| geneid | 79822 |
|---|---|
| ensemblid | ENSG00000088756.13 |
| hgncid | 25509 |
| symbol | ARHGAP28 |
| name | Rho GTPase activating protein 28 |
| refseq_nuc | NM_001366230.1 |
| refseq_prot | NP_001353159.1 |
| ensembl_nuc | ENST00000383472.9 |
| ensembl_prot | ENSP00000372964.4 |
| mane_status | MANE Select |
| chr | chr18 |
| start | 6729716 |
| end | 6915716 |
| strand | + |
| ver | v1.2 |
| region | chr18:6729716-6915716 |
| region5000 | chr18:6724716-6920716 |
| regionname0 | ARHGAP28_chr18_6729716_6915716 |
| regionname5000 | ARHGAP28_chr18_6724716_6920716 |
| 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 | 0/1 | 729 | 130 | 58 | 21 | 25 | 8 | 17 | 17 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| a0002 | 1/0 | 729 | 56 | 9 | 5 | 30 | 1 | 10 | 20 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| a0003 | 0/0 | 729 | 41 | 2 | 4 | 32 | 0 | 3 | 21 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| a0004 | 0/0 | 729 | 5 | 1 | 0 | 4 | 0 | 0 | 3 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| a0005 | 0/0 | 729 | 5 | 0 | 0 | 5 | 0 | 0 | 5 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| a0006 | 0/0 | 729 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| a0007 | 0/0 | 729 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| a0008 | 0/0 | 729 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| a0009 | 0/0 | 729 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| a0010 | 0/0 | 729 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| 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 | 0/1 | 2190 | 85 | 32 | 10 | 24 | 6 | 12 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| c0002 | 1/0 | 2190 | 45 | 7 | 5 | 23 | 1 | 8 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| c0003 | 0/0 | 2190 | 36 | 18 | 10 | 1 | 2 | 5 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| c0004 | 0/0 | 2190 | 36 | 1 | 4 | 30 | 0 | 1 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| c0005 | 0/0 | 2190 | 10 | 1 | 0 | 7 | 0 | 2 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| c0006 | 0/0 | 2190 | 5 | 0 | 0 | 5 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| c0007 | 0/0 | 2190 | 5 | 1 | 0 | 4 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| c0008 | 0/0 | 2190 | 3 | 2 | 1 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| c0009 | 0/0 | 2190 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| c0010 | 0/0 | 2190 | 3 | 2 | 1 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| c0011 | 0/0 | 2190 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| c0012 | 0/0 | 2190 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| c0013 | 0/0 | 2190 | 2 | 0 | 0 | 0 | 0 | 2 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| c0014 | 0/0 | 2190 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| c0015 | 0/0 | 2190 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| c0016 | 0/0 | 2190 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| c0017 | 0/0 | 2190 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| c0018 | 0/0 | 2190 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| c0019 | 0/0 | 2190 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| c0020 | 0/0 | 2190 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| c0021 | 0/0 | 2190 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| c0022 | 0/0 | 2190 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| c0023 | 0/0 | 2190 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| 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 | 3665 | 111 | 21 | 14 | 56 | 7 | 12 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| t0002 | 1/0 | 3669 | 56 | 7 | 6 | 31 | 1 | 10 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| t0003 | 0/0 | 3665 | 45 | 22 | 10 | 6 | 2 | 5 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| t0004 | 0/0 | 3669 | 4 | 4 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| t0005 | 0/0 | 3666 | 4 | 4 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| t0006 | 0/0 | 3664 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| t0007 | 0/0 | 3665 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| t0008 | 0/0 | 3665 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| t0009 | 0/0 | 3665 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| t0010 | 0/0 | 3669 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| t0011 | 0/0 | 3665 | 2 | 0 | 0 | 0 | 0 | 2 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| t0012 | 0/0 | 3669 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| t0013 | 0/0 | 3669 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| t0014 | 0/0 | 3665 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| t0015 | 0/0 | 3665 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| t0016 | 0/0 | 3665 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| t0017 | 0/0 | 3665 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| t0018 | 0/0 | 3665 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| t0019 | 0/0 | 3665 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| t0020 | 0/0 | 3665 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| t0021 | 0/0 | 3665 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| t0022 | 0/0 | 3669 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| t0023 | 0/0 | 3666 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0012 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0018 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0160 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| 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 | 0/1 | 2190 | 85 | 32 | 10 | 24 | 6 | 12 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| a0001c0003 | 0/0 | 2190 | 36 | 18 | 10 | 1 | 2 | 5 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| a0001c0010 | 0/0 | 2190 | 3 | 2 | 1 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| a0001c0012 | 0/0 | 2190 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| a0001c0015 | 0/0 | 2190 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| a0001c0018 | 0/0 | 2190 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| a0001c0019 | 0/0 | 2190 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| a0001c0020 | 0/0 | 2190 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| a0002c0002 | 1/0 | 2190 | 45 | 7 | 5 | 23 | 1 | 8 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| a0002c0005 | 0/0 | 2190 | 10 | 1 | 0 | 7 | 0 | 2 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| a0002c0017 | 0/0 | 2190 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| a0003c0004 | 0/0 | 2190 | 36 | 1 | 4 | 30 | 0 | 1 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| a0003c0013 | 0/0 | 2190 | 2 | 0 | 0 | 0 | 0 | 2 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| a0003c0021 | 0/0 | 2190 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| a0003c0022 | 0/0 | 2190 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| a0003c0023 | 0/0 | 2190 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| a0004c0007 | 0/0 | 2190 | 5 | 1 | 0 | 4 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| a0005c0006 | 0/0 | 2190 | 5 | 0 | 0 | 5 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| a0006c0009 | 0/0 | 2190 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| a0007c0008 | 0/0 | 2190 | 3 | 2 | 1 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| a0008c0011 | 0/0 | 2190 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| a0009c0016 | 0/0 | 2190 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| a0010c0014 | 0/0 | 2190 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 5854 | 69 | 18 | 9 | 24 | 6 | 11 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| a0001c0001t0006 | 0/0 | 5853 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| a0001c0001t0007 | 0/0 | 5854 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| a0001c0001t0008 | 0/0 | 5854 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| a0001c0001t0009 | 0/0 | 5854 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| a0001c0001t0016 | 0/0 | 5854 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| a0001c0001t0017 | 0/0 | 5854 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| a0001c0001t0018 | 0/0 | 5854 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| a0001c0001t0019 | 0/0 | 5854 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| a0001c0001t0022 | 0/0 | 5858 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| a0001c0003t0001 | 0/0 | 5854 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| a0001c0003t0003 | 0/0 | 5854 | 34 | 18 | 9 | 0 | 2 | 5 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| a0001c0003t0015 | 0/0 | 5854 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| a0001c0010t0003 | 0/0 | 5854 | 3 | 2 | 1 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| a0001c0012t0001 | 0/0 | 5854 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| a0001c0012t0014 | 0/0 | 5854 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| a0001c0015t0003 | 0/0 | 5854 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| a0001c0018t0020 | 0/0 | 5854 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| a0001c0019t0021 | 0/0 | 5854 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| a0001c0020t0023 | 0/0 | 5855 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| a0002c0002t0002 | 1/0 | 5858 | 38 | 3 | 5 | 20 | 1 | 8 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| a0002c0002t0004 | 0/0 | 5858 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| a0002c0002t0010 | 0/0 | 5858 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| a0002c0002t0012 | 0/0 | 5858 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| a0002c0002t0013 | 0/0 | 5858 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| a0002c0005t0002 | 0/0 | 5858 | 10 | 1 | 0 | 7 | 0 | 2 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| a0002c0017t0002 | 0/0 | 5858 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| a0003c0004t0001 | 0/0 | 5854 | 36 | 1 | 4 | 30 | 0 | 1 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| a0003c0013t0011 | 0/0 | 5854 | 2 | 0 | 0 | 0 | 0 | 2 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| a0003c0021t0001 | 0/0 | 5854 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| a0003c0022t0003 | 0/0 | 5854 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| a0003c0023t0001 | 0/0 | 5854 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| a0004c0007t0002 | 0/0 | 5858 | 4 | 0 | 0 | 4 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| a0004c0007t0004 | 0/0 | 5858 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| a0005c0006t0003 | 0/0 | 5854 | 5 | 0 | 0 | 5 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| a0006c0009t0003 | 0/0 | 5854 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| a0006c0009t0005 | 0/0 | 5855 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| a0006c0009t0009 | 0/0 | 5854 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| a0007c0008t0002 | 0/0 | 5858 | 3 | 2 | 1 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| a0008c0011t0005 | 0/0 | 5855 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| a0009c0016t0001 | 0/0 | 5854 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| a0010c0014t0001 | 0/0 | 5854 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | copy fasta | chr18 | 6724716 | 6920716 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0001t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0001t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0001t0001g0018 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0001t0006g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0001t0006g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0001t0006g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0001t0007g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0001t0007g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0001t0007g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0001t0008g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0001t0008g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0001t0008g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0001t0009g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0001t0009g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0001t0016g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0001t0017g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0001t0018g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0001t0019g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0001t0022g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0003t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0003t0003g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0003t0003g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0003t0003g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0003t0003g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0003t0003g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0003t0003g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0003t0003g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0003t0003g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0003t0003g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0003t0003g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0003t0003g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0003t0003g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0003t0003g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0003t0003g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0003t0003g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0003t0003g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0003t0003g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0003t0003g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0003t0003g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0003t0003g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0003t0003g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0003t0003g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0003t0003g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0003t0003g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0003t0003g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0003t0003g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0003t0003g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0003t0003g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0003t0003g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0003t0003g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0003t0003g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0003t0003g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0003t0003g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0003t0003g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0003t0015g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0010t0003g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0010t0003g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0010t0003g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0012t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0012t0014g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0015t0003g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0018t0020g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0019t0021g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0001c0020t0023g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0002c0002t0002g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0002c0002t0002g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0002c0002t0002g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0002c0002t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0002c0002t0002g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0002c0002t0002g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0002c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0002c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0002c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0002c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0002c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0002c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0002c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0002c0002t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0002c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0002c0002t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0002c0002t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0002c0002t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0002c0002t0002g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0002c0002t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0002c0002t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0002c0002t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0002c0002t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0002c0002t0002g0160 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0002c0002t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0002c0002t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0002c0002t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0002c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0002c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0002c0002t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0002c0002t0002g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0002c0002t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0002c0002t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0002c0002t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0002c0002t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0002c0002t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0002c0002t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0002c0002t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0002c0002t0004g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0002c0002t0004g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0002c0002t0004g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0002c0002t0010g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0002c0002t0010g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0002c0002t0012g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0002c0002t0013g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0002c0005t0002g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0002c0005t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0002c0005t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0002c0005t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0002c0005t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0002c0005t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0002c0005t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0002c0005t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0002c0005t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0002c0005t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0002c0017t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0003c0004t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0003c0004t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0003c0004t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0003c0004t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0003c0004t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0003c0004t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0003c0004t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0003c0004t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0003c0004t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0003c0004t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0003c0004t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0003c0004t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0003c0004t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0003c0004t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0003c0004t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0003c0004t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0003c0004t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0003c0004t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0003c0004t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0003c0004t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0003c0004t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0003c0004t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0003c0004t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0003c0004t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0003c0004t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0003c0004t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0003c0004t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0003c0004t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0003c0004t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0003c0004t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0003c0004t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0003c0004t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0003c0004t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0003c0004t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0003c0004t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0003c0004t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0003c0013t0011g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0003c0013t0011g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0003c0021t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0003c0022t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0003c0023t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0004c0007t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0004c0007t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0004c0007t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0004c0007t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0004c0007t0004g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0005c0006t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0005c0006t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0005c0006t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0005c0006t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0005c0006t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0006c0009t0003g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0006c0009t0005g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0006c0009t0009g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0007c0008t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0007c0008t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0007c0008t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0008c0011t0005g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0008c0011t0005g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0008c0011t0005g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0009c0016t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| a0010c0014t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0009 | c0016 | t0001 | g0092 | EUR | GBR | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0012 | EUR | GBR | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0236 | EUR | GBR | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG00140 | hp2 | a0002 | c0002 | t0002 | g0023 | EUR | GBR | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0071 | EUR | FIN | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG00280 | hp2 | a0001 | c0003 | t0003 | g0235 | EUR | FIN | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG00408 | hp1 | a0002 | c0002 | t0002 | g0134 | EAS | CHS | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG00408 | hp2 | a0003 | c0004 | t0001 | g0039 | EAS | CHS | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG00423 | hp1 | a0003 | c0004 | t0001 | g0227 | EAS | CHS | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | CHS | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG00438 | hp1 | a0002 | c0002 | t0002 | g0083 | EAS | CHS | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG00438 | hp2 | a0003 | c0004 | t0001 | g0193 | EAS | CHS | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | CHS | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | CHS | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG00558 | hp1 | a0003 | c0004 | t0001 | g0020 | EAS | CHS | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG00558 | hp2 | a0003 | c0004 | t0001 | g0032 | EAS | CHS | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG00597 | hp1 | a0003 | c0004 | t0001 | g0183 | EAS | CHS | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG00597 | hp2 | a0002 | c0002 | t0002 | g0224 | EAS | CHS | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG00621 | hp1 | a0003 | c0004 | t0001 | g0048 | EAS | CHS | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG00621 | hp2 | a0003 | c0004 | t0001 | g0093 | EAS | CHS | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG00735 | hp2 | a0001 | c0001 | t0016 | g0081 | AMR | PUR | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG00741 | hp1 | a0002 | c0002 | t0002 | g0099 | AMR | PUR | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG00741 | hp2 | a0001 | c0003 | t0003 | g0027 | AMR | PUR | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG01081 | hp1 | a0001 | c0003 | t0003 | g0222 | AMR | PUR | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG01081 | hp2 | a0001 | c0010 | t0003 | g0114 | AMR | PUR | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG01099 | hp1 | a0001 | c0003 | t0003 | g0110 | AMR | PUR | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG01106 | hp1 | a0010 | c0014 | t0001 | g0142 | AMR | PUR | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG01106 | hp2 | a0001 | c0003 | t0015 | g0028 | AMR | PUR | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | PUR | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG01175 | hp2 | a0001 | c0003 | t0003 | g0105 | AMR | PUR | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG01256 | hp1 | a0001 | c0003 | t0003 | g0077 | AMR | CLM | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | CLM | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | CLM | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | CLM | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG01346 | hp1 | a0002 | c0002 | t0002 | g0148 | AMR | CLM | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG01346 | hp2 | a0001 | c0003 | t0003 | g0201 | AMR | CLM | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | CLM | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG01496 | hp2 | a0001 | c0003 | t0003 | g0231 | AMR | CLM | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0203 | EUR | IBS | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG01884 | hp1 | a0004 | c0007 | t0004 | g0115 | AFR | ACB | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG01884 | hp2 | a0001 | c0001 | t0006 | g0164 | AFR | ACB | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG01891 | hp1 | a0001 | c0001 | t0009 | g0005 | AFR | ACB | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG01891 | hp2 | a0002 | c0002 | t0002 | g0157 | AFR | ACB | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG01943 | hp1 | a0002 | c0002 | t0002 | g0009 | AMR | PEL | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG01943 | hp2 | a0001 | c0003 | t0003 | g0013 | AMR | PEL | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG01952 | hp1 | a0003 | c0004 | t0001 | g0024 | AMR | PEL | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG01952 | hp2 | a0007 | c0008 | t0002 | g0166 | AMR | PEL | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG01993 | hp1 | a0001 | c0003 | t0003 | g0190 | AMR | PEL | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG01993 | hp2 | a0003 | c0004 | t0001 | g0200 | AMR | PEL | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | KHV | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG02040 | hp2 | a0002 | c0002 | t0002 | g0066 | EAS | KHV | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG02055 | hp1 | a0002 | c0005 | t0002 | g0158 | AFR | ACB | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG02055 | hp2 | a0001 | c0001 | t0006 | g0176 | AFR | ACB | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | KHV | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG02071 | hp2 | a0004 | c0007 | t0002 | g0036 | EAS | KHV | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG02080 | hp1 | a0002 | c0002 | t0002 | g0137 | EAS | KHV | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG02080 | hp2 | a0003 | c0004 | t0001 | g0058 | EAS | KHV | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG02129 | hp1 | a0003 | c0004 | t0001 | g0195 | EAS | KHV | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG02129 | hp2 | a0002 | c0002 | t0002 | g0217 | EAS | KHV | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG02135 | hp1 | a0002 | c0002 | t0002 | g0214 | EAS | KHV | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | KHV | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | ACB | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | ACB | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG02155 | hp1 | a0003 | c0004 | t0001 | g0125 | EAS | CDX | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG02155 | hp2 | a0002 | c0002 | t0002 | g0015 | EAS | CDX | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG02258 | hp1 | a0001 | c0001 | t0006 | g0155 | AFR | ACB | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | ACB | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG02273 | hp1 | a0003 | c0004 | t0001 | g0010 | AMR | PEL | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG02273 | hp2 | a0002 | c0002 | t0002 | g0033 | AMR | PEL | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | ACB | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG02280 | hp2 | a0002 | c0002 | t0004 | g0147 | AFR | ACB | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG02300 | hp1 | a0003 | c0004 | t0001 | g0025 | AMR | PEL | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG02300 | hp2 | a0002 | c0002 | t0002 | g0199 | AMR | PEL | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | ACB | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG02451 | hp2 | a0002 | c0002 | t0004 | g0059 | AFR | ACB | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG02523 | hp1 | a0002 | c0002 | t0002 | g0096 | EAS | KHV | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | KHV | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG02602 | hp1 | a0001 | c0001 | t0017 | g0118 | SAS | PJL | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG02615 | hp1 | a0006 | c0009 | t0005 | g0144 | AFR | GWD | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | GWD | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG02630 | hp1 | a0001 | c0001 | t0022 | g0067 | AFR | GWD | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG02630 | hp2 | a0008 | c0011 | t0005 | g0016 | AFR | GWD | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG02647 | hp2 | a0002 | c0002 | t0002 | g0163 | AFR | GWD | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG02723 | hp1 | a0001 | c0003 | t0003 | g0122 | AFR | GWD | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG02723 | hp2 | a0002 | c0002 | t0002 | g0229 | AFR | GWD | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG02735 | hp1 | a0001 | c0003 | t0003 | g0060 | SAS | PJL | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG02735 | hp2 | a0002 | c0002 | t0002 | g0135 | SAS | PJL | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG02818 | hp1 | a0001 | c0003 | t0003 | g0154 | AFR | GWD | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG02818 | hp2 | a0001 | c0001 | t0018 | g0111 | AFR | GWD | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG02886 | hp2 | a0001 | c0001 | t0019 | g0008 | AFR | GWD | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG02895 | hp1 | a0001 | c0003 | t0003 | g0094 | AFR | GWD | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG02895 | hp2 | a0001 | c0001 | t0009 | g0245 | AFR | GWD | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG02896 | hp1 | a0001 | c0001 | t0007 | g0116 | AFR | GWD | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG02896 | hp2 | a0001 | c0012 | t0001 | g0210 | AFR | GWD | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG02897 | hp1 | a0001 | c0003 | t0003 | g0095 | AFR | GWD | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG02897 | hp2 | a0001 | c0001 | t0007 | g0117 | AFR | GWD | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG02922 | hp1 | a0002 | c0017 | t0002 | g0086 | AFR | ESN | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG02922 | hp2 | a0007 | c0008 | t0002 | g0146 | AFR | ESN | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | ESN | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG02965 | hp2 | a0001 | c0003 | t0003 | g0170 | AFR | ESN | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG02970 | hp1 | a0001 | c0010 | t0003 | g0098 | AFR | ESN | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG02976 | hp1 | a0001 | c0003 | t0003 | g0123 | AFR | ESN | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG02976 | hp2 | a0001 | c0003 | t0003 | g0084 | AFR | ESN | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG03041 | hp1 | a0003 | c0023 | t0001 | g0120 | AFR | GWD | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG03041 | hp2 | a0006 | c0009 | t0003 | g0162 | AFR | GWD | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | MSL | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG03098 | hp2 | a0001 | c0001 | t0008 | g0074 | AFR | MSL | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG03130 | hp1 | a0001 | c0003 | t0003 | g0169 | AFR | ESN | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG03130 | hp2 | a0002 | c0002 | t0012 | g0088 | AFR | ESN | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | ESN | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG03139 | hp2 | a0001 | c0018 | t0020 | g0007 | AFR | ESN | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG03209 | hp1 | a0007 | c0008 | t0002 | g0069 | AFR | MSL | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG03209 | hp2 | a0001 | c0003 | t0003 | g0091 | AFR | MSL | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG03239 | hp1 | a0002 | c0002 | t0002 | g0046 | SAS | PJL | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG03239 | hp2 | a0002 | c0005 | t0002 | g0017 | SAS | PJL | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG03453 | hp1 | a0001 | c0010 | t0003 | g0089 | AFR | MSL | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG03453 | hp2 | a0001 | c0001 | t0008 | g0171 | AFR | MSL | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | MSL | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | MSL | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG03490 | hp1 | a0003 | c0013 | t0011 | g0063 | SAS | PJL | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0232 | SAS | PJL | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG03491 | hp1 | a0001 | c0003 | t0003 | g0233 | SAS | PJL | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG03491 | hp2 | a0002 | c0005 | t0002 | g0057 | SAS | PJL | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG03492 | hp1 | a0003 | c0013 | t0011 | g0062 | SAS | PJL | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG03492 | hp2 | a0001 | c0003 | t0003 | g0234 | SAS | PJL | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG03516 | hp1 | a0001 | c0003 | t0003 | g0087 | AFR | ESN | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG03516 | hp2 | a0001 | c0003 | t0003 | g0076 | AFR | ESN | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG03540 | hp1 | a0001 | c0001 | t0008 | g0143 | AFR | GWD | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG03540 | hp2 | a0001 | c0001 | t0007 | g0212 | AFR | GWD | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | MSL | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG03579 | hp2 | a0001 | c0003 | t0003 | g0119 | AFR | MSL | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0070 | SAS | PJL | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG03704 | hp2 | a0002 | c0002 | t0002 | g0078 | SAS | PJL | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG03710 | hp1 | a0003 | c0004 | t0001 | g0242 | SAS | PJL | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG03710 | hp2 | a0002 | c0002 | t0002 | g0103 | SAS | PJL | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG03834 | hp1 | a0002 | c0002 | t0002 | g0172 | SAS | BEB | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0237 | SAS | BEB | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG03942 | hp1 | a0001 | c0003 | t0003 | g0208 | SAS | BEB | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG03942 | hp2 | a0002 | c0002 | t0002 | g0207 | SAS | BEB | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | STU | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | STU | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | BEB | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG04184 | hp2 | a0002 | c0002 | t0002 | g0011 | SAS | BEB | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG04204 | hp1 | a0001 | c0003 | t0003 | g0079 | SAS | STU | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG04204 | hp2 | a0002 | c0002 | t0002 | g0047 | SAS | STU | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0209 | SAS | STU | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0082 | SAS | STU | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| NA18747 | hp1 | a0002 | c0002 | t0002 | g0131 | EAS | CHB | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | CHB | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| NA18906 | hp1 | a0001 | c0015 | t0003 | g0167 | AFR | YRI | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| NA18906 | hp2 | a0001 | c0003 | t0003 | g0145 | AFR | YRI | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| NA18940 | hp2 | a0004 | c0007 | t0002 | g0238 | EAS | JPT | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| NA18941 | hp2 | a0002 | c0002 | t0010 | g0206 | EAS | JPT | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| NA18943 | hp1 | a0003 | c0004 | t0001 | g0109 | EAS | JPT | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| NA18947 | hp1 | a0003 | c0004 | t0001 | g0064 | EAS | JPT | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| NA18947 | hp2 | a0002 | c0005 | t0002 | g0133 | EAS | JPT | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| NA18950 | hp1 | a0005 | c0006 | t0003 | g0180 | EAS | JPT | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| NA18953 | hp1 | a0002 | c0005 | t0002 | g0140 | EAS | JPT | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| NA18956 | hp1 | a0003 | c0004 | t0001 | g0045 | EAS | JPT | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| NA18966 | hp1 | a0003 | c0004 | t0001 | g0248 | EAS | JPT | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| NA18966 | hp2 | a0002 | c0002 | t0010 | g0246 | EAS | JPT | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| NA18967 | hp1 | a0003 | c0004 | t0001 | g0175 | EAS | JPT | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| NA18967 | hp2 | a0002 | c0002 | t0002 | g0244 | EAS | JPT | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| NA18968 | hp1 | a0003 | c0004 | t0001 | g0173 | EAS | JPT | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| NA18968 | hp2 | a0003 | c0004 | t0001 | g0218 | EAS | JPT | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| NA18971 | hp1 | a0003 | c0004 | t0001 | g0051 | EAS | JPT | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| NA18971 | hp2 | a0002 | c0005 | t0002 | g0240 | EAS | JPT | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| NA18973 | hp1 | a0003 | c0022 | t0003 | g0132 | EAS | JPT | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| NA18973 | hp2 | a0003 | c0004 | t0001 | g0021 | EAS | JPT | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| NA18977 | hp1 | a0002 | c0005 | t0002 | g0061 | EAS | JPT | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| NA18977 | hp2 | a0005 | c0006 | t0003 | g0177 | EAS | JPT | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| NA18983 | hp2 | a0002 | c0002 | t0002 | g0014 | EAS | JPT | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| NA18986 | hp1 | a0003 | c0004 | t0001 | g0247 | EAS | JPT | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| NA18986 | hp2 | a0003 | c0004 | t0001 | g0112 | EAS | JPT | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| NA18988 | hp1 | a0002 | c0002 | t0002 | g0213 | EAS | JPT | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| NA18989 | hp2 | a0002 | c0005 | t0002 | g0041 | EAS | JPT | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| NA18991 | hp2 | a0002 | c0002 | t0013 | g0022 | EAS | JPT | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| NA18995 | hp1 | a0005 | c0006 | t0003 | g0226 | EAS | JPT | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| NA18995 | hp2 | a0002 | c0002 | t0002 | g0065 | EAS | JPT | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| NA19003 | hp2 | a0002 | c0002 | t0002 | g0243 | EAS | JPT | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| NA19010 | hp2 | a0002 | c0002 | t0002 | g0138 | EAS | JPT | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| NA19011 | hp1 | a0005 | c0006 | t0003 | g0031 | EAS | JPT | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| NA19011 | hp2 | a0003 | c0004 | t0001 | g0187 | EAS | JPT | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| NA19012 | hp1 | a0002 | c0002 | t0002 | g0196 | EAS | JPT | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| NA19012 | hp2 | a0002 | c0005 | t0002 | g0043 | EAS | JPT | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| NA19043 | hp1 | a0001 | c0003 | t0003 | g0085 | AFR | LWK | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| NA19043 | hp2 | a0001 | c0020 | t0023 | g0101 | AFR | LWK | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| NA19063 | hp1 | a0004 | c0007 | t0002 | g0178 | EAS | JPT | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| NA19066 | hp1 | a0003 | c0004 | t0001 | g0030 | EAS | JPT | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| NA19066 | hp2 | a0002 | c0002 | t0002 | g0197 | EAS | JPT | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| NA19070 | hp1 | a0001 | c0003 | t0001 | g0050 | EAS | JPT | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| NA19070 | hp2 | a0003 | c0004 | t0001 | g0219 | EAS | JPT | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| NA19081 | hp1 | a0004 | c0007 | t0002 | g0056 | EAS | JPT | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| NA19081 | hp2 | a0003 | c0004 | t0001 | g0136 | EAS | JPT | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| NA19082 | hp1 | a0002 | c0002 | t0002 | g0126 | EAS | JPT | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| NA19082 | hp2 | a0003 | c0004 | t0001 | g0220 | EAS | JPT | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| NA19086 | hp1 | a0002 | c0002 | t0002 | g0174 | EAS | JPT | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| NA19086 | hp2 | a0003 | c0021 | t0001 | g0053 | EAS | JPT | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| NA19087 | hp1 | a0005 | c0006 | t0003 | g0127 | EAS | JPT | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| NA19087 | hp2 | a0003 | c0004 | t0001 | g0241 | EAS | JPT | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| NA19090 | hp1 | a0002 | c0005 | t0002 | g0108 | EAS | JPT | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| NA19090 | hp2 | a0003 | c0004 | t0001 | g0130 | EAS | JPT | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| NA19091 | hp2 | a0003 | c0004 | t0001 | g0192 | EAS | JPT | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| NA19240 | hp1 | a0001 | c0003 | t0003 | g0104 | AFR | YRI | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| NA19240 | hp2 | a0008 | c0011 | t0005 | g0090 | AFR | YRI | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| NA20129 | hp1 | a0001 | c0019 | t0021 | g0073 | AFR | ASW | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | ASW | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0181 | EUR | TSI | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| NA20752 | hp2 | a0001 | c0003 | t0003 | g0055 | EUR | TSI | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | ACB | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG02109 | hp2 | a0001 | c0003 | t0003 | g0156 | AFR | ACB | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG02559 | hp1 | a0002 | c0002 | t0004 | g0006 | AFR | ACB | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG02559 | hp2 | a0001 | c0012 | t0014 | g0159 | AFR | ACB | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG03471 | hp1 | a0001 | c0003 | t0003 | g0002 | AFR | MSL | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG03471 | hp2 | a0008 | c0011 | t0005 | g0152 | AFR | MSL | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG06807 | hp1 | a0001 | c0003 | t0003 | g0068 | AFR | USA | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | USA | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| NA20300 | hp1 | a0006 | c0009 | t0009 | g0153 | AFR | USA | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| NA20300 | hp2 | a0003 | c0004 | t0001 | g0191 | AFR | USA | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0018 | REF | REF | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| homoSapiens_grch38 | hp1 | a0002 | c0002 | t0002 | g0160 | REF | REF | ARHGAP28_chr18_6724716_6920716 | ARHGAP28 | chr18 | 6724716 | 6920716 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:6729843
|
G | A | 1 | a0010 | 1 | HG01106.hp1 | missense_variant | MODERATE | c.22G>A | p.Gly8Ser | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/18 | 128/5858 | 22/2190 | 8/729 | chr18 | 6729843 | ||
| chr18:6851059
|
C | G | 2 | a0003a0004 | 46 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(43): Show |
missense_variant | MODERATE | c.569C>G | p.Thr190Ser | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/18 | 675/5858 | 569/2190 | 190/729 | chr18 | 6851059 | ||
| chr18:6851070
|
G | A | 1 | a0009 | 1 | HG00099.hp1 | missense_variant | MODERATE | c.580G>A | p.Asp194Asn | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/18 | 686/5858 | 580/2190 | 194/729 | chr18 | 6851070 | ||
| chr18:6890044
|
A | G | 1 | a0008 | 3 | HG02630.hp2 HG03471.hp2 NA19240.hp2 |
missense_variant | MODERATE | c.1693A>G | p.Ile565Val | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 13/18 | 1799/5858 | 1693/2190 | 565/729 | chr18 | 6890044 | ||
| chr18:6890539
|
G | T | 1 | a0005 | 5 | NA18950.hp1 NA18977.hp2 NA18995.hp1 others(2): Show |
missense_variant | MODERATE | c.1844G>T | p.Arg615Leu | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 14/18 | 1950/5858 | 1844/2190 | 615/729 | chr18 | 6890539 | ||
| chr18:6908977
|
G | A | 2 | a0006a0007 | 6 | HG01952.hp2 HG02615.hp1 HG02922.hp2 others(3): Show |
missense_variant | MODERATE | c.2048G>A | p.Cys683Tyr | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 17/18 | 2154/5858 | 2048/2190 | 683/729 | chr18 | 6908977 | ||
| chr18:6912144
|
A | C | 7 | a0001a0003a0005others(4): Show | 184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
missense_variant | MODERATE | c.2180A>C | p.Gln727Pro | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 18/18 | 2286/5858 | 2180/2190 | 727/729 | chr18 | 6912144 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:6824951
|
C | T | 1 | a0003c0023 | 1 | HG03041.hp1 | synonymous_variant | LOW | c.312C>T | p.Val104Val | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/18 | 418/5858 | 312/2190 | 104/729 | chr18 | 6824951 | ||
| chr18:6837393
|
T | C | 1 | a0001c0015 | 1 | NA18906.hp1 | synonymous_variant | LOW | c.522T>C | p.Ile174Ile | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/18 | 628/5858 | 522/2190 | 174/729 | chr18 | 6837393 | ||
| chr18:6868200
|
G | A | 1 | a0003c0021 | 1 | NA19086.hp2 | synonymous_variant | LOW | c.777G>A | p.Pro259Pro | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 6/18 | 883/5858 | 777/2190 | 259/729 | chr18 | 6868200 | ||
| chr18:6873727
|
T | A | 2 | a0001c0018a0002c0017 | 2 | HG02922.hp1 HG03139.hp2 |
synonymous_variant | LOW | c.1164T>A | p.Gly388Gly | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 9/18 | 1270/5858 | 1164/2190 | 388/729 | chr18 | 6873727 | ||
| chr18:6882226
|
A | G | 1 | a0001c0020 | 1 | NA19043.hp2 | synonymous_variant | LOW | c.1380A>G | p.Lys460Lys | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 11/18 | 1486/5858 | 1380/2190 | 460/729 | chr18 | 6882226 | ||
| chr18:6882229
|
G | A | 1 | a0001c0019 | 1 | NA20129.hp1 | synonymous_variant | LOW | c.1383G>A | p.Ala461Ala | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 11/18 | 1489/5858 | 1383/2190 | 461/729 | chr18 | 6882229 | ||
| chr18:6889974
|
A | G | 12 | a0001c0001a0001c0012a0001c0018others(9): Show | 147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): Show |
synonymous_variant | LOW | c.1623A>G | p.Pro541Pro | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 13/18 | 1729/5858 | 1623/2190 | 541/729 | chr18 | 6889974 | ||
| chr18:6890435
|
A | G | 15 | a0001c0001a0001c0010a0001c0012others(12): Show | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
synonymous_variant | LOW | c.1740A>G | p.Pro580Pro | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 14/18 | 1846/5858 | 1740/2190 | 580/729 | chr18 | 6890435 | ||
| chr18:6912100
|
A | G | 4 | a0001c0012a0003c0013a0003c0023others(1): Show | 6 | HG01106.hp1 HG02559.hp2 HG02896.hp2 others(3): Show |
synonymous_variant | LOW | c.2136A>G | p.Val712Val | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 18/18 | 2242/5858 | 2136/2190 | 712/729 | chr18 | 6912100 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:6912318
|
C | T | 32 | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(29): Show | 184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
3_prime_UTR_variant | MODIFIER | c.*164C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 18/18 | 164 | chr18 | 6912318 | |||||
| chr18:6912333
|
A | G | 32 | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(29): Show | 184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
3_prime_UTR_variant | MODIFIER | c.*179A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 18/18 | 179 | chr18 | 6912333 | |||||
| chr18:6912945
|
C | G | 32 | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(29): Show | 184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
3_prime_UTR_variant | MODIFIER | c.*791C>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 18/18 | 791 | chr18 | 6912945 | |||||
| chr18:6913017
|
A | G | 32 | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(29): Show | 184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
3_prime_UTR_variant | MODIFIER | c.*863A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 18/18 | 863 | chr18 | 6913017 | |||||
| chr18:6913145
|
G | C | 1 | a0001c0012t0014 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*991G>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 18/18 | 991 | chr18 | 6913145 | |||||
| chr18:6913192
|
T | C | 1 | a0001c0003t0015 | 1 | HG01106.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1038T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 18/18 | 1038 | chr18 | 6913192 | |||||
| chr18:6913355
|
G | A | 1 | a0003c0013t0011 | 2 | HG03490.hp1 HG03492.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1201G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 18/18 | 1201 | chr18 | 6913355 | |||||
| chr18:6913379
|
A | G | 32 | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(29): Show | 184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
3_prime_UTR_variant | MODIFIER | c.*1225A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 18/18 | 1225 | chr18 | 6913379 | |||||
| chr18:6913421
|
T | C | 33 | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(30): Show | 186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
3_prime_UTR_variant | MODIFIER | c.*1267T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 18/18 | 1267 | chr18 | 6913421 | |||||
| chr18:6913448
|
T | C | 32 | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(29): Show | 184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
3_prime_UTR_variant | MODIFIER | c.*1294T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 18/18 | 1294 | chr18 | 6913448 | |||||
| chr18:6913535
|
C | T | 8 | a0001c0003t0003a0001c0003t0015a0001c0010t0003others(5): Show | 47 | HG00280.hp2 HG00741.hp2 HG01081.hp1 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*1381C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 18/18 | 1381 | chr18 | 6913535 | |||||
| chr18:6913574
|
C | A | 31 | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(28): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
3_prime_UTR_variant | MODIFIER | c.*1420C>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 18/18 | 1420 | chr18 | 6913574 | |||||
| chr18:6913627
|
AT | A | 31 | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(28): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
3_prime_UTR_variant | MODIFIER | c.*1475delT | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 18/18 | 1475 | INFO_REALIGN_3_PRIME | chr18 | 6913627 | ||||
| chr18:6913672
|
T | C | 31 | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(28): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
3_prime_UTR_variant | MODIFIER | c.*1518T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 18/18 | 1518 | chr18 | 6913672 | |||||
| chr18:6913675
|
A | G | 31 | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(28): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
3_prime_UTR_variant | MODIFIER | c.*1521A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 18/18 | 1521 | chr18 | 6913675 | |||||
| chr18:6913717
|
A | G | 31 | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(28): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
3_prime_UTR_variant | MODIFIER | c.*1563A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 18/18 | 1563 | chr18 | 6913717 | |||||
| chr18:6913734
|
A | AT | 27 | a0001c0001t0001a0001c0001t0007a0001c0001t0008others(24): Show | 175 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(172): Show |
3_prime_UTR_variant | MODIFIER | c.*1591dupT | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 18/18 | 1592 | INFO_REALIGN_3_PRIME | chr18 | 6913734 | ||||
| chr18:6913734
|
A | ATT | 3 | a0001c0020t0023a0006c0009t0005a0008c0011t0005 | 5 | HG02615.hp1 HG02630.hp2 HG03471.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1590_*1591dupTT | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 18/18 | 1592 | INFO_REALIGN_3_PRIME | chr18 | 6913734 | ||||
| chr18:6913842
|
A | G | 31 | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(28): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
3_prime_UTR_variant | MODIFIER | c.*1688A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 18/18 | 1688 | chr18 | 6913842 | |||||
| chr18:6913857
|
G | T | 1 | a0001c0019t0021 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1703G>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 18/18 | 1703 | chr18 | 6913857 | |||||
| chr18:6913976
|
G | A | 31 | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(28): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
3_prime_UTR_variant | MODIFIER | c.*1822G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 18/18 | 1822 | chr18 | 6913976 | |||||
| chr18:6914034
|
A | G | 31 | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(28): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
3_prime_UTR_variant | MODIFIER | c.*1880A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 18/18 | 1880 | chr18 | 6914034 | |||||
| chr18:6914055
|
C | G | 31 | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(28): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
3_prime_UTR_variant | MODIFIER | c.*1901C>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 18/18 | 1901 | chr18 | 6914055 | |||||
| chr18:6914094
|
G | A | 2 | a0006c0009t0005a0008c0011t0005 | 4 | HG02615.hp1 HG02630.hp2 HG03471.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1940G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 18/18 | 1940 | chr18 | 6914094 | |||||
| chr18:6914264
|
G | A | 1 | a0002c0002t0012 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2110G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 18/18 | 2110 | chr18 | 6914264 | |||||
| chr18:6914300
|
G | A | 1 | a0002c0002t0013 | 1 | NA18991.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2146G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 18/18 | 2146 | chr18 | 6914300 | |||||
| chr18:6914338
|
G | T | 1 | a0001c0018t0020 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2184G>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 18/18 | 2184 | chr18 | 6914338 | |||||
| chr18:6914399
|
C | G | 1 | a0001c0001t0019 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2245C>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 18/18 | 2245 | chr18 | 6914399 | |||||
| chr18:6914459
|
T | C | 30 | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(27): Show | 182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
3_prime_UTR_variant | MODIFIER | c.*2305T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 18/18 | 2305 | chr18 | 6914459 | |||||
| chr18:6914460
|
T | C | 1 | a0001c0001t0018 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2306T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 18/18 | 2306 | chr18 | 6914460 | |||||
| chr18:6914589
|
TA | T | 31 | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(28): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
3_prime_UTR_variant | MODIFIER | c.*2436delA | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 18/18 | 2436 | chr18 | 6914589 | |||||
| chr18:6914679
|
A | G | 1 | a0001c0001t0017 | 1 | HG02602.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2525A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 18/18 | 2525 | chr18 | 6914679 | |||||
| chr18:6914983
|
A | C | 2 | a0001c0001t0009a0006c0009t0009 | 3 | HG01891.hp1 HG02895.hp2 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2829A>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 18/18 | 2829 | chr18 | 6914983 | |||||
| chr18:6915214
|
G | T | 2 | a0001c0001t0008a0001c0001t0018 | 4 | HG02818.hp2 HG03098.hp2 HG03453.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3060G>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 18/18 | 3060 | chr18 | 6915214 | |||||
| chr18:6915220
|
A | G | 31 | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(28): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
3_prime_UTR_variant | MODIFIER | c.*3066A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 18/18 | 3066 | chr18 | 6915220 | |||||
| chr18:6915275
|
G | A | 1 | a0001c0001t0016 | 1 | HG00735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3121G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 18/18 | 3121 | chr18 | 6915275 | |||||
| chr18:6915519
|
A | AT | 31 | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(28): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
3_prime_UTR_variant | MODIFIER | c.*3372dupT | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 18/18 | 3373 | INFO_REALIGN_3_PRIME | chr18 | 6915519 | ||||
| chr18:6915542
|
CAACT | C | 31 | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(28): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
3_prime_UTR_variant | MODIFIER | c.*3390_*3393delACTA | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 18/18 | 3390 | INFO_REALIGN_3_PRIME | chr18 | 6915542 | ||||
| chr18:6915587
|
C | T | 1 | a0001c0001t0007 | 3 | HG02896.hp1 HG02897.hp2 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3433C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 18/18 | 3433 | chr18 | 6915587 | |||||
| chr18:6915624
|
A | G | 2 | a0002c0002t0004a0004c0007t0004 | 4 | HG01884.hp1 HG02280.hp2 HG02451.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3470A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 18/18 | 3470 | chr18 | 6915624 | |||||
| chr18:6915640
|
T | C | 31 | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(28): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
3_prime_UTR_variant | MODIFIER | c.*3486T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 18/18 | 3486 | chr18 | 6915640 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr18:6730017
|
G | C | 142 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(139): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.122+74G>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6730017 | ||||||
| chr18:6730171
|
TAGCA | T | 136 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0019others(133): Show | 136 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(133): Show |
intron_variant | MODIFIER | c.122+233_122+236del others(4): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6730171 | |||||
| chr18:6730188
|
G | A | 136 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0019others(133): Show | 136 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(133): Show |
intron_variant | MODIFIER | c.122+245G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6730188 | ||||||
| chr18:6730216
|
C | CATATATA others(13): Show |
1 | a0001c0018t0020g0007 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.122+275_122+276ins others(20): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6730216 | |||||
| chr18:6730216
|
C | CATATATG others(21): Show |
1 | a0001c0001t0019g0008 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.122+275_122+276ins others(28): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6730216 | |||||
| chr18:6730219
|
G | A | 2 | a0001c0001t0019g0008a0001c0018t0020g0007 | 2 | HG02886.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.122+276G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6730219 | ||||||
| chr18:6730219
|
G | GTA | 56 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0019others(53): Show | 56 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(53): Show |
intron_variant | MODIFIER | c.122+277_122+278ins others(2): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6730219 | |||||
| chr18:6730219
|
G | GTATATAT others(21): Show |
1 | a0002c0002t0002g0009 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.122+277_122+278ins others(28): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6730219 | |||||
| chr18:6730219
|
G | GTATATAT others(3): Show |
2 | a0001c0001t0022g0067a0001c0003t0003g0068 | 2 | HG02630.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.122+277_122+278ins others(10): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6730219 | |||||
| chr18:6730219
|
G | GTATATAT others(7): Show |
3 | a0001c0001t0001g0070a0001c0001t0001g0071a0007c0008t0002g0069 | 3 | HG00280.hp1 HG03209.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.122+277_122+278ins others(14): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6730219 | |||||
| chr18:6730219
|
G | GTATATAT others(9): Show |
2 | a0001c0001t0001g0072a0001c0019t0021g0073 | 2 | HG03579.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.122+277_122+278ins others(16): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6730219 | |||||
| chr18:6730219
|
G | GTATATAT others(11): Show |
7 | a0001c0001t0001g0080a0001c0001t0001g0082a0001c0001t0016g0081others(4): Show | 7 | HG00438.hp1 HG00735.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.122+277_122+278ins others(18): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6730219 | |||||
| chr18:6730219
|
G | GTATATAT others(13): Show |
7 | a0001c0003t0003g0087a0001c0003t0003g0091a0001c0010t0003g0089others(4): Show | 7 | HG00099.hp1 HG02922.hp1 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.122+277_122+278ins others(20): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6730219 | |||||
| chr18:6730219
|
G | GTATATAT others(15): Show |
5 | a0001c0001t0001g0097a0001c0003t0003g0094a0001c0003t0003g0095others(2): Show | 5 | HG02523.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.122+277_122+278ins others(22): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6730219 | |||||
| chr18:6730219
|
G | GTATATAT others(17): Show |
3 | a0001c0001t0001g0100a0001c0001t0001g0102a0001c0020t0023g0101 | 3 | HG02451.hp1 HG04184.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.122+277_122+278ins others(24): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6730219 | |||||
| chr18:6730219
|
G | GTATATAT others(19): Show |
7 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0003t0003g0104others(4): Show | 7 | HG01099.hp1 HG01175.hp2 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.122+277_122+278ins others(26): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6730219 | |||||
| chr18:6730219
|
G | GTATATAT others(21): Show |
3 | a0001c0001t0001g0113a0001c0001t0018g0111a0003c0004t0001g0112 | 3 | HG02818.hp2 HG04115.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.122+277_122+278ins others(28): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6730219 | |||||
| chr18:6730219
|
G | GTATATAT others(23): Show |
1 | a0001c0010t0003g0114 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.122+277_122+278ins others(30): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6730219 | |||||
| chr18:6730219
|
G | GTATGTAT others(9): Show |
1 | a0004c0007t0004g0115 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.122+277_122+278ins others(16): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6730219 | |||||
| chr18:6730219
|
G | GTATGTAT others(11): Show |
2 | a0001c0001t0007g0116a0001c0001t0007g0117 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.122+277_122+278ins others(18): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6730219 | |||||
| chr18:6730219
|
G | GTATGTAT others(19): Show |
1 | a0001c0001t0017g0118 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.122+277_122+278ins others(26): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6730219 | |||||
| chr18:6730219
|
G | GTATGTAT others(23): Show |
1 | a0001c0003t0003g0119 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.122+277_122+278ins others(30): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6730219 | |||||
| chr18:6730219
|
G | GTATGTAT others(25): Show |
1 | a0003c0023t0001g0120 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.122+277_122+278ins others(32): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6730219 | |||||
| chr18:6730219
|
G | GTATGTAT others(27): Show |
2 | a0001c0001t0001g0121a0001c0003t0003g0122 | 2 | HG02615.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.122+277_122+278ins others(34): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6730219 | |||||
| chr18:6730219
|
G | GTATGTAT others(29): Show |
1 | a0001c0003t0003g0123 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.122+277_122+278ins others(36): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6730219 | |||||
| chr18:6730219
|
G | GTATGTAT others(31): Show |
1 | a0001c0001t0001g0124 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.122+277_122+278ins others(38): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6730219 | |||||
| chr18:6730219
|
G | GTATGTAT others(23): Show |
1 | a0003c0004t0001g0125 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.122+277_122+278ins others(30): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6730219 | |||||
| chr18:6730219
|
G | GTATGTAT others(27): Show |
5 | a0001c0001t0001g0128a0001c0001t0001g0129a0002c0002t0002g0126others(2): Show | 5 | NA18956.hp2 NA18959.hp1 NA19082.hp1 others(2): Show |
intron_variant | MODIFIER | c.122+277_122+278ins others(34): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6730219 | |||||
| chr18:6730219
|
G | GTATGTAT others(29): Show |
5 | a0002c0002t0002g0131a0002c0002t0002g0134a0002c0002t0002g0135others(2): Show | 5 | HG00408.hp1 HG02735.hp2 NA18747.hp1 others(2): Show |
intron_variant | MODIFIER | c.122+277_122+278ins others(36): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6730219 | |||||
| chr18:6730219
|
G | GTATGTAT others(31): Show |
3 | a0002c0002t0002g0137a0002c0002t0002g0138a0003c0004t0001g0136 | 3 | HG02080.hp1 NA19010.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.122+277_122+278ins others(38): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6730219 | |||||
| chr18:6730219
|
G | GTATGTAT others(33): Show |
1 | a0001c0001t0001g0139 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.122+277_122+278ins others(40): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6730219 | |||||
| chr18:6730219
|
G | GTATGTAT others(35): Show |
1 | a0002c0005t0002g0140 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.122+277_122+278ins others(42): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6730219 | |||||
| chr18:6730219
|
G | GTATGTAT others(31): Show |
1 | a0001c0001t0001g0141 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.122+277_122+278ins others(38): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6730219 | |||||
| chr18:6730221
|
G | A | 135 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0019others(132): Show | 135 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.122+278G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6730221 | ||||||
| chr18:6730221
|
