
| chr10:24661775
|
T | C | 3 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0255 | 3 | HG02622.hp1 HG02970.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.268+5210A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24661775 | ||||||
| chr10:24662049
|
T | C | 2 | a0001c0014t0004g0286a0005c0005t0004g0287 | 2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.268+4936A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24662049 | ||||||
| chr10:24662113
|
G | A | 2 | a0001c0001t0002g0316a0001c0001t0002g0326 | 2 | HG02155.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.268+4872C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24662113 | ||||||
| chr10:24662118
|
G | A | 1 | a0001c0001t0002g0313 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.268+4867C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24662118 | ||||||
| chr10:24662489
|
G | T | 1 | a0002c0002t0001g0139 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.268+4496C>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24662489 | ||||||
| chr10:24662549
|
C | T | 2 | a0002c0002t0001g0071a0020c0019t0001g0066 | 2 | HG00642.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.268+4436G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24662549 | ||||||
| chr10:24662846
|
T | G | 1 | a0002c0002t0001g0098 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.268+4139A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24662846 | ||||||
| chr10:24662877
|
C | T | 171 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(168): Show | 171 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.268+4108G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24662877 | ||||||
| chr10:24662964
|
A | AT | 247 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(244): Show | 247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.268+4020dupA | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24662964 | ||||||
| chr10:24662964
|
A | ATT | 10 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0183others(7): Show | 10 | HG00423.hp1 HG01175.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.268+4019_268+4020d others(4): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24662964 | ||||||
| chr10:24662964
|
AT | A | 7 | a0001c0001t0001g0171a0001c0001t0002g0343a0001c0001t0004g0296others(4): Show | 7 | HG01891.hp2 HG02723.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.268+4020delA | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24662964 | ||||||
| chr10:24663007
|
C | T | 1 | a0001c0001t0001g0275 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.268+3978G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24663007 | ||||||
| chr10:24663099
|
C | T | 2 | a0002c0002t0001g0078a0002c0002t0001g0079 | 2 | HG01975.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.268+3886G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24663099 | ||||||
| chr10:24663360
|
C | T | 1 | a0005c0005t0001g0102 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.268+3625G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24663360 | ||||||
| chr10:24663482
|
A | G | 288 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(285): Show | 288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.268+3503T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24663482 | ||||||
| chr10:24663531
|
CTAT | C | 3 | a0001c0001t0001g0171a0001c0001t0004g0297a0001c0001t0004g0298 | 3 | HG01891.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.268+3451_268+3453d others(5): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24663531 | ||||||
| chr10:24663604
|
C | T | 4 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(1): Show | 4 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.268+3381G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24663604 | ||||||
| chr10:24663615
|
G | C | 2 | a0002c0002t0001g0056a0002c0002t0001g0285 | 2 | HG00408.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.268+3370C>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24663615 | ||||||
| chr10:24663822
|
C | T | 4 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(1): Show | 4 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.268+3163G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24663822 | ||||||
| chr10:24664219
|
C | T | 1 | a0002c0015t0001g0161 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.268+2766G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24664219 | ||||||
| chr10:24664259
|
A | G | 1 | a0003c0003t0001g0277 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.268+2726T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24664259 | ||||||
| chr10:24664328
|
A | G | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.268+2657T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24664328 | ||||||
| chr10:24664419
|
G | T | 1 | a0001c0001t0002g0317 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.268+2566C>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24664419 | ||||||
| chr10:24664445
|
C | A | 2 | a0002c0002t0001g0030a0002c0002t0001g0040 | 2 | NA19003.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.268+2540G>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24664445 | ||||||
| chr10:24664518
|
T | C | 1 | a0003c0003t0001g0276 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.268+2467A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24664518 | ||||||
| chr10:24664554
|
C | CA | 7 | a0006c0006t0002g0350a0007c0007t0006g0291a0007c0007t0006g0292others(4): Show | 7 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(4): Show |
intron_variant | MODIFIER | c.268+2430dupT | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24664554 | ||||||
| chr10:24664566
|
AT | A | 5 | a0001c0001t0002g0344a0004c0004t0001g0091a0005c0005t0001g0137others(2): Show | 5 | HG02109.hp1 HG02896.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.268+2418delA | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24664566 | ||||||
| chr10:24664567
|
T | A | 166 | a0001c0001t0001g0160a0001c0001t0001g0162a0001c0001t0001g0163others(163): Show | 166 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.268+2418A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24664567 | ||||||
| chr10:24664570
|
T | A | 16 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0199others(13): Show | 16 | HG00642.hp2 HG01123.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.268+2415A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24664570 | ||||||
| chr10:24664573
|
T | A | 1 | a0001c0001t0001g0257 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.268+2412A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24664573 | ||||||
| chr10:24664609
|
G | A | 288 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(285): Show | 288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.268+2376C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24664609 | ||||||
| chr10:24664646
|
T | A | 1 | a0002c0002t0001g0126 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.268+2339A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24664646 | ||||||
| chr10:24664723
|
C | CTTTT | 295 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(292): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.268+2261_268+2262i others(6): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24664723 | ||||||
| chr10:24664758
|
T | C | 1 | a0001c0001t0001g0160 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.268+2227A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24664758 | ||||||
| chr10:24665164
|
T | C | 1 | a0002c0002t0001g0081 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.268+1821A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24665164 | ||||||
| chr10:24665500
|
A | G | 1 | a0001c0001t0001g0217 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.268+1485T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24665500 | ||||||
| chr10:24665690
|
G | A | 1 | a0001c0001t0002g0340 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.268+1295C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24665690 | ||||||
| chr10:24665726
|
C | T | 1 | a0005c0005t0003g0147 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.268+1259G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24665726 | ||||||
| chr10:24665984
|
A | C | 1 | a0001c0001t0001g0239 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.268+1001T>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24665984 | ||||||
| chr10:24666030
|
T | G | 1 | a0003c0003t0001g0211 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.268+955A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24666030 | ||||||
| chr10:24666042
|
T | G | 1 | a0002c0002t0001g0123 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.268+943A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24666042 | ||||||
| chr10:24666189
|
C | A | 1 | a0003c0003t0001g0208 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.268+796G>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24666189 | ||||||
| chr10:24666277
|
G | A | 1 | a0002c0021t0001g0084 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.268+708C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24666277 | ||||||
| chr10:24666322
|
G | A | 2 | a0001c0014t0004g0286a0005c0005t0004g0287 | 2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.268+663C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24666322 | ||||||
| chr10:24666325
|
C | T | 170 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(167): Show | 170 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.268+660G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24666325 | ||||||
| chr10:24666343
|
G | A | 1 | a0003c0003t0001g0223 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.268+642C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24666343 | ||||||
| chr10:24666535
|
T | C | 1 | a0019c0020t0001g0112 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.268+450A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24666535 | ||||||
| chr10:24666544
|
T | C | 1 | a0001c0001t0001g0143 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.268+441A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24666544 | ||||||
| chr10:24666547
|
G | A | 2 | a0001c0001t0002g0304a0001c0001t0002g0309 | 2 | NA18959.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.268+438C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | 24666547 | ||||||
| chr10:24667095
|
C | T | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.244-86G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 3/25 | chr10 | 24667095 | ||||||
| chr10:24667112
|
G | A | 3 | a0004c0004t0001g0068a0004c0004t0001g0069a0004c0004t0001g0100 | 3 | HG02559.hp2 HG02809.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.244-103C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 3/25 | chr10 | 24667112 | ||||||
| chr10:24667188
|
C | T | 1 | a0001c0001t0001g0233 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.244-179G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 3/25 | chr10 | 24667188 | ||||||
| chr10:24667352
|
A | C | 1 | a0001c0001t0001g0142 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.244-343T>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 3/25 | chr10 | 24667352 | ||||||
| chr10:24667427
|
CTT | C | 4 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(1): Show | 4 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.244-420_244-419del others(2): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 3/25 | chr10 | 24667427 | ||||||
| chr10:24667484
|
G | A | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.244-475C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 3/25 | chr10 | 24667484 | ||||||
| chr10:24667585
|
G | T | 1 | a0003c0003t0001g0011 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.244-576C>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 3/25 | chr10 | 24667585 | ||||||
| chr10:24667713
|
A | G | 1 | a0002c0002t0001g0093 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.244-704T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 3/25 | chr10 | 24667713 | ||||||
| chr10:24668217
|
G | A | 2 | a0011c0011t0001g0258a0011c0011t0001g0259 | 2 | HG02818.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.244-1208C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 3/25 | chr10 | 24668217 | ||||||
| chr10:24668969
|
T | C | 1 | a0002c0002t0001g0148 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.243+1249A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 3/25 | chr10 | 24668969 | ||||||
| chr10:24668977
|
G | C | 17 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(14): Show | 17 | HG02129.hp2 HG02280.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.243+1241C>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 3/25 | chr10 | 24668977 | ||||||
| chr10:24668999
|
A | G | 2 | a0001c0001t0001g0253a0001c0001t0013g0254 | 2 | HG02630.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.243+1219T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 3/25 | chr10 | 24668999 | ||||||
| chr10:24669105
|
T | C | 2 | a0001c0001t0002g0342a0001c0001t0002g0346 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.243+1113A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 3/25 | chr10 | 24669105 | ||||||
| chr10:24669230
|
C | T | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.243+988G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 3/25 | chr10 | 24669230 | ||||||
| chr10:24669389
|
A | G | 6 | a0001c0001t0001g0270a0001c0001t0001g0271a0001c0001t0001g0272others(3): Show | 6 | HG00423.hp2 NA18943.hp2 NA18964.hp1 others(3): Show |
intron_variant | MODIFIER | c.243+829T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 3/25 | chr10 | 24669389 | ||||||
| chr10:24669528
|
T | C | 1 | a0015c0023t0001g0090 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.243+690A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 3/25 | chr10 | 24669528 | ||||||
| chr10:24669587
|
T | C | 1 | a0001c0001t0005g0006 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.243+631A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 3/25 | chr10 | 24669587 | ||||||
| chr10:24669779
|
T | C | 4 | a0002c0002t0001g0020a0002c0002t0001g0138a0002c0002t0001g0139others(1): Show | 4 | HG02615.hp1 HG02922.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.243+439A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 3/25 | chr10 | 24669779 | ||||||
| chr10:24670145
|
A | G | 1 | a0001c0001t0001g0192 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.243+73T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 3/25 | chr10 | 24670145 | ||||||
| chr10:24670199
|
C | A | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.243+19G>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 3/25 | chr10 | 24670199 | ||||||
| chr10:24670536
|
T | C | 1 | a0002c0002t0001g0283 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.64-139A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24670536 | ||||||
| chr10:24670807
|
T | C | 11 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(8): Show | 11 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.64-410A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24670807 | ||||||
| chr10:24671140
|
C | G | 1 | a0007c0007t0006g0293 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.64-743G>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24671140 | ||||||
| chr10:24671254
|
C | T | 38 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(35): Show | 38 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(35): Show |
intron_variant | MODIFIER | c.64-857G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24671254 | ||||||
| chr10:24671372
|
T | C | 23 | a0002c0002t0001g0017a0002c0002t0001g0117a0002c0002t0001g0118others(20): Show | 23 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(20): Show |
intron_variant | MODIFIER | c.64-975A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24671372 | ||||||
| chr10:24671723
|
A | AT | 15 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(12): Show | 15 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.64-1327dupA | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24671723 | ||||||
| chr10:24671723
|
AT | A | 20 | a0001c0001t0001g0185a0001c0001t0001g0250a0001c0001t0001g0251others(17): Show | 20 | HG01081.hp1 HG01169.hp2 HG01256.hp1 others(17): Show |
intron_variant | MODIFIER | c.64-1327delA | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24671723 | ||||||
| chr10:24671775
|
T | G | 1 | a0001c0001t0005g0006 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.64-1378A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24671775 | ||||||
| chr10:24671798
|
