Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 57569 |
|---|---|
| ensemblid | ENSG00000137727.13 |
| hgncid | 18357 |
| symbol | ARHGAP20 |
| name | Rho GTPase activating protein 20 |
| refseq_nuc | NM_001384657.1 |
| refseq_prot | NP_001371586.1 |
| ensembl_nuc | ENST00000683387.1 |
| ensembl_prot | ENSP00000507405.1 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 110577043 |
| end | 110712437 |
| strand | - |
| ver | v1.2 |
| region | chr11:110577043-110712437 |
| region5000 | chr11:110572043-110717437 |
| regionname0 | ARHGAP20_chr11_110577043_110712437 |
| regionname5000 | ARHGAP20_chr11_110572043_110717437 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1191 | 203 | 49 | 40 | 84 | 8 | 20 | 56 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| a0002 | 0/0 | 1191 | 7 | 5 | 1 | 0 | 0 | 1 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| a0003 | 0/0 | 1191 | 3 | 1 | 0 | 0 | 0 | 2 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| a0004 | 0/0 | 1191 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| a0005 | 0/0 | 1191 | 2 | 0 | 1 | 1 | 0 | 0 | 1 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| a0006 | 0/0 | 1191 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| a0007 | 0/0 | 1191 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| a0008 | 0/0 | 1191 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| a0009 | 0/0 | 1191 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| a0010 | 0/0 | 1191 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| a0011 | 0/0 | 1191 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| a0012 | 0/0 | 1191 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| a0013 | 0/0 | 1191 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 3576 | 187 | 45 | 39 | 76 | 7 | 18 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| c0002 | 0/0 | 3576 | 8 | 2 | 1 | 3 | 1 | 1 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| c0003 | 0/0 | 3576 | 4 | 4 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| c0004 | 0/0 | 3576 | 3 | 1 | 0 | 0 | 0 | 2 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| c0005 | 0/0 | 3576 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| c0006 | 0/0 | 3576 | 2 | 1 | 0 | 0 | 0 | 1 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| c0007 | 0/0 | 3576 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| c0008 | 0/0 | 3576 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| c0009 | 0/0 | 3576 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| c0010 | 0/0 | 3576 | 2 | 0 | 1 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| c0011 | 0/0 | 3576 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| c0012 | 0/0 | 3576 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| c0013 | 0/0 | 3576 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| c0014 | 0/0 | 3576 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| c0015 | 0/0 | 3576 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| c0016 | 0/0 | 3576 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| c0017 | 0/0 | 3576 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| c0018 | 0/0 | 3576 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| c0019 | 0/0 | 3576 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| c0020 | 0/0 | 3576 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| c0021 | 0/0 | 3576 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| 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 | 0/1 | 2533 | 72 | 9 | 20 | 29 | 5 | 8 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| t0002 | 1/0 | 2534 | 58 | 21 | 6 | 24 | 1 | 5 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| t0003 | 0/0 | 2533 | 41 | 2 | 11 | 21 | 1 | 6 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| t0004 | 0/0 | 2533 | 11 | 11 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| t0005 | 0/0 | 2533 | 11 | 4 | 1 | 3 | 1 | 2 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| t0006 | 0/0 | 2533 | 6 | 4 | 1 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| t0007 | 0/0 | 2533 | 4 | 4 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| t0008 | 0/0 | 2533 | 4 | 0 | 0 | 4 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| t0009 | 0/0 | 2537 | 3 | 0 | 2 | 0 | 0 | 1 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| t0010 | 0/0 | 2534 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| t0011 | 0/0 | 2533 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| t0012 | 0/0 | 2533 | 2 | 1 | 0 | 0 | 0 | 1 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| t0013 | 0/0 | 2533 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| t0014 | 0/0 | 2534 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| t0015 | 0/0 | 2533 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| t0016 | 0/0 | 2534 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| t0017 | 0/0 | 2534 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| t0018 | 0/0 | 2533 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| t0019 | 0/0 | 2534 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| t0020 | 0/0 | 2533 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| t0021 | 0/0 | 2534 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| 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 | 3 | 0 | 3 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0002 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0138 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0173 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 3576 | 187 | 45 | 39 | 76 | 7 | 18 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| a0001c0002 | 0/0 | 3576 | 8 | 2 | 1 | 3 | 1 | 1 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| a0001c0005 | 0/0 | 3576 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| a0001c0008 | 0/0 | 3576 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| a0001c0009 | 0/0 | 3576 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| a0001c0012 | 0/0 | 3576 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| a0001c0013 | 0/0 | 3576 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| a0002c0003 | 0/0 | 3576 | 4 | 4 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| a0002c0006 | 0/0 | 3576 | 2 | 1 | 0 | 0 | 0 | 1 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| a0002c0014 | 0/0 | 3576 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| a0003c0004 | 0/0 | 3576 | 3 | 1 | 0 | 0 | 0 | 2 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| a0004c0011 | 0/0 | 3576 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| a0005c0010 | 0/0 | 3576 | 2 | 0 | 1 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| a0006c0007 | 0/0 | 3576 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| a0007c0020 | 0/0 | 3576 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| a0008c0017 | 0/0 | 3576 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| a0009c0015 | 0/0 | 3576 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| a0010c0016 | 0/0 | 3576 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| a0011c0018 | 0/0 | 3576 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| a0012c0019 | 0/0 | 3576 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| a0013c0021 | 0/0 | 3576 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 6108 | 70 | 9 | 19 | 28 | 5 | 8 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| a0001c0001t0002 | 1/0 | 6109 | 49 | 20 | 6 | 18 | 1 | 3 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| a0001c0001t0003 | 0/0 | 6108 | 38 | 2 | 11 | 19 | 1 | 5 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| a0001c0001t0004 | 0/0 | 6108 | 9 | 9 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| a0001c0001t0006 | 0/0 | 6108 | 6 | 4 | 1 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| a0001c0001t0008 | 0/0 | 6108 | 4 | 0 | 0 | 4 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| a0001c0001t0009 | 0/0 | 6112 | 3 | 0 | 2 | 0 | 0 | 1 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| a0001c0001t0011 | 0/0 | 6108 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| a0001c0001t0013 | 0/0 | 6108 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| a0001c0001t0014 | 0/0 | 6109 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| a0001c0001t0016 | 0/0 | 6109 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| a0001c0001t0018 | 0/0 | 6108 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| a0001c0001t0021 | 0/0 | 6109 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| a0001c0002t0005 | 0/0 | 6108 | 8 | 2 | 1 | 3 | 1 | 1 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| a0001c0005t0005 | 0/0 | 6108 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| a0001c0008t0003 | 0/0 | 6108 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| a0001c0009t0002 | 0/0 | 6109 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| a0001c0012t0002 | 0/0 | 6109 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| a0001c0013t0003 | 0/0 | 6108 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| a0002c0003t0007 | 0/0 | 6108 | 4 | 4 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| a0002c0006t0012 | 0/0 | 6108 | 2 | 1 | 0 | 0 | 0 | 1 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| a0002c0014t0019 | 0/0 | 6109 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| a0003c0004t0002 | 0/0 | 6109 | 2 | 0 | 0 | 0 | 0 | 2 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| a0003c0004t0017 | 0/0 | 6109 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| a0004c0011t0002 | 0/0 | 6109 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| a0005c0010t0001 | 0/0 | 6108 | 2 | 0 | 1 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| a0006c0007t0010 | 0/0 | 6109 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| a0007c0020t0020 | 0/0 | 6108 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| a0008c0017t0002 | 0/0 | 6109 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| a0009c0015t0004 | 0/0 | 6108 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| a0010c0016t0002 | 0/0 | 6109 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| a0011c0018t0015 | 0/0 | 6108 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| a0012c0019t0004 | 0/0 | 6108 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| a0013c0021t0005 | 0/0 | 6108 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | copy fasta | chr11 | 110572043 | 110717437 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0173 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0002g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0002g0138 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0003g0001 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0003g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0003g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0003g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0003g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0003g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0003g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0003g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0003g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0003g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0003g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0003g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0003g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0004g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0004g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0004g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0004g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0004g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0004g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0004g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0004g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0006g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0006g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0006g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0006g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0006g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0006g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0008g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0008g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0008g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0008g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0009g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0009g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0011g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0011g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0013g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0013g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0014g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0016g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0018g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0021g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0002t0005g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0002t0005g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0002t0005g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0002t0005g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0002t0005g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0002t0005g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0002t0005g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0002t0005g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0005t0005g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0005t0005g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0008t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0008t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0009t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0009t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0012t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0013t0003g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0002c0003t0007g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0002c0003t0007g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0002c0003t0007g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0002c0003t0007g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0002c0006t0012g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0002c0006t0012g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0002c0014t0019g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0003c0004t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0003c0004t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0003c0004t0017g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0004c0011t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0004c0011t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0005c0010t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0005c0010t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0006c0007t0010g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0006c0007t0010g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0007c0020t0020g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0008c0017t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0009c0015t0004g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0010c0016t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0011c0018t0015g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0012c0019t0004g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0013c0021t0005g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0124 | EUR | GBR | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0210 | EUR | GBR | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0117 | EUR | FIN | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG00280 | hp2 | a0001 | c0002 | t0005 | g0209 | EUR | FIN | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG00323 | hp1 | a0001 | c0001 | t0003 | g0054 | EUR | FIN | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0071 | EUR | FIN | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | CHS | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | CHS | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | CHS | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG00621 | hp2 | a0001 | c0001 | t0003 | g0135 | EAS | CHS | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG00639 | hp1 | a0001 | c0001 | t0009 | g0003 | AMR | PUR | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0094 | EAS | CHS | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0160 | EAS | CHS | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG00733 | hp1 | a0001 | c0002 | t0005 | g0113 | AMR | PUR | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG00735 | hp1 | a0001 | c0001 | t0009 | g0003 | AMR | PUR | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0050 | AMR | PUR | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0076 | AMR | PUR | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0204 | AMR | PUR | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0052 | AMR | PUR | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0133 | AMR | PUR | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0067 | AMR | PUR | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0107 | AMR | PUR | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0063 | AMR | PUR | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | CLM | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG01261 | hp2 | a0001 | c0001 | t0003 | g0064 | AMR | CLM | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG01346 | hp1 | a0001 | c0001 | t0003 | g0091 | AMR | CLM | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | CLM | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | CLM | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0121 | AMR | CLM | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG01361 | hp1 | a0001 | c0001 | t0006 | g0172 | AMR | CLM | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | CLM | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | CLM | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG01433 | hp2 | a0001 | c0001 | t0003 | g0013 | AMR | CLM | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0127 | EUR | IBS | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0134 | EUR | IBS | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG01891 | hp1 | a0001 | c0005 | t0005 | g0142 | AFR | ACB | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0205 | AFR | ACB | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | PEL | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG01928 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | PEL | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG01952 | hp2 | a0002 | c0014 | t0019 | g0207 | AMR | PEL | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG01981 | hp1 | a0005 | c0010 | t0001 | g0161 | AMR | PEL | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG01981 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02004 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | PEL | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02015 | hp1 | a0001 | c0002 | t0005 | g0217 | EAS | KHV | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02015 | hp2 | a0001 | c0001 | t0013 | g0110 | EAS | KHV | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0158 | EAS | KHV | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0102 | EAS | KHV | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02055 | hp1 | a0002 | c0006 | t0012 | g0111 | AFR | ACB | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0112 | AFR | ACB | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02071 | hp1 | a0001 | c0001 | t0003 | g0097 | EAS | KHV | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0165 | EAS | KHV | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | KHV | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02074 | hp2 | a0001 | c0001 | t0018 | g0095 | EAS | KHV | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02080 | hp1 | a0001 | c0002 | t0005 | g0218 | EAS | KHV | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | KHV | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0166 | EAS | KHV | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | KHV | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02135 | hp1 | a0001 | c0001 | t0003 | g0198 | EAS | KHV | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02135 | hp2 | a0001 | c0002 | t0005 | g0211 | EAS | KHV | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0053 | AFR | ACB | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02145 | hp2 | a0001 | c0001 | t0004 | g0012 | AFR | ACB | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02155 | hp1 | a0001 | c0001 | t0011 | g0017 | EAS | CDX | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02155 | hp2 | a0001 | c0001 | t0003 | g0216 | EAS | CDX | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | CDX | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | CDX | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02257 | hp1 | a0002 | c0003 | t0007 | g0150 | AFR | ACB | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0062 | AFR | ACB | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02273 | hp1 | a0001 | c0001 | t0003 | g0109 | AMR | PEL | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02273 | hp2 | a0001 | c0001 | t0003 | g0049 | AMR | PEL | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | ACB | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0023 | AFR | ACB | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | ACB | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02451 | hp2 | a0001 | c0005 | t0005 | g0197 | AFR | ACB | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | KHV | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | KHV | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0079 | SAS | PJL | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | PJL | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02622 | hp2 | a0006 | c0007 | t0010 | g0147 | AFR | GWD | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02647 | hp1 | a0001 | c0001 | t0004 | g0009 | AFR | GWD | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0122 | AFR | GWD | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02683 | hp1 | a0001 | c0001 | t0003 | g0065 | SAS | PJL | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0152 | SAS | PJL | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02723 | hp1 | a0002 | c0003 | t0007 | g0208 | AFR | GWD | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0026 | AFR | GWD | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02738 | hp1 | a0001 | c0001 | t0003 | g0093 | SAS | PJL | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0168 | SAS | PJL | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02809 | hp1 | a0011 | c0018 | t0015 | g0007 | AFR | GWD | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02809 | hp2 | a0001 | c0001 | t0004 | g0082 | AFR | GWD | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0033 | AFR | GWD | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02896 | hp2 | a0001 | c0001 | t0004 | g0010 | AFR | GWD | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02922 | hp1 | a0002 | c0003 | t0007 | g0203 | AFR | ESN | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0051 | AFR | ESN | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0032 | AFR | ESN | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02965 | hp2 | a0001 | c0001 | t0004 | g0011 | AFR | ESN | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02970 | hp1 | a0001 | c0001 | t0006 | g0201 | AFR | ESN | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02970 | hp2 | a0010 | c0016 | t0002 | g0060 | AFR | ESN | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG03017 | hp2 | a0002 | c0006 | t0012 | g0140 | SAS | PJL | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0022 | AFR | GWD | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | MSL | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG03098 | hp2 | a0001 | c0001 | t0004 | g0143 | AFR | MSL | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0059 | AFR | ESN | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG03139 | hp2 | a0002 | c0003 | t0007 | g0202 | AFR | ESN | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0206 | AFR | MSL | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | MSL | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0034 | AFR | MSL | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG03225 | hp2 | a0001 | c0001 | t0004 | g0146 | AFR | MSL | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG03239 | hp1 | a0001 | c0001 | t0009 | g0120 | SAS | PJL | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG03239 | hp2 | a0001 | c0001 | t0016 | g0057 | SAS | PJL | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG03491 | hp1 | a0003 | c0004 | t0002 | g0162 | SAS | PJL | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0030 | SAS | PJL | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG03516 | hp1 | a0001 | c0001 | t0004 | g0004 | AFR | ESN | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0070 | AFR | ESN | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0031 | AFR | GWD | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG03540 | hp2 | a0006 | c0007 | t0010 | g0148 | AFR | GWD | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0213 | AFR | MSL | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | MSL | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG03688 | hp1 | a0003 | c0004 | t0002 | g0144 | SAS | STU | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | STU | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG03831 | hp1 | a0013 | c0021 | t0005 | g0220 | SAS | BEB | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0181 | SAS | BEB | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0195 | SAS | BEB | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG03834 | hp2 | a0001 | c0013 | t0003 | g0092 | SAS | BEB | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0024 | SAS | BEB | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG03942 | hp2 | a0001 | c0001 | t0003 | g0100 | SAS | BEB | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0185 | SAS | STU | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0069 | SAS | STU | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG04199 | hp1 | a0001 | c0002 | t0005 | g0215 | SAS | STU | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0123 | SAS | STU | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | CHB | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | CHB | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA18940 | hp1 | a0001 | c0001 | t0013 | g0190 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA18942 | hp2 | a0001 | c0001 | t0003 | g0118 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA18948 | hp1 | a0001 | c0001 | t0003 | g0119 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA18951 | hp1 | a0001 | c0001 | t0003 | g0096 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA18953 | hp2 | a0001 | c0001 | t0003 | g0126 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA18954 | hp1 | a0001 | c0001 | t0003 | g0099 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA18962 | hp1 | a0005 | c0010 | t0001 | g0180 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA18962 | hp2 | a0001 | c0001 | t0003 | g0108 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA18972 | hp2 | a0001 | c0001 | t0011 | g0018 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA18978 | hp2 | a0001 | c0009 | t0002 | g0196 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA18983 | hp1 | a0001 | c0001 | t0006 | g0186 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA18983 | hp2 | a0001 | c0001 | t0003 | g0130 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA18997 | hp1 | a0001 | c0001 | t0008 | g0014 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA18999 | hp1 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA19000 | hp1 | a0001 | c0001 | t0021 | g0178 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA19000 | hp2 | a0001 | c0008 | t0003 | g0086 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA19002 | hp1 | a0001 | c0009 | t0002 | g0188 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA19003 | hp1 | a0001 | c0008 | t0003 | g0085 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA19003 | hp2 | a0001 | c0001 | t0008 | g0015 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA19030 | hp1 | a0009 | c0015 | t0004 | g0153 | AFR | LWK | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA19030 | hp2 | a0003 | c0004 | t0017 | g0145 | AFR | LWK | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | LWK | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0084 | AFR | LWK | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA19057 | hp2 | a0001 | c0001 | t0008 | g0019 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA19060 | hp2 | a0001 | c0001 | t0003 | g0098 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA19063 | hp1 | a0001 | c0001 | t0003 | g0132 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA19066 | hp2 | a0001 | c0001 | t0003 | g0038 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA19067 | hp1 | a0008 | c0017 | t0002 | g0141 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA19075 | hp1 | a0001 | c0012 | t0002 | g0189 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA19075 | hp2 | a0004 | c0011 | t0002 | g0128 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA19078 | hp1 | a0001 | c0001 | t0003 | g0104 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA19082 | hp1 | a0001 | c0001 | t0003 | g0045 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA19084 | hp2 | a0001 | c0001 | t0008 | g0088 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA19086 | hp1 | a0004 | c0011 | t0002 | g0028 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA19091 | hp1 | a0001 | c0001 | t0003 | g0089 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA19240 | hp1 | a0001 | c0002 | t0005 | g0214 | AFR | YRI | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA19240 | hp2 | a0012 | c0019 | t0004 | g0151 | AFR | YRI | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA20129 | hp1 | a0001 | c0001 | t0003 | g0101 | AFR | ASW | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA20129 | hp2 | a0001 | c0002 | t0005 | g0212 | AFR | ASW | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02109 | hp1 | a0001 | c0001 | t0006 | g0199 | AFR | ACB | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0061 | AFR | ACB | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0029 | AFR | ACB | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02486 | hp2 | a0001 | c0001 | t0006 | g0200 | AFR | ACB | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02559 | hp2 | a0001 | c0001 | t0006 | g0156 | AFR | ACB | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG06807 | hp1 | a0007 | c0020 | t0020 | g0149 | AFR | USA | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG06807 | hp2 | a0001 | c0001 | t0004 | g0004 | AFR | USA | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | LWK | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA21309 | hp2 | a0001 | c0001 | t0014 | g0006 | AFR | LWK | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0173 | REF | REF | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0138 | REF | REF | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:110579620
|
C | T | 1 | a0010 | 1 | HG02970.hp2 | missense_variant | MODERATE | c.3326G>A | p.Arg1109Lys | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 15/15 | 3532/6109 | 3326/3576 | 1109/1191 | chr11 | 110579620 | ||
| chr11:110579639
|
G | C | 2 | a0009a0012 | 2 | NA19030.hp1 NA19240.hp2 |
missense_variant | MODERATE | c.3307C>G | p.Pro1103Ala | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 15/15 | 3513/6109 | 3307/3576 | 1103/1191 | chr11 | 110579639 | ||
| chr11:110579872
|
G | A | 1 | a0008 | 1 | NA19067.hp1 | missense_variant | MODERATE | c.3074C>T | p.Ser1025Leu | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 15/15 | 3280/6109 | 3074/3576 | 1025/1191 | chr11 | 110579872 | ||
| chr11:110580287
|
G | A | 1 | a0005 | 2 | HG01981.hp1 NA18962.hp1 |
missense_variant | MODERATE | c.2659C>T | p.Arg887Trp | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 15/15 | 2865/6109 | 2659/3576 | 887/1191 | chr11 | 110580287 | ||
| chr11:110580781
|
T | C | 1 | a0004 | 2 | NA19075.hp2 NA19086.hp1 |
missense_variant | MODERATE | c.2165A>G | p.Tyr722Cys | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 15/15 | 2371/6109 | 2165/3576 | 722/1191 | chr11 | 110580781 | ||
| chr11:110580997
|
T | G | 3 | a0003a0006a0008 | 6 | HG02622.hp2 HG03491.hp1 HG03540.hp2 others(3): Show |
missense_variant | MODERATE | c.1949A>C | p.Gln650Pro | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 15/15 | 2155/6109 | 1949/3576 | 650/1191 | chr11 | 110580997 | ||
| chr11:110583589
|
C | T | 3 | a0002a0006a0007 | 10 | HG01952.hp2 HG02055.hp1 HG02257.hp1 others(7): Show |
missense_variant | MODERATE | c.1564G>A | p.Ala522Thr | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 13/15 | 1770/6109 | 1564/3576 | 522/1191 | chr11 | 110583589 | ||
| chr11:110606665
|
G | C | 1 | a0011 | 1 | HG02809.hp1 | missense_variant | MODERATE | c.860C>G | p.Pro287Arg | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/15 | 1066/6109 | 860/3576 | 287/1191 | chr11 | 110606665 | ||
| chr11:110624214
|
T | C | 1 | a0012 | 1 | NA19240.hp2 | missense_variant | MODERATE | c.451A>G | p.Met151Val | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/15 | 657/6109 | 451/3576 | 151/1191 | chr11 | 110624214 | ||
| chr11:110690551
|
T | C | 1 | a0007 | 1 | HG06807.hp1 | missense_variant | MODERATE | c.184A>G | p.Thr62Ala | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/15 | 390/6109 | 184/3576 | 62/1191 | chr11 | 110690551 | ||
| chr11:110712146
|
C | A | 1 | a0013 | 1 | HG03831.hp1 | missense_variant | MODERATE | c.86G>T | p.Gly29Val | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/15 | 292/6109 | 86/3576 | 29/1191 | chr11 | 110712146 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:110579439
|
C | T | 1 | a0001c0008 | 2 | NA19000.hp2 NA19003.hp1 |
synonymous_variant | LOW | c.3507G>A | p.Ala1169Ala | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 15/15 | 3713/6109 | 3507/3576 | 1169/1191 | chr11 | 110579439 | ||
| chr11:110579940
|
G | A | 2 | a0001c0009a0010c0016 | 3 | HG02970.hp2 NA18978.hp2 NA19002.hp1 |
synonymous_variant | LOW | c.3006C>T | p.Pro1002Pro | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 15/15 | 3212/6109 | 3006/3576 | 1002/1191 | chr11 | 110579940 | ||
| chr11:110580696
|
C | T | 2 | a0002c0006a0002c0014 | 3 | HG01952.hp2 HG02055.hp1 HG03017.hp2 |
synonymous_variant | LOW | c.2250G>A | p.Gln750Gln | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 15/15 | 2456/6109 | 2250/3576 | 750/1191 | chr11 | 110580696 | ||
| chr11:110581161
|
A | G | 4 | a0001c0002a0001c0005a0011c0018others(1): Show | 12 | HG00280.hp2 HG00733.hp1 HG01891.hp1 others(9): Show |
synonymous_variant | LOW | c.1785T>C | p.Asp595Asp | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 15/15 | 1991/6109 | 1785/3576 | 595/1191 | chr11 | 110581161 | ||
| chr11:110582396
|
T | G | 1 | a0012c0019 | 1 | NA19240.hp2 | synonymous_variant | LOW | c.1645A>C | p.Arg549Arg | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 14/15 | 1851/6109 | 1645/3576 | 549/1191 | chr11 | 110582396 | ||
| chr11:110583566
|
T | C | 1 | a0002c0014 | 1 | HG01952.hp2 | synonymous_variant | LOW | c.1587A>G | p.Glu529Glu | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 13/15 | 1793/6109 | 1587/3576 | 529/1191 | chr11 | 110583566 | ||
| chr11:110583614
|
G | A | 2 | a0002c0003a0007c0020 | 5 | HG02257.hp1 HG02723.hp1 HG02922.hp1 others(2): Show |
synonymous_variant | LOW | c.1539C>T | p.Val513Val | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 13/15 | 1745/6109 | 1539/3576 | 513/1191 | chr11 | 110583614 | ||
| chr11:110592031
|
A | G | 1 | a0001c0013 | 1 | HG03834.hp2 | synonymous_variant | LOW | c.1089T>C | p.Phe363Phe | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 10/15 | 1295/6109 | 1089/3576 | 363/1191 | chr11 | 110592031 | ||
| chr11:110624278
|
A | T | 1 | a0001c0005 | 2 | HG01891.hp1 HG02451.hp2 |
synonymous_variant | LOW | c.387T>A | p.Ile129Ile | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/15 | 593/6109 | 387/3576 | 129/1191 | chr11 | 110624278 | ||
| chr11:110624296
|
A | G | 1 | a0001c0012 | 1 | NA19075.hp1 | synonymous_variant | LOW | c.369T>C | p.Phe123Phe | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/15 | 575/6109 | 369/3576 | 123/1191 | chr11 | 110624296 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:110577231
|
C | A | 1 | a0001c0001t0013 | 2 | HG02015.hp2 NA18940.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2139G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 15/15 | 2139 | chr11 | 110577231 | |||||
| chr11:110577357
|
G | T | 1 | a0001c0001t0016 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2013C>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 15/15 | 2013 | chr11 | 110577357 | |||||
| chr11:110577471
|
GA | G | 21 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(18): Show | 161 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(158): Show |
3_prime_UTR_variant | MODIFIER | c.*1898delT | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 15/15 | 1898 | chr11 | 110577471 | |||||
| chr11:110577502
|
A | C | 1 | a0001c0001t0011 | 2 | HG02155.hp1 NA18972.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1868T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 15/15 | 1868 | chr11 | 110577502 | |||||
| chr11:110577616
|
T | G | 6 | a0001c0001t0001a0001c0001t0006a0001c0001t0009others(3): Show | 84 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(81): Show |
3_prime_UTR_variant | MODIFIER | c.*1754A>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 15/15 | 1754 | chr11 | 110577616 | |||||
| chr11:110577654
|
G | A | 1 | a0003c0004t0017 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1716C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 15/15 | 1716 | chr11 | 110577654 | |||||
| chr11:110577960
|
G | A | 1 | a0001c0001t0018 | 1 | HG02074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1410C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 15/15 | 1410 | chr11 | 110577960 | |||||
| chr11:110578165
|
G | A | 6 | a0001c0001t0003a0001c0001t0008a0001c0001t0011others(3): Show | 48 | HG00323.hp1 HG00621.hp2 HG00673.hp1 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*1205C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 15/15 | 1205 | chr11 | 110578165 | |||||
| chr11:110578317
|
G | A | 4 | a0001c0002t0005a0001c0005t0005a0011c0018t0015others(1): Show | 12 | HG00280.hp2 HG00733.hp1 HG01891.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1053C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 15/15 | 1053 | chr11 | 110578317 | |||||
| chr11:110578395
|
G | T | 1 | a0006c0007t0010 | 2 | HG02622.hp2 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*975C>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 15/15 | 975 | chr11 | 110578395 | |||||
| chr11:110578481
|
G | T | 4 | a0002c0003t0007a0002c0006t0012a0002c0014t0019others(1): Show | 8 | HG01952.hp2 HG02055.hp1 HG02257.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*889C>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 15/15 | 889 | chr11 | 110578481 | |||||
| chr11:110578498
|
G | C | 1 | a0001c0001t0008 | 4 | NA18997.hp1 NA19003.hp2 NA19057.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*872C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 15/15 | 872 | chr11 | 110578498 | |||||
| chr11:110578507
|
G | GTCTT | 1 | a0001c0001t0009 | 3 | HG00639.hp1 HG00735.hp1 HG03239.hp1 |
3_prime_UTR_variant | MODIFIER | c.*859_*862dupAAGA | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 15/15 | 862 | chr11 | 110578507 | |||||
| chr11:110578702
|
A | G | 2 | a0002c0003t0007a0007c0020t0020 | 5 | HG02257.hp1 HG02723.hp1 HG02922.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*668T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 15/15 | 668 | chr11 | 110578702 | |||||
| chr11:110578834
|
T | G | 2 | a0002c0006t0012a0002c0014t0019 | 3 | HG01952.hp2 HG02055.hp1 HG03017.hp2 |
3_prime_UTR_variant | MODIFIER | c.*536A>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 15/15 | 536 | chr11 | 110578834 | |||||
| chr11:110579079
|
G | A | 1 | a0007c0020t0020 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*291C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 15/15 | 291 | chr11 | 110579079 | |||||
| chr11:110579139
|
C | A | 5 | a0001c0001t0001a0001c0001t0009a0001c0001t0013others(2): Show | 78 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*231G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 15/15 | 231 | chr11 | 110579139 | |||||
| chr11:110712314
|
G | T | 1 | a0011c0018t0015 | 1 | HG02809.hp1 | 5_prime_UTR_variant | MODIFIER | c.-83C>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/15 | 83 | chr11 | 110712314 | |||||
| chr11:110712388
|
G | T | 1 | a0001c0001t0014 | 1 | NA21309.hp2 | 5_prime_UTR_variant | MODIFIER | c.-157C>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/15 | 157 | chr11 | 110712388 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:110581289
|
A | G | 3 | a0001c0001t0001g0005a0001c0001t0001g0174a0001c0001t0001g0193 | 4 | HG02622.hp1 HG03041.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1721-64T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 14/14 | chr11 | 110581289 | ||||||
| chr11:110581295
|
A | AAACTATG others(11): Show |
10 | a0002c0003t0007g0150a0002c0003t0007g0202a0002c0003t0007g0203others(7): Show | 10 | HG01952.hp2 HG02055.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1721-71_1721-70ins others(18): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 14/14 | chr11 | 110581295 | ||||||
| chr11:110581705
|
C | T | 162 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0016others(159): Show | 168 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.1721-480G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 14/14 | chr11 | 110581705 | ||||||
| chr11:110581815
|
G | C | 1 | a0001c0001t0001g0192 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1720+506C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 14/14 | chr11 | 110581815 | ||||||
| chr11:110581825
|
G | A | 2 | a0004c0011t0002g0028a0004c0011t0002g0128 | 2 | NA19075.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.1720+496C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 14/14 | chr11 | 110581825 | ||||||
| chr11:110581878
|
A | G | 8 | a0001c0001t0004g0004a0001c0001t0004g0009a0001c0001t0004g0010others(5): Show | 9 | HG02145.hp2 HG02647.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.1720+443T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 14/14 | chr11 | 110581878 | ||||||
| chr11:110581897
|
G | A | 1 | a0001c0002t0005g0214 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1720+424C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 14/14 | chr11 | 110581897 | ||||||
| chr11:110581930
|
C | CA | 6 | a0001c0001t0002g0053a0001c0001t0002g0205a0001c0001t0004g0012others(3): Show | 6 | HG01891.hp2 HG02145.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.1720+390dupT | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 14/14 | chr11 | 110581930 | ||||||
| chr11:110581930
|
CA | C | 82 | a0001c0001t0001g0068a0001c0001t0001g0134a0001c0001t0002g0024others(79): Show | 84 | HG00323.hp1 HG00558.hp2 HG00621.hp2 others(81): Show |
intron_variant | MODIFIER | c.1720+390delT | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 14/14 | chr11 | 110581930 | ||||||
| chr11:110582106
|
C | T | 162 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0016others(159): Show | 168 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.1720+215G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 14/14 | chr11 | 110582106 | ||||||
| chr11:110582164
|
C | T | 2 | a0009c0015t0004g0153a0012c0019t0004g0151 | 2 | NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1720+157G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 14/14 | chr11 | 110582164 | ||||||
| chr11:110582262
|
C | T | 8 | a0001c0001t0004g0004a0001c0001t0004g0009a0001c0001t0004g0010others(5): Show | 9 | HG02145.hp2 HG02647.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.1720+59G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 14/14 | chr11 | 110582262 | ||||||
| chr11:110582275
|
C | A | 161 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0016others(158): Show | 167 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.1720+46G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 14/14 | chr11 | 110582275 | ||||||
| chr11:110582285
|
G | A | 156 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0016others(153): Show | 162 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.1720+36C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 14/14 | chr11 | 110582285 | ||||||
| chr11:110582526
|
C | G | 162 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0016others(159): Show | 168 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.1606-91G>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 13/14 | chr11 | 110582526 | ||||||
| chr11:110582815
|
T | C | 1 | a0001c0001t0001g0181 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1606-380A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 13/14 | chr11 | 110582815 | ||||||
| chr11:110582973
|
C | G | 12 | a0001c0002t0005g0113a0001c0002t0005g0209a0001c0002t0005g0211others(9): Show | 12 | HG00280.hp2 HG00733.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.1606-538G>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 13/14 | chr11 | 110582973 | ||||||
| chr11:110583089
|
C | T | 1 | a0001c0001t0001g0025 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1605+459G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 13/14 | chr11 | 110583089 | ||||||
| chr11:110583504
|
G | A | 1 | a0001c0001t0001g0184 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1605+44C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 13/14 | chr11 | 110583504 | ||||||
| chr11:110584028
|
G | A | 3 | a0002c0006t0012g0111a0002c0006t0012g0140a0002c0014t0019g0207 | 3 | HG01952.hp2 HG02055.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.1416-291C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 12/14 | chr11 | 110584028 | ||||||
| chr11:110584077
|
T | C | 1 | a0001c0001t0001g0173 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1416-340A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 12/14 | chr11 | 110584077 | ||||||
| chr11:110584084
|
C | G | 47 | a0001c0001t0003g0001a0001c0001t0003g0013a0001c0001t0003g0021others(44): Show | 49 | HG00323.hp1 HG00621.hp2 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.1416-347G>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 12/14 | chr11 | 110584084 | ||||||
| chr11:110584152
|
C | A | 82 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0016others(79): Show | 85 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.1416-415G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 12/14 | chr11 | 110584152 | ||||||
| chr11:110584196
|
A | G | 6 | a0003c0004t0002g0144a0003c0004t0002g0162a0003c0004t0017g0145others(3): Show | 6 | HG02622.hp2 HG03491.hp1 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.1416-459T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 12/14 | chr11 | 110584196 | ||||||
| chr11:110584214
|
T | C | 8 | a0001c0001t0004g0004a0001c0001t0004g0009a0001c0001t0004g0010others(5): Show | 9 | HG02145.hp2 HG02647.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.1416-477A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 12/14 | chr11 | 110584214 | ||||||
| chr11:110584361
|
T | C | 3 | a0001c0001t0006g0199a0001c0001t0006g0200a0001c0001t0006g0201 | 3 | HG02109.hp1 HG02486.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1416-624A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 12/14 | chr11 | 110584361 | ||||||
| chr11:110584386
|
C | A | 219 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0016others(216): Show | 225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.1416-649G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 12/14 | chr11 | 110584386 | ||||||
| chr11:110584392
|
G | GT | 219 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0016others(216): Show | 225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.1416-656dupA | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 12/14 | chr11 | 110584392 | ||||||
| chr11:110584649
|
C | T | 2 | a0001c0001t0008g0014a0001c0001t0008g0019 | 2 | NA18997.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.1416-912G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 12/14 | chr11 | 110584649 | ||||||
| chr11:110584844
|
C | CAT | 48 | a0001c0001t0003g0001a0001c0001t0003g0013a0001c0001t0003g0021others(45): Show | 50 | HG00323.hp1 HG00621.hp2 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.1416-1109_1416-110 others(6): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 12/14 | chr11 | 110584844 | ||||||
| chr11:110584861
|
A | G | 1 | a0001c0001t0002g0024 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1416-1124T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 12/14 | chr11 | 110584861 | ||||||
| chr11:110584876
|
T | C | 2 | a0006c0007t0010g0147a0006c0007t0010g0148 | 2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1416-1139A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 12/14 | chr11 | 110584876 | ||||||
| chr11:110584908
|
T | TATATATA others(3): Show |