G | GTA | 6 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0008g0171others(3): Show | 6 | HG01891.hp1 HG02559.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.122+293_122+294dup others(2): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6730221 | |||||
| chr18:6730221
|
G | GTATA | 69 | a0001c0001t0001g0179a0001c0001t0001g0181a0001c0001t0001g0182others(66): Show | 69 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.122+291_122+294dup others(4): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6730221 | |||||
| chr18:6730221
|
G | GTATATA | 8 | a0001c0001t0009g0245a0002c0002t0002g0243a0002c0002t0002g0244others(5): Show | 8 | HG02895.hp2 HG03710.hp1 NA18966.hp1 others(5): Show |
intron_variant | MODIFIER | c.122+289_122+294dup others(6): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6730221 | |||||
| chr18:6730221
|
G | GTATATAT others(21): Show |
1 | a0010c0014t0001g0142 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.122+294_122+295ins others(28): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6730221 | |||||
| chr18:6730234
|
T | TATATATA others(19): Show |
1 | a0003c0004t0001g0093 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.122+294_122+295ins others(26): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6730234 | |||||
| chr18:6730236
|
T | TATATATA others(13): Show |
4 | a0001c0001t0001g0075a0001c0001t0008g0074a0001c0003t0003g0076others(1): Show | 4 | HG01256.hp1 HG02965.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.122+294_122+295ins others(20): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6730236 | |||||
| chr18:6730236
|
T | TATATATA others(15): Show |
1 | a0001c0003t0003g0085 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.122+294_122+295ins others(22): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6730236 | |||||
| chr18:6730236
|
T | TATATATA others(19): Show |
1 | a0002c0002t0002g0099 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.122+294_122+295ins others(26): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6730236 | |||||
| chr18:6730236
|
T | TATATATA others(21): Show |
1 | a0002c0002t0002g0103 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.122+294_122+295ins others(28): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6730236 | |||||
| chr18:6730461
|
T | C | 12 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(9): Show | 12 | HG01243.hp2 HG01346.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.122+518T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6730461 | ||||||
| chr18:6730501
|
CATT | C | 7 | a0001c0001t0007g0116a0001c0001t0007g0117a0001c0001t0022g0067others(4): Show | 7 | HG01884.hp1 HG02630.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.122+562_122+564del others(3): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6730501 | |||||
| chr18:6730712
|
A | G | 64 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0019others(61): Show | 64 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(61): Show |
intron_variant | MODIFIER | c.122+769A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6730712 | ||||||
| chr18:6730717
|
A | C | 136 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0019others(133): Show | 136 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(133): Show |
intron_variant | MODIFIER | c.122+774A>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6730717 | ||||||
| chr18:6730720
|
A | C | 136 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0019others(133): Show | 136 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(133): Show |
intron_variant | MODIFIER | c.122+777A>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6730720 | ||||||
| chr18:6730805
|
G | A | 12 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(9): Show | 12 | HG01243.hp2 HG01346.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.122+862G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6730805 | ||||||
| chr18:6730904
|
G | A | 2 | a0001c0001t0006g0155a0001c0003t0003g0156 | 2 | HG02109.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.122+961G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6730904 | ||||||
| chr18:6730947
|
T | C | 64 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0019others(61): Show | 64 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(61): Show |
intron_variant | MODIFIER | c.122+1004T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6730947 | ||||||
| chr18:6731041
|
A | G | 1 | a0002c0005t0002g0240 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.122+1098A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6731041 | ||||||
| chr18:6731042
|
T | C | 1 | a0002c0002t0002g0011 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.122+1099T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6731042 | ||||||
| chr18:6731103
|
C | A | 1 | a0010c0014t0001g0142 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.122+1160C>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6731103 | ||||||
| chr18:6731133
|
C | A | 234 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(231): Show | 234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.122+1190C>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6731133 | ||||||
| chr18:6731136
|
A | G | 12 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(9): Show | 12 | HG01243.hp2 HG01346.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.122+1193A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6731136 | ||||||
| chr18:6731136
|
AT | A | 64 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0019others(61): Show | 64 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(61): Show |
intron_variant | MODIFIER | c.122+1201delT | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6731136 | |||||
| chr18:6731291
|
C | CGT | 85 | a0001c0001t0001g0072a0001c0001t0001g0100a0001c0001t0001g0179others(82): Show | 85 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.122+1369_122+1370d others(4): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6731291 | |||||
| chr18:6731291
|
CGT | C | 6 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(3): Show | 6 | HG01515.hp1 HG01891.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.122+1369_122+1370d others(4): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6731291 | |||||
| chr18:6731291
|
CGTGT | C | 7 | a0001c0001t0007g0116a0001c0001t0007g0117a0001c0001t0022g0067others(4): Show | 7 | HG01884.hp1 HG02630.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.122+1367_122+1370d others(6): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6731291 | |||||
| chr18:6731524
|
G | C | 1 | a0001c0001t0008g0171 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.122+1581G>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6731524 | ||||||
| chr18:6731526
|
G | A | 10 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0018g0111others(7): Show | 10 | HG01175.hp2 HG01243.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.122+1583G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6731526 | ||||||
| chr18:6731526
|
G | C | 1 | a0001c0003t0003g0002 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.122+1583G>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6731526 | ||||||
| chr18:6731533
|
G | A | 1 | a0001c0003t0003g0091 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.122+1590G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6731533 | ||||||
| chr18:6731656
|
A | G | 63 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0026others(60): Show | 63 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(60): Show |
intron_variant | MODIFIER | c.122+1713A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6731656 | ||||||
| chr18:6731942
|
G | A | 7 | a0001c0001t0007g0116a0001c0001t0007g0117a0001c0001t0022g0067others(4): Show | 7 | HG01884.hp1 HG02630.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.122+1999G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6731942 | ||||||
| chr18:6732102
|
GT | G | 216 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(213): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.122+2170delT | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6732102 | |||||
| chr18:6732200
|
C | T | 1 | a0002c0002t0002g0066 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.122+2257C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6732200 | ||||||
| chr18:6732211
|
C | G | 3 | a0001c0003t0003g0077a0002c0002t0002g0099a0002c0002t0002g0103 | 3 | HG00741.hp1 HG01256.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.122+2268C>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6732211 | ||||||
| chr18:6732271
|
A | T | 4 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0009g0005others(1): Show | 4 | HG01891.hp1 HG02559.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.122+2328A>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6732271 | ||||||
| chr18:6732462
|
A | G | 65 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0019others(62): Show | 65 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(62): Show |
intron_variant | MODIFIER | c.122+2519A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6732462 | ||||||
| chr18:6732512
|
T | C | 1 | a0002c0002t0002g0172 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.122+2569T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6732512 | ||||||
| chr18:6732630
|
T | C | 234 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(231): Show | 234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.122+2687T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6732630 | ||||||
| chr18:6732657
|
A | G | 2 | a0002c0002t0002g0099a0002c0002t0002g0103 | 2 | HG00741.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.122+2714A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6732657 | ||||||
| chr18:6732754
|
A | G | 1 | a0001c0001t0019g0008 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.122+2811A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6732754 | ||||||
| chr18:6732847
|
A | G | 64 | a0001c0001t0001g0072a0001c0001t0001g0075a0001c0001t0001g0080others(61): Show | 64 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.122+2904A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6732847 | ||||||
| chr18:6732864
|
G | A | 1 | a0003c0004t0001g0173 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.122+2921G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6732864 | ||||||
| chr18:6733012
|
A | C | 129 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0019others(126): Show | 129 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.122+3069A>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6733012 | ||||||
| chr18:6733042
|
C | T | 13 | a0001c0001t0001g0080a0001c0001t0001g0106a0001c0001t0001g0107others(10): Show | 13 | HG01175.hp2 HG01243.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.122+3099C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6733042 | ||||||
| chr18:6733059
|
C | T | 1 | a0002c0002t0002g0065 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.122+3116C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6733059 | ||||||
| chr18:6733282
|
T | C | 1 | a0010c0014t0001g0142 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.122+3339T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6733282 | ||||||
| chr18:6733371
|
T | C | 1 | a0002c0002t0002g0174 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.122+3428T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6733371 | ||||||
| chr18:6733416
|
G | A | 64 | a0001c0001t0001g0072a0001c0001t0001g0075a0001c0001t0001g0080others(61): Show | 64 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.122+3473G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6733416 | ||||||
| chr18:6733454
|
C | T | 1 | a0003c0004t0001g0125 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.122+3511C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6733454 | ||||||
| chr18:6733597
|
A | C | 65 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0019others(62): Show | 65 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(62): Show |
intron_variant | MODIFIER | c.122+3654A>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6733597 | ||||||
| chr18:6733690
|
A | G | 2 | a0001c0001t0006g0155a0001c0003t0003g0156 | 2 | HG02109.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.122+3747A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6733690 | ||||||
| chr18:6733836
|
C | A | 65 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0019others(62): Show | 65 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(62): Show |
intron_variant | MODIFIER | c.122+3893C>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6733836 | ||||||
| chr18:6733895
|
AC | A | 7 | a0001c0001t0007g0116a0001c0001t0007g0117a0001c0001t0022g0067others(4): Show | 7 | HG01884.hp1 HG02630.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.122+3954delC | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6733895 | |||||
| chr18:6734036
|
A | G | 1 | a0004c0007t0002g0238 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.122+4093A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6734036 | ||||||
| chr18:6734087
|
A | G | 1 | a0001c0003t0003g0123 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.122+4144A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6734087 | ||||||
| chr18:6734129
|
C | G | 82 | a0001c0001t0001g0168a0001c0001t0001g0179a0001c0001t0001g0181others(79): Show | 82 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.122+4186C>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6734129 | ||||||
| chr18:6734211
|
T | A | 6 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(3): Show | 6 | HG01515.hp1 HG01891.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.122+4268T>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6734211 | ||||||
| chr18:6734218
|
A | G | 9 | a0001c0001t0001g0230a0001c0001t0001g0232a0001c0001t0001g0236others(6): Show | 9 | HG00140.hp1 HG00280.hp2 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.122+4275A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6734218 | ||||||
| chr18:6734222
|
A | G | 1 | a0002c0002t0002g0083 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.122+4279A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6734222 | ||||||
| chr18:6734342
|
A | G | 1 | a0003c0004t0001g0064 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.122+4399A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6734342 | ||||||
| chr18:6734693
|
C | T | 64 | a0001c0001t0001g0072a0001c0001t0001g0075a0001c0001t0001g0080others(61): Show | 64 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.122+4750C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6734693 | ||||||
| chr18:6735033
|
C | T | 2 | a0003c0013t0011g0062a0003c0013t0011g0063 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.122+5090C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6735033 | ||||||
| chr18:6735326
|
C | T | 1 | a0010c0014t0001g0142 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.122+5383C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6735326 | ||||||
| chr18:6735356
|
A | G | 2 | a0001c0001t0001g0080a0001c0010t0003g0098 | 2 | HG02258.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.122+5413A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6735356 | ||||||
| chr18:6735364
|
C | T | 6 | a0001c0001t0001g0072a0001c0001t0001g0100a0001c0003t0003g0087others(3): Show | 6 | HG01081.hp2 HG02451.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.122+5421C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6735364 | ||||||
| chr18:6735424
|
C | T | 1 | a0001c0001t0001g0237 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.122+5481C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6735424 | ||||||
| chr18:6735468
|
C | T | 65 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0019others(62): Show | 65 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(62): Show |
intron_variant | MODIFIER | c.122+5525C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6735468 | ||||||
| chr18:6735493
|
A | T | 1 | a0001c0001t0001g0124 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.122+5550A>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6735493 | ||||||
| chr18:6735555
|
GT | G | 43 | a0001c0001t0001g0072a0001c0001t0001g0075a0001c0001t0001g0080others(40): Show | 43 | HG00099.hp1 HG00621.hp2 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.122+5629delT | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6735555 | |||||
| chr18:6735555
|
GTT | G | 39 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(36): Show | 39 | HG00408.hp1 HG00544.hp1 HG01243.hp2 others(36): Show |
intron_variant | MODIFIER | c.122+5628_122+5629d others(4): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6735555 | |||||
| chr18:6735674
|
C | T | 1 | a0010c0014t0001g0142 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.122+5731C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6735674 | ||||||
| chr18:6735678
|
C | G | 1 | a0001c0003t0003g0123 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.122+5735C>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6735678 | ||||||
| chr18:6735766
|
G | A | 5 | a0001c0001t0007g0116a0001c0001t0007g0117a0001c0001t0022g0067others(2): Show | 5 | HG01884.hp1 HG02630.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.122+5823G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6735766 | ||||||
| chr18:6735869
|
C | A | 1 | a0010c0014t0001g0142 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.122+5926C>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6735869 | ||||||
| chr18:6735869
|
C | T | 1 | a0001c0003t0003g0077 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.122+5926C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6735869 | ||||||
| chr18:6735932
|
C | T | 14 | a0001c0001t0001g0080a0001c0001t0001g0106a0001c0001t0001g0107others(11): Show | 14 | HG01175.hp2 HG01243.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.122+5989C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6735932 | ||||||
| chr18:6735944
|
A | C | 1 | a0001c0001t0001g0228 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.122+6001A>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6735944 | ||||||
| chr18:6735945
|
C | A | 6 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(3): Show | 6 | HG01515.hp1 HG01891.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.122+6002C>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6735945 | ||||||
| chr18:6735949
|
C | T | 2 | a0001c0003t0003g0169a0001c0003t0003g0170 | 2 | HG02965.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.122+6006C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6735949 | ||||||
| chr18:6735972
|
G | A | 12 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(9): Show | 12 | HG01243.hp2 HG01346.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.122+6029G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6735972 | ||||||
| chr18:6736014
|
C | T | 1 | a0002c0005t0002g0061 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.122+6071C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6736014 | ||||||
| chr18:6736121
|
C | G | 52 | a0001c0001t0001g0072a0001c0001t0001g0075a0001c0001t0001g0082others(49): Show | 52 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.122+6178C>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6736121 | ||||||
| chr18:6736126
|
A | G | 77 | a0001c0001t0001g0179a0001c0001t0001g0181a0001c0001t0001g0182others(74): Show | 77 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.122+6183A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6736126 | ||||||
| chr18:6736134
|
A | G | 1 | a0001c0003t0003g0060 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.122+6191A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6736134 | ||||||
| chr18:6736241
|
T | C | 234 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(231): Show | 234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.122+6298T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6736241 | ||||||
| chr18:6736457
|
C | T | 2 | a0001c0001t0006g0155a0001c0003t0003g0156 | 2 | HG02109.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.122+6514C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6736457 | ||||||
| chr18:6736515
|
G | A | 6 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(3): Show | 6 | HG01515.hp1 HG01891.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.122+6572G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6736515 | ||||||
| chr18:6736530
|
G | A | 1 | a0001c0003t0003g0091 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.122+6587G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6736530 | ||||||
| chr18:6736533
|
A | G | 1 | a0003c0004t0001g0227 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.122+6590A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6736533 | ||||||
| chr18:6736538
|
G | A | 1 | a0001c0001t0001g0139 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.122+6595G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6736538 | ||||||
| chr18:6736578
|
TA | T | 78 | a0001c0001t0001g0179a0001c0001t0001g0181a0001c0001t0001g0182others(75): Show | 78 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.122+6647delA | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6736578 | |||||
| chr18:6736591
|
T | A | 14 | a0001c0001t0001g0080a0001c0001t0001g0106a0001c0001t0001g0107others(11): Show | 14 | HG01175.hp2 HG01243.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.122+6648T>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6736591 | ||||||
| chr18:6736603
|
C | T | 1 | a0005c0006t0003g0226 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.122+6660C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6736603 | ||||||
| chr18:6736607
|
C | T | 1 | a0001c0001t0008g0171 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.122+6664C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6736607 | ||||||
| chr18:6736619
|
C | T | 1 | a0002c0002t0002g0135 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.122+6676C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6736619 | ||||||
| chr18:6736672
|
A | T | 2 | a0001c0001t0001g0075a0001c0003t0003g0076 | 2 | HG02965.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.122+6729A>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6736672 | ||||||
| chr18:6736681
|
A | G | 1 | a0002c0002t0004g0059 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.122+6738A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6736681 | ||||||
| chr18:6736747
|
C | CA | 18 | a0001c0001t0001g0080a0001c0001t0001g0106a0001c0001t0001g0107others(15): Show | 18 | HG01175.hp2 HG01243.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.122+6815dupA | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6736747 | |||||
| chr18:6736747
|
C | CAA | 71 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0019others(68): Show | 71 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(68): Show |
intron_variant | MODIFIER | c.122+6814_122+6815d others(4): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6736747 | |||||
| chr18:6736758
|
AC | A | 44 | a0001c0001t0001g0075a0001c0001t0001g0097a0001c0001t0001g0100others(41): Show | 44 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.122+6816delC | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6736758 | ||||||
| chr18:6736759
|
C | A | 188 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(185): Show | 188 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.122+6816C>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6736759 | ||||||
| chr18:6736780
|
A | ATTAAATG others(25): Show |
12 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(9): Show | 12 | HG01243.hp2 HG01346.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.122+6844_122+6875d others(34): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6736780 | |||||
| chr18:6736950
|
A | G | 2 | a0001c0001t0006g0155a0001c0003t0003g0156 | 2 | HG02109.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.122+7007A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6736950 | ||||||
| chr18:6736993
|
TCATTCCA others(8): Show |
T | 64 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0019others(61): Show | 64 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(61): Show |
intron_variant | MODIFIER | c.122+7052_122+7066d others(17): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6736993 | |||||
| chr18:6737073
|
G | A | 234 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(231): Show | 234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.122+7130G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6737073 | ||||||
| chr18:6737092
|
A | G | 15 | a0001c0001t0001g0082a0001c0001t0001g0097a0001c0001t0001g0102others(12): Show | 15 | HG00099.hp1 HG00621.hp2 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.122+7149A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6737092 | ||||||
| chr18:6737591
|
T | C | 21 | a0001c0001t0001g0080a0001c0001t0001g0106a0001c0001t0001g0107others(18): Show | 21 | HG01175.hp2 HG01243.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.122+7648T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6737591 | ||||||
| chr18:6737647
|
T | G | 1 | a0005c0006t0003g0177 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.122+7704T>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6737647 | ||||||
| chr18:6737711
|
A | C | 51 | a0001c0001t0001g0072a0001c0001t0001g0075a0001c0001t0001g0082others(48): Show | 51 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(48): Show |
intron_variant | MODIFIER | c.122+7768A>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6737711 | ||||||
| chr18:6737788
|
C | G | 50 | a0001c0001t0001g0072a0001c0001t0001g0075a0001c0001t0001g0097others(47): Show | 50 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.122+7845C>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6737788 | ||||||
| chr18:6737805
|
A | G | 51 | a0001c0001t0001g0072a0001c0001t0001g0075a0001c0001t0001g0082others(48): Show | 51 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(48): Show |
intron_variant | MODIFIER | c.122+7862A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6737805 | ||||||
| chr18:6737831
|
C | T | 1 | a0001c0001t0001g0100 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.122+7888C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6737831 | ||||||
| chr18:6738551
|
G | C | 2 | a0004c0007t0002g0178a0005c0006t0003g0177 | 2 | NA18977.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.122+8608G>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6738551 | ||||||
| chr18:6738608
|
TA | T | 116 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0018others(113): Show | 116 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(113): Show |
intron_variant | MODIFIER | c.122+8669delA | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6738608 | |||||
| chr18:6738917
|
A | G | 1 | a0001c0003t0003g0085 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.122+8974A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6738917 | ||||||
| chr18:6738944
|
C | T | 1 | a0010c0014t0001g0142 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.122+9001C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6738944 | ||||||
| chr18:6739102
|
C | T | 15 | a0001c0001t0001g0082a0001c0001t0001g0097a0001c0001t0001g0102others(12): Show | 15 | HG00099.hp1 HG00621.hp2 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.122+9159C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6739102 | ||||||
| chr18:6739291
|
A | T | 64 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0019others(61): Show | 64 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(61): Show |
intron_variant | MODIFIER | c.122+9348A>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6739291 | ||||||
| chr18:6739339
|
T | A | 21 | a0001c0001t0001g0080a0001c0001t0001g0106a0001c0001t0001g0107others(18): Show | 21 | HG01175.hp2 HG01243.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.122+9396T>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6739339 | ||||||
| chr18:6739519
|
A | G | 17 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0139others(14): Show | 17 | HG00408.hp1 HG00544.hp1 HG02080.hp1 others(14): Show |
intron_variant | MODIFIER | c.122+9576A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6739519 | ||||||
| chr18:6739537
|
A | C | 1 | a0003c0004t0001g0241 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.122+9594A>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6739537 | ||||||
| chr18:6739625
|
A | T | 21 | a0001c0001t0001g0080a0001c0001t0001g0106a0001c0001t0001g0107others(18): Show | 21 | HG01175.hp2 HG01243.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.122+9682A>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6739625 | ||||||
| chr18:6739645
|
T | TTC | 16 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0106others(13): Show | 16 | HG01175.hp2 HG01243.hp1 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.122+9728_122+9729d others(4): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6739645 | |||||
| chr18:6739645
|
T | TTCTC | 90 | a0001c0001t0001g0080a0001c0001t0001g0179a0001c0001t0001g0181others(87): Show | 90 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.122+9726_122+9729d others(6): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6739645 | |||||
| chr18:6739645
|
T | TTCTCTCT others(3): Show |
2 | a0001c0001t0001g0151a0008c0011t0005g0152 | 2 | HG01243.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.122+9720_122+9729d others(12): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6739645 | |||||
| chr18:6739645
|
T | TTCTCTCT others(7): Show |
6 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0008g0143others(3): Show | 6 | HG01346.hp1 HG02280.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.122+9716_122+9729d others(16): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6739645 | |||||
| chr18:6739645
|
T | TTCTCTCT others(9): Show |
2 | a0001c0003t0003g0145a0007c0008t0002g0146 | 2 | HG02922.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.122+9714_122+9729d others(18): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6739645 | |||||
| chr18:6739714
|
G | A | 2 | a0002c0002t0002g0014a0002c0002t0002g0015 | 2 | HG02155.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.122+9771G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6739714 | ||||||
| chr18:6739855
|
C | CT | 7 | a0001c0001t0007g0116a0001c0001t0007g0117a0001c0001t0022g0067others(4): Show | 7 | HG01884.hp1 HG02630.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.122+9928dupT | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6739855 | |||||
| chr18:6739855
|
CT | C | 72 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(69): Show | 72 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(69): Show |
intron_variant | MODIFIER | c.122+9928delT | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6739855 | |||||
| chr18:6739876
|
C | T | 96 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(93): Show | 96 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.122+9933C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6739876 | ||||||
| chr18:6739981
|
A | G | 2 | a0002c0002t0002g0224a0003c0004t0001g0248 | 2 | HG00597.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.122+10038A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6739981 | ||||||
| chr18:6740003
|
C | T | 1 | a0007c0008t0002g0166 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.122+10060C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6740003 | ||||||
| chr18:6740143
|
T | C | 232 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(229): Show | 232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.122+10200T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6740143 | ||||||
| chr18:6740268
|
A | G | 232 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(229): Show | 232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.122+10325A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6740268 | ||||||
| chr18:6740279
|
G | T | 64 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0019others(61): Show | 64 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(61): Show |
intron_variant | MODIFIER | c.122+10336G>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6740279 | ||||||
| chr18:6740332
|
C | A | 14 | a0001c0001t0001g0080a0001c0001t0001g0106a0001c0001t0001g0107others(11): Show | 14 | HG01175.hp2 HG01243.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.122+10389C>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6740332 | ||||||
| chr18:6740453
|
T | G | 79 | a0001c0001t0001g0179a0001c0001t0001g0181a0001c0001t0001g0182others(76): Show | 79 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.122+10510T>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6740453 | ||||||
| chr18:6740592
|
A | G | 34 | a0001c0001t0001g0211a0001c0001t0001g0215a0001c0001t0001g0216others(31): Show | 34 | HG00140.hp1 HG00280.hp2 HG00597.hp2 others(31): Show |
intron_variant | MODIFIER | c.122+10649A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6740592 | ||||||
| chr18:6740786
|
T | C | 97 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(94): Show | 97 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.122+10843T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6740786 | ||||||
| chr18:6740797
|
A | G | 2 | a0001c0001t0001g0075a0001c0003t0003g0076 | 2 | HG02965.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.122+10854A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6740797 | ||||||
| chr18:6740877
|
T | G | 234 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(231): Show | 234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.122+10934T>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6740877 | ||||||
| chr18:6740924
|
C | T | 10 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0018g0111others(7): Show | 10 | HG01175.hp2 HG01243.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.122+10981C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6740924 | ||||||
| chr18:6741258
|
G | T | 1 | a0004c0007t0002g0056 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.122+11315G>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6741258 | ||||||
| chr18:6741349
|
G | A | 64 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0019others(61): Show | 64 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(61): Show |
intron_variant | MODIFIER | c.122+11406G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6741349 | ||||||
| chr18:6741488
|
G | A | 17 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0139others(14): Show | 17 | HG00408.hp1 HG00544.hp1 HG02080.hp1 others(14): Show |
intron_variant | MODIFIER | c.122+11545G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6741488 | ||||||
| chr18:6741503
|
C | G | 3 | a0001c0001t0001g0012a0001c0001t0001g0054a0001c0003t0003g0055 | 3 | HG00099.hp2 HG01496.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.122+11560C>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6741503 | ||||||
| chr18:6741565
|
C | A | 65 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0019others(62): Show | 65 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(62): Show |
intron_variant | MODIFIER | c.122+11622C>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6741565 | ||||||
| chr18:6741650
|
A | AT | 12 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(9): Show | 12 | HG01243.hp2 HG01346.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.122+11709dupT | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6741650 | |||||
| chr18:6741752
|
C | T | 12 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(9): Show | 12 | HG01243.hp2 HG01346.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.122+11809C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6741752 | ||||||
| chr18:6741787
|
C | T | 2 | a0001c0003t0003g0084a0001c0019t0021g0073 | 2 | HG02976.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.122+11844C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6741787 | ||||||
| chr18:6741914
|
C | T | 6 | a0001c0001t0001g0072a0001c0001t0001g0100a0001c0003t0003g0087others(3): Show | 6 | HG01081.hp2 HG02451.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.122+11971C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6741914 | ||||||
| chr18:6741960
|
A | C | 8 | a0001c0001t0001g0072a0001c0001t0001g0100a0001c0003t0003g0087others(5): Show | 8 | HG01081.hp2 HG01106.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.122+12017A>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6741960 | ||||||
| chr18:6741975
|
T | C | 65 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0019others(62): Show | 65 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(62): Show |
intron_variant | MODIFIER | c.122+12032T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6741975 | ||||||
| chr18:6742116
|
T | G | 21 | a0001c0001t0001g0080a0001c0001t0001g0106a0001c0001t0001g0107others(18): Show | 21 | HG01175.hp2 HG01243.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.122+12173T>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6742116 | ||||||
| chr18:6742169
|
C | CT | 10 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0102others(7): Show | 10 | HG00280.hp1 HG00438.hp1 HG00735.hp2 others(7): Show |
intron_variant | MODIFIER | c.122+12240dupT | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6742169 | |||||
| chr18:6742169
|
C | CTT | 57 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0019others(54): Show | 57 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.122+12239_122+1224 others(6): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6742169 | |||||
| chr18:6742358
|
T | C | 234 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(231): Show | 234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.122+12415T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6742358 | ||||||
| chr18:6742400
|
C | T | 1 | a0001c0003t0003g0123 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.122+12457C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6742400 | ||||||
| chr18:6742421
|
C | T | 1 | a0002c0002t0002g0083 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.122+12478C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6742421 | ||||||
| chr18:6742450
|
G | A | 2 | a0001c0001t0006g0155a0001c0003t0003g0156 | 2 | HG02109.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.122+12507G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6742450 | ||||||
| chr18:6742460
|
G | A | 2 | a0002c0002t0002g0099a0002c0002t0002g0103 | 2 | HG00741.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.122+12517G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6742460 | ||||||
| chr18:6742516
|
T | C | 1 | a0010c0014t0001g0142 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.122+12573T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6742516 | ||||||
| chr18:6742556
|
T | A | 5 | a0001c0001t0007g0116a0001c0001t0007g0117a0001c0001t0022g0067others(2): Show | 5 | HG01884.hp1 HG02630.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.122+12613T>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6742556 | ||||||
| chr18:6742575
|
A | G | 1 | a0001c0001t0001g0236 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.122+12632A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6742575 | ||||||
| chr18:6742612
|
T | C | 1 | a0001c0001t0001g0179 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.122+12669T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6742612 | ||||||
| chr18:6742690
|
G | A | 2 | a0001c0001t0001g0018a0001c0001t0001g0019 | 2 | HG00735.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.122+12747G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6742690 | ||||||
| chr18:6742846
|
A | G | 3 | a0001c0003t0003g0060a0001c0003t0003g0119a0001c0003t0003g0122 | 3 | HG02723.hp1 HG02735.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.122+12903A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6742846 | ||||||
| chr18:6742959
|
A | C | 50 | a0001c0001t0001g0072a0001c0001t0001g0075a0001c0001t0001g0097others(47): Show | 50 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.122+13016A>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6742959 | ||||||
| chr18:6743012
|
G | A | 2 | a0003c0004t0001g0020a0003c0004t0001g0021 | 2 | HG00558.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.122+13069G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6743012 | ||||||
| chr18:6743017
|
G | A | 234 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(231): Show | 234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.122+13074G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6743017 | ||||||
| chr18:6743429
|
T | A | 12 | a0001c0001t0001g0080a0001c0001t0001g0106a0001c0001t0001g0107others(9): Show | 12 | HG01175.hp2 HG01243.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.122+13486T>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6743429 | ||||||
| chr18:6743458
|
G | A | 49 | a0001c0001t0001g0072a0001c0001t0001g0075a0001c0001t0001g0097others(46): Show | 49 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.122+13515G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6743458 | ||||||
| chr18:6743704
|
T | A | 2 | a0001c0001t0019g0008a0001c0018t0020g0007 | 2 | HG02886.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.122+13761T>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6743704 | ||||||
| chr18:6743760
|
CAAG | C | 12 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(9): Show | 12 | HG01243.hp2 HG01346.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.122+13823_122+1382 others(7): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6743760 | |||||
| chr18:6743879
|
G | C | 1 | a0003c0004t0001g0173 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.122+13936G>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6743879 | ||||||
| chr18:6743881
|
C | T | 1 | a0002c0002t0002g0243 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.122+13938C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6743881 | ||||||
| chr18:6743916
|
C | T | 3 | a0001c0001t0001g0113a0001c0001t0016g0081a0002c0005t0002g0017 | 3 | HG00735.hp2 HG03239.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.122+13973C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6743916 | ||||||
| chr18:6743966
|
T | G | 1 | a0002c0002t0002g0244 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.122+14023T>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6743966 | ||||||
| chr18:6744248
|
G | A | 2 | a0001c0001t0006g0155a0001c0003t0003g0156 | 2 | HG02109.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.122+14305G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6744248 | ||||||
| chr18:6744260
|
A | C | 12 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(9): Show | 12 | HG01243.hp2 HG01346.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.122+14317A>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6744260 | ||||||
| chr18:6744431
|
C | T | 1 | a0004c0007t0002g0238 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.122+14488C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6744431 | ||||||
| chr18:6744646
|
A | G | 1 | a0001c0001t0001g0100 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.122+14703A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6744646 | ||||||
| chr18:6744938
|
G | A | 50 | a0001c0001t0001g0072a0001c0001t0001g0075a0001c0001t0001g0097others(47): Show | 50 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.122+14995G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6744938 | ||||||
| chr18:6744941
|
TTAA | T | 12 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(9): Show | 12 | HG01243.hp2 HG01346.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.122+15003_122+1500 others(7): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6744941 | |||||
| chr18:6745069
|
G | A | 6 | a0001c0001t0001g0075a0001c0001t0008g0074a0001c0003t0003g0076others(3): Show | 6 | HG00741.hp1 HG02965.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.122+15126G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6745069 | ||||||
| chr18:6745585
|
T | C | 2 | a0001c0001t0006g0155a0001c0003t0003g0156 | 2 | HG02109.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.122+15642T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6745585 | ||||||
| chr18:6745633
|
T | C | 1 | a0001c0003t0003g0123 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.122+15690T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6745633 | ||||||
| chr18:6745700
|
G | C | 66 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0019others(63): Show | 66 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(63): Show |
intron_variant | MODIFIER | c.122+15757G>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6745700 | ||||||
| chr18:6745714
|
A | G | 77 | a0001c0001t0001g0179a0001c0001t0001g0181a0001c0001t0001g0182others(74): Show | 77 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.122+15771A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6745714 | ||||||
| chr18:6745787
|
C | G | 2 | a0001c0001t0006g0155a0001c0003t0003g0156 | 2 | HG02109.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.122+15844C>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6745787 | ||||||
| chr18:6746259
|
T | C | 1 | a0010c0014t0001g0142 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.122+16316T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6746259 | ||||||
| chr18:6746318
|
C | T | 15 | a0001c0001t0001g0082a0001c0001t0001g0097a0001c0001t0001g0102others(12): Show | 15 | HG00099.hp1 HG00621.hp2 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.122+16375C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6746318 | ||||||
| chr18:6746393
|
A | G | 1 | a0001c0003t0003g0235 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.122+16450A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6746393 | ||||||
| chr18:6746395
|
T | C | 1 | a0002c0002t0013g0022 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.122+16452T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6746395 | ||||||
| chr18:6746407
|
T | G | 117 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(114): Show | 117 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.122+16464T>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6746407 | ||||||
| chr18:6746935
|
G | GCACTGTA others(2): Show |
76 | a0001c0001t0001g0179a0001c0001t0001g0181a0001c0001t0001g0182others(73): Show | 76 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.122+16993_122+1700 others(13): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6746935 | |||||
| chr18:6747071
|
C | CT | 11 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0008g0143others(8): Show | 11 | HG01346.hp1 HG02280.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.122+17144dupT | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6747071 | |||||
| chr18:6747071
|
CT | C | 93 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0019others(90): Show | 93 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(90): Show |
intron_variant | MODIFIER | c.122+17144delT | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6747071 | |||||
| chr18:6747071
|
CTT | C | 5 | a0001c0001t0001g0102a0001c0003t0003g0077a0001c0003t0003g0079others(2): Show | 5 | HG01256.hp1 HG02040.hp2 HG03704.hp2 others(2): Show |
intron_variant | MODIFIER | c.122+17143_122+1714 others(6): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6747071 | |||||
| chr18:6747196
|
G | A | 1 | a0002c0002t0002g0157 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.122+17253G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6747196 | ||||||
| chr18:6747219
|
G | A | 23 | a0001c0001t0001g0121a0001c0001t0001g0124a0001c0001t0001g0128others(20): Show | 23 | HG00408.hp1 HG00544.hp1 HG02080.hp1 others(20): Show |
intron_variant | MODIFIER | c.122+17276G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6747219 | ||||||
| chr18:6747327
|
C | T | 2 | a0001c0001t0001g0075a0001c0003t0003g0076 | 2 | HG02965.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.122+17384C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6747327 | ||||||
| chr18:6747358
|
A | G | 1 | a0002c0002t0004g0059 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.122+17415A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6747358 | ||||||
| chr18:6747554
|
A | G | 117 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0019others(114): Show | 117 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(114): Show |
intron_variant | MODIFIER | c.122+17611A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6747554 | ||||||
| chr18:6747727
|
G | A | 66 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0019others(63): Show | 66 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(63): Show |
intron_variant | MODIFIER | c.122+17784G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6747727 | ||||||
| chr18:6747729
|
A | T | 117 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0019others(114): Show | 117 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(114): Show |
intron_variant | MODIFIER | c.122+17786A>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6747729 | ||||||
| chr18:6747772
|
T | C | 2 | a0001c0003t0003g0119a0001c0003t0003g0122 | 2 | HG02723.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.122+17829T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6747772 | ||||||
| chr18:6748030
|
A | G | 7 | a0001c0001t0007g0116a0001c0001t0007g0117a0001c0001t0022g0067others(4): Show | 7 | HG01884.hp1 HG02630.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.122+18087A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6748030 | ||||||
| chr18:6748162
|
A | T | 82 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(79): Show | 82 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.122+18219A>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6748162 | ||||||
| chr18:6748348
|
G | C | 7 | a0001c0001t0007g0116a0001c0001t0007g0117a0001c0001t0022g0067others(4): Show | 7 | HG01884.hp1 HG02630.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.122+18405G>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6748348 | ||||||
| chr18:6748748
|
C | G | 14 | a0001c0001t0001g0080a0001c0001t0001g0106a0001c0001t0001g0107others(11): Show | 14 | HG01175.hp2 HG01243.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.122+18805C>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6748748 | ||||||
| chr18:6748900
|
G | A | 1 | a0007c0008t0002g0069 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.122+18957G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6748900 | ||||||
| chr18:6749033
|
G | A | 116 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0019others(113): Show | 116 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(113): Show |
intron_variant | MODIFIER | c.122+19090G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6749033 | ||||||
| chr18:6749270
|
T | C | 1 | a0002c0002t0012g0088 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.122+19327T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6749270 | ||||||
| chr18:6749320
|
C | G | 6 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(3): Show | 6 | HG01515.hp1 HG01891.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.122+19377C>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6749320 | ||||||
| chr18:6749386
|
G | A | 6 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(3): Show | 6 | HG01515.hp1 HG01891.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.122+19443G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6749386 | ||||||
| chr18:6749537
|
T | A | 1 | a0001c0001t0001g0121 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.122+19594T>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6749537 | ||||||
| chr18:6749563
|
G | T | 2 | a0001c0003t0003g0084a0001c0019t0021g0073 | 2 | HG02976.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.122+19620G>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6749563 | ||||||
| chr18:6749876
|
T | G | 25 | a0001c0001t0001g0012a0001c0001t0001g0026a0001c0001t0001g0054others(22): Show | 25 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(22): Show |
intron_variant | MODIFIER | c.122+19933T>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6749876 | ||||||
| chr18:6749881
|
A | G | 1 | a0001c0018t0020g0007 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.122+19938A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6749881 | ||||||
| chr18:6750088
|
C | T | 2 | a0001c0001t0006g0155a0001c0003t0003g0156 | 2 | HG02109.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.122+20145C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6750088 | ||||||
| chr18:6750372
|
T | C | 2 | a0001c0001t0001g0080a0001c0010t0003g0098 | 2 | HG02258.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.122+20429T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6750372 | ||||||
| chr18:6750390
|
G | A | 12 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(9): Show | 12 | HG01243.hp2 HG01346.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.122+20447G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6750390 | ||||||
| chr18:6750640
|
G | T | 1 | a0005c0006t0003g0226 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.122+20697G>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6750640 | ||||||
| chr18:6750897
|
G | T | 2 | a0001c0001t0006g0155a0001c0003t0003g0156 | 2 | HG02109.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.122+20954G>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6750897 | ||||||
| chr18:6751144
|
T | C | 1 | a0001c0001t0001g0124 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.122+21201T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6751144 | ||||||
| chr18:6751145
|
T | G | 1 | a0010c0014t0001g0142 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.122+21202T>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6751145 | ||||||
| chr18:6751331
|
G | GA | 9 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0003t0003g0094others(6): Show | 9 | HG01175.hp2 HG01243.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.122+21400dupA | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6751331 | |||||
| chr18:6751422
|
C | G | 23 | a0001c0001t0001g0080a0001c0001t0001g0106a0001c0001t0001g0107others(20): Show | 23 | HG01175.hp2 HG01243.hp1 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.122+21479C>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6751422 | ||||||
| chr18:6751457
|
C | G | 1 | a0001c0001t0008g0171 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.122+21514C>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6751457 | ||||||
| chr18:6751460
|
G | A | 1 | a0001c0001t0001g0181 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.122+21517G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6751460 | ||||||
| chr18:6751620
|
T | C | 234 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(231): Show | 234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.122+21677T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6751620 | ||||||
| chr18:6751747
|
G | A | 14 | a0001c0001t0001g0097a0001c0001t0001g0102a0001c0001t0017g0118others(11): Show | 14 | HG00099.hp1 HG00621.hp2 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.122+21804G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6751747 | ||||||
| chr18:6751752
|
A | G | 1 | a0001c0001t0008g0171 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.122+21809A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6751752 | ||||||
| chr18:6751926
|
A | G | 23 | a0001c0001t0001g0121a0001c0001t0001g0124a0001c0001t0001g0128others(20): Show | 23 | HG00408.hp1 HG00544.hp1 HG02080.hp1 others(20): Show |
intron_variant | MODIFIER | c.122+21983A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6751926 | ||||||
| chr18:6752031
|
G | A | 17 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0139others(14): Show | 17 | HG00408.hp1 HG00544.hp1 HG02080.hp1 others(14): Show |
intron_variant | MODIFIER | c.122+22088G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6752031 | ||||||
| chr18:6752093
|
G | A | 1 | a0001c0001t0001g0029 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.122+22150G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6752093 | ||||||
| chr18:6752134
|
T | C | 1 | a0002c0002t0002g0023 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.122+22191T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6752134 | ||||||
| chr18:6752150
|
G | T | 1 | a0001c0003t0015g0028 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.122+22207G>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6752150 | ||||||
| chr18:6752266
|
A | G | 234 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(231): Show | 234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.122+22323A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6752266 | ||||||
| chr18:6752332
|
T | A | 3 | a0001c0001t0001g0102a0001c0003t0003g0079a0002c0002t0002g0078 | 3 | HG03704.hp2 HG04184.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.122+22389T>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6752332 | ||||||
| chr18:6752440
|
C | A | 6 | a0001c0001t0001g0075a0001c0001t0008g0074a0001c0003t0003g0076others(3): Show | 6 | HG00741.hp1 HG02965.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.122+22497C>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6752440 | ||||||
| chr18:6752599
|
C | T | 14 | a0001c0001t0001g0097a0001c0001t0001g0102a0001c0001t0017g0118others(11): Show | 14 | HG00099.hp1 HG00621.hp2 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.122+22656C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6752599 | ||||||
| chr18:6752662
|
T | C | 1 | a0001c0001t0001g0230 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.122+22719T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6752662 | ||||||
| chr18:6752784
|
G | A | 1 | a0002c0002t0002g0099 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.122+22841G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6752784 | ||||||
| chr18:6752950
|
C | CT | 200 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(197): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.122+23017dupT | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6752950 | |||||
| chr18:6752960
|
T | C | 14 | a0001c0001t0001g0080a0001c0001t0001g0106a0001c0001t0001g0107others(11): Show | 14 | HG01175.hp2 HG01243.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.122+23017T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6752960 | ||||||
| chr18:6752960
|
T | TC | 7 | a0001c0001t0007g0116a0001c0001t0007g0117a0001c0001t0019g0008others(4): Show | 7 | HG01884.hp1 HG02630.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.122+23018dupC | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6752960 | |||||
| chr18:6753196
|
G | T | 12 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(9): Show | 12 | HG01243.hp2 HG01346.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.122+23253G>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6753196 | ||||||
| chr18:6753321
|
T | C | 2 | a0001c0003t0003g0013a0003c0004t0001g0024 | 2 | HG01943.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.122+23378T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6753321 | ||||||
| chr18:6753379
|
A | G | 1 | a0001c0001t0008g0074 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.122+23436A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6753379 | ||||||
| chr18:6753408
|
T | A | 1 | a0001c0001t0001g0182 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.122+23465T>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6753408 | ||||||
| chr18:6753622
|
G | T | 1 | a0001c0003t0003g0085 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.122+23679G>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6753622 | ||||||
| chr18:6753668
|
A | T | 6 | a0001c0001t0001g0075a0001c0001t0008g0074a0001c0003t0003g0076others(3): Show | 6 | HG00741.hp1 HG02965.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.122+23725A>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6753668 | ||||||
| chr18:6753739
|
G | A | 61 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0026others(58): Show | 61 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(58): Show |
intron_variant | MODIFIER | c.122+23796G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6753739 | ||||||
| chr18:6753771
|
G | A | 1 | a0001c0003t0003g0091 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.122+23828G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6753771 | ||||||
| chr18:6753790
|
T | G | 5 | a0001c0001t0007g0116a0001c0001t0007g0117a0001c0001t0022g0067others(2): Show | 5 | HG01884.hp1 HG02630.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.122+23847T>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6753790 | ||||||
| chr18:6753797
|
C | T | 28 | a0001c0001t0001g0075a0001c0001t0001g0121a0001c0001t0001g0124others(25): Show | 28 | HG00408.hp1 HG00544.hp1 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.122+23854C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6753797 | ||||||
| chr18:6754101
|
T | A | 12 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(9): Show | 12 | HG01243.hp2 HG01346.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.122+24158T>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6754101 | ||||||
| chr18:6754167
|
C | T | 1 | a0001c0003t0003g0123 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.122+24224C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6754167 | ||||||
| chr18:6754353
|
C | T | 6 | a0001c0001t0001g0075a0001c0001t0008g0074a0001c0003t0003g0076others(3): Show | 6 | HG00741.hp1 HG02965.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.122+24410C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6754353 | ||||||
| chr18:6754476
|
C | T | 5 | a0001c0001t0007g0116a0001c0001t0007g0117a0001c0001t0022g0067others(2): Show | 5 | HG01884.hp1 HG02630.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.122+24533C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6754476 | ||||||
| chr18:6754477
|
G | A | 14 | a0001c0001t0001g0080a0001c0001t0001g0106a0001c0001t0001g0107others(11): Show | 14 | HG01175.hp2 HG01243.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.122+24534G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6754477 | ||||||
| chr18:6754709
|
A | T | 1 | a0001c0001t0001g0168 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.122+24766A>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6754709 | ||||||
| chr18:6755462
|
G | A | 1 | a0002c0005t0002g0057 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.122+25519G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6755462 | ||||||
| chr18:6755699
|
C | G | 82 | a0001c0001t0001g0012a0001c0001t0001g0179a0001c0001t0001g0181others(79): Show | 82 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.122+25756C>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6755699 | ||||||
| chr18:6755721
|
A | G | 2 | a0001c0001t0006g0155a0001c0003t0003g0156 | 2 | HG02109.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.122+25778A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6755721 | ||||||
| chr18:6755791
|
A | G | 1 | a0001c0001t0019g0008 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.122+25848A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6755791 | ||||||
| chr18:6755911
|
G | A | 1 | a0010c0014t0001g0142 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.122+25968G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6755911 | ||||||
| chr18:6755964
|
A | G | 104 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(101): Show | 104 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(101): Show |
intron_variant | MODIFIER | c.122+26021A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6755964 | ||||||
| chr18:6756034
|
T | C | 23 | a0001c0001t0001g0121a0001c0001t0001g0124a0001c0001t0001g0128others(20): Show | 23 | HG00408.hp1 HG00544.hp1 HG02080.hp1 others(20): Show |
intron_variant | MODIFIER | c.122+26091T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6756034 | ||||||
| chr18:6756209
|
G | T | 3 | a0001c0001t0001g0223a0002c0002t0002g0174a0003c0004t0001g0173 | 3 | NA18968.hp1 NA19063.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.122+26266G>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6756209 | ||||||
| chr18:6756348
|
T | C | 20 | a0001c0001t0001g0121a0001c0001t0001g0128a0001c0001t0001g0129others(17): Show | 20 | HG00408.hp1 HG00544.hp1 HG02080.hp1 others(17): Show |
intron_variant | MODIFIER | c.122+26405T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6756348 | ||||||
| chr18:6756352
|
A | G | 1 | a0008c0011t0005g0090 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.122+26409A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6756352 | ||||||
| chr18:6756581
|
G | C | 7 | a0001c0001t0007g0116a0001c0001t0007g0117a0001c0001t0022g0067others(4): Show | 7 | HG01884.hp1 HG02630.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.122+26638G>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6756581 | ||||||
| chr18:6756662
|
A | G | 155 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0019others(152): Show | 155 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.122+26719A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6756662 | ||||||
| chr18:6756700
|
C | T | 49 | a0001c0001t0001g0179a0001c0001t0001g0181a0001c0001t0001g0182others(46): Show | 49 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(46): Show |
intron_variant | MODIFIER | c.122+26757C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6756700 | ||||||
| chr18:6756949
|
C | T | 8 | a0001c0001t0001g0004a0001c0001t0001g0075a0001c0001t0008g0074others(5): Show | 8 | HG00741.hp1 HG01891.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.122+27006C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6756949 | ||||||
| chr18:6757108
|
G | A | 50 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0072others(47): Show | 50 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.122+27165G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6757108 | ||||||
| chr18:6757109
|
C | A | 50 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0072others(47): Show | 50 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.122+27166C>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6757109 | ||||||
| chr18:6757245
|
C | T | 1 | a0001c0001t0001g0052 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.122+27302C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6757245 | ||||||
| chr18:6757350
|
T | G | 6 | a0001c0001t0001g0124a0001c0001t0008g0143a0001c0001t0008g0171others(3): Show | 6 | HG01106.hp1 HG02145.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.122+27407T>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6757350 | ||||||
| chr18:6757548
|
T | C | 1 | a0001c0001t0001g0004 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.122+27605T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6757548 | ||||||
| chr18:6757847
|
T | C | 2 | a0001c0001t0001g0075a0001c0003t0003g0123 | 2 | HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.122+27904T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6757847 | ||||||
| chr18:6757986
|
G | A | 1 | a0003c0004t0001g0025 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.122+28043G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6757986 | ||||||
| chr18:6758123
|
C | T | 1 | a0002c0002t0002g0134 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.122+28180C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6758123 | ||||||
| chr18:6758156
|
G | A | 1 | a0001c0001t0001g0102 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.122+28213G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6758156 | ||||||
| chr18:6758177
|
C | G | 4 | a0001c0001t0001g0230a0001c0003t0003g0233a0001c0003t0003g0234others(1): Show | 4 | HG00140.hp2 HG01261.hp1 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.122+28234C>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6758177 | ||||||
| chr18:6758227
|
G | C | 2 | a0003c0004t0001g0136a0004c0007t0002g0178 | 2 | NA19063.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.122+28284G>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6758227 | ||||||
| chr18:6758289
|
T | C | 1 | a0001c0001t0019g0008 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.122+28346T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6758289 | ||||||
| chr18:6758393
|
G | A | 30 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0070others(27): Show | 30 | HG00558.hp2 HG00597.hp1 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.122+28450G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6758393 | ||||||
| chr18:6758409
|
T | C | 10 | a0001c0001t0001g0001a0001c0001t0008g0143a0001c0001t0022g0067others(7): Show | 10 | HG01515.hp1 HG02280.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.122+28466T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6758409 | ||||||
| chr18:6758416
|
C | A | 2 | a0001c0003t0003g0002a0001c0003t0003g0104 | 2 | HG03471.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.122+28473C>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6758416 | ||||||
| chr18:6758424
|