C | T | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.64-1401G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24671798 | ||||||
| chr10:24671805
|
C | T | 5 | a0001c0001t0001g0189a0001c0001t0001g0241a0001c0001t0001g0242others(2): Show | 5 | HG00140.hp1 HG00323.hp1 HG00741.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-1408G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24671805 | ||||||
| chr10:24671884
|
A | AT | 34 | a0001c0001t0001g0012a0001c0001t0001g0162a0001c0001t0001g0166others(31): Show | 34 | HG00423.hp2 HG00621.hp1 HG01433.hp2 others(31): Show |
intron_variant | MODIFIER | c.64-1488dupA | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24671884 | ||||||
| chr10:24671884
|
AT | A | 125 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0170others(122): Show | 125 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(122): Show |
intron_variant | MODIFIER | c.64-1488delA | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24671884 | ||||||
| chr10:24671884
|
ATT | A | 6 | a0002c0002t0001g0018a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02523.hp2 NA18747.hp1 NA18989.hp1 others(3): Show |
intron_variant | MODIFIER | c.64-1489_64-1488del others(2): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24671884 | ||||||
| chr10:24671915
|
A | C | 1 | a0002c0002t0001g0093 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.64-1518T>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24671915 | ||||||
| chr10:24671987
|
C | T | 1 | a0002c0002t0001g0146 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.64-1590G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24671987 | ||||||
| chr10:24672055
|
C | A | 7 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0164others(4): Show | 7 | HG02559.hp1 HG02572.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.64-1658G>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24672055 | ||||||
| chr10:24672244
|
A | G | 1 | a0001c0001t0001g0224 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.64-1847T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24672244 | ||||||
| chr10:24672359
|
C | T | 2 | a0002c0002t0001g0087a0013c0027t0001g0065 | 2 | HG02109.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.64-1962G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24672359 | ||||||
| chr10:24672371
|
T | C | 4 | a0006c0006t0002g0348a0006c0006t0002g0349a0006c0006t0002g0350others(1): Show | 4 | NA18957.hp1 NA18992.hp1 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.64-1974A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24672371 | ||||||
| chr10:24672474
|
T | C | 2 | a0001c0001t0001g0141a0001c0001t0001g0144 | 2 | HG02280.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.64-2077A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24672474 | ||||||
| chr10:24672522
|
T | C | 1 | a0002c0002t0007g0009 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.64-2125A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24672522 | ||||||
| chr10:24672577
|
T | C | 7 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0164others(4): Show | 7 | HG02559.hp1 HG02572.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.64-2180A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24672577 | ||||||
| chr10:24672739
|
A | G | 1 | a0001c0001t0008g0306 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.64-2342T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24672739 | ||||||
| chr10:24672845
|
G | A | 1 | a0002c0002t0001g0096 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.64-2448C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24672845 | ||||||
| chr10:24673096
|
T | G | 17 | a0002c0002t0001g0019a0002c0002t0001g0106a0002c0002t0001g0107others(14): Show | 17 | HG01261.hp2 HG01496.hp1 HG01516.hp2 others(14): Show |
intron_variant | MODIFIER | c.64-2699A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24673096 | ||||||
| chr10:24673319
|
G | A | 4 | a0001c0001t0001g0162a0001c0001t0001g0166a0001c0001t0001g0168others(1): Show | 4 | HG02559.hp1 HG03130.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.64-2922C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24673319 | ||||||
| chr10:24673477
|
C | T | 1 | a0002c0002t0004g0295 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.64-3080G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24673477 | ||||||
| chr10:24673495
|
T | C | 2 | a0001c0001t0001g0196a0001c0001t0001g0246 | 2 | HG03239.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.64-3098A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24673495 | ||||||
| chr10:24673519
|
A | G | 2 | a0011c0011t0001g0258a0011c0011t0001g0259 | 2 | HG02818.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.64-3122T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24673519 | ||||||
| chr10:24673589
|
T | C | 8 | a0001c0014t0004g0286a0005c0005t0004g0287a0007c0007t0006g0291others(5): Show | 8 | HG02129.hp2 HG02523.hp2 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-3192A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24673589 | ||||||
| chr10:24673721
|
G | T | 1 | a0002c0002t0001g0280 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.64-3324C>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24673721 | ||||||
| chr10:24673831
|
C | T | 34 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0176others(31): Show | 34 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(31): Show |
intron_variant | MODIFIER | c.64-3434G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24673831 | ||||||
| chr10:24674012
|
C | A | 1 | a0002c0002t0001g0280 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.64-3615G>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24674012 | ||||||
| chr10:24674053
|
A | T | 11 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(8): Show | 11 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.64-3656T>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24674053 | ||||||
| chr10:24674057
|
A | G | 1 | a0007c0007t0015g0288 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.64-3660T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24674057 | ||||||
| chr10:24674252
|
A | G | 106 | a0002c0002t0001g0010a0002c0002t0001g0018a0002c0002t0001g0020others(103): Show | 106 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.64-3855T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24674252 | ||||||
| chr10:24674296
|
G | A | 8 | a0001c0014t0004g0286a0005c0005t0004g0287a0007c0007t0006g0291others(5): Show | 8 | HG02129.hp2 HG02523.hp2 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-3899C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24674296 | ||||||
| chr10:24674336
|
C | T | 1 | a0002c0021t0001g0084 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.64-3939G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24674336 | ||||||
| chr10:24674380
|
A | G | 2 | a0005c0005t0001g0102a0005c0005t0001g0103 | 2 | HG02451.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.64-3983T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24674380 | ||||||
| chr10:24674424
|
C | T | 4 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(1): Show | 4 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.64-4027G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24674424 | ||||||
| chr10:24674531
|
A | C | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.64-4134T>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24674531 | ||||||
| chr10:24674615
|
G | T | 1 | a0005c0005t0001g0137 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.64-4218C>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24674615 | ||||||
| chr10:24674701
|
T | C | 4 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(1): Show | 4 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.64-4304A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24674701 | ||||||
| chr10:24674714
|
T | TAC | 8 | a0001c0014t0004g0286a0005c0005t0004g0287a0007c0007t0006g0291others(5): Show | 8 | HG02129.hp2 HG02523.hp2 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-4319_64-4318dup others(2): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24674714 | ||||||
| chr10:24674724
|
C | T | 2 | a0001c0001t0002g0337a0001c0001t0002g0338 | 2 | NA18964.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.64-4327G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24674724 | ||||||
| chr10:24674907
|
T | C | 1 | a0002c0002t0001g0099 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.64-4510A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24674907 | ||||||
| chr10:24674979
|
C | T | 150 | a0002c0002t0001g0010a0002c0002t0001g0017a0002c0002t0001g0018others(147): Show | 150 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.64-4582G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24674979 | ||||||
| chr10:24675123
|
T | G | 3 | a0001c0001t0002g0336a0001c0001t0002g0342a0001c0001t0002g0346 | 3 | HG03490.hp1 HG03492.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.64-4726A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24675123 | ||||||
| chr10:24675124
|
G | T | 3 | a0001c0001t0002g0336a0001c0001t0002g0342a0001c0001t0002g0346 | 3 | HG03490.hp1 HG03492.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.64-4727C>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24675124 | ||||||
| chr10:24675139
|
A | G | 288 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(285): Show | 288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.64-4742T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24675139 | ||||||
| chr10:24675147
|
C | G | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.64-4750G>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24675147 | ||||||
| chr10:24675148
|
A | G | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.64-4751T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24675148 | ||||||
| chr10:24675456
|
T | G | 8 | a0001c0014t0004g0286a0005c0005t0004g0287a0007c0007t0006g0291others(5): Show | 8 | HG02129.hp2 HG02523.hp2 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-5059A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24675456 | ||||||
| chr10:24675524
|
T | C | 1 | a0003c0003t0001g0265 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.64-5127A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24675524 | ||||||
| chr10:24675542
|
C | A | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.64-5145G>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24675542 | ||||||
| chr10:24675637
|
A | C | 7 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0164others(4): Show | 7 | HG02559.hp1 HG02572.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.64-5240T>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24675637 | ||||||
| chr10:24675715
|
T | G | 120 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(117): Show | 120 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.64-5318A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24675715 | ||||||
| chr10:24676108
|
G | A | 13 | a0002c0002t0001g0117a0002c0002t0001g0118a0002c0002t0001g0119others(10): Show | 13 | HG00438.hp2 HG00673.hp1 HG00735.hp1 others(10): Show |
intron_variant | MODIFIER | c.64-5711C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24676108 | ||||||
| chr10:24676150
|
G | A | 1 | a0002c0002t0001g0119 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.64-5753C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24676150 | ||||||
| chr10:24676246
|
C | A | 3 | a0001c0001t0002g0300a0001c0001t0002g0340a0001c0001t0002g0341 | 3 | HG01169.hp1 HG01934.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.64-5849G>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24676246 | ||||||
| chr10:24676281
|
C | G | 269 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(266): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.64-5884G>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24676281 | ||||||
| chr10:24676445
|
A | G | 1 | a0006c0006t0002g0348 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.64-6048T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24676445 | ||||||
| chr10:24676481
|
C | A | 1 | a0004c0004t0001g0070 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.64-6084G>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24676481 | ||||||
| chr10:24676538
|
G | A | 5 | a0001c0001t0001g0171a0001c0001t0004g0296a0001c0001t0004g0297others(2): Show | 5 | HG01891.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-6141C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24676538 | ||||||
| chr10:24676792
|
G | A | 2 | a0001c0001t0002g0315a0001c0001t0002g0325 | 2 | HG00733.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.64-6395C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24676792 | ||||||
| chr10:24676892
|
T | C | 78 | a0001c0001t0001g0160a0001c0001t0001g0174a0001c0001t0001g0181others(75): Show | 78 | HG00408.hp2 HG00423.hp1 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.64-6495A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24676892 | ||||||
| chr10:24677107
|
C | T | 4 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(1): Show | 4 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.64-6710G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24677107 | ||||||
| chr10:24677265
|
T | C | 2 | a0001c0014t0004g0286a0005c0005t0004g0287 | 2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.64-6868A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24677265 | ||||||
| chr10:24677384
|
T | C | 1 | a0001c0001t0001g0244 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.64-6987A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24677384 | ||||||
| chr10:24677584
|
A | G | 1 | a0002c0002t0004g0295 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.64-7187T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24677584 | ||||||
| chr10:24677658
|
C | T | 1 | a0002c0015t0001g0161 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.64-7261G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24677658 | ||||||
| chr10:24677876
|
C | A | 1 | a0003c0003t0001g0179 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.64-7479G>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24677876 | ||||||
| chr10:24678059
|
C | T | 2 | a0001c0001t0002g0320a0001c0001t0002g0345 | 2 | NA18954.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.64-7662G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24678059 | ||||||
| chr10:24678163
|
C | T | 169 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(166): Show | 169 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.64-7766G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24678163 | ||||||
| chr10:24678247
|
G | A | 1 | a0001c0001t0001g0192 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.64-7850C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24678247 | ||||||
| chr10:24678297
|
G | A | 167 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(164): Show | 167 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.64-7900C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24678297 | ||||||
| chr10:24678360
|
C | T | 2 | a0002c0002t0001g0107a0002c0002t0001g0111 | 2 | HG02258.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.64-7963G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24678360 | ||||||
| chr10:24678964
|
T | A | 1 | a0003c0003t0001g0116 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.64-8567A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24678964 | ||||||
| chr10:24679131
|
G | A | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.64-8734C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24679131 | ||||||
| chr10:24679267
|
C | T | 13 | a0002c0002t0001g0071a0002c0002t0001g0088a0004c0004t0001g0031others(10): Show | 13 | HG00642.hp2 HG01123.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.64-8870G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24679267 | ||||||
| chr10:24679357
|
C | A | 2 | a0002c0002t0001g0146a0002c0002t0001g0148 | 2 | NA18963.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.64-8960G>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24679357 | ||||||
| chr10:24679642
|
A | AT | 8 | a0001c0014t0004g0286a0005c0005t0004g0287a0007c0007t0006g0291others(5): Show | 8 | HG02129.hp2 HG02523.hp2 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-9246dupA | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24679642 | ||||||
| chr10:24679681
|
G | T | 15 | a0002c0002t0001g0035a0002c0002t0001g0036a0002c0002t0001g0064others(12): Show | 15 | HG00609.hp2 HG02083.hp1 NA18939.hp2 others(12): Show |
intron_variant | MODIFIER | c.64-9284C>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24679681 | ||||||
| chr10:24680032
|