7 | a0002c0003t0007g0150a0002c0003t0007g0202a0002c0003t0007g0203others(4): Show | 7 | HG02257.hp1 HG02622.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1416-1181_1416-117 others(14): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 12/14 | chr11 | 110584908 | ||||||
| chr11:110584908
|
T | TATATATG others(1): Show |
47 | a0001c0001t0003g0001a0001c0001t0003g0013a0001c0001t0003g0021others(44): Show | 49 | HG00323.hp1 HG00621.hp2 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.1416-1172_1416-117 others(12): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 12/14 | chr11 | 110584908 | ||||||
| chr11:110584951
|
A | ATG | 52 | a0001c0001t0003g0001a0001c0001t0003g0013a0001c0001t0003g0021others(49): Show | 54 | HG00323.hp1 HG00621.hp2 HG00673.hp1 others(51): Show |
intron_variant | MODIFIER | c.1416-1216_1416-121 others(6): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 12/14 | chr11 | 110584951 | ||||||
| chr11:110584961
|
G | A | 5 | a0002c0003t0007g0150a0002c0003t0007g0202a0002c0003t0007g0203others(2): Show | 5 | HG02257.hp1 HG02723.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1416-1224C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 12/14 | chr11 | 110584961 | ||||||
| chr11:110584965
|
A | ATATG | 5 | a0002c0003t0007g0150a0002c0003t0007g0202a0002c0003t0007g0203others(2): Show | 5 | HG02257.hp1 HG02723.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1416-1229_1416-122 others(8): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 12/14 | chr11 | 110584965 | ||||||
| chr11:110584966
|
T | TATATATG others(9): Show |
2 | a0006c0007t0010g0147a0006c0007t0010g0148 | 2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1416-1230_1416-122 others(20): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 12/14 | chr11 | 110584966 | ||||||
| chr11:110584966
|
T | TATATGA | 59 | a0001c0001t0003g0001a0001c0001t0003g0013a0001c0001t0003g0021others(56): Show | 62 | HG00323.hp1 HG00621.hp2 HG00673.hp1 others(59): Show |
intron_variant | MODIFIER | c.1416-1235_1416-123 others(10): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 12/14 | chr11 | 110584966 | ||||||
| chr11:110584966
|
T | TATATGTG others(9): Show |
2 | a0009c0015t0004g0153a0012c0019t0004g0151 | 2 | NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1416-1230_1416-122 others(20): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 12/14 | chr11 | 110584966 | ||||||
| chr11:110584969
|
A | G | 5 | a0002c0003t0007g0150a0002c0003t0007g0202a0002c0003t0007g0203others(2): Show | 5 | HG02257.hp1 HG02723.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1416-1232T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 12/14 | chr11 | 110584969 | ||||||
| chr11:110584971
|
G | GTGAATAT others(11): Show |
79 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0016others(76): Show | 82 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.1416-1235_1416-123 others(22): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 12/14 | chr11 | 110584971 | ||||||
| chr11:110584971
|
GAATATAT others(15): Show |
G | 1 | a0001c0001t0001g0037 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1415+1223_1416-123 others(26): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 12/14 | chr11 | 110584971 | ||||||
| chr11:110584972
|
A | T | 79 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0016others(76): Show | 82 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.1416-1235T>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 12/14 | chr11 | 110584972 | ||||||
| chr11:110585018
|
CATATATG others(3): Show |
C | 3 | a0002c0006t0012g0140a0002c0014t0019g0207a0013c0021t0005g0220 | 3 | HG01952.hp2 HG03017.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.1415+1188_1415+119 others(14): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 12/14 | chr11 | 110585018 | ||||||
| chr11:110585025
|
G | GTGAATAT others(3): Show |
80 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0020others(77): Show | 82 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.1415+1190_1415+119 others(14): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 12/14 | chr11 | 110585025 | ||||||
| chr11:110585025
|
G | GTGAATAT others(27): Show |
2 | a0001c0001t0003g0100a0001c0013t0003g0092 | 2 | HG03834.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1415+1190_1415+119 others(38): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 12/14 | chr11 | 110585025 | ||||||
| chr11:110585030
|
TATATGTG others(11): Show |
T | 1 | a0002c0006t0012g0111 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1415+1168_1415+118 others(22): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 12/14 | chr11 | 110585030 | ||||||
| chr11:110585032
|
T | TATATGA | 45 | a0001c0001t0003g0001a0001c0001t0003g0013a0001c0001t0003g0021others(42): Show | 47 | HG00323.hp1 HG00621.hp2 HG00673.hp1 others(44): Show |
intron_variant | MODIFIER | c.1415+1183_1415+118 others(10): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 12/14 | chr11 | 110585032 | ||||||
| chr11:110585035
|
G | A | 9 | a0001c0001t0001g0005a0001c0001t0001g0072a0001c0001t0001g0115others(6): Show | 10 | HG00280.hp1 HG00738.hp1 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1415+1181C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 12/14 | chr11 | 110585035 | ||||||
| chr11:110585038
|
AATAT | A | 3 | a0003c0004t0002g0144a0003c0004t0002g0162a0008c0017t0002g0141 | 3 | HG03491.hp1 HG03688.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.1415+1174_1415+117 others(8): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 12/14 | chr11 | 110585038 | ||||||
| chr11:110585040
|
T | C | 2 | a0001c0001t0003g0100a0001c0013t0003g0092 | 2 | HG03834.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1415+1176A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 12/14 | chr11 | 110585040 | ||||||
| chr11:110585040
|
T | TATATATG others(21): Show |
1 | a0003c0004t0017g0145 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1415+1148_1415+117 others(32): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 12/14 | chr11 | 110585040 | ||||||
| chr11:110585040
|
TATATATG others(1): Show |
T | 2 | a0001c0001t0002g0084a0001c0001t0002g0206 | 2 | HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1415+1168_1415+117 others(12): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 12/14 | chr11 | 110585040 | ||||||
| chr11:110585045
|
A | G | 5 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(2): Show | 5 | HG00280.hp1 HG01074.hp2 HG01346.hp2 others(2): Show |
intron_variant | MODIFIER | c.1415+1171T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 12/14 | chr11 | 110585045 | ||||||
| chr11:110585048
|
A | AAT | 5 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(2): Show | 5 | HG00280.hp1 HG01074.hp2 HG01346.hp2 others(2): Show |
intron_variant | MODIFIER | c.1415+1166_1415+116 others(6): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 12/14 | chr11 | 110585048 | ||||||
| chr11:110585068
|
CATATATG others(11): Show |
C | 1 | a0001c0001t0002g0008 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1415+1130_1415+114 others(22): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 12/14 | chr11 | 110585068 | ||||||
| chr11:110585080
|
CATGAATA others(11): Show |
C | 1 | a0001c0002t0005g0212 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1415+1118_1415+113 others(22): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 12/14 | chr11 | 110585080 | ||||||
| chr11:110585095
|
AT | A | 2 | a0006c0007t0010g0147a0006c0007t0010g0148 | 2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1415+1120delA | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 12/14 | chr11 | 110585095 | ||||||
| chr11:110585227
|
G | A | 27 | a0001c0001t0004g0004a0001c0001t0004g0009a0001c0001t0004g0010others(24): Show | 28 | HG00280.hp2 HG00733.hp1 HG01891.hp1 others(25): Show |
intron_variant | MODIFIER | c.1415+989C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 12/14 | chr11 | 110585227 | ||||||
| chr11:110585228
|
A | T | 5 | a0002c0003t0007g0150a0002c0003t0007g0202a0002c0003t0007g0203others(2): Show | 5 | HG02257.hp1 HG02723.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1415+988T>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 12/14 | chr11 | 110585228 | ||||||
| chr11:110585286
|
T | C | 1 | a0001c0001t0001g0114 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1415+930A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 12/14 | chr11 | 110585286 | ||||||
| chr11:110585378
|
T | C | 5 | a0002c0003t0007g0150a0002c0003t0007g0202a0002c0003t0007g0203others(2): Show | 5 | HG02257.hp1 HG02723.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1415+838A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 12/14 | chr11 | 110585378 | ||||||
| chr11:110585408
|
C | CCTTGGTT others(13): Show |
4 | a0003c0004t0002g0144a0003c0004t0002g0162a0003c0004t0017g0145others(1): Show | 4 | HG03491.hp1 HG03688.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1415+788_1415+807d others(22): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 12/14 | chr11 | 110585408 | ||||||
| chr11:110585496
|
A | G | 8 | a0001c0001t0004g0004a0001c0001t0004g0009a0001c0001t0004g0010others(5): Show | 9 | HG02145.hp2 HG02647.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.1415+720T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 12/14 | chr11 | 110585496 | ||||||
| chr11:110585529
|
A | G | 81 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0016others(78): Show | 84 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(81): Show |
intron_variant | MODIFIER | c.1415+687T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 12/14 | chr11 | 110585529 | ||||||
| chr11:110585579
|
A | C | 1 | a0001c0001t0001g0115 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1415+637T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 12/14 | chr11 | 110585579 | ||||||
| chr11:110585649
|
C | T | 2 | a0009c0015t0004g0153a0012c0019t0004g0151 | 2 | NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1415+567G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 12/14 | chr11 | 110585649 | ||||||
| chr11:110585726
|
C | G | 1 | a0003c0004t0017g0145 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1415+490G>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 12/14 | chr11 | 110585726 | ||||||
| chr11:110585914
|
G | A | 5 | a0002c0003t0007g0150a0002c0003t0007g0202a0002c0003t0007g0203others(2): Show | 5 | HG02257.hp1 HG02723.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1415+302C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 12/14 | chr11 | 110585914 | ||||||
| chr11:110586484
|
GA | G | 5 | a0002c0003t0007g0150a0002c0003t0007g0202a0002c0003t0007g0203others(2): Show | 5 | HG02257.hp1 HG02723.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1306-160delT | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 11/14 | chr11 | 110586484 | ||||||
| chr11:110586611
|
T | A | 2 | a0001c0005t0005g0142a0001c0005t0005g0197 | 2 | HG01891.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1306-286A>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 11/14 | chr11 | 110586611 | ||||||
| chr11:110586650
|
C | T | 1 | a0001c0002t0005g0212 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1306-325G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 11/14 | chr11 | 110586650 | ||||||
| chr11:110586748
|
C | A | 2 | a0006c0007t0010g0147a0006c0007t0010g0148 | 2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1306-423G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 11/14 | chr11 | 110586748 | ||||||
| chr11:110586776
|
T | C | 2 | a0006c0007t0010g0147a0006c0007t0010g0148 | 2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1306-451A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 11/14 | chr11 | 110586776 | ||||||
| chr11:110586920
|
GGA | G | 12 | a0001c0002t0005g0113a0001c0002t0005g0209a0001c0002t0005g0211others(9): Show | 12 | HG00280.hp2 HG00733.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.1306-597_1306-596d others(4): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 11/14 | chr11 | 110586920 | ||||||
| chr11:110587086
|
C | CACAA | 3 | a0003c0004t0002g0144a0003c0004t0002g0162a0008c0017t0002g0141 | 3 | HG03491.hp1 HG03688.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.1306-765_1306-762d others(6): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 11/14 | chr11 | 110587086 | ||||||
| chr11:110587461
|
C | T | 163 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0016others(160): Show | 169 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.1306-1136G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 11/14 | chr11 | 110587461 | ||||||
| chr11:110587535
|
G | T | 3 | a0002c0006t0012g0111a0002c0006t0012g0140a0002c0014t0019g0207 | 3 | HG01952.hp2 HG02055.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.1306-1210C>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 11/14 | chr11 | 110587535 | ||||||
| chr11:110587577
|
C | T | 2 | a0009c0015t0004g0153a0012c0019t0004g0151 | 2 | NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1306-1252G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 11/14 | chr11 | 110587577 | ||||||
| chr11:110587660
|
T | C | 1 | a0001c0001t0003g0099 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1306-1335A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 11/14 | chr11 | 110587660 | ||||||
| chr11:110587763
|
C | CT | 55 | a0001c0001t0003g0001a0001c0001t0003g0013a0001c0001t0003g0021others(52): Show | 57 | HG00323.hp1 HG00621.hp2 HG00673.hp1 others(54): Show |
intron_variant | MODIFIER | c.1306-1439dupA | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 11/14 | chr11 | 110587763 | ||||||
| chr11:110587893
|
C | A | 5 | a0002c0003t0007g0150a0002c0003t0007g0202a0002c0003t0007g0203others(2): Show | 5 | HG02257.hp1 HG02723.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1306-1568G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 11/14 | chr11 | 110587893 | ||||||
| chr11:110587910
|
T | A | 5 | a0002c0003t0007g0150a0002c0003t0007g0202a0002c0003t0007g0203others(2): Show | 5 | HG02257.hp1 HG02723.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1306-1585A>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 11/14 | chr11 | 110587910 | ||||||
| chr11:110587912
|
G | T | 1 | a0001c0001t0001g0083 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1306-1587C>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 11/14 | chr11 | 110587912 | ||||||
| chr11:110588111
|
G | A | 34 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0037others(31): Show | 36 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(33): Show |
intron_variant | MODIFIER | c.1306-1786C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 11/14 | chr11 | 110588111 | ||||||
| chr11:110588162
|
C | A | 218 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0016others(215): Show | 224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.1306-1837G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 11/14 | chr11 | 110588162 | ||||||
| chr11:110588167
|
T | C | 8 | a0001c0001t0002g0081a0001c0001t0002g0158a0001c0001t0002g0159others(5): Show | 8 | HG00673.hp2 HG02040.hp1 HG02071.hp2 others(5): Show |
intron_variant | MODIFIER | c.1306-1842A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 11/14 | chr11 | 110588167 | ||||||
| chr11:110588196
|
G | T | 3 | a0002c0003t0007g0202a0002c0003t0007g0203a0002c0003t0007g0208 | 3 | HG02723.hp1 HG02922.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1306-1871C>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 11/14 | chr11 | 110588196 | ||||||
| chr11:110588237
|
T | C | 3 | a0001c0001t0006g0199a0001c0001t0006g0200a0001c0001t0006g0201 | 3 | HG02109.hp1 HG02486.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1306-1912A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 11/14 | chr11 | 110588237 | ||||||
| chr11:110588264
|
A | C | 2 | a0009c0015t0004g0153a0012c0019t0004g0151 | 2 | NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1306-1939T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 11/14 | chr11 | 110588264 | ||||||
| chr11:110588336
|
C | T | 80 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0016others(77): Show | 83 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(80): Show |
intron_variant | MODIFIER | c.1306-2011G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 11/14 | chr11 | 110588336 | ||||||
| chr11:110588419
|
T | C | 81 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0016others(78): Show | 84 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(81): Show |
intron_variant | MODIFIER | c.1306-2094A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 11/14 | chr11 | 110588419 | ||||||
| chr11:110588511
|
A | G | 1 | a0001c0001t0003g0013 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1305+2137T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 11/14 | chr11 | 110588511 | ||||||
| chr11:110588868
|
G | A | 1 | a0001c0001t0001g0083 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1305+1780C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 11/14 | chr11 | 110588868 | ||||||
| chr11:110588898
|
C | T | 1 | a0001c0002t0005g0211 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1305+1750G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 11/14 | chr11 | 110588898 | ||||||
| chr11:110588931
|
G | A | 1 | a0001c0001t0001g0080 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1305+1717C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 11/14 | chr11 | 110588931 | ||||||
| chr11:110589026
|
C | T | 46 | a0001c0001t0003g0001a0001c0001t0003g0013a0001c0001t0003g0021others(43): Show | 48 | HG00323.hp1 HG00621.hp2 HG00673.hp1 others(45): Show |
intron_variant | MODIFIER | c.1305+1622G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 11/14 | chr11 | 110589026 | ||||||
| chr11:110589058
|
T | C | 139 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0016others(136): Show | 144 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.1305+1590A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 11/14 | chr11 | 110589058 | ||||||
| chr11:110589067
|
G | A | 46 | a0001c0001t0003g0001a0001c0001t0003g0013a0001c0001t0003g0021others(43): Show | 48 | HG00323.hp1 HG00621.hp2 HG00673.hp1 others(45): Show |
intron_variant | MODIFIER | c.1305+1581C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 11/14 | chr11 | 110589067 | ||||||
| chr11:110589108
|
T | C | 1 | a0001c0001t0002g0127 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1305+1540A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 11/14 | chr11 | 110589108 | ||||||
| chr11:110589143
|
T | C | 3 | a0002c0006t0012g0111a0002c0006t0012g0140a0002c0014t0019g0207 | 3 | HG01952.hp2 HG02055.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.1305+1505A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 11/14 | chr11 | 110589143 | ||||||
| chr11:110589355
|
G | A | 1 | a0001c0001t0003g0091 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1305+1293C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 11/14 | chr11 | 110589355 | ||||||
| chr11:110589653
|
T | C | 3 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0042 | 3 | NA18940.hp2 NA18978.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.1305+995A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 11/14 | chr11 | 110589653 | ||||||
| chr11:110589817
|
A | G | 1 | a0012c0019t0004g0151 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1305+831T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 11/14 | chr11 | 110589817 | ||||||
| chr11:110590042
|
A | T | 1 | a0001c0001t0001g0117 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1305+606T>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 11/14 | chr11 | 110590042 | ||||||
| chr11:110590116
|
G | A | 1 | a0001c0001t0001g0181 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1305+532C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 11/14 | chr11 | 110590116 | ||||||
| chr11:110590120
|
C | CA | 17 | a0001c0001t0001g0137a0001c0001t0001g0139a0001c0001t0001g0181others(14): Show | 17 | HG00323.hp1 HG00735.hp2 HG01099.hp2 others(14): Show |
intron_variant | MODIFIER | c.1305+527dupT | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 11/14 | chr11 | 110590120 | ||||||
| chr11:110590120
|
CA | C | 14 | a0001c0001t0002g0084a0001c0001t0002g0122a0001c0002t0005g0113others(11): Show | 14 | HG00280.hp2 HG00733.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.1305+527delT | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 11/14 | chr11 | 110590120 | ||||||
| chr11:110590820
|
G | A | 2 | a0006c0007t0010g0147a0006c0007t0010g0148 | 2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1144-11C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 10/14 | chr11 | 110590820 | ||||||
| chr11:110590865
|
T | C | 2 | a0006c0007t0010g0147a0006c0007t0010g0148 | 2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1144-56A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 10/14 | chr11 | 110590865 | ||||||
| chr11:110590903
|
C | T | 1 | a0001c0001t0002g0022 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1144-94G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 10/14 | chr11 | 110590903 | ||||||
| chr11:110590947
|
G | A | 2 | a0001c0001t0003g0001a0001c0001t0003g0049 | 4 | HG01928.hp2 HG01981.hp2 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.1144-138C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 10/14 | chr11 | 110590947 | ||||||
| chr11:110591224
|
C | A | 2 | a0009c0015t0004g0153a0012c0019t0004g0151 | 2 | NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1144-415G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 10/14 | chr11 | 110591224 | ||||||
| chr11:110591540
|
T | C | 1 | a0001c0001t0002g0069 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1143+437A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 10/14 | chr11 | 110591540 | ||||||
| chr11:110591582
|
G | A | 1 | a0011c0018t0015g0007 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1143+395C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 10/14 | chr11 | 110591582 | ||||||
| chr11:110591762
|
G | A | 2 | a0006c0007t0010g0147a0006c0007t0010g0148 | 2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1143+215C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 10/14 | chr11 | 110591762 | ||||||
| chr11:110591791
|
T | C | 8 | a0001c0001t0004g0004a0001c0001t0004g0009a0001c0001t0004g0010others(5): Show | 9 | HG02145.hp2 HG02647.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.1143+186A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 10/14 | chr11 | 110591791 | ||||||
| chr11:110592262
|
G | C | 53 | a0001c0001t0001g0134a0001c0001t0003g0001a0001c0001t0003g0013others(50): Show | 55 | HG00323.hp1 HG00621.hp2 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.965-107C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110592262 | ||||||
| chr11:110592370
|
G | T | 1 | a0001c0001t0002g0033 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.965-215C>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110592370 | ||||||
| chr11:110592375
|
T | C | 4 | a0001c0001t0006g0156a0001c0001t0006g0199a0001c0001t0006g0200others(1): Show | 4 | HG02109.hp1 HG02486.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.965-220A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110592375 | ||||||
| chr11:110592825
|
T | C | 1 | a0001c0001t0003g0104 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.965-670A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110592825 | ||||||
| chr11:110593045
|
T | C | 3 | a0002c0006t0012g0140a0002c0014t0019g0207a0003c0004t0017g0145 | 3 | HG01952.hp2 HG03017.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.965-890A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110593045 | ||||||
| chr11:110593270
|
C | T | 2 | a0006c0007t0010g0147a0006c0007t0010g0148 | 2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.965-1115G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110593270 | ||||||
| chr11:110593510
|
T | C | 1 | a0001c0001t0001g0175 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.965-1355A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110593510 | ||||||
| chr11:110593647
|
A | G | 1 | a0002c0003t0007g0202 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.965-1492T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110593647 | ||||||
| chr11:110593904
|
T | G | 131 | a0001c0001t0001g0134a0001c0001t0001g0163a0001c0001t0001g0210others(128): Show | 134 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.965-1749A>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110593904 | ||||||
| chr11:110593976
|
T | C | 1 | a0001c0001t0001g0152 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.965-1821A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110593976 | ||||||
| chr11:110594300
|
C | A | 8 | a0001c0001t0004g0004a0001c0001t0004g0009a0001c0001t0004g0010others(5): Show | 9 | HG02145.hp2 HG02647.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.965-2145G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110594300 | ||||||
| chr11:110594327
|
C | T | 26 | a0001c0001t0001g0210a0001c0001t0003g0216a0001c0001t0004g0004others(23): Show | 27 | HG00099.hp2 HG00280.hp2 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.965-2172G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110594327 | ||||||
| chr11:110594493
|
A | G | 4 | a0001c0001t0006g0156a0001c0001t0006g0199a0001c0001t0006g0200others(1): Show | 4 | HG02109.hp1 HG02486.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.965-2338T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110594493 | ||||||
| chr11:110594587
|
C | T | 1 | a0001c0001t0001g0117 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.965-2432G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110594587 | ||||||
| chr11:110594668
|
G | C | 4 | a0001c0001t0006g0156a0001c0001t0006g0199a0001c0001t0006g0200others(1): Show | 4 | HG02109.hp1 HG02486.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.965-2513C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110594668 | ||||||
| chr11:110594805
|
C | G | 3 | a0001c0001t0003g0118a0001c0001t0003g0119a0001c0001t0003g0126 | 3 | NA18942.hp2 NA18948.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.965-2650G>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110594805 | ||||||
| chr11:110594819
|
T | G | 1 | a0001c0001t0001g0152 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.965-2664A>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110594819 | ||||||
| chr11:110594833
|
CA | C | 75 | a0001c0001t0001g0210a0001c0001t0002g0008a0001c0001t0002g0022others(72): Show | 76 | HG00099.hp2 HG00280.hp2 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.965-2679delT | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110594833 | ||||||
| chr11:110594951
|
C | A | 130 | a0001c0001t0001g0134a0001c0001t0001g0163a0001c0001t0001g0210others(127): Show | 133 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.965-2796G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110594951 | ||||||
| chr11:110594992
|
C | T | 50 | a0001c0001t0001g0134a0001c0001t0001g0163a0001c0001t0003g0001others(47): Show | 53 | HG00323.hp1 HG00621.hp2 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.965-2837G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110594992 | ||||||
| chr11:110595137
|
C | T | 27 | a0001c0001t0001g0210a0001c0001t0003g0216a0001c0001t0004g0004others(24): Show | 28 | HG00099.hp2 HG00280.hp2 HG01891.hp1 others(25): Show |
intron_variant | MODIFIER | c.965-2982G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110595137 | ||||||
| chr11:110595208
|
G | T | 1 | a0001c0001t0001g0171 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.965-3053C>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110595208 | ||||||
| chr11:110595217
|
A | C | 1 | a0001c0001t0002g0008 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.965-3062T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110595217 | ||||||
| chr11:110595533
|
C | A | 1 | a0001c0001t0001g0056 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.965-3378G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110595533 | ||||||
| chr11:110595544
|
T | C | 1 | a0001c0001t0003g0094 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.965-3389A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110595544 | ||||||
| chr11:110595614
|
C | T | 7 | a0001c0001t0004g0004a0001c0001t0004g0009a0001c0001t0004g0010others(4): Show | 8 | HG02145.hp2 HG02647.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.965-3459G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110595614 | ||||||
| chr11:110595730
|
A | G | 44 | a0001c0001t0001g0134a0001c0001t0001g0163a0001c0001t0003g0001others(41): Show | 46 | HG00323.hp1 HG00621.hp2 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.965-3575T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110595730 | ||||||
| chr11:110595752
|
C | G | 3 | a0001c0001t0001g0129a0001c0008t0003g0085a0001c0008t0003g0086 | 3 | NA19000.hp2 NA19003.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.965-3597G>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110595752 | ||||||
| chr11:110595874
|
C | T | 2 | a0003c0004t0002g0144a0008c0017t0002g0141 | 2 | HG03688.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.965-3719G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110595874 | ||||||
| chr11:110595899
|
C | T | 1 | a0002c0006t0012g0111 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.965-3744G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110595899 | ||||||
| chr11:110595923
|
A | G | 1 | a0002c0006t0012g0140 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.965-3768T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110595923 | ||||||
| chr11:110595976
|
T | C | 79 | a0001c0001t0001g0210a0001c0001t0002g0008a0001c0001t0002g0022others(76): Show | 80 | HG00099.hp2 HG00280.hp2 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.965-3821A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110595976 | ||||||
| chr11:110595989
|
A | G | 130 | a0001c0001t0001g0134a0001c0001t0001g0163a0001c0001t0001g0210others(127): Show | 133 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.965-3834T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110595989 | ||||||
| chr11:110596025
|
C | G | 9 | a0001c0001t0002g0026a0001c0001t0002g0029a0001c0001t0002g0031others(6): Show | 9 | HG01109.hp2 HG02486.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.965-3870G>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110596025 | ||||||
| chr11:110596035
|
C | A | 1 | a0001c0001t0001g0155 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.965-3880G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110596035 | ||||||
| chr11:110596070
|
C | T | 26 | a0001c0001t0001g0210a0001c0001t0003g0216a0001c0001t0004g0004others(23): Show | 27 | HG00099.hp2 HG00280.hp2 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.965-3915G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110596070 | ||||||
| chr11:110596076
|
A | G | 51 | a0001c0001t0001g0134a0001c0001t0001g0163a0001c0001t0002g0204others(48): Show | 53 | HG00323.hp1 HG00621.hp2 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.965-3921T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110596076 | ||||||
| chr11:110596239
|
G | A | 1 | a0001c0002t0005g0214 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.965-4084C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110596239 | ||||||
| chr11:110596273
|
CA | C | 45 | a0001c0001t0002g0008a0001c0001t0002g0022a0001c0001t0002g0023others(42): Show | 45 | HG00558.hp2 HG00738.hp2 HG01099.hp1 others(42): Show |
intron_variant | MODIFIER | c.965-4119delT | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110596273 | ||||||
| chr11:110596276
|
G | A | 7 | a0001c0001t0002g0204a0001c0001t0002g0205a0001c0001t0002g0206others(4): Show | 7 | HG01074.hp1 HG01891.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.965-4121C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110596276 | ||||||
| chr11:110596277
|
G | A | 7 | a0001c0001t0002g0204a0001c0001t0002g0205a0001c0001t0002g0206others(4): Show | 7 | HG01074.hp1 HG01891.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.965-4122C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110596277 | ||||||
| chr11:110596310
|
A | G | 124 | a0001c0001t0001g0134a0001c0001t0001g0163a0001c0001t0001g0210others(121): Show | 127 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.965-4155T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110596310 | ||||||
| chr11:110596313
|
G | A | 2 | a0003c0004t0002g0144a0008c0017t0002g0141 | 2 | HG03688.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.965-4158C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110596313 | ||||||
| chr11:110596365
|
A | G | 126 | a0001c0001t0001g0134a0001c0001t0001g0163a0001c0001t0001g0210others(123): Show | 129 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.965-4210T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110596365 | ||||||
| chr11:110596376
|
C | A | 1 | a0001c0001t0001g0025 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.965-4221G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110596376 | ||||||
| chr11:110596387
|
C | T | 47 | a0001c0001t0002g0008a0001c0001t0002g0022a0001c0001t0002g0023others(44): Show | 47 | HG00558.hp2 HG00738.hp2 HG01099.hp1 others(44): Show |
intron_variant | MODIFIER | c.965-4232G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110596387 | ||||||
| chr11:110596426
|
G | A | 130 | a0001c0001t0001g0134a0001c0001t0001g0163a0001c0001t0001g0210others(127): Show | 133 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.965-4271C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110596426 | ||||||
| chr11:110596427
|
T | A | 4 | a0001c0001t0006g0156a0001c0001t0006g0199a0001c0001t0006g0200others(1): Show | 4 | HG02109.hp1 HG02486.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.965-4272A>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110596427 | ||||||
| chr11:110596438
|
G | A | 130 | a0001c0001t0001g0134a0001c0001t0001g0163a0001c0001t0001g0210others(127): Show | 133 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.965-4283C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110596438 | ||||||
| chr11:110596477
|
A | G | 10 | a0001c0001t0001g0210a0001c0001t0003g0216a0001c0002t0005g0209others(7): Show | 10 | HG00099.hp2 HG00280.hp2 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.965-4322T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110596477 | ||||||
| chr11:110596556
|
C | G | 9 | a0001c0001t0001g0175a0001c0001t0001g0176a0001c0001t0001g0177others(6): Show | 9 | HG01981.hp1 HG02040.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.965-4401G>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110596556 | ||||||
| chr11:110596615
|
G | A | 2 | a0002c0006t0012g0140a0002c0014t0019g0207 | 2 | HG01952.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.965-4460C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110596615 | ||||||
| chr11:110596668
|
C | T | 25 | a0001c0001t0001g0210a0001c0001t0003g0216a0001c0001t0004g0004others(22): Show | 26 | HG00099.hp2 HG00280.hp2 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.965-4513G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110596668 | ||||||
| chr11:110596729
|
A | G | 131 | a0001c0001t0001g0134a0001c0001t0001g0163a0001c0001t0001g0210others(128): Show | 134 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.965-4574T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110596729 | ||||||
| chr11:110596734
|
G | A | 26 | a0001c0001t0001g0210a0001c0001t0003g0216a0001c0001t0004g0004others(23): Show | 27 | HG00099.hp2 HG00280.hp2 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.965-4579C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110596734 | ||||||
| chr11:110596825
|
T | C | 2 | a0001c0001t0001g0169a0001c0001t0001g0171 | 2 | HG01169.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.965-4670A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110596825 | ||||||
| chr11:110596904
|
G | A | 2 | a0001c0001t0001g0027a0001c0001t0001g0139 | 2 | HG00735.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.965-4749C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110596904 | ||||||
| chr11:110596975
|
GTTCAT | G | 3 | a0009c0015t0004g0153a0011c0018t0015g0007a0012c0019t0004g0151 | 3 | HG02809.hp1 NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.965-4825_965-4821d others(7): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110596975 | ||||||
| chr11:110597035
|
G | A | 5 | a0001c0001t0001g0187a0001c0001t0002g0043a0001c0001t0003g0013others(2): Show | 5 | HG01261.hp2 HG01433.hp2 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.965-4880C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110597035 | ||||||
| chr11:110597056
|
C | T | 50 | a0001c0001t0001g0134a0001c0001t0001g0163a0001c0001t0002g0204others(47): Show | 52 | HG00323.hp1 HG00621.hp2 HG00673.hp1 others(49): Show |
intron_variant | MODIFIER | c.965-4901G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110597056 | ||||||
| chr11:110597136
|
G | A | 1 | a0001c0001t0002g0112 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.965-4981C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110597136 | ||||||
| chr11:110597139
|
G | T | 1 | a0001c0001t0001g0058 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.965-4984C>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110597139 | ||||||
| chr11:110597145
|
T | TG | 8 | a0001c0001t0001g0080a0001c0001t0001g0131a0001c0001t0002g0069others(5): Show | 8 | HG02602.hp2 HG03017.hp2 HG03239.hp2 others(5): Show |
intron_variant | MODIFIER | c.965-4991dupC | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110597145 | ||||||
| chr11:110597294
|
T | TA | 19 | a0001c0001t0001g0210a0001c0001t0003g0104a0001c0001t0003g0216others(16): Show | 19 | HG00099.hp2 HG00280.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.965-5140dupT | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110597294 | ||||||
| chr11:110597294
|
T | TAA | 45 | a0001c0001t0002g0008a0001c0001t0002g0022a0001c0001t0002g0023others(42): Show | 45 | HG00558.hp2 HG00738.hp2 HG01099.hp1 others(42): Show |
intron_variant | MODIFIER | c.965-5141_965-5140d others(4): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110597294 | ||||||
| chr11:110597294
|
TA | T | 5 | a0001c0001t0003g0021a0001c0001t0003g0098a0001c0001t0003g0099others(2): Show | 5 | HG03834.hp2 HG03942.hp2 NA18954.hp1 others(2): Show |
intron_variant | MODIFIER | c.965-5140delT | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110597294 | ||||||
| chr11:110597394
|
T | C | 1 | a0001c0001t0003g0038 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.965-5239A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110597394 | ||||||
| chr11:110597471
|
T | C | 1 | a0009c0015t0004g0153 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.965-5316A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110597471 | ||||||
| chr11:110597565
|
T | C | 7 | a0001c0001t0004g0004a0001c0001t0004g0009a0001c0001t0004g0010others(4): Show | 8 | HG02145.hp2 HG02647.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.965-5410A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110597565 | ||||||
| chr11:110598137
|
G | A | 2 | a0001c0001t0003g0065a0001c0001t0003g0123 | 2 | HG02683.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.965-5982C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110598137 | ||||||
| chr11:110598172
|
C | CT | 123 | a0001c0001t0001g0114a0001c0001t0001g0134a0001c0001t0001g0163others(120): Show | 126 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.965-6018dupA | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110598172 | ||||||
| chr11:110598185
|
T | TC | 4 | a0001c0005t0005g0142a0001c0005t0005g0197a0003c0004t0002g0144others(1): Show | 4 | HG01891.hp1 HG02451.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-6031dupG | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110598185 | ||||||
| chr11:110598602
|
A | G | 75 | a0001c0001t0001g0210a0001c0001t0002g0008a0001c0001t0002g0022others(72): Show | 76 | HG00099.hp2 HG00280.hp2 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.965-6447T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110598602 | ||||||
| chr11:110598744
|
T | C | 1 | a0002c0003t0007g0150 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.965-6589A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110598744 | ||||||
| chr11:110598773
|
G | A | 75 | a0001c0001t0001g0210a0001c0001t0002g0008a0001c0001t0002g0022others(72): Show | 76 | HG00099.hp2 HG00280.hp2 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.965-6618C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110598773 | ||||||
| chr11:110598886
|
G | A | 1 | a0002c0006t0012g0111 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.965-6731C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110598886 | ||||||
| chr11:110598901
|
C | T | 2 | a0006c0007t0010g0147a0006c0007t0010g0148 | 2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.965-6746G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110598901 | ||||||
| chr11:110599182
|
A | G | 1 | a0001c0001t0003g0094 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.965-7027T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110599182 | ||||||
| chr11:110599231
|
C | G | 3 | a0001c0001t0006g0199a0001c0001t0006g0200a0001c0001t0006g0201 | 3 | HG02109.hp1 HG02486.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.965-7076G>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110599231 | ||||||
| chr11:110599386
|
C | A | 23 | a0001c0001t0001g0210a0001c0001t0003g0216a0001c0001t0004g0004others(20): Show | 24 | HG00099.hp2 HG00280.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.964+7175G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110599386 | ||||||
| chr11:110599402
|
AC | A | 4 | a0001c0001t0002g0008a0001c0001t0002g0022a0001c0001t0002g0023others(1): Show | 4 | HG02280.hp2 HG03041.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.964+7158delG | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110599402 | ||||||
| chr11:110599425
|
G | A | 1 | a0001c0001t0001g0155 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.964+7136C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110599425 | ||||||
| chr11:110599434
|
C | T | 2 | a0006c0007t0010g0147a0006c0007t0010g0148 | 2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.964+7127G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110599434 | ||||||
| chr11:110599456
|
G | T | 1 | a0001c0001t0001g0020 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.964+7105C>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110599456 | ||||||
| chr11:110599498
|
G | A | 2 | a0001c0001t0003g0089a0001c0001t0003g0096 | 2 | NA18951.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.964+7063C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110599498 | ||||||
| chr11:110599766
|
GACTACCC | G | 7 | a0001c0001t0002g0204a0001c0001t0002g0205a0001c0001t0002g0206others(4): Show | 7 | HG01074.hp1 HG01891.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.964+6788_964+6794d others(9): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110599766 | ||||||
| chr11:110599831
|
G | A | 2 | a0002c0006t0012g0140a0002c0014t0019g0207 | 2 | HG01952.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.964+6730C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110599831 | ||||||
| chr11:110599862
|
C | G | 129 | a0001c0001t0001g0134a0001c0001t0001g0163a0001c0001t0001g0210others(126): Show | 132 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.964+6699G>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110599862 | ||||||
| chr11:110599867
|
C | T | 2 | a0001c0001t0001g0055a0001c0001t0001g0056 | 2 | HG01261.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.964+6694G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110599867 | ||||||
| chr11:110599915
|
G | T | 4 | a0001c0001t0003g0216a0001c0002t0005g0211a0001c0002t0005g0217others(1): Show | 4 | HG02015.hp1 HG02080.hp1 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.964+6646C>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110599915 | ||||||
| chr11:110600088
|
C | G | 2 | a0003c0004t0002g0144a0008c0017t0002g0141 | 2 | HG03688.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.964+6473G>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110600088 | ||||||
| chr11:110600190
|
G | T | 1 | a0001c0001t0001g0066 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.964+6371C>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110600190 | ||||||
| chr11:110600235
|
T | G | 2 | a0001c0001t0003g0091a0001c0001t0003g0101 | 2 | HG01346.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.964+6326A>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110600235 | ||||||
| chr11:110600327
|
T | C | 4 | a0001c0001t0006g0156a0001c0001t0006g0199a0001c0001t0006g0200others(1): Show | 4 | HG02109.hp1 HG02486.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.964+6234A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110600327 | ||||||
| chr11:110600404
|
A | C | 47 | a0001c0001t0002g0008a0001c0001t0002g0022a0001c0001t0002g0023others(44): Show | 47 | HG00558.hp2 HG00738.hp2 HG01099.hp1 others(44): Show |
intron_variant | MODIFIER | c.964+6157T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110600404 | ||||||
| chr11:110600443
|
C | T | 1 | a0001c0001t0002g0070 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.964+6118G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110600443 | ||||||
| chr11:110600510
|
G | A | 1 | a0003c0004t0002g0162 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.964+6051C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110600510 | ||||||
| chr11:110600514
|
C | A | 30 | a0001c0001t0001g0210a0001c0001t0003g0216a0001c0001t0004g0004others(27): Show | 31 | HG00099.hp2 HG00280.hp2 HG01891.hp1 others(28): Show |
intron_variant | MODIFIER | c.964+6047G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110600514 | ||||||
| chr11:110600588
|
T | G | 79 | a0001c0001t0001g0210a0001c0001t0002g0008a0001c0001t0002g0022others(76): Show | 80 | HG00099.hp2 HG00280.hp2 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.964+5973A>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110600588 | ||||||
| chr11:110600700
|
ATAACAGT others(12): Show |
A | 10 | a0001c0001t0001g0210a0001c0001t0003g0216a0001c0002t0005g0209others(7): Show | 10 | HG00099.hp2 HG00280.hp2 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.964+5842_964+5860d others(21): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110600700 | ||||||
| chr11:110600753
|
G | T | 1 | a0005c0010t0001g0180 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.964+5808C>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110600753 | ||||||
| chr11:110600812
|
GA | G | 7 | a0001c0001t0002g0204a0001c0001t0002g0205a0001c0001t0002g0206others(4): Show | 7 | HG01074.hp1 HG01891.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.964+5748delT | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110600812 | ||||||
| chr11:110601107
|
G | A | 2 | a0002c0006t0012g0140a0002c0014t0019g0207 | 2 | HG01952.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.964+5454C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110601107 | ||||||
| chr11:110601306
|
T | C | 43 | a0001c0001t0001g0134a0001c0001t0001g0163a0001c0001t0003g0001others(40): Show | 45 | HG00323.hp1 HG00621.hp2 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.964+5255A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110601306 | ||||||
| chr11:110601444
|
A | G | 13 | a0001c0001t0001g0210a0001c0001t0003g0216a0001c0002t0005g0209others(10): Show | 13 | HG00099.hp2 HG00280.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.964+5117T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110601444 | ||||||
| chr11:110601763
|
C | A | 1 | a0001c0005t0005g0197 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.964+4798G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110601763 | ||||||
| chr11:110601829
|
C | CA | 7 | a0001c0001t0004g0004a0001c0001t0004g0009a0001c0001t0004g0010others(4): Show | 8 | HG02145.hp2 HG02647.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.964+4731dupT | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110601829 | ||||||
| chr11:110601835
|
A | T | 1 | a0001c0001t0003g0097 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.964+4726T>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110601835 | ||||||
| chr11:110601837
|
A | G | 45 | a0001c0001t0002g0008a0001c0001t0002g0022a0001c0001t0002g0023others(42): Show | 45 | HG00558.hp2 HG00738.hp2 HG01099.hp1 others(42): Show |
intron_variant | MODIFIER | c.964+4724T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110601837 | ||||||
| chr11:110601898
|
GA | G | 4 | a0001c0001t0001g0047a0001c0001t0001g0068a0001c0001t0001g0083others(1): Show | 4 | HG01928.hp1 NA18948.hp2 NA18997.hp2 others(1): Show |
intron_variant | MODIFIER | c.964+4662delT | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110601898 | ||||||
| chr11:110601981
|
C | CA | 14 | a0001c0001t0001g0131a0001c0001t0002g0204a0001c0001t0002g0205others(11): Show | 14 | HG01074.hp1 HG01891.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.964+4579dupT | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110601981 | ||||||
| chr11:110601981
|
CA | C | 67 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0106others(64): Show | 67 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.964+4579delT | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110601981 | ||||||
| chr11:110601998
|
A | T | 1 | a0002c0014t0019g0207 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.964+4563T>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110601998 | ||||||