A | G | 17 | a0001c0001t0001g0107a0001c0001t0001g0165a0001c0001t0001g0203others(14): Show | 17 | HG00280.hp2 HG01081.hp1 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.122+28481A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6758424 | ||||||
| chr18:6758495
|
C | T | 59 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(56): Show | 59 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.122+28552C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6758495 | ||||||
| chr18:6758575
|
C | T | 1 | a0001c0001t0001g0236 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.122+28632C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6758575 | ||||||
| chr18:6758629
|
C | A | 1 | a0001c0001t0001g0185 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.122+28686C>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6758629 | ||||||
| chr18:6758657
|
C | T | 2 | a0001c0003t0003g0002a0001c0003t0003g0104 | 2 | HG03471.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.122+28714C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6758657 | ||||||
| chr18:6758922
|
G | A | 136 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0029others(133): Show | 136 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.122+28979G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6758922 | ||||||
| chr18:6758974
|
A | G | 6 | a0001c0001t0001g0124a0001c0001t0001g0149a0001c0001t0001g0150others(3): Show | 6 | HG02055.hp2 HG02145.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.122+29031A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6758974 | ||||||
| chr18:6759006
|
A | G | 103 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(100): Show | 103 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.122+29063A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6759006 | ||||||
| chr18:6759260
|
G | A | 106 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.122+29317G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6759260 | ||||||
| chr18:6759295
|
C | CAA | 106 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.122+29355_122+2935 others(6): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6759295 | |||||
| chr18:6759322
|
G | C | 3 | a0001c0001t0001g0106a0001c0003t0003g0122a0002c0002t0004g0059 | 3 | HG02451.hp2 HG02647.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.122+29379G>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6759322 | ||||||
| chr18:6759363
|
C | T | 91 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(88): Show | 91 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.122+29420C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6759363 | ||||||
| chr18:6759451
|
T | C | 106 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.122+29508T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6759451 | ||||||
| chr18:6759515
|
G | A | 106 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.122+29572G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6759515 | ||||||
| chr18:6759652
|
G | C | 148 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(145): Show | 148 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.122+29709G>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6759652 | ||||||
| chr18:6759703
|
T | C | 1 | a0002c0002t0002g0023 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.122+29760T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6759703 | ||||||
| chr18:6759763
|
G | A | 87 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0029others(84): Show | 87 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.122+29820G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6759763 | ||||||
| chr18:6759807
|
A | AC | 106 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.122+29868dupC | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6759807 | |||||
| chr18:6759819
|
C | T | 30 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0026others(27): Show | 30 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(27): Show |
intron_variant | MODIFIER | c.122+29876C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6759819 | ||||||
| chr18:6759826
|
C | A | 1 | a0001c0001t0001g0204 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.122+29883C>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6759826 | ||||||
| chr18:6759891
|
A | C | 108 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(105): Show | 108 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.122+29948A>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6759891 | ||||||
| chr18:6759924
|
G | A | 1 | a0001c0020t0023g0101 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.122+29981G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6759924 | ||||||
| chr18:6760079
|
A | G | 40 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0070others(37): Show | 40 | HG00558.hp2 HG00597.hp1 HG01175.hp2 others(37): Show |
intron_variant | MODIFIER | c.122+30136A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6760079 | ||||||
| chr18:6760106
|
G | A | 2 | a0001c0003t0003g0002a0001c0003t0003g0104 | 2 | HG03471.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.122+30163G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6760106 | ||||||
| chr18:6760124
|
A | G | 106 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.122+30181A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6760124 | ||||||
| chr18:6760254
|
A | T | 106 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.122+30311A>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6760254 | ||||||
| chr18:6760341
|
C | A | 105 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(102): Show | 105 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.122+30398C>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6760341 | ||||||
| chr18:6760382
|
G | A | 3 | a0001c0001t0007g0116a0001c0001t0007g0117a0002c0005t0002g0158 | 3 | HG02055.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.122+30439G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6760382 | ||||||
| chr18:6760411
|
C | G | 105 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(102): Show | 105 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.122+30468C>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6760411 | ||||||
| chr18:6760438
|
G | T | 104 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(101): Show | 104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.122+30495G>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6760438 | ||||||
| chr18:6760446
|
T | C | 2 | a0001c0001t0001g0075a0001c0003t0003g0076 | 2 | HG02965.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.122+30503T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6760446 | ||||||
| chr18:6760527
|
G | C | 101 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0019others(98): Show | 101 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.122+30584G>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6760527 | ||||||
| chr18:6760556
|
T | C | 1 | a0002c0002t0002g0229 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.122+30613T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6760556 | ||||||
| chr18:6760602
|
G | A | 1 | a0003c0004t0001g0030 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.122+30659G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6760602 | ||||||
| chr18:6760969
|
C | T | 1 | a0003c0004t0001g0173 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.122+31026C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6760969 | ||||||
| chr18:6761095
|
T | C | 1 | a0001c0001t0009g0005 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.122+31152T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6761095 | ||||||
| chr18:6761137
|
G | A | 3 | a0001c0001t0001g0106a0001c0003t0003g0122a0002c0002t0004g0059 | 3 | HG02451.hp2 HG02647.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.122+31194G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6761137 | ||||||
| chr18:6761228
|
T | C | 2 | a0001c0003t0003g0084a0001c0019t0021g0073 | 2 | HG02976.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.122+31285T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6761228 | ||||||
| chr18:6761295
|
A | T | 45 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0052others(42): Show | 45 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.122+31352A>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6761295 | ||||||
| chr18:6761510
|
G | T | 2 | a0001c0003t0003g0002a0001c0003t0003g0104 | 2 | HG03471.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.122+31567G>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6761510 | ||||||
| chr18:6761887
|
G | A | 1 | a0001c0001t0001g0186 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.122+31944G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6761887 | ||||||
| chr18:6761921
|
T | A | 8 | a0001c0001t0001g0107a0001c0001t0001g0165a0001c0001t0001g0211others(5): Show | 8 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.122+31978T>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6761921 | ||||||
| chr18:6762056
|
G | C | 173 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0029others(170): Show | 173 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.122+32113G>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6762056 | ||||||
| chr18:6762200
|
C | A | 173 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0029others(170): Show | 173 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.122+32257C>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6762200 | ||||||
| chr18:6762204
|
T | C | 174 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0029others(171): Show | 174 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.122+32261T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6762204 | ||||||
| chr18:6762281
|
A | G | 173 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0029others(170): Show | 173 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.122+32338A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6762281 | ||||||
| chr18:6762357
|
C | T | 1 | a0001c0001t0008g0074 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.122+32414C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6762357 | ||||||
| chr18:6762371
|
G | A | 242 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(239): Show | 242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.122+32428G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6762371 | ||||||
| chr18:6762448
|
T | G | 9 | a0001c0001t0001g0107a0001c0001t0001g0165a0001c0001t0001g0211others(6): Show | 9 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.122+32505T>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6762448 | ||||||
| chr18:6762475
|
C | T | 2 | a0001c0003t0003g0094a0001c0003t0003g0095 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.122+32532C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6762475 | ||||||
| chr18:6762487
|
C | G | 1 | a0002c0002t0002g0066 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.122+32544C>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6762487 | ||||||
| chr18:6762638
|
G | A | 1 | a0001c0001t0001g0165 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.122+32695G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6762638 | ||||||
| chr18:6762723
|
T | G | 1 | a0001c0001t0001g0184 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.122+32780T>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6762723 | ||||||
| chr18:6762862
|
G | C | 233 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(230): Show | 233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.122+32919G>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6762862 | ||||||
| chr18:6762886
|
C | G | 148 | a0001c0001t0001g0018a0001c0001t0001g0029a0001c0001t0001g0037others(145): Show | 148 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.122+32943C>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6762886 | ||||||
| chr18:6762960
|
G | A | 1 | a0006c0009t0009g0153 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.122+33017G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6762960 | ||||||
| chr18:6762972
|
C | T | 173 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0029others(170): Show | 173 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.122+33029C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6762972 | ||||||
| chr18:6763081
|
G | GTTGT | 23 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0019others(20): Show | 23 | HG00099.hp2 HG00408.hp1 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.122+33161_122+3316 others(8): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6763081 | |||||
| chr18:6763303
|
G | A | 10 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0026others(7): Show | 10 | HG00099.hp2 HG00408.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.122+33360G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6763303 | ||||||
| chr18:6763367
|
G | A | 1 | a0004c0007t0004g0115 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.122+33424G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6763367 | ||||||
| chr18:6763439
|
A | T | 173 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0029others(170): Show | 173 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.122+33496A>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6763439 | ||||||
| chr18:6763945
|
C | T | 5 | a0001c0001t0001g0001a0001c0001t0008g0143a0001c0003t0003g0154others(2): Show | 5 | HG01515.hp1 HG02818.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.122+34002C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6763945 | ||||||
| chr18:6764064
|
T | C | 238 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(235): Show | 238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.122+34121T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6764064 | ||||||
| chr18:6764148
|
G | A | 1 | a0002c0002t0002g0083 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.122+34205G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6764148 | ||||||
| chr18:6764182
|
G | T | 1 | a0001c0001t0001g0012 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.122+34239G>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6764182 | ||||||
| chr18:6764298
|
G | A | 172 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0029others(169): Show | 172 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.122+34355G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6764298 | ||||||
| chr18:6764444
|
G | T | 20 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(17): Show | 20 | HG00099.hp2 HG00408.hp1 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.122+34501G>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6764444 | ||||||
| chr18:6764571
|
C | T | 1 | a0002c0005t0002g0017 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.122+34628C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6764571 | ||||||
| chr18:6764634
|
A | C | 191 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0018others(188): Show | 191 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.122+34691A>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6764634 | ||||||
| chr18:6765220
|
T | C | 5 | a0001c0001t0001g0072a0001c0001t0006g0155a0001c0003t0003g0084others(2): Show | 5 | HG02258.hp1 HG02976.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.122+35277T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6765220 | ||||||
| chr18:6765240
|
G | A | 82 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0035others(79): Show | 82 | HG00280.hp1 HG00438.hp1 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.122+35297G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6765240 | ||||||
| chr18:6765328
|
G | T | 1 | a0001c0001t0017g0118 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.122+35385G>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6765328 | ||||||
| chr18:6765330
|
C | T | 1 | a0002c0005t0002g0108 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.122+35387C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6765330 | ||||||
| chr18:6765440
|
A | G | 1 | a0001c0001t0001g0049 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.122+35497A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6765440 | ||||||
| chr18:6765476
|
C | A | 173 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0029others(170): Show | 173 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.122+35533C>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6765476 | ||||||
| chr18:6765575
|
A | T | 1 | a0001c0001t0001g0003 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.122+35632A>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6765575 | ||||||
| chr18:6766003
|
A | T | 8 | a0001c0001t0001g0107a0001c0001t0001g0165a0001c0001t0001g0211others(5): Show | 8 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.122+36060A>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6766003 | ||||||
| chr18:6766188
|
G | A | 1 | a0001c0001t0001g0107 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.122+36245G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6766188 | ||||||
| chr18:6766271
|
A | G | 8 | a0001c0001t0001g0107a0001c0001t0001g0165a0001c0001t0001g0211others(5): Show | 8 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.122+36328A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6766271 | ||||||
| chr18:6766274
|
A | G | 174 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0029others(171): Show | 174 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.122+36331A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6766274 | ||||||
| chr18:6766840
|
C | T | 1 | a0003c0004t0001g0048 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.122+36897C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6766840 | ||||||
| chr18:6766917
|
C | T | 9 | a0002c0002t0002g0174a0002c0002t0002g0243a0002c0005t0002g0043others(6): Show | 9 | HG00423.hp1 NA18947.hp2 NA18968.hp1 others(6): Show |
intron_variant | MODIFIER | c.122+36974C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6766917 | ||||||
| chr18:6767057
|
C | T | 42 | a0001c0001t0001g0049a0001c0001t0001g0071a0001c0001t0001g0128others(39): Show | 42 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(39): Show |
intron_variant | MODIFIER | c.122+37114C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6767057 | ||||||
| chr18:6767058
|
G | A | 20 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(17): Show | 20 | HG00099.hp2 HG00408.hp1 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.122+37115G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6767058 | ||||||
| chr18:6767121
|
C | T | 3 | a0002c0002t0002g0174a0003c0004t0001g0173a0003c0004t0001g0227 | 3 | HG00423.hp1 NA18968.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.122+37178C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6767121 | ||||||
| chr18:6767330
|
A | C | 1 | a0003c0004t0001g0193 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.122+37387A>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6767330 | ||||||
| chr18:6767437
|
G | A | 54 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0035others(51): Show | 54 | HG00558.hp2 HG00597.hp1 HG01346.hp1 others(51): Show |
intron_variant | MODIFIER | c.122+37494G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6767437 | ||||||
| chr18:6767703
|
A | G | 1 | a0001c0003t0003g0231 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.122+37760A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6767703 | ||||||
| chr18:6767771
|
A | G | 3 | a0001c0001t0001g0107a0001c0001t0001g0165a0008c0011t0005g0016 | 3 | HG01243.hp1 HG02109.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.122+37828A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6767771 | ||||||
| chr18:6767905
|
G | C | 174 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0029others(171): Show | 174 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.122+37962G>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6767905 | ||||||
| chr18:6767966
|
T | C | 174 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0029others(171): Show | 174 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.122+38023T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6767966 | ||||||
| chr18:6767986
|
C | T | 3 | a0001c0003t0003g0002a0001c0003t0003g0104a0001c0015t0003g0167 | 3 | HG03471.hp1 NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.122+38043C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6767986 | ||||||
| chr18:6767990
|
G | A | 1 | a0001c0003t0003g0027 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.122+38047G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6767990 | ||||||
| chr18:6768125
|
T | G | 1 | a0010c0014t0001g0142 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.122+38182T>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6768125 | ||||||
| chr18:6768148
|
A | G | 1 | a0001c0001t0001g0204 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.122+38205A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6768148 | ||||||
| chr18:6768580
|
C | T | 176 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0029others(173): Show | 176 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.122+38637C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6768580 | ||||||
| chr18:6768668
|
T | A | 1 | a0002c0002t0002g0217 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.122+38725T>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6768668 | ||||||
| chr18:6768827
|
G | T | 167 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0029others(164): Show | 167 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.122+38884G>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6768827 | ||||||
| chr18:6768975
|
A | T | 8 | a0001c0001t0001g0107a0001c0001t0001g0165a0001c0001t0001g0211others(5): Show | 8 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.122+39032A>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6768975 | ||||||
| chr18:6769246
|
G | T | 1 | a0006c0009t0009g0153 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.122+39303G>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6769246 | ||||||
| chr18:6769261
|
C | T | 23 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(20): Show | 23 | HG00099.hp2 HG00408.hp1 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.122+39318C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6769261 | ||||||
| chr18:6769339
|
C | T | 1 | a0002c0002t0013g0022 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.122+39396C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6769339 | ||||||
| chr18:6769541
|
A | G | 1 | a0001c0001t0001g0225 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.122+39598A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6769541 | ||||||
| chr18:6769575
|
A | G | 2 | a0001c0001t0001g0150a0006c0009t0005g0144 | 2 | HG02615.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.122+39632A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6769575 | ||||||
| chr18:6769630
|
A | G | 1 | a0001c0003t0003g0085 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.122+39687A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6769630 | ||||||
| chr18:6769638
|
A | G | 1 | a0001c0015t0003g0167 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.122+39695A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6769638 | ||||||
| chr18:6769757
|
A | G | 175 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0029others(172): Show | 175 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.122+39814A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6769757 | ||||||
| chr18:6769768
|
C | T | 8 | a0001c0001t0001g0107a0001c0001t0001g0165a0001c0001t0001g0211others(5): Show | 8 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.122+39825C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6769768 | ||||||
| chr18:6769826
|
C | T | 2 | a0001c0001t0001g0044a0002c0002t0002g0138 | 2 | NA18950.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.122+39883C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6769826 | ||||||
| chr18:6770060
|
T | C | 9 | a0001c0001t0001g0107a0001c0001t0001g0165a0001c0001t0001g0211others(6): Show | 9 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.122+40117T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6770060 | ||||||
| chr18:6770071
|
A | T | 24 | a0001c0001t0001g0029a0001c0001t0001g0037a0001c0001t0001g0038others(21): Show | 24 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(21): Show |
intron_variant | MODIFIER | c.122+40128A>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6770071 | ||||||
| chr18:6770097
|
T | C | 9 | a0001c0001t0001g0107a0001c0001t0001g0165a0001c0001t0001g0211others(6): Show | 9 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.122+40154T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6770097 | ||||||
| chr18:6770368
|
A | G | 3 | a0001c0003t0003g0002a0001c0003t0003g0104a0001c0015t0003g0167 | 3 | HG03471.hp1 NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.122+40425A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6770368 | ||||||
| chr18:6770494
|
G | T | 1 | a0001c0003t0003g0060 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.122+40551G>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6770494 | ||||||
| chr18:6770583
|
T | C | 5 | a0001c0001t0001g0072a0001c0001t0006g0155a0001c0003t0003g0084others(2): Show | 5 | HG02258.hp1 HG02976.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.122+40640T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6770583 | ||||||
| chr18:6770621
|
T | G | 2 | a0001c0003t0003g0085a0010c0014t0001g0142 | 2 | HG01106.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.122+40678T>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6770621 | ||||||
| chr18:6770702
|
C | G | 1 | a0001c0003t0003g0156 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.122+40759C>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6770702 | ||||||
| chr18:6770721
|
T | C | 49 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0035others(46): Show | 49 | HG00558.hp2 HG00597.hp1 HG01346.hp1 others(46): Show |
intron_variant | MODIFIER | c.122+40778T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6770721 | ||||||
| chr18:6770749
|
G | A | 164 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0029others(161): Show | 164 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.122+40806G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6770749 | ||||||
| chr18:6770875
|
G | A | 175 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0029others(172): Show | 175 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.122+40932G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6770875 | ||||||
| chr18:6771493
|
G | A | 1 | a0001c0003t0003g0145 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.122+41550G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6771493 | ||||||
| chr18:6771606
|
G | A | 175 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0029others(172): Show | 175 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.122+41663G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6771606 | ||||||
| chr18:6771741
|
G | T | 1 | a0001c0003t0003g0079 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.122+41798G>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6771741 | ||||||
| chr18:6771742
|
C | T | 1 | a0001c0003t0003g0079 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.122+41799C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6771742 | ||||||
| chr18:6771773
|
T | C | 5 | a0001c0001t0001g0072a0001c0001t0006g0155a0001c0003t0003g0084others(2): Show | 5 | HG02258.hp1 HG02976.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.122+41830T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6771773 | ||||||
| chr18:6771821
|
A | G | 3 | a0001c0001t0001g0204a0002c0002t0002g0014a0003c0004t0001g0183 | 3 | HG00597.hp1 NA18983.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.122+41878A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6771821 | ||||||
| chr18:6772252
|
C | T | 3 | a0001c0003t0003g0002a0001c0003t0003g0104a0001c0015t0003g0167 | 3 | HG03471.hp1 NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.122+42309C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6772252 | ||||||
| chr18:6772521
|
T | C | 1 | a0001c0020t0023g0101 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.122+42578T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6772521 | ||||||
| chr18:6772546
|
A | T | 3 | a0002c0002t0002g0224a0003c0004t0001g0021a0003c0004t0001g0093 | 3 | HG00597.hp2 HG00621.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.122+42603A>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6772546 | ||||||
| chr18:6772594
|
G | A | 166 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0029others(163): Show | 166 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.122+42651G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6772594 | ||||||
| chr18:6772619
|
G | C | 1 | a0003c0004t0001g0173 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.122+42676G>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6772619 | ||||||
| chr18:6772629
|
A | G | 1 | a0002c0002t0002g0224 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.122+42686A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6772629 | ||||||
| chr18:6772709
|
A | G | 9 | a0001c0001t0001g0106a0001c0001t0001g0161a0001c0001t0006g0164others(6): Show | 9 | HG01884.hp2 HG01952.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.122+42766A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6772709 | ||||||
| chr18:6772720
|
GTTTTATT others(10): Show |
G | 2 | a0001c0003t0003g0085a0010c0014t0001g0142 | 2 | HG01106.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.122+42792_122+4280 others(21): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6772720 | |||||
| chr18:6772765
|
G | A | 3 | a0001c0001t0001g0165a0002c0002t0013g0022a0008c0011t0005g0016 | 3 | HG02109.hp1 HG02630.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.122+42822G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6772765 | ||||||
| chr18:6772961
|
G | A | 172 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0029others(169): Show | 172 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.122+43018G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6772961 | ||||||
| chr18:6773000
|
T | C | 176 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0029others(173): Show | 176 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.122+43057T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6773000 | ||||||
| chr18:6773033
|
C | T | 1 | a0001c0001t0008g0074 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.122+43090C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6773033 | ||||||
| chr18:6773140
|
C | T | 16 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0019others(13): Show | 16 | HG00099.hp2 HG00408.hp1 HG00735.hp1 others(13): Show |
intron_variant | MODIFIER | c.122+43197C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6773140 | ||||||
| chr18:6773270
|
A | G | 8 | a0001c0001t0001g0107a0001c0001t0001g0165a0001c0001t0001g0211others(5): Show | 8 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.122+43327A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6773270 | ||||||
| chr18:6773631
|
T | G | 1 | a0001c0015t0003g0167 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.122+43688T>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6773631 | ||||||
| chr18:6774098
|
T | C | 176 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0029others(173): Show | 176 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.122+44155T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6774098 | ||||||
| chr18:6774154
|
T | C | 176 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0029others(173): Show | 176 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.122+44211T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6774154 | ||||||
| chr18:6774271
|
A | C | 1 | a0001c0001t0001g0168 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.122+44328A>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6774271 | ||||||
| chr18:6774290
|
A | G | 176 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0029others(173): Show | 176 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.122+44347A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6774290 | ||||||
| chr18:6774367
|
T | C | 1 | a0001c0003t0003g0085 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.122+44424T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6774367 | ||||||
| chr18:6774608
|
T | C | 6 | a0001c0001t0001g0001a0001c0001t0008g0143a0001c0003t0003g0154others(3): Show | 6 | HG01515.hp1 HG02818.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.122+44665T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6774608 | ||||||
| chr18:6774830
|
G | A | 1 | a0003c0004t0001g0173 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.122+44887G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6774830 | ||||||
| chr18:6775028
|
C | T | 10 | a0001c0001t0001g0107a0001c0001t0001g0165a0001c0001t0001g0211others(7): Show | 10 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.122+45085C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6775028 | ||||||
| chr18:6775040
|
A | G | 1 | a0001c0001t0001g0225 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.122+45097A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6775040 | ||||||
| chr18:6775192
|
G | T | 2 | a0001c0003t0003g0002a0001c0003t0003g0104 | 2 | HG03471.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.122+45249G>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6775192 | ||||||
| chr18:6775278
|
C | T | 2 | a0001c0001t0001g0026a0001c0003t0003g0110 | 2 | HG01099.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.122+45335C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6775278 | ||||||
| chr18:6775513
|
TTTTG | T | 9 | a0001c0001t0001g0106a0001c0001t0001g0161a0001c0001t0006g0164others(6): Show | 9 | HG01884.hp2 HG01952.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.122+45582_122+4558 others(8): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6775513 | |||||
| chr18:6775812
|
G | A | 1 | a0002c0002t0002g0103 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.122+45869G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6775812 | ||||||
| chr18:6776037
|
G | A | 121 | a0001c0001t0001g0018a0001c0001t0001g0029a0001c0001t0001g0037others(118): Show | 121 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(118): Show |
intron_variant | MODIFIER | c.122+46094G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6776037 | ||||||
| chr18:6776182
|
G | A | 1 | a0002c0002t0002g0137 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.122+46239G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6776182 | ||||||
| chr18:6776247
|
GCCT | G | 41 | a0001c0001t0001g0049a0001c0001t0001g0071a0001c0001t0001g0128others(38): Show | 41 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(38): Show |
intron_variant | MODIFIER | c.122+46311_122+4631 others(7): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6776247 | |||||
| chr18:6776448
|
C | T | 3 | a0001c0001t0018g0111a0002c0002t0004g0006a0002c0002t0004g0147 | 3 | HG02280.hp2 HG02559.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.122+46505C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6776448 | ||||||
| chr18:6776562
|
G | C | 1 | a0001c0001t0001g0003 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.122+46619G>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6776562 | ||||||
| chr18:6776592
|
C | T | 131 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0018others(128): Show | 131 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.122+46649C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6776592 | ||||||
| chr18:6776682
|
A | G | 50 | a0001c0001t0001g0049a0001c0001t0001g0071a0001c0001t0001g0107others(47): Show | 50 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.122+46739A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6776682 | ||||||
| chr18:6776741
|
A | C | 2 | a0001c0015t0003g0167a0010c0014t0001g0142 | 2 | HG01106.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.122+46798A>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6776741 | ||||||
| chr18:6776747
|
T | C | 5 | a0001c0001t0001g0072a0001c0001t0006g0155a0001c0003t0003g0002others(2): Show | 5 | HG02258.hp1 HG03209.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.122+46804T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6776747 | ||||||
| chr18:6776760
|
G | A | 184 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(181): Show | 184 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.122+46817G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6776760 | ||||||
| chr18:6776768
|
A | G | 166 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(163): Show | 166 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.122+46825A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6776768 | ||||||
| chr18:6776787
|
C | T | 160 | a0001c0001t0001g0018a0001c0001t0001g0029a0001c0001t0001g0034others(157): Show | 160 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.122+46844C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6776787 | ||||||
| chr18:6776864
|
T | G | 47 | a0001c0001t0001g0049a0001c0001t0001g0071a0001c0001t0001g0082others(44): Show | 47 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(44): Show |
intron_variant | MODIFIER | c.122+46921T>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6776864 | ||||||
| chr18:6776882
|
A | C | 182 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0029others(179): Show | 182 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.122+46939A>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6776882 | ||||||
| chr18:6777026
|
A | C | 1 | a0001c0015t0003g0167 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.122+47083A>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6777026 | ||||||
| chr18:6777182
|
A | G | 14 | a0001c0001t0001g0080a0001c0001t0001g0106a0001c0001t0001g0161others(11): Show | 14 | HG01884.hp2 HG01952.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.122+47239A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6777182 | ||||||
| chr18:6777280
|
A | G | 2 | a0001c0003t0003g0084a0001c0019t0021g0073 | 2 | HG02976.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.122+47337A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6777280 | ||||||
| chr18:6777283
|
G | A | 217 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(214): Show | 217 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.122+47340G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6777283 | ||||||
| chr18:6777323
|
A | T | 7 | a0001c0001t0001g0107a0001c0001t0001g0165a0001c0001t0001g0211others(4): Show | 7 | HG01243.hp1 HG02109.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.122+47380A>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6777323 | ||||||
| chr18:6777457
|
T | G | 1 | a0001c0001t0006g0176 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.123-47305T>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6777457 | ||||||
| chr18:6777475
|
C | T | 1 | a0001c0003t0003g0145 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.123-47287C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6777475 | ||||||
| chr18:6777500
|
T | A | 83 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(80): Show | 83 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(80): Show |
intron_variant | MODIFIER | c.123-47262T>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6777500 | ||||||
| chr18:6777510
|
C | T | 2 | a0001c0003t0003g0002a0001c0003t0003g0104 | 2 | HG03471.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.123-47252C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6777510 | ||||||
| chr18:6777680
|
G | A | 17 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0019others(14): Show | 17 | HG00099.hp2 HG00408.hp1 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.123-47082G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6777680 | ||||||
| chr18:6777724
|
C | T | 1 | a0001c0001t0001g0018 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.123-47038C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6777724 | ||||||
| chr18:6777749
|
A | G | 1 | a0001c0003t0003g0145 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.123-47013A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6777749 | ||||||
| chr18:6777750
|
G | A | 63 | a0001c0001t0001g0035a0001c0001t0001g0049a0001c0001t0001g0071others(60): Show | 63 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.123-47012G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6777750 | ||||||
| chr18:6777754
|
A | ATGAG | 42 | a0001c0001t0001g0035a0001c0001t0001g0049a0001c0001t0001g0071others(39): Show | 42 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(39): Show |
intron_variant | MODIFIER | c.123-47005_123-4700 others(8): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6777754 | |||||
| chr18:6777754
|
A | G | 21 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0161others(18): Show | 21 | HG01106.hp1 HG01243.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.123-47008A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6777754 | ||||||
| chr18:6777786
|
C | A | 2 | a0001c0003t0003g0002a0001c0003t0003g0104 | 2 | HG03471.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.123-46976C>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6777786 | ||||||
| chr18:6777835
|
G | C | 4 | a0001c0001t0001g0080a0001c0001t0001g0168a0001c0010t0003g0098others(1): Show | 4 | HG02258.hp2 HG02970.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.123-46927G>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6777835 | ||||||
| chr18:6778213
|
G | T | 5 | a0001c0001t0001g0034a0003c0004t0001g0030a0003c0004t0001g0187others(2): Show | 5 | NA18940.hp2 NA18941.hp1 NA19011.hp1 others(2): Show |
intron_variant | MODIFIER | c.123-46549G>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6778213 | ||||||
| chr18:6778456
|
A | T | 1 | a0001c0001t0001g0194 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.123-46306A>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6778456 | ||||||
| chr18:6778473
|
C | G | 52 | a0001c0001t0001g0035a0001c0001t0001g0049a0001c0001t0001g0071others(49): Show | 52 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.123-46289C>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6778473 | ||||||
| chr18:6778503
|
A | G | 3 | a0001c0003t0003g0085a0008c0011t0005g0016a0010c0014t0001g0142 | 3 | HG01106.hp1 HG02630.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.123-46259A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6778503 | ||||||
| chr18:6778783
|
G | A | 1 | a0001c0003t0003g0145 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.123-45979G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6778783 | ||||||
| chr18:6779164
|
C | T | 9 | a0001c0001t0001g0106a0001c0001t0001g0161a0001c0001t0006g0164others(6): Show | 9 | HG01884.hp2 HG01952.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.123-45598C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6779164 | ||||||
| chr18:6779422
|
C | T | 5 | a0001c0001t0001g0072a0001c0001t0006g0155a0001c0003t0003g0084others(2): Show | 5 | HG02258.hp1 HG02976.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.123-45340C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6779422 | ||||||
| chr18:6779485
|
G | A | 1 | a0001c0012t0014g0159 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.123-45277G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6779485 | ||||||
| chr18:6779529
|
A | T | 54 | a0001c0001t0001g0035a0001c0001t0001g0049a0001c0001t0001g0071others(51): Show | 54 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.123-45233A>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6779529 | ||||||
| chr18:6779608
|
A | G | 7 | a0001c0001t0001g0107a0001c0001t0001g0165a0001c0001t0001g0211others(4): Show | 7 | HG01243.hp1 HG02109.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.123-45154A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6779608 | ||||||
| chr18:6779691
|
A | G | 1 | a0001c0001t0022g0067 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.123-45071A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6779691 | ||||||
| chr18:6779901
|
A | G | 1 | a0008c0011t0005g0016 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.123-44861A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6779901 | ||||||
| chr18:6779953
|
C | G | 1 | a0001c0015t0003g0167 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.123-44809C>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6779953 | ||||||
| chr18:6780090
|
C | T | 1 | a0003c0004t0001g0219 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.123-44672C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6780090 | ||||||
| chr18:6780103
|
C | T | 4 | a0001c0001t0001g0080a0001c0001t0001g0168a0001c0010t0003g0098others(1): Show | 4 | HG02258.hp2 HG02970.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.123-44659C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6780103 | ||||||
| chr18:6780153
|
G | A | 1 | a0001c0001t0001g0003 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.123-44609G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6780153 | ||||||
| chr18:6780189
|
G | A | 1 | a0001c0001t0001g0003 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.123-44573G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6780189 | ||||||
| chr18:6780214
|
C | G | 1 | a0001c0001t0001g0100 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.123-44548C>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6780214 | ||||||
| chr18:6780463
|
C | T | 1 | a0001c0001t0001g0054 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.123-44299C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6780463 | ||||||
| chr18:6780464
|
G | A | 56 | a0001c0001t0001g0035a0001c0001t0001g0049a0001c0001t0001g0071others(53): Show | 56 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(53): Show |
intron_variant | MODIFIER | c.123-44298G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6780464 | ||||||
| chr18:6780588
|
A | G | 51 | a0001c0001t0001g0035a0001c0001t0001g0049a0001c0001t0001g0071others(48): Show | 51 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(48): Show |
intron_variant | MODIFIER | c.123-44174A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6780588 | ||||||
| chr18:6780631
|
G | A | 1 | a0001c0015t0003g0167 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.123-44131G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6780631 | ||||||
| chr18:6780786
|
C | T | 1 | a0001c0001t0001g0202 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.123-43976C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6780786 | ||||||
| chr18:6780879
|
G | A | 1 | a0001c0003t0003g0060 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.123-43883G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6780879 | ||||||
| chr18:6780894
|
C | CA | 15 | a0001c0001t0001g0106a0001c0001t0001g0161a0001c0001t0001g0221others(12): Show | 15 | HG01175.hp1 HG01175.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.123-43851dupA | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6780894 | |||||
| chr18:6780894
|
CA | C | 19 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0019others(16): Show | 19 | HG00099.hp2 HG00408.hp1 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.123-43851delA | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6780894 | |||||
| chr18:6781017
|
G | A | 82 | a0001c0001t0001g0003a0001c0001t0001g0035a0001c0001t0001g0049others(79): Show | 82 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.123-43745G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6781017 | ||||||
| chr18:6781338
|
T | G | 83 | a0001c0001t0001g0003a0001c0001t0001g0035a0001c0001t0001g0049others(80): Show | 83 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.123-43424T>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6781338 | ||||||
| chr18:6781454
|
C | T | 86 | a0001c0001t0001g0003a0001c0001t0001g0035a0001c0001t0001g0049others(83): Show | 86 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.123-43308C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6781454 | ||||||
| chr18:6781509
|
C | G | 3 | a0001c0001t0001g0182a0002c0002t0010g0206a0002c0002t0010g0246 | 3 | HG02040.hp1 NA18941.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.123-43253C>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6781509 | ||||||
| chr18:6781630
|
T | G | 1 | a0002c0002t0002g0135 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.123-43132T>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6781630 | ||||||
| chr18:6781696
|
C | T | 51 | a0001c0001t0001g0035a0001c0001t0001g0049a0001c0001t0001g0071others(48): Show | 51 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(48): Show |
intron_variant | MODIFIER | c.123-43066C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6781696 | ||||||
| chr18:6781918
|
A | G | 21 | a0001c0001t0001g0003a0001c0001t0001g0072a0001c0001t0001g0100others(18): Show | 21 | HG01175.hp2 HG01346.hp1 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.123-42844A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6781918 | ||||||
| chr18:6782148
|
T | G | 2 | a0001c0001t0001g0075a0001c0003t0003g0076 | 2 | HG02965.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.123-42614T>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6782148 | ||||||
| chr18:6782406
|
C | G | 1 | a0002c0002t0002g0135 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.123-42356C>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6782406 | ||||||
| chr18:6782518
|
A | G | 1 | a0001c0001t0001g0107 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.123-42244A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6782518 | ||||||
| chr18:6782574
|
C | T | 4 | a0001c0001t0001g0080a0001c0001t0001g0168a0001c0010t0003g0098others(1): Show | 4 | HG02258.hp2 HG02970.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.123-42188C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6782574 | ||||||
| chr18:6782590
|
G | T | 3 | a0001c0001t0001g0080a0001c0010t0003g0098a0001c0018t0020g0007 | 3 | HG02258.hp2 HG02970.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.123-42172G>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6782590 | ||||||
| chr18:6782592
|
A | AT | 23 | a0001c0001t0001g0001a0001c0001t0001g0097a0001c0001t0001g0184others(20): Show | 23 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(20): Show |
intron_variant | MODIFIER | c.123-42133dupT | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6782592 | |||||
| chr18:6782592
|
A | ATT | 34 | a0001c0001t0001g0029a0001c0001t0001g0038a0001c0001t0001g0040others(31): Show | 34 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(31): Show |
intron_variant | MODIFIER | c.123-42134_123-4213 others(6): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6782592 | |||||
| chr18:6782592
|
A | ATTT | 17 | a0001c0001t0001g0042a0001c0001t0001g0129a0001c0001t0001g0189others(14): Show | 17 | HG00280.hp2 HG00558.hp2 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.123-42135_123-4213 others(7): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6782592 | |||||
| chr18:6782592
|
A | ATTTT | 18 | a0001c0001t0001g0018a0001c0001t0001g0070a0001c0001t0001g0082others(15): Show | 18 | HG01993.hp1 HG02055.hp2 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.123-42136_123-4213 others(8): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6782592 | |||||
| chr18:6782592
|
A | ATTTTT | 13 | a0001c0001t0001g0034a0001c0001t0001g0185a0001c0001t0017g0118others(10): Show | 13 | HG01943.hp2 HG02080.hp1 HG02602.hp1 others(10): Show |
intron_variant | MODIFIER | c.123-42137_123-4213 others(9): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6782592 | |||||
| chr18:6782592
|
A | T | 4 | a0001c0001t0001g0080a0001c0001t0001g0168a0001c0010t0003g0098others(1): Show | 4 | HG02258.hp2 HG02970.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.123-42170A>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6782592 | ||||||
| chr18:6782592
|
AT | A | 10 | a0001c0001t0001g0037a0001c0001t0001g0054a0001c0001t0001g0198others(7): Show | 10 | HG00099.hp1 HG01496.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.123-42133delT | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6782592 | |||||
| chr18:6782592
|
ATTTTT | A | 7 | a0001c0001t0007g0116a0001c0001t0007g0117a0001c0003t0003g0119others(4): Show | 7 | HG02451.hp2 HG02559.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.123-42137_123-4213 others(9): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6782592 | |||||
| chr18:6782592
|
ATTTTTTT | A | 11 | a0001c0001t0001g0019a0001c0001t0001g0072a0001c0001t0006g0155others(8): Show | 11 | HG00735.hp1 HG01346.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.123-42139_123-4213 others(11): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6782592 | |||||
| chr18:6782592
|
ATTTTTTT others(1): Show |
A | 31 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0026others(28): Show | 31 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(28): Show |
intron_variant | MODIFIER | c.123-42140_123-4213 others(12): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6782592 | |||||
| chr18:6782592
|
ATTTTTTT others(2): Show |
A | 30 | a0001c0001t0001g0035a0001c0001t0001g0049a0001c0001t0001g0071others(27): Show | 30 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(27): Show |
intron_variant | MODIFIER | c.123-42141_123-4213 others(13): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6782592 | |||||
| chr18:6782592
|
ATTTTTTT others(3): Show |
A | 7 | a0001c0001t0001g0107a0001c0001t0001g0165a0001c0001t0001g0211others(4): Show | 7 | HG01243.hp1 HG02109.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.123-42142_123-4213 others(14): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6782592 | |||||
| chr18:6782592
|
ATTTTTTT others(4): Show |
A | 3 | a0001c0003t0003g0085a0001c0003t0003g0104a0010c0014t0001g0142 | 3 | HG01106.hp1 NA19043.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.123-42143_123-4213 others(15): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6782592 | |||||
| chr18:6782592
|
ATTTTTTT others(5): Show |
A | 2 | a0001c0001t0001g0141a0001c0015t0003g0167 | 2 | HG04115.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.123-42144_123-4213 others(16): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6782592 | |||||
| chr18:6782592
|
ATTTTTTT others(11): Show |
A | 1 | a0008c0011t0005g0016 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.123-42150_123-4213 others(22): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6782592 | |||||
| chr18:6782592
|
ATTTTTTT others(12): Show |
A | 5 | a0001c0001t0001g0161a0001c0001t0006g0164a0002c0002t0002g0163others(2): Show | 5 | HG01884.hp2 HG01952.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.123-42151_123-4213 others(23): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6782592 | |||||
| chr18:6782675
|
C | T | 1 | a0001c0003t0003g0208 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.123-42087C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6782675 | ||||||
| chr18:6782732
|
G | A | 1 | a0001c0001t0006g0155 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.123-42030G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6782732 | ||||||
| chr18:6782745
|
C | T | 1 | a0001c0001t0001g0102 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.123-42017C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6782745 | ||||||
| chr18:6782913
|
C | T | 9 | a0001c0001t0001g0106a0001c0001t0001g0161a0001c0001t0006g0164others(6): Show | 9 | HG01884.hp2 HG01952.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.123-41849C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6782913 | ||||||
| chr18:6782917
|
A | G | 76 | a0001c0001t0001g0003a0001c0001t0001g0035a0001c0001t0001g0049others(73): Show | 76 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.123-41845A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6782917 | ||||||
| chr18:6783178
|
G | A | 52 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(49): Show | 52 | HG00099.hp2 HG00408.hp1 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.123-41584G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6783178 | ||||||
| chr18:6783239
|
G | A | 4 | a0001c0001t0001g0080a0001c0001t0001g0168a0001c0010t0003g0098others(1): Show | 4 | HG02258.hp2 HG02970.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.123-41523G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6783239 | ||||||
| chr18:6783303
|
C | CT | 6 | a0001c0001t0001g0165a0001c0001t0019g0008a0001c0003t0003g0002others(3): Show | 6 | HG02109.hp1 HG02630.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.123-41444dupT | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6783303 | |||||
| chr18:6783303
|
CT | C | 14 | a0001c0001t0001g0029a0001c0001t0001g0038a0001c0001t0001g0040others(11): Show | 14 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(11): Show |
intron_variant | MODIFIER | c.123-41444delT | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6783303 | |||||
| chr18:6783335
|
CTT | C | 53 | a0001c0001t0001g0035a0001c0001t0001g0049a0001c0001t0001g0071others(50): Show | 53 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.123-41426_123-4142 others(6): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6783335 | ||||||
| chr18:6783364
|
C | T | 1 | a0003c0004t0001g0025 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.123-41398C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6783364 | ||||||
| chr18:6783368
|
C | T | 6 | a0001c0001t0001g0034a0002c0002t0002g0033a0002c0002t0002g0126others(3): Show | 6 | HG02273.hp2 NA18940.hp2 NA18941.hp1 others(3): Show |
intron_variant | MODIFIER | c.123-41394C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6783368 | ||||||
| chr18:6783431
|
AGCTGGGA others(127): Show |
A | 10 | a0001c0001t0001g0072a0001c0001t0001g0100a0001c0001t0006g0155others(7): Show | 10 | HG01175.hp2 HG01346.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.123-41315_123-4118 others(4): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6783431 | |||||
| chr18:6783499
|
C | G | 1 | a0001c0001t0008g0143 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.123-41263C>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6783499 | ||||||
| chr18:6783628
|
T | G | 1 | a0001c0001t0001g0003 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.123-41134T>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6783628 | ||||||
| chr18:6783689
|
C | T | 7 | a0001c0001t0001g0211a0001c0001t0007g0116a0001c0001t0007g0117others(4): Show | 7 | HG02647.hp2 HG02895.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.123-41073C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6783689 | ||||||
| chr18:6783760
|
G | A | 158 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0018others(155): Show | 158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
intron_variant | MODIFIER | c.123-41002G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6783760 | ||||||
| chr18:6783819
|
A | C | 197 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(194): Show | 197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.123-40943A>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6783819 | ||||||
| chr18:6783829
|
C | T | 167 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(164): Show | 167 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.123-40933C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6783829 | ||||||
| chr18:6784083
|
A | G | 30 | a0001c0001t0001g0001a0001c0001t0001g0044a0001c0001t0001g0052others(27): Show | 30 | HG00099.hp1 HG00280.hp2 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.123-40679A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6784083 | ||||||
| chr18:6784094
|
C | T | 1 | a0001c0001t0001g0070 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.123-40668C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6784094 | ||||||
| chr18:6784138
|
C | G | 1 | a0008c0011t0005g0016 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.123-40624C>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6784138 | ||||||
| chr18:6784139
|
C | T | 2 | a0001c0001t0001g0194a0002c0002t0002g0196 | 2 | HG02071.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.123-40623C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6784139 | ||||||
| chr18:6784169
|
C | A | 1 | a0004c0007t0004g0115 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.123-40593C>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6784169 | ||||||
| chr18:6784343
|
A | G | 1 | a0001c0001t0001g0168 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.123-40419A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6784343 | ||||||
| chr18:6784420
|
C | T | 1 | a0001c0001t0001g0189 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.123-40342C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6784420 | ||||||
| chr18:6784693
|
A | G | 194 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(191): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.123-40069A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6784693 | ||||||
| chr18:6784815
|
G | A | 2 | a0003c0004t0001g0241a0003c0004t0001g0248 | 2 | NA18966.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.123-39947G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6784815 | ||||||
| chr18:6784990
|
T | C | 5 | a0001c0001t0001g0211a0001c0001t0007g0212a0001c0001t0009g0245others(2): Show | 5 | HG02886.hp2 HG02895.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.123-39772T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6784990 | ||||||
| chr18:6785067
|
T | C | 1 | a0002c0002t0002g0066 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.123-39695T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6785067 | ||||||
| chr18:6785070
|
C | T | 1 | a0001c0001t0001g0102 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.123-39692C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6785070 | ||||||
| chr18:6785156
|
C | A | 1 | a0001c0001t0001g0003 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.123-39606C>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6785156 | ||||||
| chr18:6785338
|
A | G | 6 | a0001c0001t0001g0106a0001c0003t0003g0085a0001c0003t0003g0122others(3): Show | 6 | HG01106.hp1 HG02451.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.123-39424A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6785338 | ||||||
| chr18:6785362
|
A | G | 1 | a0003c0004t0001g0220 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.123-39400A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6785362 | ||||||
| chr18:6785633
|
T | C | 7 | a0001c0001t0001g0004a0001c0001t0001g0080a0001c0003t0003g0119others(4): Show | 7 | HG01081.hp2 HG02258.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.123-39129T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6785633 | ||||||
| chr18:6785635
|
G | A | 7 | a0001c0001t0001g0004a0001c0001t0001g0080a0001c0003t0003g0119others(4): Show | 7 | HG01081.hp2 HG02258.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.123-39127G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6785635 | ||||||
| chr18:6786086
|
G | C | 1 | a0002c0005t0002g0061 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.123-38676G>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6786086 | ||||||
| chr18:6786184
|
G | A | 8 | a0001c0001t0001g0100a0001c0003t0003g0002a0001c0003t0003g0084others(5): Show | 8 | HG01175.hp2 HG01346.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.123-38578G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6786184 | ||||||
| chr18:6786220
|
G | A | 2 | a0002c0002t0002g0014a0003c0004t0001g0183 | 2 | HG00597.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.123-38542G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6786220 | ||||||
| chr18:6786298
|
GT | G | 7 | a0001c0001t0001g0004a0001c0001t0001g0080a0001c0003t0003g0119others(4): Show | 7 | HG01081.hp2 HG02258.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.123-38460delT | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6786298 | |||||
| chr18:6786568
|
T | C | 1 | a0001c0001t0008g0074 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.123-38194T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6786568 | ||||||
| chr18:6786769
|
A | C | 24 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0026others(21): Show | 24 | HG00099.hp2 HG00408.hp1 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.123-37993A>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6786769 | ||||||
| chr18:6786793
|
GA | G | 14 | a0001c0001t0001g0100a0001c0001t0001g0121a0001c0001t0001g0124others(11): Show | 14 | HG01175.hp2 HG01346.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.123-37959delA | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6786793 | |||||
| chr18:6786994
|
C | T | 1 | a0001c0001t0001g0215 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.123-37768C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6786994 | ||||||
| chr18:6787023
|
C | G | 8 | a0001c0001t0001g0204a0001c0001t0001g0216a0002c0002t0002g0014others(5): Show | 8 | HG00597.hp1 HG02040.hp2 NA18966.hp1 others(5): Show |
intron_variant | MODIFIER | c.123-37739C>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6787023 | ||||||
| chr18:6787093
|
G | A | 62 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(59): Show | 62 | HG00099.hp2 HG00408.hp1 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.123-37669G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6787093 | ||||||
| chr18:6787155
|
G | C | 1 | a0001c0003t0003g0208 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.123-37607G>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6787155 | ||||||
| chr18:6787212
|
C | T | 4 | a0001c0001t0001g0106a0001c0003t0003g0122a0001c0012t0014g0159others(1): Show | 4 | HG02451.hp2 HG02559.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.123-37550C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6787212 | ||||||
| chr18:6787219
|
TA | T | 55 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(52): Show | 55 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(52): Show |
intron_variant | MODIFIER | c.123-37520delA | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6787219 | |||||
| chr18:6787219
|
TAAAAAAA others(5): Show |
T | 4 | a0001c0001t0008g0143a0001c0003t0003g0154a0001c0003t0003g0169others(1): Show | 4 | HG02818.hp1 HG02965.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.123-37531_123-3752 others(16): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6787219 | |||||
| chr18:6787281
|
GA | G | 9 | a0001c0001t0001g0071a0001c0001t0001g0106a0001c0003t0003g0085others(6): Show | 9 | HG00280.hp1 HG00438.hp2 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.123-37469delA | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6787281 | |||||
| chr18:6787282
|
A | G | 1 | a0005c0006t0003g0177 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.123-37480A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6787282 | ||||||
| chr18:6787362
|
C | T | 1 | a0002c0002t0002g0207 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.123-37400C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6787362 | ||||||
| chr18:6787552
|
C | T | 1 | a0008c0011t0005g0016 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.123-37210C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6787552 | ||||||
| chr18:6787582
|
A | T | 1 | a0008c0011t0005g0016 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.123-37180A>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6787582 | ||||||
| chr18:6787881
|
A | AT | 7 | a0001c0001t0001g0004a0001c0001t0001g0080a0001c0003t0003g0119others(4): Show | 7 | HG01081.hp2 HG02258.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.123-36879dupT | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6787881 | |||||
| chr18:6787952
|
A | G | 1 | a0002c0002t0002g0163 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.123-36810A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6787952 | ||||||
| chr18:6788270
|
C | T | 1 | a0001c0001t0001g0139 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.123-36492C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6788270 | ||||||
| chr18:6788390
|
A | T | 5 | a0001c0001t0008g0143a0001c0003t0003g0154a0001c0003t0003g0169others(2): Show | 5 | HG02818.hp1 HG02965.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.123-36372A>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6788390 | ||||||
| chr18:6788446
|
G | GT | 8 | a0001c0001t0001g0165a0001c0001t0001g0168a0001c0001t0008g0143others(5): Show | 8 | HG02109.hp1 HG02818.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.123-36309dupT | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6788446 | |||||
| chr18:6788462
|
T | G | 58 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(55): Show | 58 | HG00099.hp2 HG00408.hp1 HG00735.hp1 others(55): Show |
intron_variant | MODIFIER | c.123-36300T>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6788462 | ||||||
| chr18:6788544
|
C | T | 4 | a0002c0002t0002g0243a0002c0005t0002g0108a0002c0005t0002g0133others(1): Show | 4 | NA18947.hp2 NA18968.hp2 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.123-36218C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6788544 | ||||||