A | T | 8 | a0001c0014t0004g0286a0005c0005t0004g0287a0007c0007t0006g0291others(5): Show | 8 | HG02129.hp2 HG02523.hp2 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-9635T>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24680032 | ||||||
| chr10:24680086
|
C | T | 171 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(168): Show | 171 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.64-9689G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24680086 | ||||||
| chr10:24680199
|
T | C | 1 | a0003c0003t0001g0011 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.64-9802A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24680199 | ||||||
| chr10:24680242
|
T | TAG | 8 | a0001c0014t0004g0286a0005c0005t0004g0287a0007c0007t0006g0291others(5): Show | 8 | HG02129.hp2 HG02523.hp2 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-9846_64-9845ins others(2): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24680242 | ||||||
| chr10:24680357
|
T | C | 1 | a0001c0014t0004g0286 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.64-9960A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24680357 | ||||||
| chr10:24680829
|
T | A | 2 | a0002c0002t0001g0128a0002c0002t0001g0129 | 2 | HG01175.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.64-10432A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24680829 | ||||||
| chr10:24680837
|
C | T | 4 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0183others(1): Show | 4 | HG01884.hp2 HG02615.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.64-10440G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24680837 | ||||||
| chr10:24680864
|
G | C | 7 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0164others(4): Show | 7 | HG02559.hp1 HG02572.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.64-10467C>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24680864 | ||||||
| chr10:24680975
|
G | T | 1 | a0011c0011t0001g0259 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.64-10578C>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24680975 | ||||||
| chr10:24681272
|
G | A | 11 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(8): Show | 11 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.64-10875C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24681272 | ||||||
| chr10:24681279
|
T | C | 1 | a0002c0002t0001g0092 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.64-10882A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24681279 | ||||||
| chr10:24681522
|
T | C | 1 | a0001c0001t0002g0317 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.64-11125A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24681522 | ||||||
| chr10:24681597
|
G | C | 2 | a0012c0010t0001g0266a0012c0010t0001g0267 | 2 | HG02109.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.64-11200C>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24681597 | ||||||
| chr10:24681640
|
C | CT | 9 | a0001c0001t0003g0216a0001c0014t0004g0286a0005c0005t0004g0287others(6): Show | 9 | HG02129.hp2 HG02523.hp2 HG03209.hp1 others(6): Show |
intron_variant | MODIFIER | c.64-11244dupA | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24681640 | ||||||
| chr10:24681802
|
G | A | 1 | a0003c0003t0001g0011 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.64-11405C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24681802 | ||||||
| chr10:24681872
|
T | G | 1 | a0001c0001t0001g0197 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.64-11475A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24681872 | ||||||
| chr10:24681887
|
T | C | 8 | a0001c0014t0004g0286a0005c0005t0004g0287a0007c0007t0006g0291others(5): Show | 8 | HG02129.hp2 HG02523.hp2 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-11490A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24681887 | ||||||
| chr10:24682067
|
G | A | 1 | a0001c0001t0001g0192 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.64-11670C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24682067 | ||||||
| chr10:24682166
|
C | T | 1 | a0007c0007t0006g0292 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.64-11769G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24682166 | ||||||
| chr10:24682292
|
G | T | 5 | a0001c0001t0001g0170a0001c0001t0001g0176a0001c0001t0001g0177others(2): Show | 5 | HG01261.hp1 HG02486.hp2 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.64-11895C>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24682292 | ||||||
| chr10:24682669
|
A | T | 6 | a0001c0001t0005g0001a0001c0001t0005g0005a0001c0001t0005g0006others(3): Show | 6 | HG01981.hp1 HG03927.hp2 NA18995.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-12272T>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24682669 | ||||||
| chr10:24682698
|
T | C | 6 | a0001c0001t0005g0001a0001c0001t0005g0005a0001c0001t0005g0006others(3): Show | 6 | HG01981.hp1 HG03927.hp2 NA18995.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-12301A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24682698 | ||||||
| chr10:24682862
|
G | A | 1 | a0002c0002t0001g0132 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.64-12465C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24682862 | ||||||
| chr10:24683095
|
C | CA | 6 | a0001c0001t0001g0171a0001c0001t0001g0185a0001c0001t0002g0311others(3): Show | 6 | HG00733.hp1 HG01169.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-12699dupT | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24683095 | ||||||
| chr10:24683095
|
CAAAAA | C | 65 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(62): Show | 65 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.64-12703_64-12699d others(7): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24683095 | ||||||
| chr10:24683457
|
T | C | 1 | a0002c0002t0001g0093 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.64-13060A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24683457 | ||||||
| chr10:24683620
|
T | G | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.64-13223A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24683620 | ||||||
| chr10:24683657
|
T | C | 1 | a0001c0001t0002g0325 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.64-13260A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24683657 | ||||||
| chr10:24683743
|
C | T | 2 | a0001c0001t0001g0141a0001c0001t0001g0144 | 2 | HG02280.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.64-13346G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24683743 | ||||||
| chr10:24683795
|
C | T | 1 | a0001c0001t0002g0329 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.64-13398G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24683795 | ||||||
| chr10:24683799
|
T | A | 1 | a0011c0011t0001g0258 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.64-13402A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24683799 | ||||||
| chr10:24684243
|
T | C | 286 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(283): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.64-13846A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24684243 | ||||||
| chr10:24684302
|
C | A | 1 | a0011c0011t0001g0258 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.64-13905G>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24684302 | ||||||
| chr10:24684416
|
C | T | 1 | a0002c0002t0001g0278 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.64-14019G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24684416 | ||||||
| chr10:24684498
|
T | C | 1 | a0001c0001t0001g0171 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.64-14101A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24684498 | ||||||
| chr10:24684586
|
G | C | 2 | a0010c0012t0010g0015a0010c0012t0010g0016 | 2 | HG02723.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.64-14189C>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24684586 | ||||||
| chr10:24684604
|
C | A | 2 | a0001c0001t0001g0243a0001c0001t0001g0245 | 2 | HG00323.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.64-14207G>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24684604 | ||||||
| chr10:24684799
|
C | T | 1 | a0002c0002t0001g0130 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.64-14402G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24684799 | ||||||
| chr10:24684840
|
C | T | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.64-14443G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24684840 | ||||||
| chr10:24685281
|
G | A | 1 | a0002c0002t0001g0121 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.64-14884C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24685281 | ||||||
| chr10:24685342
|
T | C | 1 | a0002c0002t0001g0279 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.64-14945A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24685342 | ||||||
| chr10:24685471
|
C | A | 1 | a0002c0002t0001g0136 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.64-15074G>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24685471 | ||||||
| chr10:24685487
|
T | C | 1 | a0003c0003t0001g0268 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.64-15090A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24685487 | ||||||
| chr10:24685608
|
G | A | 3 | a0002c0002t0001g0107a0002c0002t0001g0108a0002c0002t0001g0111 | 3 | HG02258.hp1 HG02630.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.64-15211C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24685608 | ||||||
| chr10:24685650
|
C | T | 2 | a0010c0012t0010g0015a0010c0012t0010g0016 | 2 | HG02723.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.64-15253G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24685650 | ||||||
| chr10:24685704
|
C | T | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.64-15307G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24685704 | ||||||
| chr10:24685886
|
A | G | 5 | a0001c0001t0002g0322a0001c0001t0002g0323a0001c0001t0002g0335others(2): Show | 5 | HG01099.hp2 HG01255.hp2 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.64-15489T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24685886 | ||||||
| chr10:24686013
|
C | T | 1 | a0003c0003t0001g0011 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.64-15616G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24686013 | ||||||
| chr10:24686096
|
G | T | 8 | a0001c0014t0004g0286a0005c0005t0004g0287a0007c0007t0006g0291others(5): Show | 8 | HG02129.hp2 HG02523.hp2 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-15699C>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24686096 | ||||||
| chr10:24686153
|
G | A | 2 | a0010c0012t0010g0015a0010c0012t0010g0016 | 2 | HG02723.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.64-15756C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24686153 | ||||||
| chr10:24686223
|
G | A | 164 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(161): Show | 164 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.64-15826C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24686223 | ||||||
| chr10:24686531
|
C | G | 2 | a0001c0014t0004g0286a0005c0005t0004g0287 | 2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.64-16134G>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24686531 | ||||||
| chr10:24686688
|
G | A | 61 | a0001c0001t0001g0160a0001c0001t0001g0174a0001c0001t0001g0197others(58): Show | 61 | HG00408.hp2 HG00423.hp1 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.64-16291C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24686688 | ||||||
| chr10:24686718
|
C | T | 1 | a0002c0002t0001g0279 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.64-16321G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24686718 | ||||||
| chr10:24687127
|
G | GATCGC | 293 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(290): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.64-16731_64-16730i others(7): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24687127 | ||||||
| chr10:24687128
|
G | T | 293 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(290): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.64-16731C>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24687128 | ||||||
| chr10:24687371
|
C | A | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.64-16974G>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24687371 | ||||||
| chr10:24687371
|
C | T | 1 | a0003c0003t0001g0201 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.64-16974G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24687371 | ||||||
| chr10:24687735
|
G | T | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.64-17338C>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24687735 | ||||||
| chr10:24687744
|
T | A | 3 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014 | 3 | HG02965.hp1 HG03225.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.64-17347A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24687744 | ||||||
| chr10:24687923
|
A | C | 1 | a0001c0001t0004g0299 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.64-17526T>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24687923 | ||||||
| chr10:24687934
|
T | C | 3 | a0003c0003t0001g0209a0003c0003t0001g0210a0003c0003t0001g0231 | 3 | NA18947.hp1 NA19007.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.64-17537A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24687934 | ||||||
| chr10:24688030
|
G | C | 1 | a0001c0001t0002g0321 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.64-17633C>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24688030 | ||||||
| chr10:24688117
|
G | A | 1 | a0001c0001t0001g0264 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.64-17720C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24688117 | ||||||
| chr10:24688221
|
T | C | 7 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0164others(4): Show | 7 | HG02559.hp1 HG02572.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.64-17824A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24688221 | ||||||
| chr10:24688260
|
G | A | 11 | a0001c0001t0001g0269a0002c0002t0001g0057a0002c0002t0001g0058others(8): Show | 11 | HG00597.hp1 HG00639.hp1 HG00735.hp2 others(8): Show |
intron_variant | MODIFIER | c.64-17863C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24688260 | ||||||
| chr10:24688275
|
C | T | 2 | a0012c0010t0001g0266a0012c0010t0001g0267 | 2 | HG02109.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.64-17878G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24688275 | ||||||
| chr10:24688368
|
G | A | 2 | a0010c0012t0010g0015a0010c0012t0010g0016 | 2 | HG02723.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.64-17971C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24688368 | ||||||
| chr10:24688500
|
C | T | 1 | a0002c0002t0001g0106 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.64-18103G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24688500 | ||||||
| chr10:24688543
|
G | C | 1 | a0003c0003t0001g0211 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.64-18146C>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24688543 | ||||||
| chr10:24688703
|
G | A | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.64-18306C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24688703 | ||||||
| chr10:24688855
|
C | G | 169 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(166): Show | 169 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.64-18458G>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24688855 | ||||||
| chr10:24688991
|
G | C | 4 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(1): Show | 4 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.64-18594C>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24688991 | ||||||
| chr10:24689488
|
C | A | 150 | a0002c0002t0001g0010a0002c0002t0001g0017a0002c0002t0001g0018others(147): Show | 150 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.64-19091G>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24689488 | ||||||
| chr10:24689697
|
C | T | 1 | a0013c0027t0001g0065 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.64-19300G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24689697 | ||||||
| chr10:24689758
|
C | G | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.64-19361G>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24689758 | ||||||
| chr10:24689841
|
TATATGTA others(27): Show |
T | 2 | a0002c0002t0001g0071a0019c0020t0001g0112 | 2 | HG01123.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.64-19478_64-19445d others(36): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24689841 | ||||||
| chr10:24689843
|
TATGTATA others(25): Show |
T | 138 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0164others(135): Show | 138 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.64-19478_64-19447d others(34): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24689843 | ||||||