| chr11:110602112
|
T | A | 1 | a0011c0018t0015g0007 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.964+4449A>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110602112 | ||||||
| chr11:110602214
|
C | T | 2 | a0006c0007t0010g0147a0006c0007t0010g0148 | 2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.964+4347G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110602214 | ||||||
| chr11:110602222
|
C | CT | 123 | a0001c0001t0001g0134a0001c0001t0001g0163a0001c0001t0001g0210others(120): Show | 126 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.964+4338dupA | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110602222 | ||||||
| chr11:110602399
|
T | C | 1 | a0001c0001t0001g0184 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.964+4162A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110602399 | ||||||
| chr11:110602513
|
T | C | 2 | a0006c0007t0010g0147a0006c0007t0010g0148 | 2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.964+4048A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110602513 | ||||||
| chr11:110602999
|
G | C | 75 | a0001c0001t0001g0210a0001c0001t0002g0008a0001c0001t0002g0022others(72): Show | 76 | HG00099.hp2 HG00280.hp2 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.964+3562C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110602999 | ||||||
| chr11:110603251
|
T | C | 2 | a0001c0005t0005g0142a0001c0005t0005g0197 | 2 | HG01891.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.964+3310A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110603251 | ||||||
| chr11:110603359
|
A | G | 7 | a0001c0001t0004g0004a0001c0001t0004g0009a0001c0001t0004g0010others(4): Show | 8 | HG02145.hp2 HG02647.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.964+3202T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110603359 | ||||||
| chr11:110603555
|
T | A | 4 | a0001c0001t0006g0156a0001c0001t0006g0199a0001c0001t0006g0200others(1): Show | 4 | HG02109.hp1 HG02486.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.964+3006A>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110603555 | ||||||
| chr11:110603574
|
T | C | 2 | a0001c0001t0001g0169a0001c0001t0001g0171 | 2 | HG01169.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.964+2987A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110603574 | ||||||
| chr11:110603803
|
C | A | 43 | a0001c0001t0001g0134a0001c0001t0001g0163a0001c0001t0003g0001others(40): Show | 45 | HG00323.hp1 HG00621.hp2 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.964+2758G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110603803 | ||||||
| chr11:110604064
|
T | C | 1 | a0003c0004t0017g0145 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.964+2497A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110604064 | ||||||
| chr11:110604250
|
G | A | 1 | a0007c0020t0020g0149 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.964+2311C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110604250 | ||||||
| chr11:110604271
|
C | T | 1 | a0003c0004t0017g0145 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.964+2290G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110604271 | ||||||
| chr11:110604585
|
T | C | 13 | a0001c0001t0001g0210a0001c0001t0003g0216a0001c0002t0005g0209others(10): Show | 13 | HG00099.hp2 HG00280.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.964+1976A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110604585 | ||||||
| chr11:110604684
|
A | G | 75 | a0001c0001t0001g0210a0001c0001t0002g0008a0001c0001t0002g0022others(72): Show | 76 | HG00099.hp2 HG00280.hp2 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.964+1877T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110604684 | ||||||
| chr11:110604761
|
G | A | 75 | a0001c0001t0001g0210a0001c0001t0002g0008a0001c0001t0002g0022others(72): Show | 76 | HG00099.hp2 HG00280.hp2 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.964+1800C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110604761 | ||||||
| chr11:110604766
|
T | C | 30 | a0001c0001t0001g0210a0001c0001t0003g0216a0001c0001t0004g0004others(27): Show | 31 | HG00099.hp2 HG00280.hp2 HG01891.hp1 others(28): Show |
intron_variant | MODIFIER | c.964+1795A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110604766 | ||||||
| chr11:110604814
|
C | G | 2 | a0004c0011t0002g0028a0004c0011t0002g0128 | 2 | NA19075.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.964+1747G>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110604814 | ||||||
| chr11:110604996
|
A | G | 2 | a0003c0004t0002g0144a0008c0017t0002g0141 | 2 | HG03688.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.964+1565T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110604996 | ||||||
| chr11:110605010
|
G | A | 1 | a0001c0001t0003g0093 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.964+1551C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110605010 | ||||||
| chr11:110605176
|
T | A | 1 | a0001c0001t0001g0080 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.964+1385A>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110605176 | ||||||
| chr11:110605202
|
T | A | 2 | a0001c0001t0002g0205a0001c0001t0002g0206 | 2 | HG01891.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.964+1359A>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110605202 | ||||||
| chr11:110605335
|
T | C | 49 | a0001c0001t0002g0008a0001c0001t0002g0022a0001c0001t0002g0023others(46): Show | 49 | HG00558.hp2 HG00738.hp2 HG01099.hp1 others(46): Show |
intron_variant | MODIFIER | c.964+1226A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110605335 | ||||||
| chr11:110605516
|
G | A | 3 | a0009c0015t0004g0153a0011c0018t0015g0007a0012c0019t0004g0151 | 3 | HG02809.hp1 NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.964+1045C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110605516 | ||||||
| chr11:110605724
|
T | G | 3 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117 | 3 | HG00280.hp1 HG01074.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.964+837A>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110605724 | ||||||
| chr11:110605812
|
C | T | 47 | a0001c0001t0002g0008a0001c0001t0002g0022a0001c0001t0002g0023others(44): Show | 47 | HG00558.hp2 HG00738.hp2 HG01099.hp1 others(44): Show |
intron_variant | MODIFIER | c.964+749G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110605812 | ||||||
| chr11:110605822
|
C | G | 43 | a0001c0001t0001g0134a0001c0001t0001g0163a0001c0001t0003g0001others(40): Show | 45 | HG00323.hp1 HG00621.hp2 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.964+739G>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110605822 | ||||||
| chr11:110605823
|
G | A | 1 | a0003c0004t0017g0145 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.964+738C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110605823 | ||||||
| chr11:110605870
|
T | C | 1 | a0002c0006t0012g0140 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.964+691A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110605870 | ||||||
| chr11:110605907
|
AC | A | 7 | a0001c0001t0002g0204a0001c0001t0002g0205a0001c0001t0002g0206others(4): Show | 7 | HG01074.hp1 HG01891.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.964+653delG | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110605907 | ||||||
| chr11:110605961
|
G | A | 43 | a0001c0001t0001g0134a0001c0001t0001g0163a0001c0001t0003g0001others(40): Show | 45 | HG00323.hp1 HG00621.hp2 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.964+600C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110605961 | ||||||
| chr11:110606148
|
A | G | 2 | a0002c0006t0012g0140a0002c0014t0019g0207 | 2 | HG01952.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.964+413T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110606148 | ||||||
| chr11:110606167
|
A | G | 1 | a0001c0001t0001g0103 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.964+394T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110606167 | ||||||
| chr11:110606191
|
T | C | 1 | a0001c0001t0011g0017 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.964+370A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110606191 | ||||||
| chr11:110606202
|
C | T | 1 | a0001c0001t0001g0103 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.964+359G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110606202 | ||||||
| chr11:110606309
|
T | C | 1 | a0002c0014t0019g0207 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.964+252A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110606309 | ||||||
| chr11:110606488
|
C | A | 36 | a0001c0001t0002g0024a0001c0001t0002g0026a0001c0001t0002g0029others(33): Show | 36 | HG00558.hp2 HG01109.hp2 HG01192.hp2 others(33): Show |
intron_variant | MODIFIER | c.964+73G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110606488 | ||||||
| chr11:110606546
|
C | T | 1 | a0001c0001t0003g0065 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.964+15G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110606546 | ||||||
| chr11:110607075
|
T | C | 23 | a0001c0001t0001g0210a0001c0001t0003g0216a0001c0001t0004g0004others(20): Show | 24 | HG00099.hp2 HG00280.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.776-326A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 8/14 | chr11 | 110607075 | ||||||
| chr11:110607183
|
A | G | 2 | a0006c0007t0010g0147a0006c0007t0010g0148 | 2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.776-434T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 8/14 | chr11 | 110607183 | ||||||
| chr11:110607484
|
G | A | 1 | a0003c0004t0017g0145 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.776-735C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 8/14 | chr11 | 110607484 | ||||||
| chr11:110607673
|
A | G | 1 | a0001c0001t0006g0156 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.776-924T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 8/14 | chr11 | 110607673 | ||||||
| chr11:110607816
|
A | G | 1 | a0002c0006t0012g0111 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.776-1067T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 8/14 | chr11 | 110607816 | ||||||
| chr11:110607868
|
A | G | 51 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0025others(48): Show | 52 | HG00621.hp1 HG00639.hp2 HG00673.hp2 others(49): Show |
intron_variant | MODIFIER | c.775+1116T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 8/14 | chr11 | 110607868 | ||||||
| chr11:110607929
|
A | C | 1 | a0009c0015t0004g0153 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.775+1055T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 8/14 | chr11 | 110607929 | ||||||
| chr11:110607998
|
C | T | 79 | a0001c0001t0001g0210a0001c0001t0002g0008a0001c0001t0002g0022others(76): Show | 80 | HG00099.hp2 HG00280.hp2 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.775+986G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 8/14 | chr11 | 110607998 | ||||||
| chr11:110608147
|
A | T | 49 | a0001c0001t0002g0008a0001c0001t0002g0022a0001c0001t0002g0023others(46): Show | 49 | HG00558.hp2 HG00738.hp2 HG01099.hp1 others(46): Show |
intron_variant | MODIFIER | c.775+837T>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 8/14 | chr11 | 110608147 | ||||||
| chr11:110608839
|
T | C | 2 | a0006c0007t0010g0147a0006c0007t0010g0148 | 2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.775+145A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 8/14 | chr11 | 110608839 | ||||||
| chr11:110609072
|
T | C | 2 | a0006c0007t0010g0147a0006c0007t0010g0148 | 2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.709-22A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 7/14 | chr11 | 110609072 | ||||||
| chr11:110609115
|
A | ATT | 23 | a0001c0001t0001g0210a0001c0001t0002g0024a0001c0001t0003g0216others(20): Show | 24 | HG00099.hp2 HG00280.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.709-67_709-66dupAA | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 7/14 | chr11 | 110609115 | ||||||
| chr11:110609115
|
ATTT | A | 43 | a0001c0001t0001g0134a0001c0001t0001g0163a0001c0001t0003g0001others(40): Show | 45 | HG00323.hp1 HG00621.hp2 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.709-68_709-66delAA others(1): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 7/14 | chr11 | 110609115 | ||||||
| chr11:110609120
|
T | A | 4 | a0001c0001t0006g0156a0001c0001t0006g0199a0001c0001t0006g0200others(1): Show | 4 | HG02109.hp1 HG02486.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.709-70A>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 7/14 | chr11 | 110609120 | ||||||
| chr11:110609305
|
T | C | 1 | a0001c0001t0002g0204 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.709-255A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 7/14 | chr11 | 110609305 | ||||||
| chr11:110609681
|
T | C | 8 | a0001c0001t0004g0004a0001c0001t0004g0009a0001c0001t0004g0010others(5): Show | 9 | HG02145.hp2 HG02647.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.709-631A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 7/14 | chr11 | 110609681 | ||||||
| chr11:110609692
|
C | A | 4 | a0001c0001t0006g0156a0001c0001t0006g0199a0001c0001t0006g0200others(1): Show | 4 | HG02109.hp1 HG02486.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.709-642G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 7/14 | chr11 | 110609692 | ||||||
| chr11:110609797
|
T | C | 2 | a0006c0007t0010g0147a0006c0007t0010g0148 | 2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.709-747A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 7/14 | chr11 | 110609797 | ||||||
| chr11:110609833
|
C | T | 2 | a0003c0004t0002g0144a0008c0017t0002g0141 | 2 | HG03688.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.709-783G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 7/14 | chr11 | 110609833 | ||||||
| chr11:110610051
|
A | T | 2 | a0002c0006t0012g0140a0002c0014t0019g0207 | 2 | HG01952.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.709-1001T>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 7/14 | chr11 | 110610051 | ||||||
| chr11:110610082
|
A | T | 1 | a0003c0004t0017g0145 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.709-1032T>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 7/14 | chr11 | 110610082 | ||||||
| chr11:110610310
|
C | CAATT | 131 | a0001c0001t0001g0037a0001c0001t0001g0134a0001c0001t0001g0163others(128): Show | 134 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.708+998_708+999ins others(4): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 7/14 | chr11 | 110610310 | ||||||
| chr11:110610326
|
T | C | 3 | a0001c0001t0003g0021a0001c0001t0003g0098a0001c0001t0003g0099 | 3 | NA18954.hp1 NA18999.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.708+983A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 7/14 | chr11 | 110610326 | ||||||
| chr11:110610391
|
T | A | 1 | a0001c0001t0001g0157 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.708+918A>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 7/14 | chr11 | 110610391 | ||||||
| chr11:110610430
|
T | A | 2 | a0002c0006t0012g0140a0002c0014t0019g0207 | 2 | HG01952.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.708+879A>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 7/14 | chr11 | 110610430 | ||||||
| chr11:110610431
|
G | T | 2 | a0002c0006t0012g0140a0002c0014t0019g0207 | 2 | HG01952.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.708+878C>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 7/14 | chr11 | 110610431 | ||||||
| chr11:110610554
|
T | C | 1 | a0001c0001t0001g0090 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.708+755A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 7/14 | chr11 | 110610554 | ||||||
| chr11:110610647
|
C | G | 1 | a0012c0019t0004g0151 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.708+662G>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 7/14 | chr11 | 110610647 | ||||||
| chr11:110610658
|
C | G | 2 | a0003c0004t0002g0144a0008c0017t0002g0141 | 2 | HG03688.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.708+651G>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 7/14 | chr11 | 110610658 | ||||||
| chr11:110610659
|
T | C | 1 | a0001c0001t0002g0084 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.708+650A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 7/14 | chr11 | 110610659 | ||||||
| chr11:110611032
|
A | G | 16 | a0001c0001t0001g0210a0001c0001t0003g0216a0001c0001t0006g0156others(13): Show | 16 | HG00099.hp2 HG00280.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.708+277T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 7/14 | chr11 | 110611032 | ||||||
| chr11:110611420
|
A | G | 4 | a0001c0001t0002g0205a0001c0001t0002g0206a0002c0003t0007g0203others(1): Show | 4 | HG01891.hp2 HG02723.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.631-34T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 6/14 | chr11 | 110611420 | ||||||
| chr11:110611470
|
G | A | 2 | a0009c0015t0004g0153a0012c0019t0004g0151 | 2 | NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.631-84C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 6/14 | chr11 | 110611470 | ||||||
| chr11:110611505
|
C | A | 79 | a0001c0001t0001g0134a0001c0001t0001g0163a0001c0001t0001g0210others(76): Show | 82 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.631-119G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 6/14 | chr11 | 110611505 | ||||||
| chr11:110611574
|
C | T | 1 | a0001c0002t0005g0211 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.631-188G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 6/14 | chr11 | 110611574 | ||||||
| chr11:110611602
|
T | C | 1 | a0002c0006t0012g0140 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.631-216A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 6/14 | chr11 | 110611602 | ||||||
| chr11:110611748
|
G | A | 2 | a0001c0005t0005g0142a0001c0005t0005g0197 | 2 | HG01891.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.631-362C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 6/14 | chr11 | 110611748 | ||||||
| chr11:110611789
|
A | G | 1 | a0001c0001t0001g0210 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.631-403T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 6/14 | chr11 | 110611789 | ||||||
| chr11:110611818
|
C | CAGG | 79 | a0001c0001t0001g0134a0001c0001t0001g0163a0001c0001t0001g0210others(76): Show | 82 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.631-433_631-432ins others(3): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 6/14 | chr11 | 110611818 | ||||||
| chr11:110612137
|
A | T | 4 | a0001c0001t0006g0156a0001c0001t0006g0199a0001c0001t0006g0200others(1): Show | 4 | HG02109.hp1 HG02486.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.631-751T>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 6/14 | chr11 | 110612137 | ||||||
| chr11:110612214
|
C | A | 1 | a0001c0001t0001g0134 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.631-828G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 6/14 | chr11 | 110612214 | ||||||
| chr11:110612254
|
T | TAA | 52 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0025others(49): Show | 53 | HG00099.hp2 HG00621.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.631-870_631-869dup others(2): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 6/14 | chr11 | 110612254 | ||||||
| chr11:110612317
|
A | G | 6 | a0001c0001t0002g0204a0001c0001t0002g0205a0001c0001t0002g0206others(3): Show | 6 | HG01074.hp1 HG01891.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.631-931T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 6/14 | chr11 | 110612317 | ||||||
| chr11:110612347
|
G | A | 1 | a0001c0001t0001g0080 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.631-961C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 6/14 | chr11 | 110612347 | ||||||
| chr11:110612357
|
G | A | 1 | a0003c0004t0017g0145 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.631-971C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 6/14 | chr11 | 110612357 | ||||||
| chr11:110612560
|
C | T | 2 | a0001c0008t0003g0085a0001c0008t0003g0086 | 2 | NA19000.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.631-1174G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 6/14 | chr11 | 110612560 | ||||||
| chr11:110612875
|
G | A | 44 | a0001c0001t0001g0134a0001c0001t0001g0163a0001c0001t0002g0102others(41): Show | 46 | HG00323.hp1 HG00621.hp2 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.631-1489C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 6/14 | chr11 | 110612875 | ||||||
| chr11:110612899
|
C | T | 50 | a0001c0001t0001g0134a0001c0001t0001g0163a0001c0001t0002g0102others(47): Show | 52 | HG00323.hp1 HG00621.hp2 HG00673.hp1 others(49): Show |
intron_variant | MODIFIER | c.631-1513G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 6/14 | chr11 | 110612899 | ||||||
| chr11:110612916
|
C | T | 1 | a0008c0017t0002g0141 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.631-1530G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 6/14 | chr11 | 110612916 | ||||||
| chr11:110612983
|
C | T | 2 | a0001c0005t0005g0142a0001c0005t0005g0197 | 2 | HG01891.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.630+1578G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 6/14 | chr11 | 110612983 | ||||||
| chr11:110613040
|
T | C | 3 | a0001c0001t0001g0005a0001c0001t0001g0174a0001c0001t0001g0193 | 4 | HG02622.hp1 HG03041.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.630+1521A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 6/14 | chr11 | 110613040 | ||||||
| chr11:110613421
|
C | T | 1 | a0001c0001t0004g0143 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.630+1140G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 6/14 | chr11 | 110613421 | ||||||
| chr11:110613529
|
T | G | 19 | a0001c0001t0001g0210a0001c0001t0003g0216a0001c0001t0006g0156others(16): Show | 19 | HG00099.hp2 HG00280.hp2 HG02015.hp1 others(16): Show |
intron_variant | MODIFIER | c.630+1032A>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 6/14 | chr11 | 110613529 | ||||||
| chr11:110613697
|
A | G | 2 | a0001c0001t0006g0200a0001c0001t0006g0201 | 2 | HG02486.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.630+864T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 6/14 | chr11 | 110613697 | ||||||
| chr11:110613827
|
C | A | 51 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0025others(48): Show | 52 | HG00621.hp1 HG00639.hp2 HG00673.hp2 others(49): Show |
intron_variant | MODIFIER | c.630+734G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 6/14 | chr11 | 110613827 | ||||||
| chr11:110613883
|
T | C | 2 | a0006c0007t0010g0147a0006c0007t0010g0148 | 2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.630+678A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 6/14 | chr11 | 110613883 | ||||||
| chr11:110614038
|
C | T | 1 | a0001c0001t0006g0156 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.630+523G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 6/14 | chr11 | 110614038 | ||||||
| chr11:110614175
|
TTAA | T | 10 | a0001c0001t0004g0004a0001c0001t0004g0009a0001c0001t0004g0010others(7): Show | 11 | HG01891.hp1 HG02145.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.630+383_630+385del others(3): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 6/14 | chr11 | 110614175 | ||||||
| chr11:110614266
|
A | G | 2 | a0006c0007t0010g0147a0006c0007t0010g0148 | 2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.630+295T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 6/14 | chr11 | 110614266 | ||||||
| chr11:110614417
|
C | T | 4 | a0002c0003t0007g0150a0009c0015t0004g0153a0011c0018t0015g0007others(1): Show | 4 | HG02257.hp1 HG02809.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.630+144G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 6/14 | chr11 | 110614417 | ||||||
| chr11:110614466
|
A | AGCCT | 6 | a0001c0001t0002g0204a0001c0001t0002g0205a0001c0001t0002g0206others(3): Show | 6 | HG01074.hp1 HG01891.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.630+91_630+94dupAG others(2): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 6/14 | chr11 | 110614466 | ||||||
| chr11:110614502
|
G | A | 1 | a0002c0003t0007g0202 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.630+59C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 6/14 | chr11 | 110614502 | ||||||
| chr11:110614508
|
T | C | 1 | a0001c0001t0003g0049 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.630+53A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 6/14 | chr11 | 110614508 | ||||||
| chr11:110614660
|
C | T | 2 | a0001c0005t0005g0142a0001c0005t0005g0197 | 2 | HG01891.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.546-15G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 5/14 | chr11 | 110614660 | ||||||
| chr11:110614670
|
A | G | 1 | a0001c0001t0001g0025 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.546-25T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 5/14 | chr11 | 110614670 | ||||||
| chr11:110614771
|
T | C | 1 | a0007c0020t0020g0149 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.546-126A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 5/14 | chr11 | 110614771 | ||||||
| chr11:110615019
|
A | T | 7 | a0001c0001t0004g0004a0001c0001t0004g0009a0001c0001t0004g0010others(4): Show | 8 | HG02145.hp2 HG02647.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.546-374T>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 5/14 | chr11 | 110615019 | ||||||
| chr11:110615279
|
G | A | 1 | a0001c0001t0003g0094 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.545+274C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 5/14 | chr11 | 110615279 | ||||||
| chr11:110615327
|
C | T | 1 | a0002c0006t0012g0111 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.545+226G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 5/14 | chr11 | 110615327 | ||||||
| chr11:110615396
|
G | C | 45 | a0001c0001t0001g0037a0001c0001t0002g0008a0001c0001t0002g0022others(42): Show | 45 | HG00558.hp2 HG00738.hp2 HG01099.hp1 others(42): Show |
intron_variant | MODIFIER | c.545+157C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 5/14 | chr11 | 110615396 | ||||||
| chr11:110615746
|
C | G | 29 | a0001c0001t0001g0210a0001c0001t0003g0216a0001c0001t0004g0004others(26): Show | 30 | HG00099.hp2 HG00280.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.504-152G>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110615746 | ||||||
| chr11:110615892
|
T | A | 1 | a0002c0006t0012g0111 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.504-298A>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110615892 | ||||||
| chr11:110616096
|
G | C | 1 | a0001c0002t0005g0217 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.504-502C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110616096 | ||||||
| chr11:110616155
|
T | TA | 43 | a0001c0001t0001g0134a0001c0001t0001g0163a0001c0001t0002g0102others(40): Show | 45 | HG00323.hp1 HG00621.hp2 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.504-562dupT | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110616155 | ||||||
| chr11:110616427
|
T | C | 46 | a0001c0001t0001g0037a0001c0001t0002g0008a0001c0001t0002g0022others(43): Show | 46 | HG00558.hp2 HG00738.hp2 HG01099.hp1 others(43): Show |
intron_variant | MODIFIER | c.504-833A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110616427 | ||||||
| chr11:110616507
|
A | G | 83 | a0001c0001t0001g0134a0001c0001t0001g0163a0001c0001t0001g0210others(80): Show | 86 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.504-913T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110616507 | ||||||
| chr11:110616686
|
C | CT | 59 | a0001c0001t0001g0134a0001c0001t0001g0163a0001c0001t0001g0210others(56): Show | 61 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.504-1093dupA | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110616686 | ||||||
| chr11:110616686
|
C | T | 1 | a0001c0001t0003g0132 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.504-1092G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110616686 | ||||||
| chr11:110616686
|
CT | C | 17 | a0001c0001t0001g0194a0001c0001t0004g0004a0001c0001t0004g0009others(14): Show | 18 | HG01952.hp2 HG02145.hp2 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.504-1093delA | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110616686 | ||||||
| chr11:110617120
|
G | A | 1 | a0001c0002t0005g0209 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.504-1526C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110617120 | ||||||
| chr11:110617419
|
C | T | 2 | a0006c0007t0010g0147a0006c0007t0010g0148 | 2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.504-1825G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110617419 | ||||||
| chr11:110617515
|
C | G | 83 | a0001c0001t0001g0134a0001c0001t0001g0163a0001c0001t0001g0210others(80): Show | 86 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.504-1921G>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110617515 | ||||||
| chr11:110617824
|
C | A | 2 | a0002c0006t0012g0140a0002c0014t0019g0207 | 2 | HG01952.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.504-2230G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110617824 | ||||||
| chr11:110617891
|
C | T | 3 | a0001c0001t0006g0199a0001c0001t0006g0200a0001c0001t0006g0201 | 3 | HG02109.hp1 HG02486.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.504-2297G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110617891 | ||||||
| chr11:110618161
|
G | GA | 28 | a0001c0001t0001g0210a0001c0001t0003g0216a0001c0001t0004g0004others(25): Show | 29 | HG00099.hp2 HG00280.hp2 HG01891.hp1 others(26): Show |
intron_variant | MODIFIER | c.504-2568dupT | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110618161 | ||||||
| chr11:110618161
|
G | GAAAAAAA others(13): Show |
1 | a0001c0002t0005g0215 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.504-2568_504-2567i others(22): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110618161 | ||||||
| chr11:110618190
|
A | G | 29 | a0001c0001t0001g0210a0001c0001t0003g0216a0001c0001t0004g0004others(26): Show | 30 | HG00099.hp2 HG00280.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.504-2596T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110618190 | ||||||
| chr11:110618291
|
C | G | 2 | a0003c0004t0002g0144a0008c0017t0002g0141 | 2 | HG03688.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.504-2697G>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110618291 | ||||||
| chr11:110618449
|
G | T | 85 | a0001c0001t0001g0134a0001c0001t0001g0163a0001c0001t0001g0210others(82): Show | 88 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.504-2855C>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110618449 | ||||||
| chr11:110618491
|
C | T | 1 | a0001c0001t0001g0154 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.504-2897G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110618491 | ||||||
| chr11:110618501
|
G | A | 2 | a0009c0015t0004g0153a0012c0019t0004g0151 | 2 | NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.504-2907C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110618501 | ||||||
| chr11:110618543
|
T | C | 1 | a0001c0002t0005g0214 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.504-2949A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110618543 | ||||||
| chr11:110618546
|
G | A | 1 | a0001c0002t0005g0214 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.504-2952C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110618546 | ||||||
| chr11:110618581
|
TAGTGATA others(10): Show |
T | 4 | a0002c0006t0012g0140a0002c0014t0019g0207a0006c0007t0010g0147others(1): Show | 4 | HG01952.hp2 HG02622.hp2 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.504-3004_504-2988d others(19): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110618581 | ||||||
| chr11:110618655
|
T | C | 2 | a0003c0004t0002g0144a0008c0017t0002g0141 | 2 | HG03688.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.504-3061A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110618655 | ||||||
| chr11:110618671
|
ATAGAGTA others(223): Show |
A | 5 | a0001c0001t0001g0075a0001c0001t0002g0008a0001c0001t0002g0022others(2): Show | 5 | HG02280.hp2 HG03017.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.504-3307_504-3078d others(2): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110618671 | ||||||
| chr11:110618751
|
G | A | 2 | a0001c0005t0005g0142a0001c0005t0005g0197 | 2 | HG01891.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.504-3157C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110618751 | ||||||
| chr11:110618761
|
ATATGTAG others(10): Show |
A | 1 | a0001c0008t0003g0085 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.504-3184_504-3168d others(19): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110618761 | ||||||
| chr11:110618783
|
CAGTGATA others(436): Show |
C | 7 | a0001c0001t0004g0004a0001c0001t0004g0009a0001c0001t0004g0010others(4): Show | 8 | HG02145.hp2 HG02647.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.504-3632_504-3190d others(2): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110618783 | ||||||
| chr11:110618809
|
AGT | A | 2 | a0001c0005t0005g0142a0001c0005t0005g0197 | 2 | HG01891.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.504-3217_504-3216d others(4): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110618809 | ||||||
| chr11:110618871
|
A | C | 3 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0219 | 3 | HG00099.hp1 HG00741.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.504-3277T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110618871 | ||||||
| chr11:110618871
|
AGTATATG others(453): Show |
A | 76 | a0001c0001t0001g0134a0001c0001t0001g0163a0001c0001t0001g0210others(73): Show | 78 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.504-3737_504-3278d others(2): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110618871 | ||||||
| chr11:110618874
|
ATATGCAG others(161): Show |
A | 1 | a0007c0020t0020g0149 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.504-3448_504-3281d others(2): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110618874 | ||||||
| chr11:110618896
|
C | T | 1 | a0011c0018t0015g0007 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.504-3302G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110618896 | ||||||
| chr11:110618901
|
G | A | 1 | a0011c0018t0015g0007 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.504-3307C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110618901 | ||||||
| chr11:110618905
|
A | C | 1 | a0011c0018t0015g0007 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.504-3311T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110618905 | ||||||
| chr11:110618906
|
G | A | 1 | a0011c0018t0015g0007 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.504-3312C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110618906 | ||||||
| chr11:110618906
|
GTATATGC others(453): Show |
G | 2 | a0001c0001t0002g0031a0001c0001t0014g0006 | 2 | HG03540.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.504-3772_504-3313d others(2): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110618906 | ||||||
| chr11:110618912
|
GCAGTGAT others(470): Show |
G | 1 | a0011c0018t0015g0007 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.504-3795_504-3319d others(2): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110618912 | ||||||
| chr11:110618996
|
TAGTGATA others(10): Show |
T | 1 | a0001c0008t0003g0085 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.504-3419_504-3403d others(19): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110618996 | ||||||
| chr11:110619008
|
G | A | 4 | a0001c0001t0002g0008a0001c0001t0002g0022a0001c0001t0002g0023others(1): Show | 4 | HG02280.hp2 HG03041.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.504-3414C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110619008 | ||||||
| chr11:110619038
|
G | C | 1 | a0001c0001t0001g0152 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.504-3444C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110619038 | ||||||
| chr11:110619059
|
A | G | 1 | a0001c0001t0002g0122 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.504-3465T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110619059 | ||||||
| chr11:110619064
|
C | T | 1 | a0007c0020t0020g0149 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.504-3470G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110619064 | ||||||
| chr11:110619087
|
G | A | 1 | a0007c0020t0020g0149 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.504-3493C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110619087 | ||||||
| chr11:110619101
|
AGTATATG others(223): Show |
A | 127 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0016others(124): Show | 130 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.504-3737_504-3508d others(2): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110619101 | ||||||
| chr11:110619160
|
C | T | 1 | a0007c0020t0020g0149 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.504-3566G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110619160 | ||||||
| chr11:110619169
|
A | T | 1 | a0007c0020t0020g0149 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.504-3575T>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110619169 | ||||||
| chr11:110619172
|
ATATGCAG others(138): Show |
A | 1 | a0007c0020t0020g0149 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.504-3723_504-3579d others(2): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110619172 | ||||||
| chr11:110619322
|
C | T | 1 | a0007c0020t0020g0149 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.504-3728G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110619322 | ||||||
| chr11:110619331
|
G | A | 12 | a0001c0001t0002g0008a0001c0001t0002g0022a0001c0001t0002g0023others(9): Show | 13 | HG02145.hp2 HG02280.hp2 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.504-3737C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110619331 | ||||||
| chr11:110619360
|
G | A | 2 | a0006c0007t0010g0147a0006c0007t0010g0148 | 2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.504-3766C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110619360 | ||||||
| chr11:110619361
|
ATAGCATA others(4): Show |
A | 1 | a0007c0020t0020g0149 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.504-3778_504-3768d others(13): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110619361 | ||||||
| chr11:110619376
|
A | G | 1 | a0007c0020t0020g0149 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.504-3782T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110619376 | ||||||
| chr11:110619393
|
A | G | 1 | a0007c0020t0020g0149 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.504-3799T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110619393 | ||||||
| chr11:110619406
|
ATAGAGTA others(10): Show |
A | 1 | a0007c0020t0020g0149 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.504-3829_504-3813d others(19): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110619406 | ||||||
| chr11:110619440
|
A | G | 4 | a0001c0001t0002g0062a0002c0006t0012g0140a0002c0014t0019g0207others(1): Show | 4 | HG01952.hp2 HG02257.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.504-3846T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110619440 | ||||||
| chr11:110619467
|
T | G | 1 | a0013c0021t0005g0220 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.504-3873A>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110619467 | ||||||
| chr11:110619571
|
T | C | 2 | a0002c0006t0012g0140a0002c0014t0019g0207 | 2 | HG01952.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.504-3977A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110619571 | ||||||
| chr11:110619580
|
C | A | 2 | a0002c0006t0012g0140a0002c0014t0019g0207 | 2 | HG01952.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.504-3986G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110619580 | ||||||
| chr11:110619597
|
A | C | 2 | a0002c0006t0012g0140a0002c0014t0019g0207 | 2 | HG01952.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.504-4003T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110619597 | ||||||
| chr11:110619600
|
G | A | 2 | a0002c0006t0012g0140a0002c0014t0019g0207 | 2 | HG01952.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.504-4006C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110619600 | ||||||
| chr11:110619634
|
A | G | 17 | a0001c0001t0001g0210a0001c0001t0003g0216a0001c0001t0006g0156others(14): Show | 17 | HG00099.hp2 HG00280.hp2 HG01952.hp2 others(14): Show |
intron_variant | MODIFIER | c.504-4040T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110619634 | ||||||
| chr11:110619645
|
T | C | 1 | a0003c0004t0017g0145 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.504-4051A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110619645 | ||||||
| chr11:110619656
|
T | C | 2 | a0002c0006t0012g0140a0002c0014t0019g0207 | 2 | HG01952.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.504-4062A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110619656 | ||||||
| chr11:110619673
|
C | T | 4 | a0001c0001t0003g0216a0001c0002t0005g0211a0001c0002t0005g0217others(1): Show | 4 | HG02015.hp1 HG02080.hp1 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.504-4079G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110619673 | ||||||
| chr11:110619673
|
CAGTGATA others(10): Show |
C | 50 | a0001c0001t0001g0134a0001c0001t0001g0163a0001c0001t0002g0102others(47): Show | 52 | HG00323.hp1 HG00621.hp2 HG00673.hp1 others(49): Show |
intron_variant | MODIFIER | c.504-4096_504-4080d others(19): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110619673 | ||||||
| chr11:110619690
|
T | C | 2 | a0002c0006t0012g0140a0002c0014t0019g0207 | 2 | HG01952.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.504-4096A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110619690 | ||||||
| chr11:110619705
|
T | C | 1 | a0001c0001t0002g0039 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.504-4111A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110619705 | ||||||
| chr11:110619706
|
A | G | 2 | a0002c0006t0012g0140a0002c0014t0019g0207 | 2 | HG01952.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.504-4112T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110619706 | ||||||
| chr11:110619707
|
C | CAGTGATA others(10): Show |
3 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0042 | 3 | NA18940.hp2 NA18978.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.504-4130_504-4114d others(19): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110619707 | ||||||
| chr11:110619707
|
C | T | 2 | a0002c0006t0012g0140a0002c0014t0019g0207 | 2 | HG01952.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.504-4113G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110619707 | ||||||
| chr11:110619769
|
T | C | 2 | a0001c0001t0006g0156a0008c0017t0002g0141 | 2 | HG02559.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.504-4175A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110619769 | ||||||
| chr11:110619958
|
T | C | 2 | a0001c0001t0004g0009a0001c0001t0004g0010 | 2 | HG02647.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.503+4204A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110619958 | ||||||
| chr11:110620217
|
GA | G | 44 | a0001c0001t0001g0134a0001c0001t0001g0163a0001c0001t0002g0102others(41): Show | 46 | HG00323.hp1 HG00621.hp2 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.503+3944delT | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110620217 | ||||||
| chr11:110620351
|
A | G | 1 | a0001c0001t0001g0182 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.503+3811T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110620351 | ||||||
| chr11:110620353
|
A | G | 1 | a0013c0021t0005g0220 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.503+3809T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110620353 | ||||||
| chr11:110620374
|
CT | C | 2 | a0001c0008t0003g0085a0001c0008t0003g0086 | 2 | NA19000.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.503+3787delA | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110620374 | ||||||
| chr11:110620376
|
C | A | 2 | a0001c0008t0003g0085a0001c0008t0003g0086 | 2 | NA19000.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.503+3786G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110620376 | ||||||
| chr11:110620405
|
C | T | 10 | a0001c0001t0004g0004a0001c0001t0004g0009a0001c0001t0004g0010others(7): Show | 11 | HG01891.hp1 HG02145.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.503+3757G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110620405 | ||||||
| chr11:110620682
|
T | C | 1 | a0001c0001t0003g0038 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.503+3480A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110620682 | ||||||
| chr11:110620687
|
A | T | 1 | a0001c0001t0001g0115 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.503+3475T>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110620687 | ||||||
| chr11:110620800
|
G | A | 8 | a0001c0001t0002g0081a0001c0001t0002g0158a0001c0001t0002g0159others(5): Show | 8 | HG00673.hp2 HG02040.hp1 HG02071.hp2 others(5): Show |
intron_variant | MODIFIER | c.503+3362C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110620800 | ||||||
| chr11:110620995
|
A | C | 4 | a0002c0006t0012g0140a0002c0014t0019g0207a0003c0004t0002g0144others(1): Show | 4 | HG01952.hp2 HG03017.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.503+3167T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110620995 | ||||||
| chr11:110621071
|
T | C | 4 | a0002c0003t0007g0150a0009c0015t0004g0153a0011c0018t0015g0007others(1): Show | 4 | HG02257.hp1 HG02809.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.503+3091A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110621071 | ||||||
| chr11:110621074
|
C | CA | 127 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0020others(124): Show | 131 | HG00099.hp1 HG00323.hp2 HG00558.hp1 others(128): Show |
intron_variant | MODIFIER | c.503+3087dupT | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110621074 | ||||||
| chr11:110621074
|
C | CAA | 17 | a0001c0001t0001g0016a0001c0001t0001g0056a0001c0001t0001g0103others(14): Show | 17 | HG00280.hp1 HG00733.hp1 HG01074.hp2 others(14): Show |
intron_variant | MODIFIER | c.503+3086_503+3087d others(4): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110621074 | ||||||
| chr11:110621232
|
G | A | 65 | a0001c0001t0001g0134a0001c0001t0001g0163a0001c0001t0001g0210others(62): Show | 67 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.503+2930C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110621232 | ||||||
| chr11:110621292
|
T | A | 1 | a0001c0002t0005g0113 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.503+2870A>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110621292 | ||||||
| chr11:110621356
|
C | T | 2 | a0006c0007t0010g0147a0006c0007t0010g0148 | 2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.503+2806G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110621356 | ||||||
| chr11:110621359
|
G | A | 44 | a0001c0001t0001g0134a0001c0001t0001g0163a0001c0001t0002g0102others(41): Show | 46 | HG00323.hp1 HG00621.hp2 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.503+2803C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110621359 | ||||||
| chr11:110621403
|
G | C | 1 | a0001c0001t0002g0063 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.503+2759C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110621403 | ||||||
| chr11:110621452
|
C | CT | 65 | a0001c0001t0001g0134a0001c0001t0001g0163a0001c0001t0001g0210others(62): Show | 67 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.503+2709dupA | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110621452 | ||||||
| chr11:110621678
|
C | T | 4 | a0001c0001t0006g0156a0001c0001t0006g0199a0001c0001t0006g0200others(1): Show | 4 | HG02109.hp1 HG02486.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.503+2484G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110621678 | ||||||
| chr11:110621746
|
A | AAGATTGG others(61): Show |
1 | a0001c0001t0008g0014 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.503+2348_503+2415d others(70): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110621746 | ||||||
| chr11:110621947
|
G | A | 79 | a0001c0001t0001g0134a0001c0001t0001g0163a0001c0001t0001g0210others(76): Show | 82 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.503+2215C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110621947 | ||||||
| chr11:110621957
|
G | A | 79 | a0001c0001t0001g0134a0001c0001t0001g0163a0001c0001t0001g0210others(76): Show | 82 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.503+2205C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110621957 | ||||||
| chr11:110622705
|
A | G | 1 | a0001c0001t0011g0018 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.503+1457T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110622705 | ||||||
| chr11:110622999
|
T | TAAAATTA others(6945): Show |
1 | a0009c0015t0004g0153 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.503+1162_503+1163i others(6954): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110622999 | ||||||
| chr11:110623237
|
T | C | 79 | a0001c0001t0001g0134a0001c0001t0001g0163a0001c0001t0001g0210others(76): Show | 82 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.503+925A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110623237 | ||||||
| chr11:110623371
|
G | A | 1 | a0001c0001t0001g0210 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.503+791C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110623371 | ||||||