| chr18:6788578
|
C | T | 8 | a0001c0001t0001g0165a0001c0001t0001g0168a0001c0001t0008g0143others(5): Show | 8 | HG02109.hp1 HG02818.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.123-36184C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6788578 | ||||||
| chr18:6788635
|
T | G | 2 | a0001c0001t0001g0194a0002c0002t0002g0196 | 2 | HG02071.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.123-36127T>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6788635 | ||||||
| chr18:6788706
|
C | A | 1 | a0001c0001t0022g0067 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.123-36056C>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6788706 | ||||||
| chr18:6788873
|
G | C | 1 | a0001c0001t0001g0168 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.123-35889G>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6788873 | ||||||
| chr18:6788894
|
G | C | 1 | a0001c0001t0001g0184 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.123-35868G>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6788894 | ||||||
| chr18:6789007
|
A | T | 2 | a0001c0003t0003g0119a0001c0018t0020g0007 | 2 | HG03139.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.123-35755A>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6789007 | ||||||
| chr18:6789027
|
G | C | 58 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(55): Show | 58 | HG00099.hp2 HG00408.hp1 HG00735.hp1 others(55): Show |
intron_variant | MODIFIER | c.123-35735G>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6789027 | ||||||
| chr18:6789150
|
G | A | 1 | a0004c0007t0002g0056 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.123-35612G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6789150 | ||||||
| chr18:6789300
|
G | A | 36 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0019others(33): Show | 36 | HG00099.hp2 HG00408.hp1 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.123-35462G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6789300 | ||||||
| chr18:6789553
|
C | T | 7 | a0001c0001t0001g0004a0001c0001t0001g0080a0001c0003t0003g0119others(4): Show | 7 | HG01081.hp2 HG02258.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.123-35209C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6789553 | ||||||
| chr18:6789741
|
A | C | 7 | a0001c0001t0001g0004a0001c0001t0001g0080a0001c0003t0003g0119others(4): Show | 7 | HG01081.hp2 HG02258.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.123-35021A>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6789741 | ||||||
| chr18:6789755
|
C | T | 7 | a0001c0001t0001g0165a0001c0001t0008g0143a0001c0003t0003g0154others(4): Show | 7 | HG02109.hp1 HG02818.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.123-35007C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6789755 | ||||||
| chr18:6789835
|
G | GT | 56 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(53): Show | 56 | HG00099.hp2 HG00408.hp1 HG00735.hp1 others(53): Show |
intron_variant | MODIFIER | c.123-34917dupT | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6789835 | |||||
| chr18:6789943
|
G | A | 1 | a0002c0002t0002g0207 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.123-34819G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6789943 | ||||||
| chr18:6789947
|
C | G | 7 | a0001c0001t0001g0165a0001c0001t0008g0143a0001c0003t0003g0154others(4): Show | 7 | HG02109.hp1 HG02818.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.123-34815C>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6789947 | ||||||
| chr18:6789951
|
C | G | 7 | a0001c0001t0001g0165a0001c0001t0008g0143a0001c0003t0003g0154others(4): Show | 7 | HG02109.hp1 HG02818.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.123-34811C>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6789951 | ||||||
| chr18:6790036
|
A | C | 43 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0019others(40): Show | 43 | HG00099.hp2 HG00408.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.123-34726A>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6790036 | ||||||
| chr18:6790119
|
G | A | 2 | a0001c0001t0001g0205a0003c0022t0003g0132 | 2 | NA18940.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.123-34643G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6790119 | ||||||
| chr18:6790382
|
G | A | 1 | a0003c0022t0003g0132 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.123-34380G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6790382 | ||||||
| chr18:6790733
|
A | G | 65 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(62): Show | 65 | HG00099.hp2 HG00408.hp1 HG00735.hp1 others(62): Show |
intron_variant | MODIFIER | c.123-34029A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6790733 | ||||||
| chr18:6790759
|
G | A | 2 | a0001c0003t0003g0233a0001c0003t0003g0234 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.123-34003G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6790759 | ||||||
| chr18:6790842
|
G | A | 1 | a0008c0011t0005g0016 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.123-33920G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6790842 | ||||||
| chr18:6791110
|
C | A | 13 | a0001c0001t0001g0004a0001c0001t0001g0080a0001c0001t0001g0106others(10): Show | 13 | HG01081.hp2 HG01106.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.123-33652C>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6791110 | ||||||
| chr18:6791204
|
C | G | 1 | a0003c0023t0001g0120 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.123-33558C>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6791204 | ||||||
| chr18:6791354
|
C | T | 24 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0026others(21): Show | 24 | HG00099.hp2 HG00408.hp1 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.123-33408C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6791354 | ||||||
| chr18:6791568
|
G | A | 9 | a0001c0001t0001g0165a0001c0001t0001g0168a0001c0001t0008g0143others(6): Show | 9 | HG02109.hp1 HG02630.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.123-33194G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6791568 | ||||||
| chr18:6791679
|
T | C | 1 | a0001c0001t0009g0245 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.123-33083T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6791679 | ||||||
| chr18:6791819
|
C | CT | 9 | a0001c0001t0001g0165a0001c0001t0001g0168a0001c0001t0008g0143others(6): Show | 9 | HG02109.hp1 HG02630.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.123-32933dupT | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6791819 | |||||
| chr18:6791838
|
G | T | 6 | a0001c0001t0001g0052a0001c0001t0016g0081a0001c0003t0003g0201others(3): Show | 6 | HG00735.hp2 HG01346.hp2 HG01943.hp1 others(3): Show |
intron_variant | MODIFIER | c.123-32924G>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6791838 | ||||||
| chr18:6791839
|
G | T | 240 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(237): Show | 240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.123-32923G>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6791839 | ||||||
| chr18:6791844
|
T | G | 1 | a0001c0003t0003g0060 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.123-32918T>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6791844 | ||||||
| chr18:6791959
|
C | T | 2 | a0001c0003t0003g0002a0001c0003t0003g0104 | 2 | HG03471.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.123-32803C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6791959 | ||||||
| chr18:6791985
|
C | T | 1 | a0001c0001t0016g0081 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.123-32777C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6791985 | ||||||
| chr18:6792211
|
G | A | 9 | a0001c0001t0001g0165a0001c0001t0001g0168a0001c0001t0008g0143others(6): Show | 9 | HG02109.hp1 HG02630.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.123-32551G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6792211 | ||||||
| chr18:6792397
|
A | C | 9 | a0001c0001t0001g0165a0001c0001t0001g0168a0001c0001t0008g0143others(6): Show | 9 | HG02109.hp1 HG02630.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.123-32365A>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6792397 | ||||||
| chr18:6792463
|
G | T | 8 | a0001c0001t0001g0165a0001c0001t0001g0168a0001c0001t0008g0143others(5): Show | 8 | HG02109.hp1 HG02818.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.123-32299G>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6792463 | ||||||
| chr18:6792555
|
T | C | 6 | a0001c0001t0001g0003a0001c0001t0001g0072a0001c0001t0006g0155others(3): Show | 6 | HG02258.hp1 HG02630.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.123-32207T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6792555 | ||||||
| chr18:6792842
|
G | A | 1 | a0006c0009t0009g0153 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.123-31920G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6792842 | ||||||
| chr18:6793029
|
C | T | 1 | a0003c0004t0001g0045 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.123-31733C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6793029 | ||||||
| chr18:6793113
|
T | G | 1 | a0001c0003t0003g0105 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.123-31649T>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6793113 | ||||||
| chr18:6793133
|
T | C | 2 | a0001c0001t0001g0100a0001c0003t0003g0145 | 2 | HG02451.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.123-31629T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6793133 | ||||||
| chr18:6793240
|
G | A | 1 | a0003c0004t0001g0032 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.123-31522G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6793240 | ||||||
| chr18:6793294
|
C | G | 6 | a0001c0001t0001g0106a0001c0003t0003g0085a0001c0003t0003g0122others(3): Show | 6 | HG01106.hp1 HG02451.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.123-31468C>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6793294 | ||||||
| chr18:6793664
|
T | A | 1 | a0003c0004t0001g0173 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.123-31098T>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6793664 | ||||||
| chr18:6793863
|
G | A | 3 | a0001c0001t0001g0106a0001c0003t0003g0122a0002c0002t0004g0059 | 3 | HG02451.hp2 HG02647.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.123-30899G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6793863 | ||||||
| chr18:6793916
|
G | A | 7 | a0001c0001t0001g0004a0001c0001t0001g0080a0001c0003t0003g0119others(4): Show | 7 | HG01081.hp2 HG02258.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.123-30846G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6793916 | ||||||
| chr18:6794012
|
A | C | 1 | a0001c0001t0001g0168 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.123-30750A>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6794012 | ||||||
| chr18:6794022
|
T | G | 42 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0019others(39): Show | 42 | HG00099.hp2 HG00408.hp1 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.123-30740T>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6794022 | ||||||
| chr18:6794063
|
A | C | 7 | a0001c0001t0001g0004a0001c0001t0001g0080a0001c0003t0003g0119others(4): Show | 7 | HG01081.hp2 HG02258.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.123-30699A>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6794063 | ||||||
| chr18:6794218
|
A | G | 5 | a0001c0001t0001g0128a0002c0002t0002g0224a0003c0004t0001g0021others(2): Show | 5 | HG00597.hp2 HG00621.hp2 HG02129.hp1 others(2): Show |
intron_variant | MODIFIER | c.123-30544A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6794218 | ||||||
| chr18:6794273
|
T | C | 13 | a0001c0001t0001g0004a0001c0001t0001g0080a0001c0001t0001g0106others(10): Show | 13 | HG01081.hp2 HG01106.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.123-30489T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6794273 | ||||||
| chr18:6794703
|
T | TA | 64 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(61): Show | 64 | HG00099.hp2 HG00408.hp1 HG00735.hp1 others(61): Show |
intron_variant | MODIFIER | c.123-30059_123-3005 others(5): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6794703 | ||||||
| chr18:6794767
|
C | T | 1 | a0004c0007t0004g0115 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.123-29995C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6794767 | ||||||
| chr18:6795270
|
G | A | 62 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(59): Show | 62 | HG00099.hp2 HG00408.hp1 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.123-29492G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6795270 | ||||||
| chr18:6795310
|
G | A | 5 | a0001c0001t0001g0211a0001c0001t0007g0212a0001c0001t0009g0245others(2): Show | 5 | HG02886.hp2 HG02895.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.123-29452G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6795310 | ||||||
| chr18:6795329
|
G | A | 7 | a0001c0001t0001g0004a0001c0001t0001g0080a0001c0003t0003g0119others(4): Show | 7 | HG01081.hp2 HG02258.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.123-29433G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6795329 | ||||||
| chr18:6795820
|
A | G | 1 | a0003c0004t0001g0024 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.123-28942A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6795820 | ||||||
| chr18:6795870
|
C | T | 1 | a0002c0002t0002g0103 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.123-28892C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6795870 | ||||||
| chr18:6795912
|
A | G | 6 | a0001c0001t0001g0001a0001c0001t0001g0203a0001c0003t0003g0027others(3): Show | 6 | HG00280.hp2 HG00741.hp2 HG01081.hp1 others(3): Show |
intron_variant | MODIFIER | c.123-28850A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6795912 | ||||||
| chr18:6795935
|
G | A | 63 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(60): Show | 63 | HG00099.hp2 HG00408.hp1 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.123-28827G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6795935 | ||||||
| chr18:6796111
|
T | A | 63 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(60): Show | 63 | HG00099.hp2 HG00408.hp1 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.123-28651T>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6796111 | ||||||
| chr18:6796126
|
C | T | 1 | a0001c0003t0003g0154 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.123-28636C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6796126 | ||||||
| chr18:6796297
|
G | A | 1 | a0001c0019t0021g0073 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.123-28465G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6796297 | ||||||
| chr18:6796371
|
C | T | 13 | a0001c0001t0001g0004a0001c0001t0001g0080a0001c0001t0001g0106others(10): Show | 13 | HG01081.hp2 HG01106.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.123-28391C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6796371 | ||||||
| chr18:6796440
|
T | C | 201 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(198): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.123-28322T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6796440 | ||||||
| chr18:6796482
|
T | C | 42 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0019others(39): Show | 42 | HG00099.hp2 HG00408.hp1 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.123-28280T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6796482 | ||||||
| chr18:6796524
|
G | A | 13 | a0001c0001t0001g0100a0001c0001t0001g0211a0001c0001t0007g0212others(10): Show | 13 | HG01175.hp2 HG01346.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.123-28238G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6796524 | ||||||
| chr18:6796543
|
G | A | 62 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(59): Show | 62 | HG00099.hp2 HG00408.hp1 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.123-28219G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6796543 | ||||||
| chr18:6796609
|
G | A | 1 | a0003c0004t0001g0030 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.123-28153G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6796609 | ||||||
| chr18:6796781
|
C | T | 1 | a0005c0006t0003g0127 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.123-27981C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6796781 | ||||||
| chr18:6796821
|
T | TAC | 39 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0019others(36): Show | 39 | HG00099.hp2 HG00408.hp1 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.123-27935_123-2793 others(6): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6796821 | |||||
| chr18:6796821
|
T | TACAC | 3 | a0001c0003t0003g0084a0002c0002t0002g0148a0007c0008t0002g0146 | 3 | HG01346.hp1 HG02922.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.123-27937_123-2793 others(8): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6796821 | |||||
| chr18:6796829
|
T | C | 63 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(60): Show | 63 | HG00099.hp2 HG00408.hp1 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.123-27933T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6796829 | ||||||
| chr18:6797028
|
A | G | 1 | a0003c0004t0001g0200 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.123-27734A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6797028 | ||||||
| chr18:6797245
|
A | C | 4 | a0001c0001t0001g0106a0001c0003t0003g0122a0001c0012t0014g0159others(1): Show | 4 | HG02451.hp2 HG02559.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.123-27517A>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6797245 | ||||||
| chr18:6797512
|
C | T | 1 | a0003c0004t0001g0191 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.123-27250C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6797512 | ||||||
| chr18:6797513
|
G | A | 58 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(55): Show | 58 | HG00099.hp2 HG00408.hp1 HG00735.hp1 others(55): Show |
intron_variant | MODIFIER | c.123-27249G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6797513 | ||||||
| chr18:6797558
|
T | G | 1 | a0001c0001t0001g0239 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.123-27204T>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6797558 | ||||||
| chr18:6797677
|
T | C | 1 | a0004c0007t0002g0056 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.123-27085T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6797677 | ||||||
| chr18:6797687
|
A | G | 130 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0029others(127): Show | 130 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.123-27075A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6797687 | ||||||
| chr18:6797695
|
T | G | 1 | a0001c0001t0001g0161 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.123-27067T>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6797695 | ||||||
| chr18:6797882
|
G | A | 5 | a0001c0001t0001g0139a0001c0001t0001g0186a0002c0002t0002g0244others(2): Show | 5 | HG00423.hp2 HG00544.hp1 HG02080.hp2 others(2): Show |
intron_variant | MODIFIER | c.123-26880G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6797882 | ||||||
| chr18:6797946
|
C | G | 1 | a0001c0001t0001g0165 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.123-26816C>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6797946 | ||||||
| chr18:6797950
|
G | A | 7 | a0001c0001t0001g0004a0001c0001t0001g0080a0001c0003t0003g0119others(4): Show | 7 | HG01081.hp2 HG02258.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.123-26812G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6797950 | ||||||
| chr18:6798067
|
TAAAAA | T | 128 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0029others(125): Show | 128 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.123-26694_123-2669 others(9): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6798067 | ||||||
| chr18:6798254
|
C | T | 4 | a0001c0001t0001g0106a0001c0003t0003g0122a0001c0012t0014g0159others(1): Show | 4 | HG02451.hp2 HG02559.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.123-26508C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6798254 | ||||||
| chr18:6798282
|
C | T | 23 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0026others(20): Show | 23 | HG00099.hp2 HG00408.hp1 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.123-26480C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6798282 | ||||||
| chr18:6798304
|
C | T | 1 | a0003c0004t0001g0010 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.123-26458C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6798304 | ||||||
| chr18:6798338
|
C | G | 61 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(58): Show | 61 | HG00099.hp2 HG00408.hp1 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.123-26424C>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6798338 | ||||||
| chr18:6798386
|
G | A | 1 | a0003c0004t0001g0219 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.123-26376G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6798386 | ||||||
| chr18:6798435
|
C | T | 1 | a0002c0002t0002g0096 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.123-26327C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6798435 | ||||||
| chr18:6798441
|
G | A | 7 | a0001c0001t0001g0165a0001c0001t0008g0143a0001c0003t0003g0154others(4): Show | 7 | HG02109.hp1 HG02818.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.123-26321G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6798441 | ||||||
| chr18:6798515
|
C | G | 7 | a0001c0001t0001g0165a0001c0001t0008g0143a0001c0003t0003g0154others(4): Show | 7 | HG02109.hp1 HG02818.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.123-26247C>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6798515 | ||||||
| chr18:6798571
|
A | T | 62 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(59): Show | 62 | HG00099.hp2 HG00408.hp1 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.123-26191A>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6798571 | ||||||
| chr18:6798808
|
G | A | 61 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(58): Show | 61 | HG00099.hp2 HG00408.hp1 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.123-25954G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6798808 | ||||||
| chr18:6798821
|
G | T | 6 | a0001c0001t0001g0106a0001c0003t0003g0085a0001c0003t0003g0122others(3): Show | 6 | HG01106.hp1 HG02451.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.123-25941G>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6798821 | ||||||
| chr18:6798854
|
T | C | 4 | a0001c0001t0001g0128a0002c0002t0002g0224a0003c0004t0001g0021others(1): Show | 4 | HG00597.hp2 HG00621.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.123-25908T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6798854 | ||||||
| chr18:6798917
|
G | A | 1 | a0008c0011t0005g0016 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.123-25845G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6798917 | ||||||
| chr18:6799052
|
C | A | 7 | a0001c0001t0001g0004a0001c0001t0001g0080a0001c0003t0003g0119others(4): Show | 7 | HG01081.hp2 HG02258.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.123-25710C>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6799052 | ||||||
| chr18:6799323
|
GT | G | 41 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0019others(38): Show | 41 | HG00099.hp2 HG00408.hp1 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.123-25438delT | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6799323 | ||||||
| chr18:6799456
|
C | T | 2 | a0001c0001t0001g0168a0001c0015t0003g0167 | 2 | HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.123-25306C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6799456 | ||||||
| chr18:6799481
|
A | G | 1 | a0008c0011t0005g0016 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.123-25281A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6799481 | ||||||
| chr18:6799519
|
G | A | 2 | a0001c0003t0003g0085a0010c0014t0001g0142 | 2 | HG01106.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.123-25243G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6799519 | ||||||
| chr18:6799656
|
T | C | 1 | a0003c0004t0001g0020 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.123-25106T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6799656 | ||||||
| chr18:6799781
|
G | A | 1 | a0001c0001t0001g0225 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.123-24981G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6799781 | ||||||
| chr18:6799782
|
T | C | 1 | a0001c0001t0001g0225 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.123-24980T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6799782 | ||||||
| chr18:6800518
|
A | C | 21 | a0001c0001t0001g0004a0001c0001t0001g0080a0001c0001t0001g0100others(18): Show | 21 | HG01081.hp2 HG01106.hp1 HG01175.hp2 others(18): Show |
intron_variant | MODIFIER | c.123-24244A>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6800518 | ||||||
| chr18:6800604
|
CAAG | C | 3 | a0001c0003t0003g0084a0002c0002t0002g0148a0007c0008t0002g0146 | 3 | HG01346.hp1 HG02922.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.123-24155_123-2415 others(7): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6800604 | |||||
| chr18:6800652
|
C | T | 1 | a0003c0004t0001g0227 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.123-24110C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6800652 | ||||||
| chr18:6800823
|
T | C | 1 | a0002c0002t0002g0199 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.123-23939T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6800823 | ||||||
| chr18:6801019
|
G | T | 22 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0026others(19): Show | 22 | HG00099.hp2 HG00408.hp1 HG00735.hp1 others(19): Show |
intron_variant | MODIFIER | c.123-23743G>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6801019 | ||||||
| chr18:6801279
|
T | C | 196 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(193): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.123-23483T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6801279 | ||||||
| chr18:6801371
|
T | C | 22 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0026others(19): Show | 22 | HG00099.hp2 HG00408.hp1 HG00735.hp1 others(19): Show |
intron_variant | MODIFIER | c.123-23391T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6801371 | ||||||
| chr18:6801663
|
T | G | 7 | a0001c0001t0001g0165a0001c0001t0008g0143a0001c0001t0022g0067others(4): Show | 7 | HG02109.hp1 HG02630.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.123-23099T>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6801663 | ||||||
| chr18:6801751
|
C | G | 5 | a0001c0001t0001g0107a0001c0001t0007g0116a0001c0001t0007g0117others(2): Show | 5 | HG01243.hp1 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.123-23011C>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6801751 | ||||||
| chr18:6801793
|
T | G | 6 | a0001c0001t0001g0003a0001c0001t0001g0072a0001c0001t0006g0155others(3): Show | 6 | HG02258.hp1 HG02630.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.123-22969T>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6801793 | ||||||
| chr18:6801953
|
C | G | 2 | a0001c0003t0003g0085a0010c0014t0001g0142 | 2 | HG01106.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.123-22809C>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6801953 | ||||||
| chr18:6802107
|
T | G | 22 | a0001c0001t0001g0004a0001c0001t0001g0080a0001c0001t0001g0106others(19): Show | 22 | HG01081.hp2 HG01106.hp1 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.123-22655T>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6802107 | ||||||
| chr18:6802132
|
A | G | 2 | a0001c0003t0003g0002a0001c0003t0003g0104 | 2 | HG03471.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.123-22630A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6802132 | ||||||
| chr18:6802159
|
T | A | 1 | a0002c0002t0002g0099 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.123-22603T>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6802159 | ||||||
| chr18:6802335
|
C | CT | 38 | a0001c0001t0001g0054a0001c0001t0001g0070a0001c0001t0001g0072others(35): Show | 38 | HG00099.hp1 HG00597.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.123-22399dupT | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6802335 | |||||
| chr18:6802335
|
C | CTT | 27 | a0001c0001t0001g0001a0001c0001t0001g0044a0001c0001t0001g0052others(24): Show | 27 | HG00280.hp2 HG00735.hp2 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.123-22400_123-2239 others(6): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6802335 | |||||
| chr18:6802335
|
C | CTTT | 9 | a0001c0001t0001g0124a0001c0001t0001g0149a0001c0001t0001g0184others(6): Show | 9 | HG01175.hp2 HG02109.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.123-22401_123-2239 others(7): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6802335 | |||||
| chr18:6802335
|
CT | C | 16 | a0001c0001t0001g0004a0001c0001t0001g0080a0001c0001t0001g0106others(13): Show | 16 | HG01081.hp2 HG01256.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.123-22399delT | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6802335 | |||||
| chr18:6802335
|
CTTTTTTT others(3): Show |
C | 1 | a0008c0011t0005g0016 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.123-22408_123-2239 others(14): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6802335 | |||||
| chr18:6802492
|
C | T | 1 | a0003c0004t0001g0020 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.123-22270C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6802492 | ||||||
| chr18:6802796
|
C | T | 1 | a0002c0002t0002g0172 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.123-21966C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6802796 | ||||||
| chr18:6802830
|
C | A | 9 | a0001c0001t0001g0004a0001c0001t0001g0080a0001c0003t0003g0085others(6): Show | 9 | HG01081.hp2 HG01106.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.123-21932C>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6802830 | ||||||
| chr18:6802909
|
G | A | 3 | a0001c0001t0001g0106a0001c0003t0003g0122a0001c0012t0014g0159 | 3 | HG02559.hp2 HG02647.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.123-21853G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6802909 | ||||||
| chr18:6803168
|
A | G | 2 | a0001c0001t0001g0168a0001c0015t0003g0167 | 2 | HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.123-21594A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6803168 | ||||||
| chr18:6803172
|
T | C | 1 | a0002c0005t0002g0061 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.123-21590T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6803172 | ||||||
| chr18:6803189
|
G | A | 1 | a0004c0007t0004g0115 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.123-21573G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6803189 | ||||||
| chr18:6803375
|
G | A | 11 | a0001c0001t0001g0106a0001c0001t0001g0165a0001c0001t0001g0168others(8): Show | 11 | HG02109.hp1 HG02559.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.123-21387G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6803375 | ||||||
| chr18:6803513
|
T | C | 1 | a0002c0002t0002g0015 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.123-21249T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6803513 | ||||||
| chr18:6803813
|
C | G | 1 | a0001c0001t0001g0168 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.123-20949C>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6803813 | ||||||
| chr18:6803814
|
T | C | 7 | a0001c0001t0001g0004a0001c0001t0001g0080a0001c0003t0003g0119others(4): Show | 7 | HG01081.hp2 HG02258.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.123-20948T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6803814 | ||||||
| chr18:6803839
|
C | T | 3 | a0001c0001t0001g0106a0001c0003t0003g0122a0001c0012t0014g0159 | 3 | HG02559.hp2 HG02647.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.123-20923C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6803839 | ||||||
| chr18:6803841
|
C | T | 2 | a0001c0003t0003g0085a0003c0004t0001g0064 | 2 | NA18947.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.123-20921C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6803841 | ||||||
| chr18:6803981
|
G | A | 1 | a0001c0015t0003g0167 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.123-20781G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6803981 | ||||||
| chr18:6804058
|
C | T | 22 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0026others(19): Show | 22 | HG00099.hp2 HG00408.hp1 HG00735.hp1 others(19): Show |
intron_variant | MODIFIER | c.123-20704C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6804058 | ||||||
| chr18:6804282
|
T | C | 1 | a0003c0004t0001g0032 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.123-20480T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6804282 | ||||||
| chr18:6804406
|
C | CT | 12 | a0001c0001t0001g0106a0001c0001t0001g0165a0001c0001t0001g0168others(9): Show | 12 | HG02109.hp1 HG02559.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.123-20347dupT | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6804406 | |||||
| chr18:6804570
|
A | G | 12 | a0001c0001t0001g0106a0001c0001t0001g0165a0001c0001t0001g0168others(9): Show | 12 | HG02109.hp1 HG02559.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.123-20192A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6804570 | ||||||
| chr18:6804813
|
T | G | 1 | a0008c0011t0005g0016 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.123-19949T>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6804813 | ||||||
| chr18:6804888
|
A | T | 3 | a0002c0002t0002g0214a0004c0007t0002g0036a0005c0006t0003g0226 | 3 | HG02071.hp2 HG02135.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.123-19874A>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6804888 | ||||||
| chr18:6804935
|
T | A | 3 | a0001c0001t0001g0204a0002c0002t0002g0014a0003c0004t0001g0183 | 3 | HG00597.hp1 NA18983.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.123-19827T>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6804935 | ||||||
| chr18:6804939
|
G | A | 1 | a0008c0011t0005g0016 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.123-19823G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6804939 | ||||||
| chr18:6804941
|
A | G | 1 | a0002c0002t0002g0009 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.123-19821A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6804941 | ||||||
| chr18:6805392
|
C | T | 3 | a0001c0001t0001g0182a0002c0002t0002g0083a0002c0002t0010g0206 | 3 | HG00438.hp1 HG02040.hp1 NA18941.hp2 |
intron_variant | MODIFIER | c.123-19370C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6805392 | ||||||
| chr18:6805479
|
C | CT | 38 | a0001c0001t0001g0003a0001c0001t0001g0044a0001c0001t0001g0072others(35): Show | 38 | HG00597.hp1 HG01175.hp2 HG01346.hp1 others(35): Show |
intron_variant | MODIFIER | c.123-19260dupT | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6805479 | |||||
| chr18:6805479
|
C | CTT | 17 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0026others(14): Show | 17 | HG00099.hp2 HG00408.hp1 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.123-19261_123-1926 others(6): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6805479 | |||||
| chr18:6805479
|
C | CTTT | 5 | a0001c0001t0001g0209a0001c0001t0008g0074a0001c0001t0018g0111others(2): Show | 5 | HG01891.hp2 HG02559.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.123-19262_123-1926 others(7): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6805479 | |||||
| chr18:6805479
|
CT | C | 6 | a0001c0001t0001g0038a0001c0001t0001g0128a0001c0001t0009g0005others(3): Show | 6 | HG01081.hp1 HG01891.hp1 HG02040.hp2 others(3): Show |
intron_variant | MODIFIER | c.123-19260delT | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6805479 | |||||
| chr18:6805479
|
CTTTTTTT | C | 7 | a0001c0001t0001g0004a0001c0001t0001g0080a0001c0003t0003g0119others(4): Show | 7 | HG01081.hp2 HG02258.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.123-19266_123-1926 others(11): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6805479 | |||||
| chr18:6805530
|
G | A | 1 | a0001c0001t0001g0184 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.123-19232G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6805530 | ||||||
| chr18:6805566
|
A | G | 1 | a0008c0011t0005g0016 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.123-19196A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6805566 | ||||||
| chr18:6805812
|
C | G | 1 | a0008c0011t0005g0016 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.123-18950C>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6805812 | ||||||
| chr18:6805879
|
T | C | 12 | a0001c0001t0001g0106a0001c0001t0001g0165a0001c0001t0001g0168others(9): Show | 12 | HG02109.hp1 HG02559.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.123-18883T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6805879 | ||||||
| chr18:6806013
|
T | C | 5 | a0001c0001t0001g0211a0001c0001t0007g0212a0001c0001t0009g0245others(2): Show | 5 | HG02886.hp2 HG02895.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.123-18749T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6806013 | ||||||
| chr18:6806023
|
T | C | 1 | a0008c0011t0005g0016 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.123-18739T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6806023 | ||||||
| chr18:6806107
|
T | G | 1 | a0008c0011t0005g0016 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.123-18655T>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6806107 | ||||||
| chr18:6806124
|
G | C | 12 | a0001c0001t0001g0106a0001c0001t0001g0165a0001c0001t0001g0168others(9): Show | 12 | HG02109.hp1 HG02559.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.123-18638G>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6806124 | ||||||
| chr18:6806138
|
C | T | 2 | a0001c0003t0003g0085a0010c0014t0001g0142 | 2 | HG01106.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.123-18624C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6806138 | ||||||
| chr18:6806148
|
C | T | 7 | a0001c0001t0001g0004a0001c0001t0001g0080a0001c0003t0003g0119others(4): Show | 7 | HG01081.hp2 HG02258.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.123-18614C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6806148 | ||||||
| chr18:6806170
|
A | G | 7 | a0001c0001t0001g0121a0001c0001t0001g0124a0001c0001t0001g0149others(4): Show | 7 | HG02055.hp1 HG02145.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.123-18592A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6806170 | ||||||
| chr18:6806184
|
G | A | 12 | a0001c0001t0001g0106a0001c0001t0001g0165a0001c0001t0001g0168others(9): Show | 12 | HG02109.hp1 HG02559.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.123-18578G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6806184 | ||||||
| chr18:6806189
|
T | C | 1 | a0008c0011t0005g0016 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.123-18573T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6806189 | ||||||
| chr18:6806313
|
A | G | 3 | a0001c0001t0001g0106a0001c0003t0003g0122a0001c0012t0014g0159 | 3 | HG02559.hp2 HG02647.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.123-18449A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6806313 | ||||||
| chr18:6806473
|
T | C | 1 | a0001c0001t0001g0072 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.123-18289T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6806473 | ||||||
| chr18:6806637
|
A | G | 1 | a0008c0011t0005g0016 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.123-18125A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6806637 | ||||||
| chr18:6806776
|
G | A | 1 | a0001c0015t0003g0167 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.123-17986G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6806776 | ||||||
| chr18:6806790
|
G | A | 50 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(47): Show | 50 | HG00099.hp2 HG00408.hp1 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.123-17972G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6806790 | ||||||
| chr18:6806796
|
G | T | 9 | a0001c0001t0001g0165a0001c0001t0001g0168a0001c0001t0008g0143others(6): Show | 9 | HG02109.hp1 HG02630.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.123-17966G>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6806796 | ||||||
| chr18:6806990
|
A | G | 1 | a0008c0011t0005g0016 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.123-17772A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6806990 | ||||||
| chr18:6807030
|
G | T | 1 | a0001c0001t0001g0236 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.123-17732G>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6807030 | ||||||
| chr18:6807120
|
ACTC | A | 5 | a0001c0001t0001g0003a0001c0001t0001g0072a0001c0001t0006g0155others(2): Show | 5 | HG02258.hp1 HG02886.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.123-17639_123-1763 others(7): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6807120 | |||||
| chr18:6807183
|
T | C | 1 | a0003c0004t0001g0195 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.123-17579T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6807183 | ||||||
| chr18:6807210
|
C | T | 1 | a0003c0004t0001g0024 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.123-17552C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6807210 | ||||||
| chr18:6807770
|
A | T | 1 | a0001c0001t0008g0074 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.123-16992A>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6807770 | ||||||
| chr18:6807814
|
A | C | 1 | a0008c0011t0005g0016 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.123-16948A>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6807814 | ||||||
| chr18:6807824
|
C | T | 1 | a0008c0011t0005g0016 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.123-16938C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6807824 | ||||||
| chr18:6808398
|
T | A | 2 | a0001c0003t0003g0085a0010c0014t0001g0142 | 2 | HG01106.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.123-16364T>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6808398 | ||||||
| chr18:6808431
|
T | C | 3 | a0001c0001t0001g0029a0001c0001t0001g0223a0003c0004t0001g0193 | 3 | HG00438.hp2 HG00544.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.123-16331T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6808431 | ||||||
| chr18:6808645
|
G | A | 1 | a0008c0011t0005g0016 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.123-16117G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6808645 | ||||||
| chr18:6808673
|
A | T | 2 | a0001c0003t0003g0085a0010c0014t0001g0142 | 2 | HG01106.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.123-16089A>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6808673 | ||||||
| chr18:6808790
|
A | C | 7 | a0001c0001t0001g0004a0001c0001t0001g0080a0001c0003t0003g0119others(4): Show | 7 | HG01081.hp2 HG02258.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.123-15972A>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6808790 | ||||||
| chr18:6808934
|
C | T | 2 | a0001c0001t0001g0188a0003c0004t0001g0125 | 2 | HG02155.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.123-15828C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6808934 | ||||||
| chr18:6809376
|
G | A | 2 | a0001c0003t0003g0085a0010c0014t0001g0142 | 2 | HG01106.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.123-15386G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6809376 | ||||||
| chr18:6809567
|
T | A | 1 | a0001c0001t0001g0165 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.123-15195T>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6809567 | ||||||
| chr18:6809581
|
A | G | 1 | a0002c0002t0002g0197 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.123-15181A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6809581 | ||||||
| chr18:6809671
|
A | G | 8 | a0001c0001t0001g0204a0001c0001t0001g0216a0002c0002t0002g0014others(5): Show | 8 | HG00597.hp1 HG02040.hp2 NA18966.hp1 others(5): Show |
intron_variant | MODIFIER | c.123-15091A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6809671 | ||||||
| chr18:6809682
|
G | A | 2 | a0001c0003t0003g0085a0010c0014t0001g0142 | 2 | HG01106.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.123-15080G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6809682 | ||||||
| chr18:6809746
|
C | A | 1 | a0001c0001t0008g0074 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.123-15016C>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6809746 | ||||||
| chr18:6809832
|
C | T | 9 | a0001c0001t0001g0165a0001c0001t0001g0168a0001c0001t0008g0143others(6): Show | 9 | HG02109.hp1 HG02630.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.123-14930C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6809832 | ||||||
| chr18:6809854
|
G | T | 5 | a0001c0001t0001g0211a0001c0001t0007g0212a0001c0001t0009g0245others(2): Show | 5 | HG02886.hp2 HG02895.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.123-14908G>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6809854 | ||||||
| chr18:6810013
|
A | G | 1 | a0001c0001t0001g0228 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.123-14749A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6810013 | ||||||
| chr18:6810283
|
G | T | 1 | a0002c0002t0002g0157 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.123-14479G>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6810283 | ||||||
| chr18:6810778
|
TAAAG | T | 3 | a0001c0001t0001g0106a0001c0003t0003g0122a0001c0012t0014g0159 | 3 | HG02559.hp2 HG02647.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.123-13978_123-1397 others(8): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6810778 | |||||
| chr18:6810872
|
G | C | 6 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0026others(3): Show | 6 | HG00099.hp2 HG00735.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.123-13890G>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6810872 | ||||||
| chr18:6811116
|
T | TTAC | 23 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0026others(20): Show | 23 | HG00099.hp2 HG00408.hp1 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.123-13645_123-1364 others(7): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6811116 | |||||
| chr18:6811309
|
T | C | 1 | a0001c0020t0023g0101 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.123-13453T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6811309 | ||||||
| chr18:6811328
|
A | G | 3 | a0001c0003t0003g0085a0008c0011t0005g0016a0010c0014t0001g0142 | 3 | HG01106.hp1 HG02630.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.123-13434A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6811328 | ||||||
| chr18:6811475
|
A | G | 51 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(48): Show | 51 | HG00099.hp2 HG00408.hp1 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.123-13287A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6811475 | ||||||
| chr18:6811567
|
G | A | 1 | a0001c0003t0003g0119 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.123-13195G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6811567 | ||||||
| chr18:6811655
|
G | A | 1 | a0008c0011t0005g0016 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.123-13107G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6811655 | ||||||
| chr18:6811727
|
C | CT | 27 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0072others(24): Show | 27 | HG01081.hp2 HG01106.hp1 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.123-13027dupT | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6811727 | |||||
| chr18:6811780
|
A | G | 1 | a0001c0001t0001g0211 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.123-12982A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6811780 | ||||||
| chr18:6811904
|
T | C | 1 | a0001c0012t0014g0159 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.123-12858T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6811904 | ||||||
| chr18:6811909
|
A | G | 1 | a0002c0002t0002g0126 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.123-12853A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6811909 | ||||||
| chr18:6811951
|
G | A | 1 | a0001c0015t0003g0167 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.123-12811G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6811951 | ||||||
| chr18:6812014
|
A | G | 8 | a0001c0001t0001g0100a0001c0003t0003g0002a0001c0003t0003g0084others(5): Show | 8 | HG01175.hp2 HG01346.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.123-12748A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6812014 | ||||||
| chr18:6812074
|
C | G | 1 | a0003c0004t0001g0064 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.123-12688C>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6812074 | ||||||
| chr18:6812306
|
C | G | 7 | a0001c0001t0001g0004a0001c0001t0001g0080a0001c0003t0003g0119others(4): Show | 7 | HG01081.hp2 HG02258.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.123-12456C>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6812306 | ||||||
| chr18:6812353
|
C | T | 1 | a0001c0003t0003g0235 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.123-12409C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6812353 | ||||||
| chr18:6812510
|
G | T | 38 | a0001c0001t0001g0029a0001c0001t0001g0034a0001c0001t0001g0037others(35): Show | 38 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(35): Show |
intron_variant | MODIFIER | c.123-12252G>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6812510 | ||||||
| chr18:6812605
|
CAGCTATT others(14): Show |
C | 25 | a0001c0001t0001g0003a0001c0001t0001g0072a0001c0001t0001g0100others(22): Show | 25 | HG01106.hp1 HG01175.hp2 HG01346.hp1 others(22): Show |
intron_variant | MODIFIER | c.123-12152_123-1213 others(25): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6812605 | |||||
| chr18:6812634
|
C | T | 1 | a0001c0001t0001g0003 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.123-12128C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6812634 | ||||||
| chr18:6812691
|
A | G | 20 | a0001c0001t0001g0003a0001c0001t0001g0072a0001c0001t0001g0100others(17): Show | 20 | HG01106.hp1 HG01175.hp2 HG01346.hp1 others(17): Show |
intron_variant | MODIFIER | c.123-12071A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6812691 | ||||||
| chr18:6812802
|
C | T | 1 | a0003c0004t0001g0193 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.123-11960C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6812802 | ||||||
| chr18:6812817
|
T | C | 1 | a0002c0002t0002g0134 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.123-11945T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6812817 | ||||||
| chr18:6812858
|
A | T | 7 | a0001c0001t0001g0165a0001c0001t0008g0143a0001c0001t0022g0067others(4): Show | 7 | HG02109.hp1 HG02630.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.123-11904A>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6812858 | ||||||
| chr18:6813207
|
C | T | 62 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(59): Show | 62 | HG00099.hp2 HG00408.hp1 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.123-11555C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6813207 | ||||||
| chr18:6813276
|
G | C | 1 | a0003c0004t0001g0173 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.123-11486G>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6813276 | ||||||
| chr18:6813357
|
C | A | 26 | a0001c0001t0001g0003a0001c0001t0001g0072a0001c0001t0001g0100others(23): Show | 26 | HG01106.hp1 HG01175.hp2 HG01346.hp1 others(23): Show |
intron_variant | MODIFIER | c.123-11405C>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6813357 | ||||||
| chr18:6813365
|
A | C | 1 | a0003c0004t0001g0242 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.123-11397A>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6813365 | ||||||
| chr18:6813389
|
A | T | 1 | a0001c0019t0021g0073 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.123-11373A>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6813389 | ||||||
| chr18:6813491
|
C | T | 33 | a0001c0001t0001g0003a0001c0001t0001g0072a0001c0001t0001g0100others(30): Show | 33 | HG01106.hp1 HG01175.hp2 HG01346.hp1 others(30): Show |
intron_variant | MODIFIER | c.123-11271C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6813491 | ||||||
| chr18:6813757
|
T | C | 3 | a0001c0001t0001g0106a0001c0003t0003g0122a0001c0012t0014g0159 | 3 | HG02559.hp2 HG02647.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.123-11005T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6813757 | ||||||
| chr18:6813868
|
G | A | 1 | a0008c0011t0005g0152 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.123-10894G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6813868 | ||||||
| chr18:6813946
|
T | C | 1 | a0001c0001t0001g0102 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.123-10816T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6813946 | ||||||
| chr18:6814033
|
G | A | 2 | a0001c0001t0001g0001a0001c0001t0001g0203 | 2 | HG01515.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.123-10729G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6814033 | ||||||
| chr18:6814133
|
C | T | 14 | a0001c0001t0001g0004a0001c0001t0001g0080a0001c0001t0001g0165others(11): Show | 14 | HG01081.hp2 HG02109.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.123-10629C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6814133 | ||||||
| chr18:6814244
|
C | T | 1 | a0001c0012t0014g0159 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.123-10518C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6814244 | ||||||
| chr18:6814327
|
C | T | 1 | a0001c0001t0019g0008 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.123-10435C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6814327 | ||||||
| chr18:6814567
|
A | T | 1 | a0001c0003t0003g0231 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.123-10195A>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6814567 | ||||||
| chr18:6814616
|
G | A | 14 | a0001c0001t0001g0004a0001c0001t0001g0080a0001c0001t0001g0165others(11): Show | 14 | HG01081.hp2 HG02109.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.123-10146G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6814616 | ||||||
| chr18:6814740
|
A | G | 7 | a0001c0001t0001g0004a0001c0001t0001g0080a0001c0003t0003g0119others(4): Show | 7 | HG01081.hp2 HG02258.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.123-10022A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6814740 | ||||||
| chr18:6814803
|
A | C | 2 | a0001c0001t0001g0168a0001c0015t0003g0167 | 2 | HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.123-9959A>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6814803 | ||||||
| chr18:6814846
|
C | T | 1 | a0001c0003t0003g0208 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.123-9916C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6814846 | ||||||
| chr18:6814861
|
T | C | 1 | a0001c0001t0006g0176 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.123-9901T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6814861 | ||||||
| chr18:6814862
|
C | T | 40 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0072others(37): Show | 40 | HG01081.hp2 HG01106.hp1 HG01175.hp2 others(37): Show |
intron_variant | MODIFIER | c.123-9900C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6814862 | ||||||
| chr18:6814932
|
G | C | 1 | a0002c0002t0002g0134 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.123-9830G>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6814932 | ||||||
| chr18:6814936
|
C | A | 3 | a0001c0003t0003g0156a0008c0011t0005g0090a0008c0011t0005g0152 | 3 | HG02109.hp2 HG03471.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.123-9826C>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6814936 | ||||||
| chr18:6815106
|
G | A | 2 | a0001c0010t0003g0089a0001c0010t0003g0114 | 2 | HG01081.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.123-9656G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6815106 | ||||||
| chr18:6815469
|
T | C | 3 | a0001c0003t0003g0156a0008c0011t0005g0090a0008c0011t0005g0152 | 3 | HG02109.hp2 HG03471.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.123-9293T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6815469 | ||||||
| chr18:6815523
|
T | G | 4 | a0001c0001t0001g0034a0001c0001t0001g0038a0001c0001t0001g0042others(1): Show | 4 | HG00408.hp2 NA18941.hp1 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.123-9239T>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6815523 | ||||||
| chr18:6815549
|
C | T | 1 | a0003c0004t0001g0219 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.123-9213C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6815549 | ||||||
| chr18:6815658
|
A | G | 63 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(60): Show | 63 | HG00099.hp2 HG00408.hp1 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.123-9104A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6815658 | ||||||
| chr18:6815782
|
A | G | 49 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0019others(46): Show | 49 | HG00099.hp2 HG00408.hp1 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.123-8980A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6815782 | ||||||
| chr18:6815835
|
A | G | 1 | a0001c0001t0001g0128 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.123-8927A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6815835 | ||||||
| chr18:6815905
|
G | GT | 36 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0026others(33): Show | 36 | HG00099.hp2 HG00408.hp1 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.123-8844dupT | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6815905 | |||||
| chr18:6816164
|
G | A | 34 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0019others(31): Show | 34 | HG00099.hp2 HG00408.hp1 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.123-8598G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6816164 | ||||||
| chr18:6816236
|
T | C | 1 | a0001c0001t0001g0181 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.123-8526T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6816236 | ||||||
| chr18:6816489
|
G | A | 1 | a0001c0001t0001g0121 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.123-8273G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6816489 | ||||||
| chr18:6816527
|
G | C | 9 | a0001c0001t0001g0165a0001c0001t0001g0168a0001c0001t0008g0143others(6): Show | 9 | HG02109.hp1 HG02630.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.123-8235G>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6816527 | ||||||
| chr18:6816548
|
C | T | 2 | a0001c0001t0001g0026a0001c0003t0003g0110 | 2 | HG01099.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.123-8214C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6816548 | ||||||
| chr18:6816601
|
C | A | 1 | a0001c0001t0006g0155 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.123-8161C>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6816601 | ||||||
| chr18:6816602
|
G | A | 42 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0019others(39): Show | 42 | HG00099.hp2 HG00408.hp1 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.123-8160G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6816602 | ||||||
| chr18:6816725
|
A | C | 1 | a0001c0001t0001g0194 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.123-8037A>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6816725 | ||||||
| chr18:6816799
|
C | G | 62 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(59): Show | 62 | HG00099.hp2 HG00408.hp1 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.123-7963C>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6816799 | ||||||
| chr18:6816868
|
G | A | 1 | a0001c0001t0001g0165 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.123-7894G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6816868 | ||||||
| chr18:6816924
|
C | T | 9 | a0001c0001t0001g0165a0001c0001t0001g0168a0001c0001t0008g0143others(6): Show | 9 | HG02109.hp1 HG02630.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.123-7838C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6816924 | ||||||
| chr18:6817066
|
G | C | 7 | a0001c0001t0001g0004a0001c0001t0001g0080a0001c0003t0003g0119others(4): Show | 7 | HG01081.hp2 HG02258.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.123-7696G>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6817066 | ||||||
| chr18:6817085
|
TA | T | 6 | a0001c0001t0009g0245a0001c0003t0003g0013a0001c0003t0003g0077others(3): Show | 6 | HG01256.hp1 HG01943.hp1 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.123-7662delA | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6817085 | |||||
| chr18:6817090
|
A | C | 8 | a0001c0001t0001g0100a0001c0003t0003g0002a0001c0003t0003g0084others(5): Show | 8 | HG01175.hp2 HG01346.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.123-7672A>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6817090 | ||||||
| chr18:6817157
|
A | T | 42 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0019others(39): Show | 42 | HG00099.hp2 HG00408.hp1 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.123-7605A>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6817157 | ||||||
| chr18:6817175
|
A | G | 3 | a0001c0001t0001g0106a0001c0003t0003g0122a0001c0012t0014g0159 | 3 | HG02559.hp2 HG02647.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.123-7587A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6817175 | ||||||
| chr18:6817332
|
C | A | 1 | a0001c0001t0001g0216 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.123-7430C>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6817332 | ||||||
| chr18:6817332
|
C | CA | 37 | a0001c0001t0001g0001a0001c0001t0001g0044a0001c0001t0001g0052others(34): Show | 37 | HG00099.hp1 HG00280.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.123-7420dupA | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6817332 | |||||
| chr18:6817338
|
A | C | 7 | a0001c0001t0001g0004a0001c0001t0001g0080a0001c0003t0003g0119others(4): Show | 7 | HG01081.hp2 HG02258.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.123-7424A>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6817338 | ||||||
| chr18:6817482
|
C | G | 2 | a0001c0001t0001g0080a0001c0018t0020g0007 | 2 | HG02258.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.123-7280C>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6817482 | ||||||
| chr18:6817553
|
G | A | 9 | a0001c0001t0001g0165a0001c0001t0001g0168a0001c0001t0008g0143others(6): Show | 9 | HG02109.hp1 HG02630.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.123-7209G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6817553 | ||||||
| chr18:6817575
|
C | G | 1 | a0002c0002t0002g0196 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.123-7187C>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6817575 | ||||||
| chr18:6817648
|
T | C | 2 | a0001c0001t0001g0107a0001c0001t0008g0171 | 2 | HG01243.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.123-7114T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6817648 | ||||||
| chr18:6817664
|
C | T | 4 | a0001c0001t0008g0143a0001c0003t0003g0154a0001c0003t0003g0169others(1): Show | 4 | HG02818.hp1 HG02965.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.123-7098C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6817664 | ||||||
| chr18:6817703
|
G | C | 7 | a0001c0001t0001g0003a0001c0001t0001g0106a0001c0001t0008g0074others(4): Show | 7 | HG01106.hp1 HG02559.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.123-7059G>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6817703 | ||||||
| chr18:6817832
|
G | C | 2 | a0001c0001t0001g0230a0002c0002t0002g0023 | 2 | HG00140.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.123-6930G>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6817832 | ||||||
| chr18:6818026
|
C | G | 18 | a0001c0001t0001g0004a0001c0001t0001g0080a0001c0001t0001g0100others(15): Show | 18 | HG01081.hp2 HG01175.hp2 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.123-6736C>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6818026 | ||||||
| chr18:6818076
|
T | A | 22 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0026others(19): Show | 22 | HG00099.hp2 HG00408.hp1 HG00735.hp1 others(19): Show |
intron_variant | MODIFIER | c.123-6686T>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6818076 | ||||||
| chr18:6818118
|
C | T | 1 | a0001c0001t0001g0037 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.123-6644C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6818118 | ||||||
| chr18:6818151
|
G | C | 137 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0029others(134): Show | 137 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.123-6611G>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6818151 | ||||||
| chr18:6818176
|
C | T | 1 | a0005c0006t0003g0180 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.123-6586C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6818176 | ||||||
| chr18:6818324
|
G | C | 1 | a0001c0001t0001g0168 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.123-6438G>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6818324 | ||||||
| chr18:6818339
|
A | G | 7 | a0001c0001t0001g0004a0001c0001t0001g0080a0001c0003t0003g0119others(4): Show | 7 | HG01081.hp2 HG02258.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.123-6423A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6818339 | ||||||
| chr18:6818440
|
C | T | 1 | a0001c0003t0003g0208 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.123-6322C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6818440 | ||||||
| chr18:6818560
|
T | G | 1 | a0001c0001t0001g0168 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.123-6202T>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6818560 | ||||||
| chr18:6818627
|
A | G | 3 | a0001c0001t0001g0072a0001c0001t0006g0155a0007c0008t0002g0069 | 3 | HG02258.hp1 HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.123-6135A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6818627 | ||||||
| chr18:6818666
|
A | G | 1 | a0001c0001t0001g0003 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.123-6096A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6818666 | ||||||
| chr18:6818825
|
C | T | 6 | a0001c0001t0001g0211a0001c0001t0007g0116a0001c0001t0007g0117others(3): Show | 6 | HG02895.hp2 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.123-5937C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6818825 | ||||||
| chr18:6818927
|
A | G | 7 | a0001c0001t0001g0004a0001c0001t0001g0080a0001c0003t0003g0119others(4): Show | 7 | HG01081.hp2 HG02258.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.123-5835A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6818927 | ||||||
| chr18:6819001
|
G | C | 1 | a0001c0003t0015g0028 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.123-5761G>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6819001 | ||||||
| chr18:6819048
|
C | T | 154 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0018others(151): Show | 154 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.123-5714C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6819048 | ||||||
| chr18:6819060
|
A | G | 5 | a0001c0001t0001g0128a0002c0002t0002g0224a0003c0004t0001g0021others(2): Show | 5 | HG00597.hp2 HG00621.hp2 HG02129.hp1 others(2): Show |
intron_variant | MODIFIER | c.123-5702A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6819060 | ||||||
| chr18:6819326
|
A | G | 4 | a0001c0001t0001g0121a0001c0001t0001g0151a0001c0001t0008g0074others(1): Show | 4 | HG01243.hp2 HG02615.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.123-5436A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6819326 | ||||||
| chr18:6819460
|
T | A | 6 | a0001c0001t0001g0075a0001c0001t0001g0230a0001c0003t0003g0076others(3): Show | 6 | HG00140.hp2 HG01261.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.123-5302T>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6819460 | ||||||
| chr18:6819528
|
G | A | 1 | a0010c0014t0001g0142 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.123-5234G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6819528 | ||||||
| chr18:6819529
|
G | A | 3 | a0002c0002t0002g0131a0003c0004t0001g0136a0004c0007t0002g0178 | 3 | NA18747.hp1 NA19063.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.123-5233G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6819529 | ||||||
| chr18:6819664
|
G | C | 1 | a0001c0001t0001g0168 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.123-5098G>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6819664 | ||||||
| chr18:6819697
|
C | T | 18 | a0001c0001t0001g0003a0001c0001t0001g0072a0001c0001t0001g0106others(15): Show | 18 | HG01106.hp1 HG01175.hp2 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.123-5065C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6819697 | ||||||
| chr18:6819829
|
A | G | 2 | a0001c0001t0001g0165a0002c0002t0004g0059 | 2 | HG02109.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.123-4933A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6819829 | ||||||
| chr18:6819914
|