| chr10:24689889
|
T | C | 2 | a0012c0010t0001g0266a0012c0010t0001g0267 | 2 | HG02109.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.64-19492A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24689889 | ||||||
| chr10:24689894
|
ATGTGTAT others(33): Show |
A | 10 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(7): Show | 10 | HG02129.hp2 HG02280.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.64-19537_64-19498d others(42): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24689894 | ||||||
| chr10:24689898
|
G | A | 16 | a0002c0002t0001g0018a0002c0002t0001g0073a0002c0002t0001g0074others(13): Show | 16 | HG02145.hp1 HG02559.hp2 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.64-19501C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24689898 | ||||||
| chr10:24689902
|
A | G | 16 | a0002c0002t0001g0018a0002c0002t0001g0073a0002c0002t0001g0074others(13): Show | 16 | HG02145.hp1 HG02559.hp2 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.64-19505T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24689902 | ||||||
| chr10:24689904
|
ATACATGT others(23): Show |
A | 16 | a0002c0002t0001g0018a0002c0002t0001g0073a0002c0002t0001g0074others(13): Show | 16 | HG02145.hp1 HG02559.hp2 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.64-19537_64-19508d others(32): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24689904 | ||||||
| chr10:24689933
|
T | A | 5 | a0005c0005t0001g0102a0005c0005t0001g0103a0005c0005t0001g0104others(2): Show | 5 | HG02055.hp1 HG02451.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-19536A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24689933 | ||||||
| chr10:24689942
|
G | A | 262 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(259): Show | 262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.64-19545C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24689942 | ||||||
| chr10:24689944
|
A | G | 262 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(259): Show | 262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.64-19547T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24689944 | ||||||
| chr10:24689946
|
A | G | 2 | a0001c0001t0001g0228a0011c0011t0001g0258 | 2 | HG02818.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.64-19549T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24689946 | ||||||
| chr10:24689946
|
ATG | A | 6 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(3): Show | 6 | HG00733.hp1 HG02280.hp1 HG02300.hp1 others(3): Show |
intron_variant | MODIFIER | c.64-19551_64-19550d others(4): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24689946 | ||||||
| chr10:24689946
|
ATGTG | A | 22 | a0002c0002t0001g0018a0002c0002t0001g0073a0002c0002t0001g0074others(19): Show | 22 | HG02129.hp2 HG02145.hp1 HG02523.hp2 others(19): Show |
intron_variant | MODIFIER | c.64-19553_64-19550d others(6): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24689946 | ||||||
| chr10:24689948
|
G | A | 264 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(261): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.64-19551C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24689948 | ||||||
| chr10:24689950
|
G | A | 2 | a0001c0001t0001g0228a0011c0011t0001g0258 | 2 | HG02818.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.64-19553C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24689950 | ||||||
| chr10:24689964
|
G | A | 177 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(174): Show | 177 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.64-19567C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24689964 | ||||||
| chr10:24690252
|
T | C | 2 | a0002c0002t0001g0150a0002c0002t0001g0151 | 2 | NA18941.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.64-19855A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24690252 | ||||||
| chr10:24690421
|
T | C | 2 | a0002c0002t0001g0109a0002c0002t0001g0110 | 2 | HG02148.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.64-20024A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24690421 | ||||||
| chr10:24690604
|
A | G | 293 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(290): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.64-20207T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24690604 | ||||||
| chr10:24690609
|
A | T | 2 | a0002c0002t0001g0130a0002c0002t0001g0131 | 2 | HG00323.hp2 HG00733.hp2 |
intron_variant | MODIFIER | c.64-20212T>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24690609 | ||||||
| chr10:24690705
|
G | A | 1 | a0006c0006t0002g0349 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.64-20308C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24690705 | ||||||
| chr10:24690827
|
C | CA | 9 | a0001c0001t0001g0171a0001c0001t0004g0296a0001c0001t0004g0297others(6): Show | 9 | HG01891.hp2 HG02818.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.64-20431dupT | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24690827 | ||||||
| chr10:24690827
|
CA | C | 146 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(143): Show | 146 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.64-20431delT | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24690827 | ||||||
| chr10:24690835
|
A | T | 1 | a0003c0003t0001g0247 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.64-20438T>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24690835 | ||||||
| chr10:24690837
|
A | AT | 6 | a0001c0001t0002g0303a0001c0001t0002g0304a0001c0001t0002g0305others(3): Show | 6 | HG01168.hp2 HG01928.hp2 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-20441_64-20440i others(3): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24690837 | ||||||
| chr10:24690837
|
A | T | 19 | a0001c0001t0001g0160a0001c0001t0001g0264a0001c0001t0001g0270others(16): Show | 19 | HG01261.hp2 HG01496.hp1 HG01516.hp2 others(16): Show |
intron_variant | MODIFIER | c.64-20440T>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24690837 | ||||||
| chr10:24690838
|
AT | A | 5 | a0002c0002t0001g0018a0002c0002t0001g0073a0002c0002t0001g0074others(2): Show | 5 | NA18957.hp2 NA18978.hp2 NA19058.hp1 others(2): Show |
intron_variant | MODIFIER | c.64-20442delA | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24690838 | ||||||
| chr10:24690839
|
T | A | 15 | a0001c0001t0001g0162a0001c0001t0001g0181a0001c0001t0001g0182others(12): Show | 15 | HG00639.hp2 HG01257.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.64-20442A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24690839 | ||||||
| chr10:24690841
|
T | A | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.64-20444A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24690841 | ||||||
| chr10:24690855
|
C | T | 2 | a0001c0001t0003g0154a0024c0026t0003g0156 | 2 | HG01081.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.64-20458G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24690855 | ||||||
| chr10:24690859
|
T | C | 1 | a0002c0002t0001g0126 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.64-20462A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24690859 | ||||||
| chr10:24691081
|
C | A | 3 | a0001c0001t0002g0337a0001c0001t0002g0338a0016c0022t0002g0339 | 3 | HG01109.hp1 NA18964.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.64-20684G>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24691081 | ||||||
| chr10:24691116
|
G | C | 1 | a0002c0002t0001g0281 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.64-20719C>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24691116 | ||||||
| chr10:24691154
|
T | C | 1 | a0001c0001t0001g0192 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.64-20757A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24691154 | ||||||
| chr10:24691235
|
C | T | 1 | a0001c0001t0002g0311 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.64-20838G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24691235 | ||||||
| chr10:24691335
|
A | G | 3 | a0003c0003t0001g0201a0003c0003t0001g0202a0003c0003t0001g0203 | 3 | HG01123.hp1 HG02004.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.64-20938T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24691335 | ||||||
| chr10:24691355
|
T | C | 2 | a0011c0011t0001g0258a0011c0011t0001g0259 | 2 | HG02818.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.64-20958A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24691355 | ||||||
| chr10:24691472
|
TA | T | 7 | a0002c0002t0001g0118a0002c0002t0001g0119a0002c0002t0001g0120others(4): Show | 7 | HG00438.hp2 HG00673.hp1 HG00735.hp1 others(4): Show |
intron_variant | MODIFIER | c.64-21076delT | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24691472 | ||||||
| chr10:24691563
|
G | A | 4 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(1): Show | 4 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.64-21166C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24691563 | ||||||
| chr10:24691655
|
T | G | 115 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(112): Show | 115 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.64-21258A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24691655 | ||||||
| chr10:24691739
|
TAAATGTT others(11): Show |
T | 5 | a0001c0001t0001g0171a0001c0001t0004g0296a0001c0001t0004g0297others(2): Show | 5 | HG01891.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-21360_64-21343d others(20): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24691739 | ||||||
| chr10:24692249
|
C | T | 2 | a0001c0001t0001g0142a0001c0001t0001g0143 | 2 | HG02451.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.64-21852G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24692249 | ||||||
| chr10:24692279
|
T | C | 1 | a0003c0003t0001g0180 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.64-21882A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24692279 | ||||||
| chr10:24692314
|
G | A | 1 | a0001c0001t0001g0264 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.64-21917C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24692314 | ||||||
| chr10:24692491
|
A | G | 7 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0164others(4): Show | 7 | HG02559.hp1 HG02572.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.64-22094T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24692491 | ||||||
| chr10:24692544
|
T | C | 4 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(1): Show | 4 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.64-22147A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24692544 | ||||||
| chr10:24692548
|
T | C | 4 | a0002c0002t0001g0020a0002c0002t0001g0138a0002c0002t0001g0139others(1): Show | 4 | HG02615.hp1 HG02922.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.64-22151A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24692548 | ||||||
| chr10:24692554
|
A | G | 1 | a0005c0005t0001g0284 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.64-22157T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24692554 | ||||||
| chr10:24692843
|
AT | A | 5 | a0001c0001t0001g0189a0001c0001t0001g0241a0001c0001t0001g0242others(2): Show | 5 | HG00140.hp1 HG00323.hp1 HG00741.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-22447delA | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24692843 | ||||||
| chr10:24692845
|
A | T | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.64-22448T>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24692845 | ||||||
| chr10:24692854
|
A | T | 2 | a0001c0001t0002g0319a0002c0030t0001g0022 | 2 | HG02071.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.64-22457T>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24692854 | ||||||
| chr10:24693047
|
T | C | 5 | a0005c0005t0001g0102a0005c0005t0001g0103a0005c0005t0001g0104others(2): Show | 5 | HG02055.hp1 HG02451.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-22650A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24693047 | ||||||
| chr10:24693125
|
C | T | 1 | a0011c0011t0001g0259 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.64-22728G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24693125 | ||||||
| chr10:24693126
|
G | A | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.64-22729C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24693126 | ||||||
| chr10:24693253
|
C | G | 1 | a0002c0002t0001g0278 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.64-22856G>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24693253 | ||||||
| chr10:24693278
|
C | T | 2 | a0010c0012t0010g0015a0010c0012t0010g0016 | 2 | HG02723.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.64-22881G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24693278 | ||||||
| chr10:24693317
|
C | T | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.64-22920G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24693317 | ||||||
| chr10:24693325
|
A | C | 270 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(267): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.64-22928T>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24693325 | ||||||
| chr10:24693338
|
C | CT | 10 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0164others(7): Show | 10 | HG02559.hp1 HG02572.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.64-22942dupA | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24693338 | ||||||
| chr10:24693454
|
A | G | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.64-23057T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24693454 | ||||||
| chr10:24693512
|
G | A | 2 | a0002c0002t0007g0007a0002c0002t0007g0008 | 2 | HG00280.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.64-23115C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24693512 | ||||||
| chr10:24693596
|
G | A | 52 | a0002c0002t0001g0018a0002c0002t0001g0021a0002c0002t0001g0027others(49): Show | 52 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(49): Show |
intron_variant | MODIFIER | c.64-23199C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24693596 | ||||||
| chr10:24693684
|
C | G | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.64-23287G>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24693684 | ||||||
| chr10:24693763
|
C | T | 7 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0164others(4): Show | 7 | HG02559.hp1 HG02572.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.64-23366G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24693763 | ||||||
| chr10:24693891
|
T | C | 1 | a0002c0002t0004g0295 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.64-23494A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24693891 | ||||||
| chr10:24693929
|
A | C | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.64-23532T>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24693929 | ||||||
| chr10:24694146
|
A | G | 21 | a0001c0001t0001g0232a0001c0001t0002g0302a0001c0001t0002g0310others(18): Show | 21 | HG00673.hp2 HG00733.hp1 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.64-23749T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24694146 | ||||||
| chr10:24694174
|
C | G | 3 | a0009c0008t0001g0261a0009c0008t0001g0262a0009c0008t0004g0347 | 3 | NA18941.hp2 NA18974.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.64-23777G>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24694174 | ||||||
| chr10:24694370
|
G | A | 8 | a0001c0001t0001g0197a0001c0001t0001g0224a0001c0001t0001g0225others(5): Show | 8 | HG00621.hp1 HG02040.hp1 NA18954.hp2 others(5): Show |
intron_variant | MODIFIER | c.64-23973C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24694370 | ||||||
| chr10:24694461
|
G | A | 6 | a0001c0001t0005g0001a0001c0001t0005g0005a0001c0001t0005g0006others(3): Show | 6 | HG01981.hp1 HG03927.hp2 NA18995.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-24064C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24694461 | ||||||
| chr10:24694612
|
C | T | 1 | a0002c0002t0001g0017 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.64-24215G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24694612 | ||||||
| chr10:24694649
|
C | A | 1 | a0002c0002t0001g0017 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.64-24252G>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24694649 | ||||||
| chr10:24694790
|
G | A | 1 | a0003c0003t0001g0236 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.64-24393C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24694790 | ||||||
| chr10:24694901
|
A | T | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.64-24504T>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24694901 | ||||||
| chr10:24695044
|
C | T | 1 | a0003c0003t0001g0198 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.64-24647G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24695044 | ||||||