| chr11:110623377
|
T | C | 1 | a0003c0004t0017g0145 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.503+785A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110623377 | ||||||
| chr11:110623379
|
G | A | 2 | a0002c0006t0012g0140a0002c0014t0019g0207 | 2 | HG01952.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.503+783C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110623379 | ||||||
| chr11:110623624
|
CTATT | C | 2 | a0001c0005t0005g0142a0001c0005t0005g0197 | 2 | HG01891.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.503+534_503+537del others(4): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110623624 | ||||||
| chr11:110623724
|
T | C | 1 | a0007c0020t0020g0149 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.503+438A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110623724 | ||||||
| chr11:110623788
|
GA | G | 50 | a0001c0001t0001g0134a0001c0001t0001g0163a0001c0001t0002g0102others(47): Show | 52 | HG00323.hp1 HG00621.hp2 HG00673.hp1 others(49): Show |
intron_variant | MODIFIER | c.503+373delT | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110623788 | ||||||
| chr11:110623852
|
CTGTTGTT others(2): Show |
C | 19 | a0001c0001t0001g0210a0001c0001t0003g0216a0001c0001t0006g0156others(16): Show | 19 | HG00099.hp2 HG00280.hp2 HG02015.hp1 others(16): Show |
intron_variant | MODIFIER | c.503+301_503+309del others(9): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110623852 | ||||||
| chr11:110624000
|
T | C | 35 | a0001c0001t0001g0210a0001c0001t0002g0204a0001c0001t0002g0205others(32): Show | 36 | HG00099.hp2 HG00280.hp2 HG01074.hp1 others(33): Show |
intron_variant | MODIFIER | c.503+162A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110624000 | ||||||
| chr11:110624150
|
T | C | 6 | a0001c0001t0002g0204a0001c0001t0002g0205a0001c0001t0002g0206others(3): Show | 6 | HG01074.hp1 HG01891.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.503+12A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110624150 | ||||||
| chr11:110624515
|
G | C | 6 | a0001c0001t0002g0204a0001c0001t0002g0205a0001c0001t0002g0206others(3): Show | 6 | HG01074.hp1 HG01891.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.354-204C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110624515 | ||||||
| chr11:110624552
|
T | A | 2 | a0003c0004t0002g0144a0008c0017t0002g0141 | 2 | HG03688.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.354-241A>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110624552 | ||||||
| chr11:110624560
|
A | T | 85 | a0001c0001t0001g0134a0001c0001t0001g0163a0001c0001t0001g0210others(82): Show | 88 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.354-249T>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110624560 | ||||||
| chr11:110624583
|
G | A | 2 | a0001c0005t0005g0142a0001c0005t0005g0197 | 2 | HG01891.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.354-272C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110624583 | ||||||
| chr11:110624589
|
C | T | 2 | a0001c0001t0002g0062a0010c0016t0002g0060 | 2 | HG02257.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.354-278G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110624589 | ||||||
| chr11:110624617
|
A | G | 35 | a0001c0001t0001g0210a0001c0001t0002g0204a0001c0001t0002g0205others(32): Show | 36 | HG00099.hp2 HG00280.hp2 HG01074.hp1 others(33): Show |
intron_variant | MODIFIER | c.354-306T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110624617 | ||||||
| chr11:110624626
|
G | GT | 42 | a0001c0001t0001g0037a0001c0001t0002g0026a0001c0001t0002g0029others(39): Show | 43 | HG00558.hp2 HG01109.hp2 HG01192.hp2 others(40): Show |
intron_variant | MODIFIER | c.354-316dupA | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110624626 | ||||||
| chr11:110624633
|
T | C | 6 | a0001c0001t0001g0027a0001c0001t0001g0139a0002c0006t0012g0140others(3): Show | 6 | HG00735.hp2 HG01496.hp2 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.354-322A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110624633 | ||||||
| chr11:110624829
|
T | G | 19 | a0001c0001t0001g0210a0001c0001t0003g0216a0001c0001t0006g0156others(16): Show | 19 | HG00099.hp2 HG00280.hp2 HG02015.hp1 others(16): Show |
intron_variant | MODIFIER | c.354-518A>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110624829 | ||||||
| chr11:110624845
|
C | T | 1 | a0001c0001t0001g0194 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.354-534G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110624845 | ||||||
| chr11:110624877
|
G | C | 1 | a0011c0018t0015g0007 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.354-566C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110624877 | ||||||
| chr11:110625012
|
T | TA | 16 | a0001c0001t0002g0102a0001c0001t0003g0001a0001c0001t0003g0021others(13): Show | 18 | HG00323.hp1 HG01099.hp2 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.354-702_354-701ins others(1): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110625012 | ||||||
| chr11:110625012
|
TTTTTTTT others(7): Show |
T | 4 | a0002c0003t0007g0150a0009c0015t0004g0153a0011c0018t0015g0007others(1): Show | 4 | HG02257.hp1 HG02809.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.354-715_354-702del others(14): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110625012 | ||||||
| chr11:110625016
|
T | A | 16 | a0001c0001t0002g0102a0001c0001t0003g0001a0001c0001t0003g0021others(13): Show | 18 | HG00323.hp1 HG01099.hp2 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.354-705A>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110625016 | ||||||
| chr11:110625016
|
T | TA | 28 | a0001c0001t0001g0134a0001c0001t0001g0163a0001c0001t0003g0013others(25): Show | 28 | HG00621.hp2 HG00673.hp1 HG01261.hp2 others(25): Show |
intron_variant | MODIFIER | c.354-706_354-705ins others(1): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110625016 | ||||||
| chr11:110625017
|
TTTATTTT others(8): Show |
T | 31 | a0001c0001t0001g0210a0001c0001t0002g0204a0001c0001t0002g0205others(28): Show | 32 | HG00099.hp2 HG00280.hp2 HG01074.hp1 others(29): Show |
intron_variant | MODIFIER | c.354-721_354-707del others(15): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110625017 | ||||||
| chr11:110625024
|
T | A | 44 | a0001c0001t0001g0134a0001c0001t0001g0163a0001c0001t0002g0102others(41): Show | 46 | HG00323.hp1 HG00621.hp2 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.354-713A>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110625024 | ||||||
| chr11:110625026
|
A | T | 44 | a0001c0001t0001g0134a0001c0001t0001g0163a0001c0001t0002g0102others(41): Show | 46 | HG00323.hp1 HG00621.hp2 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.354-715T>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110625026 | ||||||
| chr11:110625028
|
T | A | 44 | a0001c0001t0001g0134a0001c0001t0001g0163a0001c0001t0002g0102others(41): Show | 46 | HG00323.hp1 HG00621.hp2 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.354-717A>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110625028 | ||||||
| chr11:110625032
|
A | T | 1 | a0001c0001t0001g0037 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.354-721T>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110625032 | ||||||
| chr11:110625033
|
T | A | 35 | a0001c0001t0001g0210a0001c0001t0002g0204a0001c0001t0002g0205others(32): Show | 36 | HG00099.hp2 HG00280.hp2 HG01074.hp1 others(33): Show |
intron_variant | MODIFIER | c.354-722A>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110625033 | ||||||
| chr11:110625033
|
T | TTTA | 44 | a0001c0001t0001g0134a0001c0001t0001g0163a0001c0001t0002g0102others(41): Show | 46 | HG00323.hp1 HG00621.hp2 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.354-723_354-722ins others(3): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110625033 | ||||||
| chr11:110625034
|
T | A | 31 | a0001c0001t0001g0210a0001c0001t0002g0204a0001c0001t0002g0205others(28): Show | 32 | HG00099.hp2 HG00280.hp2 HG01074.hp1 others(29): Show |
intron_variant | MODIFIER | c.354-723A>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110625034 | ||||||
| chr11:110625035
|
T | A | 1 | a0001c0001t0021g0178 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.354-724A>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110625035 | ||||||
| chr11:110625036
|
T | A | 5 | a0001c0001t0001g0184a0001c0001t0002g0035a0002c0006t0012g0140others(2): Show | 5 | HG00733.hp2 HG01952.hp2 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.354-725A>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110625036 | ||||||
| chr11:110625037
|
T | A | 39 | a0001c0001t0001g0134a0001c0001t0001g0163a0001c0001t0002g0102others(36): Show | 41 | HG00323.hp1 HG00621.hp2 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.354-726A>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110625037 | ||||||
| chr11:110625038
|
T | A | 7 | a0001c0001t0001g0027a0001c0001t0001g0139a0001c0001t0001g0154others(4): Show | 7 | HG00735.hp2 HG01496.hp2 HG03579.hp2 others(4): Show |
intron_variant | MODIFIER | c.354-727A>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110625038 | ||||||
| chr11:110625040
|
T | C | 10 | a0001c0001t0001g0210a0001c0001t0003g0216a0001c0002t0005g0209others(7): Show | 10 | HG00099.hp2 HG00280.hp2 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.354-729A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110625040 | ||||||
| chr11:110625054
|
G | A | 1 | a0001c0001t0002g0121 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.354-743C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110625054 | ||||||
| chr11:110625056
|
A | G | 2 | a0006c0007t0010g0147a0006c0007t0010g0148 | 2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.354-745T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110625056 | ||||||
| chr11:110625095
|
T | C | 11 | a0001c0001t0001g0210a0001c0001t0003g0216a0001c0002t0005g0209others(8): Show | 11 | HG00099.hp2 HG00280.hp2 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.354-784A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110625095 | ||||||
| chr11:110625123
|
C | T | 44 | a0001c0001t0001g0134a0001c0001t0001g0163a0001c0001t0002g0102others(41): Show | 46 | HG00323.hp1 HG00621.hp2 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.354-812G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110625123 | ||||||
| chr11:110625192
|
C | T | 44 | a0001c0001t0001g0134a0001c0001t0001g0163a0001c0001t0002g0102others(41): Show | 46 | HG00323.hp1 HG00621.hp2 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.354-881G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110625192 | ||||||
| chr11:110625239
|
T | C | 1 | a0007c0020t0020g0149 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.354-928A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110625239 | ||||||
| chr11:110625283
|
C | T | 7 | a0001c0001t0004g0004a0001c0001t0004g0009a0001c0001t0004g0010others(4): Show | 8 | HG02145.hp2 HG02647.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.354-972G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110625283 | ||||||
| chr11:110625305
|
G | T | 44 | a0001c0001t0001g0134a0001c0001t0001g0163a0001c0001t0002g0102others(41): Show | 46 | HG00323.hp1 HG00621.hp2 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.354-994C>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110625305 | ||||||
| chr11:110625328
|
T | C | 87 | a0001c0001t0001g0027a0001c0001t0001g0134a0001c0001t0001g0139others(84): Show | 90 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.354-1017A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110625328 | ||||||
| chr11:110625333
|
A | G | 79 | a0001c0001t0001g0134a0001c0001t0001g0163a0001c0001t0001g0210others(76): Show | 82 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.354-1022T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110625333 | ||||||
| chr11:110625378
|
G | A | 4 | a0001c0001t0001g0027a0001c0001t0001g0139a0003c0004t0002g0144others(1): Show | 4 | HG00735.hp2 HG01496.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.354-1067C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110625378 | ||||||
| chr11:110625470
|
G | C | 3 | a0001c0001t0003g0021a0001c0001t0003g0098a0001c0001t0003g0099 | 3 | NA18954.hp1 NA18999.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.354-1159C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110625470 | ||||||
| chr11:110625541
|
G | C | 35 | a0001c0001t0001g0210a0001c0001t0002g0204a0001c0001t0002g0205others(32): Show | 36 | HG00099.hp2 HG00280.hp2 HG01074.hp1 others(33): Show |
intron_variant | MODIFIER | c.354-1230C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110625541 | ||||||
| chr11:110625553
|
A | C | 1 | a0001c0001t0008g0014 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.354-1242T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110625553 | ||||||
| chr11:110625662
|
G | A | 2 | a0001c0001t0003g0065a0001c0001t0003g0123 | 2 | HG02683.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.354-1351C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110625662 | ||||||
| chr11:110625676
|
A | T | 2 | a0006c0007t0010g0147a0006c0007t0010g0148 | 2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.354-1365T>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110625676 | ||||||
| chr11:110625688
|
C | T | 1 | a0001c0002t0005g0212 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.354-1377G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110625688 | ||||||
| chr11:110625707
|
CAT | C | 44 | a0001c0001t0001g0134a0001c0001t0001g0163a0001c0001t0002g0102others(41): Show | 46 | HG00323.hp1 HG00621.hp2 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.354-1398_354-1397d others(4): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110625707 | ||||||
| chr11:110625956
|
G | A | 35 | a0001c0001t0001g0210a0001c0001t0002g0204a0001c0001t0002g0205others(32): Show | 36 | HG00099.hp2 HG00280.hp2 HG01074.hp1 others(33): Show |
intron_variant | MODIFIER | c.354-1645C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110625956 | ||||||
| chr11:110626248
|
G | A | 2 | a0006c0007t0010g0147a0006c0007t0010g0148 | 2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.354-1937C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110626248 | ||||||
| chr11:110626281
|
C | T | 4 | a0001c0001t0002g0008a0001c0001t0002g0022a0001c0001t0002g0023others(1): Show | 4 | HG02280.hp2 HG03041.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.354-1970G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110626281 | ||||||
| chr11:110626312
|
A | C | 1 | a0001c0001t0001g0072 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.354-2001T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110626312 | ||||||
| chr11:110626586
|
T | C | 1 | a0001c0001t0001g0090 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.354-2275A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110626586 | ||||||
| chr11:110626734
|
C | CT | 7 | a0001c0001t0002g0204a0001c0001t0002g0205a0001c0001t0002g0206others(4): Show | 7 | HG01074.hp1 HG01891.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.354-2424dupA | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110626734 | ||||||
| chr11:110626908
|
T | C | 6 | a0001c0001t0002g0204a0001c0001t0002g0205a0001c0001t0002g0206others(3): Show | 6 | HG01074.hp1 HG01891.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.354-2597A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110626908 | ||||||
| chr11:110626980
|
T | A | 1 | a0001c0001t0002g0029 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.354-2669A>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110626980 | ||||||
| chr11:110627099
|
T | TA | 35 | a0001c0001t0001g0210a0001c0001t0002g0204a0001c0001t0002g0205others(32): Show | 36 | HG00099.hp2 HG00280.hp2 HG01074.hp1 others(33): Show |
intron_variant | MODIFIER | c.354-2789_354-2788i others(3): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110627099 | ||||||
| chr11:110627249
|
C | T | 43 | a0001c0001t0001g0134a0001c0001t0001g0163a0001c0001t0002g0102others(40): Show | 45 | HG00323.hp1 HG00621.hp2 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.354-2938G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110627249 | ||||||
| chr11:110627423
|
A | G | 19 | a0001c0001t0001g0210a0001c0001t0003g0216a0001c0001t0006g0156others(16): Show | 19 | HG00099.hp2 HG00280.hp2 HG02015.hp1 others(16): Show |
intron_variant | MODIFIER | c.354-3112T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110627423 | ||||||
| chr11:110627515
|
A | G | 1 | a0001c0001t0001g0105 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.353+3113T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110627515 | ||||||
| chr11:110627551
|
G | A | 6 | a0001c0001t0002g0204a0001c0001t0002g0205a0001c0001t0002g0206others(3): Show | 6 | HG01074.hp1 HG01891.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.353+3077C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110627551 | ||||||
| chr11:110627599
|
C | T | 43 | a0001c0001t0001g0134a0001c0001t0001g0163a0001c0001t0002g0102others(40): Show | 45 | HG00323.hp1 HG00621.hp2 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.353+3029G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110627599 | ||||||
| chr11:110627720
|
G | A | 3 | a0001c0001t0002g0164a0001c0001t0002g0165a0001c0001t0002g0166 | 3 | HG02071.hp2 HG02132.hp1 NA18942.hp1 |
intron_variant | MODIFIER | c.353+2908C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110627720 | ||||||
| chr11:110627921
|
C | A | 1 | a0001c0001t0008g0014 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.353+2707G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110627921 | ||||||
| chr11:110627922
|
A | C | 1 | a0001c0001t0008g0014 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.353+2706T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110627922 | ||||||
| chr11:110627995
|
T | C | 35 | a0001c0001t0001g0210a0001c0001t0002g0204a0001c0001t0002g0205others(32): Show | 36 | HG00099.hp2 HG00280.hp2 HG01074.hp1 others(33): Show |
intron_variant | MODIFIER | c.353+2633A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110627995 | ||||||
| chr11:110628042
|
A | T | 86 | a0001c0001t0001g0027a0001c0001t0001g0134a0001c0001t0001g0139others(83): Show | 89 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.353+2586T>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110628042 | ||||||
| chr11:110628063
|
C | T | 12 | a0001c0001t0002g0070a0001c0001t0004g0004a0001c0001t0004g0009others(9): Show | 13 | HG01891.hp1 HG02055.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.353+2565G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110628063 | ||||||
| chr11:110628130
|
T | A | 86 | a0001c0001t0001g0027a0001c0001t0001g0134a0001c0001t0001g0139others(83): Show | 89 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.353+2498A>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110628130 | ||||||
| chr11:110628283
|
C | T | 1 | a0003c0004t0017g0145 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.353+2345G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110628283 | ||||||
| chr11:110628457
|
T | C | 7 | a0001c0001t0004g0004a0001c0001t0004g0009a0001c0001t0004g0010others(4): Show | 8 | HG02145.hp2 HG02647.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.353+2171A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110628457 | ||||||
| chr11:110628482
|
A | T | 1 | a0002c0014t0019g0207 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.353+2146T>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110628482 | ||||||
| chr11:110628527
|
A | C | 1 | a0001c0001t0002g0039 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.353+2101T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110628527 | ||||||
| chr11:110628530
|
A | C | 73 | a0001c0001t0001g0037a0001c0001t0001g0155a0001c0001t0002g0008others(70): Show | 74 | HG00558.hp2 HG00673.hp2 HG00738.hp2 others(71): Show |
intron_variant | MODIFIER | c.353+2098T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110628530 | ||||||
| chr11:110628533
|
C | A | 2 | a0002c0006t0012g0140a0002c0014t0019g0207 | 2 | HG01952.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.353+2095G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110628533 | ||||||
| chr11:110628609
|
G | A | 5 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0042others(2): Show | 5 | NA18940.hp2 NA18978.hp1 NA18994.hp1 others(2): Show |
intron_variant | MODIFIER | c.353+2019C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110628609 | ||||||
| chr11:110628742
|
AAAGTT | A | 4 | a0001c0001t0001g0027a0001c0001t0001g0139a0003c0004t0002g0144others(1): Show | 4 | HG00735.hp2 HG01496.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.353+1881_353+1885d others(7): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110628742 | ||||||
| chr11:110628813
|
A | G | 2 | a0001c0001t0001g0136a0001c0001t0001g0137 | 2 | NA19065.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.353+1815T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110628813 | ||||||
| chr11:110628871
|
C | A | 2 | a0006c0007t0010g0147a0006c0007t0010g0148 | 2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.353+1757G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110628871 | ||||||
| chr11:110628965
|
C | A | 78 | a0001c0001t0001g0134a0001c0001t0001g0163a0001c0001t0001g0210others(75): Show | 81 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.353+1663G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110628965 | ||||||
| chr11:110629030
|
G | C | 1 | a0001c0001t0002g0039 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.353+1598C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110629030 | ||||||
| chr11:110629038
|
A | C | 6 | a0001c0001t0002g0204a0001c0001t0002g0205a0001c0001t0002g0206others(3): Show | 6 | HG01074.hp1 HG01891.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.353+1590T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110629038 | ||||||
| chr11:110629158
|
CTATT | C | 43 | a0001c0001t0001g0134a0001c0001t0001g0163a0001c0001t0002g0102others(40): Show | 45 | HG00323.hp1 HG00621.hp2 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.353+1466_353+1469d others(6): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110629158 | ||||||
| chr11:110629227
|
C | T | 1 | a0001c0001t0003g0013 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.353+1401G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110629227 | ||||||
| chr11:110629498
|
C | A | 1 | a0001c0001t0008g0014 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.353+1130G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110629498 | ||||||
| chr11:110629528
|
A | T | 86 | a0001c0001t0001g0027a0001c0001t0001g0134a0001c0001t0001g0139others(83): Show | 89 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.353+1100T>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110629528 | ||||||
| chr11:110629551
|
T | TA | 64 | a0001c0001t0001g0134a0001c0001t0001g0163a0001c0001t0001g0210others(61): Show | 66 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(63): Show |
intron_variant | MODIFIER | c.353+1076dupT | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110629551 | ||||||
| chr11:110629561
|
T | A | 86 | a0001c0001t0001g0027a0001c0001t0001g0134a0001c0001t0001g0139others(83): Show | 89 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.353+1067A>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110629561 | ||||||
| chr11:110629597
|
G | T | 15 | a0001c0001t0001g0210a0001c0001t0003g0216a0001c0001t0006g0156others(12): Show | 15 | HG00099.hp2 HG00280.hp2 HG02015.hp1 others(12): Show |
intron_variant | MODIFIER | c.353+1031C>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110629597 | ||||||
| chr11:110629602
|
G | A | 78 | a0001c0001t0001g0134a0001c0001t0001g0163a0001c0001t0001g0210others(75): Show | 81 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.353+1026C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110629602 | ||||||
| chr11:110629881
|
G | T | 2 | a0001c0005t0005g0142a0001c0005t0005g0197 | 2 | HG01891.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.353+747C>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110629881 | ||||||
| chr11:110629987
|
A | G | 1 | a0002c0003t0007g0150 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.353+641T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110629987 | ||||||
| chr11:110630036
|
T | C | 1 | a0001c0001t0002g0032 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.353+592A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110630036 | ||||||
| chr11:110630245
|
T | C | 1 | a0001c0001t0001g0182 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.353+383A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110630245 | ||||||
| chr11:110630275
|
A | G | 64 | a0001c0001t0001g0134a0001c0001t0001g0163a0001c0001t0001g0210others(61): Show | 66 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(63): Show |
intron_variant | MODIFIER | c.353+353T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110630275 | ||||||
| chr11:110630312
|
C | T | 1 | a0001c0001t0003g0038 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.353+316G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110630312 | ||||||
| chr11:110630421
|
CATGGCAC others(7): Show |
C | 14 | a0001c0001t0004g0004a0001c0001t0004g0009a0001c0001t0004g0010others(11): Show | 15 | HG01891.hp1 HG02145.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.353+193_353+206del others(14): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110630421 | ||||||
| chr11:110630473
|
AT | A | 43 | a0001c0001t0001g0134a0001c0001t0001g0163a0001c0001t0002g0102others(40): Show | 45 | HG00323.hp1 HG00621.hp2 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.353+154delA | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110630473 | ||||||
| chr11:110630975
|
T | C | 16 | a0001c0001t0002g0204a0001c0001t0002g0205a0001c0001t0002g0206others(13): Show | 16 | HG01074.hp1 HG01891.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.189-183A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110630975 | ||||||
| chr11:110631049
|
C | T | 86 | a0001c0001t0001g0027a0001c0001t0001g0134a0001c0001t0001g0139others(83): Show | 89 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.189-257G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110631049 | ||||||
| chr11:110631106
|
T | C | 10 | a0001c0001t0006g0156a0001c0001t0006g0199a0001c0001t0006g0200others(7): Show | 10 | HG02109.hp1 HG02257.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.189-314A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110631106 | ||||||
| chr11:110631160
|
T | G | 62 | a0001c0001t0001g0134a0001c0001t0001g0163a0001c0001t0002g0102others(59): Show | 64 | HG00323.hp1 HG00621.hp2 HG00673.hp1 others(61): Show |
intron_variant | MODIFIER | c.189-368A>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110631160 | ||||||
| chr11:110631203
|
C | A | 26 | a0001c0001t0001g0210a0001c0001t0002g0204a0001c0001t0002g0205others(23): Show | 27 | HG00099.hp2 HG00280.hp2 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.189-411G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110631203 | ||||||
| chr11:110631383
|
T | C | 44 | a0001c0001t0001g0134a0001c0001t0001g0163a0001c0001t0002g0102others(41): Show | 46 | HG00323.hp1 HG00621.hp2 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.189-591A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110631383 | ||||||
| chr11:110631550
|
C | G | 1 | a0001c0001t0001g0179 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.189-758G>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110631550 | ||||||
| chr11:110631693
|
T | C | 1 | a0003c0004t0017g0145 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.189-901A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110631693 | ||||||
| chr11:110631736
|
C | T | 1 | a0003c0004t0017g0145 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.189-944G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110631736 | ||||||
| chr11:110631943
|
C | A | 1 | a0010c0016t0002g0060 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.189-1151G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110631943 | ||||||
| chr11:110632230
|
A | T | 2 | a0006c0007t0010g0147a0006c0007t0010g0148 | 2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.189-1438T>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110632230 | ||||||
| chr11:110632233
|
A | T | 123 | a0001c0001t0001g0037a0001c0001t0001g0047a0001c0001t0001g0134others(120): Show | 125 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.189-1441T>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110632233 | ||||||
| chr11:110632352
|
C | G | 1 | a0001c0001t0001g0163 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.189-1560G>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110632352 | ||||||
| chr11:110632587
|
T | A | 1 | a0001c0001t0001g0155 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.189-1795A>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110632587 | ||||||
| chr11:110632625
|
G | A | 2 | a0001c0001t0002g0205a0001c0001t0002g0206 | 2 | HG01891.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.189-1833C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110632625 | ||||||
| chr11:110632743
|
T | C | 1 | a0001c0001t0001g0168 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.189-1951A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110632743 | ||||||
| chr11:110632803
|
G | C | 5 | a0001c0001t0004g0009a0001c0001t0004g0010a0001c0001t0004g0011others(2): Show | 5 | HG02145.hp2 HG02647.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.189-2011C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110632803 | ||||||
| chr11:110632817
|
G | A | 129 | a0001c0001t0001g0037a0001c0001t0001g0047a0001c0001t0001g0134others(126): Show | 132 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.189-2025C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110632817 | ||||||
| chr11:110632898
|
AT | A | 4 | a0001c0001t0004g0004a0001c0001t0004g0143a0002c0006t0012g0140others(1): Show | 5 | HG01952.hp2 HG03017.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.189-2107delA | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110632898 | ||||||
| chr11:110632902
|
GTTTTGGA others(5): Show |
G | 2 | a0001c0005t0005g0142a0001c0005t0005g0197 | 2 | HG01891.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.189-2122_189-2111d others(14): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110632902 | ||||||
| chr11:110633048
|
C | T | 1 | a0003c0004t0002g0144 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.189-2256G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110633048 | ||||||
| chr11:110633321
|
T | C | 62 | a0001c0001t0001g0134a0001c0001t0001g0163a0001c0001t0001g0210others(59): Show | 64 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.189-2529A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110633321 | ||||||
| chr11:110633347
|
C | T | 1 | a0003c0004t0017g0145 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.189-2555G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110633347 | ||||||
| chr11:110633582
|
A | G | 6 | a0001c0001t0002g0204a0001c0001t0002g0205a0001c0001t0002g0206others(3): Show | 6 | HG01074.hp1 HG01891.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.189-2790T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110633582 | ||||||
| chr11:110633710
|
G | A | 1 | a0001c0001t0003g0093 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.189-2918C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110633710 | ||||||
| chr11:110634034
|
C | A | 1 | a0001c0001t0001g0125 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.189-3242G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110634034 | ||||||
| chr11:110634088
|
A | G | 1 | a0003c0004t0017g0145 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.189-3296T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110634088 | ||||||
| chr11:110634148
|
A | G | 4 | a0001c0001t0001g0027a0001c0001t0001g0139a0003c0004t0002g0144others(1): Show | 4 | HG00735.hp2 HG01496.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.189-3356T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110634148 | ||||||
| chr11:110634289
|
G | A | 43 | a0001c0001t0001g0134a0001c0001t0001g0163a0001c0001t0002g0102others(40): Show | 45 | HG00323.hp1 HG00621.hp2 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.189-3497C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110634289 | ||||||
| chr11:110634656
|
A | C | 1 | a0003c0004t0017g0145 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.189-3864T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110634656 | ||||||
| chr11:110634742
|
C | T | 1 | a0003c0004t0017g0145 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.189-3950G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110634742 | ||||||
| chr11:110634942
|
GT | G | 123 | a0001c0001t0001g0037a0001c0001t0001g0047a0001c0001t0001g0134others(120): Show | 125 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.189-4151delA | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110634942 | ||||||
| chr11:110634970
|
T | C | 3 | a0001c0001t0006g0199a0001c0001t0006g0200a0001c0001t0006g0201 | 3 | HG02109.hp1 HG02486.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.189-4178A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110634970 | ||||||
| chr11:110634998
|
G | A | 123 | a0001c0001t0001g0037a0001c0001t0001g0047a0001c0001t0001g0134others(120): Show | 125 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.189-4206C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110634998 | ||||||
| chr11:110635096
|
C | A | 1 | a0001c0001t0002g0121 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.189-4304G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110635096 | ||||||
| chr11:110635438
|
T | A | 1 | a0003c0004t0017g0145 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.189-4646A>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110635438 | ||||||
| chr11:110635438
|
T | G | 122 | a0001c0001t0001g0037a0001c0001t0001g0047a0001c0001t0001g0134others(119): Show | 124 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.189-4646A>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110635438 | ||||||
| chr11:110635683
|
T | A | 123 | a0001c0001t0001g0037a0001c0001t0001g0047a0001c0001t0001g0134others(120): Show | 125 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.189-4891A>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110635683 | ||||||
| chr11:110635785
|
T | A | 4 | a0001c0001t0004g0004a0001c0001t0004g0143a0002c0006t0012g0140others(1): Show | 5 | HG01952.hp2 HG03017.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.189-4993A>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110635785 | ||||||
| chr11:110635790
|
G | GA | 6 | a0001c0001t0002g0204a0001c0001t0002g0205a0001c0001t0002g0206others(3): Show | 6 | HG01074.hp1 HG01891.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.189-4999dupT | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110635790 | ||||||
| chr11:110636201
|
G | A | 1 | a0002c0003t0007g0208 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.189-5409C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110636201 | ||||||
| chr11:110636217
|
G | A | 123 | a0001c0001t0001g0037a0001c0001t0001g0047a0001c0001t0001g0134others(120): Show | 125 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.189-5425C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110636217 | ||||||
| chr11:110636276
|
G | A | 123 | a0001c0001t0001g0037a0001c0001t0001g0047a0001c0001t0001g0134others(120): Show | 125 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.189-5484C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110636276 | ||||||
| chr11:110636306
|
T | A | 1 | a0001c0001t0002g0039 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.189-5514A>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110636306 | ||||||
| chr11:110636542
|
C | G | 1 | a0003c0004t0017g0145 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.189-5750G>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110636542 | ||||||
| chr11:110636750
|
C | A | 2 | a0006c0007t0010g0147a0006c0007t0010g0148 | 2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.189-5958G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110636750 | ||||||
| chr11:110636967
|
C | A | 8 | a0001c0001t0003g0001a0001c0001t0003g0021a0001c0001t0003g0049others(5): Show | 10 | HG01928.hp2 HG01981.hp2 HG02004.hp1 others(7): Show |
intron_variant | MODIFIER | c.189-6175G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110636967 | ||||||
| chr11:110637009
|
C | T | 4 | a0001c0001t0004g0004a0001c0001t0004g0143a0002c0006t0012g0140others(1): Show | 5 | HG01952.hp2 HG03017.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.189-6217G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110637009 | ||||||
| chr11:110637153
|
C | T | 72 | a0001c0001t0001g0037a0001c0001t0001g0047a0001c0001t0001g0210others(69): Show | 72 | HG00099.hp2 HG00280.hp2 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.189-6361G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110637153 | ||||||
| chr11:110637317
|
G | A | 51 | a0001c0001t0001g0134a0001c0001t0001g0163a0001c0001t0002g0102others(48): Show | 53 | HG00323.hp1 HG00621.hp2 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.189-6525C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110637317 | ||||||
| chr11:110637423
|
C | T | 1 | a0001c0001t0002g0121 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.189-6631G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110637423 | ||||||
| chr11:110637435
|
ATTAG | A | 2 | a0001c0001t0002g0069a0001c0001t0016g0057 | 2 | HG03239.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.189-6647_189-6644d others(6): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110637435 | ||||||
| chr11:110637444
|
A | T | 122 | a0001c0001t0001g0037a0001c0001t0001g0047a0001c0001t0001g0134others(119): Show | 124 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.189-6652T>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110637444 | ||||||
| chr11:110637526
|
G | A | 4 | a0001c0001t0004g0004a0001c0001t0004g0143a0002c0006t0012g0140others(1): Show | 5 | HG01952.hp2 HG03017.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.189-6734C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110637526 | ||||||
| chr11:110637611
|
G | A | 2 | a0001c0001t0013g0110a0001c0001t0013g0190 | 2 | HG02015.hp2 NA18940.hp1 |
intron_variant | MODIFIER | c.189-6819C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110637611 | ||||||
| chr11:110637617
|
A | T | 123 | a0001c0001t0001g0037a0001c0001t0001g0047a0001c0001t0001g0134others(120): Show | 125 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.189-6825T>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110637617 | ||||||
| chr11:110637738
|
A | G | 123 | a0001c0001t0001g0037a0001c0001t0001g0047a0001c0001t0001g0134others(120): Show | 125 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.189-6946T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110637738 | ||||||
| chr11:110638130
|
T | G | 1 | a0001c0001t0001g0025 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.189-7338A>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110638130 | ||||||
| chr11:110638341
|
A | T | 8 | a0001c0001t0002g0081a0001c0001t0002g0158a0001c0001t0002g0159others(5): Show | 8 | HG00673.hp2 HG02040.hp1 HG02071.hp2 others(5): Show |
intron_variant | MODIFIER | c.189-7549T>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110638341 | ||||||
| chr11:110638444
|
C | T | 120 | a0001c0001t0001g0037a0001c0001t0001g0047a0001c0001t0001g0134others(117): Show | 122 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.189-7652G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110638444 | ||||||
| chr11:110638512
|
G | A | 1 | a0001c0001t0001g0066 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.189-7720C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110638512 | ||||||
| chr11:110638604
|
C | G | 1 | a0003c0004t0017g0145 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.189-7812G>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110638604 | ||||||
| chr11:110638618
|
G | A | 1 | a0001c0001t0004g0011 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.189-7826C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110638618 | ||||||
| chr11:110638751
|
C | CA | 10 | a0001c0001t0001g0210a0001c0001t0003g0216a0001c0002t0005g0209others(7): Show | 10 | HG00099.hp2 HG00280.hp2 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.189-7960dupT | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110638751 | ||||||
| chr11:110638788
|
G | T | 1 | a0001c0001t0001g0173 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.189-7996C>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110638788 | ||||||
| chr11:110638814
|
T | C | 117 | a0001c0001t0001g0037a0001c0001t0001g0047a0001c0001t0001g0134others(114): Show | 119 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.189-8022A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110638814 | ||||||
| chr11:110638887
|
T | C | 7 | a0001c0001t0002g0205a0001c0001t0002g0206a0001c0001t0004g0004others(4): Show | 8 | HG01891.hp2 HG01952.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.189-8095A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110638887 | ||||||
| chr11:110639033
|
C | T | 2 | a0006c0007t0010g0147a0006c0007t0010g0148 | 2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.189-8241G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110639033 | ||||||
| chr11:110639141
|
C | T | 1 | a0003c0004t0017g0145 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.189-8349G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110639141 | ||||||
| chr11:110639201
|
G | A | 2 | a0006c0007t0010g0147a0006c0007t0010g0148 | 2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.189-8409C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110639201 | ||||||
| chr11:110639238
|
AC | A | 13 | a0001c0001t0002g0204a0001c0001t0002g0205a0001c0001t0002g0206others(10): Show | 14 | HG01074.hp1 HG01891.hp2 HG01952.hp2 others(11): Show |
intron_variant | MODIFIER | c.189-8447delG | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110639238 | ||||||
| chr11:110639238
|
ACC | A | 64 | a0001c0001t0001g0037a0001c0001t0001g0047a0001c0001t0001g0210others(61): Show | 64 | HG00099.hp2 HG00280.hp2 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.189-8448_189-8447d others(4): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110639238 | ||||||
| chr11:110639247
|
C | CG | 9 | a0001c0001t0003g0064a0001c0001t0006g0156a0001c0001t0006g0199others(6): Show | 9 | HG01261.hp2 HG02109.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.189-8456_189-8455i others(3): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110639247 | ||||||
| chr11:110639247
|
C | G | 43 | a0001c0001t0001g0134a0001c0001t0001g0163a0001c0001t0002g0102others(40): Show | 45 | HG00323.hp1 HG00621.hp2 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.189-8455G>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110639247 | ||||||
| chr11:110639249
|
A | AC | 3 | a0001c0001t0001g0005a0001c0001t0001g0174a0001c0001t0001g0193 | 4 | HG02622.hp1 HG03041.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.189-8458dupG | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110639249 | ||||||
| chr11:110639307
|
T | C | 4 | a0001c0001t0001g0027a0001c0001t0001g0139a0003c0004t0002g0144others(1): Show | 4 | HG00735.hp2 HG01496.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.189-8515A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110639307 | ||||||
| chr11:110639381
|
CT | C | 12 | a0001c0001t0001g0027a0001c0001t0001g0139a0001c0001t0003g0065others(9): Show | 12 | HG00735.hp2 HG01496.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.189-8590delA | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110639381 | ||||||
| chr11:110639444
|
T | C | 1 | a0001c0005t0005g0197 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.189-8652A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110639444 | ||||||
| chr11:110639484
|
C | T | 133 | a0001c0001t0001g0027a0001c0001t0001g0037a0001c0001t0001g0047others(130): Show | 136 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.189-8692G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110639484 | ||||||
| chr11:110639578
|
A | G | 7 | a0001c0001t0002g0205a0001c0001t0002g0206a0001c0001t0004g0004others(4): Show | 8 | HG01891.hp2 HG01952.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.189-8786T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110639578 | ||||||
| chr11:110639579
|
T | C | 3 | a0001c0001t0002g0204a0002c0003t0007g0202a0002c0003t0007g0208 | 3 | HG01074.hp1 HG02723.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.189-8787A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110639579 | ||||||
| chr11:110639637
|
T | A | 1 | a0001c0001t0003g0064 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.189-8845A>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110639637 | ||||||
| chr11:110639753
|
G | T | 1 | a0003c0004t0017g0145 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.189-8961C>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110639753 | ||||||
| chr11:110639791
|
A | G | 1 | a0003c0004t0017g0145 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.189-8999T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110639791 | ||||||
| chr11:110639804
|
C | T | 3 | a0001c0001t0002g0204a0002c0003t0007g0202a0002c0003t0007g0208 | 3 | HG01074.hp1 HG02723.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.189-9012G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110639804 | ||||||
| chr11:110639992
|
T | G | 55 | a0001c0001t0001g0134a0001c0001t0001g0163a0001c0001t0002g0102others(52): Show | 57 | HG00323.hp1 HG00621.hp2 HG00673.hp1 others(54): Show |
intron_variant | MODIFIER | c.189-9200A>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110639992 | ||||||
| chr11:110640129
|
T | A | 4 | a0001c0001t0004g0004a0001c0001t0004g0143a0002c0006t0012g0140others(1): Show | 5 | HG01952.hp2 HG03017.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.189-9337A>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110640129 | ||||||
| chr11:110640191
|
C | G | 2 | a0006c0007t0010g0147a0006c0007t0010g0148 | 2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.189-9399G>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110640191 | ||||||
| chr11:110640325
|
C | G | 20 | a0001c0001t0001g0037a0001c0001t0001g0047a0001c0001t0002g0024others(17): Show | 20 | HG00558.hp2 HG01358.hp2 HG02080.hp2 others(17): Show |
intron_variant | MODIFIER | c.189-9533G>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110640325 | ||||||
| chr11:110640423
|
G | C | 3 | a0001c0001t0002g0204a0002c0003t0007g0202a0002c0003t0007g0208 | 3 | HG01074.hp1 HG02723.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.189-9631C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110640423 | ||||||
| chr11:110640527
|
C | T | 1 | a0007c0020t0020g0149 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.189-9735G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110640527 | ||||||
| chr11:110640867
|
C | T | 66 | a0001c0001t0001g0134a0001c0001t0001g0210a0001c0001t0002g0008others(63): Show | 68 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.189-10075G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110640867 | ||||||
| chr11:110640876
|
C | T | 81 | a0001c0001t0001g0134a0001c0001t0001g0163a0001c0001t0001g0210others(78): Show | 83 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.189-10084G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110640876 | ||||||
| chr11:110640899
|
T | C | 1 | a0003c0004t0017g0145 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.189-10107A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110640899 | ||||||
| chr11:110641088
|
A | G | 44 | a0001c0001t0001g0134a0001c0001t0001g0163a0001c0001t0002g0102others(41): Show | 46 | HG00323.hp1 HG00621.hp2 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.189-10296T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110641088 | ||||||
| chr11:110641099
|
C | T | 1 | a0003c0004t0017g0145 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.189-10307G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110641099 | ||||||
| chr11:110641606
|
G | C | 1 | a0001c0001t0003g0045 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.189-10814C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110641606 | ||||||
| chr11:110641755
|
T | C | 7 | a0001c0001t0006g0156a0001c0001t0006g0199a0001c0001t0006g0200others(4): Show | 7 | HG02109.hp1 HG02257.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.189-10963A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110641755 | ||||||
| chr11:110641906
|
T | C | 91 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0025others(88): Show | 93 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(90): Show |
intron_variant | MODIFIER | c.189-11114A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110641906 | ||||||
| chr11:110641913
|
G | A | 91 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0025others(88): Show | 93 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(90): Show |
intron_variant | MODIFIER | c.189-11121C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110641913 | ||||||
| chr11:110641923
|
T | C | 1 | a0003c0004t0017g0145 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.189-11131A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110641923 | ||||||
| chr11:110642068
|
G | A | 1 | a0001c0001t0003g0097 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.189-11276C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110642068 | ||||||