T | G | 4 | a0001c0003t0003g0013a0003c0004t0001g0010a0003c0004t0001g0191others(1): Show | 4 | HG01943.hp2 HG01993.hp2 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.123-4848T>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6819914 | ||||||
| chr18:6820046
|
T | C | 143 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0018others(140): Show | 143 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.123-4716T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6820046 | ||||||
| chr18:6820126
|
T | G | 4 | a0001c0001t0001g0121a0001c0001t0001g0151a0001c0001t0008g0074others(1): Show | 4 | HG01243.hp2 HG02615.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.123-4636T>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6820126 | ||||||
| chr18:6820188
|
T | G | 167 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(164): Show | 167 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.123-4574T>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6820188 | ||||||
| chr18:6820507
|
A | G | 2 | a0001c0001t0001g0026a0001c0003t0003g0110 | 2 | HG01099.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.123-4255A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6820507 | ||||||
| chr18:6820594
|
C | T | 4 | a0001c0001t0001g0034a0001c0001t0001g0038a0001c0001t0001g0042others(1): Show | 4 | HG00408.hp2 NA18941.hp1 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.123-4168C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6820594 | ||||||
| chr18:6820698
|
G | C | 1 | a0003c0004t0001g0173 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.123-4064G>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6820698 | ||||||
| chr18:6821095
|
C | T | 3 | a0001c0001t0001g0165a0001c0001t0001g0168a0002c0002t0004g0059 | 3 | HG02109.hp1 HG02451.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.123-3667C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6821095 | ||||||
| chr18:6821142
|
C | T | 1 | a0001c0001t0001g0003 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.123-3620C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6821142 | ||||||
| chr18:6821246
|
A | G | 6 | a0001c0001t0001g0075a0001c0001t0001g0230a0001c0003t0003g0076others(3): Show | 6 | HG00140.hp2 HG01261.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.123-3516A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6821246 | ||||||
| chr18:6821457
|
C | G | 4 | a0001c0001t0001g0121a0001c0001t0001g0151a0001c0001t0008g0074others(1): Show | 4 | HG01243.hp2 HG02615.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.123-3305C>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6821457 | ||||||
| chr18:6821491
|
G | A | 2 | a0001c0001t0001g0165a0002c0002t0004g0059 | 2 | HG02109.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.123-3271G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6821491 | ||||||
| chr18:6821699
|
C | A | 2 | a0001c0001t0001g0165a0002c0002t0004g0059 | 2 | HG02109.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.123-3063C>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6821699 | ||||||
| chr18:6821738
|
T | C | 4 | a0001c0001t0001g0106a0001c0003t0003g0105a0001c0003t0003g0122others(1): Show | 4 | HG01175.hp2 HG02559.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.123-3024T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6821738 | ||||||
| chr18:6821851
|
T | G | 6 | a0001c0001t0001g0124a0001c0001t0001g0149a0001c0001t0001g0150others(3): Show | 6 | HG02055.hp1 HG02145.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.123-2911T>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6821851 | ||||||
| chr18:6821871
|
T | C | 1 | a0010c0014t0001g0142 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.123-2891T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6821871 | ||||||
| chr18:6821920
|
A | G | 1 | a0001c0003t0003g0060 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.123-2842A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6821920 | ||||||
| chr18:6821986
|
A | G | 1 | a0001c0003t0003g0085 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.123-2776A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6821986 | ||||||
| chr18:6822278
|
G | GA | 4 | a0001c0001t0001g0106a0001c0003t0003g0105a0001c0003t0003g0122others(1): Show | 4 | HG01175.hp2 HG02559.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.123-2478dupA | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6822278 | |||||
| chr18:6822527
|
T | C | 1 | a0001c0001t0001g0054 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.123-2235T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6822527 | ||||||
| chr18:6822582
|
G | A | 3 | a0001c0003t0003g0156a0008c0011t0005g0090a0008c0011t0005g0152 | 3 | HG02109.hp2 HG03471.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.123-2180G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6822582 | ||||||
| chr18:6822596
|
G | A | 1 | a0001c0003t0003g0145 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.123-2166G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6822596 | ||||||
| chr18:6822602
|
C | T | 4 | a0001c0003t0003g0002a0001c0003t0003g0085a0001c0003t0003g0104others(1): Show | 4 | HG01106.hp1 HG03471.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.123-2160C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6822602 | ||||||
| chr18:6822604
|
G | A | 27 | a0001c0001t0001g0003a0001c0001t0001g0072a0001c0001t0001g0075others(24): Show | 27 | HG00140.hp2 HG01106.hp1 HG01261.hp1 others(24): Show |
intron_variant | MODIFIER | c.123-2158G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6822604 | ||||||
| chr18:6822632
|
C | A | 1 | a0001c0003t0003g0145 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.123-2130C>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6822632 | ||||||
| chr18:6822770
|
A | T | 1 | a0001c0001t0022g0067 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.123-1992A>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6822770 | ||||||
| chr18:6822952
|
G | A | 1 | a0001c0001t0001g0044 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.123-1810G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6822952 | ||||||
| chr18:6823012
|
G | A | 3 | a0001c0003t0003g0087a0001c0003t0003g0123a0002c0017t0002g0086 | 3 | HG02922.hp1 HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.123-1750G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6823012 | ||||||
| chr18:6823066
|
T | A | 1 | a0001c0001t0001g0184 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.123-1696T>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6823066 | ||||||
| chr18:6823088
|
T | G | 1 | a0002c0002t0002g0217 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.123-1674T>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6823088 | ||||||
| chr18:6823140
|
C | G | 152 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0018others(149): Show | 152 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.123-1622C>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6823140 | ||||||
| chr18:6823196
|
C | T | 1 | a0001c0001t0001g0097 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.123-1566C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6823196 | ||||||
| chr18:6823215
|
T | C | 137 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0029others(134): Show | 137 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.123-1547T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6823215 | ||||||
| chr18:6823282
|
G | T | 1 | a0001c0003t0003g0104 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.123-1480G>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6823282 | ||||||
| chr18:6823601
|
AT | A | 64 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0070others(61): Show | 64 | HG00140.hp2 HG00597.hp1 HG01243.hp1 others(61): Show |
intron_variant | MODIFIER | c.123-1142delT | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6823601 | |||||
| chr18:6823601
|
ATT | A | 13 | a0001c0001t0001g0004a0001c0001t0001g0100a0001c0001t0001g0106others(10): Show | 13 | HG01081.hp2 HG01175.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.123-1143_123-1142d others(4): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | 6823601 | |||||
| chr18:6823810
|
T | A | 1 | a0001c0001t0001g0211 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.123-952T>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6823810 | ||||||
| chr18:6823963
|
T | C | 128 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0029others(125): Show | 128 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.123-799T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6823963 | ||||||
| chr18:6824018
|
C | T | 25 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0026others(22): Show | 25 | HG00099.hp2 HG00408.hp1 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.123-744C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6824018 | ||||||
| chr18:6824220
|
C | T | 6 | a0001c0001t0001g0075a0001c0001t0001g0230a0001c0003t0003g0076others(3): Show | 6 | HG00140.hp2 HG01261.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.123-542C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6824220 | ||||||
| chr18:6824244
|
C | G | 143 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0018others(140): Show | 143 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.123-518C>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6824244 | ||||||
| chr18:6824405
|
C | T | 127 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0029others(124): Show | 127 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.123-357C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6824405 | ||||||
| chr18:6824485
|
C | T | 6 | a0001c0001t0001g0075a0001c0001t0001g0230a0001c0003t0003g0076others(3): Show | 6 | HG00140.hp2 HG01261.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.123-277C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6824485 | ||||||
| chr18:6824492
|
G | A | 6 | a0001c0001t0001g0075a0001c0001t0001g0230a0001c0003t0003g0076others(3): Show | 6 | HG00140.hp2 HG01261.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.123-270G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6824492 | ||||||
| chr18:6824626
|
C | T | 4 | a0001c0001t0001g0100a0001c0001t0001g0107a0001c0001t0008g0171others(1): Show | 4 | HG01243.hp1 HG02451.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.123-136C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6824626 | ||||||
| chr18:6824716
|
T | C | 1 | a0002c0002t0002g0083 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.123-46T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6824716 | ||||||
| chr18:6824730
|
G | A | 6 | a0001c0001t0001g0100a0001c0001t0001g0107a0001c0001t0008g0171others(3): Show | 6 | HG01243.hp1 HG02451.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.123-32G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | chr18 | 6824730 | ||||||
| chr18:6825097
|
TC | T | 3 | a0001c0001t0001g0165a0001c0001t0001g0168a0002c0002t0004g0059 | 3 | HG02109.hp1 HG02451.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.325+134delC | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6825097 | ||||||
| chr18:6825120
|
A | G | 1 | a0002c0002t0013g0022 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.325+156A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6825120 | ||||||
| chr18:6825267
|
G | C | 205 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(202): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.325+303G>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6825267 | ||||||
| chr18:6825409
|
T | A | 1 | a0002c0002t0002g0138 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.325+445T>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6825409 | ||||||
| chr18:6825628
|
T | C | 11 | a0001c0001t0001g0003a0001c0001t0001g0072a0001c0001t0001g0075others(8): Show | 11 | HG00140.hp2 HG01261.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.325+664T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6825628 | ||||||
| chr18:6825641
|
G | T | 4 | a0001c0001t0001g0121a0001c0001t0001g0151a0001c0001t0008g0074others(1): Show | 4 | HG01243.hp2 HG02615.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.325+677G>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6825641 | ||||||
| chr18:6825908
|
G | A | 6 | a0001c0001t0001g0100a0001c0001t0001g0107a0001c0001t0008g0171others(3): Show | 6 | HG01243.hp1 HG02451.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.325+944G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6825908 | ||||||
| chr18:6825928
|
T | G | 7 | a0001c0001t0001g0004a0001c0001t0001g0080a0001c0003t0003g0119others(4): Show | 7 | HG01081.hp2 HG02258.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.325+964T>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6825928 | ||||||
| chr18:6825932
|
T | A | 1 | a0001c0001t0016g0081 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.325+968T>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6825932 | ||||||
| chr18:6826063
|
A | C | 134 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0029others(131): Show | 134 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.325+1099A>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6826063 | ||||||
| chr18:6826117
|
G | GT | 145 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0018others(142): Show | 145 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.325+1168dupT | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr18 | 6826117 | |||||
| chr18:6826117
|
GT | G | 10 | a0001c0001t0001g0003a0001c0001t0001g0075a0001c0001t0001g0165others(7): Show | 10 | HG00140.hp2 HG01261.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.325+1168delT | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr18 | 6826117 | |||||
| chr18:6826357
|
C | G | 7 | a0001c0001t0001g0004a0001c0001t0001g0080a0001c0003t0003g0119others(4): Show | 7 | HG01081.hp2 HG02258.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.325+1393C>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6826357 | ||||||
| chr18:6826476
|
GT | G | 9 | a0001c0001t0001g0019a0001c0001t0008g0143a0001c0001t0022g0067others(6): Show | 9 | HG00735.hp1 HG01346.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.325+1524delT | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr18 | 6826476 | |||||
| chr18:6826488
|
T | A | 147 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0018others(144): Show | 147 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.325+1524T>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6826488 | ||||||
| chr18:6826488
|
T | TA | 3 | a0001c0001t0001g0165a0001c0001t0001g0168a0002c0002t0004g0059 | 3 | HG02109.hp1 HG02451.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.325+1526dupA | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr18 | 6826488 | |||||
| chr18:6826488
|
T | TTA | 7 | a0001c0001t0001g0004a0001c0001t0001g0080a0001c0003t0003g0119others(4): Show | 7 | HG01081.hp2 HG02258.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.325+1524_325+1525i others(4): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6826488 | ||||||
| chr18:6826605
|
G | A | 133 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0029others(130): Show | 133 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.325+1641G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6826605 | ||||||
| chr18:6826683
|
C | CT | 135 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0018others(132): Show | 135 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.325+1742dupT | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr18 | 6826683 | |||||
| chr18:6826683
|
C | CTT | 24 | a0001c0001t0001g0004a0001c0001t0001g0075a0001c0001t0001g0124others(21): Show | 24 | HG00140.hp2 HG01081.hp2 HG01175.hp1 others(21): Show |
intron_variant | MODIFIER | c.325+1741_325+1742d others(4): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr18 | 6826683 | |||||
| chr18:6826706
|
T | A | 5 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0026others(2): Show | 5 | HG00099.hp2 HG00735.hp1 HG01099.hp1 others(2): Show |
intron_variant | MODIFIER | c.325+1742T>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6826706 | ||||||
| chr18:6826748
|
C | T | 2 | a0001c0001t0001g0236a0002c0002t0002g0011 | 2 | HG00140.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.325+1784C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6826748 | ||||||
| chr18:6826895
|
G | C | 1 | a0001c0001t0001g0165 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.325+1931G>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6826895 | ||||||
| chr18:6826900
|
C | T | 11 | a0001c0001t0001g0003a0001c0001t0001g0072a0001c0001t0001g0075others(8): Show | 11 | HG00140.hp2 HG01261.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.325+1936C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6826900 | ||||||
| chr18:6826901
|
T | G | 11 | a0001c0001t0001g0003a0001c0001t0001g0072a0001c0001t0001g0075others(8): Show | 11 | HG00140.hp2 HG01261.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.325+1937T>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6826901 | ||||||
| chr18:6826942
|
A | G | 145 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0018others(142): Show | 145 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.325+1978A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6826942 | ||||||
| chr18:6826961
|
A | C | 1 | a0001c0019t0021g0073 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.325+1997A>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6826961 | ||||||
| chr18:6827027
|
C | T | 1 | a0001c0001t0001g0198 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.325+2063C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6827027 | ||||||
| chr18:6827222
|
G | A | 130 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0029others(127): Show | 130 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.325+2258G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6827222 | ||||||
| chr18:6827298
|
C | T | 19 | a0001c0001t0001g0003a0001c0001t0001g0072a0001c0001t0001g0075others(16): Show | 19 | HG00140.hp2 HG01175.hp2 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.325+2334C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6827298 | ||||||
| chr18:6827304
|
GCCGGGCG others(218): Show |
G | 1 | a0009c0016t0001g0092 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.325+2357_325+2581d others(2): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr18 | 6827304 | |||||
| chr18:6827311
|
G | A | 4 | a0001c0003t0003g0002a0001c0003t0003g0085a0001c0003t0003g0104others(1): Show | 4 | HG01106.hp1 HG03471.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.325+2347G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6827311 | ||||||
| chr18:6827317
|
C | CTGACCCC others(91): Show |
1 | a0001c0001t0001g0018 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.325+2356_325+2357i others(100): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr18 | 6827317 | |||||
| chr18:6827321
|
A | C | 158 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(155): Show | 158 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.325+2357A>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6827321 | ||||||
| chr18:6827325
|
T | C | 158 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(155): Show | 158 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.325+2361T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6827325 | ||||||
| chr18:6827368
|
G | A | 1 | a0001c0003t0003g0145 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.325+2404G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6827368 | ||||||
| chr18:6827413
|
G | C | 1 | a0003c0004t0001g0173 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.325+2449G>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6827413 | ||||||
| chr18:6827440
|
C | T | 1 | a0001c0003t0003g0055 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.325+2476C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6827440 | ||||||
| chr18:6827446
|
G | A | 3 | a0001c0001t0001g0165a0001c0001t0001g0168a0002c0002t0004g0059 | 3 | HG02109.hp1 HG02451.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.325+2482G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6827446 | ||||||
| chr18:6827548
|
C | A | 2 | a0001c0019t0021g0073a0003c0023t0001g0120 | 2 | HG03041.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.325+2584C>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6827548 | ||||||
| chr18:6827574
|
A | G | 182 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(179): Show | 182 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.325+2610A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6827574 | ||||||
| chr18:6827584
|
T | C | 159 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(156): Show | 159 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.325+2620T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6827584 | ||||||
| chr18:6827631
|
AG | A | 7 | a0001c0001t0001g0211a0001c0001t0007g0116a0001c0001t0007g0117others(4): Show | 7 | HG02895.hp2 HG02896.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.325+2673delG | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr18 | 6827631 | |||||
| chr18:6827641
|
AC | A | 161 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(158): Show | 161 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.325+2687delC | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr18 | 6827641 | |||||
| chr18:6827646
|
C | A | 7 | a0001c0001t0001g0004a0001c0001t0001g0080a0001c0003t0003g0119others(4): Show | 7 | HG01081.hp2 HG02258.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.325+2682C>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6827646 | ||||||
| chr18:6827649
|
C | T | 6 | a0001c0001t0001g0211a0001c0001t0007g0116a0001c0001t0007g0117others(3): Show | 6 | HG02895.hp2 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.325+2685C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6827649 | ||||||
| chr18:6827679
|
T | C | 162 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(159): Show | 162 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.325+2715T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6827679 | ||||||
| chr18:6827763
|
C | T | 1 | a0001c0001t0001g0168 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.325+2799C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6827763 | ||||||
| chr18:6827793
|
G | T | 1 | a0001c0003t0003g0190 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.325+2829G>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6827793 | ||||||
| chr18:6827828
|
G | T | 1 | a0004c0007t0002g0056 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.325+2864G>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6827828 | ||||||
| chr18:6827885
|
C | T | 2 | a0008c0011t0005g0090a0008c0011t0005g0152 | 2 | HG03471.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.325+2921C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6827885 | ||||||
| chr18:6827916
|
G | A | 5 | a0001c0001t0001g0003a0001c0001t0001g0072a0001c0001t0006g0155others(2): Show | 5 | HG02258.hp1 HG02630.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.325+2952G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6827916 | ||||||
| chr18:6827925
|
C | T | 1 | a0001c0001t0001g0003 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.325+2961C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6827925 | ||||||
| chr18:6827943
|
C | T | 7 | a0001c0001t0001g0004a0001c0001t0001g0080a0001c0003t0003g0119others(4): Show | 7 | HG01081.hp2 HG02258.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.325+2979C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6827943 | ||||||
| chr18:6828027
|
C | T | 2 | a0002c0002t0002g0199a0002c0005t0002g0017 | 2 | HG02300.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.325+3063C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6828027 | ||||||
| chr18:6828028
|
G | A | 1 | a0001c0001t0001g0054 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.325+3064G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6828028 | ||||||
| chr18:6828086
|
C | T | 2 | a0001c0001t0001g0165a0002c0002t0004g0059 | 2 | HG02109.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.325+3122C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6828086 | ||||||
| chr18:6828098
|
C | T | 2 | a0001c0001t0001g0179a0003c0004t0001g0045 | 2 | NA18956.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.325+3134C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6828098 | ||||||
| chr18:6828106
|
T | C | 20 | a0001c0001t0001g0003a0001c0001t0001g0072a0001c0001t0001g0075others(17): Show | 20 | HG00140.hp2 HG01175.hp2 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.325+3142T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6828106 | ||||||
| chr18:6828115
|
G | C | 1 | a0001c0015t0003g0167 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.325+3151G>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6828115 | ||||||
| chr18:6828135
|
G | A | 131 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0029others(128): Show | 131 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.325+3171G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6828135 | ||||||
| chr18:6828158
|
G | A | 1 | a0002c0002t0002g0217 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.325+3194G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6828158 | ||||||
| chr18:6828178
|
G | A | 1 | a0001c0003t0003g0145 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.325+3214G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6828178 | ||||||
| chr18:6828222
|
G | A | 1 | a0001c0003t0003g0085 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.325+3258G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6828222 | ||||||
| chr18:6828223
|
C | A | 1 | a0001c0003t0003g0085 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.325+3259C>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6828223 | ||||||
| chr18:6828223
|
C | T | 3 | a0001c0001t0018g0111a0002c0002t0004g0006a0002c0002t0004g0147 | 3 | HG02280.hp2 HG02559.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.325+3259C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6828223 | ||||||
| chr18:6828316
|
G | A | 4 | a0001c0001t0001g0121a0001c0001t0001g0151a0001c0001t0008g0074others(1): Show | 4 | HG01243.hp2 HG02615.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.325+3352G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6828316 | ||||||
| chr18:6828320
|
C | G | 6 | a0001c0001t0001g0128a0002c0002t0002g0224a0003c0004t0001g0021others(3): Show | 6 | HG00597.hp2 HG00621.hp1 HG00621.hp2 others(3): Show |
intron_variant | MODIFIER | c.325+3356C>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6828320 | ||||||
| chr18:6828380
|
C | A | 133 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0029others(130): Show | 133 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.325+3416C>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6828380 | ||||||
| chr18:6828380
|
C | G | 27 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0072others(24): Show | 27 | HG00140.hp2 HG01081.hp2 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.325+3416C>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6828380 | ||||||
| chr18:6828384
|
G | GGAGGAGA | 16 | a0001c0001t0001g0003a0001c0001t0001g0072a0001c0001t0001g0075others(13): Show | 16 | HG01175.hp2 HG01243.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.325+3445_325+3451d others(9): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr18 | 6828384 | |||||
| chr18:6828384
|
GGAGGAGA others(7): Show |
G | 6 | a0001c0001t0001g0124a0001c0001t0001g0149a0001c0001t0001g0150others(3): Show | 6 | HG02055.hp1 HG02145.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.325+3438_325+3451d others(16): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr18 | 6828384 | |||||
| chr18:6828397
|
G | C | 1 | a0003c0004t0001g0173 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.325+3433G>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6828397 | ||||||
| chr18:6828504
|
A | T | 4 | a0001c0001t0001g0106a0001c0003t0003g0105a0001c0003t0003g0122others(1): Show | 4 | HG01175.hp2 HG02559.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.325+3540A>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6828504 | ||||||
| chr18:6828569
|
A | G | 1 | a0002c0002t0002g0134 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.325+3605A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6828569 | ||||||
| chr18:6828697
|
T | A | 1 | a0001c0001t0001g0168 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.325+3733T>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6828697 | ||||||
| chr18:6829026
|
G | A | 1 | a0002c0002t0013g0022 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.325+4062G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6829026 | ||||||
| chr18:6829067
|
C | T | 4 | a0001c0001t0001g0121a0001c0001t0001g0151a0001c0001t0008g0074others(1): Show | 4 | HG01243.hp2 HG02615.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.325+4103C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6829067 | ||||||
| chr18:6829080
|
A | G | 2 | a0001c0003t0003g0222a0001c0003t0003g0235 | 2 | HG00280.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.325+4116A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6829080 | ||||||
| chr18:6829354
|
C | T | 2 | a0002c0002t0002g0126a0002c0005t0002g0140 | 2 | NA18953.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.325+4390C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6829354 | ||||||
| chr18:6829854
|
A | G | 4 | a0001c0001t0001g0165a0001c0001t0001g0168a0001c0015t0003g0167others(1): Show | 4 | HG02109.hp1 HG02451.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.325+4890A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6829854 | ||||||
| chr18:6830143
|
T | C | 4 | a0001c0001t0001g0121a0001c0001t0001g0151a0001c0001t0008g0074others(1): Show | 4 | HG01243.hp2 HG02615.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.325+5179T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6830143 | ||||||
| chr18:6830249
|
C | T | 1 | a0001c0001t0001g0216 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.325+5285C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6830249 | ||||||
| chr18:6830282
|
CTCTT | C | 5 | a0001c0001t0001g0205a0001c0003t0003g0002a0001c0003t0003g0085others(2): Show | 5 | HG01106.hp1 HG03471.hp1 NA18940.hp1 others(2): Show |
intron_variant | MODIFIER | c.325+5324_325+5327d others(6): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr18 | 6830282 | |||||
| chr18:6830619
|
C | T | 2 | a0001c0003t0003g0094a0001c0003t0003g0095 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.325+5655C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6830619 | ||||||
| chr18:6830702
|
A | G | 1 | a0001c0001t0001g0165 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.325+5738A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6830702 | ||||||
| chr18:6830931
|
A | G | 131 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0029others(128): Show | 131 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.325+5967A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6830931 | ||||||
| chr18:6830938
|
T | C | 6 | a0001c0001t0001g0189a0001c0001t0001g0215a0002c0002t0002g0065others(3): Show | 6 | NA18747.hp2 NA18943.hp1 NA18986.hp2 others(3): Show |
intron_variant | MODIFIER | c.325+5974T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6830938 | ||||||
| chr18:6831292
|
T | C | 131 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0029others(128): Show | 131 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.326-5905T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6831292 | ||||||
| chr18:6831351
|
C | G | 26 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0026others(23): Show | 26 | HG00099.hp2 HG00408.hp1 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.326-5846C>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6831351 | ||||||
| chr18:6831421
|
T | A | 208 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(205): Show | 208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.326-5776T>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6831421 | ||||||
| chr18:6831471
|
GT | G | 14 | a0001c0001t0001g0004a0001c0001t0001g0075a0001c0001t0001g0080others(11): Show | 14 | HG00140.hp2 HG01243.hp2 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.326-5710delT | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr18 | 6831471 | |||||
| chr18:6831471
|
GTT | G | 133 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0029others(130): Show | 133 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.326-5711_326-5710d others(4): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr18 | 6831471 | |||||
| chr18:6831471
|
GTTT | G | 7 | a0001c0001t0001g0003a0001c0001t0001g0100a0001c0001t0001g0107others(4): Show | 7 | HG01243.hp1 HG02451.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.326-5712_326-5710d others(5): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr18 | 6831471 | |||||
| chr18:6831473
|
T | G | 1 | a0002c0002t0002g0148 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.326-5724T>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6831473 | ||||||
| chr18:6831481
|
T | C | 6 | a0001c0001t0001g0075a0001c0001t0001g0230a0001c0003t0003g0076others(3): Show | 6 | HG00140.hp2 HG01261.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.326-5716T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6831481 | ||||||
| chr18:6831485
|
TTTC | T | 10 | a0001c0001t0001g0124a0001c0001t0001g0149a0001c0001t0001g0150others(7): Show | 10 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.326-5709_326-5707d others(5): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr18 | 6831485 | |||||
| chr18:6831487
|
T | C | 1 | a0003c0004t0001g0220 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.326-5710T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6831487 | ||||||
| chr18:6831488
|
C | CTTTTTTT others(9): Show |
4 | a0001c0003t0003g0002a0001c0003t0003g0085a0001c0003t0003g0104others(1): Show | 4 | HG01106.hp1 HG03471.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.326-5696_326-5695i others(18): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr18 | 6831488 | |||||
| chr18:6831488
|
C | T | 1 | a0003c0004t0001g0220 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.326-5709C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6831488 | ||||||
| chr18:6831489
|
T | C | 10 | a0001c0001t0001g0124a0001c0001t0001g0149a0001c0001t0001g0150others(7): Show | 10 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.326-5708T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6831489 | ||||||
| chr18:6831522
|
G | A | 1 | a0002c0002t0004g0059 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.326-5675G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6831522 | ||||||
| chr18:6831563
|
T | C | 1 | a0001c0015t0003g0167 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.326-5634T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6831563 | ||||||
| chr18:6831851
|
T | G | 1 | a0001c0015t0003g0167 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.326-5346T>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6831851 | ||||||
| chr18:6831879
|
G | C | 172 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(169): Show | 172 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.326-5318G>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6831879 | ||||||
| chr18:6832291
|
TTTTGAAA others(19): Show |
T | 1 | a0001c0019t0021g0073 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.326-4904_326-4879d others(28): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr18 | 6832291 | |||||
| chr18:6832423
|
G | A | 1 | a0002c0002t0002g0197 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.326-4774G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6832423 | ||||||
| chr18:6832472
|
T | A | 4 | a0001c0003t0003g0002a0001c0003t0003g0085a0001c0003t0003g0104others(1): Show | 4 | HG01106.hp1 HG03471.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.326-4725T>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6832472 | ||||||
| chr18:6832612
|
C | G | 1 | a0001c0003t0001g0050 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.326-4585C>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6832612 | ||||||
| chr18:6832680
|
C | A | 1 | a0002c0002t0004g0059 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.326-4517C>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6832680 | ||||||
| chr18:6832766
|
C | T | 3 | a0002c0002t0002g0163a0006c0009t0003g0162a0007c0008t0002g0166 | 3 | HG01952.hp2 HG02647.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.326-4431C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6832766 | ||||||
| chr18:6832780
|
T | C | 172 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(169): Show | 172 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.326-4417T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6832780 | ||||||
| chr18:6832801
|
T | C | 1 | a0001c0001t0001g0205 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.326-4396T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6832801 | ||||||
| chr18:6832833
|
C | T | 7 | a0001c0001t0001g0211a0001c0001t0007g0116a0001c0001t0007g0117others(4): Show | 7 | HG02895.hp2 HG02896.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.326-4364C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6832833 | ||||||
| chr18:6833067
|
TTTAAG | T | 4 | a0001c0003t0003g0002a0001c0003t0003g0085a0001c0003t0003g0104others(1): Show | 4 | HG01106.hp1 HG03471.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.326-4127_326-4123d others(7): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr18 | 6833067 | |||||
| chr18:6833341
|
A | G | 12 | a0001c0001t0001g0106a0001c0001t0001g0121a0001c0001t0001g0151others(9): Show | 12 | HG01106.hp1 HG01175.hp2 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.326-3856A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6833341 | ||||||
| chr18:6833447
|
T | C | 1 | a0001c0015t0003g0167 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.326-3750T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6833447 | ||||||
| chr18:6833609
|
C | T | 1 | a0001c0001t0008g0074 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.326-3588C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6833609 | ||||||
| chr18:6833610
|
A | G | 3 | a0002c0002t0002g0174a0003c0004t0001g0173a0003c0004t0001g0227 | 3 | HG00423.hp1 NA18968.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.326-3587A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6833610 | ||||||
| chr18:6833715
|
T | C | 1 | a0001c0015t0003g0167 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.326-3482T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6833715 | ||||||
| chr18:6833746
|
G | A | 3 | a0001c0003t0003g0002a0001c0003t0003g0104a0010c0014t0001g0142 | 3 | HG01106.hp1 HG03471.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.326-3451G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6833746 | ||||||
| chr18:6833806
|
G | C | 1 | a0001c0001t0001g0003 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.326-3391G>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6833806 | ||||||
| chr18:6833880
|
C | G | 130 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0029others(127): Show | 130 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.326-3317C>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6833880 | ||||||
| chr18:6834032
|
A | T | 6 | a0001c0001t0001g0100a0001c0001t0001g0107a0001c0001t0008g0171others(3): Show | 6 | HG01243.hp1 HG02451.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.326-3165A>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6834032 | ||||||
| chr18:6834086
|
G | A | 7 | a0001c0001t0001g0004a0001c0001t0001g0080a0001c0003t0003g0119others(4): Show | 7 | HG01081.hp2 HG02258.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.326-3111G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6834086 | ||||||
| chr18:6834162
|
T | G | 1 | a0001c0015t0003g0167 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.326-3035T>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6834162 | ||||||
| chr18:6834162
|
T | TA | 130 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0029others(127): Show | 130 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.326-3026dupA | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr18 | 6834162 | |||||
| chr18:6834197
|
A | T | 9 | a0001c0001t0001g0106a0001c0003t0003g0002a0001c0003t0003g0085others(6): Show | 9 | HG01106.hp1 HG01175.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.326-3000A>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6834197 | ||||||
| chr18:6834230
|
AAATAATA others(10): Show |
A | 1 | a0001c0001t0001g0168 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.326-2966_326-2950d others(19): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6834230 | ||||||
| chr18:6834563
|
T | G | 1 | a0001c0001t0001g0168 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.326-2634T>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6834563 | ||||||
| chr18:6834652
|
T | C | 172 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(169): Show | 172 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.326-2545T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6834652 | ||||||
| chr18:6834850
|
A | C | 4 | a0001c0001t0001g0121a0001c0001t0001g0151a0001c0001t0008g0074others(1): Show | 4 | HG01243.hp2 HG02615.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.326-2347A>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6834850 | ||||||
| chr18:6834886
|
C | T | 8 | a0001c0001t0001g0106a0001c0003t0003g0002a0001c0003t0003g0085others(5): Show | 8 | HG01106.hp1 HG01175.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.326-2311C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6834886 | ||||||
| chr18:6834911
|
T | G | 4 | a0001c0001t0001g0230a0001c0003t0003g0233a0001c0003t0003g0234others(1): Show | 4 | HG00140.hp2 HG01261.hp1 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.326-2286T>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6834911 | ||||||
| chr18:6835170
|
A | C | 1 | a0001c0015t0003g0167 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.326-2027A>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6835170 | ||||||
| chr18:6835271
|
A | G | 4 | a0001c0003t0003g0013a0003c0004t0001g0010a0003c0004t0001g0191others(1): Show | 4 | HG01943.hp2 HG01993.hp2 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.326-1926A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6835271 | ||||||
| chr18:6835321
|
T | C | 176 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(173): Show | 176 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.326-1876T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6835321 | ||||||
| chr18:6835477
|
T | G | 4 | a0001c0001t0001g0121a0001c0001t0001g0151a0001c0001t0008g0074others(1): Show | 4 | HG01243.hp2 HG02615.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.326-1720T>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6835477 | ||||||
| chr18:6835478
|
A | C | 2 | a0001c0001t0001g0161a0001c0001t0019g0008 | 2 | HG02145.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.326-1719A>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6835478 | ||||||
| chr18:6836055
|
A | G | 1 | a0001c0015t0003g0167 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.326-1142A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6836055 | ||||||
| chr18:6836140
|
G | C | 1 | a0008c0011t0005g0016 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.326-1057G>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6836140 | ||||||
| chr18:6836364
|
C | G | 12 | a0001c0001t0001g0003a0001c0001t0001g0072a0001c0001t0001g0165others(9): Show | 12 | HG01106.hp1 HG02109.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.326-833C>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6836364 | ||||||
| chr18:6836543
|
T | C | 16 | a0001c0001t0001g0124a0001c0001t0001g0149a0001c0001t0001g0150others(13): Show | 16 | HG01106.hp1 HG02055.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.326-654T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6836543 | ||||||
| chr18:6836587
|
G | C | 1 | a0001c0001t0001g0168 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.326-610G>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6836587 | ||||||
| chr18:6836715
|
A | G | 4 | a0001c0001t0001g0121a0001c0001t0001g0151a0001c0001t0008g0074others(1): Show | 4 | HG01243.hp2 HG02615.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.326-482A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6836715 | ||||||
| chr18:6836756
|
G | T | 1 | a0001c0003t0003g0091 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.326-441G>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6836756 | ||||||
| chr18:6836781
|
G | A | 12 | a0001c0001t0001g0075a0001c0001t0001g0211a0001c0001t0001g0230others(9): Show | 12 | HG00140.hp2 HG01261.hp1 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.326-416G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6836781 | ||||||
| chr18:6836815
|
T | A | 1 | a0004c0007t0002g0036 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.326-382T>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6836815 | ||||||
| chr18:6836824
|
C | T | 4 | a0001c0003t0003g0002a0001c0003t0003g0085a0001c0003t0003g0104others(1): Show | 4 | HG01106.hp1 HG03471.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.326-373C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6836824 | ||||||
| chr18:6836857
|
A | G | 3 | a0001c0001t0001g0165a0001c0001t0001g0168a0002c0002t0004g0059 | 3 | HG02109.hp1 HG02451.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.326-340A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6836857 | ||||||
| chr18:6836866
|
T | C | 4 | a0001c0003t0003g0002a0001c0003t0003g0085a0001c0003t0003g0104others(1): Show | 4 | HG01106.hp1 HG03471.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.326-331T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6836866 | ||||||
| chr18:6836884
|
G | C | 1 | a0009c0016t0001g0092 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.326-313G>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6836884 | ||||||
| chr18:6836887
|
T | A | 1 | a0009c0016t0001g0092 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.326-310T>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6836887 | ||||||
| chr18:6837019
|
A | G | 4 | a0001c0003t0003g0002a0001c0003t0003g0085a0001c0003t0003g0104others(1): Show | 4 | HG01106.hp1 HG03471.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.326-178A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6837019 | ||||||
| chr18:6837090
|
GA | G | 8 | a0001c0001t0001g0121a0001c0001t0001g0151a0001c0001t0001g0165others(5): Show | 8 | HG01243.hp2 HG02109.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.326-99delA | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr18 | 6837090 | |||||
| chr18:6837091
|
A | G | 1 | a0001c0001t0001g0184 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.326-106A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | chr18 | 6837091 | ||||||
| chr18:6837447
|
G | A | 31 | a0001c0001t0001g0001a0001c0001t0001g0044a0001c0001t0001g0052others(28): Show | 31 | HG00099.hp1 HG00280.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.543+33G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6837447 | ||||||
| chr18:6837531
|
T | G | 5 | a0001c0001t0001g0003a0001c0001t0001g0072a0001c0001t0006g0155others(2): Show | 5 | HG02258.hp1 HG02630.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.543+117T>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6837531 | ||||||
| chr18:6837623
|
T | G | 4 | a0001c0001t0001g0106a0001c0003t0003g0105a0001c0003t0003g0122others(1): Show | 4 | HG01175.hp2 HG02559.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.543+209T>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6837623 | ||||||
| chr18:6837712
|
T | C | 1 | a0001c0001t0017g0118 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.543+298T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6837712 | ||||||
| chr18:6837809
|
G | A | 4 | a0001c0001t0001g0106a0001c0003t0003g0105a0001c0003t0003g0122others(1): Show | 4 | HG01175.hp2 HG02559.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.543+395G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6837809 | ||||||
| chr18:6837838
|
T | C | 8 | a0001c0001t0008g0143a0001c0001t0022g0067a0001c0003t0003g0084others(5): Show | 8 | HG01346.hp1 HG02630.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.543+424T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6837838 | ||||||
| chr18:6837846
|
T | A | 1 | a0001c0003t0003g0145 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.543+432T>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6837846 | ||||||
| chr18:6838279
|
T | C | 40 | a0001c0001t0001g0004a0001c0001t0001g0075a0001c0001t0001g0080others(37): Show | 40 | HG00140.hp2 HG00741.hp1 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.543+865T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6838279 | ||||||
| chr18:6838291
|
T | C | 156 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(153): Show | 156 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.543+877T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6838291 | ||||||
| chr18:6838337
|
C | T | 1 | a0004c0007t0002g0056 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.543+923C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6838337 | ||||||
| chr18:6838465
|
T | C | 30 | a0001c0001t0001g0001a0001c0001t0001g0044a0001c0001t0001g0052others(27): Show | 30 | HG00099.hp1 HG00280.hp2 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.543+1051T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6838465 | ||||||
| chr18:6838516
|
G | A | 6 | a0001c0001t0001g0100a0001c0001t0001g0107a0001c0001t0008g0171others(3): Show | 6 | HG01243.hp1 HG02451.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.543+1102G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6838516 | ||||||
| chr18:6838681
|
T | A | 4 | a0001c0001t0001g0121a0001c0001t0001g0151a0001c0001t0008g0074others(1): Show | 4 | HG01243.hp2 HG02615.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.543+1267T>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6838681 | ||||||
| chr18:6838735
|
T | G | 7 | a0001c0001t0001g0075a0001c0001t0001g0230a0001c0003t0003g0076others(4): Show | 7 | HG00140.hp2 HG00741.hp1 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.543+1321T>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6838735 | ||||||
| chr18:6838820
|
T | C | 2 | a0001c0001t0001g0230a0002c0002t0002g0023 | 2 | HG00140.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.543+1406T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6838820 | ||||||
| chr18:6838882
|
A | C | 4 | a0001c0001t0001g0121a0001c0001t0001g0151a0001c0001t0008g0074others(1): Show | 4 | HG01243.hp2 HG02615.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.543+1468A>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6838882 | ||||||
| chr18:6838961
|
T | C | 32 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0026others(29): Show | 32 | HG00099.hp2 HG00408.hp1 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.543+1547T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6838961 | ||||||
| chr18:6838987
|
G | A | 7 | a0001c0001t0001g0004a0001c0001t0001g0080a0001c0003t0003g0119others(4): Show | 7 | HG01081.hp2 HG02258.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.543+1573G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6838987 | ||||||
| chr18:6839095
|
CA | C | 13 | a0001c0001t0001g0072a0001c0001t0001g0121a0001c0001t0001g0151others(10): Show | 13 | HG01106.hp1 HG01243.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.543+1683delA | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr18 | 6839095 | |||||
| chr18:6839134
|
A | G | 1 | a0001c0012t0014g0159 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.543+1720A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6839134 | ||||||
| chr18:6839164
|
C | T | 17 | a0001c0001t0001g0035a0001c0001t0001g0182a0001c0001t0001g0188others(14): Show | 17 | HG00438.hp1 HG01952.hp1 HG02040.hp1 others(14): Show |
intron_variant | MODIFIER | c.543+1750C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6839164 | ||||||
| chr18:6839200
|
T | C | 13 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0075others(10): Show | 13 | HG00741.hp1 HG01081.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.543+1786T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6839200 | ||||||
| chr18:6839228
|
A | G | 1 | a0003c0004t0001g0183 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.543+1814A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6839228 | ||||||
| chr18:6839255
|
A | G | 2 | a0001c0001t0001g0004a0001c0001t0001g0080 | 2 | HG02258.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.543+1841A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6839255 | ||||||
| chr18:6839279
|
A | G | 5 | a0001c0001t0001g0003a0001c0001t0001g0075a0001c0001t0001g0151others(2): Show | 5 | HG00741.hp1 HG01243.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.543+1865A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6839279 | ||||||
| chr18:6839292
|
A | AT | 30 | a0001c0001t0001g0003a0001c0001t0001g0080a0001c0001t0001g0102others(27): Show | 30 | HG00423.hp1 HG00438.hp2 HG01175.hp2 others(27): Show |
intron_variant | MODIFIER | c.543+1897dupT | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr18 | 6839292 | |||||
| chr18:6839292
|
A | ATT | 49 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0019others(46): Show | 49 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(46): Show |
intron_variant | MODIFIER | c.543+1896_543+1897d others(4): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr18 | 6839292 | |||||
| chr18:6839292
|
AT | A | 15 | a0001c0001t0001g0100a0001c0001t0001g0107a0001c0001t0001g0179others(12): Show | 15 | HG01106.hp1 HG01243.hp1 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.543+1897delT | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr18 | 6839292 | |||||
| chr18:6839317
|
A | G | 164 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0012others(161): Show | 164 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(161): Show |
intron_variant | MODIFIER | c.543+1903A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6839317 | ||||||
| chr18:6839329
|
T | C | 3 | a0001c0001t0001g0037a0002c0002t0002g0172a0003c0004t0001g0025 | 3 | HG02300.hp1 HG02523.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.543+1915T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6839329 | ||||||
| chr18:6839332
|
C | G | 1 | a0001c0001t0001g0035 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.543+1918C>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6839332 | ||||||
| chr18:6839345
|
G | C | 1 | a0002c0002t0002g0099 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.543+1931G>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6839345 | ||||||
| chr18:6839354
|
C | T | 3 | a0001c0003t0003g0233a0001c0003t0003g0234a0002c0002t0002g0099 | 3 | HG00741.hp1 HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.543+1940C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6839354 | ||||||
| chr18:6839380
|
G | A | 2 | a0001c0003t0003g0002a0001c0003t0003g0104 | 2 | HG03471.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.543+1966G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6839380 | ||||||
| chr18:6839382
|
C | T | 6 | a0001c0001t0001g0003a0001c0001t0006g0164a0001c0003t0003g0105others(3): Show | 6 | HG01175.hp2 HG01884.hp2 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.543+1968C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6839382 | ||||||
| chr18:6839399
|
T | C | 3 | a0001c0001t0001g0232a0001c0001t0008g0143a0001c0003t0003g0027 | 3 | HG00741.hp2 HG03490.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.543+1985T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6839399 | ||||||
| chr18:6839405
|
C | A | 1 | a0001c0001t0001g0097 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.543+1991C>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6839405 | ||||||
| chr18:6839405
|
C | T | 2 | a0001c0003t0003g0060a0001c0003t0015g0028 | 2 | HG01106.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.543+1991C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6839405 | ||||||
| chr18:6839406
|
C | G | 3 | a0001c0001t0001g0097a0001c0003t0003g0060a0001c0003t0015g0028 | 3 | HG01106.hp2 HG02735.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.543+1992C>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6839406 | ||||||
| chr18:6839431
|
C | T | 3 | a0001c0003t0003g0201a0002c0002t0002g0009a0002c0002t0002g0033 | 3 | HG01346.hp2 HG01943.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.543+2017C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6839431 | ||||||
| chr18:6839434
|
T | C | 10 | a0001c0001t0001g0001a0001c0001t0001g0054a0001c0001t0001g0070others(7): Show | 10 | HG00099.hp1 HG00140.hp1 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.543+2020T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6839434 | ||||||
| chr18:6839442
|
A | C | 44 | a0001c0001t0001g0001a0001c0001t0001g0072a0001c0001t0001g0121others(41): Show | 44 | HG00741.hp1 HG01081.hp2 HG01106.hp1 others(41): Show |
intron_variant | MODIFIER | c.543+2028A>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6839442 | ||||||
| chr18:6839443
|
G | A | 4 | a0001c0001t0001g0124a0001c0001t0001g0149a0001c0001t0001g0150others(1): Show | 4 | HG02145.hp1 HG02615.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.543+2029G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6839443 | ||||||
| chr18:6839445
|
C | T | 2 | a0001c0001t0001g0209a0002c0002t0002g0174 | 2 | HG04228.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.543+2031C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6839445 | ||||||
| chr18:6839454
|
T | C | 1 | a0003c0004t0001g0024 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.543+2040T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6839454 | ||||||
| chr18:6839460
|
A | G | 1 | a0001c0015t0003g0167 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.543+2046A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6839460 | ||||||
| chr18:6839488
|
A | G | 1 | a0001c0001t0016g0081 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.543+2074A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6839488 | ||||||
| chr18:6839499
|
C | G | 1 | a0001c0001t0001g0188 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.543+2085C>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6839499 | ||||||
| chr18:6839540
|
G | A | 1 | a0001c0001t0001g0198 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.543+2126G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6839540 | ||||||
| chr18:6839569
|
T | C | 1 | a0001c0001t0001g0129 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.543+2155T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6839569 | ||||||
| chr18:6839578
|
T | C | 15 | a0001c0001t0001g0100a0001c0001t0001g0107a0001c0001t0006g0155others(12): Show | 15 | HG01243.hp1 HG01891.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.543+2164T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6839578 | ||||||
| chr18:6839585
|
C | G | 1 | a0003c0004t0001g0064 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.543+2171C>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6839585 | ||||||
| chr18:6839586
|
T | C | 75 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0018others(72): Show | 75 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.543+2172T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6839586 | ||||||
| chr18:6839587
|
G | A | 1 | a0003c0004t0001g0064 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.543+2173G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6839587 | ||||||
| chr18:6839589
|
G | A | 1 | a0001c0003t0003g0110 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.543+2175G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6839589 | ||||||
| chr18:6839592
|
C | T | 3 | a0001c0001t0001g0029a0001c0001t0001g0128a0003c0004t0001g0195 | 3 | HG00544.hp2 HG02129.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.543+2178C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6839592 | ||||||
| chr18:6839593
|
G | A | 3 | a0001c0001t0001g0161a0001c0001t0001g0185a0002c0002t0002g0137 | 3 | HG02080.hp1 HG02145.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.543+2179G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6839593 | ||||||
| chr18:6839593
|
G | C | 1 | a0001c0003t0003g0079 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.543+2179G>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6839593 | ||||||
| chr18:6839597
|
A | T | 1 | a0002c0002t0002g0135 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.543+2183A>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6839597 | ||||||
| chr18:6839645
|
C | T | 3 | a0001c0001t0001g0072a0001c0001t0006g0155a0007c0008t0002g0069 | 3 | HG02258.hp1 HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.543+2231C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6839645 | ||||||
| chr18:6839790
|
G | T | 1 | a0002c0002t0010g0246 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.543+2376G>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6839790 | ||||||
| chr18:6839812
|
A | G | 3 | a0001c0001t0001g0072a0001c0001t0006g0155a0007c0008t0002g0069 | 3 | HG02258.hp1 HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.543+2398A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6839812 | ||||||
| chr18:6839996
|
G | T | 1 | a0002c0002t0002g0148 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.543+2582G>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6839996 | ||||||
| chr18:6840064
|
G | A | 173 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(170): Show | 173 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.543+2650G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6840064 | ||||||
| chr18:6840149
|
C | T | 40 | a0001c0001t0001g0003a0001c0001t0001g0029a0001c0001t0001g0040others(37): Show | 40 | HG00544.hp2 HG00558.hp2 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.543+2735C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6840149 | ||||||
| chr18:6840196
|
A | G | 1 | a0002c0002t0013g0022 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.543+2782A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6840196 | ||||||
| chr18:6840358
|
C | A | 1 | a0003c0004t0001g0025 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.543+2944C>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6840358 | ||||||
| chr18:6840377
|
T | C | 1 | a0002c0005t0002g0017 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.543+2963T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6840377 | ||||||
| chr18:6840521
|
A | G | 2 | a0001c0012t0014g0159a0008c0011t0005g0016 | 2 | HG02559.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.543+3107A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6840521 | ||||||
| chr18:6840599
|
G | T | 1 | a0001c0003t0003g0085 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.543+3185G>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6840599 | ||||||
| chr18:6840751
|
G | A | 2 | a0001c0003t0003g0145a0001c0019t0021g0073 | 2 | NA18906.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.543+3337G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6840751 | ||||||
| chr18:6840760
|
A | G | 1 | a0004c0007t0002g0238 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.543+3346A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6840760 | ||||||
| chr18:6840860
|
A | G | 2 | a0002c0002t0002g0137a0003c0004t0001g0048 | 2 | HG00621.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.543+3446A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6840860 | ||||||
| chr18:6840868
|
C | G | 8 | a0001c0001t0001g0106a0001c0001t0009g0245a0001c0003t0003g0068others(5): Show | 8 | HG02451.hp2 HG02647.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.543+3454C>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6840868 | ||||||
| chr18:6840952
|
A | G | 2 | a0008c0011t0005g0090a0008c0011t0005g0152 | 2 | HG03471.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.543+3538A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6840952 | ||||||
| chr18:6841119
|
T | TTC | 8 | a0001c0001t0008g0074a0001c0003t0003g0002a0001c0003t0003g0076others(5): Show | 8 | HG01106.hp1 HG02922.hp1 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.543+3718_543+3719d others(4): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr18 | 6841119 | |||||
| chr18:6841119
|
T | TTCTCTCT others(99): Show |
1 | a0002c0002t0002g0131 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.543+3742_543+3743i others(108): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr18 | 6841119 | |||||
| chr18:6841119
|
T | TTCTCTCT others(48): Show |
2 | a0001c0003t0003g0123a0008c0011t0005g0152 | 2 | HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.543+3712_543+3766d others(57): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr18 | 6841119 | |||||
| chr18:6841119
|
T | TTCTCTCT others(118): Show |
1 | a0008c0011t0005g0090 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.543+3766_543+3767i others(127): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr18 | 6841119 | |||||
| chr18:6841125
|
C | CTCTCTCT others(12): Show |
7 | a0001c0001t0001g0019a0001c0001t0001g0035a0001c0001t0001g0202others(4): Show | 7 | HG00099.hp1 HG00735.hp1 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.543+3724_543+3742d others(21): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr18 | 6841125 | |||||
| chr18:6841141
|
A | T | 1 | a0001c0012t0014g0159 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.543+3727A>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6841141 | ||||||
| chr18:6841144
|
G | C | 1 | a0001c0012t0014g0159 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.543+3730G>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6841144 | ||||||
| chr18:6841144
|
G | GTCTCTCT others(8): Show |
3 | a0001c0001t0001g0001a0001c0001t0001g0054a0001c0003t0003g0077 | 3 | HG01256.hp1 HG01496.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.543+3743_543+3757d others(17): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr18 | 6841144 | |||||
| chr18:6841144
|
GTCTCTCT others(8): Show |
G | 3 | a0001c0001t0001g0186a0003c0004t0001g0058a0003c0004t0001g0219 | 3 | HG00423.hp2 HG02080.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.543+3743_543+3757d others(17): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr18 | 6841144 | |||||
| chr18:6841152
|
C | CTCTCTCT others(161): Show |
1 | a0001c0012t0014g0159 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.543+3738_543+3739i others(170): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6841152 | ||||||
| chr18:6841155
|
CTT | C | 3 | a0001c0001t0001g0075a0001c0001t0001g0211a0003c0004t0001g0175 | 3 | HG02965.hp1 HG03486.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.543+3743_543+3744d others(4): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr18 | 6841155 | |||||
| chr18:6841156
|
T | TCTCACTG others(23): Show |
1 | a0002c0002t0002g0011 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.543+3742_543+3743i others(32): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6841156 | ||||||
| chr18:6841157
|
T | C | 20 | a0001c0001t0001g0052a0001c0001t0001g0071a0001c0001t0001g0072others(17): Show | 20 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(17): Show |
intron_variant | MODIFIER | c.543+3743T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6841157 | ||||||
| chr18:6841157
|
T | TTCTCTCT others(30): Show |
1 | a0001c0012t0001g0210 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.543+3777_543+3778i others(39): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr18 | 6841157 | |||||
| chr18:6841157
|
TTCTCTCT others(6): Show |
T | 2 | a0001c0003t0003g0119a0002c0017t0002g0086 | 2 | HG02922.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.543+3767_543+3779d others(15): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr18 | 6841157 | |||||
| chr18:6841159
|
C | CACTG | 17 | a0001c0001t0001g0052a0001c0001t0001g0071a0001c0001t0001g0072others(14): Show | 17 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(14): Show |
intron_variant | MODIFIER | c.543+3745_543+3746i others(6): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6841159 | ||||||
| chr18:6841165
|
CTCCTCTC others(10): Show |
C | 1 | a0001c0001t0001g0215 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.543+3752_543+3768d others(19): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6841165 | ||||||
| chr18:6841167
|
C | CTCCTCTC others(261): Show |
1 | a0001c0003t0003g0156 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.543+3753_543+3754i others(270): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6841167 | ||||||
| chr18:6841167
|
CCTCTCTC others(12): Show |
C | 1 | a0001c0001t0009g0005 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.543+3767_543+3785d others(21): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr18 | 6841167 | |||||
| chr18:6841168