| chr10:24695050
|
CAAAAA | C | 14 | a0001c0001t0002g0308a0001c0001t0002g0309a0001c0001t0002g0322others(11): Show | 14 | HG01081.hp1 HG01258.hp2 HG01928.hp2 others(11): Show |
intron_variant | MODIFIER | c.64-24658_64-24654d others(7): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24695050 | ||||||
| chr10:24695050
|
CAAAAAA | C | 14 | a0001c0001t0001g0232a0001c0001t0002g0303a0001c0001t0002g0304others(11): Show | 14 | HG01109.hp1 HG01168.hp2 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.64-24659_64-24654d others(8): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24695050 | ||||||
| chr10:24695050
|
CAAAAAAA | C | 10 | a0001c0001t0002g0302a0001c0001t0002g0311a0001c0001t0002g0317others(7): Show | 10 | HG00673.hp2 HG01169.hp1 HG02698.hp1 others(7): Show |
intron_variant | MODIFIER | c.64-24660_64-24654d others(9): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24695050 | ||||||
| chr10:24695050
|
CAAAAAAA others(3): Show |
C | 3 | a0001c0001t0001g0226a0001c0001t0001g0234a0012c0010t0001g0267 | 3 | HG02109.hp1 NA19065.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.64-24663_64-24654d others(12): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24695050 | ||||||
| chr10:24695050
|
CAAAAAAA others(4): Show |
C | 14 | a0001c0001t0001g0174a0001c0001t0001g0220a0001c0001t0001g0222others(11): Show | 14 | HG00621.hp1 HG01981.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.64-24664_64-24654d others(13): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24695050 | ||||||
| chr10:24695050
|
CAAAAAAA others(5): Show |
C | 19 | a0001c0001t0001g0197a0001c0001t0001g0217a0001c0001t0001g0219others(16): Show | 19 | HG00423.hp1 HG01069.hp2 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.64-24665_64-24654d others(14): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24695050 | ||||||
| chr10:24695050
|
CAAAAAAA others(6): Show |
C | 16 | a0001c0001t0001g0160a0001c0001t0001g0170a0001c0001t0001g0199others(13): Show | 16 | HG00408.hp2 HG01952.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.64-24666_64-24654d others(15): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24695050 | ||||||
| chr10:24695050
|
CAAAAAAA others(7): Show |
C | 1 | a0003c0003t0001g0230 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.64-24667_64-24654d others(16): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24695050 | ||||||
| chr10:24695050
|
CAAAAAAA others(8): Show |
C | 7 | a0001c0001t0001g0244a0007c0007t0006g0292a0007c0007t0015g0288others(4): Show | 7 | HG02818.hp2 HG03486.hp2 HG04228.hp1 others(4): Show |
intron_variant | MODIFIER | c.64-24668_64-24654d others(17): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24695050 | ||||||
| chr10:24695050
|
CAAAAAAA others(9): Show |
C | 4 | a0001c0001t0001g0171a0001c0014t0004g0286a0005c0005t0004g0287others(1): Show | 4 | HG01891.hp2 HG02523.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.64-24669_64-24654d others(18): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24695050 | ||||||
| chr10:24695050
|
CAAAAAAA others(10): Show |
C | 4 | a0001c0001t0002g0310a0001c0001t0004g0297a0001c0001t0004g0298others(1): Show | 4 | HG02895.hp1 HG02897.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.64-24670_64-24654d others(19): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24695050 | ||||||
| chr10:24695050
|
CAAAAAAA others(12): Show |
C | 2 | a0001c0001t0002g0337a0001c0001t0002g0338 | 2 | NA18964.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.64-24672_64-24654d others(21): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24695050 | ||||||
| chr10:24695050
|
CAAAAAAA others(13): Show |
C | 1 | a0001c0001t0002g0300 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.64-24673_64-24654d others(22): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24695050 | ||||||
| chr10:24695050
|
CAAAAAAA others(14): Show |
C | 7 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0164others(4): Show | 7 | HG02559.hp1 HG02572.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.64-24674_64-24654d others(23): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24695050 | ||||||
| chr10:24695050
|
CAAAAAAA others(16): Show |
C | 1 | a0003c0003t0001g0210 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.64-24676_64-24654d others(25): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24695050 | ||||||
| chr10:24695050
|
CAAAAAAA others(17): Show |
C | 20 | a0001c0001t0001g0177a0001c0001t0001g0190a0001c0001t0004g0296others(17): Show | 20 | HG00609.hp1 HG01123.hp1 HG02004.hp1 others(17): Show |
intron_variant | MODIFIER | c.64-24677_64-24654d others(26): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24695050 | ||||||
| chr10:24695050
|
CAAAAAAA others(18): Show |
C | 36 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(33): Show | 36 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(33): Show |
intron_variant | MODIFIER | c.64-24678_64-24654d others(27): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24695050 | ||||||
| chr10:24695050
|
CAAAAAAA others(22): Show |
C | 3 | a0002c0002t0001g0082a0002c0002t0001g0123a0002c0002t0001g0152 | 3 | HG00099.hp2 HG01099.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.64-24682_64-24654d others(31): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24695050 | ||||||
| chr10:24695050
|
CAAAAAAA others(23): Show |
C | 158 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(155): Show | 158 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.64-24683_64-24654d others(32): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24695050 | ||||||
| chr10:24695050
|
CAAAAAAA others(24): Show |
C | 1 | a0001c0001t0001g0144 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.64-24684_64-24654d others(33): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24695050 | ||||||
| chr10:24695098
|
G | A | 2 | a0001c0001t0001g0274a0002c0002t0001g0256 | 2 | HG00423.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.64-24701C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24695098 | ||||||
| chr10:24695335
|
G | A | 2 | a0011c0011t0001g0258a0011c0011t0001g0259 | 2 | HG02818.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.64-24938C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24695335 | ||||||
| chr10:24695398
|
G | A | 6 | a0001c0001t0001g0270a0001c0001t0001g0271a0001c0001t0001g0272others(3): Show | 6 | HG00423.hp2 NA18943.hp2 NA18964.hp1 others(3): Show |
intron_variant | MODIFIER | c.64-25001C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24695398 | ||||||
| chr10:24695405
|
C | A | 1 | a0005c0005t0001g0137 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.64-25008G>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24695405 | ||||||
| chr10:24695477
|
G | A | 1 | a0001c0001t0002g0317 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.64-25080C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24695477 | ||||||
| chr10:24695564
|
G | A | 1 | a0001c0001t0002g0318 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.64-25167C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24695564 | ||||||
| chr10:24695566
|
C | CA | 87 | a0001c0001t0001g0144a0001c0001t0002g0319a0001c0001t0002g0340others(84): Show | 87 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.64-25170dupT | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24695566 | ||||||
| chr10:24695566
|
C | CAAA | 7 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0164others(4): Show | 7 | HG02559.hp1 HG02572.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.64-25172_64-25170d others(5): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24695566 | ||||||
| chr10:24695585
|
T | C | 3 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143 | 3 | HG02280.hp1 HG02451.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.64-25188A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24695585 | ||||||
| chr10:24695962
|
T | C | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.64-25565A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24695962 | ||||||
| chr10:24696061
|
T | A | 1 | a0001c0001t0002g0340 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.64-25664A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24696061 | ||||||
| chr10:24696063
|
T | G | 1 | a0001c0001t0002g0340 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.64-25666A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24696063 | ||||||
| chr10:24696066
|
C | G | 1 | a0001c0001t0002g0340 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.64-25669G>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24696066 | ||||||
| chr10:24696068
|
C | G | 274 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(271): Show | 274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.64-25671G>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24696068 | ||||||
| chr10:24696068
|
C | T | 1 | a0001c0001t0002g0340 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.64-25671G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24696068 | ||||||
| chr10:24696069
|
C | G | 1 | a0001c0001t0002g0340 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.64-25672G>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24696069 | ||||||
| chr10:24696070
|
A | T | 1 | a0001c0001t0002g0340 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.64-25673T>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24696070 | ||||||
| chr10:24696071
|
A | T | 1 | a0001c0001t0002g0340 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.64-25674T>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24696071 | ||||||
| chr10:24696237
|
G | A | 10 | a0002c0002t0001g0010a0002c0002t0001g0019a0002c0002t0001g0113others(7): Show | 10 | HG01496.hp1 HG01516.hp2 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.63+25600C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24696237 | ||||||
| chr10:24696277
|
T | C | 1 | a0005c0005t0001g0104 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.63+25560A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24696277 | ||||||
| chr10:24696426
|
G | C | 5 | a0002c0002t0001g0010a0002c0002t0001g0113a0002c0002t0001g0114others(2): Show | 5 | HG02027.hp2 HG02074.hp1 NA18995.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+25411C>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24696426 | ||||||
| chr10:24696472
|
A | T | 1 | a0001c0001t0001g0174 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.63+25365T>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24696472 | ||||||
| chr10:24696511
|
C | T | 1 | a0001c0001t0008g0306 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.63+25326G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24696511 | ||||||
| chr10:24696764
|
G | A | 103 | a0001c0001t0001g0144a0002c0002t0001g0018a0002c0002t0001g0020others(100): Show | 103 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.63+25073C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24696764 | ||||||
| chr10:24696861
|
C | T | 1 | a0002c0002t0001g0034 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.63+24976G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24696861 | ||||||
| chr10:24696974
|
T | A | 3 | a0008c0009t0005g0002a0008c0009t0005g0003a0008c0009t0005g0004 | 3 | NA18995.hp2 NA19004.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.63+24863A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24696974 | ||||||
| chr10:24697210
|
C | T | 13 | a0001c0001t0002g0303a0001c0001t0002g0304a0001c0001t0002g0305others(10): Show | 13 | HG01168.hp2 HG01928.hp2 HG01975.hp2 others(10): Show |
intron_variant | MODIFIER | c.63+24627G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24697210 | ||||||
| chr10:24697217
|
A | G | 282 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(279): Show | 282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.63+24620T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24697217 | ||||||
| chr10:24697455
|
C | G | 1 | a0002c0002t0001g0117 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.63+24382G>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24697455 | ||||||
| chr10:24697457
|
T | C | 282 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(279): Show | 282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.63+24380A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24697457 | ||||||
| chr10:24697673
|
A | G | 1 | a0001c0001t0001g0143 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.63+24164T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24697673 | ||||||
| chr10:24697768
|
G | A | 5 | a0001c0001t0001g0171a0001c0001t0004g0296a0001c0001t0004g0297others(2): Show | 5 | HG01891.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.63+24069C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24697768 | ||||||
| chr10:24697833
|
C | T | 1 | a0002c0002t0001g0064 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.63+24004G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24697833 | ||||||
| chr10:24697834
|
T | C | 1 | a0002c0002t0001g0064 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.63+24003A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24697834 | ||||||
| chr10:24697839
|
G | A | 5 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(2): Show | 5 | HG02129.hp2 HG02523.hp2 NA18989.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+23998C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24697839 | ||||||
| chr10:24697949
|
T | C | 1 | a0002c0002t0001g0063 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.63+23888A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24697949 | ||||||
| chr10:24698001
|
T | C | 4 | a0002c0002t0001g0010a0002c0002t0001g0113a0002c0002t0001g0114others(1): Show | 4 | HG02074.hp1 NA18995.hp1 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+23836A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24698001 | ||||||
| chr10:24698213
|
C | T | 3 | a0002c0002t0001g0107a0002c0002t0001g0108a0002c0002t0001g0111 | 3 | HG02258.hp1 HG02630.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.63+23624G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24698213 | ||||||
| chr10:24698483
|
A | G | 2 | a0001c0001t0001g0142a0001c0001t0001g0143 | 2 | HG02451.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.63+23354T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24698483 | ||||||
| chr10:24698738
|
T | C | 1 | a0002c0021t0001g0084 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.63+23099A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24698738 | ||||||
| chr10:24698783
|
A | G | 3 | a0002c0002t0001g0064a0002c0002t0001g0096a0002c0002t0001g0145 | 3 | NA18988.hp2 NA18992.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.63+23054T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24698783 | ||||||
| chr10:24699336
|
A | T | 2 | a0001c0001t0001g0233a0001c0001t0001g0234 | 2 | NA18970.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.63+22501T>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24699336 | ||||||
| chr10:24699339
|
T | A | 2 | a0001c0001t0002g0300a0009c0008t0001g0262 | 2 | NA18974.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.63+22498A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24699339 | ||||||
| chr10:24699388
|
G | A | 4 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(1): Show | 4 | HG02280.hp1 HG02451.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+22449C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24699388 | ||||||
| chr10:24699580
|
C | A | 2 | a0010c0012t0010g0015a0010c0012t0010g0016 | 2 | HG02723.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.63+22257G>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24699580 | ||||||
| chr10:24699802
|
G | A | 1 | a0001c0001t0001g0169 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.63+22035C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24699802 | ||||||
| chr10:24700203
|
G | A | 6 | a0001c0001t0005g0001a0001c0001t0005g0005a0001c0001t0005g0006others(3): Show | 6 | HG01981.hp1 HG03927.hp2 NA18995.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+21634C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24700203 | ||||||
| chr10:24700516
|
G | A | 1 | a0002c0002t0004g0295 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.63+21321C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24700516 | ||||||
| chr10:24700522
|
G | A | 5 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(2): Show | 5 | HG02129.hp2 HG02523.hp2 NA18989.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+21315C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24700522 | ||||||
| chr10:24700589
|