| chr11:110642072
|
T | G | 98 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0025others(95): Show | 100 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(97): Show |
intron_variant | MODIFIER | c.189-11280A>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110642072 | ||||||
| chr11:110642167
|
T | G | 13 | a0001c0001t0001g0027a0001c0001t0001g0139a0001c0001t0002g0205others(10): Show | 14 | HG00735.hp2 HG01496.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.189-11375A>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110642167 | ||||||
| chr11:110642218
|
G | A | 4 | a0001c0001t0002g0204a0002c0003t0007g0202a0002c0003t0007g0208others(1): Show | 4 | HG01074.hp1 HG01952.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.189-11426C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110642218 | ||||||
| chr11:110642230
|
C | T | 1 | a0001c0001t0001g0105 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.189-11438G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110642230 | ||||||
| chr11:110642326
|
G | A | 1 | a0003c0004t0017g0145 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.189-11534C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110642326 | ||||||
| chr11:110642353
|
C | T | 1 | a0003c0004t0017g0145 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.189-11561G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110642353 | ||||||
| chr11:110642469
|
C | T | 4 | a0001c0001t0001g0027a0001c0001t0001g0139a0003c0004t0002g0144others(1): Show | 4 | HG00735.hp2 HG01496.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.189-11677G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110642469 | ||||||
| chr11:110642698
|
C | T | 96 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0025others(93): Show | 98 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.189-11906G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110642698 | ||||||
| chr11:110642701
|
G | A | 1 | a0001c0001t0018g0095 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.189-11909C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110642701 | ||||||
| chr11:110642827
|
C | T | 1 | a0001c0001t0004g0082 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.189-12035G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110642827 | ||||||
| chr11:110642979
|
G | A | 1 | a0011c0018t0015g0007 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.189-12187C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110642979 | ||||||
| chr11:110642984
|
A | G | 5 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0021g0178others(2): Show | 5 | HG01981.hp1 NA18962.hp1 NA18999.hp2 others(2): Show |
intron_variant | MODIFIER | c.189-12192T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110642984 | ||||||
| chr11:110643012
|
C | T | 6 | a0001c0001t0001g0027a0001c0001t0001g0139a0003c0004t0002g0144others(3): Show | 6 | HG00735.hp2 HG01496.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.189-12220G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110643012 | ||||||
| chr11:110643201
|
G | C | 10 | a0001c0001t0001g0027a0001c0001t0001g0139a0001c0001t0004g0004others(7): Show | 11 | HG00735.hp2 HG01496.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.189-12409C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110643201 | ||||||
| chr11:110643233
|
T | C | 93 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0025others(90): Show | 95 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(92): Show |
intron_variant | MODIFIER | c.189-12441A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110643233 | ||||||
| chr11:110643373
|
G | C | 1 | a0001c0001t0009g0003 | 2 | HG00639.hp1 HG00735.hp1 |
intron_variant | MODIFIER | c.189-12581C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110643373 | ||||||
| chr11:110643394
|
G | T | 1 | a0001c0001t0001g0181 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.189-12602C>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110643394 | ||||||
| chr11:110643408
|
C | T | 92 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0025others(89): Show | 94 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(91): Show |
intron_variant | MODIFIER | c.189-12616G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110643408 | ||||||
| chr11:110643453
|
G | C | 1 | a0001c0001t0016g0057 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.189-12661C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110643453 | ||||||
| chr11:110643489
|
C | T | 1 | a0002c0003t0007g0203 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.189-12697G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110643489 | ||||||
| chr11:110643594
|
A | T | 10 | a0001c0001t0001g0210a0001c0001t0003g0216a0001c0002t0005g0209others(7): Show | 10 | HG00099.hp2 HG00280.hp2 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.189-12802T>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110643594 | ||||||
| chr11:110643611
|
T | C | 10 | a0001c0001t0001g0210a0001c0001t0003g0216a0001c0002t0005g0209others(7): Show | 10 | HG00099.hp2 HG00280.hp2 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.189-12819A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110643611 | ||||||
| chr11:110643643
|
AT | A | 4 | a0001c0001t0004g0004a0001c0001t0004g0143a0001c0005t0005g0142others(1): Show | 5 | HG01891.hp1 HG03017.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.189-12852delA | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110643643 | ||||||
| chr11:110644115
|
A | T | 96 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0025others(93): Show | 98 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.189-13323T>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110644115 | ||||||
| chr11:110644337
|
G | A | 1 | a0001c0001t0001g0179 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.189-13545C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110644337 | ||||||
| chr11:110644341
|
T | G | 13 | a0001c0001t0001g0027a0001c0001t0001g0139a0001c0001t0002g0205others(10): Show | 14 | HG00735.hp2 HG01496.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.189-13549A>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110644341 | ||||||
| chr11:110644362
|
A | G | 2 | a0001c0001t0002g0205a0001c0001t0002g0206 | 2 | HG01891.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.189-13570T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110644362 | ||||||
| chr11:110644532
|
G | A | 4 | a0001c0001t0002g0204a0002c0003t0007g0202a0002c0003t0007g0208others(1): Show | 4 | HG01074.hp1 HG01952.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.189-13740C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110644532 | ||||||
| chr11:110644544
|
A | G | 85 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0025others(82): Show | 86 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.189-13752T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110644544 | ||||||
| chr11:110644785
|
T | A | 96 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0025others(93): Show | 98 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.189-13993A>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110644785 | ||||||
| chr11:110644997
|
T | TTCTATCT others(9): Show |
2 | a0006c0007t0010g0147a0006c0007t0010g0148 | 2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.189-14206_189-1420 others(20): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110644997 | ||||||
| chr11:110644997
|
T | TTCTC | 78 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0025others(75): Show | 79 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.189-14209_189-1420 others(8): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110644997 | ||||||
| chr11:110644997
|
T | TTCTCTC | 131 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0027others(128): Show | 135 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.189-14211_189-1420 others(10): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110644997 | ||||||
| chr11:110644997
|
T | TTCTCTCT others(3): Show |
3 | a0001c0001t0002g0205a0001c0001t0002g0206a0002c0003t0007g0203 | 3 | HG01891.hp2 HG02922.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.189-14215_189-1420 others(14): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110644997 | ||||||
| chr11:110644997
|
T | TTCTCTCT others(5): Show |
4 | a0001c0001t0004g0004a0001c0001t0004g0143a0001c0005t0005g0142others(1): Show | 5 | HG01891.hp1 HG03017.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.189-14217_189-1420 others(16): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110644997 | ||||||
| chr11:110645171
|
C | T | 1 | a0001c0001t0001g0152 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.189-14379G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110645171 | ||||||
| chr11:110645302
|
G | A | 4 | a0001c0001t0001g0027a0001c0001t0001g0139a0003c0004t0002g0144others(1): Show | 4 | HG00735.hp2 HG01496.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.189-14510C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110645302 | ||||||
| chr11:110645505
|
C | A | 5 | a0001c0001t0004g0009a0001c0001t0004g0010a0001c0001t0004g0011others(2): Show | 5 | HG02145.hp2 HG02647.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.189-14713G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110645505 | ||||||
| chr11:110645547
|
T | C | 1 | a0001c0001t0002g0063 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.189-14755A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110645547 | ||||||
| chr11:110645652
|
G | C | 1 | a0001c0002t0005g0209 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.189-14860C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110645652 | ||||||
| chr11:110645763
|
T | C | 1 | a0003c0004t0017g0145 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.189-14971A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110645763 | ||||||
| chr11:110645847
|
T | C | 1 | a0001c0005t0005g0197 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.189-15055A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110645847 | ||||||
| chr11:110645887
|
A | G | 81 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0025others(78): Show | 82 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.189-15095T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110645887 | ||||||
| chr11:110645959
|
A | G | 77 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0025others(74): Show | 78 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(75): Show |
intron_variant | MODIFIER | c.189-15167T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110645959 | ||||||
| chr11:110646002
|
A | G | 1 | a0001c0001t0003g0093 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.189-15210T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110646002 | ||||||
| chr11:110646012
|
G | C | 53 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0025others(50): Show | 54 | HG00621.hp1 HG00639.hp2 HG00673.hp2 others(51): Show |
intron_variant | MODIFIER | c.189-15220C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110646012 | ||||||
| chr11:110646100
|
T | A | 77 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0025others(74): Show | 78 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(75): Show |
intron_variant | MODIFIER | c.189-15308A>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110646100 | ||||||
| chr11:110646401
|
G | C | 1 | a0001c0001t0001g0117 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.189-15609C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110646401 | ||||||
| chr11:110646439
|
C | T | 1 | a0001c0001t0003g0101 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.189-15647G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110646439 | ||||||
| chr11:110646529
|
T | C | 10 | a0001c0001t0001g0210a0001c0001t0003g0216a0001c0002t0005g0209others(7): Show | 10 | HG00099.hp2 HG00280.hp2 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.189-15737A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110646529 | ||||||
| chr11:110646570
|
A | C | 93 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0025others(90): Show | 95 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(92): Show |
intron_variant | MODIFIER | c.189-15778T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110646570 | ||||||
| chr11:110646952
|
A | C | 1 | a0003c0004t0017g0145 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.189-16160T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110646952 | ||||||
| chr11:110647159
|
T | TTG | 6 | a0001c0001t0004g0009a0001c0001t0004g0010a0001c0001t0004g0011others(3): Show | 6 | HG02145.hp2 HG02647.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.189-16369_189-1636 others(6): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110647159 | ||||||
| chr11:110647516
|
G | C | 1 | a0002c0003t0007g0208 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.189-16724C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110647516 | ||||||
| chr11:110647705
|
A | C | 89 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0025others(86): Show | 91 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(88): Show |
intron_variant | MODIFIER | c.189-16913T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110647705 | ||||||
| chr11:110647816
|
C | T | 4 | a0001c0001t0001g0027a0001c0001t0001g0139a0003c0004t0002g0144others(1): Show | 4 | HG00735.hp2 HG01496.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.189-17024G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110647816 | ||||||
| chr11:110647954
|
A | C | 1 | a0001c0001t0001g0074 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.189-17162T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110647954 | ||||||
| chr11:110648153
|
T | TAATATAT others(31): Show |
1 | a0001c0001t0003g0076 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.189-17399_189-1736 others(42): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648153 | ||||||
| chr11:110648154
|
AAT | A | 2 | a0001c0005t0005g0197a0011c0018t0015g0007 | 2 | HG02451.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.189-17364_189-1736 others(6): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648154 | ||||||
| chr11:110648154
|
AATATATA others(13): Show |
A | 1 | a0001c0001t0011g0018 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.189-17382_189-1736 others(24): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648154 | ||||||
| chr11:110648166
|
TATGTAA | T | 6 | a0001c0001t0004g0009a0001c0001t0004g0010a0001c0001t0004g0011others(3): Show | 6 | HG00280.hp2 HG02145.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.189-17380_189-1737 others(10): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648166 | ||||||
| chr11:110648167
|
A | G | 63 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0025others(60): Show | 64 | HG00099.hp2 HG00621.hp1 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.189-17375T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648167 | ||||||
| chr11:110648168
|
TGTAA | T | 63 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0025others(60): Show | 64 | HG00099.hp2 HG00621.hp1 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.189-17380_189-1737 others(8): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648168 | ||||||
| chr11:110648170
|
TA | T | 4 | a0001c0001t0002g0127a0001c0001t0003g0013a0001c0001t0003g0132others(1): Show | 4 | HG01433.hp2 HG01516.hp1 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.189-17379delT | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648170 | ||||||
| chr11:110648172
|
A | AAT | 8 | a0001c0001t0001g0027a0001c0001t0001g0068a0001c0001t0001g0073others(5): Show | 8 | HG00735.hp2 HG01496.hp2 HG01928.hp1 others(5): Show |
intron_variant | MODIFIER | c.189-17382_189-1738 others(6): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648172 | ||||||
| chr11:110648172
|
A | AATATATA others(33): Show |
1 | a0001c0001t0001g0078 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.189-17420_189-1738 others(44): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648172 | ||||||
| chr11:110648172
|
A | C | 4 | a0001c0005t0005g0197a0006c0007t0010g0147a0006c0007t0010g0148others(1): Show | 4 | HG02451.hp2 HG02622.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.189-17380T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648172 | ||||||
| chr11:110648172
|
AAT | A | 41 | a0001c0001t0001g0083a0001c0001t0001g0134a0001c0001t0002g0022others(38): Show | 43 | HG00323.hp1 HG00621.hp2 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.189-17382_189-1738 others(6): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648172 | ||||||
| chr11:110648173
|
A | G | 6 | a0001c0001t0004g0009a0001c0001t0004g0010a0001c0001t0004g0011others(3): Show | 6 | HG00280.hp2 HG02145.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.189-17381T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648173 | ||||||
| chr11:110648174
|
T | C | 63 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0025others(60): Show | 64 | HG00099.hp2 HG00621.hp1 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.189-17382A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648174 | ||||||
| chr11:110648174
|
TATATATA others(73): Show |
T | 1 | a0011c0018t0015g0007 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.189-17462_189-1738 others(84): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648174 | ||||||
| chr11:110648176
|
T | C | 6 | a0001c0001t0004g0009a0001c0001t0004g0010a0001c0001t0004g0011others(3): Show | 6 | HG00280.hp2 HG02145.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.189-17384A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648176 | ||||||
| chr11:110648176
|
TATATATA others(9): Show |
T | 1 | a0002c0003t0007g0202 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.189-17400_189-1738 others(20): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648176 | ||||||
| chr11:110648176
|
TATATATA others(71): Show |
T | 1 | a0003c0004t0017g0145 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.189-17462_189-1738 others(82): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648176 | ||||||
| chr11:110648187
|
A | G | 4 | a0001c0001t0003g0064a0001c0001t0003g0079a0006c0007t0010g0147others(1): Show | 4 | HG01261.hp2 HG02602.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.189-17395T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648187 | ||||||
| chr11:110648188
|
TGTAA | T | 2 | a0006c0007t0010g0147a0006c0007t0010g0148 | 2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.189-17400_189-1739 others(8): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648188 | ||||||
| chr11:110648189
|
G | A | 2 | a0001c0001t0003g0064a0001c0001t0003g0079 | 2 | HG01261.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.189-17397C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648189 | ||||||
| chr11:110648190
|
T | A | 2 | a0001c0001t0003g0064a0001c0001t0003g0079 | 2 | HG01261.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.189-17398A>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648190 | ||||||
| chr11:110648192
|
A | C | 78 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0025others(75): Show | 80 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.189-17400T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648192 | ||||||
| chr11:110648192
|
A | T | 2 | a0001c0001t0003g0064a0001c0001t0003g0079 | 2 | HG01261.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.189-17400T>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648192 | ||||||
| chr11:110648192
|
AAT | A | 5 | a0001c0001t0001g0083a0001c0001t0002g0053a0001c0001t0003g0107others(2): Show | 5 | HG01192.hp1 HG02145.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.189-17402_189-1740 others(6): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648192 | ||||||
| chr11:110648194
|
T | C | 2 | a0006c0007t0010g0147a0006c0007t0010g0148 | 2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.189-17402A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648194 | ||||||
| chr11:110648194
|
TATATATA others(53): Show |
T | 70 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0025others(67): Show | 71 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(68): Show |
intron_variant | MODIFIER | c.189-17462_189-1740 others(64): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648194 | ||||||
| chr11:110648198
|
TATATATA others(5): Show |
T | 1 | a0001c0001t0002g0008 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.189-17418_189-1740 others(16): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648198 | ||||||
| chr11:110648205
|
A | G | 4 | a0001c0001t0004g0004a0001c0001t0004g0143a0001c0005t0005g0142others(1): Show | 5 | HG01891.hp1 HG03017.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.189-17413T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648205 | ||||||
| chr11:110648207
|
G | A | 4 | a0001c0001t0004g0004a0001c0001t0004g0143a0001c0005t0005g0142others(1): Show | 5 | HG01891.hp1 HG03017.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.189-17415C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648207 | ||||||
| chr11:110648208
|
T | C | 4 | a0001c0001t0004g0004a0001c0001t0004g0143a0001c0005t0005g0142others(1): Show | 5 | HG01891.hp1 HG03017.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.189-17416A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648208 | ||||||
| chr11:110648210
|
A | T | 4 | a0001c0001t0004g0004a0001c0001t0004g0143a0001c0005t0005g0142others(1): Show | 5 | HG01891.hp1 HG03017.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.189-17418T>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648210 | ||||||
| chr11:110648210
|
AATATATA others(5): Show |
A | 1 | a0001c0001t0003g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.189-17430_189-1741 others(16): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648210 | ||||||
| chr11:110648210
|
AATATATA others(9): Show |
A | 1 | a0001c0001t0003g0109 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.189-17434_189-1741 others(20): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648210 | ||||||
| chr11:110648210
|
AATATATA others(11): Show |
A | 6 | a0001c0001t0002g0204a0001c0001t0002g0205a0001c0001t0002g0206others(3): Show | 6 | HG01074.hp1 HG01891.hp2 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.189-17436_189-1741 others(22): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648210 | ||||||
| chr11:110648215
|
ATATATG | A | 6 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116others(3): Show | 7 | HG00280.hp1 HG00639.hp1 HG00733.hp1 others(4): Show |
intron_variant | MODIFIER | c.189-17429_189-1742 others(10): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648215 | ||||||
| chr11:110648221
|
G | A | 10 | a0001c0001t0001g0027a0001c0001t0001g0139a0002c0003t0007g0150others(7): Show | 10 | HG00735.hp2 HG01496.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.189-17429C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648221 | ||||||
| chr11:110648221
|
GTA | G | 58 | a0001c0001t0001g0072a0001c0001t0001g0083a0001c0001t0001g0134others(55): Show | 60 | HG00621.hp2 HG00673.hp1 HG00738.hp1 others(57): Show |
intron_variant | MODIFIER | c.189-17431_189-1743 others(6): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648221 | ||||||
| chr11:110648221
|
GTATA | G | 4 | a0001c0001t0001g0080a0001c0001t0003g0093a0001c0001t0003g0118others(1): Show | 4 | HG02602.hp2 HG02738.hp1 NA18942.hp2 others(1): Show |
intron_variant | MODIFIER | c.189-17433_189-1743 others(8): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648221 | ||||||
| chr11:110648223
|
A | G | 10 | a0001c0001t0001g0027a0001c0001t0001g0105a0001c0001t0001g0139others(7): Show | 10 | HG00735.hp2 HG01496.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.189-17431T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648223 | ||||||
| chr11:110648224
|
T | A | 2 | a0001c0001t0002g0008a0001c0001t0006g0156 | 2 | HG02559.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.189-17432A>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648224 | ||||||
| chr11:110648224
|
T | C | 7 | a0001c0001t0004g0004a0001c0001t0004g0143a0001c0001t0006g0199others(4): Show | 8 | HG01891.hp1 HG02109.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.189-17432A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648224 | ||||||
| chr11:110648225
|
A | G | 1 | a0002c0003t0007g0202 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.189-17433T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648225 | ||||||
| chr11:110648226
|
T | C | 9 | a0001c0001t0001g0027a0001c0001t0001g0139a0002c0003t0007g0150others(6): Show | 9 | HG00735.hp2 HG01496.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.189-17434A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648226 | ||||||
| chr11:110648226
|
T | TATATATA others(19): Show |
1 | a0001c0001t0002g0023 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.189-17435_189-1743 others(30): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648226 | ||||||
| chr11:110648226
|
TATATATA others(7): Show |
T | 7 | a0001c0001t0004g0004a0001c0001t0004g0143a0001c0001t0006g0199others(4): Show | 8 | HG01891.hp1 HG02109.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.189-17448_189-1743 others(18): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648226 | ||||||
| chr11:110648228
|
T | A | 1 | a0002c0003t0007g0202 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.189-17436A>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648228 | ||||||
| chr11:110648228
|
TATATATA others(5): Show |
T | 3 | a0002c0003t0007g0150a0009c0015t0004g0153a0012c0019t0004g0151 | 3 | HG02257.hp1 NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.189-17448_189-1743 others(16): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648228 | ||||||
| chr11:110648237
|
G | T | 2 | a0006c0007t0010g0147a0006c0007t0010g0148 | 2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.189-17445C>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648237 | ||||||
| chr11:110648240
|
A | C | 15 | a0001c0001t0001g0027a0001c0001t0001g0139a0001c0001t0002g0008others(12): Show | 15 | HG00735.hp2 HG01074.hp1 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.189-17448T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648240 | ||||||
| chr11:110648242
|
TATATATA others(5): Show |
T | 2 | a0006c0007t0010g0147a0006c0007t0010g0148 | 2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.189-17462_189-1745 others(16): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648242 | ||||||
| chr11:110648244
|
TATATATG others(3): Show |
T | 4 | a0001c0001t0001g0027a0001c0001t0001g0139a0003c0004t0002g0144others(1): Show | 4 | HG00735.hp2 HG01496.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.189-17462_189-1745 others(14): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648244 | ||||||
| chr11:110648254
|
A | C | 4 | a0001c0001t0004g0004a0001c0001t0004g0143a0001c0005t0005g0142others(1): Show | 5 | HG01891.hp1 HG03017.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.189-17462T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648254 | ||||||
| chr11:110648265
|
G | T | 71 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0025others(68): Show | 72 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.189-17473C>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648265 | ||||||
| chr11:110648268
|
A | C | 79 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0025others(76): Show | 81 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.189-17476T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648268 | ||||||
| chr11:110648348
|
G | A | 1 | a0003c0004t0017g0145 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.189-17556C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648348 | ||||||
| chr11:110648351
|
T | C | 1 | a0003c0004t0017g0145 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.189-17559A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648351 | ||||||
| chr11:110648353
|
C | CAT | 188 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0025others(185): Show | 192 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.189-17563_189-1756 others(6): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648353 | ||||||
| chr11:110648353
|
C | T | 1 | a0003c0004t0017g0145 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.189-17561G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648353 | ||||||
| chr11:110648484
|
A | AT | 48 | a0001c0001t0001g0047a0001c0001t0001g0083a0001c0001t0001g0129others(45): Show | 50 | HG00323.hp1 HG00621.hp2 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.189-17693dupA | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648484 | ||||||
| chr11:110648484
|
AT | A | 65 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0025others(62): Show | 67 | HG00621.hp1 HG00639.hp2 HG00673.hp2 others(64): Show |
intron_variant | MODIFIER | c.189-17693delA | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648484 | ||||||
| chr11:110648615
|
A | G | 85 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0025others(82): Show | 87 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(84): Show |
intron_variant | MODIFIER | c.189-17823T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648615 | ||||||
| chr11:110648671
|
C | T | 71 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0025others(68): Show | 72 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.189-17879G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648671 | ||||||
| chr11:110648979
|
T | C | 5 | a0001c0001t0004g0009a0001c0001t0004g0010a0001c0001t0004g0011others(2): Show | 5 | HG02145.hp2 HG02647.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.189-18187A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648979 | ||||||
| chr11:110649201
|
C | CT | 14 | a0001c0001t0001g0037a0001c0001t0001g0131a0001c0001t0002g0026others(11): Show | 14 | HG00673.hp1 HG01109.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.189-18410dupA | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110649201 | ||||||
| chr11:110649201
|
CT | C | 23 | a0001c0001t0001g0134a0001c0001t0001g0154a0001c0001t0002g0030others(20): Show | 23 | HG00280.hp2 HG01074.hp1 HG01516.hp1 others(20): Show |
intron_variant | MODIFIER | c.189-18410delA | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110649201 | ||||||
| chr11:110649201
|
CTT | C | 15 | a0001c0001t0001g0027a0001c0001t0001g0137a0001c0001t0001g0139others(12): Show | 16 | HG00735.hp2 HG01496.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.189-18411_189-1841 others(6): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110649201 | ||||||
| chr11:110649201
|
CTTT | C | 43 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0025others(40): Show | 44 | HG00621.hp1 HG00639.hp2 HG00673.hp2 others(41): Show |
intron_variant | MODIFIER | c.189-18412_189-1841 others(7): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110649201 | ||||||
| chr11:110649201
|
CTTTTTTT others(5): Show |
C | 9 | a0001c0001t0001g0157a0001c0001t0001g0167a0001c0001t0001g0175others(6): Show | 9 | HG01981.hp1 HG02165.hp1 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.189-18421_189-1841 others(16): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110649201 | ||||||
| chr11:110649369
|
A | C | 1 | a0001c0005t0005g0197 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.189-18577T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110649369 | ||||||
| chr11:110649394
|
G | A | 71 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0025others(68): Show | 72 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.189-18602C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110649394 | ||||||
| chr11:110649417
|
A | T | 1 | a0001c0001t0001g0167 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.189-18625T>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110649417 | ||||||
| chr11:110649567
|
G | A | 4 | a0001c0001t0001g0027a0001c0001t0001g0139a0003c0004t0002g0144others(1): Show | 4 | HG00735.hp2 HG01496.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.189-18775C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110649567 | ||||||
| chr11:110649635
|
G | A | 1 | a0003c0004t0017g0145 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.189-18843C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110649635 | ||||||
| chr11:110649656
|
G | C | 5 | a0001c0001t0002g0029a0001c0001t0002g0033a0001c0001t0002g0034others(2): Show | 5 | HG01109.hp2 HG02486.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.189-18864C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110649656 | ||||||
| chr11:110649828
|
A | G | 1 | a0001c0001t0001g0071 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.189-19036T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110649828 | ||||||
| chr11:110650146
|
T | C | 9 | a0001c0001t0002g0026a0001c0001t0002g0029a0001c0001t0002g0031others(6): Show | 9 | HG01109.hp2 HG02486.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.189-19354A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110650146 | ||||||
| chr11:110650215
|
T | C | 98 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0025others(95): Show | 100 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(97): Show |
intron_variant | MODIFIER | c.189-19423A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110650215 | ||||||
| chr11:110650218
|
T | C | 2 | a0006c0007t0010g0147a0006c0007t0010g0148 | 2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.189-19426A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110650218 | ||||||
| chr11:110650237
|
C | A | 1 | a0004c0011t0002g0128 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.189-19445G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110650237 | ||||||
| chr11:110650424
|
G | C | 7 | a0001c0001t0004g0009a0001c0001t0004g0010a0001c0001t0004g0011others(4): Show | 7 | HG02145.hp2 HG02451.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.189-19632C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110650424 | ||||||
| chr11:110650703
|
T | C | 4 | a0001c0001t0001g0027a0001c0001t0001g0139a0003c0004t0002g0144others(1): Show | 4 | HG00735.hp2 HG01496.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.189-19911A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110650703 | ||||||
| chr11:110650741
|
A | G | 1 | a0003c0004t0017g0145 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.189-19949T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110650741 | ||||||
| chr11:110650837
|
A | G | 7 | a0001c0001t0002g0204a0001c0001t0002g0205a0001c0001t0002g0206others(4): Show | 7 | HG01074.hp1 HG01891.hp2 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.189-20045T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110650837 | ||||||
| chr11:110650852
|
G | A | 2 | a0006c0007t0010g0147a0006c0007t0010g0148 | 2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.189-20060C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110650852 | ||||||
| chr11:110650884
|
T | C | 68 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0025others(65): Show | 69 | HG00621.hp1 HG00639.hp2 HG00673.hp2 others(66): Show |
intron_variant | MODIFIER | c.189-20092A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110650884 | ||||||
| chr11:110650904
|
C | T | 1 | a0002c0003t0007g0208 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.189-20112G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110650904 | ||||||
| chr11:110650909
|
A | G | 2 | a0006c0007t0010g0147a0006c0007t0010g0148 | 2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.189-20117T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110650909 | ||||||
| chr11:110651035
|
G | C | 1 | a0003c0004t0017g0145 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.189-20243C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110651035 | ||||||
| chr11:110651193
|
A | C | 1 | a0001c0001t0006g0156 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.189-20401T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110651193 | ||||||
| chr11:110651324
|
C | A | 1 | a0003c0004t0017g0145 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.189-20532G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110651324 | ||||||
| chr11:110651400
|
C | A | 70 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0025others(67): Show | 71 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(68): Show |
intron_variant | MODIFIER | c.189-20608G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110651400 | ||||||
| chr11:110651453
|
T | G | 4 | a0001c0001t0001g0027a0001c0001t0001g0139a0003c0004t0002g0144others(1): Show | 4 | HG00735.hp2 HG01496.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.189-20661A>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110651453 | ||||||
| chr11:110651747
|
C | CA | 19 | a0001c0001t0001g0027a0001c0001t0001g0139a0001c0001t0002g0026others(16): Show | 19 | HG00735.hp2 HG01074.hp1 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.189-20956dupT | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110651747 | ||||||
| chr11:110651747
|
CA | C | 73 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0025others(70): Show | 74 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.189-20956delT | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110651747 | ||||||
| chr11:110651747
|
CAA | C | 6 | a0001c0001t0001g0194a0001c0001t0004g0011a0001c0001t0004g0012others(3): Show | 6 | HG02145.hp2 HG02809.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.189-20957_189-2095 others(6): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110651747 | ||||||
| chr11:110651856
|
G | C | 1 | a0001c0001t0001g0020 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.189-21064C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110651856 | ||||||
| chr11:110651873
|
C | T | 7 | a0001c0001t0004g0009a0001c0001t0004g0010a0001c0001t0004g0011others(4): Show | 7 | HG02145.hp2 HG02451.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.189-21081G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110651873 | ||||||
| chr11:110651886
|
T | C | 80 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0025others(77): Show | 81 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.189-21094A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110651886 | ||||||
| chr11:110652093
|
T | C | 6 | a0001c0001t0004g0004a0001c0001t0004g0143a0001c0005t0005g0142others(3): Show | 7 | HG01891.hp1 HG02622.hp2 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.189-21301A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110652093 | ||||||
| chr11:110652101
|
T | C | 79 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0025others(76): Show | 80 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.189-21309A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110652101 | ||||||
| chr11:110652304
|
G | A | 1 | a0003c0004t0017g0145 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.189-21512C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110652304 | ||||||
| chr11:110652321
|
C | G | 1 | a0007c0020t0020g0149 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.189-21529G>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110652321 | ||||||
| chr11:110652490
|
C | T | 1 | a0011c0018t0015g0007 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.189-21698G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110652490 | ||||||
| chr11:110652709
|
A | G | 79 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0025others(76): Show | 80 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.189-21917T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110652709 | ||||||
| chr11:110652780
|
A | G | 2 | a0006c0007t0010g0147a0006c0007t0010g0148 | 2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.189-21988T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110652780 | ||||||
| chr11:110652792
|
A | G | 90 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0025others(87): Show | 92 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.189-22000T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110652792 | ||||||
| chr11:110652847
|
G | A | 1 | a0003c0004t0017g0145 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.189-22055C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110652847 | ||||||
| chr11:110652871
|
T | C | 61 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0025others(58): Show | 62 | HG00621.hp1 HG00639.hp2 HG00673.hp2 others(59): Show |
intron_variant | MODIFIER | c.189-22079A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110652871 | ||||||
| chr11:110652875
|
T | C | 4 | a0001c0001t0004g0004a0001c0001t0004g0143a0001c0005t0005g0142others(1): Show | 5 | HG01891.hp1 HG03017.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.189-22083A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110652875 | ||||||
| chr11:110653130
|
T | G | 1 | a0003c0004t0017g0145 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.189-22338A>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110653130 | ||||||
| chr11:110653178
|
G | A | 1 | a0001c0001t0003g0045 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.189-22386C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110653178 | ||||||
| chr11:110653208
|
G | A | 1 | a0003c0004t0017g0145 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.189-22416C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110653208 | ||||||
| chr11:110653213
|
T | C | 1 | a0001c0002t0005g0211 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.189-22421A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110653213 | ||||||
| chr11:110653224
|
G | A | 1 | a0003c0004t0017g0145 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.189-22432C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110653224 | ||||||
| chr11:110653297
|
G | A | 3 | a0001c0001t0004g0004a0001c0001t0004g0143a0001c0005t0005g0142 | 4 | HG01891.hp1 HG03098.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.189-22505C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110653297 | ||||||
| chr11:110653391
|
C | T | 1 | a0002c0014t0019g0207 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.189-22599G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110653391 | ||||||
| chr11:110653727
|
T | TAC | 7 | a0001c0001t0002g0204a0001c0001t0002g0205a0001c0001t0002g0206others(4): Show | 7 | HG01074.hp1 HG01891.hp2 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.189-22937_189-2293 others(6): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110653727 | ||||||
| chr11:110653814
|
T | C | 78 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0025others(75): Show | 79 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.189-23022A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110653814 | ||||||
| chr11:110653914
|
A | G | 60 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0025others(57): Show | 61 | HG00621.hp1 HG00639.hp2 HG00673.hp2 others(58): Show |
intron_variant | MODIFIER | c.189-23122T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110653914 | ||||||
| chr11:110653946
|
A | G | 98 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0025others(95): Show | 100 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(97): Show |
intron_variant | MODIFIER | c.189-23154T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110653946 | ||||||
| chr11:110653969
|
C | T | 5 | a0001c0001t0004g0009a0001c0001t0004g0010a0001c0001t0004g0011others(2): Show | 5 | HG02145.hp2 HG02647.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.189-23177G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110653969 | ||||||
| chr11:110653971
|
A | G | 3 | a0001c0001t0004g0004a0001c0001t0004g0143a0001c0005t0005g0142 | 4 | HG01891.hp1 HG03098.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.189-23179T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110653971 | ||||||
| chr11:110654083
|
T | C | 1 | a0001c0001t0002g0059 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.189-23291A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110654083 | ||||||
| chr11:110654436
|
A | T | 1 | a0003c0004t0002g0144 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.189-23644T>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110654436 | ||||||
| chr11:110654472
|
A | G | 10 | a0001c0001t0001g0210a0001c0001t0003g0216a0001c0002t0005g0209others(7): Show | 10 | HG00099.hp2 HG00280.hp2 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.189-23680T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110654472 | ||||||
| chr11:110654487
|
A | C | 10 | a0001c0001t0001g0027a0001c0001t0001g0139a0001c0001t0004g0004others(7): Show | 11 | HG00735.hp2 HG01496.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.189-23695T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110654487 | ||||||
| chr11:110654590
|
T | C | 7 | a0001c0001t0002g0204a0001c0001t0002g0205a0001c0001t0002g0206others(4): Show | 7 | HG01074.hp1 HG01891.hp2 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.189-23798A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110654590 | ||||||
| chr11:110654652
|
G | C | 5 | a0001c0001t0002g0008a0001c0001t0006g0156a0001c0001t0006g0199others(2): Show | 5 | HG02109.hp1 HG02486.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.189-23860C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110654652 | ||||||
| chr11:110654670
|
C | T | 1 | a0003c0004t0017g0145 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.189-23878G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110654670 | ||||||
| chr11:110654902
|
G | A | 4 | a0001c0001t0004g0004a0001c0001t0004g0143a0001c0005t0005g0142others(1): Show | 5 | HG01891.hp1 HG03017.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.189-24110C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110654902 | ||||||
| chr11:110654958
|
C | A | 1 | a0001c0001t0002g0008 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.189-24166G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110654958 | ||||||
| chr11:110655103
|
T | G | 7 | a0001c0001t0002g0204a0001c0001t0002g0205a0001c0001t0002g0206others(4): Show | 7 | HG01074.hp1 HG01891.hp2 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.189-24311A>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110655103 | ||||||
| chr11:110655104
|
A | C | 7 | a0001c0001t0002g0204a0001c0001t0002g0205a0001c0001t0002g0206others(4): Show | 7 | HG01074.hp1 HG01891.hp2 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.189-24312T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110655104 | ||||||
| chr11:110655251
|
T | TA | 5 | a0001c0001t0004g0009a0001c0001t0004g0010a0001c0001t0004g0011others(2): Show | 5 | HG02145.hp2 HG02647.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.189-24460dupT | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110655251 | ||||||
| chr11:110655443
|
T | C | 1 | a0001c0001t0011g0018 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.189-24651A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110655443 | ||||||
| chr11:110655449
|
T | C | 10 | a0001c0001t0001g0210a0001c0001t0003g0216a0001c0002t0005g0209others(7): Show | 10 | HG00099.hp2 HG00280.hp2 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.189-24657A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110655449 | ||||||
| chr11:110655453
|
G | A | 1 | a0003c0004t0017g0145 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.189-24661C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110655453 | ||||||
| chr11:110655610
|
G | A | 4 | a0001c0001t0001g0037a0001c0001t0002g0043a0001c0001t0002g0044others(1): Show | 4 | HG02080.hp2 NA18989.hp1 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.189-24818C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110655610 | ||||||
| chr11:110655644
|
G | A | 1 | a0001c0001t0003g0126 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.189-24852C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110655644 | ||||||
| chr11:110655666
|
G | A | 1 | a0001c0001t0004g0146 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.189-24874C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110655666 | ||||||
| chr11:110655700
|
G | C | 2 | a0006c0007t0010g0147a0006c0007t0010g0148 | 2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.189-24908C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110655700 | ||||||
| chr11:110655809
|
T | C | 10 | a0001c0001t0001g0210a0001c0001t0003g0216a0001c0002t0005g0209others(7): Show | 10 | HG00099.hp2 HG00280.hp2 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.189-25017A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110655809 | ||||||
| chr11:110655835
|
T | C | 2 | a0001c0001t0002g0043a0001c0001t0002g0044 | 2 | NA18989.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.189-25043A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110655835 | ||||||
| chr11:110655959
|
G | A | 1 | a0001c0001t0002g0063 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.189-25167C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110655959 | ||||||
| chr11:110656029
|
C | T | 10 | a0001c0001t0001g0027a0001c0001t0001g0139a0001c0001t0004g0004others(7): Show | 11 | HG00735.hp2 HG01496.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.189-25237G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110656029 | ||||||
| chr11:110656079
|
G | A | 1 | a0001c0001t0002g0063 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.189-25287C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110656079 | ||||||
| chr11:110656107
|
T | C | 2 | a0006c0007t0010g0147a0006c0007t0010g0148 | 2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.189-25315A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110656107 | ||||||