|
C | T | 1 | a0006c0009t0005g0144 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.543+3754C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6841168 | ||||||
| chr18:6841169
|
T | C | 1 | a0006c0009t0005g0144 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.543+3755T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6841169 | ||||||
| chr18:6841169
|
TCTCTCTC others(4): Show |
T | 1 | a0003c0004t0001g0039 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.543+3767_543+3777d others(13): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr18 | 6841169 | |||||
| chr18:6841170
|
C | CTT | 10 | a0001c0001t0001g0052a0001c0001t0001g0071a0001c0001t0001g0082others(7): Show | 10 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(7): Show |
intron_variant | MODIFIER | c.543+3757_543+3758i others(4): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr18 | 6841170 | |||||
| chr18:6841171
|
TCTCTCTC others(2): Show |
T | 5 | a0001c0001t0001g0003a0001c0003t0003g0002a0001c0003t0003g0068others(2): Show | 5 | HG01175.hp2 HG02886.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.543+3767_543+3775d others(11): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr18 | 6841171 | |||||
| chr18:6841172
|
C | T | 4 | a0001c0003t0003g0091a0001c0003t0003g0122a0002c0002t0002g0065others(1): Show | 4 | HG02723.hp1 HG03209.hp2 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.543+3758C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6841172 | ||||||
| chr18:6841173
|
T | TC | 3 | a0003c0004t0001g0125a0003c0004t0001g0193a0004c0007t0002g0056 | 3 | HG00438.hp2 HG02155.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.543+3760dupC | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr18 | 6841173 | |||||
| chr18:6841175
|
T | TCTCTCTC others(77): Show |
1 | a0001c0001t0001g0165 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.543+3766_543+3767i others(86): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr18 | 6841175 | |||||
| chr18:6841179
|
TC | T | 4 | a0001c0001t0001g0194a0001c0003t0003g0122a0002c0002t0002g0065others(1): Show | 4 | HG02071.hp1 HG02723.hp1 NA18968.hp1 others(1): Show |
intron_variant | MODIFIER | c.543+3767delC | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr18 | 6841179 | |||||
| chr18:6841180
|
C | CCTCTCTC others(32): Show |
1 | a0002c0005t0002g0158 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.543+3777_543+3778i others(41): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr18 | 6841180 | |||||
| chr18:6841180
|
C | CCTCTCTC others(26): Show |
2 | a0003c0013t0011g0062a0003c0013t0011g0063 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.543+3777_543+3778i others(35): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr18 | 6841180 | |||||
| chr18:6841180
|
C | CCTCTCTC others(89): Show |
1 | a0001c0010t0003g0089 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.543+3783_543+3784i others(98): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr18 | 6841180 | |||||
| chr18:6841180
|
C | CT | 8 | a0001c0001t0001g0004a0001c0001t0001g0038a0001c0001t0001g0075others(5): Show | 8 | HG00544.hp1 HG01243.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.543+3766_543+3767i others(3): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6841180 | ||||||
| chr18:6841180
|
C | CTCT | 7 | a0001c0001t0001g0019a0001c0001t0001g0034a0001c0001t0001g0035others(4): Show | 7 | HG00735.hp1 HG01099.hp2 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.543+3766_543+3767i others(5): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6841180 | ||||||
| chr18:6841180
|
C | CTCTCT | 3 | a0001c0001t0001g0042a0001c0012t0014g0159a0002c0005t0002g0017 | 3 | HG02559.hp2 HG03239.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.543+3766_543+3767i others(7): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6841180 | ||||||
| chr18:6841180
|
C | CTCTCTCC others(283): Show |
1 | a0001c0020t0023g0101 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.543+3766_543+3767i others(292): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6841180 | ||||||
| chr18:6841180
|
C | CTCTCTCT others(113): Show |
1 | a0001c0001t0006g0176 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.543+3766_543+3767i others(122): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6841180 | ||||||
| chr18:6841180
|
C | CTCTCTCT others(6): Show |
1 | a0001c0001t0001g0228 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.543+3766_543+3767i others(15): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6841180 | ||||||
| chr18:6841180
|
C | CTCTCTCT others(53): Show |
1 | a0002c0002t0004g0059 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.543+3766_543+3767i others(62): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6841180 | ||||||
| chr18:6841180
|
C | CTCTCTCT others(60): Show |
1 | a0001c0003t0003g0076 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.543+3766_543+3767i others(69): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6841180 | ||||||
| chr18:6841180
|
CCT | C | 12 | a0001c0001t0001g0128a0001c0001t0001g0216a0001c0001t0001g0223others(9): Show | 12 | HG00597.hp1 HG00621.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.543+3788_543+3789d others(4): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr18 | 6841180 | |||||
| chr18:6841180
|
CCTCT | C | 5 | a0001c0003t0003g0208a0003c0004t0001g0020a0003c0004t0001g0136others(2): Show | 5 | HG00558.hp1 HG03942.hp1 NA19063.hp1 others(2): Show |
intron_variant | MODIFIER | c.543+3786_543+3789d others(6): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr18 | 6841180 | |||||
| chr18:6841181
|
C | T | 2 | a0005c0006t0003g0177a0005c0006t0003g0180 | 2 | NA18950.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.543+3767C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6841181 | ||||||
| chr18:6841182
|
T | C | 2 | a0005c0006t0003g0177a0005c0006t0003g0180 | 2 | NA18950.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.543+3768T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6841182 | ||||||
| chr18:6841182
|
T | TCTCTCTC others(88): Show |
2 | a0001c0010t0003g0098a0001c0010t0003g0114 | 2 | HG01081.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.543+3783_543+3784i others(97): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr18 | 6841182 | |||||
| chr18:6841184
|
T | TTTCTCTC others(4): Show |
1 | a0003c0004t0001g0045 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.543+3770_543+3771i others(13): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6841184 | ||||||
| chr18:6841186
|
T | TCTCTCTC others(229): Show |
1 | a0001c0001t0001g0168 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.543+3781_543+3782i others(238): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr18 | 6841186 | |||||
| chr18:6841186
|
T | TCTCTCTC others(19): Show |
3 | a0001c0003t0003g0087a0001c0003t0003g0169a0001c0003t0003g0170 | 3 | HG02965.hp2 HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.543+3783_543+3784i others(28): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr18 | 6841186 | |||||
| chr18:6841188
|
T | TCCTCTCT others(73): Show |
1 | a0006c0009t0005g0144 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.543+3775_543+3776i others(82): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr18 | 6841188 | |||||
| chr18:6841188
|
T | TCTCTC | 3 | a0001c0001t0001g0071a0001c0001t0001g0209a0003c0004t0001g0187 | 3 | HG00280.hp1 HG04228.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.543+3775_543+3779d others(7): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr18 | 6841188 | |||||
| chr18:6841190
|
T | TCTC | 3 | a0001c0001t0018g0111a0002c0002t0004g0006a0002c0002t0004g0147 | 3 | HG02280.hp2 HG02559.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.543+3777_543+3779d others(5): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr18 | 6841190 | |||||
| chr18:6841190
|
T | TCTCTCTC others(177): Show |
1 | a0001c0003t0003g0094 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.543+3783_543+3784i others(186): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr18 | 6841190 | |||||
| chr18:6841190
|
T | TCTCTCTC others(176): Show |
1 | a0001c0003t0003g0095 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.543+3783_543+3784i others(185): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr18 | 6841190 | |||||
| chr18:6841190
|
T | TCTCTCTC others(63): Show |
2 | a0001c0001t0007g0116a0001c0001t0007g0117 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.543+3789_543+3790i others(72): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr18 | 6841190 | |||||
| chr18:6841190
|
TCTCTCTC others(11): Show |
T | 3 | a0001c0003t0003g0222a0002c0002t0002g0196a0004c0007t0002g0036 | 3 | HG01081.hp1 HG02071.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.543+3790_543+3807d others(20): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr18 | 6841190 | |||||
| chr18:6841192
|
TCTCTCTC others(4): Show |
T | 3 | a0002c0002t0002g0046a0002c0002t0002g0047a0002c0005t0002g0057 | 3 | HG03239.hp1 HG03491.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.543+3784_543+3794d others(13): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr18 | 6841192 | |||||
| chr18:6841196
|
TCTCTCTC others(5): Show |
T | 2 | a0002c0002t0002g0224a0003c0004t0001g0227 | 2 | HG00423.hp1 HG00597.hp2 |
intron_variant | MODIFIER | c.543+3790_543+3801d others(14): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr18 | 6841196 | |||||
| chr18:6841197
|
CTCTCTCC others(6): Show |
C | 8 | a0001c0003t0003g0013a0001c0003t0003g0201a0002c0002t0002g0083others(5): Show | 8 | HG00438.hp1 HG01346.hp2 HG01943.hp2 others(5): Show |
intron_variant | MODIFIER | c.543+3784_543+3796d others(15): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6841197 | ||||||
| chr18:6841197
|
CTCTCTCC others(8): Show |
C | 1 | a0003c0004t0001g0125 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.543+3784_543+3798d others(17): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6841197 | ||||||
| chr18:6841198
|
TCTCTCCT others(3): Show |
T | 1 | a0002c0005t0002g0043 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.543+3790_543+3799d others(12): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr18 | 6841198 | |||||
| chr18:6841202
|
T | C | 1 | a0006c0009t0005g0144 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.543+3788T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6841202 | ||||||
| chr18:6841202
|
TC | T | 27 | a0001c0001t0001g0072a0001c0001t0001g0107a0001c0001t0001g0149others(24): Show | 27 | HG00099.hp1 HG00408.hp1 HG00558.hp2 others(24): Show |
intron_variant | MODIFIER | c.543+3790delC | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr18 | 6841202 | |||||
| chr18:6841202
|
TCCTCTC | T | 16 | a0001c0001t0001g0003a0001c0001t0001g0121a0001c0001t0001g0179others(13): Show | 16 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(13): Show |
intron_variant | MODIFIER | c.543+3790_543+3795d others(8): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr18 | 6841202 | |||||
| chr18:6841203
|
C | CT | 55 | a0001c0001t0001g0019a0001c0001t0001g0034a0001c0001t0001g0035others(52): Show | 55 | HG00280.hp1 HG00544.hp1 HG00735.hp1 others(52): Show |
intron_variant | MODIFIER | c.543+3789_543+3790i others(3): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6841203 | ||||||
| chr18:6841203
|
C | CTCT | 7 | a0001c0001t0001g0001a0001c0001t0001g0037a0001c0001t0001g0040others(4): Show | 7 | HG01515.hp1 HG02523.hp2 HG03492.hp2 others(4): Show |
intron_variant | MODIFIER | c.543+3789_543+3790i others(5): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6841203 | ||||||
| chr18:6841203
|
C | CTCTCTCC others(87): Show |
1 | a0001c0001t0007g0212 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.543+3789_543+3790i others(96): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6841203 | ||||||
| chr18:6841203
|
C | CTCTCTCT others(9): Show |
2 | a0001c0001t0001g0106a0006c0009t0003g0162 | 2 | HG02647.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.543+3789_543+3790i others(18): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6841203 | ||||||
| chr18:6841203
|
C | CTCTCTCT others(62): Show |
1 | a0001c0003t0003g0154 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.543+3789_543+3790i others(71): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6841203 | ||||||
| chr18:6841203
|
C | CTCTCTCT others(6): Show |
1 | a0003c0004t0001g0024 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.543+3789_543+3790i others(15): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6841203 | ||||||
| chr18:6841203
|
C | CTCTCTCT others(12): Show |
1 | a0001c0001t0022g0067 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.543+3789_543+3790i others(21): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6841203 | ||||||
| chr18:6841203
|
C | CTCTCTCT others(20): Show |
1 | a0001c0001t0001g0102 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.543+3789_543+3790i others(29): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6841203 | ||||||
| chr18:6841203
|
CCTCT | C | 13 | a0001c0001t0001g0029a0001c0001t0001g0188a0001c0001t0017g0118others(10): Show | 13 | HG00140.hp2 HG00544.hp2 HG02135.hp1 others(10): Show |
intron_variant | MODIFIER | c.543+3791_543+3794d others(6): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr18 | 6841203 | |||||
| chr18:6841207
|
TC | T | 27 | a0001c0001t0001g0038a0001c0001t0001g0107a0001c0001t0001g0139others(24): Show | 27 | HG00408.hp1 HG00544.hp1 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.543+3795delC | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr18 | 6841207 | |||||
| chr18:6841208
|
C | CCTCTCTC others(78): Show |
1 | a0001c0003t0003g0190 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.543+3807_543+3808i others(87): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr18 | 6841208 | |||||
| chr18:6841208
|
C | CCTCTCTC others(7): Show |
1 | a0001c0003t0003g0235 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.543+3796_543+3809d others(16): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr18 | 6841208 | |||||
| chr18:6841208
|
C | CT | 50 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0026others(47): Show | 50 | HG00280.hp1 HG00423.hp2 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.543+3794_543+3795i others(3): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6841208 | ||||||
| chr18:6841208
|
C | CTCTCTCT others(4): Show |
1 | a0001c0001t0001g0228 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.543+3794_543+3795i others(13): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6841208 | ||||||
| chr18:6841208
|
C | CTCTCTCT others(56): Show |
1 | a0001c0003t0003g0145 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.543+3794_543+3795i others(65): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6841208 | ||||||
| chr18:6841208
|
C | CTCTCTCT others(16): Show |
1 | a0001c0001t0009g0245 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.543+3794_543+3795i others(25): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6841208 | ||||||
| chr18:6841208
|
C | T | 13 | a0001c0001t0001g0029a0001c0001t0001g0188a0001c0001t0017g0118others(10): Show | 13 | HG00140.hp2 HG00544.hp2 HG02135.hp1 others(10): Show |
intron_variant | MODIFIER | c.543+3794C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6841208 | ||||||
| chr18:6841208
|
CCTCT | C | 10 | a0001c0001t0001g0124a0001c0001t0001g0149a0001c0001t0001g0150others(7): Show | 10 | HG00558.hp1 HG01884.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.543+3806_543+3809d others(6): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr18 | 6841208 | |||||
| chr18:6841209
|
C | T | 2 | a0001c0001t0001g0072a0001c0003t0003g0154 | 2 | HG02818.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.543+3795C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6841209 | ||||||
| chr18:6841210
|
T | C | 3 | a0001c0001t0001g0072a0001c0003t0003g0122a0001c0003t0003g0154 | 3 | HG02723.hp1 HG02818.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.543+3796T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6841210 | ||||||
| chr18:6841210
|
T | TCTCTCTC others(40): Show |
1 | a0001c0001t0001g0151 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.543+3809_543+3810i others(49): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr18 | 6841210 | |||||
| chr18:6841212
|
T | TC | 3 | a0003c0004t0001g0175a0003c0004t0001g0241a0003c0004t0001g0248 | 3 | NA18966.hp1 NA18967.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.543+3799dupC | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr18 | 6841212 | |||||
| chr18:6841212
|
T | TCTCTCTC others(6): Show |
2 | a0003c0004t0001g0032a0003c0004t0001g0048 | 2 | HG00558.hp2 HG00621.hp1 |
intron_variant | MODIFIER | c.543+3809_543+3810i others(15): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr18 | 6841212 | |||||
| chr18:6841222
|
T | TCTCTCAT others(135): Show |
1 | a0001c0001t0001g0203 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.543+3809_543+3810i others(144): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr18 | 6841222 | |||||
| chr18:6841223
|
C | CT | 6 | a0001c0001t0001g0202a0001c0001t0009g0245a0001c0001t0019g0008others(3): Show | 6 | HG01099.hp2 HG02886.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.543+3809_543+3810i others(3): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6841223 | ||||||
| chr18:6841265
|
CCCTTGGT others(13): Show |
C | 1 | a0002c0002t0002g0096 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.543+3856_543+3875d others(22): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr18 | 6841265 | |||||
| chr18:6841355
|
C | T | 1 | a0001c0003t0003g0087 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.543+3941C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6841355 | ||||||
| chr18:6841480
|
A | G | 2 | a0002c0002t0002g0148a0002c0002t0012g0088 | 2 | HG01346.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.543+4066A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6841480 | ||||||
| chr18:6841501
|
T | A | 1 | a0010c0014t0001g0142 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.543+4087T>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6841501 | ||||||
| chr18:6842194
|
T | A | 3 | a0001c0001t0001g0161a0001c0001t0009g0245a0001c0003t0003g0122 | 3 | HG02145.hp2 HG02723.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.543+4780T>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6842194 | ||||||
| chr18:6842224
|
G | A | 46 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0038others(43): Show | 46 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(43): Show |
intron_variant | MODIFIER | c.543+4810G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6842224 | ||||||
| chr18:6842225
|
T | C | 7 | a0001c0001t0018g0111a0001c0003t0003g0094a0001c0003t0003g0095others(4): Show | 7 | HG02055.hp1 HG02280.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.543+4811T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6842225 | ||||||
| chr18:6842309
|
G | C | 1 | a0001c0001t0019g0008 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.543+4895G>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6842309 | ||||||
| chr18:6842343
|
G | C | 1 | a0001c0019t0021g0073 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.543+4929G>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6842343 | ||||||
| chr18:6842409
|
G | A | 1 | a0001c0015t0003g0167 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.543+4995G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6842409 | ||||||
| chr18:6842452
|
C | T | 1 | a0001c0001t0001g0026 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.543+5038C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6842452 | ||||||
| chr18:6842670
|
T | C | 7 | a0001c0003t0003g0002a0001c0003t0003g0076a0001c0003t0003g0104others(4): Show | 7 | HG01106.hp1 HG02922.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.543+5256T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6842670 | ||||||
| chr18:6842684
|
A | G | 1 | a0001c0019t0021g0073 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.543+5270A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6842684 | ||||||
| chr18:6842750
|
C | T | 1 | a0004c0007t0002g0036 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.543+5336C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6842750 | ||||||
| chr18:6842854
|
A | T | 7 | a0001c0001t0018g0111a0001c0003t0003g0094a0001c0003t0003g0095others(4): Show | 7 | HG02055.hp1 HG02280.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.543+5440A>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6842854 | ||||||
| chr18:6842906
|
A | G | 7 | a0001c0001t0018g0111a0001c0003t0003g0094a0001c0003t0003g0095others(4): Show | 7 | HG02055.hp1 HG02280.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.543+5492A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6842906 | ||||||
| chr18:6843008
|
A | G | 1 | a0001c0003t0003g0085 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.543+5594A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6843008 | ||||||
| chr18:6843260
|
G | A | 46 | a0001c0001t0001g0044a0001c0001t0001g0049a0001c0001t0001g0070others(43): Show | 46 | HG00140.hp2 HG00597.hp2 HG01891.hp2 others(43): Show |
intron_variant | MODIFIER | c.543+5846G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6843260 | ||||||
| chr18:6843286
|
G | A | 1 | a0001c0015t0003g0167 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.543+5872G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6843286 | ||||||
| chr18:6843340
|
T | C | 4 | a0001c0001t0008g0143a0001c0001t0009g0005a0001c0003t0003g0145others(1): Show | 4 | HG01891.hp1 HG03130.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.543+5926T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6843340 | ||||||
| chr18:6843529
|
C | G | 47 | a0002c0002t0010g0246a0003c0004t0001g0010a0003c0004t0001g0020others(44): Show | 47 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(44): Show |
intron_variant | MODIFIER | c.543+6115C>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6843529 | ||||||
| chr18:6843530
|
T | G | 47 | a0002c0002t0010g0246a0003c0004t0001g0010a0003c0004t0001g0020others(44): Show | 47 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(44): Show |
intron_variant | MODIFIER | c.543+6116T>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6843530 | ||||||
| chr18:6843797
|
G | A | 14 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0072others(11): Show | 14 | HG01346.hp1 HG01884.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.543+6383G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6843797 | ||||||
| chr18:6843873
|
A | G | 10 | a0001c0001t0001g0165a0001c0001t0006g0176a0001c0001t0008g0143others(7): Show | 10 | HG01175.hp2 HG02055.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.543+6459A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6843873 | ||||||
| chr18:6843953
|
C | T | 7 | a0001c0001t0018g0111a0001c0003t0003g0094a0001c0003t0003g0095others(4): Show | 7 | HG02055.hp1 HG02280.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.543+6539C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6843953 | ||||||
| chr18:6843965
|
G | A | 3 | a0001c0001t0001g0161a0001c0001t0009g0245a0001c0003t0003g0122 | 3 | HG02145.hp2 HG02723.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.543+6551G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6843965 | ||||||
| chr18:6843978
|
T | C | 1 | a0003c0004t0001g0247 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.543+6564T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6843978 | ||||||
| chr18:6844025
|
C | T | 47 | a0001c0001t0001g0044a0001c0001t0001g0049a0001c0001t0001g0070others(44): Show | 47 | HG00140.hp2 HG00408.hp1 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.543+6611C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6844025 | ||||||
| chr18:6844308
|
A | G | 2 | a0001c0001t0001g0121a0001c0001t0001g0168 | 2 | HG02615.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.544-6726A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6844308 | ||||||
| chr18:6844495
|
G | A | 1 | a0002c0002t0002g0174 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.544-6539G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6844495 | ||||||
| chr18:6844504
|
G | C | 1 | a0002c0002t0002g0229 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.544-6530G>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6844504 | ||||||
| chr18:6844608
|
T | A | 49 | a0001c0003t0003g0123a0001c0015t0003g0167a0002c0002t0010g0246others(46): Show | 49 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(46): Show |
intron_variant | MODIFIER | c.544-6426T>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6844608 | ||||||
| chr18:6844705
|
G | A | 2 | a0001c0003t0003g0094a0001c0003t0003g0095 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.544-6329G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6844705 | ||||||
| chr18:6844743
|
T | G | 1 | a0001c0001t0001g0026 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.544-6291T>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6844743 | ||||||
| chr18:6844792
|
A | G | 49 | a0001c0003t0003g0123a0002c0002t0002g0134a0002c0002t0010g0246others(46): Show | 49 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(46): Show |
intron_variant | MODIFIER | c.544-6242A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6844792 | ||||||
| chr18:6844885
|
T | G | 13 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0072others(10): Show | 13 | HG01346.hp1 HG01884.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.544-6149T>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6844885 | ||||||
| chr18:6844926
|
G | A | 1 | a0001c0001t0001g0182 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.544-6108G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6844926 | ||||||
| chr18:6845271
|
G | A | 193 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(190): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.544-5763G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6845271 | ||||||
| chr18:6845341
|
C | T | 14 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0072others(11): Show | 14 | HG01346.hp1 HG01884.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.544-5693C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6845341 | ||||||
| chr18:6845342
|
A | G | 121 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0044others(118): Show | 121 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.544-5692A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6845342 | ||||||
| chr18:6845439
|
T | C | 1 | a0001c0001t0001g0070 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.544-5595T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6845439 | ||||||
| chr18:6845566
|
C | T | 2 | a0001c0003t0003g0094a0001c0003t0003g0095 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.544-5468C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6845566 | ||||||
| chr18:6845926
|
T | C | 1 | a0001c0003t0003g0085 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.544-5108T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6845926 | ||||||
| chr18:6845983
|
C | T | 2 | a0001c0001t0001g0228a0009c0016t0001g0092 | 2 | HG00099.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.544-5051C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6845983 | ||||||
| chr18:6846034
|
T | C | 3 | a0001c0001t0001g0034a0001c0001t0001g0038a0001c0001t0001g0042 | 3 | NA18941.hp1 NA18983.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.544-5000T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6846034 | ||||||
| chr18:6846066
|
T | A | 51 | a0001c0001t0001g0044a0001c0001t0001g0049a0001c0001t0001g0070others(48): Show | 51 | HG00140.hp2 HG00408.hp1 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.544-4968T>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6846066 | ||||||
| chr18:6846087
|
G | A | 1 | a0001c0019t0021g0073 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.544-4947G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6846087 | ||||||
| chr18:6846683
|
C | T | 47 | a0001c0001t0001g0044a0001c0001t0001g0049a0001c0001t0001g0070others(44): Show | 47 | HG00140.hp2 HG00408.hp1 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.544-4351C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6846683 | ||||||
| chr18:6846703
|
A | G | 192 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(189): Show | 192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.544-4331A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6846703 | ||||||
| chr18:6846708
|
G | A | 1 | a0010c0014t0001g0142 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.544-4326G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6846708 | ||||||
| chr18:6846739
|
A | G | 106 | a0001c0001t0001g0044a0001c0001t0001g0049a0001c0001t0001g0070others(103): Show | 106 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.544-4295A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6846739 | ||||||
| chr18:6846962
|
G | A | 14 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0072others(11): Show | 14 | HG01346.hp1 HG01884.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.544-4072G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6846962 | ||||||
| chr18:6847053
|
A | C | 1 | a0001c0012t0014g0159 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.544-3981A>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6847053 | ||||||
| chr18:6847177
|
C | T | 3 | a0001c0001t0001g0161a0001c0001t0009g0245a0001c0003t0003g0122 | 3 | HG02145.hp2 HG02723.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.544-3857C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6847177 | ||||||
| chr18:6847254
|
A | T | 1 | a0001c0015t0003g0167 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.544-3780A>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6847254 | ||||||
| chr18:6847277
|
C | T | 1 | a0001c0001t0001g0070 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.544-3757C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6847277 | ||||||
| chr18:6847296
|
C | T | 62 | a0001c0001t0001g0044a0001c0001t0001g0049a0001c0001t0001g0070others(59): Show | 62 | HG00140.hp2 HG00408.hp1 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.544-3738C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6847296 | ||||||
| chr18:6847350
|
G | A | 1 | a0001c0003t0003g0076 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.544-3684G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6847350 | ||||||
| chr18:6847354
|
C | T | 1 | a0001c0003t0003g0055 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.544-3680C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6847354 | ||||||
| chr18:6847622
|
A | T | 1 | a0001c0003t0003g0079 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.544-3412A>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6847622 | ||||||
| chr18:6847624
|
A | G | 1 | a0001c0003t0003g0079 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.544-3410A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6847624 | ||||||
| chr18:6847626
|
T | G | 1 | a0001c0003t0003g0079 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.544-3408T>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6847626 | ||||||
| chr18:6847628
|
G | GGT | 9 | a0001c0001t0001g0121a0001c0001t0001g0161a0001c0001t0009g0245others(6): Show | 9 | HG01081.hp2 HG02145.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.544-3405_544-3404i others(4): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr18 | 6847628 | |||||
| chr18:6847628
|
G | GGTGT | 50 | a0001c0001t0001g0049a0001c0001t0001g0070a0001c0001t0001g0124others(47): Show | 50 | HG00140.hp2 HG00408.hp1 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.544-3405_544-3404i others(6): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr18 | 6847628 | |||||
| chr18:6847628
|
G | T | 2 | a0001c0003t0003g0079a0002c0002t0002g0172 | 2 | HG03834.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.544-3406G>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6847628 | ||||||
| chr18:6847630
|
G | GGT | 70 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0072others(67): Show | 70 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.544-3383_544-3382d others(4): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr18 | 6847630 | |||||
| chr18:6847630
|
G | GGTGT | 55 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0034others(52): Show | 55 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(52): Show |
intron_variant | MODIFIER | c.544-3385_544-3382d others(6): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr18 | 6847630 | |||||
| chr18:6847630
|
G | GGTGTGT | 6 | a0001c0001t0018g0111a0001c0003t0003g0094a0001c0003t0003g0095others(3): Show | 6 | HG02055.hp1 HG02280.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.544-3387_544-3382d others(8): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr18 | 6847630 | |||||
| chr18:6847630
|
G | T | 62 | a0001c0001t0001g0044a0001c0001t0001g0049a0001c0001t0001g0070others(59): Show | 62 | HG00140.hp2 HG00408.hp1 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.544-3404G>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6847630 | ||||||
| chr18:6847670
|
A | G | 1 | a0001c0003t0003g0077 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.544-3364A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6847670 | ||||||
| chr18:6847718
|
T | C | 2 | a0001c0001t0008g0143a0001c0003t0003g0105 | 2 | HG01175.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.544-3316T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6847718 | ||||||
| chr18:6847888
|
G | A | 1 | a0001c0012t0014g0159 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.544-3146G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6847888 | ||||||
| chr18:6847940
|
T | C | 190 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(187): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.544-3094T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6847940 | ||||||
| chr18:6848021
|
T | C | 190 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(187): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.544-3013T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6848021 | ||||||
| chr18:6848087
|
C | T | 1 | a0001c0001t0001g0236 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.544-2947C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6848087 | ||||||
| chr18:6848123
|
A | G | 2 | a0001c0001t0008g0143a0001c0003t0003g0105 | 2 | HG01175.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.544-2911A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6848123 | ||||||
| chr18:6848131
|
G | A | 3 | a0001c0001t0006g0155a0001c0001t0006g0164a0001c0001t0008g0074 | 3 | HG01884.hp2 HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.544-2903G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6848131 | ||||||
| chr18:6848213
|
G | A | 190 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(187): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.544-2821G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6848213 | ||||||
| chr18:6848324
|
C | T | 190 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(187): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.544-2710C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6848324 | ||||||
| chr18:6848463
|
G | A | 190 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(187): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.544-2571G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6848463 | ||||||
| chr18:6848519
|
T | G | 46 | a0002c0002t0010g0246a0003c0004t0001g0010a0003c0004t0001g0020others(43): Show | 46 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(43): Show |
intron_variant | MODIFIER | c.544-2515T>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6848519 | ||||||
| chr18:6848607
|
G | A | 190 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(187): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.544-2427G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6848607 | ||||||
| chr18:6848627
|
T | C | 190 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(187): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.544-2407T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6848627 | ||||||
| chr18:6848635
|
C | T | 1 | a0001c0003t0003g0145 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.544-2399C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6848635 | ||||||
| chr18:6848810
|
T | G | 46 | a0002c0002t0010g0246a0003c0004t0001g0010a0003c0004t0001g0020others(43): Show | 46 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(43): Show |
intron_variant | MODIFIER | c.544-2224T>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6848810 | ||||||
| chr18:6848893
|
T | C | 1 | a0001c0019t0021g0073 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.544-2141T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6848893 | ||||||
| chr18:6848914
|
A | C | 1 | a0001c0003t0003g0085 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.544-2120A>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6848914 | ||||||
| chr18:6848914
|
A | G | 3 | a0001c0001t0001g0097a0001c0001t0001g0107a0001c0001t0001g0221 | 3 | HG01175.hp1 HG01243.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.544-2120A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6848914 | ||||||
| chr18:6849252
|
C | CA | 9 | a0001c0001t0001g0026a0001c0001t0001g0107a0001c0001t0001g0151others(6): Show | 9 | HG01175.hp1 HG01243.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.544-1759dupA | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr18 | 6849252 | |||||
| chr18:6849252
|
CA | C | 76 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0034others(73): Show | 76 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(73): Show |
intron_variant | MODIFIER | c.544-1759delA | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr18 | 6849252 | |||||
| chr18:6849252
|
CAA | C | 109 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0044others(106): Show | 109 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.544-1760_544-1759d others(4): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr18 | 6849252 | |||||
| chr18:6849252
|
CAAA | C | 6 | a0001c0003t0003g0094a0001c0003t0003g0095a0001c0003t0003g0123others(3): Show | 6 | HG02040.hp2 HG02523.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.544-1761_544-1759d others(5): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr18 | 6849252 | |||||
| chr18:6849453
|
G | A | 1 | a0001c0015t0003g0167 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.544-1581G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6849453 | ||||||
| chr18:6849458
|
A | C | 1 | a0002c0002t0012g0088 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.544-1576A>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6849458 | ||||||
| chr18:6849506
|
ATCT | A | 43 | a0001c0001t0001g0044a0001c0001t0001g0049a0001c0001t0001g0070others(40): Show | 43 | HG00140.hp2 HG00408.hp1 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.544-1523_544-1521d others(5): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr18 | 6849506 | |||||
| chr18:6849525
|
C | A | 1 | a0006c0009t0005g0144 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.544-1509C>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6849525 | ||||||
| chr18:6849834
|
A | G | 2 | a0001c0001t0001g0003a0001c0001t0001g0072 | 2 | HG02886.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.544-1200A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6849834 | ||||||
| chr18:6849896
|
G | T | 189 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(186): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.544-1138G>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6849896 | ||||||
| chr18:6850080
|
C | T | 3 | a0001c0001t0001g0161a0001c0001t0009g0245a0001c0003t0003g0122 | 3 | HG02145.hp2 HG02723.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.544-954C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6850080 | ||||||
| chr18:6850126
|
A | G | 1 | a0003c0023t0001g0120 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.544-908A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6850126 | ||||||
| chr18:6850355
|
T | C | 1 | a0001c0001t0001g0239 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.544-679T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6850355 | ||||||
| chr18:6850429
|
T | C | 1 | a0002c0002t0002g0126 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.544-605T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6850429 | ||||||
| chr18:6850544
|
T | C | 10 | a0001c0001t0001g0165a0001c0001t0006g0176a0001c0001t0008g0143others(7): Show | 10 | HG01175.hp2 HG02055.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.544-490T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6850544 | ||||||
| chr18:6850570
|
C | T | 1 | a0002c0002t0002g0134 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.544-464C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | 6850570 | ||||||
| chr18:6850854
|
T | TCAATGTA others(325): Show |
6 | a0001c0001t0001g0100a0001c0001t0006g0155a0001c0001t0006g0164others(3): Show | 6 | HG01346.hp1 HG01884.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.544-168_544-167ins others(332): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr18 | 6850854 | |||||
| chr18:6850854
|
T | TCAATGTA others(325): Show |
2 | a0001c0001t0001g0003a0001c0001t0001g0072 | 2 | HG02886.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.544-168_544-167ins others(332): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr18 | 6850854 | |||||
| chr18:6850854
|
T | TCAATGTA others(325): Show |
5 | a0001c0001t0001g0004a0001c0001t0001g0080a0001c0001t0001g0106others(2): Show | 5 | HG02258.hp2 HG02615.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.544-168_544-167ins others(332): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr18 | 6850854 | |||||
| chr18:6850854
|
T | TCAATGTA others(326): Show |
1 | a0001c0001t0001g0168 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.544-168_544-167ins others(333): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr18 | 6850854 | |||||
| chr18:6851260
|
C | T | 1 | a0001c0003t0003g0085 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.636+134C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | chr18 | 6851260 | ||||||
| chr18:6851268
|
G | A | 192 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(189): Show | 192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.636+142G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | chr18 | 6851268 | ||||||
| chr18:6851360
|
T | C | 132 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(129): Show | 132 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(129): Show |
intron_variant | MODIFIER | c.636+234T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | chr18 | 6851360 | ||||||
| chr18:6851361
|
G | A | 57 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0034others(54): Show | 57 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(54): Show |
intron_variant | MODIFIER | c.636+235G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | chr18 | 6851361 | ||||||
| chr18:6851362
|
C | T | 4 | a0001c0003t0003g0077a0001c0003t0003g0110a0001c0003t0003g0222others(1): Show | 4 | HG01081.hp1 HG01099.hp1 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.636+236C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | chr18 | 6851362 | ||||||
| chr18:6851558
|
C | T | 116 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0034others(113): Show | 116 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(113): Show |
intron_variant | MODIFIER | c.636+432C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | chr18 | 6851558 | ||||||
| chr18:6851998
|
A | G | 10 | a0001c0001t0001g0165a0001c0001t0006g0176a0001c0001t0008g0143others(7): Show | 10 | HG01175.hp2 HG02055.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.636+872A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | chr18 | 6851998 | ||||||
| chr18:6852060
|
A | G | 47 | a0002c0002t0010g0246a0003c0004t0001g0010a0003c0004t0001g0020others(44): Show | 47 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(44): Show |
intron_variant | MODIFIER | c.636+934A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | chr18 | 6852060 | ||||||
| chr18:6852099
|
A | G | 3 | a0001c0001t0009g0005a0001c0003t0003g0145a0002c0002t0012g0088 | 3 | HG01891.hp1 HG03130.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.636+973A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | chr18 | 6852099 | ||||||
| chr18:6852359
|
T | C | 1 | a0001c0003t0003g0084 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.636+1233T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | chr18 | 6852359 | ||||||
| chr18:6852380
|
T | G | 65 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0072others(62): Show | 65 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.636+1254T>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | chr18 | 6852380 | ||||||
| chr18:6852392
|
A | G | 1 | a0001c0001t0001g0026 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.636+1266A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | chr18 | 6852392 | ||||||
| chr18:6852479
|
T | C | 2 | a0002c0002t0002g0065a0002c0002t0002g0174 | 2 | NA18995.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.636+1353T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | chr18 | 6852479 | ||||||
| chr18:6852557
|
C | T | 116 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0034others(113): Show | 116 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(113): Show |
intron_variant | MODIFIER | c.636+1431C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | chr18 | 6852557 | ||||||
| chr18:6852628
|
C | G | 120 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(117): Show | 120 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(117): Show |
intron_variant | MODIFIER | c.636+1502C>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | chr18 | 6852628 | ||||||
| chr18:6852654
|
C | G | 67 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0034others(64): Show | 67 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(64): Show |
intron_variant | MODIFIER | c.636+1528C>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | chr18 | 6852654 | ||||||
| chr18:6852674
|
G | A | 1 | a0001c0003t0003g0079 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.636+1548G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | chr18 | 6852674 | ||||||
| chr18:6852772
|
G | A | 1 | a0001c0003t0003g0085 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.636+1646G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | chr18 | 6852772 | ||||||
| chr18:6852894
|
C | T | 2 | a0001c0003t0003g0094a0001c0003t0003g0095 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.636+1768C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | chr18 | 6852894 | ||||||
| chr18:6853167
|
A | G | 5 | a0001c0001t0018g0111a0001c0012t0001g0210a0002c0002t0004g0006others(2): Show | 5 | HG02055.hp1 HG02280.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.636+2041A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | chr18 | 6853167 | ||||||
| chr18:6853196
|
A | G | 64 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0072others(61): Show | 64 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.636+2070A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | chr18 | 6853196 | ||||||
| chr18:6853309
|
T | C | 7 | a0001c0001t0018g0111a0001c0003t0003g0094a0001c0003t0003g0095others(4): Show | 7 | HG02055.hp1 HG02280.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.636+2183T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | chr18 | 6853309 | ||||||
| chr18:6853357
|
T | C | 67 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0034others(64): Show | 67 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(64): Show |
intron_variant | MODIFIER | c.636+2231T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | chr18 | 6853357 | ||||||
| chr18:6853386
|
T | C | 67 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0034others(64): Show | 67 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(64): Show |
intron_variant | MODIFIER | c.636+2260T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | chr18 | 6853386 | ||||||
| chr18:6853414
|
G | A | 117 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0034others(114): Show | 117 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(114): Show |
intron_variant | MODIFIER | c.636+2288G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | chr18 | 6853414 | ||||||
| chr18:6853415
|
C | T | 117 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0034others(114): Show | 117 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(114): Show |
intron_variant | MODIFIER | c.636+2289C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | chr18 | 6853415 | ||||||
| chr18:6853474
|
A | AT | 102 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0034others(99): Show | 102 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(99): Show |
intron_variant | MODIFIER | c.636+2362dupT | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr18 | 6853474 | |||||
| chr18:6853474
|
A | ATT | 15 | a0001c0001t0001g0165a0001c0001t0006g0176a0001c0001t0008g0143others(12): Show | 15 | HG01175.hp2 HG02055.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.636+2361_636+2362d others(4): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr18 | 6853474 | |||||
| chr18:6853488
|
TG | T | 7 | a0001c0003t0003g0002a0001c0003t0003g0076a0001c0003t0003g0104others(4): Show | 7 | HG01106.hp1 HG02922.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.636+2364delG | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr18 | 6853488 | |||||
| chr18:6853704
|
A | G | 50 | a0001c0001t0001g0161a0001c0001t0009g0245a0001c0003t0003g0122others(47): Show | 50 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.636+2578A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | chr18 | 6853704 | ||||||
| chr18:6853742
|
T | A | 117 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0034others(114): Show | 117 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(114): Show |
intron_variant | MODIFIER | c.636+2616T>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | chr18 | 6853742 | ||||||
| chr18:6853800
|
C | T | 1 | a0001c0015t0003g0167 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.636+2674C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | chr18 | 6853800 | ||||||
| chr18:6853901
|
T | C | 1 | a0001c0003t0003g0085 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.636+2775T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | chr18 | 6853901 | ||||||
| chr18:6853958
|
G | A | 1 | a0001c0003t0003g0085 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.636+2832G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | chr18 | 6853958 | ||||||
| chr18:6853979
|
A | G | 50 | a0001c0001t0001g0161a0001c0001t0009g0245a0001c0003t0003g0122others(47): Show | 50 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.636+2853A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | chr18 | 6853979 | ||||||
| chr18:6854267
|
T | C | 67 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0034others(64): Show | 67 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(64): Show |
intron_variant | MODIFIER | c.636+3141T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | chr18 | 6854267 | ||||||
| chr18:6854454
|
A | C | 117 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0034others(114): Show | 117 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(114): Show |
intron_variant | MODIFIER | c.636+3328A>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | chr18 | 6854454 | ||||||
| chr18:6854519
|
C | G | 1 | a0001c0003t0003g0122 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.636+3393C>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | chr18 | 6854519 | ||||||
| chr18:6854571
|
A | G | 75 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0044others(72): Show | 75 | HG00140.hp2 HG00408.hp1 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.636+3445A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | chr18 | 6854571 | ||||||
| chr18:6854618
|
C | T | 1 | a0002c0005t0002g0057 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.636+3492C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | chr18 | 6854618 | ||||||
| chr18:6854622
|
T | C | 1 | a0001c0001t0001g0188 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.636+3496T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | chr18 | 6854622 | ||||||
| chr18:6854645
|
G | A | 1 | a0001c0001t0001g0018 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.636+3519G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | chr18 | 6854645 | ||||||
| chr18:6854706
|
A | T | 1 | a0001c0003t0003g0085 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.636+3580A>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | chr18 | 6854706 | ||||||
| chr18:6854742
|
G | GCTGCAGC others(7): Show |
1 | a0001c0001t0009g0245 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.636+3639_636+3652d others(16): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr18 | 6854742 | |||||
| chr18:6854742
|
GCTGCAGC others(7): Show |
G | 67 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0034others(64): Show | 67 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(64): Show |
intron_variant | MODIFIER | c.636+3639_636+3652d others(16): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr18 | 6854742 | |||||
| chr18:6854836
|
T | A | 2 | a0001c0001t0001g0202a0001c0003t0003g0208 | 2 | HG01099.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.636+3710T>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | chr18 | 6854836 | ||||||
| chr18:6854871
|
C | A | 75 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0044others(72): Show | 75 | HG00140.hp2 HG00408.hp1 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.636+3745C>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | chr18 | 6854871 | ||||||
| chr18:6854932
|
C | T | 1 | a0001c0001t0001g0168 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.636+3806C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | chr18 | 6854932 | ||||||
| chr18:6854979
|
C | T | 1 | a0001c0003t0003g0123 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.636+3853C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | chr18 | 6854979 | ||||||
| chr18:6855275
|
C | T | 50 | a0001c0001t0001g0044a0001c0001t0001g0049a0001c0001t0001g0070others(47): Show | 50 | HG00140.hp2 HG00408.hp1 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.636+4149C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | chr18 | 6855275 | ||||||
| chr18:6855277
|
A | G | 3 | a0001c0001t0009g0005a0001c0003t0003g0145a0002c0002t0012g0088 | 3 | HG01891.hp1 HG03130.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.636+4151A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | chr18 | 6855277 | ||||||
| chr18:6855454
|
G | C | 1 | a0001c0001t0001g0106 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.636+4328G>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | chr18 | 6855454 | ||||||
| chr18:6855620
|
C | A | 1 | a0002c0002t0002g0199 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.637-4188C>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | chr18 | 6855620 | ||||||
| chr18:6855708
|
G | T | 112 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0034others(109): Show | 112 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(109): Show |
intron_variant | MODIFIER | c.637-4100G>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | chr18 | 6855708 | ||||||
| chr18:6855747
|
C | G | 5 | a0001c0001t0001g0161a0001c0001t0009g0245a0001c0003t0003g0122others(2): Show | 5 | HG02145.hp2 HG02723.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.637-4061C>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | chr18 | 6855747 | ||||||
| chr18:6855789
|
T | C | 1 | a0001c0001t0001g0168 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.637-4019T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | chr18 | 6855789 | ||||||
| chr18:6855826
|
C | G | 1 | a0003c0004t0001g0192 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.637-3982C>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | chr18 | 6855826 | ||||||
| chr18:6855836
|
C | T | 1 | a0009c0016t0001g0092 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.637-3972C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | chr18 | 6855836 | ||||||
| chr18:6855870
|
A | C | 1 | a0001c0019t0021g0073 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.637-3938A>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | chr18 | 6855870 | ||||||
| chr18:6855900
|
C | T | 58 | a0001c0001t0001g0044a0001c0001t0001g0049a0001c0001t0001g0070others(55): Show | 58 | HG00140.hp2 HG00408.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.637-3908C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | chr18 | 6855900 | ||||||
| chr18:6855933
|
G | A | 14 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0072others(11): Show | 14 | HG01346.hp1 HG01884.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.637-3875G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | chr18 | 6855933 | ||||||
| chr18:6856094
|
G | C | 18 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0072others(15): Show | 18 | HG01346.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.637-3714G>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | chr18 | 6856094 | ||||||
| chr18:6856094
|
G | T | 1 | a0001c0015t0003g0167 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.637-3714G>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | chr18 | 6856094 | ||||||
| chr18:6856445
|
G | A | 1 | a0002c0002t0002g0137 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.637-3363G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | chr18 | 6856445 | ||||||
| chr18:6856531
|
A | C | 65 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0072others(62): Show | 65 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.637-3277A>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | chr18 | 6856531 | ||||||
| chr18:6856535
|
G | A | 1 | a0002c0002t0002g0011 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.637-3273G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | chr18 | 6856535 | ||||||
| chr18:6856558
|
G | A | 1 | a0001c0003t0003g0123 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.637-3250G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | chr18 | 6856558 | ||||||
| chr18:6856619
|
CCCT | C | 14 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0072others(11): Show | 14 | HG01346.hp1 HG01884.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.637-3184_637-3182d others(5): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr18 | 6856619 | |||||
| chr18:6856694
|
G | A | 1 | a0001c0001t0001g0168 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.637-3114G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | chr18 | 6856694 | ||||||
| chr18:6856809
|
G | A | 1 | a0001c0003t0003g0123 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.637-2999G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | chr18 | 6856809 | ||||||
| chr18:6857085
|
A | C | 1 | a0001c0001t0001g0151 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.637-2723A>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | chr18 | 6857085 | ||||||
| chr18:6857092
|
G | C | 51 | a0001c0001t0001g0161a0001c0001t0009g0245a0001c0003t0003g0122others(48): Show | 51 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.637-2716G>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | chr18 | 6857092 | ||||||
| chr18:6857133
|
G | C | 51 | a0001c0001t0001g0161a0001c0001t0009g0245a0001c0003t0003g0122others(48): Show | 51 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.637-2675G>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | chr18 | 6857133 | ||||||
| chr18:6857135
|
G | A | 1 | a0002c0002t0002g0023 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.637-2673G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | chr18 | 6857135 | ||||||
| chr18:6857341
|
A | G | 7 | a0001c0001t0018g0111a0001c0003t0003g0094a0001c0003t0003g0095others(4): Show | 7 | HG02055.hp1 HG02280.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.637-2467A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | chr18 | 6857341 | ||||||
| chr18:6857430
|
G | A | 3 | a0001c0001t0001g0161a0001c0001t0009g0245a0001c0003t0003g0122 | 3 | HG02145.hp2 HG02723.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.637-2378G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | chr18 | 6857430 | ||||||
| chr18:6857651
|
A | G | 1 | a0001c0019t0021g0073 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.637-2157A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | chr18 | 6857651 | ||||||
| chr18:6857823
|
A | G | 2 | a0001c0003t0003g0027a0001c0003t0003g0055 | 2 | HG00741.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.637-1985A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | chr18 | 6857823 | ||||||
| chr18:6857838
|
G | A | 3 | a0001c0001t0001g0097a0001c0001t0001g0107a0001c0001t0001g0221 | 3 | HG01175.hp1 HG01243.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.637-1970G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | chr18 | 6857838 | ||||||
| chr18:6857882
|
A | G | 1 | a0002c0002t0002g0126 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.637-1926A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | chr18 | 6857882 | ||||||
| chr18:6857938
|
A | G | 45 | a0003c0004t0001g0010a0003c0004t0001g0020a0003c0004t0001g0021others(42): Show | 45 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(42): Show |
intron_variant | MODIFIER | c.637-1870A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | chr18 | 6857938 | ||||||
| chr18:6857944
|
G | A | 50 | a0001c0001t0001g0044a0001c0001t0001g0049a0001c0001t0001g0070others(47): Show | 50 | HG00140.hp2 HG00408.hp1 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.637-1864G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | chr18 | 6857944 | ||||||
| chr18:6857970
|
G | T | 6 | a0001c0001t0001g0161a0001c0001t0009g0245a0001c0003t0003g0122others(3): Show | 6 | HG02145.hp2 HG02723.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.637-1838G>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | chr18 | 6857970 | ||||||
| chr18:6858079
|
T | C | 6 | a0001c0001t0001g0161a0001c0001t0009g0245a0001c0003t0003g0122others(3): Show | 6 | HG02145.hp2 HG02723.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.637-1729T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | chr18 | 6858079 | ||||||
| chr18:6858147
|
C | T | 5 | a0001c0001t0001g0161a0001c0001t0009g0245a0001c0003t0003g0122others(2): Show | 5 | HG02145.hp2 HG02723.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.637-1661C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | chr18 | 6858147 | ||||||
| chr18:6858149
|
CT | C | 7 | a0001c0001t0001g0161a0001c0001t0009g0245a0001c0003t0003g0122others(4): Show | 7 | HG02145.hp2 HG02723.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.637-1650delT | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr18 | 6858149 | |||||
| chr18:6858275
|
T | C | 6 | a0001c0001t0001g0161a0001c0001t0009g0245a0001c0003t0003g0122others(3): Show | 6 | HG02145.hp2 HG02723.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.637-1533T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | chr18 | 6858275 | ||||||
| chr18:6858427
|
T | C | 193 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(190): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.637-1381T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | chr18 | 6858427 | ||||||
| chr18:6858471
|
T | C | 2 | a0001c0003t0003g0094a0001c0003t0003g0095 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.637-1337T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | chr18 | 6858471 | ||||||
| chr18:6858528
|
C | A | 51 | a0001c0001t0001g0161a0001c0001t0009g0245a0001c0003t0003g0122others(48): Show | 51 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.637-1280C>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | chr18 | 6858528 | ||||||
| chr18:6858549
|
C | CT | 116 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0034others(113): Show | 116 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(113): Show |
intron_variant | MODIFIER | c.637-1248dupT | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr18 | 6858549 | |||||
| chr18:6858559
|
T | C | 2 | a0001c0003t0003g0094a0001c0003t0003g0095 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.637-1249T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | chr18 | 6858559 | ||||||
| chr18:6858569
|
G | A | 51 | a0001c0001t0001g0161a0001c0001t0009g0245a0001c0003t0003g0122others(48): Show | 51 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.637-1239G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | chr18 | 6858569 | ||||||
| chr18:6858574
|
G | C | 51 | a0001c0001t0001g0161a0001c0001t0009g0245a0001c0003t0003g0122others(48): Show | 51 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.637-1234G>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | chr18 | 6858574 | ||||||
| chr18:6858597
|
G | A | 74 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0044others(71): Show | 74 | HG00140.hp2 HG00408.hp1 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.637-1211G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | chr18 | 6858597 | ||||||
| chr18:6858608
|
A | G | 76 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0044others(73): Show | 76 | HG00140.hp2 HG00408.hp1 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.637-1200A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | chr18 | 6858608 | ||||||
| chr18:6858669
|
A | G | 3 | a0001c0001t0006g0155a0001c0001t0006g0164a0001c0001t0008g0074 | 3 | HG01884.hp2 HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.637-1139A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | chr18 | 6858669 | ||||||
| chr18:6858671
|
C | G | 1 | a0001c0003t0003g0085 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.637-1137C>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | chr18 | 6858671 | ||||||
| chr18:6858730
|
T | C | 51 | a0001c0001t0001g0161a0001c0001t0009g0245a0001c0003t0003g0122others(48): Show | 51 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.637-1078T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | chr18 | 6858730 | ||||||
| chr18:6858808
|
A | C | 1 | a0001c0015t0003g0167 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.637-1000A>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | chr18 | 6858808 | ||||||
| chr18:6858809
|
G | A | 1 | a0001c0015t0003g0167 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.637-999G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | chr18 | 6858809 | ||||||
| chr18:6858829
|
T | TA | 7 | a0001c0001t0018g0111a0001c0003t0003g0094a0001c0003t0003g0095others(4): Show | 7 | HG02055.hp1 HG02280.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.637-976dupA | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr18 | 6858829 | |||||
| chr18:6858869
|
T | TA | 75 | a0001c0001t0001g0004a0001c0001t0001g0044a0001c0001t0001g0049others(72): Show | 75 | HG00140.hp2 HG00408.hp1 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.637-926dupA | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr18 | 6858869 | |||||
| chr18:6858973
|
A | C | 2 | a0001c0003t0003g0094a0001c0003t0003g0095 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.637-835A>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | chr18 | 6858973 | ||||||
| chr18:6859077
|
AAAC | A | 50 | a0001c0001t0001g0044a0001c0001t0001g0049a0001c0001t0001g0070others(47): Show | 50 | HG00140.hp2 HG00408.hp1 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.637-713_637-711del others(3): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr18 | 6859077 | |||||
| chr18:6859092
|
C | A | 3 | a0001c0001t0001g0161a0001c0001t0009g0245a0001c0003t0003g0122 | 3 | HG02145.hp2 HG02723.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.637-716C>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | chr18 | 6859092 | ||||||
| chr18:6859092
|
C | CA | 109 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0034others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.637-714dupA | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr18 | 6859092 | |||||
| chr18:6859092
|
C | CAA | 3 | a0001c0003t0003g0013a0001c0003t0003g0201a0002c0002t0002g0137 | 3 | HG01346.hp2 HG01943.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.637-715_637-714dup others(2): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr18 | 6859092 | |||||
| chr18:6859095
|
C | A | 117 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0034others(114): Show | 117 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(114): Show |
intron_variant | MODIFIER | c.637-713C>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | chr18 | 6859095 | ||||||
| chr18:6859289
|
G | A | 3 | a0008c0011t0005g0016a0008c0011t0005g0090a0008c0011t0005g0152 | 3 | HG02630.hp2 HG03471.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.637-519G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | chr18 | 6859289 | ||||||
| chr18:6859506
|