G | A | 1 | a0005c0005t0001g0104 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.63+21248C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24700589 | ||||||
| chr10:24700742
|
A | C | 2 | a0003c0003t0001g0200a0003c0003t0001g0248 | 2 | NA18959.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.63+21095T>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24700742 | ||||||
| chr10:24700756
|
T | A | 5 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(2): Show | 5 | HG02129.hp2 HG02523.hp2 NA18989.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+21081A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24700756 | ||||||
| chr10:24700954
|
T | A | 1 | a0002c0002t0001g0132 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.63+20883A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24700954 | ||||||
| chr10:24701183
|
A | T | 4 | a0001c0001t0001g0171a0001c0001t0004g0296a0001c0001t0004g0297others(1): Show | 4 | HG01891.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+20654T>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24701183 | ||||||
| chr10:24701240
|
G | A | 1 | a0002c0002t0001g0071 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.63+20597C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24701240 | ||||||
| chr10:24701413
|
T | C | 1 | a0005c0005t0001g0137 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.63+20424A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24701413 | ||||||
| chr10:24701505
|
G | A | 1 | a0005c0005t0001g0137 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.63+20332C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24701505 | ||||||
| chr10:24701610
|
T | A | 1 | a0001c0001t0001g0228 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.63+20227A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24701610 | ||||||
| chr10:24701840
|
T | C | 1 | a0002c0002t0001g0110 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.63+19997A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24701840 | ||||||
| chr10:24702126
|
TC | T | 7 | a0002c0002t0001g0010a0002c0002t0001g0113a0002c0002t0001g0114others(4): Show | 7 | HG02027.hp2 HG02074.hp1 NA18953.hp2 others(4): Show |
intron_variant | MODIFIER | c.63+19710delG | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24702126 | ||||||
| chr10:24702127
|
C | CT | 24 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(21): Show | 24 | HG00733.hp2 HG01496.hp1 HG01517.hp2 others(21): Show |
intron_variant | MODIFIER | c.63+19709dupA | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24702127 | ||||||
| chr10:24702127
|
C | CTT | 219 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(216): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.63+19708_63+19709d others(4): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24702127 | ||||||
| chr10:24702127
|
C | CTTT | 20 | a0001c0001t0001g0176a0001c0001t0001g0178a0001c0001t0001g0191others(17): Show | 20 | HG00438.hp1 HG00621.hp2 HG01175.hp2 others(17): Show |
intron_variant | MODIFIER | c.63+19707_63+19709d others(5): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24702127 | ||||||
| chr10:24702127
|
C | T | 1 | a0002c0002t0014g0105 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.63+19710G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24702127 | ||||||
| chr10:24702127
|
CT | C | 11 | a0001c0001t0001g0171a0001c0001t0002g0320a0001c0001t0004g0296others(8): Show | 11 | HG01891.hp2 HG02129.hp2 HG02523.hp2 others(8): Show |
intron_variant | MODIFIER | c.63+19709delA | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24702127 | ||||||
| chr10:24702127
|
CTTTTT | C | 13 | a0002c0002t0001g0071a0002c0002t0001g0088a0002c0002t0001g0136others(10): Show | 13 | HG00642.hp2 HG01123.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.63+19705_63+19709d others(7): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24702127 | ||||||
| chr10:24702223
|
C | T | 5 | a0001c0001t0001g0171a0001c0001t0004g0296a0001c0001t0004g0297others(2): Show | 5 | HG01891.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.63+19614G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24702223 | ||||||
| chr10:24702278
|
C | T | 3 | a0002c0002t0007g0007a0002c0002t0007g0008a0002c0002t0007g0009 | 3 | HG00280.hp1 HG03017.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.63+19559G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24702278 | ||||||
| chr10:24702297
|
A | AT | 7 | a0001c0001t0001g0171a0001c0001t0004g0296a0001c0001t0004g0297others(4): Show | 7 | HG01891.hp2 HG02895.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.63+19539dupA | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24702297 | ||||||
| chr10:24702477
|
T | C | 115 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(112): Show | 115 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.63+19360A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24702477 | ||||||
| chr10:24702583
|
G | A | 1 | a0002c0002t0001g0072 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.63+19254C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24702583 | ||||||
| chr10:24702955
|
A | C | 1 | a0001c0001t0005g0005 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.63+18882T>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24702955 | ||||||
| chr10:24702980
|
T | TAC | 5 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(2): Show | 5 | HG02129.hp2 HG02523.hp2 NA18989.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+18855_63+18856d others(4): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24702980 | ||||||
| chr10:24703091
|
A | G | 1 | a0001c0001t0001g0197 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.63+18746T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24703091 | ||||||
| chr10:24703408
|
G | A | 4 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(1): Show | 4 | HG02145.hp2 HG02965.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+18429C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24703408 | ||||||
| chr10:24703960
|
T | C | 5 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(2): Show | 5 | HG02129.hp2 HG02523.hp2 NA18989.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+17877A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24703960 | ||||||
| chr10:24703994
|
G | A | 1 | a0002c0002t0004g0295 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.63+17843C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24703994 | ||||||
| chr10:24704069
|
C | T | 1 | a0001c0001t0001g0252 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.63+17768G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24704069 | ||||||
| chr10:24704193
|
G | C | 5 | a0002c0002t0001g0018a0002c0002t0001g0073a0002c0002t0001g0074others(2): Show | 5 | NA18957.hp2 NA18978.hp2 NA19058.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+17644C>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24704193 | ||||||
| chr10:24704217
|
T | A | 1 | a0003c0003t0001g0230 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.63+17620A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24704217 | ||||||
| chr10:24704289
|
C | CT | 29 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(26): Show | 29 | HG00621.hp2 HG00735.hp1 HG01169.hp1 others(26): Show |
intron_variant | MODIFIER | c.63+17547dupA | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24704289 | ||||||
| chr10:24704289
|
CT | C | 9 | a0001c0001t0001g0196a0001c0001t0002g0302a0001c0001t0002g0321others(6): Show | 9 | HG01517.hp1 HG02109.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.63+17547delA | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24704289 | ||||||
| chr10:24704294
|
T | C | 1 | a0002c0002t0001g0111 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.63+17543A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24704294 | ||||||
| chr10:24704416
|
G | A | 3 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195 | 3 | HG02280.hp2 HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.63+17421C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24704416 | ||||||
| chr10:24704465
|
A | AT | 333 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(330): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.63+17371dupA | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24704465 | ||||||
| chr10:24704683
|
G | A | 1 | a0002c0002t0001g0077 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.63+17154C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24704683 | ||||||
| chr10:24704796
|
G | T | 1 | a0002c0002t0001g0106 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.63+17041C>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24704796 | ||||||
| chr10:24704913
|
G | C | 1 | a0023c0025t0003g0029 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.63+16924C>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24704913 | ||||||
| chr10:24704993
|
G | C | 1 | a0005c0005t0001g0137 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.63+16844C>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24704993 | ||||||
| chr10:24705226
|
G | A | 6 | a0002c0002t0001g0078a0002c0002t0001g0079a0002c0002t0001g0080others(3): Show | 6 | HG00741.hp1 HG01361.hp1 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+16611C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24705226 | ||||||
| chr10:24705380
|
G | A | 1 | a0002c0002t0001g0083 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.63+16457C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24705380 | ||||||
| chr10:24705651
|
C | T | 1 | a0001c0001t0003g0155 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.63+16186G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24705651 | ||||||
| chr10:24705862
|
CAAT | C | 5 | a0001c0001t0016g0352a0006c0006t0002g0348a0006c0006t0002g0349others(2): Show | 5 | NA18957.hp1 NA18989.hp2 NA18992.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+15972_63+15974d others(5): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24705862 | ||||||
| chr10:24705998
|
A | C | 1 | a0002c0002t0004g0295 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.63+15839T>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24705998 | ||||||
| chr10:24706220
|
T | C | 1 | a0002c0002t0004g0295 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.63+15617A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24706220 | ||||||
| chr10:24706309
|
T | A | 2 | a0011c0011t0001g0258a0011c0011t0001g0259 | 2 | HG02818.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.63+15528A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24706309 | ||||||
| chr10:24706423
|
T | G | 3 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0255 | 3 | HG02622.hp1 HG02970.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.63+15414A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24706423 | ||||||
| chr10:24706512
|
C | G | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+15325G>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24706512 | ||||||
| chr10:24706655
|
G | A | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+15182C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24706655 | ||||||
| chr10:24706706
|
C | G | 1 | a0003c0003t0001g0173 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.63+15131G>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24706706 | ||||||
| chr10:24706728
|
T | C | 1 | a0005c0005t0001g0284 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.63+15109A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24706728 | ||||||
| chr10:24706769
|
C | T | 2 | a0001c0014t0004g0286a0005c0005t0004g0287 | 2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.63+15068G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24706769 | ||||||
| chr10:24706834
|
T | G | 4 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(1): Show | 4 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+15003A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24706834 | ||||||
| chr10:24707044
|
G | A | 2 | a0002c0002t0001g0125a0019c0020t0001g0112 | 2 | HG01261.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.63+14793C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24707044 | ||||||
| chr10:24707286
|
C | T | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+14551G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24707286 | ||||||
| chr10:24707291
|
A | C | 1 | a0001c0001t0002g0304 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.63+14546T>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24707291 | ||||||
| chr10:24707504
|
C | T | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+14333G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24707504 | ||||||
| chr10:24707596
|
T | C | 3 | a0001c0001t0002g0337a0001c0001t0002g0338a0016c0022t0002g0339 | 3 | HG01109.hp1 NA18964.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.63+14241A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24707596 | ||||||
| chr10:24707781
|
C | T | 148 | a0002c0002t0001g0010a0002c0002t0001g0017a0002c0002t0001g0018others(145): Show | 148 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.63+14056G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24707781 | ||||||
| chr10:24707902
|
A | G | 281 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(278): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.63+13935T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24707902 | ||||||
| chr10:24707991
|
C | CA | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+13845dupT | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24707991 | ||||||
| chr10:24708008
|
G | A | 1 | a0001c0001t0002g0294 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.63+13829C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24708008 | ||||||
| chr10:24708159
|
G | A | 2 | a0010c0012t0010g0015a0010c0012t0010g0016 | 2 | HG02723.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.63+13678C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24708159 | ||||||
| chr10:24708504
|
T | C | 287 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(284): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.63+13333A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24708504 | ||||||
| chr10:24708513
|
G | A | 1 | a0002c0021t0001g0084 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.63+13324C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24708513 | ||||||
| chr10:24708701
|
G | T | 1 | a0002c0002t0014g0105 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.63+13136C>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24708701 | ||||||
| chr10:24708771
|
T | C | 269 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(266): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.63+13066A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24708771 | ||||||
| chr10:24708854
|
G | C | 4 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(1): Show | 4 | HG02280.hp1 HG02451.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+12983C>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24708854 | ||||||
| chr10:24708938
|
T | C | 1 | a0002c0002t0004g0295 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.63+12899A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24708938 | ||||||
| chr10:24709012
|
T | C | 1 | a0007c0007t0006g0292 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.63+12825A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24709012 | ||||||
| chr10:24709032
|
A | G | 38 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(35): Show | 38 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(35): Show |
intron_variant | MODIFIER | c.63+12805T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24709032 | ||||||
| chr10:24709104
|
C | T | 3 | a0004c0004t0001g0031a0004c0004t0001g0032a0014c0024t0011g0033 | 3 | HG02647.hp1 HG02970.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.63+12733G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24709104 | ||||||
| chr10:24709721
|
A | C | 1 | a0001c0001t0001g0255 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.63+12116T>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24709721 | ||||||
| chr10:24709738
|
TA | T | 27 | a0001c0001t0001g0192a0001c0001t0002g0303a0002c0002t0001g0017others(24): Show | 27 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(24): Show |
intron_variant | MODIFIER | c.63+12098delT | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24709738 | ||||||
| chr10:24709770
|
CACAACA | C | 61 | a0001c0001t0001g0160a0001c0001t0001g0174a0001c0001t0001g0197others(58): Show | 61 | HG00408.hp2 HG00423.hp1 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.63+12061_63+12066d others(8): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24709770 | ||||||
| chr10:24709871
|