| chr11:110656238
|
T | C | 4 | a0001c0001t0001g0037a0001c0001t0002g0043a0001c0001t0002g0044others(1): Show | 4 | HG02080.hp2 NA18989.hp1 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.189-25446A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110656238 | ||||||
| chr11:110656411
|
A | G | 61 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0025others(58): Show | 62 | HG00621.hp1 HG00639.hp2 HG00673.hp2 others(59): Show |
intron_variant | MODIFIER | c.189-25619T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110656411 | ||||||
| chr11:110656455
|
G | T | 1 | a0001c0001t0003g0109 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.189-25663C>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110656455 | ||||||
| chr11:110656500
|
C | T | 2 | a0001c0001t0002g0062a0010c0016t0002g0060 | 2 | HG02257.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.189-25708G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110656500 | ||||||
| chr11:110656528
|
A | G | 1 | a0003c0004t0017g0145 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.189-25736T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110656528 | ||||||
| chr11:110656531
|
A | G | 1 | a0011c0018t0015g0007 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.189-25739T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110656531 | ||||||
| chr11:110656544
|
C | A | 1 | a0003c0004t0017g0145 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.189-25752G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110656544 | ||||||
| chr11:110656718
|
A | G | 4 | a0001c0001t0004g0004a0001c0001t0004g0143a0001c0005t0005g0142others(1): Show | 5 | HG01891.hp1 HG03017.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.189-25926T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110656718 | ||||||
| chr11:110656776
|
T | G | 5 | a0001c0001t0002g0008a0001c0001t0006g0156a0001c0001t0006g0199others(2): Show | 5 | HG02109.hp1 HG02486.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.189-25984A>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110656776 | ||||||
| chr11:110656917
|
C | T | 1 | a0001c0001t0016g0057 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.189-26125G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110656917 | ||||||
| chr11:110657201
|
G | A | 4 | a0001c0001t0004g0004a0001c0001t0004g0143a0001c0005t0005g0142others(1): Show | 5 | HG01891.hp1 HG03017.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.189-26409C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110657201 | ||||||
| chr11:110657243
|
C | A | 1 | a0002c0006t0012g0140 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.189-26451G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110657243 | ||||||
| chr11:110657291
|
T | G | 1 | a0001c0001t0002g0035 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.189-26499A>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110657291 | ||||||
| chr11:110657403
|
G | A | 1 | a0011c0018t0015g0007 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.189-26611C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110657403 | ||||||
| chr11:110657404
|
A | T | 10 | a0001c0001t0001g0027a0001c0001t0001g0139a0001c0001t0004g0004others(7): Show | 11 | HG00735.hp2 HG01496.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.189-26612T>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110657404 | ||||||
| chr11:110657514
|
C | T | 2 | a0006c0007t0010g0147a0006c0007t0010g0148 | 2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.189-26722G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110657514 | ||||||
| chr11:110657657
|
G | A | 2 | a0001c0001t0003g0100a0001c0013t0003g0092 | 2 | HG03834.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.189-26865C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110657657 | ||||||
| chr11:110657752
|
C | T | 1 | a0001c0001t0001g0187 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.189-26960G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110657752 | ||||||
| chr11:110657819
|
C | T | 4 | a0001c0001t0001g0027a0001c0001t0001g0139a0003c0004t0002g0144others(1): Show | 4 | HG00735.hp2 HG01496.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.189-27027G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110657819 | ||||||
| chr11:110657825
|
GC | G | 4 | a0001c0001t0001g0027a0001c0001t0001g0139a0003c0004t0002g0144others(1): Show | 4 | HG00735.hp2 HG01496.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.189-27034delG | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110657825 | ||||||
| chr11:110657889
|
C | T | 1 | a0001c0001t0013g0190 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.189-27097G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110657889 | ||||||
| chr11:110657920
|
G | GAGGA | 18 | a0001c0001t0001g0016a0001c0001t0001g0055a0001c0001t0001g0056others(15): Show | 18 | HG00099.hp1 HG00280.hp1 HG00558.hp1 others(15): Show |
intron_variant | MODIFIER | c.189-27132_189-2712 others(8): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110657920 | ||||||
| chr11:110657920
|
G | GAGGAAGG others(1): Show |
9 | a0001c0001t0001g0047a0001c0001t0001g0129a0001c0001t0002g0030others(6): Show | 10 | HG01891.hp1 HG02622.hp2 HG03491.hp2 others(7): Show |
intron_variant | MODIFIER | c.189-27136_189-2712 others(12): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110657920 | ||||||
| chr11:110657920
|
G | GAGGAAGG others(5): Show |
2 | a0001c0001t0004g0143a0002c0006t0012g0140 | 2 | HG03017.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.189-27140_189-2712 others(16): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110657920 | ||||||
| chr11:110657920
|
G | GAGGAAGG others(9): Show |
1 | a0001c0001t0002g0063 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.189-27144_189-2712 others(20): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110657920 | ||||||
| chr11:110657920
|
GAGGA | G | 30 | a0001c0001t0001g0103a0001c0001t0001g0134a0001c0001t0002g0031others(27): Show | 32 | HG00323.hp1 HG00621.hp2 HG01099.hp2 others(29): Show |
intron_variant | MODIFIER | c.189-27132_189-2712 others(8): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110657920 | ||||||
| chr11:110657920
|
GAGGAAGG others(1): Show |
G | 91 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0025others(88): Show | 92 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.189-27136_189-2712 others(12): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110657920 | ||||||
| chr11:110657920
|
GAGGAAGG others(5): Show |
G | 6 | a0001c0001t0001g0154a0001c0001t0001g0174a0001c0001t0001g0191others(3): Show | 6 | HG02809.hp1 HG02809.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.189-27140_189-2712 others(16): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110657920 | ||||||
| chr11:110657946
|
G | C | 1 | a0009c0015t0004g0153 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.189-27154C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110657946 | ||||||
| chr11:110657949
|
A | G | 7 | a0001c0001t0002g0204a0001c0001t0002g0205a0001c0001t0002g0206others(4): Show | 7 | HG01074.hp1 HG01891.hp2 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.189-27157T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110657949 | ||||||
| chr11:110657958
|
G | C | 86 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0025others(83): Show | 87 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(84): Show |
intron_variant | MODIFIER | c.189-27166C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110657958 | ||||||
| chr11:110658045
|
C | A | 1 | a0007c0020t0020g0149 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.189-27253G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110658045 | ||||||
| chr11:110658246
|
A | C | 2 | a0001c0001t0002g0022a0001c0001t0002g0023 | 2 | HG02280.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.189-27454T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110658246 | ||||||
| chr11:110658404
|
G | A | 5 | a0001c0001t0004g0009a0001c0001t0004g0010a0001c0001t0004g0011others(2): Show | 5 | HG02145.hp2 HG02647.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.189-27612C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110658404 | ||||||
| chr11:110658443
|
C | T | 1 | a0001c0001t0001g0182 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.189-27651G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110658443 | ||||||
| chr11:110658742
|
A | T | 2 | a0001c0001t0002g0022a0001c0001t0002g0023 | 2 | HG02280.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.189-27950T>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110658742 | ||||||
| chr11:110658780
|
A | ATTGTTTT others(3): Show |
63 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0025others(60): Show | 65 | HG00621.hp1 HG00639.hp2 HG00673.hp2 others(62): Show |
intron_variant | MODIFIER | c.189-27998_189-2798 others(14): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110658780 | ||||||
| chr11:110658780
|
A | ATTGTTTT others(8): Show |
17 | a0001c0001t0001g0027a0001c0001t0001g0139a0001c0001t0001g0210others(14): Show | 17 | HG00099.hp2 HG00280.hp2 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.189-27989_189-2798 others(19): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110658780 | ||||||
| chr11:110658780
|
A | ATTGTTTT others(13): Show |
2 | a0006c0007t0010g0147a0006c0007t0010g0148 | 2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.189-27989_189-2798 others(24): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110658780 | ||||||
| chr11:110658791
|
T | TTGTTTTG others(3): Show |
1 | a0001c0001t0001g0173 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.189-28000_189-2799 others(14): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110658791 | ||||||
| chr11:110658932
|
C | T | 2 | a0001c0001t0004g0146a0003c0004t0017g0145 | 2 | HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.189-28140G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110658932 | ||||||
| chr11:110658951
|
A | G | 1 | a0007c0020t0020g0149 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.189-28159T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110658951 | ||||||
| chr11:110659009
|
G | A | 10 | a0001c0001t0001g0027a0001c0001t0001g0139a0001c0001t0004g0082others(7): Show | 10 | HG00735.hp2 HG01496.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.189-28217C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110659009 | ||||||
| chr11:110659094
|
C | A | 10 | a0001c0001t0001g0027a0001c0001t0001g0139a0001c0001t0004g0004others(7): Show | 11 | HG00735.hp2 HG01496.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.189-28302G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110659094 | ||||||
| chr11:110659119
|
C | T | 1 | a0001c0001t0001g0168 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.189-28327G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110659119 | ||||||
| chr11:110659174
|
C | T | 1 | a0001c0005t0005g0197 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.189-28382G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110659174 | ||||||
| chr11:110659188
|
T | G | 2 | a0001c0001t0004g0146a0003c0004t0017g0145 | 2 | HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.189-28396A>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110659188 | ||||||
| chr11:110659256
|
C | G | 8 | a0001c0001t0002g0008a0001c0001t0006g0156a0001c0001t0006g0199others(5): Show | 8 | HG02109.hp1 HG02257.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.189-28464G>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110659256 | ||||||
| chr11:110659307
|
C | G | 1 | a0002c0003t0007g0150 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.189-28515G>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110659307 | ||||||
| chr11:110659396
|
T | C | 2 | a0001c0001t0004g0146a0003c0004t0017g0145 | 2 | HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.189-28604A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110659396 | ||||||
| chr11:110659446
|
G | A | 1 | a0001c0001t0002g0008 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.189-28654C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110659446 | ||||||
| chr11:110659637
|
T | G | 1 | a0001c0001t0001g0169 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.189-28845A>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110659637 | ||||||
| chr11:110659717
|
C | T | 91 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0025others(88): Show | 93 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(90): Show |
intron_variant | MODIFIER | c.189-28925G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110659717 | ||||||
| chr11:110659755
|
G | T | 2 | a0001c0001t0001g0087a0001c0001t0001g0090 | 2 | NA19057.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.189-28963C>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110659755 | ||||||
| chr11:110659876
|
G | A | 53 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0025others(50): Show | 54 | HG00621.hp1 HG00639.hp2 HG00673.hp2 others(51): Show |
intron_variant | MODIFIER | c.189-29084C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110659876 | ||||||
| chr11:110659911
|
G | A | 1 | a0001c0001t0001g0193 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.189-29119C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110659911 | ||||||
| chr11:110659918
|
T | G | 1 | a0001c0001t0002g0053 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.189-29126A>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110659918 | ||||||
| chr11:110659922
|
G | C | 1 | a0001c0001t0002g0053 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.189-29130C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110659922 | ||||||
| chr11:110660054
|
T | TAAAAAAC others(8): Show |
1 | a0008c0017t0002g0141 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.189-29277_189-2926 others(19): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110660054 | ||||||
| chr11:110660061
|
C | CA | 10 | a0001c0001t0002g0051a0001c0001t0002g0052a0001c0001t0002g0053others(7): Show | 10 | HG00323.hp1 HG01099.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.189-29270dupT | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110660061 | ||||||
| chr11:110660061
|
CAAAA | C | 7 | a0001c0001t0002g0008a0001c0001t0006g0156a0001c0001t0006g0199others(4): Show | 7 | HG02109.hp1 HG02257.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.189-29273_189-2927 others(8): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110660061 | ||||||
| chr11:110660062
|
A | AAAAAAAA others(7): Show |
3 | a0001c0001t0001g0027a0001c0001t0001g0139a0003c0004t0002g0144 | 3 | HG00735.hp2 HG01496.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.189-29271_189-2927 others(18): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110660062 | ||||||
| chr11:110660063
|
A | AAAAAAAA others(4): Show |
2 | a0001c0001t0004g0146a0003c0004t0017g0145 | 2 | HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.189-29272_189-2927 others(15): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110660063 | ||||||
| chr11:110660064
|
A | AAAAAAAA others(19): Show |
2 | a0006c0007t0010g0147a0006c0007t0010g0148 | 2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.189-29273_189-2927 others(30): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110660064 | ||||||
| chr11:110660064
|
A | AAAAAAAA others(3): Show |
1 | a0011c0018t0015g0007 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.189-29273_189-2927 others(14): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110660064 | ||||||
| chr11:110660064
|
A | ACAAAAAA others(5): Show |
53 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0025others(50): Show | 54 | HG00621.hp1 HG00639.hp2 HG00673.hp2 others(51): Show |
intron_variant | MODIFIER | c.189-29273_189-2927 others(16): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110660064 | ||||||
| chr11:110660064
|
A | ACAAAAAA others(4): Show |
5 | a0001c0001t0004g0009a0001c0001t0004g0010a0001c0001t0004g0011others(2): Show | 5 | HG02145.hp2 HG02647.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.189-29273_189-2927 others(15): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110660064 | ||||||
| chr11:110660068
|
A | AAAAAAAA others(5): Show |
4 | a0001c0001t0004g0004a0001c0001t0004g0143a0001c0005t0005g0142others(1): Show | 5 | HG01891.hp1 HG03017.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.189-29277_189-2927 others(16): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110660068 | ||||||
| chr11:110660069
|
A | AAAAAAAC others(5): Show |
9 | a0001c0001t0002g0204a0001c0001t0002g0205a0001c0001t0002g0206others(6): Show | 9 | HG01074.hp1 HG01891.hp2 HG01952.hp2 others(6): Show |
intron_variant | MODIFIER | c.189-29278_189-2927 others(16): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110660069 | ||||||
| chr11:110660069
|
A | AAAAAACA others(4): Show |
10 | a0001c0001t0001g0210a0001c0001t0003g0216a0001c0002t0005g0209others(7): Show | 10 | HG00099.hp2 HG00280.hp2 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.189-29278_189-2927 others(15): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110660069 | ||||||
| chr11:110660069
|
A | C | 58 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0025others(55): Show | 59 | HG00621.hp1 HG00639.hp2 HG00673.hp2 others(56): Show |
intron_variant | MODIFIER | c.189-29277T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110660069 | ||||||
| chr11:110660212
|
G | A | 42 | a0001c0001t0001g0134a0001c0001t0002g0102a0001c0001t0003g0001others(39): Show | 44 | HG00323.hp1 HG00621.hp2 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.189-29420C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110660212 | ||||||
| chr11:110660717
|
C | G | 1 | a0001c0001t0001g0055 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.188+29830G>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110660717 | ||||||
| chr11:110660759
|
A | C | 5 | a0001c0001t0002g0081a0001c0001t0002g0158a0001c0001t0002g0159others(2): Show | 5 | HG00673.hp2 HG02040.hp1 NA18951.hp2 others(2): Show |
intron_variant | MODIFIER | c.188+29788T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110660759 | ||||||
| chr11:110660785
|
C | CT | 5 | a0001c0001t0004g0009a0001c0001t0004g0010a0001c0001t0004g0011others(2): Show | 5 | HG02145.hp2 HG02647.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.188+29761dupA | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110660785 | ||||||
| chr11:110660828
|
G | T | 4 | a0001c0001t0004g0004a0001c0001t0004g0143a0001c0005t0005g0142others(1): Show | 5 | HG01891.hp1 HG03017.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.188+29719C>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110660828 | ||||||
| chr11:110660834
|
A | T | 8 | a0001c0001t0002g0008a0001c0001t0006g0156a0001c0001t0006g0199others(5): Show | 8 | HG02109.hp1 HG02257.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.188+29713T>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110660834 | ||||||
| chr11:110660837
|
T | C | 4 | a0001c0001t0004g0004a0001c0001t0004g0143a0001c0005t0005g0142others(1): Show | 5 | HG01891.hp1 HG03017.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.188+29710A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110660837 | ||||||
| chr11:110660896
|
G | T | 1 | a0011c0018t0015g0007 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.188+29651C>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110660896 | ||||||
| chr11:110660959
|
C | T | 1 | a0001c0001t0001g0027 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.188+29588G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110660959 | ||||||
| chr11:110661024
|
A | G | 4 | a0001c0001t0001g0027a0001c0001t0001g0139a0003c0004t0002g0144others(1): Show | 4 | HG00735.hp2 HG01496.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.188+29523T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110661024 | ||||||
| chr11:110661102
|
T | C | 1 | a0007c0020t0020g0149 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.188+29445A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110661102 | ||||||
| chr11:110661117
|
A | T | 1 | a0001c0001t0001g0131 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.188+29430T>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110661117 | ||||||
| chr11:110661208
|
A | T | 1 | a0001c0005t0005g0197 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.188+29339T>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110661208 | ||||||
| chr11:110661453
|
C | T | 1 | a0001c0001t0001g0169 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.188+29094G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110661453 | ||||||
| chr11:110661460
|
C | A | 1 | a0001c0001t0001g0131 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.188+29087G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110661460 | ||||||
| chr11:110661573
|
AT | A | 10 | a0001c0001t0001g0210a0001c0001t0003g0216a0001c0002t0005g0209others(7): Show | 10 | HG00099.hp2 HG00280.hp2 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.188+28973delA | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110661573 | ||||||
| chr11:110661625
|
C | T | 82 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0025others(79): Show | 83 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(80): Show |
intron_variant | MODIFIER | c.188+28922G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110661625 | ||||||
| chr11:110661676
|
T | C | 1 | a0011c0018t0015g0007 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.188+28871A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110661676 | ||||||
| chr11:110661740
|
T | C | 10 | a0001c0001t0001g0027a0001c0001t0001g0139a0001c0001t0004g0004others(7): Show | 11 | HG00735.hp2 HG01496.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.188+28807A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110661740 | ||||||
| chr11:110661993
|
G | A | 1 | a0007c0020t0020g0149 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.188+28554C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110661993 | ||||||
| chr11:110662093
|
A | C | 1 | a0011c0018t0015g0007 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.188+28454T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110662093 | ||||||
| chr11:110662179
|
G | A | 2 | a0001c0001t0004g0146a0003c0004t0017g0145 | 2 | HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.188+28368C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110662179 | ||||||
| chr11:110662220
|
A | G | 99 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0025others(96): Show | 101 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(98): Show |
intron_variant | MODIFIER | c.188+28327T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110662220 | ||||||
| chr11:110662476
|
T | C | 1 | a0011c0018t0015g0007 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.188+28071A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110662476 | ||||||
| chr11:110662581
|
A | C | 10 | a0001c0001t0001g0027a0001c0001t0001g0139a0001c0001t0004g0004others(7): Show | 11 | HG00735.hp2 HG01496.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.188+27966T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110662581 | ||||||
| chr11:110662658
|
C | T | 1 | a0001c0001t0002g0160 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.188+27889G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110662658 | ||||||
| chr11:110663599
|
C | T | 4 | a0001c0001t0004g0004a0001c0001t0004g0143a0001c0005t0005g0142others(1): Show | 5 | HG01891.hp1 HG03017.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.188+26948G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110663599 | ||||||
| chr11:110663795
|
C | A | 1 | a0001c0001t0001g0179 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.188+26752G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110663795 | ||||||
| chr11:110663795
|
C | G | 97 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0025others(94): Show | 99 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.188+26752G>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110663795 | ||||||
| chr11:110664054
|
T | C | 1 | a0011c0018t0015g0007 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.188+26493A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110664054 | ||||||
| chr11:110664299
|
C | T | 7 | a0001c0001t0004g0009a0001c0001t0004g0010a0001c0001t0004g0011others(4): Show | 7 | HG02145.hp2 HG02451.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.188+26248G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110664299 | ||||||
| chr11:110664349
|
C | CAT | 6 | a0001c0001t0004g0004a0001c0001t0004g0143a0001c0001t0004g0146others(3): Show | 7 | HG01891.hp1 HG03017.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.188+26196_188+2619 others(6): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110664349 | ||||||
| chr11:110664417
|
A | G | 2 | a0001c0009t0002g0188a0001c0009t0002g0196 | 2 | NA18978.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.188+26130T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110664417 | ||||||
| chr11:110664439
|
A | G | 3 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0219 | 3 | HG00099.hp1 HG00741.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.188+26108T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110664439 | ||||||
| chr11:110664449
|
C | A | 53 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0025others(50): Show | 54 | HG00621.hp1 HG00639.hp2 HG00673.hp2 others(51): Show |
intron_variant | MODIFIER | c.188+26098G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110664449 | ||||||
| chr11:110664455
|
G | A | 7 | a0001c0001t0004g0009a0001c0001t0004g0010a0001c0001t0004g0011others(4): Show | 7 | HG02145.hp2 HG02451.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.188+26092C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110664455 | ||||||
| chr11:110664491
|
G | A | 8 | a0001c0001t0002g0008a0001c0001t0006g0156a0001c0001t0006g0199others(5): Show | 8 | HG02109.hp1 HG02257.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.188+26056C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110664491 | ||||||
| chr11:110664615
|
C | G | 5 | a0001c0001t0002g0059a0001c0001t0002g0061a0001c0001t0002g0062others(2): Show | 5 | HG02055.hp2 HG02109.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.188+25932G>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110664615 | ||||||
| chr11:110664644
|
C | T | 61 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0025others(58): Show | 62 | HG00621.hp1 HG00639.hp2 HG00673.hp2 others(59): Show |
intron_variant | MODIFIER | c.188+25903G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110664644 | ||||||
| chr11:110664706
|
C | T | 7 | a0001c0001t0002g0204a0001c0001t0002g0205a0001c0001t0002g0206others(4): Show | 7 | HG01074.hp1 HG01891.hp2 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.188+25841G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110664706 | ||||||
| chr11:110664727
|
C | CA | 8 | a0001c0001t0001g0078a0001c0001t0001g0114a0001c0001t0002g0034others(5): Show | 8 | HG00733.hp1 HG01169.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.188+25819dupT | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110664727 | ||||||
| chr11:110664727
|
CA | C | 10 | a0001c0001t0001g0027a0001c0001t0001g0139a0001c0001t0004g0004others(7): Show | 11 | HG00735.hp2 HG01496.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.188+25819delT | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110664727 | ||||||
| chr11:110664727
|
CAA | C | 81 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0025others(78): Show | 82 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.188+25818_188+2581 others(6): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110664727 | ||||||
| chr11:110664727
|
CAAAAAAA | C | 7 | a0001c0001t0002g0204a0001c0001t0002g0205a0001c0001t0002g0206others(4): Show | 7 | HG01074.hp1 HG01891.hp2 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.188+25813_188+2581 others(11): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110664727 | ||||||
| chr11:110664727
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0001g0068 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.188+25810_188+2581 others(14): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110664727 | ||||||
| chr11:110664774
|
C | T | 5 | a0001c0001t0004g0009a0001c0001t0004g0010a0001c0001t0004g0011others(2): Show | 5 | HG02145.hp2 HG02647.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.188+25773G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110664774 | ||||||
| chr11:110664820
|
T | C | 1 | a0001c0001t0003g0109 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.188+25727A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110664820 | ||||||
| chr11:110665145
|
G | A | 2 | a0001c0001t0004g0146a0003c0004t0017g0145 | 2 | HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.188+25402C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110665145 | ||||||
| chr11:110665156
|
C | A | 2 | a0001c0001t0004g0146a0003c0004t0017g0145 | 2 | HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.188+25391G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110665156 | ||||||
| chr11:110665244
|
A | G | 1 | a0007c0020t0020g0149 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.188+25303T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110665244 | ||||||
| chr11:110665373
|
C | T | 2 | a0001c0001t0003g0091a0001c0001t0003g0101 | 2 | HG01346.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.188+25174G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110665373 | ||||||
| chr11:110665617
|
G | A | 4 | a0001c0001t0004g0004a0001c0001t0004g0143a0001c0005t0005g0142others(1): Show | 5 | HG01891.hp1 HG03017.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.188+24930C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110665617 | ||||||
| chr11:110665628
|
A | G | 2 | a0001c0001t0004g0146a0003c0004t0017g0145 | 2 | HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.188+24919T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110665628 | ||||||
| chr11:110665813
|
T | C | 1 | a0011c0018t0015g0007 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.188+24734A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110665813 | ||||||
| chr11:110665835
|
A | G | 4 | a0001c0001t0004g0004a0001c0001t0004g0143a0001c0005t0005g0142others(1): Show | 5 | HG01891.hp1 HG03017.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.188+24712T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110665835 | ||||||
| chr11:110665905
|
A | T | 1 | a0002c0006t0012g0140 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.188+24642T>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110665905 | ||||||
| chr11:110665970
|
TAC | T | 89 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0025others(86): Show | 91 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(88): Show |
intron_variant | MODIFIER | c.188+24575_188+2457 others(6): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110665970 | ||||||
| chr11:110665972
|
C | T | 2 | a0001c0001t0004g0146a0003c0004t0017g0145 | 2 | HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.188+24575G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110665972 | ||||||
| chr11:110665976
|
TACAC | T | 2 | a0001c0001t0004g0146a0003c0004t0017g0145 | 2 | HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.188+24567_188+2457 others(8): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110665976 | ||||||
| chr11:110665978
|
C | T | 88 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0025others(85): Show | 90 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(87): Show |
intron_variant | MODIFIER | c.188+24569G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110665978 | ||||||
| chr11:110666011
|
G | A | 1 | a0001c0001t0001g0154 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.188+24536C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110666011 | ||||||
| chr11:110666048
|
T | C | 4 | a0001c0001t0004g0004a0001c0001t0004g0143a0001c0005t0005g0142others(1): Show | 5 | HG01891.hp1 HG03017.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.188+24499A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110666048 | ||||||
| chr11:110666177
|
T | C | 8 | a0001c0001t0002g0008a0001c0001t0006g0156a0001c0001t0006g0199others(5): Show | 8 | HG02109.hp1 HG02257.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.188+24370A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110666177 | ||||||
| chr11:110666273
|
T | C | 7 | a0001c0001t0002g0204a0001c0001t0002g0205a0001c0001t0002g0206others(4): Show | 7 | HG01074.hp1 HG01891.hp2 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.188+24274A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110666273 | ||||||
| chr11:110666409
|
G | A | 91 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0025others(88): Show | 93 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(90): Show |
intron_variant | MODIFIER | c.188+24138C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110666409 | ||||||
| chr11:110666544
|
G | A | 2 | a0001c0001t0004g0146a0003c0004t0017g0145 | 2 | HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.188+24003C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110666544 | ||||||
| chr11:110666571
|
T | C | 98 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0025others(95): Show | 100 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(97): Show |
intron_variant | MODIFIER | c.188+23976A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110666571 | ||||||
| chr11:110666596
|
A | T | 1 | a0001c0001t0002g0067 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.188+23951T>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110666596 | ||||||
| chr11:110666639
|
C | A | 5 | a0001c0001t0004g0009a0001c0001t0004g0010a0001c0001t0004g0011others(2): Show | 5 | HG02145.hp2 HG02647.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.188+23908G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110666639 | ||||||
| chr11:110666784
|
C | T | 1 | a0011c0018t0015g0007 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.188+23763G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110666784 | ||||||
| chr11:110666834
|
C | T | 4 | a0001c0001t0001g0027a0001c0001t0001g0139a0003c0004t0002g0144others(1): Show | 4 | HG00735.hp2 HG01496.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.188+23713G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110666834 | ||||||
| chr11:110666849
|
T | G | 2 | a0001c0001t0002g0059a0001c0001t0002g0061 | 2 | HG02109.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.188+23698A>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110666849 | ||||||
| chr11:110666866
|
G | C | 2 | a0001c0001t0004g0146a0003c0004t0017g0145 | 2 | HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.188+23681C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110666866 | ||||||
| chr11:110667054
|
A | G | 1 | a0001c0001t0002g0084 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.188+23493T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110667054 | ||||||
| chr11:110667365
|
T | C | 4 | a0001c0001t0001g0027a0001c0001t0001g0139a0003c0004t0002g0144others(1): Show | 4 | HG00735.hp2 HG01496.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.188+23182A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110667365 | ||||||
| chr11:110667557
|
G | A | 1 | a0001c0001t0001g0183 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.188+22990C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110667557 | ||||||
| chr11:110667566
|
A | C | 86 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0025others(83): Show | 87 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(84): Show |
intron_variant | MODIFIER | c.188+22981T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110667566 | ||||||
| chr11:110667614
|
A | C | 4 | a0001c0001t0003g0216a0001c0002t0005g0211a0001c0002t0005g0217others(1): Show | 4 | HG02015.hp1 HG02080.hp1 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.188+22933T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110667614 | ||||||
| chr11:110667703
|
T | C | 8 | a0001c0001t0002g0008a0001c0001t0006g0156a0001c0001t0006g0199others(5): Show | 8 | HG02109.hp1 HG02257.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.188+22844A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110667703 | ||||||
| chr11:110668008
|
G | A | 1 | a0001c0001t0003g0100 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.188+22539C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110668008 | ||||||
| chr11:110668101
|
A | G | 6 | a0001c0001t0004g0004a0001c0001t0004g0143a0001c0005t0005g0142others(3): Show | 7 | HG01891.hp1 HG02622.hp2 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.188+22446T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110668101 | ||||||
| chr11:110668374
|
G | A | 4 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0013g0110others(1): Show | 4 | HG02015.hp2 NA18940.hp1 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.188+22173C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110668374 | ||||||
| chr11:110668467
|
G | A | 7 | a0001c0001t0002g0204a0001c0001t0002g0205a0001c0001t0002g0206others(4): Show | 7 | HG01074.hp1 HG01891.hp2 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.188+22080C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110668467 | ||||||
| chr11:110668666
|
AAAAGAAA others(2): Show |
A | 8 | a0001c0001t0002g0008a0001c0001t0006g0156a0001c0001t0006g0199others(5): Show | 8 | HG02109.hp1 HG02257.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.188+21872_188+2188 others(13): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110668666 | ||||||
| chr11:110668720
|
A | G | 3 | a0001c0001t0002g0158a0001c0001t0002g0159a0001c0012t0002g0189 | 3 | HG02040.hp1 NA18951.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.188+21827T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110668720 | ||||||
| chr11:110668785
|
T | A | 1 | a0001c0001t0001g0167 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.188+21762A>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110668785 | ||||||
| chr11:110669098
|
A | G | 2 | a0006c0007t0010g0147a0006c0007t0010g0148 | 2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.188+21449T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110669098 | ||||||
| chr11:110669117
|
A | C | 8 | a0001c0001t0002g0008a0001c0001t0006g0156a0001c0001t0006g0199others(5): Show | 8 | HG02109.hp1 HG02257.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.188+21430T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110669117 | ||||||
| chr11:110669285
|
C | T | 10 | a0001c0001t0001g0210a0001c0001t0003g0216a0001c0002t0005g0209others(7): Show | 10 | HG00099.hp2 HG00280.hp2 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.188+21262G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110669285 | ||||||
| chr11:110669411
|
C | G | 8 | a0001c0001t0002g0008a0001c0001t0006g0156a0001c0001t0006g0199others(5): Show | 8 | HG02109.hp1 HG02257.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.188+21136G>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110669411 | ||||||
| chr11:110669418
|
T | C | 78 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0025others(75): Show | 79 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.188+21129A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110669418 | ||||||
| chr11:110669483
|
C | A | 1 | a0001c0001t0001g0167 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.188+21064G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110669483 | ||||||
| chr11:110669510
|
T | C | 1 | a0011c0018t0015g0007 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.188+21037A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110669510 | ||||||
| chr11:110669573
|
A | G | 61 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0025others(58): Show | 62 | HG00621.hp1 HG00639.hp2 HG00673.hp2 others(59): Show |
intron_variant | MODIFIER | c.188+20974T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110669573 | ||||||
| chr11:110669632
|
A | G | 8 | a0001c0001t0002g0008a0001c0001t0006g0156a0001c0001t0006g0199others(5): Show | 8 | HG02109.hp1 HG02257.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.188+20915T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110669632 | ||||||
| chr11:110669818
|
T | C | 2 | a0001c0001t0004g0146a0003c0004t0017g0145 | 2 | HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.188+20729A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110669818 | ||||||
| chr11:110669904
|
A | G | 2 | a0001c0001t0004g0146a0003c0004t0017g0145 | 2 | HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.188+20643T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110669904 | ||||||
| chr11:110670032
|
C | A | 1 | a0002c0014t0019g0207 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.188+20515G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110670032 | ||||||
| chr11:110670218
|
C | T | 1 | a0001c0001t0003g0213 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.188+20329G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110670218 | ||||||
| chr11:110670329
|
AC | A | 2 | a0006c0007t0010g0147a0006c0007t0010g0148 | 2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.188+20217delG | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110670329 | ||||||
| chr11:110670331
|
T | A | 2 | a0006c0007t0010g0147a0006c0007t0010g0148 | 2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.188+20216A>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110670331 | ||||||
| chr11:110670506
|
G | A | 8 | a0001c0001t0004g0004a0001c0001t0004g0143a0001c0001t0004g0146others(5): Show | 9 | HG01891.hp1 HG02622.hp2 HG03017.hp2 others(6): Show |
intron_variant | MODIFIER | c.188+20041C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110670506 | ||||||
| chr11:110670574
|
A | G | 1 | a0007c0020t0020g0149 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.188+19973T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110670574 | ||||||
| chr11:110670655
|
C | T | 1 | a0001c0001t0001g0175 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.188+19892G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110670655 | ||||||
| chr11:110670858
|
G | A | 10 | a0001c0001t0001g0210a0001c0001t0003g0216a0001c0002t0005g0209others(7): Show | 10 | HG00099.hp2 HG00280.hp2 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.188+19689C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110670858 | ||||||
| chr11:110670867
|
C | A | 1 | a0001c0001t0001g0173 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.188+19680G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110670867 | ||||||
| chr11:110670914
|
G | T | 1 | a0002c0014t0019g0207 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.188+19633C>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110670914 | ||||||
| chr11:110671025
|
T | G | 3 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117 | 3 | HG00280.hp1 HG01074.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.188+19522A>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110671025 | ||||||
| chr11:110671229
|
G | GA | 4 | a0001c0001t0004g0004a0001c0001t0004g0143a0001c0005t0005g0142others(1): Show | 5 | HG01891.hp1 HG03017.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.188+19317dupT | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110671229 | ||||||
| chr11:110671244
|
C | T | 70 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0025others(67): Show | 71 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(68): Show |
intron_variant | MODIFIER | c.188+19303G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110671244 | ||||||
| chr11:110671396
|
T | C | 2 | a0001c0001t0001g0080a0001c0001t0003g0079 | 2 | HG02602.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.188+19151A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110671396 | ||||||
| chr11:110671403
|
T | C | 5 | a0001c0001t0004g0009a0001c0001t0004g0010a0001c0001t0004g0011others(2): Show | 5 | HG02145.hp2 HG02647.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.188+19144A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110671403 | ||||||
| chr11:110671415
|
G | T | 1 | a0001c0001t0002g0121 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.188+19132C>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110671415 | ||||||
| chr11:110671417
|
A | G | 1 | a0001c0001t0002g0164 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.188+19130T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110671417 | ||||||
| chr11:110671509
|
C | T | 4 | a0001c0001t0001g0027a0001c0001t0001g0139a0003c0004t0002g0144others(1): Show | 4 | HG00735.hp2 HG01496.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.188+19038G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110671509 | ||||||
| chr11:110671519
|
A | G | 1 | a0001c0001t0001g0134 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.188+19028T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110671519 | ||||||
| chr11:110671539
|
T | C | 2 | a0001c0001t0004g0146a0003c0004t0017g0145 | 2 | HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.188+19008A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110671539 | ||||||
| chr11:110671642
|
A | C | 2 | a0006c0007t0010g0147a0006c0007t0010g0148 | 2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.188+18905T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110671642 | ||||||
| chr11:110671865
|
G | T | 1 | a0001c0001t0004g0082 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.188+18682C>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110671865 | ||||||
| chr11:110672437
|
C | A | 1 | a0001c0002t0005g0209 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.188+18110G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110672437 | ||||||
| chr11:110672474
|
AT | A | 8 | a0001c0001t0002g0008a0001c0001t0006g0156a0001c0001t0006g0199others(5): Show | 8 | HG02109.hp1 HG02257.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.188+18072delA | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110672474 | ||||||
| chr11:110672606
|
G | A | 2 | a0006c0007t0010g0147a0006c0007t0010g0148 | 2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.188+17941C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110672606 | ||||||
| chr11:110672797
|
C | T | 71 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0025others(68): Show | 72 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.188+17750G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110672797 | ||||||
| chr11:110672893
|
G | C | 18 | a0001c0001t0001g0027a0001c0001t0001g0139a0001c0001t0002g0008others(15): Show | 19 | HG00735.hp2 HG01496.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.188+17654C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110672893 | ||||||
| chr11:110672928
|
G | A | 2 | a0001c0001t0004g0146a0003c0004t0017g0145 | 2 | HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.188+17619C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110672928 | ||||||
| chr11:110673075
|
T | A | 2 | a0001c0001t0003g0091a0001c0001t0003g0101 | 2 | HG01346.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.188+17472A>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110673075 | ||||||
| chr11:110673109
|
A | T | 4 | a0001c0001t0008g0014a0001c0001t0008g0015a0001c0001t0008g0019others(1): Show | 4 | NA18997.hp1 NA19003.hp2 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.188+17438T>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110673109 | ||||||
| chr11:110673182
|
A | G | 71 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0025others(68): Show | 72 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.188+17365T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110673182 | ||||||
| chr11:110673373
|
T | C | 1 | a0001c0005t0005g0197 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.188+17174A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110673373 | ||||||
| chr11:110673477
|
C | T | 1 | a0012c0019t0004g0151 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.188+17070G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110673477 | ||||||
| chr11:110673725
|
G | A | 2 | a0001c0001t0001g0173a0001c0001t0006g0172 | 2 | HG01361.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.188+16822C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110673725 | ||||||
| chr11:110673934
|
G | T | 2 | a0001c0001t0004g0146a0003c0004t0017g0145 | 2 | HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.188+16613C>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110673934 | ||||||
| chr11:110673941
|
A | AT | 6 | a0001c0001t0001g0105a0001c0001t0003g0104a0001c0001t0011g0018others(3): Show | 6 | HG02622.hp2 HG03540.hp2 NA18972.hp1 others(3): Show |
intron_variant | MODIFIER | c.188+16605dupA | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110673941 | ||||||
| chr11:110673941
|
AT | A | 74 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0025others(71): Show | 75 | HG00621.hp1 HG00639.hp2 HG00673.hp2 others(72): Show |
intron_variant | MODIFIER | c.188+16605delA | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110673941 | ||||||
| chr11:110673941
|
ATTT | A | 5 | a0001c0001t0004g0009a0001c0001t0004g0010a0001c0001t0004g0011others(2): Show | 5 | HG02145.hp2 HG02647.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.188+16603_188+1660 others(7): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110673941 | ||||||
| chr11:110673964
|
C | T | 1 | a0002c0003t0007g0150 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.188+16583G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110673964 | ||||||