T | C | 75 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0044others(72): Show | 75 | HG00140.hp2 HG00408.hp1 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.637-302T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | chr18 | 6859506 | ||||||
| chr18:6859926
|
T | C | 1 | a0001c0001t0001g0186 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.726+29T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 5/17 | chr18 | 6859926 | ||||||
| chr18:6859954
|
A | G | 1 | a0001c0001t0019g0008 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.726+57A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 5/17 | chr18 | 6859954 | ||||||
| chr18:6860030
|
C | T | 1 | a0001c0003t0003g0085 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.726+133C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 5/17 | chr18 | 6860030 | ||||||
| chr18:6860294
|
G | A | 1 | a0001c0015t0003g0167 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.726+397G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 5/17 | chr18 | 6860294 | ||||||
| chr18:6860348
|
T | C | 46 | a0002c0002t0013g0022a0003c0004t0001g0010a0003c0004t0001g0020others(43): Show | 46 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(43): Show |
intron_variant | MODIFIER | c.726+451T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 5/17 | chr18 | 6860348 | ||||||
| chr18:6860457
|
T | C | 116 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0029others(113): Show | 116 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.726+560T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 5/17 | chr18 | 6860457 | ||||||
| chr18:6860558
|
T | A | 45 | a0003c0004t0001g0010a0003c0004t0001g0020a0003c0004t0001g0021others(42): Show | 45 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(42): Show |
intron_variant | MODIFIER | c.726+661T>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 5/17 | chr18 | 6860558 | ||||||
| chr18:6860658
|
C | T | 1 | a0002c0002t0012g0088 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.726+761C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 5/17 | chr18 | 6860658 | ||||||
| chr18:6860675
|
A | G | 46 | a0002c0002t0002g0015a0003c0004t0001g0010a0003c0004t0001g0020others(43): Show | 46 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(43): Show |
intron_variant | MODIFIER | c.726+778A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 5/17 | chr18 | 6860675 | ||||||
| chr18:6860881
|
T | C | 45 | a0003c0004t0001g0010a0003c0004t0001g0020a0003c0004t0001g0021others(42): Show | 45 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(42): Show |
intron_variant | MODIFIER | c.726+984T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 5/17 | chr18 | 6860881 | ||||||
| chr18:6861134
|
C | G | 52 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0029others(49): Show | 52 | HG00423.hp2 HG00544.hp2 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.726+1237C>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 5/17 | chr18 | 6861134 | ||||||
| chr18:6861142
|
G | A | 2 | a0001c0012t0001g0210a0002c0005t0002g0158 | 2 | HG02055.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.726+1245G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 5/17 | chr18 | 6861142 | ||||||
| chr18:6861173
|
C | G | 2 | a0001c0001t0001g0205a0005c0006t0003g0031 | 2 | NA18940.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.726+1276C>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 5/17 | chr18 | 6861173 | ||||||
| chr18:6861173
|
C | T | 8 | a0001c0001t0001g0161a0001c0001t0009g0245a0001c0003t0003g0094others(5): Show | 8 | HG02055.hp1 HG02145.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.726+1276C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 5/17 | chr18 | 6861173 | ||||||
| chr18:6861174
|
A | G | 195 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(192): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.726+1277A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 5/17 | chr18 | 6861174 | ||||||
| chr18:6861430
|
G | A | 3 | a0001c0003t0003g0094a0001c0003t0003g0095a0001c0003t0003g0123 | 3 | HG02895.hp1 HG02897.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.726+1533G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 5/17 | chr18 | 6861430 | ||||||
| chr18:6861442
|
T | A | 1 | a0001c0001t0006g0155 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.726+1545T>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 5/17 | chr18 | 6861442 | ||||||
| chr18:6861689
|
G | C | 2 | a0001c0012t0001g0210a0002c0005t0002g0158 | 2 | HG02055.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.726+1792G>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 5/17 | chr18 | 6861689 | ||||||
| chr18:6861778
|
T | C | 104 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0029others(101): Show | 104 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.726+1881T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 5/17 | chr18 | 6861778 | ||||||
| chr18:6861788
|
T | A | 4 | a0001c0003t0003g0068a0001c0003t0003g0087a0001c0003t0003g0169others(1): Show | 4 | HG02965.hp2 HG03130.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.726+1891T>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 5/17 | chr18 | 6861788 | ||||||
| chr18:6861944
|
T | G | 5 | a0001c0001t0018g0111a0002c0002t0004g0006a0002c0002t0004g0059others(2): Show | 5 | HG02280.hp2 HG02451.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.726+2047T>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 5/17 | chr18 | 6861944 | ||||||
| chr18:6862027
|
A | C | 45 | a0003c0004t0001g0010a0003c0004t0001g0020a0003c0004t0001g0021others(42): Show | 45 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(42): Show |
intron_variant | MODIFIER | c.726+2130A>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 5/17 | chr18 | 6862027 | ||||||
| chr18:6862219
|
A | G | 55 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0029others(52): Show | 55 | HG00423.hp2 HG00544.hp2 HG00735.hp1 others(52): Show |
intron_variant | MODIFIER | c.726+2322A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 5/17 | chr18 | 6862219 | ||||||
| chr18:6862258
|
C | G | 10 | a0001c0001t0001g0165a0001c0001t0006g0176a0001c0001t0008g0143others(7): Show | 10 | HG01106.hp1 HG01175.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.726+2361C>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 5/17 | chr18 | 6862258 | ||||||
| chr18:6862325
|
C | T | 2 | a0001c0001t0001g0215a0001c0001t0001g0216 | 2 | NA18747.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.726+2428C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 5/17 | chr18 | 6862325 | ||||||
| chr18:6862339
|
C | G | 2 | a0001c0003t0003g0013a0001c0003t0003g0201 | 2 | HG01346.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.726+2442C>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 5/17 | chr18 | 6862339 | ||||||
| chr18:6862385
|
A | G | 8 | a0001c0001t0009g0005a0001c0001t0018g0111a0001c0003t0003g0145others(5): Show | 8 | HG01891.hp1 HG02280.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.726+2488A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 5/17 | chr18 | 6862385 | ||||||
| chr18:6862471
|
A | G | 118 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0018others(115): Show | 118 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(115): Show |
intron_variant | MODIFIER | c.726+2574A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 5/17 | chr18 | 6862471 | ||||||
| chr18:6862647
|
T | G | 45 | a0003c0004t0001g0010a0003c0004t0001g0020a0003c0004t0001g0021others(42): Show | 45 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(42): Show |
intron_variant | MODIFIER | c.726+2750T>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 5/17 | chr18 | 6862647 | ||||||
| chr18:6862664
|
A | T | 52 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0029others(49): Show | 52 | HG00423.hp2 HG00544.hp2 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.726+2767A>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 5/17 | chr18 | 6862664 | ||||||
| chr18:6862739
|
A | G | 1 | a0002c0005t0002g0061 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.726+2842A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 5/17 | chr18 | 6862739 | ||||||
| chr18:6863243
|
T | C | 1 | a0001c0015t0003g0167 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.726+3346T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 5/17 | chr18 | 6863243 | ||||||
| chr18:6863471
|
G | A | 1 | a0001c0001t0001g0035 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.726+3574G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 5/17 | chr18 | 6863471 | ||||||
| chr18:6863555
|
A | G | 14 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0072others(11): Show | 14 | HG01346.hp1 HG01884.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.726+3658A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 5/17 | chr18 | 6863555 | ||||||
| chr18:6863608
|
T | C | 70 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0034others(67): Show | 70 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(67): Show |
intron_variant | MODIFIER | c.726+3711T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 5/17 | chr18 | 6863608 | ||||||
| chr18:6863757
|
A | G | 66 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0034others(63): Show | 66 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(63): Show |
intron_variant | MODIFIER | c.726+3860A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 5/17 | chr18 | 6863757 | ||||||
| chr18:6863786
|
A | AT | 111 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0029others(108): Show | 111 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.726+3904dupT | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr18 | 6863786 | |||||
| chr18:6863788
|
T | TG | 14 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0072others(11): Show | 14 | HG01346.hp1 HG01884.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.726+3891_726+3892i others(3): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 5/17 | chr18 | 6863788 | ||||||
| chr18:6863885
|
C | T | 1 | a0001c0001t0022g0067 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.726+3988C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 5/17 | chr18 | 6863885 | ||||||
| chr18:6863931
|
C | T | 14 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0072others(11): Show | 14 | HG01346.hp1 HG01884.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.726+4034C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 5/17 | chr18 | 6863931 | ||||||
| chr18:6863936
|
C | G | 1 | a0001c0003t0003g0085 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.726+4039C>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 5/17 | chr18 | 6863936 | ||||||
| chr18:6863942
|
C | T | 1 | a0001c0001t0008g0171 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.726+4045C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 5/17 | chr18 | 6863942 | ||||||
| chr18:6864037
|
C | T | 1 | a0001c0003t0003g0169 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.727-4113C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 5/17 | chr18 | 6864037 | ||||||
| chr18:6864047
|
G | GTTTATT | 6 | a0001c0001t0001g0165a0001c0001t0006g0176a0001c0003t0003g0068others(3): Show | 6 | HG02055.hp2 HG02109.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.727-4088_727-4083d others(8): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr18 | 6864047 | |||||
| chr18:6864053
|
T | C | 1 | a0001c0019t0021g0073 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.727-4097T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 5/17 | chr18 | 6864053 | ||||||
| chr18:6864088
|
C | T | 1 | a0002c0002t0002g0137 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.727-4062C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 5/17 | chr18 | 6864088 | ||||||
| chr18:6864129
|
G | A | 1 | a0001c0003t0003g0222 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.727-4021G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 5/17 | chr18 | 6864129 | ||||||
| chr18:6864211
|
G | A | 66 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0034others(63): Show | 66 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(63): Show |
intron_variant | MODIFIER | c.727-3939G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 5/17 | chr18 | 6864211 | ||||||
| chr18:6864316
|
G | A | 66 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0034others(63): Show | 66 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(63): Show |
intron_variant | MODIFIER | c.727-3834G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 5/17 | chr18 | 6864316 | ||||||
| chr18:6864342
|
G | A | 1 | a0001c0003t0003g0085 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.727-3808G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 5/17 | chr18 | 6864342 | ||||||
| chr18:6864448
|
T | G | 2 | a0001c0003t0003g0084a0001c0003t0003g0154 | 2 | HG02818.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.727-3702T>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 5/17 | chr18 | 6864448 | ||||||
| chr18:6864571
|
G | T | 66 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0034others(63): Show | 66 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(63): Show |
intron_variant | MODIFIER | c.727-3579G>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 5/17 | chr18 | 6864571 | ||||||
| chr18:6864746
|
A | G | 3 | a0001c0001t0001g0034a0001c0001t0001g0038a0001c0001t0001g0042 | 3 | NA18941.hp1 NA18983.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.727-3404A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 5/17 | chr18 | 6864746 | ||||||
| chr18:6864788
|
T | C | 46 | a0001c0019t0021g0073a0003c0004t0001g0010a0003c0004t0001g0020others(43): Show | 46 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(43): Show |
intron_variant | MODIFIER | c.727-3362T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 5/17 | chr18 | 6864788 | ||||||
| chr18:6864809
|
C | T | 10 | a0001c0001t0001g0165a0001c0001t0006g0176a0001c0001t0008g0143others(7): Show | 10 | HG01106.hp1 HG01175.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.727-3341C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 5/17 | chr18 | 6864809 | ||||||
| chr18:6864827
|
C | G | 66 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0034others(63): Show | 66 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(63): Show |
intron_variant | MODIFIER | c.727-3323C>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 5/17 | chr18 | 6864827 | ||||||
| chr18:6864852
|
A | AT | 53 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0029others(50): Show | 53 | HG00423.hp2 HG00544.hp2 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.727-3287dupT | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr18 | 6864852 | |||||
| chr18:6864870
|
A | C | 1 | a0001c0015t0003g0167 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.727-3280A>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 5/17 | chr18 | 6864870 | ||||||
| chr18:6864906
|
A | G | 45 | a0003c0004t0001g0010a0003c0004t0001g0020a0003c0004t0001g0021others(42): Show | 45 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(42): Show |
intron_variant | MODIFIER | c.727-3244A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 5/17 | chr18 | 6864906 | ||||||
| chr18:6864914
|
G | A | 2 | a0001c0001t0001g0003a0001c0001t0001g0072 | 2 | HG02886.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.727-3236G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 5/17 | chr18 | 6864914 | ||||||
| chr18:6864930
|
G | A | 66 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0034others(63): Show | 66 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(63): Show |
intron_variant | MODIFIER | c.727-3220G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 5/17 | chr18 | 6864930 | ||||||
| chr18:6864939
|
T | C | 1 | a0001c0001t0001g0179 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.727-3211T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 5/17 | chr18 | 6864939 | ||||||
| chr18:6864980
|
C | T | 1 | a0001c0001t0001g0232 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.727-3170C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 5/17 | chr18 | 6864980 | ||||||
| chr18:6865166
|
A | G | 66 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0034others(63): Show | 66 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(63): Show |
intron_variant | MODIFIER | c.727-2984A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 5/17 | chr18 | 6865166 | ||||||
| chr18:6865388
|
T | C | 10 | a0001c0001t0001g0165a0001c0001t0006g0176a0001c0001t0008g0143others(7): Show | 10 | HG01106.hp1 HG01175.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.727-2762T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 5/17 | chr18 | 6865388 | ||||||
| chr18:6865659
|
C | T | 64 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0034others(61): Show | 64 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(61): Show |
intron_variant | MODIFIER | c.727-2491C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 5/17 | chr18 | 6865659 | ||||||
| chr18:6865809
|
C | G | 1 | a0002c0005t0002g0017 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.727-2341C>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 5/17 | chr18 | 6865809 | ||||||
| chr18:6865849
|
G | A | 1 | a0001c0001t0001g0037 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.727-2301G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 5/17 | chr18 | 6865849 | ||||||
| chr18:6866055
|
G | A | 3 | a0001c0003t0003g0002a0001c0003t0003g0104a0001c0003t0003g0119 | 3 | HG03471.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.727-2095G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 5/17 | chr18 | 6866055 | ||||||
| chr18:6866138
|
A | G | 65 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0018others(62): Show | 65 | HG00423.hp2 HG00544.hp2 HG00735.hp1 others(62): Show |
intron_variant | MODIFIER | c.727-2012A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 5/17 | chr18 | 6866138 | ||||||
| chr18:6866162
|
A | G | 10 | a0001c0001t0001g0165a0001c0001t0006g0176a0001c0001t0008g0143others(7): Show | 10 | HG01106.hp1 HG01175.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.727-1988A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 5/17 | chr18 | 6866162 | ||||||
| chr18:6866211
|
G | A | 1 | a0001c0019t0021g0073 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.727-1939G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 5/17 | chr18 | 6866211 | ||||||
| chr18:6866304
|
A | C | 1 | a0001c0019t0021g0073 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.727-1846A>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 5/17 | chr18 | 6866304 | ||||||
| chr18:6866793
|
G | A | 20 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0029others(17): Show | 20 | HG00423.hp2 HG00544.hp2 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.727-1357G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 5/17 | chr18 | 6866793 | ||||||
| chr18:6866797
|
A | G | 15 | a0001c0001t0001g0075a0001c0001t0001g0211a0001c0001t0001g0223others(12): Show | 15 | HG02723.hp2 HG02735.hp1 HG02965.hp1 others(12): Show |
intron_variant | MODIFIER | c.727-1353A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 5/17 | chr18 | 6866797 | ||||||
| chr18:6866833
|
G | A | 1 | a0003c0004t0001g0242 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.727-1317G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 5/17 | chr18 | 6866833 | ||||||
| chr18:6866865
|
T | C | 1 | a0001c0001t0001g0075 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.727-1285T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 5/17 | chr18 | 6866865 | ||||||
| chr18:6866984
|
G | A | 1 | a0001c0003t0003g0231 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.727-1166G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 5/17 | chr18 | 6866984 | ||||||
| chr18:6867081
|
T | C | 4 | a0003c0004t0001g0021a0003c0004t0001g0093a0003c0004t0001g0183others(1): Show | 4 | HG00597.hp1 HG00621.hp2 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.727-1069T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 5/17 | chr18 | 6867081 | ||||||
| chr18:6867224
|
A | G | 12 | a0001c0001t0001g0124a0001c0001t0001g0149a0001c0001t0001g0150others(9): Show | 12 | HG01952.hp2 HG02109.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.727-926A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 5/17 | chr18 | 6867224 | ||||||
| chr18:6867398
|
C | A | 2 | a0001c0003t0003g0094a0001c0003t0003g0095 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.727-752C>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 5/17 | chr18 | 6867398 | ||||||
| chr18:6867508
|
T | C | 191 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(188): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.727-642T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 5/17 | chr18 | 6867508 | ||||||
| chr18:6867865
|
A | G | 1 | a0002c0002t0002g0135 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.727-285A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 5/17 | chr18 | 6867865 | ||||||
| chr18:6868012
|
G | A | 1 | a0002c0002t0004g0006 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.727-138G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 5/17 | chr18 | 6868012 | ||||||
| chr18:6868610
|
T | A | 5 | a0001c0001t0018g0111a0002c0002t0004g0006a0002c0002t0004g0059others(2): Show | 5 | HG02280.hp2 HG02451.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.811+376T>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 6/17 | chr18 | 6868610 | ||||||
| chr18:6868611
|
GC | G | 190 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(187): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.811+382delC | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr18 | 6868611 | |||||
| chr18:6868647
|
C | T | 1 | a0003c0022t0003g0132 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.811+413C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 6/17 | chr18 | 6868647 | ||||||
| chr18:6868926
|
T | C | 190 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(187): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.811+692T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 6/17 | chr18 | 6868926 | ||||||
| chr18:6869137
|
C | G | 1 | a0001c0003t0003g0085 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.811+903C>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 6/17 | chr18 | 6869137 | ||||||
| chr18:6869194
|
C | T | 2 | a0001c0003t0003g0094a0001c0003t0003g0095 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.811+960C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 6/17 | chr18 | 6869194 | ||||||
| chr18:6869212
|
C | T | 2 | a0001c0003t0003g0094a0001c0003t0003g0095 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.811+978C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 6/17 | chr18 | 6869212 | ||||||
| chr18:6869251
|
TTC | T | 19 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0029others(16): Show | 19 | HG00544.hp2 HG00735.hp1 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.811+1019_811+1020d others(4): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr18 | 6869251 | |||||
| chr18:6869252
|
TC | T | 3 | a0001c0001t0001g0052a0001c0001t0001g0186a0002c0005t0002g0041 | 3 | HG00423.hp2 NA18989.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.811+1019delC | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 6/17 | chr18 | 6869252 | ||||||
| chr18:6869253
|
CT | C | 150 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(147): Show | 150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
intron_variant | MODIFIER | c.811+1043delT | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr18 | 6869253 | |||||
| chr18:6869253
|
CTT | C | 16 | a0001c0001t0009g0005a0001c0001t0009g0245a0001c0001t0018g0111others(13): Show | 16 | HG00408.hp2 HG01081.hp1 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.811+1042_811+1043d others(4): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr18 | 6869253 | |||||
| chr18:6869262
|
T | A | 1 | a0001c0003t0003g0104 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.811+1028T>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 6/17 | chr18 | 6869262 | ||||||
| chr18:6869331
|
G | C | 1 | a0001c0019t0021g0073 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.811+1097G>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 6/17 | chr18 | 6869331 | ||||||
| chr18:6869513
|
A | G | 191 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(188): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.812-1077A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 6/17 | chr18 | 6869513 | ||||||
| chr18:6869582
|
T | A | 1 | a0001c0019t0021g0073 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.812-1008T>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 6/17 | chr18 | 6869582 | ||||||
| chr18:6869733
|
G | A | 66 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0034others(63): Show | 66 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(63): Show |
intron_variant | MODIFIER | c.812-857G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 6/17 | chr18 | 6869733 | ||||||
| chr18:6870054
|
G | A | 2 | a0001c0012t0001g0210a0002c0005t0002g0158 | 2 | HG02055.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.812-536G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 6/17 | chr18 | 6870054 | ||||||
| chr18:6870108
|
C | T | 2 | a0001c0001t0001g0161a0001c0001t0009g0245 | 2 | HG02145.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.812-482C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 6/17 | chr18 | 6870108 | ||||||
| chr18:6870525
|
T | C | 53 | a0001c0001t0001g0018a0001c0001t0001g0029a0001c0001t0001g0037others(50): Show | 53 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.812-65T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 6/17 | chr18 | 6870525 | ||||||
| chr18:6870586
|
T | C | 6 | a0001c0003t0003g0002a0001c0003t0003g0076a0001c0003t0003g0104others(3): Show | 6 | HG02922.hp1 HG03139.hp2 HG03471.hp1 others(3): Show |
splice_region_variant&intron_variant | LOW | c.812-4T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 6/17 | chr18 | 6870586 | ||||||
| chr18:6870780
|
T | C | 2 | a0001c0001t0009g0005a0001c0001t0009g0245 | 2 | HG01891.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.954+48T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 7/17 | chr18 | 6870780 | ||||||
| chr18:6870836
|
A | G | 5 | a0001c0001t0007g0116a0001c0001t0007g0117a0001c0001t0007g0212others(2): Show | 5 | HG01891.hp1 HG02895.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.954+104A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 7/17 | chr18 | 6870836 | ||||||
| chr18:6870838
|
T | C | 5 | a0001c0001t0007g0116a0001c0001t0007g0117a0001c0001t0007g0212others(2): Show | 5 | HG01891.hp1 HG02895.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.954+106T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 7/17 | chr18 | 6870838 | ||||||
| chr18:6870839
|
GC | G | 5 | a0001c0001t0007g0116a0001c0001t0007g0117a0001c0001t0007g0212others(2): Show | 5 | HG01891.hp1 HG02895.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.954+111delC | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr18 | 6870839 | |||||
| chr18:6870853
|
T | C | 1 | a0001c0003t0003g0145 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.954+121T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 7/17 | chr18 | 6870853 | ||||||
| chr18:6870861
|
C | T | 1 | a0001c0001t0001g0151 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.954+129C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 7/17 | chr18 | 6870861 | ||||||
| chr18:6870863
|
C | T | 8 | a0001c0001t0001g0165a0001c0001t0001g0194a0001c0003t0003g0068others(5): Show | 8 | HG01081.hp2 HG02055.hp1 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.954+131C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 7/17 | chr18 | 6870863 | ||||||
| chr18:6870869
|
C | T | 7 | a0001c0001t0001g0165a0001c0003t0003g0068a0001c0003t0003g0156others(4): Show | 7 | HG01081.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.954+137C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 7/17 | chr18 | 6870869 | ||||||
| chr18:6870874
|
C | T | 8 | a0002c0002t0002g0131a0002c0002t0002g0172a0002c0002t0002g0244others(5): Show | 8 | HG00408.hp2 HG03834.hp1 NA18747.hp1 others(5): Show |
intron_variant | MODIFIER | c.954+142C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 7/17 | chr18 | 6870874 | ||||||
| chr18:6870886
|
T | C | 9 | a0001c0001t0001g0151a0001c0003t0003g0094a0001c0003t0003g0095others(6): Show | 9 | HG01081.hp1 HG01243.hp2 HG02155.hp2 others(6): Show |
intron_variant | MODIFIER | c.954+154T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 7/17 | chr18 | 6870886 | ||||||
| chr18:6870887
|
G | A | 1 | a0003c0004t0001g0220 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.954+155G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 7/17 | chr18 | 6870887 | ||||||
| chr18:6870890
|
T | C | 1 | a0002c0002t0002g0015 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.954+158T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 7/17 | chr18 | 6870890 | ||||||
| chr18:6870961
|
C | T | 6 | a0001c0003t0003g0002a0001c0003t0003g0076a0001c0003t0003g0104others(3): Show | 6 | HG02922.hp1 HG03139.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.954+229C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 7/17 | chr18 | 6870961 | ||||||
| chr18:6870974
|
G | T | 1 | a0003c0004t0001g0187 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.954+242G>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 7/17 | chr18 | 6870974 | ||||||
| chr18:6871052
|
G | A | 2 | a0001c0001t0001g0182a0003c0004t0001g0021 | 2 | HG02040.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.954+320G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 7/17 | chr18 | 6871052 | ||||||
| chr18:6871057
|
C | T | 1 | a0005c0006t0003g0031 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.954+325C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 7/17 | chr18 | 6871057 | ||||||
| chr18:6871058
|
T | C | 2 | a0001c0001t0001g0182a0003c0004t0001g0021 | 2 | HG02040.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.954+326T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 7/17 | chr18 | 6871058 | ||||||
| chr18:6871079
|
T | C | 7 | a0001c0001t0001g0001a0001c0001t0001g0054a0001c0001t0001g0070others(4): Show | 7 | HG00735.hp2 HG01256.hp2 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.954+347T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 7/17 | chr18 | 6871079 | ||||||
| chr18:6871087
|
G | A | 7 | a0001c0001t0001g0001a0001c0001t0001g0054a0001c0001t0001g0070others(4): Show | 7 | HG00735.hp2 HG01256.hp2 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.954+355G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 7/17 | chr18 | 6871087 | ||||||
| chr18:6871147
|
G | A | 51 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0026others(48): Show | 51 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.954+415G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 7/17 | chr18 | 6871147 | ||||||
| chr18:6871234
|
T | G | 1 | a0001c0001t0018g0111 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.954+502T>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 7/17 | chr18 | 6871234 | ||||||
| chr18:6871462
|
A | G | 1 | a0001c0019t0021g0073 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.954+730A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 7/17 | chr18 | 6871462 | ||||||
| chr18:6871549
|
C | CATT | 11 | a0001c0001t0001g0080a0001c0001t0001g0121a0001c0001t0001g0161others(8): Show | 11 | HG02145.hp2 HG02258.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.954+821_954+823dup others(3): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr18 | 6871549 | |||||
| chr18:6871775
|
G | A | 1 | a0001c0001t0016g0081 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.954+1043G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 7/17 | chr18 | 6871775 | ||||||
| chr18:6871807
|
G | A | 1 | a0001c0020t0023g0101 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.954+1075G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 7/17 | chr18 | 6871807 | ||||||
| chr18:6871910
|
G | A | 6 | a0001c0003t0003g0002a0001c0003t0003g0076a0001c0003t0003g0104others(3): Show | 6 | HG02922.hp1 HG03139.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.954+1178G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 7/17 | chr18 | 6871910 | ||||||
| chr18:6871969
|
T | C | 126 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(123): Show | 126 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.954+1237T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 7/17 | chr18 | 6871969 | ||||||
| chr18:6872169
|
G | T | 65 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0026others(62): Show | 65 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(62): Show |
intron_variant | MODIFIER | c.955-1240G>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 7/17 | chr18 | 6872169 | ||||||
| chr18:6872182
|
G | A | 1 | a0001c0015t0003g0167 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.955-1227G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 7/17 | chr18 | 6872182 | ||||||
| chr18:6872301
|
A | G | 124 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(121): Show | 124 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.955-1108A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 7/17 | chr18 | 6872301 | ||||||
| chr18:6872345
|
C | T | 6 | a0001c0003t0003g0002a0001c0003t0003g0076a0001c0003t0003g0104others(3): Show | 6 | HG02922.hp1 HG03139.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.955-1064C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 7/17 | chr18 | 6872345 | ||||||
| chr18:6872939
|
G | A | 1 | a0001c0003t0003g0154 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.955-470G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 7/17 | chr18 | 6872939 | ||||||
| chr18:6873205
|
TTTTGCTT others(4): Show |
T | 1 | a0001c0003t0003g0154 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.955-201_955-191del others(11): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr18 | 6873205 | |||||
| chr18:6873260
|
A | G | 1 | a0001c0019t0021g0073 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.955-149A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 7/17 | chr18 | 6873260 | ||||||
| chr18:6873308
|
C | T | 1 | a0001c0001t0001g0194 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.955-101C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 7/17 | chr18 | 6873308 | ||||||
| chr18:6873355
|
G | A | 65 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0026others(62): Show | 65 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(62): Show |
intron_variant | MODIFIER | c.955-54G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 7/17 | chr18 | 6873355 | ||||||
| chr18:6873610
|
C | T | 3 | a0001c0001t0007g0116a0001c0001t0007g0117a0001c0001t0007g0212 | 3 | HG02896.hp1 HG02897.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1120+36C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 8/17 | chr18 | 6873610 | ||||||
| chr18:6873647
|
CT | C | 7 | a0001c0001t0009g0005a0001c0001t0009g0245a0002c0002t0002g0046others(4): Show | 7 | HG01891.hp1 HG02630.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1121-26delT | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr18 | 6873647 | |||||
| chr18:6873658
|
T | C | 2 | a0001c0001t0001g0080a0003c0004t0001g0024 | 2 | HG01952.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.1121-26T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 8/17 | chr18 | 6873658 | ||||||
| chr18:6873934
|
A | G | 3 | a0008c0011t0005g0016a0008c0011t0005g0090a0008c0011t0005g0152 | 3 | HG02630.hp2 HG03471.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1212+159A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 9/17 | chr18 | 6873934 | ||||||
| chr18:6873948
|
C | T | 1 | a0001c0001t0001g0239 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1212+173C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 9/17 | chr18 | 6873948 | ||||||
| chr18:6873955
|
G | A | 191 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(188): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.1212+180G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 9/17 | chr18 | 6873955 | ||||||
| chr18:6874303
|
C | T | 3 | a0001c0001t0001g0124a0001c0001t0001g0149a0001c0001t0001g0150 | 3 | HG02145.hp1 HG03098.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1212+528C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 9/17 | chr18 | 6874303 | ||||||
| chr18:6874306
|
T | A | 8 | a0001c0018t0020g0007a0002c0017t0002g0086a0003c0013t0011g0062others(5): Show | 8 | HG02630.hp2 HG02922.hp1 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.1212+531T>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 9/17 | chr18 | 6874306 | ||||||
| chr18:6874630
|
T | C | 4 | a0003c0004t0001g0045a0003c0004t0001g0064a0003c0004t0001g0218others(1): Show | 4 | NA18947.hp1 NA18956.hp1 NA18968.hp2 others(1): Show |
intron_variant | MODIFIER | c.1212+855T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 9/17 | chr18 | 6874630 | ||||||
| chr18:6874760
|
A | G | 3 | a0001c0012t0001g0210a0001c0012t0014g0159a0010c0014t0001g0142 | 3 | HG01106.hp1 HG02559.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.1212+985A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 9/17 | chr18 | 6874760 | ||||||
| chr18:6874782
|
C | T | 6 | a0002c0005t0002g0043a0002c0005t0002g0061a0002c0005t0002g0108others(3): Show | 6 | NA18947.hp2 NA18953.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.1212+1007C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 9/17 | chr18 | 6874782 | ||||||
| chr18:6874783
|
G | A | 4 | a0002c0002t0004g0006a0002c0002t0004g0059a0002c0002t0004g0147others(1): Show | 4 | HG01884.hp1 HG02280.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.1212+1008G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 9/17 | chr18 | 6874783 | ||||||
| chr18:6874857
|
A | G | 115 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(112): Show | 115 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.1212+1082A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 9/17 | chr18 | 6874857 | ||||||
| chr18:6875324
|
C | A | 6 | a0001c0001t0007g0116a0001c0001t0007g0117a0001c0001t0007g0212others(3): Show | 6 | HG02896.hp1 HG02897.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1213-807C>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 9/17 | chr18 | 6875324 | ||||||
| chr18:6875343
|
T | G | 3 | a0001c0003t0003g0002a0001c0003t0003g0104a0001c0003t0003g0119 | 3 | HG03471.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1213-788T>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 9/17 | chr18 | 6875343 | ||||||
| chr18:6875420
|
A | T | 115 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(112): Show | 115 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.1213-711A>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 9/17 | chr18 | 6875420 | ||||||
| chr18:6875434
|
C | A | 6 | a0001c0003t0003g0068a0001c0003t0003g0087a0001c0003t0003g0122others(3): Show | 6 | HG02109.hp2 HG02723.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1213-697C>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 9/17 | chr18 | 6875434 | ||||||
| chr18:6875507
|
G | A | 5 | a0001c0001t0009g0005a0001c0001t0009g0245a0001c0010t0003g0089others(2): Show | 5 | HG01081.hp2 HG01891.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1213-624G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 9/17 | chr18 | 6875507 | ||||||
| chr18:6875671
|
C | T | 8 | a0001c0001t0009g0005a0001c0001t0009g0245a0001c0010t0003g0089others(5): Show | 8 | HG01081.hp2 HG01891.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1213-460C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 9/17 | chr18 | 6875671 | ||||||
| chr18:6875694
|
G | A | 98 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(95): Show | 98 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.1213-437G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 9/17 | chr18 | 6875694 | ||||||
| chr18:6875870
|
C | T | 1 | a0001c0001t0009g0005 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1213-261C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 9/17 | chr18 | 6875870 | ||||||
| chr18:6875887
|
C | T | 1 | a0002c0002t0002g0047 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1213-244C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 9/17 | chr18 | 6875887 | ||||||
| chr18:6875888
|
G | A | 3 | a0003c0013t0011g0062a0003c0013t0011g0063a0003c0023t0001g0120 | 3 | HG03041.hp1 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1213-243G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 9/17 | chr18 | 6875888 | ||||||
| chr18:6875910
|
G | A | 1 | a0001c0001t0001g0139 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1213-221G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 9/17 | chr18 | 6875910 | ||||||
| chr18:6875922
|
A | G | 2 | a0001c0001t0001g0001a0001c0001t0001g0054 | 2 | HG01496.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.1213-209A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 9/17 | chr18 | 6875922 | ||||||
| chr18:6876686
|
T | C | 1 | a0001c0015t0003g0167 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1290+478T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 10/17 | chr18 | 6876686 | ||||||
| chr18:6877083
|
CAAA | C | 3 | a0001c0018t0020g0007a0001c0019t0021g0073a0002c0017t0002g0086 | 3 | HG02922.hp1 HG03139.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1290+878_1290+880d others(5): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr18 | 6877083 | |||||
| chr18:6877193
|
C | T | 98 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(95): Show | 98 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.1290+985C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 10/17 | chr18 | 6877193 | ||||||
| chr18:6877265
|
G | A | 3 | a0008c0011t0005g0016a0008c0011t0005g0090a0008c0011t0005g0152 | 3 | HG02630.hp2 HG03471.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1290+1057G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 10/17 | chr18 | 6877265 | ||||||
| chr18:6877296
|
C | T | 1 | a0002c0002t0002g0244 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1290+1088C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 10/17 | chr18 | 6877296 | ||||||
| chr18:6877376
|
A | C | 3 | a0008c0011t0005g0016a0008c0011t0005g0090a0008c0011t0005g0152 | 3 | HG02630.hp2 HG03471.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1290+1168A>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 10/17 | chr18 | 6877376 | ||||||
| chr18:6877379
|
C | T | 3 | a0008c0011t0005g0016a0008c0011t0005g0090a0008c0011t0005g0152 | 3 | HG02630.hp2 HG03471.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1290+1171C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 10/17 | chr18 | 6877379 | ||||||
| chr18:6877452
|
C | G | 1 | a0001c0019t0021g0073 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1290+1244C>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 10/17 | chr18 | 6877452 | ||||||
| chr18:6877553
|
C | T | 3 | a0001c0001t0001g0121a0001c0001t0001g0161a0001c0001t0001g0168 | 3 | HG02145.hp2 HG02615.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1290+1345C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 10/17 | chr18 | 6877553 | ||||||
| chr18:6877560
|
C | T | 7 | a0001c0001t0001g0080a0002c0005t0002g0043a0002c0005t0002g0061others(4): Show | 7 | HG02258.hp2 NA18947.hp2 NA18953.hp1 others(4): Show |
intron_variant | MODIFIER | c.1290+1352C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 10/17 | chr18 | 6877560 | ||||||
| chr18:6877561
|
G | A | 98 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(95): Show | 98 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.1290+1353G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 10/17 | chr18 | 6877561 | ||||||
| chr18:6877596
|
G | A | 1 | a0002c0002t0002g0197 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1290+1388G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 10/17 | chr18 | 6877596 | ||||||
| chr18:6877672
|
GA | G | 3 | a0001c0001t0007g0116a0001c0001t0007g0117a0001c0001t0007g0212 | 3 | HG02896.hp1 HG02897.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1290+1467delA | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr18 | 6877672 | |||||
| chr18:6877711
|
G | T | 190 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(187): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.1290+1503G>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 10/17 | chr18 | 6877711 | ||||||
| chr18:6877999
|
C | T | 1 | a0001c0019t0021g0073 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1290+1791C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 10/17 | chr18 | 6877999 | ||||||
| chr18:6878066
|
A | G | 6 | a0001c0001t0007g0116a0001c0001t0007g0117a0001c0001t0007g0212others(3): Show | 6 | HG02896.hp1 HG02897.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1290+1858A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 10/17 | chr18 | 6878066 | ||||||
| chr18:6878074
|
G | A | 1 | a0001c0003t0003g0068 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1290+1866G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 10/17 | chr18 | 6878074 | ||||||
| chr18:6878180
|
T | C | 3 | a0005c0006t0003g0127a0005c0006t0003g0177a0005c0006t0003g0180 | 3 | NA18950.hp1 NA18977.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.1290+1972T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 10/17 | chr18 | 6878180 | ||||||
| chr18:6878262
|
G | A | 1 | a0001c0001t0001g0188 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1290+2054G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 10/17 | chr18 | 6878262 | ||||||
| chr18:6878359
|
G | C | 5 | a0003c0004t0001g0010a0003c0004t0001g0025a0003c0004t0001g0051others(2): Show | 5 | HG01993.hp2 HG02273.hp1 HG02300.hp1 others(2): Show |
intron_variant | MODIFIER | c.1290+2151G>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 10/17 | chr18 | 6878359 | ||||||
| chr18:6878435
|
T | C | 1 | a0001c0020t0023g0101 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1290+2227T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 10/17 | chr18 | 6878435 | ||||||
| chr18:6878836
|
C | T | 6 | a0001c0001t0007g0116a0001c0001t0007g0117a0001c0001t0007g0212others(3): Show | 6 | HG02896.hp1 HG02897.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1290+2628C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 10/17 | chr18 | 6878836 | ||||||
| chr18:6878891
|
A | T | 6 | a0001c0001t0007g0116a0001c0001t0007g0117a0001c0001t0007g0212others(3): Show | 6 | HG02896.hp1 HG02897.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1290+2683A>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 10/17 | chr18 | 6878891 | ||||||
| chr18:6878966
|
C | T | 62 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(59): Show | 62 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.1290+2758C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 10/17 | chr18 | 6878966 | ||||||
| chr18:6879037
|
T | A | 190 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(187): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.1290+2829T>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 10/17 | chr18 | 6879037 | ||||||
| chr18:6879071
|
G | T | 2 | a0001c0001t0009g0005a0001c0001t0009g0245 | 2 | HG01891.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1290+2863G>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 10/17 | chr18 | 6879071 | ||||||
| chr18:6879200
|
A | G | 13 | a0001c0001t0009g0005a0001c0001t0009g0245a0001c0010t0003g0089others(10): Show | 13 | HG01081.hp2 HG01891.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.1291-2937A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 10/17 | chr18 | 6879200 | ||||||
| chr18:6879354
|
C | T | 18 | a0001c0003t0003g0013a0001c0003t0003g0027a0001c0003t0003g0055others(15): Show | 18 | HG00280.hp2 HG00741.hp2 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.1291-2783C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 10/17 | chr18 | 6879354 | ||||||
| chr18:6879401
|
T | A | 2 | a0001c0003t0003g0105a0001c0003t0003g0123 | 2 | HG01175.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1291-2736T>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 10/17 | chr18 | 6879401 | ||||||
| chr18:6879521
|
C | T | 16 | a0001c0001t0007g0116a0001c0001t0007g0117a0001c0001t0007g0212others(13): Show | 16 | HG01081.hp2 HG01891.hp1 HG02630.hp2 others(13): Show |
intron_variant | MODIFIER | c.1291-2616C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 10/17 | chr18 | 6879521 | ||||||
| chr18:6879626
|
G | A | 6 | a0001c0001t0009g0005a0001c0001t0009g0245a0001c0010t0003g0089others(3): Show | 6 | HG01081.hp2 HG01891.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1291-2511G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 10/17 | chr18 | 6879626 | ||||||
| chr18:6879704
|
A | T | 1 | a0001c0019t0021g0073 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1291-2433A>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 10/17 | chr18 | 6879704 | ||||||
| chr18:6879870
|
T | C | 1 | a0001c0001t0001g0082 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1291-2267T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 10/17 | chr18 | 6879870 | ||||||
| chr18:6879915
|
G | A | 2 | a0001c0018t0020g0007a0002c0017t0002g0086 | 2 | HG02922.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1291-2222G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 10/17 | chr18 | 6879915 | ||||||
| chr18:6880092
|
T | C | 1 | a0001c0001t0001g0141 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1291-2045T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 10/17 | chr18 | 6880092 | ||||||
| chr18:6880154
|
T | C | 1 | a0001c0019t0021g0073 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1291-1983T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 10/17 | chr18 | 6880154 | ||||||
| chr18:6880180
|
C | T | 76 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0019others(73): Show | 76 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(73): Show |
intron_variant | MODIFIER | c.1291-1957C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 10/17 | chr18 | 6880180 | ||||||
| chr18:6880414
|
C | T | 105 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(102): Show | 105 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.1291-1723C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 10/17 | chr18 | 6880414 | ||||||
| chr18:6880421
|
A | G | 1 | a0002c0002t0002g0096 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1291-1716A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 10/17 | chr18 | 6880421 | ||||||
| chr18:6880429
|
G | A | 1 | a0001c0019t0021g0073 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1291-1708G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 10/17 | chr18 | 6880429 | ||||||
| chr18:6880448
|
G | A | 1 | a0001c0019t0021g0073 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1291-1689G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 10/17 | chr18 | 6880448 | ||||||
| chr18:6880770
|
G | A | 6 | a0001c0001t0007g0116a0001c0001t0007g0117a0001c0001t0007g0212others(3): Show | 6 | HG02896.hp1 HG02897.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1291-1367G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 10/17 | chr18 | 6880770 | ||||||
| chr18:6880862
|
G | A | 2 | a0001c0019t0021g0073a0002c0002t0012g0088 | 2 | HG03130.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1291-1275G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 10/17 | chr18 | 6880862 | ||||||
| chr18:6881037
|
G | A | 247 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(244): Show | 247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.1291-1100G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 10/17 | chr18 | 6881037 | ||||||
| chr18:6881091
|
G | A | 75 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0019others(72): Show | 75 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(72): Show |
intron_variant | MODIFIER | c.1291-1046G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 10/17 | chr18 | 6881091 | ||||||
| chr18:6881122
|
A | G | 3 | a0008c0011t0005g0016a0008c0011t0005g0090a0008c0011t0005g0152 | 3 | HG02630.hp2 HG03471.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1291-1015A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 10/17 | chr18 | 6881122 | ||||||
| chr18:6881183
|
A | G | 5 | a0005c0006t0003g0031a0005c0006t0003g0127a0005c0006t0003g0177others(2): Show | 5 | NA18950.hp1 NA18977.hp2 NA18995.hp1 others(2): Show |
intron_variant | MODIFIER | c.1291-954A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 10/17 | chr18 | 6881183 | ||||||
| chr18:6881268
|
T | TA | 4 | a0001c0001t0001g0124a0001c0001t0001g0149a0001c0001t0001g0150others(1): Show | 4 | HG02145.hp1 HG03098.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1291-866dupA | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr18 | 6881268 | |||||
| chr18:6881447
|
G | A | 1 | a0001c0001t0001g0012 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1291-690G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 10/17 | chr18 | 6881447 | ||||||
| chr18:6881482
|
T | G | 1 | a0003c0004t0001g0247 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1291-655T>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 10/17 | chr18 | 6881482 | ||||||
| chr18:6881615
|
G | A | 3 | a0008c0011t0005g0016a0008c0011t0005g0090a0008c0011t0005g0152 | 3 | HG02630.hp2 HG03471.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1291-522G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 10/17 | chr18 | 6881615 | ||||||
| chr18:6881678
|
T | C | 72 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0019others(69): Show | 72 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(69): Show |
intron_variant | MODIFIER | c.1291-459T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 10/17 | chr18 | 6881678 | ||||||
| chr18:6881984
|
G | A | 1 | a0001c0019t0021g0073 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1291-153G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 10/17 | chr18 | 6881984 | ||||||
| chr18:6882044
|
A | C | 1 | a0002c0002t0002g0207 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1291-93A>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 10/17 | chr18 | 6882044 | ||||||
| chr18:6882101
|
G | A | 1 | a0001c0019t0021g0073 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1291-36G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 10/17 | chr18 | 6882101 | ||||||
| chr18:6882110
|
A | C | 1 | a0001c0001t0001g0100 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1291-27A>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 10/17 | chr18 | 6882110 | ||||||
| chr18:6882313
|
G | A | 5 | a0006c0009t0003g0162a0006c0009t0009g0153a0007c0008t0002g0069others(2): Show | 5 | HG01952.hp2 HG02922.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1453+14G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 11/17 | chr18 | 6882313 | ||||||
| chr18:6882325
|
T | C | 1 | a0001c0019t0021g0073 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1453+26T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 11/17 | chr18 | 6882325 | ||||||
| chr18:6882376
|
C | T | 1 | a0001c0019t0021g0073 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1453+77C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 11/17 | chr18 | 6882376 | ||||||
| chr18:6882706
|
C | T | 3 | a0005c0006t0003g0127a0005c0006t0003g0177a0005c0006t0003g0180 | 3 | NA18950.hp1 NA18977.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.1453+407C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 11/17 | chr18 | 6882706 | ||||||
| chr18:6882792
|
G | A | 1 | a0001c0019t0021g0073 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1453+493G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 11/17 | chr18 | 6882792 | ||||||
| chr18:6882943
|
A | G | 3 | a0003c0013t0011g0062a0003c0013t0011g0063a0003c0023t0001g0120 | 3 | HG03041.hp1 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1453+644A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 11/17 | chr18 | 6882943 | ||||||
| chr18:6883116
|
A | G | 6 | a0001c0001t0007g0116a0001c0001t0007g0117a0001c0001t0007g0212others(3): Show | 6 | HG02896.hp1 HG02897.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1453+817A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 11/17 | chr18 | 6883116 | ||||||
| chr18:6883239
|
A | AT | 7 | a0002c0002t0002g0046a0002c0002t0002g0244a0002c0002t0004g0006others(4): Show | 7 | HG01884.hp1 HG02280.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1453+957dupT | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr18 | 6883239 | |||||
| chr18:6883239
|
AT | A | 6 | a0001c0001t0001g0141a0002c0002t0002g0078a0002c0002t0002g0131others(3): Show | 6 | HG02300.hp1 HG02630.hp2 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.1453+957delT | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr18 | 6883239 | |||||
| chr18:6883239
|
ATT | A | 185 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(182): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.1453+956_1453+957d others(4): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr18 | 6883239 | |||||
| chr18:6883275
|
G | A | 1 | a0001c0001t0016g0081 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1453+976G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 11/17 | chr18 | 6883275 | ||||||
| chr18:6883314
|
C | A | 190 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(187): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.1453+1015C>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 11/17 | chr18 | 6883314 | ||||||
| chr18:6883330
|
C | T | 1 | a0003c0004t0001g0048 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1453+1031C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 11/17 | chr18 | 6883330 | ||||||
| chr18:6883388
|
G | A | 6 | a0001c0001t0007g0116a0001c0001t0007g0117a0001c0001t0007g0212others(3): Show | 6 | HG02896.hp1 HG02897.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1453+1089G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 11/17 | chr18 | 6883388 | ||||||
| chr18:6883436
|
G | A | 1 | a0002c0002t0002g0135 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1453+1137G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 11/17 | chr18 | 6883436 | ||||||
| chr18:6883439
|
A | G | 6 | a0001c0001t0007g0116a0001c0001t0007g0117a0001c0001t0007g0212others(3): Show | 6 | HG02896.hp1 HG02897.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1453+1140A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 11/17 | chr18 | 6883439 | ||||||
| chr18:6883551
|
A | C | 1 | a0001c0001t0001g0128 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1453+1252A>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 11/17 | chr18 | 6883551 | ||||||
| chr18:6883568
|
G | A | 1 | a0006c0009t0005g0144 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1453+1269G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 11/17 | chr18 | 6883568 | ||||||
| chr18:6883630
|
A | G | 192 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(189): Show | 192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.1453+1331A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 11/17 | chr18 | 6883630 | ||||||
| chr18:6883672
|
A | G | 1 | a0001c0001t0001g0181 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1453+1373A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 11/17 | chr18 | 6883672 | ||||||
| chr18:6884025
|
A | T | 3 | a0003c0013t0011g0062a0003c0013t0011g0063a0003c0023t0001g0120 | 3 | HG03041.hp1 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1453+1726A>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 11/17 | chr18 | 6884025 | ||||||
| chr18:6884051
|
A | G | 75 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0019others(72): Show | 75 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(72): Show |
intron_variant | MODIFIER | c.1453+1752A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 11/17 | chr18 | 6884051 | ||||||
| chr18:6884102
|
T | C | 190 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(187): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.1453+1803T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 11/17 | chr18 | 6884102 | ||||||
| chr18:6884113
|
G | A | 3 | a0008c0011t0005g0016a0008c0011t0005g0090a0008c0011t0005g0152 | 3 | HG02630.hp2 HG03471.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1453+1814G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 11/17 | chr18 | 6884113 | ||||||
| chr18:6884201
|
C | T | 3 | a0003c0013t0011g0062a0003c0013t0011g0063a0003c0023t0001g0120 | 3 | HG03041.hp1 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1453+1902C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 11/17 | chr18 | 6884201 | ||||||
| chr18:6884302
|
C | T | 1 | a0001c0001t0001g0188 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1453+2003C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 11/17 | chr18 | 6884302 | ||||||
| chr18:6884323
|
G | A | 3 | a0003c0013t0011g0062a0003c0013t0011g0063a0003c0023t0001g0120 | 3 | HG03041.hp1 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1453+2024G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 11/17 | chr18 | 6884323 | ||||||
| chr18:6884328
|
C | G | 1 | a0001c0019t0021g0073 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1453+2029C>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 11/17 | chr18 | 6884328 | ||||||
| chr18:6884458
|
C | T | 6 | a0001c0001t0007g0116a0001c0001t0007g0117a0001c0001t0007g0212others(3): Show | 6 | HG02896.hp1 HG02897.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1453+2159C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 11/17 | chr18 | 6884458 | ||||||
| chr18:6884489
|
A | G | 190 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(187): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.1453+2190A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 11/17 | chr18 | 6884489 | ||||||
| chr18:6884496
|
G | A | 1 | a0001c0019t0021g0073 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1453+2197G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 11/17 | chr18 | 6884496 | ||||||
| chr18:6884530
|
G | A | 1 | a0001c0019t0021g0073 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1453+2231G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 11/17 | chr18 | 6884530 | ||||||
| chr18:6884538
|
A | G | 4 | a0001c0003t0003g0085a0001c0003t0003g0091a0001c0003t0003g0105others(1): Show | 4 | HG01175.hp2 HG02976.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1453+2239A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 11/17 | chr18 | 6884538 | ||||||
| chr18:6884663
|
G | A | 1 | a0002c0002t0002g0066 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1453+2364G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 11/17 | chr18 | 6884663 | ||||||
| chr18:6885243
|
T | G | 180 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(177): Show | 180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.1454-1914T>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 11/17 | chr18 | 6885243 | ||||||
| chr18:6885296
|
G | A | 2 | a0001c0018t0020g0007a0002c0017t0002g0086 | 2 | HG02922.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1454-1861G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 11/17 | chr18 | 6885296 | ||||||
| chr18:6885377
|
T | C | 189 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(186): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.1454-1780T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 11/17 | chr18 | 6885377 | ||||||
| chr18:6885523
|
A | G | 75 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0019others(72): Show | 75 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(72): Show |
intron_variant | MODIFIER | c.1454-1634A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 11/17 | chr18 | 6885523 | ||||||
| chr18:6885625
|
C | T | 2 | a0001c0018t0020g0007a0002c0017t0002g0086 | 2 | HG02922.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1454-1532C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 11/17 | chr18 | 6885625 | ||||||
| chr18:6885802
|
G | GT | 73 | a0001c0001t0001g0012a0001c0001t0001g0026a0001c0001t0001g0052others(70): Show | 73 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.1454-1340dupT | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr18 | 6885802 | |||||
| chr18:6885802
|
G | GTT | 61 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0071others(58): Show | 61 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.1454-1341_1454-134 others(6): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr18 | 6885802 | |||||
| chr18:6885962
|
C | G | 190 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(187): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.1454-1195C>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 11/17 | chr18 | 6885962 | ||||||
| chr18:6885985
|
G | A | 3 | a0001c0010t0003g0089a0001c0010t0003g0098a0001c0010t0003g0114 | 3 | HG01081.hp2 HG02970.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1454-1172G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 11/17 | chr18 | 6885985 | ||||||
| chr18:6886233
|
C | T | 3 | a0001c0001t0001g0044a0003c0004t0001g0241a0003c0004t0001g0248 | 3 | NA18950.hp2 NA18966.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.1454-924C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 11/17 | chr18 | 6886233 | ||||||
| chr18:6886349
|
T | G | 6 | a0003c0013t0011g0062a0003c0013t0011g0063a0003c0023t0001g0120others(3): Show | 6 | HG02630.hp2 HG03041.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.1454-808T>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 11/17 | chr18 | 6886349 | ||||||
| chr18:6886423
|
C | T | 1 | a0003c0004t0001g0048 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1454-734C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 11/17 | chr18 | 6886423 | ||||||
| chr18:6886453
|
G | A | 1 | a0001c0018t0020g0007 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1454-704G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 11/17 | chr18 | 6886453 | ||||||
| chr18:6886548
|
T | C | 193 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(190): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.1454-609T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 11/17 | chr18 | 6886548 | ||||||
| chr18:6886606
|
G | A | 193 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(190): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.1454-551G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 11/17 | chr18 | 6886606 | ||||||
| chr18:6886615
|
C | A | 3 | a0006c0009t0009g0153a0007c0008t0002g0069a0007c0008t0002g0146 | 3 | HG02922.hp2 HG03209.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1454-542C>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 11/17 | chr18 | 6886615 | ||||||
| chr18:6886680
|
G | A | 2 | a0001c0001t0009g0005a0001c0001t0009g0245 | 2 | HG01891.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1454-477G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 11/17 | chr18 | 6886680 | ||||||
| chr18:6887128
|
A | G | 1 | a0002c0002t0012g0088 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1454-29A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 11/17 | chr18 | 6887128 | ||||||
| chr18:6887430
|
G | GT | 43 | a0001c0001t0001g0001a0001c0001t0001g0165a0001c0001t0001g0202others(40): Show | 43 | HG00280.hp2 HG00741.hp2 HG01081.hp1 others(40): Show |
intron_variant | MODIFIER | c.1536+207dupT | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr18 | 6887430 | |||||
| chr18:6887430
|
G | GTT | 145 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0018others(142): Show | 145 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(142): Show |
intron_variant | MODIFIER | c.1536+206_1536+207d others(4): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr18 | 6887430 | |||||
| chr18:6887430
|
G | GTTT | 6 | a0001c0001t0001g0004a0001c0001t0001g0151a0001c0001t0009g0005others(3): Show | 6 | HG01243.hp2 HG01891.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1536+205_1536+207d others(5): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr18 | 6887430 | |||||
| chr18:6887494
|
G | A | 3 | a0008c0011t0005g0016a0008c0011t0005g0090a0008c0011t0005g0152 | 3 | HG02630.hp2 HG03471.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1536+255G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 12/17 | chr18 | 6887494 | ||||||
| chr18:6887523
|
C | G | 21 | a0001c0003t0003g0013a0001c0003t0003g0027a0001c0003t0003g0055others(18): Show | 21 | HG00280.hp2 HG00741.hp2 HG01081.hp1 others(18): Show |
intron_variant | MODIFIER | c.1536+284C>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 12/17 | chr18 | 6887523 | ||||||
| chr18:6887635
|
C | T | 35 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0034others(32): Show | 35 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(32): Show |
intron_variant | MODIFIER | c.1536+396C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 12/17 | chr18 | 6887635 | ||||||
| chr18:6887718
|
C | T | 9 | a0001c0001t0001g0230a0002c0002t0002g0157a0002c0002t0002g0163others(6): Show | 9 | HG01261.hp1 HG01891.hp2 HG01952.hp2 others(6): Show |