C | A | 167 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(164): Show | 167 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.63+11966G>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24709871 | ||||||
| chr10:24710102
|
C | T | 1 | a0001c0001t0001g0197 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.63+11735G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24710102 | ||||||
| chr10:24710182
|
C | T | 2 | a0001c0001t0001g0142a0001c0001t0001g0143 | 2 | HG02451.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.63+11655G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24710182 | ||||||
| chr10:24710532
|
C | T | 150 | a0002c0002t0001g0010a0002c0002t0001g0017a0002c0002t0001g0018others(147): Show | 150 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.63+11305G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24710532 | ||||||
| chr10:24710597
|
C | CT | 294 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(291): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.63+11239_63+11240i others(3): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24710597 | ||||||
| chr10:24710664
|
G | A | 40 | a0002c0002t0001g0010a0002c0002t0001g0017a0002c0002t0001g0019others(37): Show | 40 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.63+11173C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24710664 | ||||||
| chr10:24710739
|
T | G | 270 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(267): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.63+11098A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24710739 | ||||||
| chr10:24710824
|
G | A | 1 | a0001c0001t0001g0275 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.63+11013C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24710824 | ||||||
| chr10:24710888
|
G | C | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+10949C>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24710888 | ||||||
| chr10:24710993
|
C | T | 1 | a0002c0002t0001g0145 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.63+10844G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24710993 | ||||||
| chr10:24711034
|
C | G | 1 | a0002c0002t0004g0295 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.63+10803G>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24711034 | ||||||
| chr10:24711050
|
C | T | 1 | a0001c0001t0001g0187 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.63+10787G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24711050 | ||||||
| chr10:24711093
|
CA | C | 204 | a0001c0001t0001g0171a0001c0001t0001g0181a0001c0001t0001g0182others(201): Show | 204 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.63+10743delT | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24711093 | ||||||
| chr10:24711113
|
A | AGG | 7 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0164others(4): Show | 7 | HG02559.hp1 HG02572.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.63+10723_63+10724i others(4): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24711113 | ||||||
| chr10:24711114
|
A | G | 7 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0164others(4): Show | 7 | HG02559.hp1 HG02572.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.63+10723T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24711114 | ||||||
| chr10:24711116
|
G | A | 7 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0164others(4): Show | 7 | HG02559.hp1 HG02572.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.63+10721C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24711116 | ||||||
| chr10:24711168
|
AAGAAAGA others(1): Show |
A | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+10661_63+10668d others(10): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24711168 | ||||||
| chr10:24711231
|
A | G | 1 | a0001c0001t0001g0252 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.63+10606T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24711231 | ||||||
| chr10:24711269
|
T | C | 5 | a0005c0005t0001g0102a0005c0005t0001g0103a0005c0005t0001g0104others(2): Show | 5 | HG02055.hp1 HG02451.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.63+10568A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24711269 | ||||||
| chr10:24711411
|
T | C | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+10426A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24711411 | ||||||
| chr10:24711460
|
G | A | 1 | a0001c0001t0001g0142 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.63+10377C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24711460 | ||||||
| chr10:24711840
|
C | A | 6 | a0001c0001t0002g0328a0001c0001t0002g0329a0001c0001t0002g0330others(3): Show | 6 | NA18945.hp2 NA18961.hp1 NA18998.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+9997G>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24711840 | ||||||
| chr10:24711910
|
G | A | 2 | a0002c0002t0001g0128a0002c0002t0001g0129 | 2 | HG01175.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.63+9927C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24711910 | ||||||
| chr10:24711999
|
C | G | 3 | a0002c0002t0001g0280a0002c0002t0001g0281a0002c0002t0001g0282 | 3 | NA18953.hp2 NA18980.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.63+9838G>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24711999 | ||||||
| chr10:24712103
|
A | T | 3 | a0002c0002t0001g0027a0021c0016t0003g0028a0023c0025t0003g0029 | 3 | HG01433.hp1 HG02004.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.63+9734T>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24712103 | ||||||
| chr10:24712151
|
A | C | 7 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0164others(4): Show | 7 | HG02559.hp1 HG02572.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.63+9686T>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24712151 | ||||||
| chr10:24712153
|
T | A | 1 | a0001c0001t0002g0294 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.63+9684A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24712153 | ||||||
| chr10:24712218
|
G | A | 149 | a0001c0001t0001g0144a0002c0002t0001g0010a0002c0002t0001g0017others(146): Show | 149 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.63+9619C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24712218 | ||||||
| chr10:24712269
|
G | T | 1 | a0002c0002t0001g0024 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.63+9568C>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24712269 | ||||||
| chr10:24712295
|
C | A | 1 | a0002c0002t0001g0153 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.63+9542G>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24712295 | ||||||
| chr10:24712299
|
G | A | 177 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(174): Show | 177 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.63+9538C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24712299 | ||||||
| chr10:24712492
|
G | A | 1 | a0002c0002t0001g0101 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.63+9345C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24712492 | ||||||
| chr10:24712579
|
C | G | 2 | a0001c0001t0001g0184a0001c0001t0001g0185 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.63+9258G>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24712579 | ||||||
| chr10:24712980
|
T | TA | 20 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(17): Show | 20 | HG01891.hp2 HG01981.hp2 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.63+8856dupT | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24712980 | ||||||
| chr10:24713007
|
C | A | 2 | a0001c0001t0001g0196a0001c0001t0001g0246 | 2 | HG03239.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.63+8830G>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24713007 | ||||||
| chr10:24713169
|
T | C | 2 | a0001c0014t0004g0286a0005c0005t0004g0287 | 2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.63+8668A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24713169 | ||||||
| chr10:24713199
|
G | C | 1 | a0005c0005t0001g0104 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.63+8638C>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24713199 | ||||||
| chr10:24713221
|
A | G | 269 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(266): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.63+8616T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24713221 | ||||||
| chr10:24713335
|
G | A | 2 | a0001c0001t0001g0170a0001c0001t0001g0178 | 2 | HG03654.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.63+8502C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24713335 | ||||||
| chr10:24713428
|
T | C | 7 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0164others(4): Show | 7 | HG02559.hp1 HG02572.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.63+8409A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24713428 | ||||||
| chr10:24713638
|
CT | C | 6 | a0001c0001t0001g0245a0001c0001t0002g0334a0001c0001t0002g0335others(3): Show | 6 | HG00323.hp1 HG01169.hp1 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+8198delA | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24713638 | ||||||
| chr10:24713797
|
G | A | 1 | a0002c0002t0001g0092 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.63+8040C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24713797 | ||||||
| chr10:24713889
|
T | C | 7 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0164others(4): Show | 7 | HG02559.hp1 HG02572.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.63+7948A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24713889 | ||||||
| chr10:24713942
|
C | A | 1 | a0001c0001t0002g0336 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.63+7895G>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24713942 | ||||||
| chr10:24714228
|
C | G | 1 | a0003c0003t0001g0236 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.63+7609G>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24714228 | ||||||
| chr10:24714431
|
G | C | 2 | a0010c0012t0010g0015a0010c0012t0010g0016 | 2 | HG02723.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.63+7406C>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24714431 | ||||||
| chr10:24714604
|
G | A | 1 | a0002c0002t0001g0093 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.63+7233C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24714604 | ||||||
| chr10:24714772
|
C | T | 1 | a0002c0002t0004g0295 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.63+7065G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24714772 | ||||||
| chr10:24714818
|
A | G | 1 | a0001c0001t0001g0252 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.63+7019T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24714818 | ||||||
| chr10:24714862
|
C | G | 7 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0164others(4): Show | 7 | HG02559.hp1 HG02572.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.63+6975G>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24714862 | ||||||
| chr10:24714949
|
G | A | 3 | a0001c0001t0002g0337a0001c0001t0002g0338a0016c0022t0002g0339 | 3 | HG01109.hp1 NA18964.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.63+6888C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24714949 | ||||||
| chr10:24714955
|
G | A | 1 | a0001c0014t0004g0286 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.63+6882C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24714955 | ||||||
| chr10:24714969
|
T | G | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+6868A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24714969 | ||||||
| chr10:24715007
|
G | A | 3 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143 | 3 | HG02280.hp1 HG02451.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.63+6830C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24715007 | ||||||
| chr10:24715029
|
C | CA | 284 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(281): Show | 284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.63+6807dupT | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24715029 | ||||||
| chr10:24715029
|
C | CAA | 10 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(7): Show | 10 | HG02129.hp2 HG02280.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.63+6806_63+6807dup others(2): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24715029 | ||||||
| chr10:24715088
|
T | C | 1 | a0001c0001t0016g0352 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.63+6749A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24715088 | ||||||
| chr10:24715137
|
C | G | 9 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(6): Show | 9 | HG02129.hp2 HG02280.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.63+6700G>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24715137 | ||||||
| chr10:24715235
|
A | G | 3 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143 | 3 | HG02280.hp1 HG02451.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.63+6602T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24715235 | ||||||
| chr10:24715375
|
G | A | 5 | a0001c0001t0001g0171a0001c0001t0004g0296a0001c0001t0004g0297others(2): Show | 5 | HG01891.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.63+6462C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24715375 | ||||||
| chr10:24715511
|
T | C | 1 | a0003c0003t0001g0247 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.63+6326A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24715511 | ||||||
| chr10:24715512
|
G | A | 140 | a0002c0002t0001g0010a0002c0002t0001g0017a0002c0002t0001g0018others(137): Show | 140 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.63+6325C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24715512 | ||||||
| chr10:24715541
|
A | T | 3 | a0002c0002t0001g0024a0002c0002t0001g0025a0002c0002t0001g0026 | 3 | HG00621.hp2 HG02165.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.63+6296T>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24715541 | ||||||
| chr10:24715547
|
T | A | 5 | a0001c0001t0001g0170a0001c0001t0001g0176a0001c0001t0001g0177others(2): Show | 5 | HG01261.hp1 HG02486.hp2 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+6290A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24715547 | ||||||
| chr10:24715573
|
T | C | 4 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234others(1): Show | 4 | NA18970.hp1 NA18975.hp1 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+6264A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24715573 | ||||||
| chr10:24715733
|
C | T | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+6104G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24715733 | ||||||
| chr10:24715749
|
T | C | 1 | a0001c0001t0001g0171 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.63+6088A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24715749 | ||||||
| chr10:24715767
|
G | A | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+6070C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24715767 | ||||||
| chr10:24715782
|
T | C | 294 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(291): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.63+6055A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24715782 | ||||||
| chr10:24715958
|
C | G | 10 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(7): Show | 10 | HG02129.hp2 HG02280.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.63+5879G>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24715958 | ||||||
| chr10:24716000
|
C | T | 3 | a0001c0014t0004g0286a0002c0002t0001g0023a0005c0005t0004g0287 | 3 | HG03209.hp1 NA18906.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.63+5837G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24716000 | ||||||
| chr10:24716208
|
G | A | 1 | a0002c0002t0004g0295 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.63+5629C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24716208 | ||||||
| chr10:24716254
|
C | A | 1 | a0002c0002t0001g0021 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.63+5583G>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24716254 | ||||||
| chr10:24716693
|
T | C | 3 | a0001c0001t0002g0300a0001c0001t0002g0340a0001c0001t0002g0341 | 3 | HG01169.hp1 HG01934.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.63+5144A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24716693 | ||||||
| chr10:24716772
|
A | G | 5 | a0005c0005t0001g0102a0005c0005t0001g0103a0005c0005t0001g0104others(2): Show | 5 | HG02055.hp1 HG02451.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.63+5065T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24716772 | ||||||
| chr10:24716980
|
T | C | 1 | a0002c0002t0001g0094 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.63+4857A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24716980 | ||||||