| chr11:110674102
|
C | G | 53 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0025others(50): Show | 54 | HG00621.hp1 HG00639.hp2 HG00673.hp2 others(51): Show |
intron_variant | MODIFIER | c.188+16445G>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110674102 | ||||||
| chr11:110674147
|
G | A | 2 | a0001c0001t0001g0116a0001c0001t0001g0117 | 2 | HG00280.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.188+16400C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110674147 | ||||||
| chr11:110674160
|
T | C | 2 | a0001c0001t0002g0008a0001c0001t0006g0156 | 2 | HG02559.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.188+16387A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110674160 | ||||||
| chr11:110674234
|
A | G | 98 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0025others(95): Show | 100 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(97): Show |
intron_variant | MODIFIER | c.188+16313T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110674234 | ||||||
| chr11:110674282
|
A | G | 2 | a0001c0001t0002g0204a0002c0003t0007g0202 | 2 | HG01074.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.188+16265T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110674282 | ||||||
| chr11:110674630
|
T | TTA | 5 | a0001c0001t0001g0027a0001c0001t0001g0139a0003c0004t0002g0144others(2): Show | 5 | HG00735.hp2 HG01496.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.188+15915_188+1591 others(6): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110674630 | ||||||
| chr11:110674734
|
T | C | 80 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0025others(77): Show | 81 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.188+15813A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110674734 | ||||||
| chr11:110674758
|
C | G | 4 | a0001c0001t0001g0027a0001c0001t0001g0139a0003c0004t0002g0144others(1): Show | 4 | HG00735.hp2 HG01496.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.188+15789G>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110674758 | ||||||
| chr11:110674775
|
T | G | 60 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0025others(57): Show | 61 | HG00621.hp1 HG00639.hp2 HG00673.hp2 others(58): Show |
intron_variant | MODIFIER | c.188+15772A>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110674775 | ||||||
| chr11:110674807
|
T | C | 1 | a0011c0018t0015g0007 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.188+15740A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110674807 | ||||||
| chr11:110674977
|
T | C | 2 | a0001c0001t0004g0146a0003c0004t0017g0145 | 2 | HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.188+15570A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110674977 | ||||||
| chr11:110675270
|
C | T | 7 | a0001c0001t0002g0204a0001c0001t0002g0205a0001c0001t0002g0206others(4): Show | 7 | HG01074.hp1 HG01891.hp2 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.188+15277G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110675270 | ||||||
| chr11:110675347
|
C | T | 2 | a0006c0007t0010g0147a0006c0007t0010g0148 | 2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.188+15200G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110675347 | ||||||
| chr11:110675479
|
A | T | 4 | a0001c0001t0004g0004a0001c0001t0004g0143a0001c0005t0005g0142others(1): Show | 5 | HG01891.hp1 HG03017.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.188+15068T>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110675479 | ||||||
| chr11:110675490
|
G | A | 1 | a0001c0001t0001g0066 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.188+15057C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110675490 | ||||||
| chr11:110675573
|
A | G | 2 | a0001c0001t0004g0146a0003c0004t0017g0145 | 2 | HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.188+14974T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110675573 | ||||||
| chr11:110675656
|
C | T | 7 | a0001c0001t0002g0204a0001c0001t0002g0205a0001c0001t0002g0206others(4): Show | 7 | HG01074.hp1 HG01891.hp2 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.188+14891G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110675656 | ||||||
| chr11:110675675
|
C | T | 1 | a0001c0001t0003g0133 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.188+14872G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110675675 | ||||||
| chr11:110675904
|
A | T | 9 | a0001c0001t0001g0027a0001c0001t0001g0139a0001c0001t0004g0004others(6): Show | 10 | HG00735.hp2 HG01496.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.188+14643T>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110675904 | ||||||
| chr11:110676202
|
T | C | 2 | a0001c0001t0001g0027a0001c0001t0001g0139 | 2 | HG00735.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.188+14345A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110676202 | ||||||
| chr11:110676303
|
T | C | 1 | a0003c0004t0002g0162 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.188+14244A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110676303 | ||||||
| chr11:110676382
|
G | A | 1 | a0001c0001t0001g0083 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.188+14165C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110676382 | ||||||
| chr11:110676427
|
C | T | 1 | a0001c0001t0008g0014 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.188+14120G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110676427 | ||||||
| chr11:110676431
|
C | G | 1 | a0002c0006t0012g0140 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.188+14116G>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110676431 | ||||||
| chr11:110676453
|
G | A | 6 | a0001c0001t0006g0156a0001c0001t0006g0199a0001c0001t0006g0200others(3): Show | 6 | HG02109.hp1 HG02257.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.188+14094C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110676453 | ||||||
| chr11:110676523
|
A | T | 11 | a0001c0001t0001g0210a0001c0001t0003g0213a0001c0001t0003g0216others(8): Show | 11 | HG00099.hp2 HG00280.hp2 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.188+14024T>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110676523 | ||||||
| chr11:110676563
|
G | A | 3 | a0001c0001t0001g0139a0003c0004t0002g0144a0008c0017t0002g0141 | 3 | HG00735.hp2 HG03688.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.188+13984C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110676563 | ||||||
| chr11:110676588
|
T | G | 1 | a0007c0020t0020g0149 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.188+13959A>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110676588 | ||||||
| chr11:110676817
|
G | GT | 31 | a0001c0001t0001g0195a0001c0001t0001g0210a0001c0001t0002g0008others(28): Show | 32 | HG00099.hp2 HG00280.hp2 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.188+13729dupA | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110676817 | ||||||
| chr11:110676827
|
T | A | 5 | a0001c0001t0001g0139a0001c0001t0002g0084a0002c0006t0012g0140others(2): Show | 5 | HG00735.hp2 HG03017.hp2 HG03688.hp1 others(2): Show |
intron_variant | MODIFIER | c.188+13720A>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110676827 | ||||||
| chr11:110676828
|
A | T | 66 | a0001c0001t0001g0020a0001c0001t0001g0025a0001c0001t0001g0136others(63): Show | 66 | HG00280.hp2 HG00621.hp1 HG00639.hp2 others(63): Show |
intron_variant | MODIFIER | c.188+13719T>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110676828 | ||||||
| chr11:110676829
|
A | T | 1 | a0001c0001t0001g0185 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.188+13718T>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110676829 | ||||||
| chr11:110676981
|
T | C | 1 | a0001c0001t0002g0102 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.188+13566A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110676981 | ||||||
| chr11:110677036
|
C | T | 7 | a0001c0001t0001g0139a0001c0001t0004g0004a0001c0001t0004g0143others(4): Show | 8 | HG00735.hp2 HG01891.hp1 HG03017.hp2 others(5): Show |
intron_variant | MODIFIER | c.188+13511G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110677036 | ||||||
| chr11:110677112
|
A | C | 1 | a0001c0005t0005g0197 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.188+13435T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110677112 | ||||||
| chr11:110677113
|
G | C | 1 | a0009c0015t0004g0153 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.188+13434C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110677113 | ||||||
| chr11:110677387
|
C | G | 12 | a0001c0001t0001g0210a0001c0001t0003g0213a0001c0001t0003g0216others(9): Show | 12 | HG00099.hp2 HG00280.hp2 HG02015.hp1 others(9): Show |
intron_variant | MODIFIER | c.188+13160G>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110677387 | ||||||
| chr11:110677647
|
GA | G | 22 | a0001c0001t0001g0210a0001c0001t0002g0008a0001c0001t0003g0213others(19): Show | 22 | HG00099.hp2 HG00280.hp2 HG02015.hp1 others(19): Show |
intron_variant | MODIFIER | c.188+12899delT | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110677647 | ||||||
| chr11:110677735
|
G | A | 49 | a0001c0001t0001g0005a0001c0001t0001g0136a0001c0001t0001g0137others(46): Show | 50 | HG00621.hp1 HG00639.hp2 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.188+12812C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110677735 | ||||||
| chr11:110677848
|
C | T | 2 | a0001c0001t0001g0131a0001c0005t0005g0197 | 2 | HG02451.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.188+12699G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110677848 | ||||||
| chr11:110678062
|
A | G | 35 | a0001c0001t0001g0210a0001c0001t0002g0008a0001c0001t0002g0204others(32): Show | 35 | HG00099.hp2 HG00280.hp2 HG01074.hp1 others(32): Show |
intron_variant | MODIFIER | c.188+12485T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110678062 | ||||||
| chr11:110678085
|
T | C | 3 | a0001c0001t0006g0199a0001c0001t0006g0200a0001c0001t0006g0201 | 3 | HG02109.hp1 HG02486.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.188+12462A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110678085 | ||||||
| chr11:110678357
|
A | G | 9 | a0001c0001t0002g0026a0001c0001t0002g0029a0001c0001t0002g0031others(6): Show | 9 | HG01109.hp2 HG02486.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.188+12190T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110678357 | ||||||
| chr11:110678509
|
G | T | 8 | a0001c0001t0002g0008a0001c0001t0004g0009a0001c0001t0004g0010others(5): Show | 8 | HG02145.hp2 HG02647.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.188+12038C>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110678509 | ||||||
| chr11:110678545
|
G | A | 1 | a0001c0001t0002g0062 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.188+12002C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110678545 | ||||||
| chr11:110678597
|
T | C | 7 | a0001c0001t0002g0204a0001c0001t0002g0205a0001c0001t0002g0206others(4): Show | 7 | HG01074.hp1 HG01891.hp2 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.188+11950A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110678597 | ||||||
| chr11:110678755
|
A | G | 2 | a0006c0007t0010g0147a0006c0007t0010g0148 | 2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.188+11792T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110678755 | ||||||
| chr11:110678807
|
C | G | 91 | a0001c0001t0001g0005a0001c0001t0001g0136a0001c0001t0001g0137others(88): Show | 93 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(90): Show |
intron_variant | MODIFIER | c.188+11740G>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110678807 | ||||||
| chr11:110678896
|
C | T | 1 | a0001c0005t0005g0197 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.188+11651G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110678896 | ||||||
| chr11:110679288
|
C | T | 7 | a0001c0001t0001g0139a0001c0001t0004g0004a0001c0001t0004g0143others(4): Show | 8 | HG00735.hp2 HG01891.hp1 HG03017.hp2 others(5): Show |
intron_variant | MODIFIER | c.188+11259G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110679288 | ||||||
| chr11:110679348
|
G | C | 1 | a0007c0020t0020g0149 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.188+11199C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110679348 | ||||||
| chr11:110679656
|
T | C | 12 | a0001c0001t0001g0210a0001c0001t0003g0213a0001c0001t0003g0216others(9): Show | 12 | HG00099.hp2 HG00280.hp2 HG02015.hp1 others(9): Show |
intron_variant | MODIFIER | c.188+10891A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110679656 | ||||||
| chr11:110679670
|
T | C | 7 | a0001c0001t0001g0139a0001c0001t0004g0004a0001c0001t0004g0143others(4): Show | 8 | HG00735.hp2 HG01891.hp1 HG03017.hp2 others(5): Show |
intron_variant | MODIFIER | c.188+10877A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110679670 | ||||||
| chr11:110679903
|
C | A | 1 | a0001c0005t0005g0197 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.188+10644G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110679903 | ||||||
| chr11:110679915
|
T | C | 1 | a0007c0020t0020g0149 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.188+10632A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110679915 | ||||||
| chr11:110679943
|
G | A | 3 | a0001c0001t0006g0199a0001c0001t0006g0200a0001c0001t0006g0201 | 3 | HG02109.hp1 HG02486.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.188+10604C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110679943 | ||||||
| chr11:110680152
|
A | T | 91 | a0001c0001t0001g0005a0001c0001t0001g0136a0001c0001t0001g0137others(88): Show | 93 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(90): Show |
intron_variant | MODIFIER | c.188+10395T>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110680152 | ||||||
| chr11:110680214
|
G | A | 1 | a0012c0019t0004g0151 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.188+10333C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110680214 | ||||||
| chr11:110680590
|
T | G | 2 | a0001c0009t0002g0188a0001c0009t0002g0196 | 2 | NA18978.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.188+9957A>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110680590 | ||||||
| chr11:110680883
|
A | C | 1 | a0001c0001t0002g0204 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.188+9664T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110680883 | ||||||
| chr11:110680887
|
T | C | 7 | a0001c0001t0001g0139a0001c0001t0004g0004a0001c0001t0004g0143others(4): Show | 8 | HG00735.hp2 HG01891.hp1 HG03017.hp2 others(5): Show |
intron_variant | MODIFIER | c.188+9660A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110680887 | ||||||
| chr11:110680942
|
T | C | 48 | a0001c0001t0001g0005a0001c0001t0001g0136a0001c0001t0001g0137others(45): Show | 49 | HG00621.hp1 HG00639.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.188+9605A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110680942 | ||||||
| chr11:110681048
|
T | C | 4 | a0001c0001t0003g0216a0001c0002t0005g0211a0001c0002t0005g0217others(1): Show | 4 | HG02015.hp1 HG02080.hp1 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.188+9499A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110681048 | ||||||
| chr11:110681049
|
G | A | 10 | a0001c0001t0002g0008a0001c0001t0004g0009a0001c0001t0004g0010others(7): Show | 10 | HG02145.hp2 HG02622.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.188+9498C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110681049 | ||||||
| chr11:110681143
|
G | A | 1 | a0001c0005t0005g0197 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.188+9404C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110681143 | ||||||
| chr11:110681274
|
G | T | 5 | a0001c0001t0002g0008a0001c0001t0004g0009a0001c0001t0004g0010others(2): Show | 5 | HG02145.hp2 HG02647.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.188+9273C>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110681274 | ||||||
| chr11:110681398
|
T | C | 2 | a0001c0001t0002g0063a0001c0001t0002g0112 | 2 | HG01192.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.188+9149A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110681398 | ||||||
| chr11:110681549
|
T | G | 7 | a0001c0001t0001g0139a0001c0001t0004g0004a0001c0001t0004g0143others(4): Show | 8 | HG00735.hp2 HG01891.hp1 HG03017.hp2 others(5): Show |
intron_variant | MODIFIER | c.188+8998A>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110681549 | ||||||
| chr11:110681666
|
T | C | 1 | a0001c0001t0001g0155 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.188+8881A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110681666 | ||||||
| chr11:110681729
|
G | C | 4 | a0001c0001t0001g0025a0001c0001t0002g0040a0001c0001t0002g0041others(1): Show | 4 | NA18940.hp2 NA18953.hp1 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.188+8818C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110681729 | ||||||
| chr11:110682052
|
T | G | 45 | a0001c0001t0001g0005a0001c0001t0001g0136a0001c0001t0001g0137others(42): Show | 46 | HG00621.hp1 HG00639.hp2 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.188+8495A>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110682052 | ||||||
| chr11:110682278
|
A | G | 2 | a0006c0007t0010g0147a0006c0007t0010g0148 | 2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.188+8269T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110682278 | ||||||
| chr11:110682302
|
A | G | 3 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0219 | 3 | HG00099.hp1 HG00741.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.188+8245T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110682302 | ||||||
| chr11:110682448
|
A | G | 6 | a0001c0001t0006g0156a0001c0001t0006g0199a0001c0001t0006g0200others(3): Show | 6 | HG02109.hp1 HG02257.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.188+8099T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110682448 | ||||||
| chr11:110682483
|
A | T | 2 | a0001c0001t0003g0001a0001c0001t0003g0049 | 4 | HG01928.hp2 HG01981.hp2 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.188+8064T>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110682483 | ||||||
| chr11:110682715
|
T | C | 7 | a0001c0001t0001g0139a0001c0001t0004g0004a0001c0001t0004g0143others(4): Show | 8 | HG00735.hp2 HG01891.hp1 HG03017.hp2 others(5): Show |
intron_variant | MODIFIER | c.188+7832A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110682715 | ||||||
| chr11:110682863
|
G | T | 1 | a0001c0001t0001g0066 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.188+7684C>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110682863 | ||||||
| chr11:110682957
|
A | G | 3 | a0001c0001t0001g0105a0001c0001t0011g0017a0001c0001t0011g0018 | 3 | HG02155.hp1 NA18972.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.188+7590T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110682957 | ||||||
| chr11:110682999
|
T | TA | 91 | a0001c0001t0001g0005a0001c0001t0001g0136a0001c0001t0001g0137others(88): Show | 93 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(90): Show |
intron_variant | MODIFIER | c.188+7547dupT | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110682999 | ||||||
| chr11:110683744
|
T | C | 6 | a0001c0001t0006g0156a0001c0001t0006g0199a0001c0001t0006g0200others(3): Show | 6 | HG02109.hp1 HG02257.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.188+6803A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110683744 | ||||||
| chr11:110683778
|
T | C | 1 | a0001c0001t0001g0058 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.188+6769A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110683778 | ||||||
| chr11:110683793
|
C | T | 10 | a0001c0001t0001g0139a0001c0001t0002g0164a0001c0001t0002g0165others(7): Show | 11 | HG00735.hp2 HG01891.hp1 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.188+6754G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110683793 | ||||||
| chr11:110683923
|
T | C | 6 | a0001c0001t0006g0156a0001c0001t0006g0199a0001c0001t0006g0200others(3): Show | 6 | HG02109.hp1 HG02257.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.188+6624A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110683923 | ||||||
| chr11:110684035
|
C | G | 91 | a0001c0001t0001g0005a0001c0001t0001g0136a0001c0001t0001g0137others(88): Show | 93 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(90): Show |
intron_variant | MODIFIER | c.188+6512G>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110684035 | ||||||
| chr11:110684092
|
A | G | 1 | a0001c0001t0003g0104 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.188+6455T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110684092 | ||||||
| chr11:110684125
|
T | C | 8 | a0001c0001t0002g0008a0001c0001t0004g0009a0001c0001t0004g0010others(5): Show | 8 | HG02145.hp2 HG02647.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.188+6422A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110684125 | ||||||
| chr11:110684164
|
G | GT | 7 | a0001c0001t0001g0139a0001c0001t0004g0004a0001c0001t0004g0143others(4): Show | 8 | HG00735.hp2 HG01891.hp1 HG03017.hp2 others(5): Show |
intron_variant | MODIFIER | c.188+6382dupA | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110684164 | ||||||
| chr11:110684231
|
A | T | 91 | a0001c0001t0001g0005a0001c0001t0001g0136a0001c0001t0001g0137others(88): Show | 93 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(90): Show |
intron_variant | MODIFIER | c.188+6316T>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110684231 | ||||||
| chr11:110684234
|
A | C | 6 | a0001c0001t0001g0134a0001c0001t0003g0054a0001c0001t0003g0064others(3): Show | 6 | HG00323.hp1 HG01099.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.188+6313T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110684234 | ||||||
| chr11:110684266
|
T | A | 1 | a0006c0007t0010g0148 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.188+6281A>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110684266 | ||||||
| chr11:110684287
|
G | A | 29 | a0001c0001t0001g0210a0001c0001t0002g0008a0001c0001t0002g0204others(26): Show | 29 | HG00099.hp2 HG00280.hp2 HG01074.hp1 others(26): Show |
intron_variant | MODIFIER | c.188+6260C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110684287 | ||||||
| chr11:110684403
|
T | A | 1 | a0001c0001t0001g0157 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.188+6144A>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110684403 | ||||||
| chr11:110684483
|
G | T | 1 | a0001c0001t0001g0058 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.188+6064C>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110684483 | ||||||
| chr11:110684872
|
G | GGGAACAC others(2): Show |
91 | a0001c0001t0001g0005a0001c0001t0001g0136a0001c0001t0001g0137others(88): Show | 93 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(90): Show |
intron_variant | MODIFIER | c.188+5674_188+5675i others(11): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110684872 | ||||||
| chr11:110685131
|
T | C | 1 | a0001c0001t0001g0168 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.188+5416A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110685131 | ||||||
| chr11:110685138
|
T | A | 1 | a0001c0001t0003g0013 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.188+5409A>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110685138 | ||||||
| chr11:110685197
|
T | TAGA | 91 | a0001c0001t0001g0005a0001c0001t0001g0136a0001c0001t0001g0137others(88): Show | 93 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(90): Show |
intron_variant | MODIFIER | c.188+5347_188+5349d others(5): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110685197 | ||||||
| chr11:110685216
|
A | G | 12 | a0001c0001t0001g0210a0001c0001t0003g0213a0001c0001t0003g0216others(9): Show | 12 | HG00099.hp2 HG00280.hp2 HG02015.hp1 others(9): Show |
intron_variant | MODIFIER | c.188+5331T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110685216 | ||||||
| chr11:110685422
|
A | T | 1 | a0010c0016t0002g0060 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.188+5125T>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110685422 | ||||||
| chr11:110685494
|
T | TA | 81 | a0001c0001t0001g0005a0001c0001t0001g0136a0001c0001t0001g0137others(78): Show | 83 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(80): Show |
intron_variant | MODIFIER | c.188+5052dupT | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110685494 | ||||||
| chr11:110685494
|
T | TAA | 10 | a0001c0001t0002g0008a0001c0001t0004g0009a0001c0001t0004g0010others(7): Show | 10 | HG02145.hp2 HG02622.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.188+5051_188+5052d others(4): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110685494 | ||||||
| chr11:110685560
|
T | C | 49 | a0001c0001t0001g0005a0001c0001t0001g0136a0001c0001t0001g0137others(46): Show | 50 | HG00621.hp1 HG00639.hp2 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.188+4987A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110685560 | ||||||
| chr11:110685587
|
AAT | A | 7 | a0001c0001t0002g0204a0001c0001t0002g0205a0001c0001t0002g0206others(4): Show | 7 | HG01074.hp1 HG01891.hp2 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.188+4958_188+4959d others(4): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110685587 | ||||||
| chr11:110685617
|
A | C | 91 | a0001c0001t0001g0005a0001c0001t0001g0136a0001c0001t0001g0137others(88): Show | 93 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(90): Show |
intron_variant | MODIFIER | c.188+4930T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110685617 | ||||||
| chr11:110685702
|
G | A | 1 | a0001c0001t0001g0083 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.188+4845C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110685702 | ||||||
| chr11:110685759
|
G | A | 35 | a0001c0001t0001g0210a0001c0001t0002g0008a0001c0001t0002g0204others(32): Show | 35 | HG00099.hp2 HG00280.hp2 HG01074.hp1 others(32): Show |
intron_variant | MODIFIER | c.188+4788C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110685759 | ||||||
| chr11:110685936
|
C | CG | 6 | a0001c0001t0006g0156a0001c0001t0006g0199a0001c0001t0006g0200others(3): Show | 6 | HG02109.hp1 HG02257.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.188+4610dupC | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110685936 | ||||||
| chr11:110685953
|
A | G | 11 | a0001c0001t0001g0210a0001c0001t0003g0213a0001c0001t0003g0216others(8): Show | 11 | HG00099.hp2 HG00280.hp2 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.188+4594T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110685953 | ||||||
| chr11:110685972
|
C | A | 84 | a0001c0001t0001g0005a0001c0001t0001g0136a0001c0001t0001g0137others(81): Show | 86 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.188+4575G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110685972 | ||||||
| chr11:110686127
|
T | C | 2 | a0005c0010t0001g0161a0005c0010t0001g0180 | 2 | HG01981.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.188+4420A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110686127 | ||||||
| chr11:110686446
|
A | C | 6 | a0001c0001t0006g0156a0001c0001t0006g0199a0001c0001t0006g0200others(3): Show | 6 | HG02109.hp1 HG02257.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.188+4101T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110686446 | ||||||
| chr11:110686494
|
C | T | 1 | a0001c0005t0005g0197 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.188+4053G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110686494 | ||||||
| chr11:110686561
|
C | A | 12 | a0001c0001t0001g0210a0001c0001t0003g0213a0001c0001t0003g0216others(9): Show | 12 | HG00099.hp2 HG00280.hp2 HG02015.hp1 others(9): Show |
intron_variant | MODIFIER | c.188+3986G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110686561 | ||||||
| chr11:110686652
|
C | T | 7 | a0001c0001t0002g0204a0001c0001t0002g0205a0001c0001t0002g0206others(4): Show | 7 | HG01074.hp1 HG01891.hp2 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.188+3895G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110686652 | ||||||
| chr11:110686699
|
T | C | 11 | a0001c0001t0001g0210a0001c0001t0003g0213a0001c0001t0003g0216others(8): Show | 11 | HG00099.hp2 HG00280.hp2 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.188+3848A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110686699 | ||||||
| chr11:110686724
|
A | G | 1 | a0001c0001t0001g0020 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.188+3823T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110686724 | ||||||
| chr11:110686759
|
T | G | 2 | a0001c0001t0008g0014a0001c0001t0008g0019 | 2 | NA18997.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.188+3788A>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110686759 | ||||||
| chr11:110686829
|
C | T | 6 | a0001c0001t0006g0156a0001c0001t0006g0199a0001c0001t0006g0200others(3): Show | 6 | HG02109.hp1 HG02257.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.188+3718G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110686829 | ||||||
| chr11:110686943
|
A | G | 7 | a0001c0001t0001g0139a0001c0001t0004g0004a0001c0001t0004g0143others(4): Show | 8 | HG00735.hp2 HG01891.hp1 HG03017.hp2 others(5): Show |
intron_variant | MODIFIER | c.188+3604T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110686943 | ||||||
| chr11:110687010
|
G | C | 91 | a0001c0001t0001g0005a0001c0001t0001g0136a0001c0001t0001g0137others(88): Show | 93 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(90): Show |
intron_variant | MODIFIER | c.188+3537C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110687010 | ||||||
| chr11:110687035
|
C | CAT | 8 | a0001c0001t0001g0047a0001c0001t0001g0195a0001c0001t0002g0022others(5): Show | 8 | HG00558.hp2 HG02809.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.188+3510_188+3511d others(4): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110687035 | ||||||
| chr11:110687035
|
C | CATAT | 3 | a0001c0001t0001g0005a0001c0001t0001g0174a0001c0001t0001g0193 | 4 | HG02622.hp1 HG03041.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.188+3508_188+3511d others(6): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110687035 | ||||||
| chr11:110687035
|
C | CATATATA others(1): Show |
3 | a0001c0001t0004g0004a0001c0001t0004g0143a0001c0005t0005g0142 | 4 | HG01891.hp1 HG03098.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.188+3504_188+3511d others(10): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110687035 | ||||||
| chr11:110687035
|
C | CATATATA others(3): Show |
4 | a0001c0001t0002g0160a0001c0005t0005g0197a0003c0004t0002g0144others(1): Show | 4 | HG00673.hp2 HG02451.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.188+3502_188+3511d others(12): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110687035 | ||||||
| chr11:110687035
|
C | CATATATA others(5): Show |
5 | a0001c0001t0001g0155a0001c0001t0001g0173a0001c0001t0004g0011others(2): Show | 5 | HG01361.hp1 HG02280.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.188+3500_188+3511d others(14): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110687035 | ||||||
| chr11:110687035
|
C | CATATATA others(7): Show |
5 | a0001c0001t0002g0008a0001c0001t0004g0009a0001c0001t0004g0010others(2): Show | 5 | HG02109.hp1 HG02145.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.188+3498_188+3511d others(16): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110687035 | ||||||
| chr11:110687035
|
C | CATATATA others(9): Show |
4 | a0001c0001t0001g0210a0001c0001t0006g0200a0001c0001t0006g0201others(1): Show | 4 | HG00099.hp2 HG02257.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.188+3496_188+3511d others(18): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110687035 | ||||||
| chr11:110687035
|
C | CATATATA others(11): Show |
5 | a0001c0002t0005g0212a0001c0002t0005g0215a0001c0002t0005g0217others(2): Show | 5 | HG02015.hp1 HG02080.hp1 HG04199.hp1 others(2): Show |
intron_variant | MODIFIER | c.188+3494_188+3511d others(20): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110687035 | ||||||
| chr11:110687035
|
C | CATATATA others(13): Show |
8 | a0001c0001t0001g0139a0001c0001t0001g0171a0001c0001t0001g0183others(5): Show | 8 | HG00621.hp1 HG00735.hp2 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.188+3492_188+3511d others(22): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110687035 | ||||||
| chr11:110687035
|
C | CATATATA others(15): Show |
9 | a0001c0001t0001g0170a0001c0001t0001g0191a0001c0001t0002g0206others(6): Show | 9 | HG02922.hp1 HG03139.hp2 HG03209.hp1 others(6): Show |
intron_variant | MODIFIER | c.188+3511_188+3512i others(24): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110687035 | ||||||
| chr11:110687035
|
C | CATATATA others(17): Show |
8 | a0001c0001t0001g0136a0001c0001t0001g0169a0001c0001t0001g0181others(5): Show | 8 | HG00733.hp2 HG01169.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.188+3511_188+3512i others(26): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110687035 | ||||||
| chr11:110687035
|
C | CATATATA others(19): Show |
8 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0002g0164others(5): Show | 8 | HG02071.hp2 HG02132.hp1 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.188+3511_188+3512i others(28): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110687035 | ||||||
| chr11:110687035
|
C | CATATATA others(21): Show |
1 | a0001c0012t0002g0189 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.188+3511_188+3512i others(30): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110687035 | ||||||
| chr11:110687035
|
C | CATATATA others(23): Show |
5 | a0001c0001t0001g0152a0001c0001t0002g0158a0001c0001t0002g0159others(2): Show | 5 | HG01074.hp1 HG01891.hp2 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.188+3511_188+3512i others(32): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110687035 | ||||||
| chr11:110687035
|
C | CATATATA others(25): Show |
7 | a0001c0001t0001g0154a0001c0001t0001g0157a0001c0001t0001g0163others(4): Show | 7 | HG01433.hp2 HG02155.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.188+3511_188+3512i others(34): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110687035 | ||||||
| chr11:110687035
|
C | CATATATA others(27): Show |
1 | a0001c0001t0001g0137 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.188+3511_188+3512i others(36): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110687035 | ||||||
| chr11:110687035
|
C | CATATATA others(35): Show |
1 | a0003c0004t0002g0162 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.188+3511_188+3512i others(44): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110687035 | ||||||
| chr11:110687035
|
CAT | C | 3 | a0001c0001t0002g0084a0001c0001t0002g0127a0001c0001t0008g0014 | 3 | HG01516.hp1 NA18997.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.188+3510_188+3511d others(4): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110687035 | ||||||
| chr11:110687035
|
CATAT | C | 8 | a0001c0001t0001g0175a0001c0001t0001g0176a0001c0001t0001g0177others(5): Show | 8 | HG00639.hp2 HG01981.hp1 HG02165.hp1 others(5): Show |
intron_variant | MODIFIER | c.188+3508_188+3511d others(6): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110687035 | ||||||
| chr11:110687055
|
T | TATATATA others(7): Show |
1 | a0012c0019t0004g0151 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.188+3491_188+3492i others(16): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110687055 | ||||||
| chr11:110687057
|
G | C | 1 | a0012c0019t0004g0151 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.188+3490C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110687057 | ||||||
| chr11:110687057
|
G | GAC | 6 | a0001c0001t0001g0058a0001c0001t0001g0087a0001c0001t0003g0132others(3): Show | 6 | HG01358.hp1 HG02015.hp2 NA19000.hp2 others(3): Show |
intron_variant | MODIFIER | c.188+3488_188+3489d others(4): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110687057 | ||||||
| chr11:110687057
|
G | T | 69 | a0001c0001t0001g0005a0001c0001t0001g0136a0001c0001t0001g0137others(66): Show | 70 | HG00099.hp2 HG00621.hp1 HG00673.hp2 others(67): Show |
intron_variant | MODIFIER | c.188+3490C>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110687057 | ||||||
| chr11:110687057
|
GAC | G | 2 | a0001c0001t0002g0059a0001c0001t0003g0123 | 2 | HG03139.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.188+3488_188+3489d others(4): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110687057 | ||||||
| chr11:110687059
|
C | G | 69 | a0001c0001t0001g0005a0001c0001t0001g0136a0001c0001t0001g0137others(66): Show | 70 | HG00099.hp2 HG00621.hp1 HG00673.hp2 others(67): Show |
intron_variant | MODIFIER | c.188+3488G>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110687059 | ||||||
| chr11:110687061
|
CACACACA others(19): Show |
C | 1 | a0001c0001t0003g0091 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.188+3460_188+3485d others(28): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110687061 | ||||||
| chr11:110687077
|
C | T | 12 | a0001c0001t0001g0175a0001c0001t0001g0176a0001c0001t0001g0177others(9): Show | 12 | HG00280.hp2 HG00639.hp2 HG01981.hp1 others(9): Show |
intron_variant | MODIFIER | c.188+3470G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110687077 | ||||||
| chr11:110687083
|
T | TAGAC | 8 | a0001c0001t0001g0175a0001c0001t0001g0176a0001c0001t0001g0177others(5): Show | 8 | HG00639.hp2 HG01981.hp1 HG02165.hp1 others(5): Show |
intron_variant | MODIFIER | c.188+3463_188+3464i others(6): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110687083 | ||||||
| chr11:110687083
|
T | TAGACAC | 2 | a0001c0001t0001g0182a0001c0005t0005g0197 | 2 | HG02451.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.188+3463_188+3464i others(8): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110687083 | ||||||
| chr11:110687083
|
T | TAGACACA others(1): Show |
2 | a0001c0002t0005g0209a0007c0020t0020g0149 | 2 | HG00280.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.188+3463_188+3464i others(10): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110687083 | ||||||
| chr11:110687085
|
T | C | 12 | a0001c0001t0001g0175a0001c0001t0001g0176a0001c0001t0001g0177others(9): Show | 12 | HG00280.hp2 HG00639.hp2 HG01981.hp1 others(9): Show |
intron_variant | MODIFIER | c.188+3462A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110687085 | ||||||
| chr11:110687087
|
G | C | 12 | a0001c0001t0001g0175a0001c0001t0001g0176a0001c0001t0001g0177others(9): Show | 12 | HG00280.hp2 HG00639.hp2 HG01981.hp1 others(9): Show |
intron_variant | MODIFIER | c.188+3460C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110687087 | ||||||
| chr11:110687087
|
G | GAC | 4 | a0001c0001t0001g0090a0001c0001t0003g0089a0001c0001t0006g0200others(1): Show | 4 | HG02486.hp2 NA19084.hp2 NA19091.hp1 others(1): Show |
intron_variant | MODIFIER | c.188+3458_188+3459d others(4): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110687087 | ||||||
| chr11:110687087
|
G | GACAC | 47 | a0001c0001t0001g0020a0001c0001t0001g0105a0001c0001t0001g0129others(44): Show | 50 | HG00323.hp1 HG00621.hp2 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.188+3456_188+3459d others(6): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110687087 | ||||||
| chr11:110687087
|
G | GACACAC | 50 | a0001c0001t0001g0005a0001c0001t0001g0136a0001c0001t0001g0137others(47): Show | 51 | HG00621.hp1 HG00673.hp2 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.188+3454_188+3459d others(8): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110687087 | ||||||
| chr11:110687087
|
G | GACACACA others(1): Show |
6 | a0001c0001t0001g0181a0001c0001t0004g0146a0003c0004t0017g0145others(3): Show | 6 | HG02622.hp2 HG02809.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.188+3452_188+3459d others(10): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110687087 | ||||||
| chr11:110687087
|
G | GACACACA others(3): Show |
9 | a0001c0001t0001g0210a0001c0001t0002g0008a0001c0001t0003g0213others(6): Show | 9 | HG00099.hp2 HG02145.hp2 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.188+3450_188+3459d others(12): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110687087 | ||||||
| chr11:110687087
|
G | GACACACA others(5): Show |
6 | a0001c0001t0003g0216a0001c0001t0004g0009a0001c0001t0004g0010others(3): Show | 6 | HG02015.hp1 HG02080.hp1 HG02135.hp2 others(3): Show |
intron_variant | MODIFIER | c.188+3448_188+3459d others(14): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110687087 | ||||||
| chr11:110687139
|
A | G | 48 | a0001c0001t0001g0005a0001c0001t0001g0136a0001c0001t0001g0137others(45): Show | 49 | HG00621.hp1 HG00639.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.188+3408T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110687139 | ||||||
| chr11:110687472
|
G | A | 56 | a0001c0001t0001g0005a0001c0001t0001g0136a0001c0001t0001g0137others(53): Show | 58 | HG00621.hp1 HG00639.hp2 HG00673.hp2 others(55): Show |
intron_variant | MODIFIER | c.188+3075C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110687472 | ||||||
| chr11:110687574
|
G | A | 1 | a0001c0001t0001g0103 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.188+2973C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110687574 | ||||||
| chr11:110687707
|
A | C | 1 | a0001c0002t0005g0211 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.188+2840T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110687707 | ||||||
| chr11:110688013
|
T | C | 3 | a0001c0001t0001g0139a0003c0004t0002g0144a0008c0017t0002g0141 | 3 | HG00735.hp2 HG03688.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.188+2534A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110688013 | ||||||
| chr11:110688063
|
T | C | 1 | a0011c0018t0015g0007 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.188+2484A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110688063 | ||||||
| chr11:110688090
|
C | G | 28 | a0001c0001t0001g0210a0001c0001t0002g0008a0001c0001t0003g0213others(25): Show | 28 | HG00099.hp2 HG00280.hp2 HG02015.hp1 others(25): Show |
intron_variant | MODIFIER | c.188+2457G>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110688090 | ||||||
| chr11:110688095
|
G | A | 1 | a0001c0001t0003g0123 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.188+2452C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110688095 | ||||||
| chr11:110688282
|
C | G | 1 | a0001c0001t0003g0065 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.188+2265G>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110688282 | ||||||
| chr11:110688775
|
T | C | 1 | a0001c0001t0004g0011 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.188+1772A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110688775 | ||||||
| chr11:110688792
|
G | T | 1 | a0002c0003t0007g0202 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.188+1755C>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110688792 | ||||||
| chr11:110688895
|
T | C | 7 | a0001c0001t0002g0204a0001c0001t0002g0205a0001c0001t0002g0206others(4): Show | 7 | HG01074.hp1 HG01891.hp2 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.188+1652A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110688895 | ||||||
| chr11:110688999
|
G | GC | 11 | a0001c0001t0001g0210a0001c0001t0003g0213a0001c0001t0003g0216others(8): Show | 11 | HG00099.hp2 HG00280.hp2 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.188+1547_188+1548i others(3): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110688999 | ||||||
| chr11:110688999
|
G | GT | 27 | a0001c0001t0001g0219a0001c0001t0002g0008a0001c0001t0002g0053others(24): Show | 27 | HG00741.hp2 HG01074.hp1 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.188+1547dupA | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110688999 | ||||||
| chr11:110688999
|
G | GTT | 53 | a0001c0001t0001g0005a0001c0001t0001g0136a0001c0001t0001g0152others(50): Show | 55 | HG00621.hp1 HG00639.hp2 HG00673.hp2 others(52): Show |
intron_variant | MODIFIER | c.188+1546_188+1547d others(4): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110688999 | ||||||
| chr11:110689000
|
T | C | 1 | a0011c0018t0015g0007 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.188+1547A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110689000 | ||||||
| chr11:110689092
|
C | G | 1 | a0001c0001t0009g0120 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.188+1455G>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110689092 | ||||||
| chr11:110689159
|
C | T | 48 | a0001c0001t0001g0005a0001c0001t0001g0136a0001c0001t0001g0137others(45): Show | 49 | HG00621.hp1 HG00639.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.188+1388G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110689159 | ||||||
| chr11:110689236
|
C | T | 1 | a0005c0010t0001g0161 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.188+1311G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110689236 | ||||||
| chr11:110689521
|
ATAAAT | A | 2 | a0006c0007t0010g0147a0006c0007t0010g0148 | 2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.188+1021_188+1025d others(7): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110689521 | ||||||
| chr11:110689682
|
T | C | 11 | a0001c0001t0001g0210a0001c0001t0003g0213a0001c0001t0003g0216others(8): Show | 11 | HG00099.hp2 HG00280.hp2 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.188+865A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110689682 | ||||||
| chr11:110689740
|
CGGGGAAA others(17): Show |
C | 7 | a0001c0001t0002g0008a0001c0001t0004g0009a0001c0001t0004g0010others(4): Show | 7 | HG02145.hp2 HG02647.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.188+783_188+806del others(24): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110689740 | ||||||
| chr11:110689856
|
C | T | 2 | a0001c0001t0002g0024a0001c0001t0002g0030 | 2 | HG03491.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.188+691G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110689856 | ||||||
| chr11:110689869
|
T | C | 1 | a0001c0001t0001g0020 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.188+678A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110689869 | ||||||
| chr11:110689961
|
C | CA | 58 | a0001c0001t0001g0005a0001c0001t0001g0105a0001c0001t0001g0136others(55): Show | 59 | HG00621.hp1 HG00639.hp2 HG00673.hp2 others(56): Show |
intron_variant | MODIFIER | c.188+585dupT | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110689961 | ||||||
| chr11:110689994
|
T | C | 1 | a0011c0018t0015g0007 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.188+553A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110689994 | ||||||
| chr11:110690190
|
C | A | 1 | a0001c0001t0001g0219 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.188+357G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110690190 | ||||||
| chr11:110690453
|
C | T | 11 | a0001c0001t0001g0210a0001c0001t0003g0213a0001c0001t0003g0216others(8): Show | 11 | HG00099.hp2 HG00280.hp2 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.188+94G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110690453 | ||||||
| chr11:110690707
|
T | G | 1 | a0001c0001t0001g0194 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.106-78A>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110690707 | ||||||
| chr11:110690738
|
G | A | 1 | a0001c0001t0001g0154 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.106-109C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110690738 | ||||||
| chr11:110690870
|
G | C | 7 | a0001c0001t0001g0139a0001c0001t0004g0004a0001c0001t0004g0143others(4): Show | 8 | HG00735.hp2 HG01891.hp1 HG03017.hp2 others(5): Show |
intron_variant | MODIFIER | c.106-241C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110690870 | ||||||
| chr11:110690905
|
A | G | 3 | a0001c0001t0001g0139a0003c0004t0002g0144a0008c0017t0002g0141 | 3 | HG00735.hp2 HG03688.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.106-276T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110690905 | ||||||
| chr11:110691189
|
T | G | 7 | a0001c0001t0002g0204a0001c0001t0002g0205a0001c0001t0002g0206others(4): Show | 7 | HG01074.hp1 HG01891.hp2 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.106-560A>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110691189 | ||||||
| chr11:110691256
|
T | C | 2 | a0001c0001t0004g0146a0003c0004t0017g0145 | 2 | HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.106-627A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110691256 | ||||||
| chr11:110691333
|
G | C | 6 | a0001c0001t0006g0156a0001c0001t0006g0199a0001c0001t0006g0200others(3): Show | 6 | HG02109.hp1 HG02257.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.106-704C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110691333 | ||||||
| chr11:110691366
|
TA | T | 3 | a0001c0001t0006g0199a0001c0001t0006g0200a0001c0001t0006g0201 | 3 | HG02109.hp1 HG02486.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.106-738delT | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110691366 | ||||||
| chr11:110691388
|
C | T | 1 | a0001c0001t0009g0003 | 2 | HG00639.hp1 HG00735.hp1 |
intron_variant | MODIFIER | c.106-759G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110691388 | ||||||
| chr11:110691591
|
T | A | 1 | a0001c0002t0005g0209 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.106-962A>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110691591 | ||||||
| chr11:110691702
|
C | T | 2 | a0006c0007t0010g0147a0006c0007t0010g0148 | 2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.106-1073G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110691702 | ||||||
| chr11:110691855
|
A | G | 36 | a0001c0001t0001g0210a0001c0001t0002g0008a0001c0001t0002g0204others(33): Show | 36 | HG00099.hp2 HG00280.hp2 HG01074.hp1 others(33): Show |