intron_variant | MODIFIER | c.1536+479C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 12/17 | chr18 | 6887718 | ||||||
| chr18:6887722
|
C | T | 1 | a0001c0001t0001g0082 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1536+483C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 12/17 | chr18 | 6887722 | ||||||
| chr18:6888113
|
G | A | 2 | a0001c0001t0009g0005a0001c0001t0009g0245 | 2 | HG01891.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1536+874G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 12/17 | chr18 | 6888113 | ||||||
| chr18:6888148
|
T | C | 2 | a0001c0001t0009g0005a0001c0001t0009g0245 | 2 | HG01891.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1536+909T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 12/17 | chr18 | 6888148 | ||||||
| chr18:6888311
|
G | A | 1 | a0001c0001t0001g0080 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1536+1072G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 12/17 | chr18 | 6888311 | ||||||
| chr18:6888349
|
G | A | 2 | a0001c0001t0009g0005a0001c0001t0009g0245 | 2 | HG01891.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1536+1110G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 12/17 | chr18 | 6888349 | ||||||
| chr18:6888368
|
AT | A | 144 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(141): Show | 144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
intron_variant | MODIFIER | c.1536+1133delT | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr18 | 6888368 | |||||
| chr18:6888386
|
A | C | 153 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(150): Show | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.1536+1147A>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 12/17 | chr18 | 6888386 | ||||||
| chr18:6888514
|
A | C | 153 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(150): Show | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.1536+1275A>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 12/17 | chr18 | 6888514 | ||||||
| chr18:6888629
|
G | C | 153 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(150): Show | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.1537-1259G>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 12/17 | chr18 | 6888629 | ||||||
| chr18:6888749
|
A | T | 1 | a0001c0012t0014g0159 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1537-1139A>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 12/17 | chr18 | 6888749 | ||||||
| chr18:6888802
|
G | GTC | 3 | a0001c0010t0003g0089a0001c0010t0003g0098a0001c0010t0003g0114 | 3 | HG01081.hp2 HG02970.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1537-1070_1537-106 others(6): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr18 | 6888802 | |||||
| chr18:6888955
|
C | G | 3 | a0001c0001t0001g0124a0001c0001t0001g0149a0001c0001t0001g0150 | 3 | HG02145.hp1 HG03098.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1537-933C>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 12/17 | chr18 | 6888955 | ||||||
| chr18:6888977
|
G | A | 6 | a0001c0001t0001g0097a0001c0001t0001g0107a0001c0001t0001g0221others(3): Show | 6 | HG01106.hp1 HG01175.hp1 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.1537-911G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 12/17 | chr18 | 6888977 | ||||||
| chr18:6889033
|
A | T | 1 | a0002c0005t0002g0057 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1537-855A>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 12/17 | chr18 | 6889033 | ||||||
| chr18:6889075
|
A | G | 70 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0026others(67): Show | 70 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.1537-813A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 12/17 | chr18 | 6889075 | ||||||
| chr18:6889327
|
T | G | 3 | a0001c0001t0001g0034a0001c0001t0001g0038a0001c0001t0001g0042 | 3 | NA18941.hp1 NA18983.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.1537-561T>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 12/17 | chr18 | 6889327 | ||||||
| chr18:6889355
|
G | C | 1 | a0002c0005t0002g0041 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1537-533G>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 12/17 | chr18 | 6889355 | ||||||
| chr18:6889419
|
C | T | 60 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0026others(57): Show | 60 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(57): Show |
intron_variant | MODIFIER | c.1537-469C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 12/17 | chr18 | 6889419 | ||||||
| chr18:6889550
|
T | C | 1 | a0002c0002t0002g0217 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1537-338T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 12/17 | chr18 | 6889550 | ||||||
| chr18:6889595
|
T | C | 153 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(150): Show | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.1537-293T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 12/17 | chr18 | 6889595 | ||||||
| chr18:6889687
|
C | T | 153 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(150): Show | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.1537-201C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 12/17 | chr18 | 6889687 | ||||||
| chr18:6889692
|
A | G | 153 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(150): Show | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.1537-196A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 12/17 | chr18 | 6889692 | ||||||
| chr18:6889762
|
C | T | 1 | a0002c0002t0002g0148 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1537-126C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 12/17 | chr18 | 6889762 | ||||||
| chr18:6890125
|
A | G | 1 | a0001c0019t0021g0073 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1734+40A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 13/17 | chr18 | 6890125 | ||||||
| chr18:6890135
|
G | A | 1 | a0005c0006t0003g0127 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1734+50G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 13/17 | chr18 | 6890135 | ||||||
| chr18:6890412
|
G | A | 2 | a0001c0001t0001g0004a0001c0001t0001g0151 | 2 | HG01243.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1735-18G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 13/17 | chr18 | 6890412 | ||||||
| chr18:6890579
|
G | T | 3 | a0005c0006t0003g0127a0005c0006t0003g0177a0005c0006t0003g0180 | 3 | NA18950.hp1 NA18977.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.1848+36G>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 14/17 | chr18 | 6890579 | ||||||
| chr18:6890592
|
C | T | 153 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(150): Show | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.1848+49C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 14/17 | chr18 | 6890592 | ||||||
| chr18:6890710
|
G | A | 153 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(150): Show | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.1848+167G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 14/17 | chr18 | 6890710 | ||||||
| chr18:6891012
|
G | A | 2 | a0002c0005t0002g0017a0002c0005t0002g0057 | 2 | HG03239.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.1848+469G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 14/17 | chr18 | 6891012 | ||||||
| chr18:6891316
|
AT | A | 10 | a0001c0003t0003g0068a0001c0003t0003g0087a0001c0003t0003g0094others(7): Show | 10 | HG02109.hp2 HG02723.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.1848+786delT | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr18 | 6891316 | |||||
| chr18:6891761
|
A | T | 1 | a0001c0003t0003g0068 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1848+1218A>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 14/17 | chr18 | 6891761 | ||||||
| chr18:6891771
|
T | C | 37 | a0001c0003t0003g0002a0001c0003t0003g0013a0001c0003t0003g0027others(34): Show | 37 | HG00280.hp2 HG00741.hp2 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.1848+1228T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 14/17 | chr18 | 6891771 | ||||||
| chr18:6891891
|
T | C | 2 | a0001c0001t0001g0003a0001c0001t0001g0106 | 2 | HG02647.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1848+1348T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 14/17 | chr18 | 6891891 | ||||||
| chr18:6891899
|
G | A | 2 | a0001c0001t0001g0129a0001c0001t0001g0204 | 2 | NA18956.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.1848+1356G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 14/17 | chr18 | 6891899 | ||||||
| chr18:6891932
|
G | C | 25 | a0001c0003t0003g0002a0001c0003t0003g0013a0001c0003t0003g0027others(22): Show | 25 | HG00280.hp2 HG00741.hp2 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.1848+1389G>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 14/17 | chr18 | 6891932 | ||||||
| chr18:6891973
|
G | A | 63 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(60): Show | 63 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.1848+1430G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 14/17 | chr18 | 6891973 | ||||||
| chr18:6892032
|
TCTGA | T | 3 | a0003c0013t0011g0062a0003c0013t0011g0063a0003c0023t0001g0120 | 3 | HG03041.hp1 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1848+1492_1848+149 others(8): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr18 | 6892032 | |||||
| chr18:6892062
|
A | T | 3 | a0002c0002t0004g0006a0002c0002t0004g0147a0004c0007t0004g0115 | 3 | HG01884.hp1 HG02280.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1848+1519A>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 14/17 | chr18 | 6892062 | ||||||
| chr18:6892078
|
A | G | 1 | a0003c0004t0001g0112 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1848+1535A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 14/17 | chr18 | 6892078 | ||||||
| chr18:6892122
|
G | GA | 10 | a0001c0001t0001g0184a0001c0010t0003g0089a0001c0010t0003g0098others(7): Show | 10 | HG01081.hp2 HG02135.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1848+1585dupA | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr18 | 6892122 | |||||
| chr18:6892159
|
T | TTTGA | 3 | a0003c0013t0011g0062a0003c0013t0011g0063a0003c0023t0001g0120 | 3 | HG03041.hp1 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1848+1617_1848+162 others(8): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr18 | 6892159 | |||||
| chr18:6892200
|
A | G | 2 | a0001c0003t0003g0094a0001c0003t0003g0095 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1848+1657A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 14/17 | chr18 | 6892200 | ||||||
| chr18:6892602
|
G | A | 63 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(60): Show | 63 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.1848+2059G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 14/17 | chr18 | 6892602 | ||||||
| chr18:6892817
|
C | T | 1 | a0001c0001t0001g0204 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1849-2018C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 14/17 | chr18 | 6892817 | ||||||
| chr18:6892895
|
T | A | 3 | a0001c0001t0007g0116a0001c0001t0007g0117a0001c0001t0007g0212 | 3 | HG02896.hp1 HG02897.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1849-1940T>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 14/17 | chr18 | 6892895 | ||||||
| chr18:6892932
|
C | T | 2 | a0005c0006t0003g0031a0005c0006t0003g0226 | 2 | NA18995.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.1849-1903C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 14/17 | chr18 | 6892932 | ||||||
| chr18:6892982
|
T | G | 1 | a0002c0002t0002g0148 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1849-1853T>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 14/17 | chr18 | 6892982 | ||||||
| chr18:6893150
|
T | C | 1 | a0001c0003t0003g0122 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1849-1685T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 14/17 | chr18 | 6893150 | ||||||
| chr18:6893775
|
G | A | 2 | a0001c0001t0009g0005a0001c0001t0009g0245 | 2 | HG01891.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1849-1060G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 14/17 | chr18 | 6893775 | ||||||
| chr18:6893859
|
G | T | 1 | a0001c0012t0014g0159 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1849-976G>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 14/17 | chr18 | 6893859 | ||||||
| chr18:6893867
|
G | GT | 163 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(160): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
intron_variant | MODIFIER | c.1849-951dupT | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr18 | 6893867 | |||||
| chr18:6893867
|
G | GTT | 27 | a0001c0001t0001g0026a0001c0001t0001g0129a0001c0001t0001g0141others(24): Show | 27 | HG00408.hp2 HG00558.hp2 HG01175.hp1 others(24): Show |
intron_variant | MODIFIER | c.1849-952_1849-951d others(4): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr18 | 6893867 | |||||
| chr18:6893937
|
G | A | 2 | a0003c0004t0001g0218a0003c0021t0001g0053 | 2 | NA18968.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.1849-898G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 14/17 | chr18 | 6893937 | ||||||
| chr18:6894023
|
C | T | 1 | a0003c0022t0003g0132 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1849-812C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 14/17 | chr18 | 6894023 | ||||||
| chr18:6894071
|
G | A | 1 | a0001c0019t0021g0073 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1849-764G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 14/17 | chr18 | 6894071 | ||||||
| chr18:6894096
|
C | T | 1 | a0001c0019t0021g0073 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1849-739C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 14/17 | chr18 | 6894096 | ||||||
| chr18:6894122
|
C | T | 6 | a0003c0013t0011g0062a0003c0013t0011g0063a0003c0023t0001g0120others(3): Show | 6 | HG02630.hp2 HG03041.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.1849-713C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 14/17 | chr18 | 6894122 | ||||||
| chr18:6894476
|
T | C | 4 | a0003c0004t0001g0045a0003c0004t0001g0064a0003c0004t0001g0218others(1): Show | 4 | NA18947.hp1 NA18956.hp1 NA18968.hp2 others(1): Show |
intron_variant | MODIFIER | c.1849-359T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 14/17 | chr18 | 6894476 | ||||||
| chr18:6894688
|
G | A | 1 | a0001c0019t0021g0073 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1849-147G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 14/17 | chr18 | 6894688 | ||||||
| chr18:6894693
|
G | A | 3 | a0008c0011t0005g0016a0008c0011t0005g0090a0008c0011t0005g0152 | 3 | HG02630.hp2 HG03471.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1849-142G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 14/17 | chr18 | 6894693 | ||||||
| chr18:6894729
|
A | G | 1 | a0002c0002t0002g0065 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1849-106A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 14/17 | chr18 | 6894729 | ||||||
| chr18:6895146
|
T | C | 139 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(136): Show | 139 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(136): Show |
intron_variant | MODIFIER | c.1905+255T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 15/17 | chr18 | 6895146 | ||||||
| chr18:6895172
|
C | G | 190 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(187): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.1905+281C>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 15/17 | chr18 | 6895172 | ||||||
| chr18:6895220
|
G | A | 3 | a0001c0001t0001g0121a0001c0001t0001g0161a0001c0001t0001g0168 | 3 | HG02145.hp2 HG02615.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1905+329G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 15/17 | chr18 | 6895220 | ||||||
| chr18:6895492
|
T | G | 9 | a0001c0010t0003g0089a0001c0010t0003g0098a0001c0010t0003g0114others(6): Show | 9 | HG01081.hp2 HG02630.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.1905+601T>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 15/17 | chr18 | 6895492 | ||||||
| chr18:6895551
|
T | A | 1 | a0001c0018t0020g0007 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1905+660T>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 15/17 | chr18 | 6895551 | ||||||
| chr18:6895639
|
A | T | 3 | a0001c0001t0007g0116a0001c0001t0007g0117a0001c0001t0007g0212 | 3 | HG02896.hp1 HG02897.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1905+748A>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 15/17 | chr18 | 6895639 | ||||||
| chr18:6895666
|
A | T | 1 | a0001c0003t0003g0145 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1905+775A>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 15/17 | chr18 | 6895666 | ||||||
| chr18:6896020
|
G | A | 4 | a0001c0001t0018g0111a0003c0013t0011g0062a0003c0013t0011g0063others(1): Show | 4 | HG02818.hp2 HG03041.hp1 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.1906-482G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 15/17 | chr18 | 6896020 | ||||||
| chr18:6896114
|
ACT | A | 3 | a0003c0013t0011g0062a0003c0013t0011g0063a0003c0023t0001g0120 | 3 | HG03041.hp1 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1906-385_1906-384d others(4): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr18 | 6896114 | |||||
| chr18:6896376
|
A | C | 1 | a0003c0004t0001g0030 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1906-126A>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 15/17 | chr18 | 6896376 | ||||||
| chr18:6896451
|
C | T | 153 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(150): Show | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.1906-51C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 15/17 | chr18 | 6896451 | ||||||
| chr18:6896770
|
A | C | 1 | a0002c0002t0002g0196 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.2030+144A>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6896770 | ||||||
| chr18:6896899
|
C | CTTTTATT others(3): Show |
3 | a0003c0013t0011g0062a0003c0013t0011g0063a0003c0023t0001g0120 | 3 | HG03041.hp1 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2030+287_2030+296d others(12): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr18 | 6896899 | |||||
| chr18:6896899
|
C | CTTTTATT others(8): Show |
3 | a0008c0011t0005g0016a0008c0011t0005g0090a0008c0011t0005g0152 | 3 | HG02630.hp2 HG03471.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2030+282_2030+296d others(17): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr18 | 6896899 | |||||
| chr18:6897142
|
G | A | 2 | a0001c0018t0020g0007a0002c0017t0002g0086 | 2 | HG02922.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2030+516G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6897142 | ||||||
| chr18:6897172
|
C | A | 1 | a0003c0004t0001g0175 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.2030+546C>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6897172 | ||||||
| chr18:6897174
|
A | T | 1 | a0003c0004t0001g0175 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.2030+548A>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6897174 | ||||||
| chr18:6897180
|
C | A | 1 | a0003c0004t0001g0175 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.2030+554C>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6897180 | ||||||
| chr18:6897182
|
G | C | 1 | a0003c0004t0001g0175 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.2030+556G>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6897182 | ||||||
| chr18:6897184
|
G | C | 1 | a0003c0004t0001g0175 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.2030+558G>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6897184 | ||||||
| chr18:6897185
|
A | G | 1 | a0003c0004t0001g0175 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.2030+559A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6897185 | ||||||
| chr18:6897187
|
T | G | 1 | a0003c0004t0001g0175 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.2030+561T>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6897187 | ||||||
| chr18:6897188
|
A | T | 1 | a0003c0004t0001g0175 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.2030+562A>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6897188 | ||||||
| chr18:6897189
|
C | T | 1 | a0003c0004t0001g0175 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.2030+563C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6897189 | ||||||
| chr18:6897258
|
G | A | 1 | a0001c0003t0003g0201 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2030+632G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6897258 | ||||||
| chr18:6897461
|
C | T | 2 | a0001c0018t0020g0007a0002c0017t0002g0086 | 2 | HG02922.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2030+835C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6897461 | ||||||
| chr18:6897676
|
C | T | 1 | a0001c0003t0003g0068 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2030+1050C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6897676 | ||||||
| chr18:6897779
|
G | A | 25 | a0001c0003t0003g0002a0001c0003t0003g0013a0001c0003t0003g0027others(22): Show | 25 | HG00280.hp2 HG00741.hp2 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.2030+1153G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6897779 | ||||||
| chr18:6897895
|
T | TAC | 33 | a0001c0003t0003g0002a0001c0003t0003g0013a0001c0003t0003g0027others(30): Show | 33 | HG00280.hp2 HG00741.hp2 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.2030+1281_2030+128 others(6): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr18 | 6897895 | |||||
| chr18:6897992
|
T | C | 2 | a0001c0003t0003g0002a0001c0003t0003g0104 | 2 | HG03471.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2030+1366T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6897992 | ||||||
| chr18:6898115
|
A | G | 1 | a0002c0002t0002g0199 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.2030+1489A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6898115 | ||||||
| chr18:6898384
|
A | T | 1 | a0003c0004t0001g0039 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2030+1758A>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6898384 | ||||||
| chr18:6898416
|
C | T | 141 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(138): Show | 141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.2030+1790C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6898416 | ||||||
| chr18:6898445
|
C | T | 1 | a0003c0004t0001g0173 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.2030+1819C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6898445 | ||||||
| chr18:6898533
|
C | T | 3 | a0003c0013t0011g0062a0003c0013t0011g0063a0003c0023t0001g0120 | 3 | HG03041.hp1 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2030+1907C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6898533 | ||||||
| chr18:6898590
|
C | T | 3 | a0001c0001t0007g0116a0001c0001t0007g0117a0001c0001t0007g0212 | 3 | HG02896.hp1 HG02897.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2030+1964C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6898590 | ||||||
| chr18:6898890
|
G | C | 3 | a0002c0002t0002g0066a0004c0007t0002g0056a0004c0007t0002g0178 | 3 | HG02040.hp2 NA19063.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.2030+2264G>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6898890 | ||||||
| chr18:6899024
|
C | T | 1 | a0001c0001t0001g0075 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2030+2398C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6899024 | ||||||
| chr18:6899068
|
A | C | 1 | a0001c0003t0003g0084 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2030+2442A>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6899068 | ||||||
| chr18:6899126
|
T | C | 2 | a0002c0002t0010g0206a0002c0002t0010g0246 | 2 | NA18941.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.2030+2500T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6899126 | ||||||
| chr18:6899490
|
A | G | 4 | a0001c0003t0003g0085a0001c0003t0003g0091a0001c0003t0003g0105others(1): Show | 4 | HG01175.hp2 HG02976.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.2030+2864A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6899490 | ||||||
| chr18:6899538
|
G | GA | 4 | a0002c0002t0004g0006a0002c0002t0004g0059a0002c0002t0004g0147others(1): Show | 4 | HG01884.hp1 HG02280.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.2030+2918dupA | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr18 | 6899538 | |||||
| chr18:6899566
|
C | T | 1 | a0001c0003t0003g0222 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2030+2940C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6899566 | ||||||
| chr18:6899849
|
A | C | 14 | a0001c0001t0001g0102a0001c0001t0001g0141a0001c0001t0001g0215others(11): Show | 14 | HG00140.hp1 HG01261.hp2 HG01993.hp2 others(11): Show |
intron_variant | MODIFIER | c.2030+3223A>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6899849 | ||||||
| chr18:6899929
|
A | G | 1 | a0002c0002t0002g0096 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2030+3303A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6899929 | ||||||
| chr18:6899995
|
T | C | 153 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(150): Show | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.2030+3369T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6899995 | ||||||
| chr18:6900114
|
G | C | 3 | a0001c0001t0008g0143a0001c0001t0008g0171a0001c0001t0018g0111 | 3 | HG02818.hp2 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2030+3488G>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6900114 | ||||||
| chr18:6900244
|
A | G | 60 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0026others(57): Show | 60 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(57): Show |
intron_variant | MODIFIER | c.2030+3618A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6900244 | ||||||
| chr18:6900294
|
C | CACA | 153 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(150): Show | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.2030+3669_2030+367 others(7): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr18 | 6900294 | |||||
| chr18:6900638
|
G | A | 1 | a0002c0002t0002g0137 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.2030+4012G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6900638 | ||||||
| chr18:6900674
|
G | A | 2 | a0006c0009t0003g0162a0007c0008t0002g0166 | 2 | HG01952.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.2030+4048G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6900674 | ||||||
| chr18:6900696
|
TATC | T | 69 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0026others(66): Show | 69 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(66): Show |
intron_variant | MODIFIER | c.2030+4073_2030+407 others(7): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr18 | 6900696 | |||||
| chr18:6900737
|
T | C | 2 | a0001c0001t0009g0005a0001c0001t0009g0245 | 2 | HG01891.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.2030+4111T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6900737 | ||||||
| chr18:6900856
|
A | G | 64 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(61): Show | 64 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.2030+4230A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6900856 | ||||||
| chr18:6900913
|
GAA | G | 69 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0026others(66): Show | 69 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(66): Show |
intron_variant | MODIFIER | c.2030+4289_2030+429 others(6): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr18 | 6900913 | |||||
| chr18:6900928
|
A | G | 4 | a0001c0003t0003g0002a0001c0003t0003g0076a0001c0003t0003g0104others(1): Show | 4 | HG03471.hp1 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.2030+4302A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6900928 | ||||||
| chr18:6901114
|
G | C | 9 | a0001c0010t0003g0089a0001c0010t0003g0098a0001c0010t0003g0114others(6): Show | 9 | HG01081.hp2 HG02630.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.2030+4488G>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6901114 | ||||||
| chr18:6901246
|
C | T | 1 | a0001c0001t0001g0012 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2030+4620C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6901246 | ||||||
| chr18:6901347
|
A | C | 6 | a0003c0013t0011g0062a0003c0013t0011g0063a0003c0023t0001g0120others(3): Show | 6 | HG02630.hp2 HG03041.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.2030+4721A>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6901347 | ||||||
| chr18:6901506
|
A | G | 1 | a0001c0003t0003g0145 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2030+4880A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6901506 | ||||||
| chr18:6901517
|
A | C | 1 | a0001c0001t0001g0211 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2030+4891A>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6901517 | ||||||
| chr18:6901540
|
T | TA | 6 | a0001c0001t0001g0141a0001c0012t0001g0210a0001c0012t0014g0159others(3): Show | 6 | HG00140.hp2 HG01106.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.2030+4931dupA | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr18 | 6901540 | |||||
| chr18:6901540
|
TA | T | 74 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(71): Show | 74 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.2030+4931delA | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr18 | 6901540 | |||||
| chr18:6901540
|
TAA | T | 52 | a0001c0001t0001g0042a0001c0001t0009g0005a0001c0001t0009g0245others(49): Show | 52 | HG00280.hp2 HG00735.hp2 HG00741.hp2 others(49): Show |
intron_variant | MODIFIER | c.2030+4930_2030+493 others(6): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr18 | 6901540 | |||||
| chr18:6901540
|
TAAAA | T | 6 | a0001c0010t0003g0089a0001c0010t0003g0098a0001c0010t0003g0114others(3): Show | 6 | HG01081.hp2 HG02970.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.2030+4928_2030+493 others(8): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr18 | 6901540 | |||||
| chr18:6901555
|
A | C | 1 | a0001c0019t0021g0073 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2030+4929A>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6901555 | ||||||
| chr18:6901660
|
G | T | 17 | a0001c0003t0003g0013a0001c0003t0003g0027a0001c0003t0003g0055others(14): Show | 17 | HG00280.hp2 HG00741.hp2 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.2030+5034G>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6901660 | ||||||
| chr18:6901915
|
C | T | 1 | a0001c0019t0021g0073 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2030+5289C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6901915 | ||||||
| chr18:6901916
|
G | A | 3 | a0008c0011t0005g0016a0008c0011t0005g0090a0008c0011t0005g0152 | 3 | HG02630.hp2 HG03471.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2030+5290G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6901916 | ||||||
| chr18:6901959
|
T | C | 2 | a0003c0004t0001g0241a0003c0004t0001g0248 | 2 | NA18966.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.2030+5333T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6901959 | ||||||
| chr18:6902065
|
C | G | 9 | a0001c0010t0003g0089a0001c0010t0003g0098a0001c0010t0003g0114others(6): Show | 9 | HG01081.hp2 HG02630.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.2030+5439C>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6902065 | ||||||
| chr18:6902268
|
T | C | 6 | a0003c0013t0011g0062a0003c0013t0011g0063a0003c0023t0001g0120others(3): Show | 6 | HG02630.hp2 HG03041.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.2030+5642T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6902268 | ||||||
| chr18:6902365
|
T | C | 132 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(129): Show | 132 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(129): Show |
intron_variant | MODIFIER | c.2030+5739T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6902365 | ||||||
| chr18:6902473
|
A | G | 9 | a0001c0010t0003g0089a0001c0010t0003g0098a0001c0010t0003g0114others(6): Show | 9 | HG01081.hp2 HG02630.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.2030+5847A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6902473 | ||||||
| chr18:6902477
|
C | T | 9 | a0001c0010t0003g0089a0001c0010t0003g0098a0001c0010t0003g0114others(6): Show | 9 | HG01081.hp2 HG02630.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.2030+5851C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6902477 | ||||||
| chr18:6902548
|
A | G | 3 | a0008c0011t0005g0016a0008c0011t0005g0090a0008c0011t0005g0152 | 3 | HG02630.hp2 HG03471.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2030+5922A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6902548 | ||||||
| chr18:6902568
|
C | T | 130 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(127): Show | 130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.2030+5942C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6902568 | ||||||
| chr18:6902643
|
T | TA | 9 | a0001c0010t0003g0089a0001c0010t0003g0098a0001c0010t0003g0114others(6): Show | 9 | HG01081.hp2 HG02630.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.2030+6023dupA | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr18 | 6902643 | |||||
| chr18:6902810
|
C | T | 2 | a0001c0001t0009g0005a0001c0001t0009g0245 | 2 | HG01891.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.2031-6150C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6902810 | ||||||
| chr18:6902819
|
C | T | 1 | a0002c0002t0002g0217 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2031-6141C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6902819 | ||||||
| chr18:6902933
|
C | T | 3 | a0003c0013t0011g0062a0003c0013t0011g0063a0003c0023t0001g0120 | 3 | HG03041.hp1 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2031-6027C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6902933 | ||||||
| chr18:6903063
|
A | G | 1 | a0001c0020t0023g0101 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2031-5897A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6903063 | ||||||
| chr18:6903199
|
A | G | 1 | a0002c0002t0002g0229 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2031-5761A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6903199 | ||||||
| chr18:6903205
|
A | G | 9 | a0001c0010t0003g0089a0001c0010t0003g0098a0001c0010t0003g0114others(6): Show | 9 | HG01081.hp2 HG02630.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.2031-5755A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6903205 | ||||||
| chr18:6903587
|
C | G | 9 | a0001c0010t0003g0089a0001c0010t0003g0098a0001c0010t0003g0114others(6): Show | 9 | HG01081.hp2 HG02630.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.2031-5373C>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6903587 | ||||||
| chr18:6903590
|
T | A | 9 | a0001c0010t0003g0089a0001c0010t0003g0098a0001c0010t0003g0114others(6): Show | 9 | HG01081.hp2 HG02630.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.2031-5370T>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6903590 | ||||||
| chr18:6903669
|
A | G | 2 | a0001c0018t0020g0007a0002c0017t0002g0086 | 2 | HG02922.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2031-5291A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6903669 | ||||||
| chr18:6903729
|
C | T | 5 | a0001c0001t0001g0004a0001c0001t0001g0151a0001c0001t0008g0143others(2): Show | 5 | HG01243.hp2 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.2031-5231C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6903729 | ||||||
| chr18:6903786
|
G | A | 2 | a0002c0002t0002g0157a0002c0002t0002g0163 | 2 | HG01891.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.2031-5174G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6903786 | ||||||
| chr18:6903826
|
C | CA | 159 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(156): Show | 159 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(156): Show |
intron_variant | MODIFIER | c.2031-5115dupA | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr18 | 6903826 | |||||
| chr18:6903826
|
C | CAA | 16 | a0001c0001t0001g0019a0001c0001t0001g0071a0001c0001t0001g0186others(13): Show | 16 | HG00280.hp1 HG00423.hp2 HG00558.hp1 others(13): Show |
intron_variant | MODIFIER | c.2031-5116_2031-511 others(6): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr18 | 6903826 | |||||
| chr18:6903850
|
C | T | 3 | a0001c0010t0003g0089a0001c0010t0003g0098a0001c0010t0003g0114 | 3 | HG01081.hp2 HG02970.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2031-5110C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6903850 | ||||||
| chr18:6904169
|
G | A | 1 | a0001c0020t0023g0101 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2031-4791G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6904169 | ||||||
| chr18:6904407
|
T | C | 2 | a0001c0001t0009g0005a0001c0001t0009g0245 | 2 | HG01891.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.2031-4553T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6904407 | ||||||
| chr18:6904517
|
G | A | 1 | a0001c0012t0014g0159 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2031-4443G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6904517 | ||||||
| chr18:6904549
|
T | C | 1 | a0003c0004t0001g0173 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.2031-4411T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6904549 | ||||||
| chr18:6904587
|
A | G | 5 | a0001c0001t0009g0005a0001c0001t0009g0245a0001c0010t0003g0089others(2): Show | 5 | HG01081.hp2 HG01891.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.2031-4373A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6904587 | ||||||
| chr18:6904617
|
G | A | 2 | a0001c0001t0001g0236a0001c0001t0017g0118 | 2 | HG00140.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.2031-4343G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6904617 | ||||||
| chr18:6904660
|
A | C | 1 | a0002c0002t0002g0207 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2031-4300A>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6904660 | ||||||
| chr18:6904737
|
G | T | 1 | a0002c0002t0002g0103 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2031-4223G>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6904737 | ||||||
| chr18:6904839
|
C | T | 1 | a0001c0001t0001g0019 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2031-4121C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6904839 | ||||||
| chr18:6904955
|
C | T | 130 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(127): Show | 130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.2031-4005C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6904955 | ||||||
| chr18:6905063
|
T | G | 1 | a0001c0001t0001g0082 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2031-3897T>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6905063 | ||||||
| chr18:6905110
|
A | C | 1 | a0003c0004t0001g0247 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.2031-3850A>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6905110 | ||||||
| chr18:6905246
|
A | G | 2 | a0001c0001t0001g0001a0001c0001t0001g0054 | 2 | HG01496.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.2031-3714A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6905246 | ||||||
| chr18:6905491
|
G | A | 3 | a0001c0001t0007g0116a0001c0001t0007g0117a0001c0001t0007g0212 | 3 | HG02896.hp1 HG02897.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2031-3469G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6905491 | ||||||
| chr18:6905639
|
A | G | 1 | a0003c0004t0001g0175 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.2031-3321A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6905639 | ||||||
| chr18:6905738
|
T | C | 3 | a0001c0001t0001g0102a0001c0001t0001g0202a0001c0001t0001g0239 | 3 | HG01099.hp2 HG01261.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.2031-3222T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6905738 | ||||||
| chr18:6905906
|
G | A | 1 | a0001c0001t0001g0070 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2031-3054G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6905906 | ||||||
| chr18:6906185
|
A | G | 1 | a0002c0002t0002g0015 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2031-2775A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6906185 | ||||||
| chr18:6906414
|
CTA | C | 3 | a0003c0013t0011g0062a0003c0013t0011g0063a0003c0023t0001g0120 | 3 | HG03041.hp1 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2031-2543_2031-254 others(6): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr18 | 6906414 | |||||
| chr18:6906509
|
C | G | 188 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(185): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.2031-2451C>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6906509 | ||||||
| chr18:6906518
|
C | A | 1 | a0001c0001t0001g0194 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2031-2442C>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6906518 | ||||||
| chr18:6906599
|
G | C | 3 | a0001c0001t0008g0143a0001c0001t0008g0171a0001c0001t0018g0111 | 3 | HG02818.hp2 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2031-2361G>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6906599 | ||||||
| chr18:6906681
|
A | G | 1 | a0001c0001t0019g0008 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2031-2279A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6906681 | ||||||
| chr18:6906838
|
C | T | 1 | a0001c0001t0001g0221 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2031-2122C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6906838 | ||||||
| chr18:6906967
|
C | A | 9 | a0001c0010t0003g0089a0001c0010t0003g0098a0001c0010t0003g0114others(6): Show | 9 | HG01081.hp2 HG02630.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.2031-1993C>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6906967 | ||||||
| chr18:6907098
|
A | G | 9 | a0001c0010t0003g0089a0001c0010t0003g0098a0001c0010t0003g0114others(6): Show | 9 | HG01081.hp2 HG02630.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.2031-1862A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6907098 | ||||||
| chr18:6907183
|
C | T | 2 | a0001c0018t0020g0007a0002c0017t0002g0086 | 2 | HG02922.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2031-1777C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6907183 | ||||||
| chr18:6907268
|
C | T | 38 | a0001c0003t0003g0002a0001c0003t0003g0013a0001c0003t0003g0027others(35): Show | 38 | HG00280.hp2 HG00741.hp2 HG01081.hp1 others(35): Show |
intron_variant | MODIFIER | c.2031-1692C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6907268 | ||||||
| chr18:6907279
|
G | A | 2 | a0001c0018t0020g0007a0002c0017t0002g0086 | 2 | HG02922.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2031-1681G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6907279 | ||||||
| chr18:6907394
|
G | GA | 114 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0026others(111): Show | 114 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.2031-1551dupA | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr18 | 6907394 | |||||
| chr18:6907394
|
GA | G | 6 | a0001c0001t0001g0121a0001c0001t0001g0161a0001c0001t0001g0168others(3): Show | 6 | HG01891.hp1 HG02145.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.2031-1551delA | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr18 | 6907394 | |||||
| chr18:6907633
|
G | A | 3 | a0001c0010t0003g0089a0001c0010t0003g0098a0001c0010t0003g0114 | 3 | HG01081.hp2 HG02970.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2031-1327G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6907633 | ||||||
| chr18:6907667
|
G | A | 1 | a0002c0002t0002g0103 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2031-1293G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6907667 | ||||||
| chr18:6907854
|
C | T | 130 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(127): Show | 130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.2031-1106C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6907854 | ||||||
| chr18:6907868
|
G | A | 6 | a0003c0013t0011g0062a0003c0013t0011g0063a0003c0023t0001g0120others(3): Show | 6 | HG02630.hp2 HG03041.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.2031-1092G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6907868 | ||||||
| chr18:6907883
|
G | C | 1 | a0001c0001t0001g0040 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.2031-1077G>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6907883 | ||||||
| chr18:6907952
|
A | C | 2 | a0001c0001t0001g0121a0001c0001t0001g0161 | 2 | HG02145.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.2031-1008A>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6907952 | ||||||
| chr18:6908011
|
C | T | 2 | a0001c0001t0009g0005a0001c0001t0009g0245 | 2 | HG01891.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.2031-949C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6908011 | ||||||
| chr18:6908125
|
G | GTTTTA | 35 | a0001c0003t0003g0002a0001c0003t0003g0013a0001c0003t0003g0055others(32): Show | 35 | HG00280.hp2 HG01081.hp1 HG01099.hp1 others(32): Show |
intron_variant | MODIFIER | c.2031-810_2031-806d others(7): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr18 | 6908125 | |||||
| chr18:6908125
|
G | GTTTTATT others(3): Show |
3 | a0001c0003t0003g0027a0001c0003t0003g0085a0001c0003t0003g0122 | 3 | HG00741.hp2 HG02723.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2031-815_2031-806d others(12): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr18 | 6908125 | |||||
| chr18:6908125
|
GTTTTA | G | 3 | a0001c0010t0003g0089a0001c0010t0003g0098a0001c0010t0003g0114 | 3 | HG01081.hp2 HG02970.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2031-810_2031-806d others(7): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr18 | 6908125 | |||||
| chr18:6908180
|
C | T | 1 | a0002c0002t0012g0088 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2031-780C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6908180 | ||||||
| chr18:6908246
|
T | G | 9 | a0001c0010t0003g0089a0001c0010t0003g0098a0001c0010t0003g0114others(6): Show | 9 | HG01081.hp2 HG02630.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.2031-714T>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6908246 | ||||||
| chr18:6908273
|
A | G | 1 | a0001c0001t0008g0074 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2031-687A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6908273 | ||||||
| chr18:6908428
|
C | T | 3 | a0001c0010t0003g0089a0001c0010t0003g0098a0001c0010t0003g0114 | 3 | HG01081.hp2 HG02970.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2031-532C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6908428 | ||||||
| chr18:6908435
|
G | A | 3 | a0001c0001t0001g0121a0001c0001t0001g0161a0001c0001t0001g0168 | 3 | HG02145.hp2 HG02615.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2031-525G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6908435 | ||||||
| chr18:6908479
|
T | A | 1 | a0001c0001t0001g0228 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2031-481T>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6908479 | ||||||
| chr18:6908727
|
A | G | 108 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(105): Show | 108 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.2031-233A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | chr18 | 6908727 | ||||||
| chr18:6909269
|
T | G | 2 | a0001c0001t0009g0005a0001c0001t0009g0245 | 2 | HG01891.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.2095+245T>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 17/17 | chr18 | 6909269 | ||||||
| chr18:6909269
|
TCTTTG | T | 3 | a0003c0013t0011g0062a0003c0013t0011g0063a0003c0023t0001g0120 | 3 | HG03041.hp1 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2095+250_2095+254d others(7): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr18 | 6909269 | |||||
| chr18:6909274
|
G | T | 174 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(171): Show | 174 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(171): Show |
intron_variant | MODIFIER | c.2095+250G>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 17/17 | chr18 | 6909274 | ||||||
| chr18:6909275
|
CTTTTCTT others(19): Show |
C | 3 | a0001c0010t0003g0089a0001c0010t0003g0098a0001c0010t0003g0114 | 3 | HG01081.hp2 HG02970.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2095+256_2095+281d others(28): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr18 | 6909275 | |||||
| chr18:6909285
|
CTTTTCTT others(9): Show |
C | 4 | a0001c0001t0007g0116a0001c0001t0007g0117a0001c0001t0007g0212others(1): Show | 4 | HG02896.hp1 HG02897.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.2095+266_2095+281d others(18): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr18 | 6909285 | |||||
| chr18:6909290
|
CTTTTCTT others(4): Show |
C | 11 | a0001c0001t0001g0040a0001c0001t0001g0121a0001c0001t0001g0161others(8): Show | 11 | HG01261.hp1 HG01515.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.2095+271_2095+281d others(13): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr18 | 6909290 | |||||
| chr18:6909295
|
CTTTTCT | C | 71 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0029others(68): Show | 71 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.2095+276_2095+281d others(8): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr18 | 6909295 | |||||
| chr18:6909300
|
C | CTTTTCTT others(54): Show |
2 | a0001c0001t0001g0209a0002c0005t0002g0017 | 2 | HG03239.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.2095+280_2095+281i others(63): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr18 | 6909300 | |||||
| chr18:6909300
|
C | CTTTTCTT others(59): Show |
1 | a0002c0005t0002g0057 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2095+280_2095+281i others(68): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr18 | 6909300 | |||||
| chr18:6909300
|
C | CTTTTCTT others(107): Show |
1 | a0001c0001t0001g0185 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.2095+280_2095+281i others(116): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr18 | 6909300 | |||||
| chr18:6909300
|
C | CTTTTCTT others(177): Show |
1 | a0001c0001t0001g0038 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.2095+280_2095+281i others(186): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr18 | 6909300 | |||||
| chr18:6909300
|
C | CTTTTCTT others(187): Show |
1 | a0001c0001t0001g0042 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.2095+280_2095+281i others(196): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr18 | 6909300 | |||||
| chr18:6909300
|
C | CTTTTCTT others(207): Show |
1 | a0001c0001t0001g0034 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.2095+280_2095+281i others(216): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr18 | 6909300 | |||||
| chr18:6909300
|
CT | C | 23 | a0001c0001t0001g0026a0001c0001t0001g0181a0001c0001t0001g0215others(20): Show | 23 | HG00741.hp2 HG01261.hp2 HG01346.hp2 others(20): Show |
intron_variant | MODIFIER | c.2095+286delT | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr18 | 6909300 | |||||
| chr18:6909301
|
T | TTTTCTTT others(7): Show |
3 | a0001c0001t0001g0097a0001c0001t0001g0107a0001c0001t0001g0221 | 3 | HG01175.hp1 HG01243.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.2095+280_2095+281i others(16): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr18 | 6909301 | |||||
| chr18:6909301
|
T | TTTTCTTT others(12): Show |
1 | a0001c0001t0008g0171 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2095+280_2095+281i others(21): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr18 | 6909301 | |||||
| chr18:6909301
|
T | TTTTCTTT others(22): Show |
6 | a0001c0001t0001g0071a0001c0001t0001g0080a0001c0001t0001g0124others(3): Show | 6 | HG00280.hp1 HG02145.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.2095+280_2095+281i others(31): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr18 | 6909301 | |||||
| chr18:6909301
|
T | TTTTCTTT others(27): Show |
4 | a0001c0001t0001g0100a0001c0001t0001g0150a0001c0001t0001g0211others(1): Show | 4 | HG02451.hp1 HG03098.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.2095+280_2095+281i others(36): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr18 | 6909301 | |||||
| chr18:6909301
|
T | TTTTCTTT others(32): Show |
7 | a0001c0001t0001g0001a0001c0001t0001g0054a0001c0001t0001g0072others(4): Show | 7 | HG00735.hp2 HG01496.hp1 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.2095+280_2095+281i others(41): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr18 | 6909301 | |||||
| chr18:6909301
|
T | TTTTCTTT others(37): Show |
4 | a0001c0001t0001g0113a0001c0001t0001g0225a0001c0001t0006g0155others(1): Show | 4 | HG01256.hp2 HG01884.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.2095+280_2095+281i others(46): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr18 | 6909301 | |||||
| chr18:6909301
|
T | TTTTCTTT others(42): Show |
3 | a0001c0001t0001g0003a0001c0001t0001g0151a0001c0001t0006g0176 | 3 | HG01243.hp2 HG02055.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.2095+280_2095+281i others(51): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr18 | 6909301 | |||||
| chr18:6909301
|
T | TTTTCTTT others(47): Show |
7 | a0001c0001t0001g0004a0001c0001t0001g0070a0001c0001t0001g0075others(4): Show | 7 | HG02965.hp1 HG02970.hp2 HG03490.hp2 others(4): Show |
intron_variant | MODIFIER | c.2095+280_2095+281i others(56): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr18 | 6909301 | |||||
| chr18:6909301
|
T | TTTTCTTT others(52): Show |
3 | a0001c0001t0001g0012a0001c0001t0001g0189a0003c0004t0001g0193 | 3 | HG00099.hp2 HG00438.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.2095+280_2095+281i others(61): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr18 | 6909301 | |||||
| chr18:6909301
|
T | TTTTCTTT others(57): Show |
2 | a0003c0004t0001g0173a0005c0006t0003g0031 | 2 | NA18968.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.2095+280_2095+281i others(66): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr18 | 6909301 | |||||
| chr18:6909301
|
T | TTTTCTTT others(62): Show |
3 | a0001c0001t0001g0129a0001c0001t0001g0204a0005c0006t0003g0226 | 3 | NA18956.hp2 NA18989.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.2095+280_2095+281i others(71): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr18 | 6909301 | |||||
| chr18:6909301
|
T | TTTTCTTT others(72): Show |
3 | a0003c0004t0001g0030a0003c0004t0001g0219a0003c0004t0001g0220 | 3 | NA19066.hp1 NA19070.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.2095+280_2095+281i others(81): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr18 | 6909301 | |||||
| chr18:6909301
|
T | TTTTCTTT others(87): Show |
1 | a0003c0004t0001g0227 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2095+280_2095+281i others(96): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr18 | 6909301 | |||||
| chr18:6909301
|
T | TTTTCTTT others(92): Show |
1 | a0001c0001t0001g0194 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2095+280_2095+281i others(101): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr18 | 6909301 | |||||
| chr18:6909301
|
T | TTTTCTTT others(127): Show |
1 | a0003c0004t0001g0020 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2095+280_2095+281i others(136): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr18 | 6909301 | |||||
| chr18:6909301
|
T | TTTTCTTT others(172): Show |
1 | a0003c0004t0001g0109 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.2095+280_2095+281i others(181): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr18 | 6909301 | |||||
| chr18:6909301
|
T | TTTTCTTT others(222): Show |
1 | a0003c0004t0001g0048 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2095+280_2095+281i others(231): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr18 | 6909301 | |||||
| chr18:6909301
|
T | TTTTCTTT others(277): Show |
1 | a0001c0001t0001g0139 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2095+280_2095+281i others(286): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr18 | 6909301 | |||||
| chr18:6909302
|
T | TTTCTTTT others(316): Show |
1 | a0001c0001t0001g0128 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.2095+280_2095+281i others(325): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr18 | 6909302 | |||||
| chr18:6909324
|
G | T | 104 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(101): Show | 104 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.2095+300G>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 17/17 | chr18 | 6909324 | ||||||
| chr18:6909450
|
G | A | 1 | a0003c0004t0001g0187 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.2095+426G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 17/17 | chr18 | 6909450 | ||||||
| chr18:6909452
|
C | G | 2 | a0001c0001t0009g0005a0001c0001t0009g0245 | 2 | HG01891.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.2095+428C>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 17/17 | chr18 | 6909452 | ||||||
| chr18:6909456
|
A | T | 3 | a0001c0010t0003g0089a0001c0010t0003g0098a0001c0010t0003g0114 | 3 | HG01081.hp2 HG02970.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2095+432A>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 17/17 | chr18 | 6909456 | ||||||
| chr18:6909501
|
C | T | 3 | a0003c0013t0011g0062a0003c0013t0011g0063a0003c0023t0001g0120 | 3 | HG03041.hp1 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2095+477C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 17/17 | chr18 | 6909501 | ||||||
| chr18:6909512
|
C | A | 3 | a0003c0013t0011g0062a0003c0013t0011g0063a0003c0023t0001g0120 | 3 | HG03041.hp1 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2095+488C>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 17/17 | chr18 | 6909512 | ||||||
| chr18:6909561
|
G | A | 3 | a0001c0010t0003g0089a0001c0010t0003g0098a0001c0010t0003g0114 | 3 | HG01081.hp2 HG02970.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2095+537G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 17/17 | chr18 | 6909561 | ||||||
| chr18:6909809
|
C | G | 2 | a0001c0018t0020g0007a0002c0017t0002g0086 | 2 | HG02922.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2095+785C>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 17/17 | chr18 | 6909809 | ||||||
| chr18:6909829
|
C | T | 3 | a0001c0001t0007g0116a0001c0001t0007g0117a0001c0001t0007g0212 | 3 | HG02896.hp1 HG02897.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2095+805C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 17/17 | chr18 | 6909829 | ||||||
| chr18:6910186
|
C | T | 2 | a0001c0003t0003g0154a0001c0015t0003g0167 | 2 | HG02818.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2095+1162C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 17/17 | chr18 | 6910186 | ||||||
| chr18:6910212
|
G | A | 3 | a0001c0001t0001g0179a0003c0004t0001g0093a0003c0004t0001g0183 | 3 | HG00597.hp1 HG00621.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.2095+1188G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 17/17 | chr18 | 6910212 | ||||||
| chr18:6910257
|
T | A | 1 | a0001c0001t0001g0211 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2095+1233T>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 17/17 | chr18 | 6910257 | ||||||
| chr18:6910465
|
A | G | 3 | a0003c0013t0011g0062a0003c0013t0011g0063a0003c0023t0001g0120 | 3 | HG03041.hp1 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2095+1441A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 17/17 | chr18 | 6910465 | ||||||
| chr18:6910536
|
G | T | 74 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0026others(71): Show | 74 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.2095+1512G>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 17/17 | chr18 | 6910536 | ||||||
| chr18:6910541
|
A | G | 1 | a0002c0002t0002g0134 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2095+1517A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 17/17 | chr18 | 6910541 | ||||||
| chr18:6910711
|
T | C | 1 | a0001c0001t0001g0100 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2096-1349T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 17/17 | chr18 | 6910711 | ||||||
| chr18:6910828
|
TTTTTG | T | 173 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(170): Show | 173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.2096-1218_2096-121 others(9): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr18 | 6910828 | |||||
| chr18:6910842
|
T | G | 7 | a0001c0001t0001g0052a0001c0001t0007g0116a0001c0001t0007g0117others(4): Show | 7 | HG02896.hp1 HG02897.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.2096-1218T>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 17/17 | chr18 | 6910842 | ||||||
| chr18:6910843
|
G | T | 7 | a0001c0001t0001g0052a0001c0001t0007g0116a0001c0001t0007g0117others(4): Show | 7 | HG02896.hp1 HG02897.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.2096-1217G>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 17/17 | chr18 | 6910843 | ||||||
| chr18:6910847
|
GCTTT | G | 6 | a0001c0001t0007g0116a0001c0001t0007g0117a0001c0001t0007g0212others(3): Show | 6 | HG02896.hp1 HG02897.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.2096-1212_2096-120 others(8): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 17/17 | chr18 | 6910847 | ||||||
| chr18:6910848
|
C | T | 173 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(170): Show | 173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.2096-1212C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 17/17 | chr18 | 6910848 | ||||||
| chr18:6910852
|
G | T | 6 | a0001c0001t0007g0116a0001c0001t0007g0117a0001c0001t0007g0212others(3): Show | 6 | HG02896.hp1 HG02897.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.2096-1208G>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 17/17 | chr18 | 6910852 | ||||||
| chr18:6910886
|
C | T | 1 | a0003c0004t0001g0064 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.2096-1174C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 17/17 | chr18 | 6910886 | ||||||
| chr18:6910891
|
CT | C | 82 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0026others(79): Show | 82 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.2096-1168delT | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 17/17 | chr18 | 6910891 | ||||||
| chr18:6910900
|
A | G | 119 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(116): Show | 119 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.2096-1160A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 17/17 | chr18 | 6910900 | ||||||
| chr18:6910930
|
C | T | 61 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0026others(58): Show | 61 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.2096-1130C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 17/17 | chr18 | 6910930 | ||||||
| chr18:6910930
|
CGCCTCCC others(584): Show |
C | 3 | a0001c0001t0007g0116a0001c0001t0007g0117a0001c0001t0007g0212 | 3 | HG02896.hp1 HG02897.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2096-1122_2096-532 others(3): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr18 | 6910930 | |||||
| chr18:6910969
|
G | A | 176 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(173): Show | 176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.2096-1091G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 17/17 | chr18 | 6910969 | ||||||
| chr18:6910969
|
G | C | 6 | a0002c0002t0002g0131a0002c0002t0002g0207a0002c0002t0002g0214others(3): Show | 6 | HG00597.hp2 HG02135.hp1 HG03942.hp2 others(3): Show |
intron_variant | MODIFIER | c.2096-1091G>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 17/17 | chr18 | 6910969 | ||||||
| chr18:6910989
|
C | G | 179 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(176): Show | 179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.2096-1071C>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 17/17 | chr18 | 6910989 | ||||||
| chr18:6910993
|
C | T | 1 | a0001c0001t0001g0184 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2096-1067C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 17/17 | chr18 | 6910993 | ||||||
| chr18:6910994
|
A | G | 181 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(178): Show | 181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.2096-1066A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 17/17 | chr18 | 6910994 | ||||||
| chr18:6910995
|
T | C | 182 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(179): Show | 182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.2096-1065T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 17/17 | chr18 | 6910995 | ||||||
| chr18:6911024
|
T | C | 3 | a0002c0002t0002g0066a0004c0007t0002g0056a0004c0007t0002g0178 | 3 | HG02040.hp2 NA19063.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.2096-1036T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 17/17 | chr18 | 6911024 | ||||||
| chr18:6911077
|
G | A | 2 | a0001c0001t0001g0128a0001c0001t0001g0139 | 2 | HG00544.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.2096-983G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 17/17 | chr18 | 6911077 | ||||||
| chr18:6911134
|
A | C | 50 | a0001c0001t0001g0080a0001c0001t0001g0203a0001c0003t0003g0002others(47): Show | 50 | HG00280.hp2 HG00741.hp2 HG01081.hp1 others(47): Show |
intron_variant | MODIFIER | c.2096-926A>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 17/17 | chr18 | 6911134 | ||||||
| chr18:6911170
|
TTTCAAGC others(4): Show |
T | 1 | a0003c0004t0001g0130 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.2096-888_2096-878d others(13): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr18 | 6911170 | |||||
| chr18:6911244
|
G | A | 3 | a0008c0011t0005g0016a0008c0011t0005g0090a0008c0011t0005g0152 | 3 | HG02630.hp2 HG03471.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2096-816G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 17/17 | chr18 | 6911244 | ||||||
| chr18:6911269
|
G | A | 180 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(177): Show | 180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.2096-791G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 17/17 | chr18 | 6911269 | ||||||
| chr18:6911331
|
T | C | 183 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(180): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.2096-729T>C | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 17/17 | chr18 | 6911331 | ||||||
| chr18:6911378
|
A | G | 3 | a0001c0012t0001g0210a0001c0012t0014g0159a0010c0014t0001g0142 | 3 | HG01106.hp1 HG02559.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.2096-682A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 17/17 | chr18 | 6911378 | ||||||
| chr18:6911393
|
TTATATGC others(3): Show |
T | 183 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(180): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.2096-662_2096-653d others(12): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr18 | 6911393 | |||||
| chr18:6911450
|
C | CTTTTT | 182 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(179): Show | 182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.2096-607_2096-606i others(7): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr18 | 6911450 | |||||
| chr18:6911450
|
C | T | 1 | a0001c0001t0001g0037 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2096-610C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 17/17 | chr18 | 6911450 | ||||||
| chr18:6911546
|
C | T | 23 | a0001c0003t0003g0013a0001c0003t0003g0027a0001c0003t0003g0055others(20): Show | 23 | HG00280.hp2 HG00741.hp2 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.2096-514C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 17/17 | chr18 | 6911546 | ||||||
| chr18:6911558
|
C | T | 1 | a0001c0003t0003g0123 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2096-502C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 17/17 | chr18 | 6911558 | ||||||
| chr18:6911594
|
C | G | 62 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0026others(59): Show | 62 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.2096-466C>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 17/17 | chr18 | 6911594 | ||||||
| chr18:6911650
|
G | A | 184 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(181): Show | 184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.2096-410G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 17/17 | chr18 | 6911650 | ||||||
| chr18:6911695
|
C | T | 47 | a0001c0003t0003g0002a0001c0003t0003g0013a0001c0003t0003g0027others(44): Show | 47 | HG00280.hp2 HG00741.hp2 HG01081.hp1 others(44): Show |
intron_variant | MODIFIER | c.2096-365C>T | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 17/17 | chr18 | 6911695 | ||||||
| chr18:6911723
|
A | G | 184 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(181): Show | 184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.2096-337A>G | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 17/17 | chr18 | 6911723 | ||||||
| chr18:6911929
|
G | A | 1 | a0002c0002t0002g0134 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2096-131G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 17/17 | chr18 | 6911929 | ||||||
| chr18:6912005
|
G | A | 184 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(181): Show | 184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.2096-55G>A | ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 17/17 | chr18 | 6912005 |