| chr10:24717003
|
C | T | 101 | a0002c0002t0001g0018a0002c0002t0001g0020a0002c0002t0001g0021others(98): Show | 101 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.63+4834G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24717003 | ||||||
| chr10:24717035
|
T | C | 287 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(284): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.63+4802A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24717035 | ||||||
| chr10:24717205
|
A | G | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+4632T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24717205 | ||||||
| chr10:24717221
|
G | A | 1 | a0003c0003t0001g0236 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.63+4616C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24717221 | ||||||
| chr10:24717300
|
T | C | 1 | a0003c0003t0001g0276 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.63+4537A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24717300 | ||||||
| chr10:24717418
|
T | A | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+4419A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24717418 | ||||||
| chr10:24717573
|
AG | A | 3 | a0002c0002t0001g0113a0002c0002t0001g0114a0002c0002t0001g0115 | 3 | NA18995.hp1 NA19065.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.63+4263delC | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24717573 | ||||||
| chr10:24717618
|
A | G | 294 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(291): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.63+4219T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24717618 | ||||||
| chr10:24717772
|
TCAGCTGG others(4): Show |
T | 2 | a0011c0011t0001g0258a0011c0011t0001g0259 | 2 | HG02818.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.63+4054_63+4064del others(11): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24717772 | ||||||
| chr10:24717858
|
GT | G | 141 | a0002c0002t0001g0010a0002c0002t0001g0017a0002c0002t0001g0018others(138): Show | 141 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.63+3978delA | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24717858 | ||||||
| chr10:24717915
|
A | AC | 3 | a0001c0001t0001g0162a0001c0001t0002g0302a0003c0003t0001g0247 | 3 | HG02027.hp1 NA18906.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.63+3921dupG | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24717915 | ||||||
| chr10:24717952
|
T | C | 1 | a0002c0002t0004g0295 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.63+3885A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24717952 | ||||||
| chr10:24718015
|
G | A | 1 | a0002c0002t0001g0021 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.63+3822C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24718015 | ||||||
| chr10:24718037
|
T | C | 1 | a0001c0001t0004g0299 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.63+3800A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24718037 | ||||||
| chr10:24718071
|
T | C | 2 | a0001c0001t0001g0196a0001c0001t0001g0246 | 2 | HG03239.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.63+3766A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24718071 | ||||||
| chr10:24718154
|
GGAATGAC others(2): Show |
G | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+3674_63+3682del others(9): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24718154 | ||||||
| chr10:24718166
|
C | T | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+3671G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24718166 | ||||||
| chr10:24718377
|
T | C | 71 | a0001c0001t0001g0160a0001c0001t0001g0174a0001c0001t0001g0197others(68): Show | 71 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.63+3460A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24718377 | ||||||
| chr10:24718463
|
G | A | 1 | a0001c0001t0004g0299 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.63+3374C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24718463 | ||||||
| chr10:24718483
|
C | G | 4 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0183others(1): Show | 4 | HG01884.hp2 HG02615.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+3354G>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24718483 | ||||||
| chr10:24718822
|
T | A | 2 | a0001c0014t0004g0286a0005c0005t0004g0287 | 2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.63+3015A>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24718822 | ||||||
| chr10:24718822
|
T | C | 7 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0164others(4): Show | 7 | HG02559.hp1 HG02572.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.63+3015A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24718822 | ||||||
| chr10:24718916
|
T | C | 23 | a0002c0002t0001g0017a0002c0002t0001g0117a0002c0002t0001g0118others(20): Show | 23 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(20): Show |
intron_variant | MODIFIER | c.63+2921A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24718916 | ||||||
| chr10:24719094
|
G | A | 2 | a0012c0010t0001g0266a0012c0010t0001g0267 | 2 | HG02109.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.63+2743C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24719094 | ||||||
| chr10:24719098
|
T | TAC | 48 | a0001c0001t0001g0174a0001c0001t0002g0342a0001c0001t0002g0343others(45): Show | 48 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(45): Show |
intron_variant | MODIFIER | c.63+2737_63+2738dup others(2): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24719098 | ||||||
| chr10:24719098
|
T | TACAC | 13 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0170others(10): Show | 13 | HG00597.hp1 HG00609.hp1 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.63+2735_63+2738dup others(4): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24719098 | ||||||
| chr10:24719098
|
T | TACACAC | 86 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0160others(83): Show | 86 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.63+2733_63+2738dup others(6): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24719098 | ||||||
| chr10:24719098
|
T | TACACACA others(1): Show |
27 | a0001c0001t0001g0169a0001c0001t0001g0237a0001c0001t0001g0238others(24): Show | 27 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.63+2731_63+2738dup others(8): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24719098 | ||||||
| chr10:24719098
|
T | TACACACA others(3): Show |
6 | a0001c0001t0001g0252a0001c0001t0001g0253a0001c0001t0001g0264others(3): Show | 6 | HG00642.hp1 HG01993.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+2729_63+2738dup others(10): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24719098 | ||||||
| chr10:24719098
|
T | TACACACA others(5): Show |
4 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(1): Show | 4 | HG02622.hp1 HG02965.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+2727_63+2738dup others(12): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24719098 | ||||||
| chr10:24719098
|
T | TACACACA others(7): Show |
6 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0164others(3): Show | 6 | HG02559.hp1 HG02572.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+2725_63+2738dup others(14): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24719098 | ||||||
| chr10:24719098
|
T | TACACACA others(9): Show |
1 | a0001c0001t0001g0168 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.63+2723_63+2738dup others(16): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24719098 | ||||||
| chr10:24719098
|
TAC | T | 95 | a0001c0001t0016g0352a0002c0002t0001g0018a0002c0002t0001g0020others(92): Show | 95 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.63+2737_63+2738del others(2): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24719098 | ||||||
| chr10:24719129
|
A | C | 1 | a0002c0030t0001g0022 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.63+2708T>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24719129 | ||||||
| chr10:24719133
|
C | A | 1 | a0002c0015t0001g0161 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.63+2704G>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24719133 | ||||||
| chr10:24719214
|
G | A | 4 | a0002c0002t0001g0020a0002c0002t0001g0138a0002c0002t0001g0139others(1): Show | 4 | HG02615.hp1 HG02922.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+2623C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24719214 | ||||||
| chr10:24719434
|
C | T | 149 | a0002c0002t0001g0010a0002c0002t0001g0017a0002c0002t0001g0018others(146): Show | 149 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.63+2403G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24719434 | ||||||
| chr10:24719805
|
A | G | 1 | a0002c0002t0004g0295 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.63+2032T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24719805 | ||||||
| chr10:24719983
|
T | C | 270 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(267): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.63+1854A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24719983 | ||||||
| chr10:24719989
|
T | G | 7 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0164others(4): Show | 7 | HG02559.hp1 HG02572.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.63+1848A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24719989 | ||||||
| chr10:24720083
|
A | G | 1 | a0001c0001t0001g0170 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.63+1754T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24720083 | ||||||
| chr10:24720212
|
G | T | 1 | a0002c0002t0001g0021 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.63+1625C>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24720212 | ||||||
| chr10:24720244
|
C | G | 1 | a0003c0003t0001g0277 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.63+1593G>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24720244 | ||||||
| chr10:24720254
|
C | CA | 123 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(120): Show | 123 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.63+1582dupT | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24720254 | ||||||
| chr10:24720254
|
C | CAA | 159 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0164others(156): Show | 159 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.63+1581_63+1582dup others(2): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24720254 | ||||||
| chr10:24720254
|
C | CAAA | 11 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(8): Show | 11 | HG00609.hp2 HG02280.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.63+1580_63+1582dup others(3): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24720254 | ||||||
| chr10:24720288
|
C | A | 2 | a0002c0002t0001g0150a0002c0002t0001g0151 | 2 | NA18941.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.63+1549G>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24720288 | ||||||
| chr10:24720382
|
T | G | 2 | a0012c0010t0001g0266a0012c0010t0001g0267 | 2 | HG02109.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.63+1455A>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24720382 | ||||||
| chr10:24720429
|
A | T | 1 | a0002c0015t0001g0161 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.63+1408T>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24720429 | ||||||
| chr10:24720449
|
G | A | 1 | a0003c0003t0001g0268 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.63+1388C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24720449 | ||||||
| chr10:24720569
|
G | A | 2 | a0002c0002t0001g0152a0002c0002t0001g0153 | 2 | HG00099.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.63+1268C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24720569 | ||||||
| chr10:24720574
|
G | A | 7 | a0001c0001t0001g0269a0001c0001t0001g0270a0001c0001t0001g0271others(4): Show | 7 | HG00423.hp2 HG00597.hp1 NA18943.hp2 others(4): Show |
intron_variant | MODIFIER | c.63+1263C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24720574 | ||||||
| chr10:24720657
|
C | T | 167 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(164): Show | 167 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.63+1180G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24720657 | ||||||
| chr10:24720770
|
C | T | 1 | a0001c0001t0001g0160 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.63+1067G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24720770 | ||||||
| chr10:24720994
|
G | GA | 141 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(138): Show | 141 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.63+842dupT | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24720994 | ||||||
| chr10:24720997
|
A | G | 1 | a0001c0001t0002g0300 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.63+840T>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24720997 | ||||||
| chr10:24721606
|
G | A | 1 | a0003c0003t0001g0276 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.63+231C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24721606 | ||||||
| chr10:24721729
|
C | A | 5 | a0001c0001t0016g0352a0006c0006t0002g0348a0006c0006t0002g0349others(2): Show | 5 | NA18957.hp1 NA18989.hp2 NA18992.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+108G>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | 24721729 | ||||||
| chr10:24722388
|
A | C | 1 | a0002c0002t0001g0017 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-380-109T>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 1/25 | chr10 | 24722388 | ||||||
| chr10:24722477
|
C | T | 13 | a0001c0001t0004g0296a0001c0001t0004g0297a0001c0001t0004g0298others(10): Show | 13 | HG01884.hp1 HG02129.hp2 HG02523.hp2 others(10): Show |
intron_variant | MODIFIER | c.-380-198G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 1/25 | chr10 | 24722477 | ||||||
| chr10:24722586
|
T | C | 1 | a0003c0003t0001g0277 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-380-307A>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 1/25 | chr10 | 24722586 | ||||||
| chr10:24722617
|
G | C | 1 | a0003c0003t0001g0277 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-380-338C>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 1/25 | chr10 | 24722617 | ||||||
| chr10:24722758
|
G | GCCGCCCC others(1): Show |
3 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014 | 3 | HG02965.hp1 HG03225.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-380-487_-380-480d others(10): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 1/25 | chr10 | 24722758 | ||||||
| chr10:24722842
|
G | A | 2 | a0002c0002t0001g0278a0002c0002t0001g0279 | 2 | HG00099.hp1 HG00140.hp2 |
intron_variant | MODIFIER | c.-380-563C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 1/25 | chr10 | 24722842 | ||||||
| chr10:24722846
|
G | C | 3 | a0002c0002t0001g0280a0002c0002t0001g0281a0002c0002t0001g0282 | 3 | NA18953.hp2 NA18980.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.-380-567C>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 1/25 | chr10 | 24722846 | ||||||
| chr10:24722908
|
G | A | 1 | a0002c0002t0001g0283 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-380-629C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 1/25 | chr10 | 24722908 | ||||||
| chr10:24723067
|
G | C | 1 | a0005c0005t0001g0284 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-381+495C>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 1/25 | chr10 | 24723067 | ||||||
| chr10:24723073
|
C | G | 1 | a0003c0003t0001g0011 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.-381+489G>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 1/25 | chr10 | 24723073 | ||||||
| chr10:24723111
|
C | T | 1 | a0001c0001t0002g0294 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-381+451G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 1/25 | chr10 | 24723111 | ||||||
| chr10:24723137
|
G | A | 1 | a0002c0002t0001g0285 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.-381+425C>T | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 1/25 | chr10 | 24723137 | ||||||
| chr10:24723242
|
C | G | 6 | a0007c0007t0006g0291a0007c0007t0006g0292a0007c0007t0006g0293others(3): Show | 6 | HG02129.hp2 HG02523.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.-381+320G>C | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 1/25 | chr10 | 24723242 | ||||||
| chr10:24723272
|
A | C | 1 | a0002c0002t0001g0010 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-381+290T>G | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 1/25 | chr10 | 24723272 | ||||||
| chr10:24723454
|
C | T | 2 | a0001c0014t0004g0286a0005c0005t0004g0287 | 2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-381+108G>A | ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 1/25 | chr10 | 24723454 |