intron_variant | MODIFIER | c.106-1226T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110691855 | ||||||
| chr11:110691968
|
T | C | 7 | a0001c0001t0001g0139a0001c0001t0004g0004a0001c0001t0004g0143others(4): Show | 8 | HG00735.hp2 HG01891.hp1 HG03017.hp2 others(5): Show |
intron_variant | MODIFIER | c.106-1339A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110691968 | ||||||
| chr11:110691989
|
G | A | 1 | a0001c0001t0004g0012 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.106-1360C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110691989 | ||||||
| chr11:110692100
|
T | C | 1 | a0001c0001t0002g0043 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.106-1471A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110692100 | ||||||
| chr11:110692176
|
T | C | 4 | a0001c0001t0001g0027a0001c0001t0001g0106a0001c0001t0002g0127others(1): Show | 4 | HG01496.hp2 HG01516.hp1 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.106-1547A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110692176 | ||||||
| chr11:110692365
|
G | C | 7 | a0001c0001t0001g0139a0001c0001t0004g0004a0001c0001t0004g0143others(4): Show | 8 | HG00735.hp2 HG01891.hp1 HG03017.hp2 others(5): Show |
intron_variant | MODIFIER | c.106-1736C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110692365 | ||||||
| chr11:110692643
|
C | T | 91 | a0001c0001t0001g0005a0001c0001t0001g0136a0001c0001t0001g0137others(88): Show | 93 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(90): Show |
intron_variant | MODIFIER | c.106-2014G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110692643 | ||||||
| chr11:110692715
|
A | C | 7 | a0001c0001t0002g0204a0001c0001t0002g0205a0001c0001t0002g0206others(4): Show | 7 | HG01074.hp1 HG01891.hp2 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.106-2086T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110692715 | ||||||
| chr11:110692741
|
T | C | 1 | a0001c0001t0001g0154 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.106-2112A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110692741 | ||||||
| chr11:110692880
|
T | C | 7 | a0001c0001t0002g0204a0001c0001t0002g0205a0001c0001t0002g0206others(4): Show | 7 | HG01074.hp1 HG01891.hp2 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.106-2251A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110692880 | ||||||
| chr11:110692976
|
A | G | 1 | a0001c0001t0002g0029 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.106-2347T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110692976 | ||||||
| chr11:110693175
|
G | A | 5 | a0001c0001t0002g0044a0001c0001t0003g0045a0001c0001t0003g0107others(2): Show | 5 | HG01192.hp1 HG02273.hp1 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.106-2546C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110693175 | ||||||
| chr11:110693263
|
T | C | 1 | a0001c0005t0005g0197 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.106-2634A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110693263 | ||||||
| chr11:110693633
|
C | G | 1 | a0009c0015t0004g0153 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.106-3004G>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110693633 | ||||||
| chr11:110693637
|
A | C | 7 | a0001c0001t0001g0139a0001c0001t0004g0004a0001c0001t0004g0143others(4): Show | 8 | HG00735.hp2 HG01891.hp1 HG03017.hp2 others(5): Show |
intron_variant | MODIFIER | c.106-3008T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110693637 | ||||||
| chr11:110693691
|
T | C | 6 | a0001c0001t0006g0156a0001c0001t0006g0199a0001c0001t0006g0200others(3): Show | 6 | HG02109.hp1 HG02257.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.106-3062A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110693691 | ||||||
| chr11:110693825
|
T | C | 1 | a0001c0001t0013g0110 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.106-3196A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110693825 | ||||||
| chr11:110694021
|
C | T | 1 | a0001c0001t0001g0210 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.106-3392G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110694021 | ||||||
| chr11:110694325
|
G | C | 1 | a0001c0001t0006g0156 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.106-3696C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110694325 | ||||||
| chr11:110694368
|
C | A | 1 | a0002c0006t0012g0111 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.106-3739G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110694368 | ||||||
| chr11:110694458
|
TA | T | 56 | a0001c0001t0001g0005a0001c0001t0001g0136a0001c0001t0001g0137others(53): Show | 58 | HG00621.hp1 HG00639.hp2 HG00673.hp2 others(55): Show |
intron_variant | MODIFIER | c.106-3830delT | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110694458 | ||||||
| chr11:110694555
|
C | T | 84 | a0001c0001t0001g0005a0001c0001t0001g0136a0001c0001t0001g0137others(81): Show | 86 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.106-3926G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110694555 | ||||||
| chr11:110694606
|
T | C | 1 | a0001c0005t0005g0197 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.106-3977A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110694606 | ||||||
| chr11:110694713
|
A | G | 11 | a0001c0001t0001g0210a0001c0001t0003g0213a0001c0001t0003g0216others(8): Show | 11 | HG00099.hp2 HG00280.hp2 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.106-4084T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110694713 | ||||||
| chr11:110694982
|
G | C | 7 | a0001c0001t0001g0139a0001c0001t0004g0004a0001c0001t0004g0143others(4): Show | 8 | HG00735.hp2 HG01891.hp1 HG03017.hp2 others(5): Show |
intron_variant | MODIFIER | c.106-4353C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110694982 | ||||||
| chr11:110695181
|
A | G | 6 | a0001c0001t0006g0156a0001c0001t0006g0199a0001c0001t0006g0200others(3): Show | 6 | HG02109.hp1 HG02257.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.106-4552T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110695181 | ||||||
| chr11:110695402
|
A | C | 91 | a0001c0001t0001g0005a0001c0001t0001g0136a0001c0001t0001g0137others(88): Show | 93 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(90): Show |
intron_variant | MODIFIER | c.106-4773T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110695402 | ||||||
| chr11:110695419
|
T | C | 1 | a0001c0001t0001g0184 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.106-4790A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110695419 | ||||||
| chr11:110695435
|
A | G | 6 | a0001c0001t0002g0059a0001c0001t0002g0061a0001c0001t0002g0062others(3): Show | 6 | HG01192.hp2 HG02055.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.106-4806T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110695435 | ||||||
| chr11:110695497
|
T | C | 1 | a0001c0001t0002g0112 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.106-4868A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110695497 | ||||||
| chr11:110695529
|
T | C | 35 | a0001c0001t0001g0210a0001c0001t0002g0008a0001c0001t0002g0204others(32): Show | 35 | HG00099.hp2 HG00280.hp2 HG01074.hp1 others(32): Show |
intron_variant | MODIFIER | c.106-4900A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110695529 | ||||||
| chr11:110695539
|
C | T | 1 | a0004c0011t0002g0128 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.106-4910G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110695539 | ||||||
| chr11:110695550
|
T | C | 1 | a0001c0001t0001g0185 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.106-4921A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110695550 | ||||||
| chr11:110695711
|
C | T | 1 | a0001c0002t0005g0113 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.106-5082G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110695711 | ||||||
| chr11:110695903
|
C | A | 56 | a0001c0001t0001g0005a0001c0001t0001g0136a0001c0001t0001g0137others(53): Show | 58 | HG00621.hp1 HG00639.hp2 HG00673.hp2 others(55): Show |
intron_variant | MODIFIER | c.106-5274G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110695903 | ||||||
| chr11:110695978
|
G | A | 56 | a0001c0001t0001g0005a0001c0001t0001g0136a0001c0001t0001g0137others(53): Show | 58 | HG00621.hp1 HG00639.hp2 HG00673.hp2 others(55): Show |
intron_variant | MODIFIER | c.106-5349C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110695978 | ||||||
| chr11:110696264
|
T | C | 35 | a0001c0001t0001g0210a0001c0001t0002g0008a0001c0001t0002g0204others(32): Show | 35 | HG00099.hp2 HG00280.hp2 HG01074.hp1 others(32): Show |
intron_variant | MODIFIER | c.106-5635A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110696264 | ||||||
| chr11:110696280
|
C | T | 1 | a0001c0001t0001g0058 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.106-5651G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110696280 | ||||||
| chr11:110696423
|
T | G | 2 | a0001c0009t0002g0188a0001c0009t0002g0196 | 2 | NA18978.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.106-5794A>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110696423 | ||||||
| chr11:110696471
|
A | AT | 48 | a0001c0001t0001g0005a0001c0001t0001g0136a0001c0001t0001g0137others(45): Show | 49 | HG00621.hp1 HG00639.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.106-5843dupA | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110696471 | ||||||
| chr11:110696502
|
G | C | 91 | a0001c0001t0001g0005a0001c0001t0001g0136a0001c0001t0001g0137others(88): Show | 93 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(90): Show |
intron_variant | MODIFIER | c.106-5873C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110696502 | ||||||
| chr11:110696569
|
A | T | 4 | a0001c0001t0006g0156a0001c0001t0006g0199a0001c0001t0006g0200others(1): Show | 4 | HG02109.hp1 HG02486.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.106-5940T>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110696569 | ||||||
| chr11:110696583
|
T | TCATGTG | 7 | a0001c0001t0001g0139a0001c0001t0004g0004a0001c0001t0004g0143others(4): Show | 8 | HG00735.hp2 HG01891.hp1 HG03017.hp2 others(5): Show |
intron_variant | MODIFIER | c.106-5960_106-5955d others(8): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110696583 | ||||||
| chr11:110696616
|
C | T | 84 | a0001c0001t0001g0005a0001c0001t0001g0136a0001c0001t0001g0137others(81): Show | 86 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.106-5987G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110696616 | ||||||
| chr11:110696730
|
C | T | 1 | a0001c0001t0003g0123 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.106-6101G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110696730 | ||||||
| chr11:110696762
|
T | C | 35 | a0001c0001t0001g0210a0001c0001t0002g0008a0001c0001t0002g0204others(32): Show | 35 | HG00099.hp2 HG00280.hp2 HG01074.hp1 others(32): Show |
intron_variant | MODIFIER | c.106-6133A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110696762 | ||||||
| chr11:110696818
|
G | T | 1 | a0002c0003t0007g0150 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.106-6189C>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110696818 | ||||||
| chr11:110696833
|
C | T | 2 | a0001c0001t0001g0129a0001c0001t0003g0130 | 2 | NA18983.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.106-6204G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110696833 | ||||||
| chr11:110696844
|
T | C | 8 | a0001c0001t0002g0008a0001c0001t0004g0009a0001c0001t0004g0010others(5): Show | 8 | HG02145.hp2 HG02647.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.106-6215A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110696844 | ||||||
| chr11:110696872
|
C | T | 2 | a0006c0007t0010g0147a0006c0007t0010g0148 | 2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.106-6243G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110696872 | ||||||
| chr11:110696946
|
A | G | 1 | a0001c0001t0016g0057 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.106-6317T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110696946 | ||||||
| chr11:110697062
|
A | G | 1 | a0001c0001t0014g0006 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.106-6433T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110697062 | ||||||
| chr11:110697159
|
A | G | 7 | a0001c0001t0002g0204a0001c0001t0002g0205a0001c0001t0002g0206others(4): Show | 7 | HG01074.hp1 HG01891.hp2 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.106-6530T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110697159 | ||||||
| chr11:110697302
|
A | G | 56 | a0001c0001t0001g0005a0001c0001t0001g0136a0001c0001t0001g0137others(53): Show | 58 | HG00621.hp1 HG00639.hp2 HG00673.hp2 others(55): Show |
intron_variant | MODIFIER | c.106-6673T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110697302 | ||||||
| chr11:110697531
|
G | T | 7 | a0001c0001t0002g0204a0001c0001t0002g0205a0001c0001t0002g0206others(4): Show | 7 | HG01074.hp1 HG01891.hp2 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.106-6902C>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110697531 | ||||||
| chr11:110697677
|
G | A | 1 | a0011c0018t0015g0007 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.106-7048C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110697677 | ||||||
| chr11:110698018
|
T | C | 48 | a0001c0001t0001g0005a0001c0001t0001g0136a0001c0001t0001g0137others(45): Show | 49 | HG00621.hp1 HG00639.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.106-7389A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110698018 | ||||||
| chr11:110698072
|
A | G | 7 | a0001c0001t0001g0139a0001c0001t0004g0004a0001c0001t0004g0143others(4): Show | 8 | HG00735.hp2 HG01891.hp1 HG03017.hp2 others(5): Show |
intron_variant | MODIFIER | c.106-7443T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110698072 | ||||||
| chr11:110698127
|
C | T | 2 | a0006c0007t0010g0147a0006c0007t0010g0148 | 2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.106-7498G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110698127 | ||||||
| chr11:110698163
|
A | G | 35 | a0001c0001t0001g0210a0001c0001t0002g0008a0001c0001t0002g0204others(32): Show | 35 | HG00099.hp2 HG00280.hp2 HG01074.hp1 others(32): Show |
intron_variant | MODIFIER | c.106-7534T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110698163 | ||||||
| chr11:110698242
|
A | G | 7 | a0001c0001t0002g0204a0001c0001t0002g0205a0001c0001t0002g0206others(4): Show | 7 | HG01074.hp1 HG01891.hp2 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.106-7613T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110698242 | ||||||
| chr11:110698314
|
C | T | 48 | a0001c0001t0001g0005a0001c0001t0001g0136a0001c0001t0001g0137others(45): Show | 49 | HG00621.hp1 HG00639.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.106-7685G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110698314 | ||||||
| chr11:110698389
|
A | G | 91 | a0001c0001t0001g0005a0001c0001t0001g0136a0001c0001t0001g0137others(88): Show | 93 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(90): Show |
intron_variant | MODIFIER | c.106-7760T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110698389 | ||||||
| chr11:110698566
|
A | G | 1 | a0007c0020t0020g0149 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.106-7937T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110698566 | ||||||
| chr11:110698627
|
C | A | 1 | a0001c0001t0002g0053 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.106-7998G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110698627 | ||||||
| chr11:110698701
|
G | T | 1 | a0001c0001t0001g0027 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.106-8072C>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110698701 | ||||||
| chr11:110698908
|
T | C | 35 | a0001c0001t0001g0210a0001c0001t0002g0008a0001c0001t0002g0204others(32): Show | 35 | HG00099.hp2 HG00280.hp2 HG01074.hp1 others(32): Show |
intron_variant | MODIFIER | c.106-8279A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110698908 | ||||||
| chr11:110699092
|
C | T | 48 | a0001c0001t0001g0005a0001c0001t0001g0136a0001c0001t0001g0137others(45): Show | 49 | HG00621.hp1 HG00639.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.106-8463G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110699092 | ||||||
| chr11:110699114
|
A | G | 3 | a0001c0001t0006g0199a0001c0001t0006g0200a0001c0001t0006g0201 | 3 | HG02109.hp1 HG02486.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.106-8485T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110699114 | ||||||
| chr11:110699170
|
G | T | 48 | a0001c0001t0001g0005a0001c0001t0001g0136a0001c0001t0001g0137others(45): Show | 49 | HG00621.hp1 HG00639.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.106-8541C>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110699170 | ||||||
| chr11:110699305
|
G | A | 91 | a0001c0001t0001g0005a0001c0001t0001g0136a0001c0001t0001g0137others(88): Show | 93 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(90): Show |
intron_variant | MODIFIER | c.106-8676C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110699305 | ||||||
| chr11:110699548
|
TGTA | T | 2 | a0004c0011t0002g0028a0004c0011t0002g0128 | 2 | NA19075.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.106-8922_106-8920d others(5): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110699548 | ||||||
| chr11:110699602
|
T | C | 2 | a0001c0001t0001g0047a0001c0001t0002g0046 | 2 | HG00558.hp2 NA18997.hp2 |
intron_variant | MODIFIER | c.106-8973A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110699602 | ||||||
| chr11:110699604
|
T | C | 1 | a0012c0019t0004g0151 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.106-8975A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110699604 | ||||||
| chr11:110699729
|
T | C | 1 | a0007c0020t0020g0149 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.106-9100A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110699729 | ||||||
| chr11:110699765
|
C | T | 2 | a0001c0001t0004g0146a0003c0004t0017g0145 | 2 | HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.106-9136G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110699765 | ||||||
| chr11:110699863
|
T | C | 1 | a0001c0005t0005g0197 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.106-9234A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110699863 | ||||||
| chr11:110699875
|
C | T | 48 | a0001c0001t0001g0005a0001c0001t0001g0136a0001c0001t0001g0137others(45): Show | 49 | HG00621.hp1 HG00639.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.106-9246G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110699875 | ||||||
| chr11:110700323
|
T | C | 6 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116others(3): Show | 7 | HG00280.hp1 HG00639.hp1 HG00733.hp1 others(4): Show |
intron_variant | MODIFIER | c.106-9694A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110700323 | ||||||
| chr11:110700405
|
GACT | G | 6 | a0001c0001t0006g0156a0001c0001t0006g0199a0001c0001t0006g0200others(3): Show | 6 | HG02109.hp1 HG02257.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.106-9779_106-9777d others(5): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110700405 | ||||||
| chr11:110700565
|
C | A | 1 | a0001c0001t0002g0026 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.106-9936G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110700565 | ||||||
| chr11:110700565
|
CT | C | 20 | a0001c0001t0001g0139a0001c0001t0001g0210a0001c0001t0003g0213others(17): Show | 21 | HG00099.hp2 HG00280.hp2 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.106-9937delA | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110700565 | ||||||
| chr11:110700568
|
T | C | 1 | a0001c0005t0005g0197 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.106-9939A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110700568 | ||||||
| chr11:110700678
|
T | C | 84 | a0001c0001t0001g0005a0001c0001t0001g0136a0001c0001t0001g0137others(81): Show | 86 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.106-10049A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110700678 | ||||||
| chr11:110700680
|
C | A | 6 | a0001c0001t0006g0156a0001c0001t0006g0199a0001c0001t0006g0200others(3): Show | 6 | HG02109.hp1 HG02257.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.106-10051G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110700680 | ||||||
| chr11:110700738
|
C | A | 2 | a0006c0007t0010g0147a0006c0007t0010g0148 | 2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.106-10109G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110700738 | ||||||
| chr11:110700835
|
C | A | 1 | a0008c0017t0002g0141 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.106-10206G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110700835 | ||||||
| chr11:110700844
|
G | C | 6 | a0001c0001t0006g0156a0001c0001t0006g0199a0001c0001t0006g0200others(3): Show | 6 | HG02109.hp1 HG02257.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.106-10215C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110700844 | ||||||
| chr11:110701098
|
C | T | 2 | a0001c0001t0001g0055a0001c0001t0001g0056 | 2 | HG01261.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.106-10469G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110701098 | ||||||
| chr11:110701159
|
C | T | 5 | a0001c0001t0002g0008a0001c0001t0004g0009a0001c0001t0004g0010others(2): Show | 5 | HG02145.hp2 HG02647.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.106-10530G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110701159 | ||||||
| chr11:110701184
|
G | A | 1 | a0007c0020t0020g0149 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.106-10555C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110701184 | ||||||
| chr11:110701198
|
T | TCCCA | 6 | a0001c0001t0006g0156a0001c0001t0006g0199a0001c0001t0006g0200others(3): Show | 6 | HG02109.hp1 HG02257.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.106-10570_106-1056 others(8): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110701198 | ||||||
| chr11:110701220
|
T | C | 19 | a0001c0001t0001g0210a0001c0001t0002g0204a0001c0001t0002g0205others(16): Show | 19 | HG00099.hp2 HG00280.hp2 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.106-10591A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110701220 | ||||||
| chr11:110701282
|
C | G | 3 | a0001c0001t0006g0199a0001c0001t0006g0200a0001c0001t0006g0201 | 3 | HG02109.hp1 HG02486.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.106-10653G>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110701282 | ||||||
| chr11:110701333
|
C | A | 1 | a0001c0001t0002g0048 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.106-10704G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110701333 | ||||||
| chr11:110701346
|
G | A | 6 | a0001c0001t0006g0156a0001c0001t0006g0199a0001c0001t0006g0200others(3): Show | 6 | HG02109.hp1 HG02257.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.106-10717C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110701346 | ||||||
| chr11:110701507
|
G | A | 91 | a0001c0001t0001g0005a0001c0001t0001g0136a0001c0001t0001g0137others(88): Show | 93 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(90): Show |
intron_variant | MODIFIER | c.105+10620C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110701507 | ||||||
| chr11:110701523
|
T | G | 1 | a0001c0001t0003g0054 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.105+10604A>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110701523 | ||||||
| chr11:110701665
|
T | G | 1 | a0001c0001t0006g0186 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.105+10462A>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110701665 | ||||||
| chr11:110701813
|
T | C | 3 | a0001c0001t0004g0004a0001c0001t0004g0143a0001c0005t0005g0142 | 4 | HG01891.hp1 HG03098.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+10314A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110701813 | ||||||
| chr11:110701904
|
G | A | 11 | a0001c0001t0001g0210a0001c0001t0003g0213a0001c0001t0003g0216others(8): Show | 11 | HG00099.hp2 HG00280.hp2 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.105+10223C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110701904 | ||||||
| chr11:110701952
|
G | T | 7 | a0001c0001t0002g0204a0001c0001t0002g0205a0001c0001t0002g0206others(4): Show | 7 | HG01074.hp1 HG01891.hp2 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.105+10175C>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110701952 | ||||||
| chr11:110702058
|
C | T | 4 | a0001c0001t0002g0158a0001c0001t0002g0159a0001c0001t0002g0160others(1): Show | 4 | HG00673.hp2 HG02040.hp1 NA18951.hp2 others(1): Show |
intron_variant | MODIFIER | c.105+10069G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110702058 | ||||||
| chr11:110702063
|
C | T | 2 | a0001c0001t0001g0027a0009c0015t0004g0153 | 2 | HG01496.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.105+10064G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110702063 | ||||||
| chr11:110702211
|
G | A | 1 | a0002c0003t0007g0208 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.105+9916C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110702211 | ||||||
| chr11:110702220
|
G | T | 1 | a0003c0004t0017g0145 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.105+9907C>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110702220 | ||||||
| chr11:110702278
|
C | G | 1 | a0001c0001t0003g0054 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.105+9849G>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110702278 | ||||||
| chr11:110702320
|
T | G | 1 | a0007c0020t0020g0149 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.105+9807A>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110702320 | ||||||
| chr11:110702434
|
G | T | 1 | a0001c0001t0014g0006 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.105+9693C>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110702434 | ||||||
| chr11:110702538
|
C | A | 12 | a0001c0001t0001g0210a0001c0001t0003g0213a0001c0001t0003g0216others(9): Show | 12 | HG00099.hp2 HG00280.hp2 HG02015.hp1 others(9): Show |
intron_variant | MODIFIER | c.105+9589G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110702538 | ||||||
| chr11:110702718
|
C | A | 28 | a0001c0001t0001g0210a0001c0001t0002g0008a0001c0001t0003g0213others(25): Show | 28 | HG00099.hp2 HG00280.hp2 HG02015.hp1 others(25): Show |
intron_variant | MODIFIER | c.105+9409G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110702718 | ||||||
| chr11:110702743
|
G | C | 1 | a0001c0001t0001g0187 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.105+9384C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110702743 | ||||||
| chr11:110702749
|
T | C | 57 | a0001c0001t0001g0005a0001c0001t0001g0136a0001c0001t0001g0137others(54): Show | 59 | HG00621.hp1 HG00639.hp2 HG00673.hp2 others(56): Show |
intron_variant | MODIFIER | c.105+9378A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110702749 | ||||||
| chr11:110702824
|
T | C | 84 | a0001c0001t0001g0005a0001c0001t0001g0136a0001c0001t0001g0137others(81): Show | 86 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.105+9303A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110702824 | ||||||
| chr11:110702958
|
C | T | 56 | a0001c0001t0001g0005a0001c0001t0001g0136a0001c0001t0001g0137others(53): Show | 58 | HG00621.hp1 HG00639.hp2 HG00673.hp2 others(55): Show |
intron_variant | MODIFIER | c.105+9169G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110702958 | ||||||
| chr11:110703025
|
G | C | 1 | a0007c0020t0020g0149 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.105+9102C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110703025 | ||||||
| chr11:110703038
|
C | T | 4 | a0001c0001t0002g0050a0001c0001t0002g0051a0001c0001t0002g0052others(1): Show | 4 | HG00738.hp2 HG01099.hp1 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+9089G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110703038 | ||||||
| chr11:110703060
|
A | C | 91 | a0001c0001t0001g0005a0001c0001t0001g0136a0001c0001t0001g0137others(88): Show | 93 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(90): Show |
intron_variant | MODIFIER | c.105+9067T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110703060 | ||||||
| chr11:110703146
|
T | C | 1 | a0001c0005t0005g0197 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.105+8981A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110703146 | ||||||
| chr11:110703201
|
G | T | 2 | a0001c0001t0003g0001a0001c0001t0003g0049 | 4 | HG01928.hp2 HG01981.hp2 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+8926C>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110703201 | ||||||
| chr11:110703326
|
A | G | 91 | a0001c0001t0001g0005a0001c0001t0001g0136a0001c0001t0001g0137others(88): Show | 93 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(90): Show |
intron_variant | MODIFIER | c.105+8801T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110703326 | ||||||
| chr11:110703407
|
A | G | 7 | a0001c0001t0001g0139a0001c0001t0004g0004a0001c0001t0004g0143others(4): Show | 8 | HG00735.hp2 HG01891.hp1 HG03017.hp2 others(5): Show |
intron_variant | MODIFIER | c.105+8720T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110703407 | ||||||
| chr11:110703410
|
T | C | 45 | a0001c0001t0001g0005a0001c0001t0001g0136a0001c0001t0001g0137others(42): Show | 46 | HG00621.hp1 HG00639.hp2 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.105+8717A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110703410 | ||||||
| chr11:110703637
|
G | A | 1 | a0001c0001t0001g0195 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.105+8490C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110703637 | ||||||
| chr11:110703678
|
C | A | 3 | a0001c0001t0004g0146a0003c0004t0017g0145a0007c0020t0020g0149 | 3 | HG03225.hp2 HG06807.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.105+8449G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110703678 | ||||||
| chr11:110703710
|
A | G | 7 | a0001c0001t0001g0139a0001c0001t0004g0004a0001c0001t0004g0143others(4): Show | 8 | HG00735.hp2 HG01891.hp1 HG03017.hp2 others(5): Show |
intron_variant | MODIFIER | c.105+8417T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110703710 | ||||||
| chr11:110703717
|
T | C | 1 | a0001c0001t0008g0019 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.105+8410A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110703717 | ||||||
| chr11:110703823
|
C | T | 1 | a0001c0001t0001g0191 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.105+8304G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110703823 | ||||||
| chr11:110703889
|
A | G | 2 | a0006c0007t0010g0147a0006c0007t0010g0148 | 2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.105+8238T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110703889 | ||||||
| chr11:110703967
|
G | A | 48 | a0001c0001t0001g0005a0001c0001t0001g0136a0001c0001t0001g0137others(45): Show | 49 | HG00621.hp1 HG00639.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.105+8160C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110703967 | ||||||
| chr11:110704110
|
C | A | 91 | a0001c0001t0001g0005a0001c0001t0001g0136a0001c0001t0001g0137others(88): Show | 93 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(90): Show |
intron_variant | MODIFIER | c.105+8017G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110704110 | ||||||
| chr11:110704256
|
T | C | 1 | a0001c0002t0005g0209 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.105+7871A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110704256 | ||||||
| chr11:110704288
|
C | T | 2 | a0001c0001t0004g0146a0003c0004t0017g0145 | 2 | HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.105+7839G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110704288 | ||||||
| chr11:110704389
|
A | G | 12 | a0001c0001t0001g0210a0001c0001t0003g0213a0001c0001t0003g0216others(9): Show | 12 | HG00099.hp2 HG00280.hp2 HG02015.hp1 others(9): Show |
intron_variant | MODIFIER | c.105+7738T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110704389 | ||||||
| chr11:110704556
|
T | C | 35 | a0001c0001t0001g0210a0001c0001t0002g0008a0001c0001t0002g0204others(32): Show | 35 | HG00099.hp2 HG00280.hp2 HG01074.hp1 others(32): Show |
intron_variant | MODIFIER | c.105+7571A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110704556 | ||||||
| chr11:110704576
|
GC | G | 29 | a0001c0001t0001g0037a0001c0001t0001g0047a0001c0001t0002g0024others(26): Show | 29 | HG00558.hp2 HG01358.hp2 HG02080.hp2 others(26): Show |
intron_variant | MODIFIER | c.105+7550delG | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110704576 | ||||||
| chr11:110704710
|
T | G | 2 | a0001c0001t0003g0118a0001c0001t0003g0119 | 2 | NA18942.hp2 NA18948.hp1 |
intron_variant | MODIFIER | c.105+7417A>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110704710 | ||||||
| chr11:110704745
|
G | A | 19 | a0001c0001t0001g0210a0001c0001t0002g0204a0001c0001t0002g0205others(16): Show | 19 | HG00099.hp2 HG00280.hp2 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.105+7382C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110704745 | ||||||
| chr11:110704768
|
A | C | 91 | a0001c0001t0001g0005a0001c0001t0001g0136a0001c0001t0001g0137others(88): Show | 93 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(90): Show |
intron_variant | MODIFIER | c.105+7359T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110704768 | ||||||
| chr11:110704866
|
G | T | 1 | a0002c0006t0012g0140 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.105+7261C>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110704866 | ||||||
| chr11:110704990
|
A | G | 2 | a0001c0001t0001g0027a0001c0001t0002g0127 | 2 | HG01496.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.105+7137T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110704990 | ||||||
| chr11:110705009
|
C | A | 7 | a0001c0001t0002g0204a0001c0001t0002g0205a0001c0001t0002g0206others(4): Show | 7 | HG01074.hp1 HG01891.hp2 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.105+7118G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110705009 | ||||||
| chr11:110705191
|
G | A | 49 | a0001c0001t0001g0005a0001c0001t0001g0136a0001c0001t0001g0137others(46): Show | 50 | HG00621.hp1 HG00639.hp2 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.105+6936C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110705191 | ||||||
| chr11:110705207
|
C | T | 56 | a0001c0001t0001g0005a0001c0001t0001g0136a0001c0001t0001g0137others(53): Show | 58 | HG00621.hp1 HG00639.hp2 HG00673.hp2 others(55): Show |
intron_variant | MODIFIER | c.105+6920G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110705207 | ||||||
| chr11:110705302
|
A | G | 1 | a0002c0003t0007g0150 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.105+6825T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110705302 | ||||||
| chr11:110705465
|
A | G | 45 | a0001c0001t0001g0005a0001c0001t0001g0136a0001c0001t0001g0137others(42): Show | 46 | HG00621.hp1 HG00639.hp2 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.105+6662T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110705465 | ||||||
| chr11:110705549
|
C | T | 49 | a0001c0001t0001g0005a0001c0001t0001g0136a0001c0001t0001g0137others(46): Show | 50 | HG00621.hp1 HG00639.hp2 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.105+6578G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110705549 | ||||||
| chr11:110705632
|
G | A | 1 | a0001c0001t0009g0120 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.105+6495C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110705632 | ||||||
| chr11:110705727
|
C | A | 1 | a0001c0001t0002g0121 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.105+6400G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110705727 | ||||||
| chr11:110705807
|
A | C | 7 | a0001c0001t0001g0139a0001c0001t0004g0004a0001c0001t0004g0143others(4): Show | 8 | HG00735.hp2 HG01891.hp1 HG03017.hp2 others(5): Show |
intron_variant | MODIFIER | c.105+6320T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110705807 | ||||||
| chr11:110705850
|
C | T | 1 | a0001c0001t0002g0026 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.105+6277G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110705850 | ||||||
| chr11:110705871
|
G | A | 6 | a0001c0001t0006g0156a0001c0001t0006g0199a0001c0001t0006g0200others(3): Show | 6 | HG02109.hp1 HG02257.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.105+6256C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110705871 | ||||||
| chr11:110705912
|
G | A | 84 | a0001c0001t0001g0005a0001c0001t0001g0136a0001c0001t0001g0137others(81): Show | 86 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.105+6215C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110705912 | ||||||
| chr11:110706105
|
C | T | 2 | a0006c0007t0010g0147a0006c0007t0010g0148 | 2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.105+6022G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110706105 | ||||||
| chr11:110706323
|
C | T | 1 | a0001c0001t0001g0025 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.105+5804G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110706323 | ||||||
| chr11:110706362
|
T | A | 1 | a0001c0001t0001g0155 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.105+5765A>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110706362 | ||||||
| chr11:110706581
|
T | C | 1 | a0001c0001t0002g0122 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.105+5546A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110706581 | ||||||
| chr11:110706593
|
ACCTACTC others(48): Show |
A | 1 | a0001c0002t0005g0209 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.105+5479_105+5533d others(57): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110706593 | ||||||
| chr11:110707571
|
T | A | 1 | a0003c0004t0002g0144 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.105+4556A>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110707571 | ||||||
| chr11:110707575
|
C | T | 1 | a0001c0001t0002g0024 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.105+4552G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110707575 | ||||||
| chr11:110707625
|
T | C | 22 | a0001c0001t0001g0210a0001c0001t0002g0008a0001c0001t0003g0213others(19): Show | 22 | HG00099.hp2 HG00280.hp2 HG02015.hp1 others(19): Show |
intron_variant | MODIFIER | c.105+4502A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110707625 | ||||||
| chr11:110707831
|
A | C | 6 | a0001c0001t0006g0156a0001c0001t0006g0199a0001c0001t0006g0200others(3): Show | 6 | HG02109.hp1 HG02257.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.105+4296T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110707831 | ||||||
| chr11:110707863
|
GT | G | 76 | a0001c0001t0001g0005a0001c0001t0001g0136a0001c0001t0001g0137others(73): Show | 77 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.105+4263delA | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110707863 | ||||||
| chr11:110707924
|
G | A | 2 | a0001c0009t0002g0188a0001c0009t0002g0196 | 2 | NA18978.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.105+4203C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110707924 | ||||||
| chr11:110708002
|
C | T | 2 | a0001c0001t0002g0022a0001c0001t0002g0023 | 2 | HG02280.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.105+4125G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110708002 | ||||||
| chr11:110708201
|
A | C | 48 | a0001c0001t0001g0005a0001c0001t0001g0136a0001c0001t0001g0137others(45): Show | 49 | HG00621.hp1 HG00639.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.105+3926T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110708201 | ||||||
| chr11:110708246
|
T | C | 8 | a0001c0001t0002g0008a0001c0001t0004g0009a0001c0001t0004g0010others(5): Show | 8 | HG02145.hp2 HG02647.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.105+3881A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110708246 | ||||||
| chr11:110708452
|
T | TTTTA | 77 | a0001c0001t0001g0005a0001c0001t0001g0136a0001c0001t0001g0137others(74): Show | 78 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(75): Show |
intron_variant | MODIFIER | c.105+3674_105+3675i others(6): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110708452 | ||||||
| chr11:110708567
|
G | A | 4 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0219others(1): Show | 4 | HG00099.hp1 HG00741.hp2 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.105+3560C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110708567 | ||||||
| chr11:110708652
|
C | A | 1 | a0001c0002t0005g0209 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.105+3475G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110708652 | ||||||
| chr11:110708653
|
A | C | 1 | a0001c0002t0005g0209 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.105+3474T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110708653 | ||||||
| chr11:110708654
|
T | A | 1 | a0001c0002t0005g0209 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.105+3473A>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110708654 | ||||||
| chr11:110708667
|
T | A | 1 | a0001c0002t0005g0209 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.105+3460A>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110708667 | ||||||
| chr11:110708669
|
T | TTGAAGAA others(47): Show |
1 | a0001c0002t0005g0209 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.105+3457_105+3458i others(56): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110708669 | ||||||
| chr11:110708674
|
G | A | 56 | a0001c0001t0001g0005a0001c0001t0001g0136a0001c0001t0001g0137others(53): Show | 58 | HG00621.hp1 HG00639.hp2 HG00673.hp2 others(55): Show |
intron_variant | MODIFIER | c.105+3453C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110708674 | ||||||
| chr11:110708675
|
T | G | 1 | a0001c0002t0005g0209 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.105+3452A>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110708675 | ||||||
| chr11:110708714
|
T | C | 12 | a0001c0001t0001g0210a0001c0001t0003g0213a0001c0001t0003g0216others(9): Show | 12 | HG00099.hp2 HG00280.hp2 HG02015.hp1 others(9): Show |
intron_variant | MODIFIER | c.105+3413A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110708714 | ||||||
| chr11:110708726
|
G | A | 1 | a0001c0001t0003g0126 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.105+3401C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110708726 | ||||||
| chr11:110709280
|
G | A | 1 | a0001c0012t0002g0189 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.105+2847C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110709280 | ||||||
| chr11:110709363
|
G | C | 1 | a0001c0005t0005g0197 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.105+2764C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110709363 | ||||||
| chr11:110709415
|
T | A | 7 | a0001c0001t0001g0139a0001c0001t0004g0004a0001c0001t0004g0143others(4): Show | 8 | HG00735.hp2 HG01891.hp1 HG03017.hp2 others(5): Show |
intron_variant | MODIFIER | c.105+2712A>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110709415 | ||||||
| chr11:110709560
|
G | C | 2 | a0006c0007t0010g0147a0006c0007t0010g0148 | 2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.105+2567C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110709560 | ||||||
| chr11:110709874
|
A | T | 28 | a0001c0001t0001g0210a0001c0001t0002g0008a0001c0001t0003g0213others(25): Show | 28 | HG00099.hp2 HG00280.hp2 HG02015.hp1 others(25): Show |
intron_variant | MODIFIER | c.105+2253T>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110709874 | ||||||
| chr11:110709900
|
C | A | 1 | a0001c0001t0013g0190 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.105+2227G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110709900 | ||||||
| chr11:110709956
|
C | T | 1 | a0001c0001t0006g0199 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.105+2171G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110709956 | ||||||
| chr11:110709957
|
G | A | 1 | a0001c0001t0001g0191 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.105+2170C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110709957 | ||||||
| chr11:110710141
|
G | A | 91 | a0001c0001t0001g0005a0001c0001t0001g0136a0001c0001t0001g0137others(88): Show | 93 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(90): Show |
intron_variant | MODIFIER | c.105+1986C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110710141 | ||||||
| chr11:110710435
|
T | TA | 66 | a0001c0001t0001g0005a0001c0001t0001g0136a0001c0001t0001g0137others(63): Show | 68 | HG00621.hp1 HG00639.hp2 HG00673.hp2 others(65): Show |
intron_variant | MODIFIER | c.105+1691dupT | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110710435 | ||||||
| chr11:110710878
|
C | T | 19 | a0001c0001t0001g0210a0001c0001t0002g0204a0001c0001t0002g0205others(16): Show | 19 | HG00099.hp2 HG00280.hp2 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.105+1249G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110710878 | ||||||
| chr11:110711005
|
C | CA | 30 | a0001c0001t0001g0020a0001c0001t0001g0129a0001c0001t0001g0131others(27): Show | 31 | HG00099.hp2 HG00280.hp2 HG00621.hp2 others(28): Show |
intron_variant | MODIFIER | c.105+1121dupT | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110711005 | ||||||
| chr11:110711005
|
C | CAA | 17 | a0001c0001t0002g0008a0001c0001t0002g0204a0001c0001t0002g0205others(14): Show | 17 | HG01074.hp1 HG01891.hp2 HG01952.hp2 others(14): Show |
intron_variant | MODIFIER | c.105+1120_105+1121d others(4): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110711005 | ||||||
| chr11:110711005
|
C | CAAA | 9 | a0001c0001t0001g0152a0001c0001t0001g0154a0001c0001t0001g0155others(6): Show | 9 | HG02109.hp1 HG02257.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.105+1119_105+1121d others(5): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110711005 | ||||||
| chr11:110711005
|
C | CAAAA | 41 | a0001c0001t0001g0005a0001c0001t0001g0136a0001c0001t0001g0137others(38): Show | 42 | HG00639.hp2 HG00673.hp2 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.105+1118_105+1121d others(6): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110711005 | ||||||
| chr11:110711005
|
C | CAAAAA | 5 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0001g0194others(2): Show | 5 | HG00621.hp1 HG03098.hp1 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.105+1117_105+1121d others(7): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110711005 | ||||||
| chr11:110711033
|
G | T | 7 | a0001c0001t0001g0139a0001c0001t0004g0004a0001c0001t0004g0143others(4): Show | 8 | HG00735.hp2 HG01891.hp1 HG03017.hp2 others(5): Show |
intron_variant | MODIFIER | c.105+1094C>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110711033 | ||||||
| chr11:110711267
|
C | T | 1 | a0001c0001t0003g0021 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.105+860G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110711267 | ||||||
| chr11:110711352
|
A | AG | 219 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0016others(216): Show | 225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.105+774dupC | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110711352 | ||||||
| chr11:110711447
|
G | A | 1 | a0001c0005t0005g0197 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.105+680C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110711447 | ||||||
| chr11:110711587
|
T | C | 90 | a0001c0001t0001g0005a0001c0001t0001g0139a0001c0001t0001g0152others(87): Show | 92 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.105+540A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110711587 | ||||||
| chr11:110711625
|
C | G | 1 | a0001c0001t0001g0020 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.105+502G>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110711625 | ||||||
| chr11:110711645
|
C | T | 6 | a0001c0001t0001g0016a0001c0001t0008g0014a0001c0001t0008g0015others(3): Show | 6 | HG02155.hp1 NA18972.hp2 NA18997.hp1 others(3): Show |
intron_variant | MODIFIER | c.105+482G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110711645 | ||||||
| chr11:110711648
|
C | T | 1 | a0001c0001t0003g0013 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.105+479G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110711648 | ||||||
| chr11:110711807
|
C | T | 5 | a0001c0001t0002g0008a0001c0001t0004g0009a0001c0001t0004g0010others(2): Show | 5 | HG02145.hp2 HG02647.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.105+320G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110711807 | ||||||
| chr11:110711904
|
G | A | 1 | a0001c0001t0003g0198 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.105+223C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110711904 | ||||||
| chr11:110711937
|
G | C | 3 | a0001c0001t0006g0199a0001c0001t0006g0200a0001c0001t0006g0201 | 3 | HG02109.hp1 HG02486.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.105+190C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110711937 | ||||||
| chr11:110712091
|
C | A | 19 | a0001c0001t0001g0210a0001c0001t0001g0219a0001c0001t0002g0204others(16): Show | 19 | HG00099.hp2 HG00741.hp2 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.105+36G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110712091 | ||||||
| chr11:110712092
|
G | A | 20 | a0001c0001t0001g0210a0001c0001t0001g0219a0001c0001t0002g0204others(17): Show | 20 | HG00099.hp2 HG00280.hp2 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.105+35C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110712092 | ||||||
| chr11:110712111
|
C | A | 13 | a0001c0001t0001g0210a0001c0001t0001g0219a0001c0001t0003g0213others(10): Show | 13 | HG00099.hp2 HG00280.hp2 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.105+16G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110712111 |